<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[Job openings at biotechjobs]]></title><description><![CDATA[The latest job openings at biotechjobs]]></description><link>http://biotechroles.com</link><image><url>http://biotechroles.com/images/logo.png</url><title>Job openings at biotechjobs</title><link>http://biotechroles.com</link></image><generator>RSS for Node</generator><lastBuildDate>Sat, 16 May 2026 20:03:27 GMT</lastBuildDate><atom:link href="http://biotechroles.com/rss" rel="self" type="application/rss+xml"/><item><title><![CDATA[Senior Director, Cell Therapy Communications, Corporate Affairs]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b><u>Summary of Team</u></b></p><p>The Cell Therapy Communications team is responsible for developing and executing strategic communications plans that support the Company’s Cell Therapy Organization (CTO). This work spans both the U.S. and global markets, driving a comprehensive, science-forward narrative around approved products and pipeline assets. The team manages communications related to regulatory milestones, educational materials, data and medical meeting announcements, issues management, digital and social content, internal communications, executive leader support, and robust thought-leadership and reputation-building activities.</p><p></p><p><b><u>Position Overview</u></b></p><p>The Senior Director will lead the Cell Therapy Communications team, providing strategic direction and oversight for all cell therapy communications initiatives. This leader will be responsible for aligning communications strategies with organizational priorities, ensuring consistent messaging and effective engagement with key stakeholders. The Senior Director will serve as a trusted advisor to a C-suite executive and other senior leaders across CTO, building strong relationships and influencing decision-making at the highest levels. The Senior Director will enable and oversee seamless cross-functional coordination across Corporate Affairs teams and demonstrate a consistent ability to build and maintain productive relationships with a diverse group of colleagues with varying responsibilities and communications styles.</p><p></p><p>The role requires an experienced and strong communications professional who demonstrates sound business judgment and can work closely with senior leaders in various parts of the Cell Therapy Organization. Must possess the ability to think strategically, work with speed and agility, execute tactically and demonstrate a strong understanding of the science and technical aspects of the business behind the cell therapy organization, pipeline and patient landscape. </p><p>This position can be based in either Giralda, NJ or Princeton, NJ with flexibility to work at other BMS sites based on need and within the company’s Flexible Ways of Working policy of having an onsite presence at BMS sites 50% of the time over a two-week period.</p><p></p><p></p><p><b><u>Key Responsibilities</u></b></p><ul><li>Develop and implement comprehensive communications strategies that advance the CTO’s business objectives and enhance the reputation of BMS’s cell therapy portfolio.</li><li>Lead and mentor a high-performing communications team, fostering a culture of collaboration, innovation, and excellence.</li><li>Serve as a primary communications partner to CTO leadership, including the President of CTO, providing counsel and support on executive communications, media relations, and issues management.</li><li>Oversee the creation and dissemination of science-driven narratives for both internal and external audiences, including product launches, regulatory milestones, and pipeline updates.</li><li>Manage cross-functional coordination with Corporate Affairs, Advocacy, Product Development &amp; Supply, Medical, Regulatory, and Commercial teams to ensure seamless execution of communications plans.</li><li>Direct the development of digital and social media content, educational materials, and thought-leadership initiatives to build stakeholder awareness and engagement.</li><li>Support crisis and issues management, ensuring timely and effective communication in response to emerging challenges.</li><li>Represent the Cell Therapy Communications team in key meetings and forums, advocating for strategic priorities and driving alignment across the organization</li><li>Actively prepare for and mitigate challenges specific to the Cell Therapy business, brands and portfolio, across internal and external audiences</li></ul><p></p><p><b><u>Requirements:</u></b></p><ul><li>10&#43; years of professional experience in the healthcare or related industry with a focus on strategic business communications. </li><li>Self-motivated leader with proven ability to drive strategic communication initiatives aligned with broader company objectives while operating within a complex, fast paced and changing environment.</li><li>Strong commercial and development focus and business acumen, including an understanding of how policy, advocacy, pricing and access work together to implement integrated strategies.</li><li>Strong understanding of medicine and scientific approaches and/or significant in the area of the science behind medicines is critical.</li><li>Solid understanding of the changing global media environment and the role of digital media in reaching key audiences.</li><li>A strong record of success and experience in leading and advising senior and executive level employees and teams.</li><li>A strong understanding of business critical priorities, and ability to apply understanding of market dynamics into strategy.</li><li>Creative and versatile professional with experience in the development and implementation of integrated communications.</li><li>Excellent project management skills and the ability to successfully work in a matrix organization, lead cross-functional teams and manage multiple complex projects.</li><li>Master’s degree preferred.</li><li>Desired candidate will have experience working with autologous cell therapy, allogeneic cell therapy, stem cell therapy and/or CAR-T cell therapy.</li></ul><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $225,170 - $272,847 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1600720 : Senior Director, Cell Therapy Communications, Corporate Affairs]]></description><link>http://biotechroles.com/senior-director-cell-therapy-communications-corporate-affairs-bristol-myers-squibb/6a0899242f1861929d2533ab</link><guid isPermaLink="true">http://biotechroles.com/senior-director-cell-therapy-communications-corporate-affairs-bristol-myers-squibb/6a0899242f1861929d2533ab</guid><pubDate>Sat, 16 May 2026 16:19:48 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$220000-320000</salary><type>Full time</type></item><item><title><![CDATA[Lead Engineer, CSV]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Purpose of the Position:</b></p><p>The Lead CSV Engineer, Equipment Commissioning &amp; Qualification (ECQ) supports the successful configuration, implementation and support of manufacturing and laboratory equipment and computerized systems at multi-use sites through interaction with internal customers and external service providers.  With minimum supervision and given general instructions, this individual carries out routine tasks and functions and uses strong analytical skills to recognize and solve challenging problems of various degrees of complexity and scope. As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships outside the immediate organization.</p><p>The Lead CSV Engineer, through hands-on leadership, will be directly responsible for individual efforts, projects and other tasks.  The incumbent will be responsible for fostering a productive, learning environment for colleagues and reports while ensuring timely completion of assigned work. </p><p><b>Essential Functions:</b></p><p><b><u>Maintains all qualified and validated equipment and systems in compliance with policies, guidelines and procedures:</u></b></p><ul><li><p>Applies strong technical skillset to investigate and resolve complex challenges.</p><ul><li><p>Investigate and resolve Deviations, CAPA investigations and other potential issues.</p></li></ul></li><li><p>Supports equipment qualification and validation activities.</p></li><li><p>Configure and document the configuration of computerized systems to meet the requirements of CFR21 Part 11.</p></li><li><p>Supports the execution of equipment qualifications and validation protocols</p></li><li><p>Supervises vendors for qualification functions.</p></li><li><p>Completes all qualification and validation documentation with accuracy, completeness and compliance to Celgene standards.</p></li><li><p>Responsible for the delivery of all lifecycle deliverables in the Qualification of equipment and full CSV for single and multi-user Computerized Systems.</p></li><li><p>Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Validation Protocols, Traceability Matrices, Summary Reports, Change Controls.</p></li></ul><p><br /> </p><p><b><u>Initiates, manages and leads projects of moderate scope and complexity within their functional area.</u></b></p><ul><li><p>Manages projects of varying scope and complexity.</p></li><li><p>Maintains a positive relationship with all team members and site customers while promoting a positive learning, team environment.</p></li><li><p>Author quality procedures and training documents</p></li><li><p>Deliver training on procedures and best practice to an audience that may include departmental personnel and business partners.</p></li><li><p>Innovate, research and develop tools and solutions to provide more efficient and compliant solutions for department use and deployment.</p></li><li><p>Supports laboratory and manufacturing equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turn over to business area.</p></li><li><p>Support growing standardization efforts in the review and approval of Validation Deliverables</p></li></ul><p><b><u>Promotes and provides excellent customer service and support</u></b></p><ul><li><p>Provides excellent customer service and support.</p></li><li><p>Regularly reviews, prioritizes and promptly responds to customer qualification, validation and support requests.</p></li><li><p>Provides technical support and guidance on Validation, Quality Process and equipment qualification issues. Interfaces with customers to ensure all expectations are being met.</p></li></ul><p><b><u>Regulatory Responsibilities</u></b></p><ul><li><p>Ensure equipment, facilities and programs are maintained in compliance.  </p></li><li><p>Act as departmental delegate and SME in both internal and regulatory audits.</p></li></ul><p>      </p><p><b>Required Competencies-Knowledge, Skills, and Abilities:</b></p><p><b>Knowledge, Skills &amp; Abilities</b>:</p><ul><li><p>Strong working knowledge of MS Windows client and server technologies including user groups, folder permissions and windows policies.</p></li><li><p>Ability to learn new technologies while applying a strong technical skillset to configure computerized systems to meet Business and Regulatory requirements.</p></li><li><p>Excellent understanding of cGXP requirements and good documentation practices relating to systems, equipment and instrumentation within the pharmaceutical industry</p></li><li><p>Strong working knowledge of ISPE guidance and 21 CFR Part 11 compliance</p></li><li><p>Strong working knowledge of SDLC principles and standards</p></li><li><p>Ability to work with the end user to identify and document User and Functional Requirements</p></li><li><p>Knowledge of pharmaceutical laboratory and manufacturing systems.</p></li><li><p>Experience authoring and executing standard CSV deliverables</p></li><li><p>Ability to interact effectively with manufacturing, laboratory, QA, and Facilities groups</p></li><li><p>Strong ability to organize assigned tasks in a high paced environment and concurrently monitor tasks / assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously</p></li><li><p>Strong written and verbal communication skills along solid presentation skills. Proficient at writing well-formulated emails and reports. Ability to follow oral and written instructions, read and interpret engineering manuals/drawings relevant to the assigned task. Ability to effectively communicate with employees, contractors and vendors. Experience with technical writing and document development / generation</p></li><li><p>Strong computer skills in Microsoft Office Suite – Word, Excel, Visio and Outlook, and the ability to learn new software as required for equipment qualification.</p></li></ul><p><b>Competencies:</b></p><ul><li><p>Technical / Professional Knowledge</p></li><li><p>Problem Solving / Troubleshooting</p></li><li><p>Action Oriented</p></li><li><p>Attention to Detail</p></li><li><p>Multi-tasking</p></li><li><p>Building Relationships</p></li></ul><p><b>Education &amp; Experience:</b></p><ul><li><p>BS degree or equivalent experience</p></li><li><p>Minimum 5 years of experience in FDA-regulated industry</p></li></ul><p><b>Working Conditions:</b></p><p><b>Physical / Mental Demands:</b></p><ul><li><p>Occasional stooping, bending, stretching, pushing, pulling, reaching and/or lifting up to 25lbs</p></li><li><p>Ability to sit, stand, walk and move within workspace for extended periods</p></li><li><p>Ability to perform repetitive tasks including hand to finger manipulations, grasping, pushing and pulling.</p></li></ul><p><b>Environmental Conditions:</b></p><ul><li><p>Primarily an office environment.  Will be required to enter laboratory or GMP process areas donning proper gowning / lab coats or PPE such as safety glasses and shoes.</p></li><li><p>Ability to work safely and effectively when working alone or working with others.</p></li></ul><p> </p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Summit West - NJ - US: $86,490 - $104,803&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602403 : Lead Engineer, CSV]]></description><link>http://biotechroles.com/lead-engineer-csv-bristol-myers-squibb/6a0899242f1861929d2533aa</link><guid isPermaLink="true">http://biotechroles.com/lead-engineer-csv-bristol-myers-squibb/6a0899242f1861929d2533aa</guid><pubDate>Sat, 16 May 2026 16:19:48 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Summit West - NJ - US</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Hematology - Ann Arbor, MI, Flint, MI, Bay City, MI, Saginaw, MI,Bowling Green, OH & Toledo, OH]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p><b><span>Position Summary</span></b><span> </span></p></div><div><p><span><span>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for<span> </span></span><span>appropriate patients</span><span>. </span></span><span> </span></p></div><div><p></p><p><span><span>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the<span> </span></span><span>appropriate patients</span><span>. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (</span><span>Cx</span><span>) through deeper scientific dialogue on and consistent with label,<span> </span></span><span>leveraging</span><span><span> </span>new ways of working and CE^3.</span></span><span> </span></p></div><div><p></p><p><span><span>The role builds and<span> </span></span><span>maintains</span><span><span> </span>strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact.</span></span><span> </span></p></div><div><p></p><p><span><span>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (</span><span>Cx</span><span>) – by meeting HCP needs in<span> </span></span><span>a timely</span><span><span> </span>and scientific manner. This role will prioritize the safe and<span> </span></span><span>appropriate use</span><span><span> </span>of BMS products while also focusing on overall business results and performance<span> </span></span><span>objectives</span><span><span> </span>while exemplifying BMS values. </span></span><span> </span></p></div><div><p></p><p><span><span>The TAS role is<span> </span></span><span>field-based</span><span>. A TAS is<span> </span></span><span>anticipated</span><span><span> </span>to spend 100% of their time in the field with external customers.</span></span><span> </span></p></div><div><p><b><span>Key Responsibilities:</span></b><span> </span></p></div><div><ul><li><p><b><span>Portfolio Promotion</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in<span> </span></span><span>appropriate patients</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages with and continuously<span> </span></span><span>maintains</span><span>/grows<span> </span></span><span>a high level</span><span><span> </span>of scientific<span> </span></span><span>expertise</span><span><span> </span>in all assigned products and therapeutic areas.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Prepares and successfully implements comprehensive territory and account plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Fair &amp; Balanced Scientific Dialogue</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrates scientific<span> </span></span><span>expertise</span><span><span> </span>and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with<span> </span></span><span>label</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and<span> </span></span><span>facilitating</span><span><span> </span>scheduling and<span> </span></span><span>logistics</span><span>.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Maintains<span> </span></span><span>a high level</span><span><span> </span>of working<span> </span></span><span>expertise</span><span><span> </span>on emerging data for approved indications.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages real-time medical support through<span> </span></span><span>Medical on</span><span><span> </span>Call to reactively answer unsolicited questions and complex technical inquiries.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Cross-functional collaboration</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proactively collaborates with other field teams to ensure the best Customer Experience (</span><span>Cx</span><span>) for HCPs. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Gathers and shares relevant insights and information internally with the<span> </span></span><span>appropriate stakeholders</span><span><span> </span>to enable BMS to better serve its customers.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Complies with</span><span><span> </span>all laws, regulations, and policies that govern the conduct of BMS.</span></b><span> </span></p></li></ul></div><div><p><b><span>Required Qualifications &amp; Experience</span></b><span> </span></p></div><div><ul><li><p><span><span>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated experience building and<span> </span></span><span>maintaining</span><span><span> </span>strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (</span><span>Cx</span><span>).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in Hematology/Oncology<span> </span></span><span>required</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance<span> </span></span><span>track record</span><span><span> </span>of meeting or exceeding goals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong selling and promotional skills proven through<span> </span></span><span>a track record</span><span><span> </span>of performance.</span></span><span> </span></p></li></ul></div><div><p><b><span>Key Competencies Desired</span></b><span> </span></p></div><div><ul><li><p><b><span>Customer/commercial mindset</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to drive business results.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience<span> </span></span><span>identifying</span><span>, engaging, and cultivating credibility with customers across the patient care journey.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated resourcefulness and ability to connect with customers.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><b><span>Patient centricity </span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understands the<span> </span></span><span>patient</span><span><span> </span>journey and experience.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a patient-focused mindset.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Scientific Agility </span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Analytical Capability:</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understanding how to interpret and analyze data related to BMS products, customer preferences</span><span>, clinical</span><span><span> </span>data.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use CE^3 to generate insights<span> </span></span><span>and do</span><span><span> </span>dynamic call planning.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Technological Agility:</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and<span> </span></span><span>maintain</span><span><span> </span>effective communication.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in<span> </span></span><span>a timely</span><span><span> </span>and compliant manner, track interactions, and plan future engagements with healthcare professionals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use the Medical on Call technology effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Keeping up to date with technological advancements and changes.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Teamwork/Enterprise mindset</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong business acumen to understand and<span> </span></span><span>analyze business and market drivers</span><span><span> </span>and develop, execute, and adjust business plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrates<span> </span></span><span>a strong sense</span><span><span> </span>of learning agility. Seeks out and learns from unfamiliar<span> </span></span><span>experiences, and</span><span><span> </span>then applies those lessons to achieve better results in<span> </span></span><span>subsequent</span><span><span> </span>situations.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Track record</span><span><span> </span>of balancing individual drive and collaborative attitude.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Holds<span> </span></span><span>a high level</span><span><span> </span>of integrity and good judgment,<span> </span></span><span>in order to</span><span><span> </span>navigate the requirements of the role effectively and compliantly<span> </span></span><span>in accordance with</span><span><span> </span>BMS policies and procedures.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company.</span></span><span> </span></p></li></ul></div><div><p><span><span>#LI-Remote</span></span><span> </span></p></div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602434 : Senior Therapeutic Area Specialist, Hematology - Ann Arbor, MI, Flint, MI, Bay City, MI, Saginaw, MI,Bowling Green, OH &amp; Toledo, OH]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-hematology-ann-arbor-mi-flint-mi-bay-city-mi-saginaw-mibowling-green-oh-and-toledo-oh-bristol-myers-squibb/6a0899232f1861929d2533a9</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-hematology-ann-arbor-mi-flint-mi-bay-city-mi-saginaw-mibowling-green-oh-and-toledo-oh-bristol-myers-squibb/6a0899232f1861929d2533a9</guid><pubDate>Sat, 16 May 2026 16:19:47 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Ann Arbor - MI - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Radiopharmaceuticals Applications Liaison]]></title><description><![CDATA[<p><span>At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: </span><a href="https://careers.bms.com/rayzebio/" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>https://careers.bms.com/rayzebio/</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a></p><p></p><p><b>Radiopharmaceutical Applications Liaison</b></p><p></p><p>At RayzeBio, every day is a chance to make a meaningful difference. As a wholly owned subsidiary of Bristol Myers Squibb, RayzeBio combines the agility and entrepreneurial mindset of an emerging biotech with the expertise and resources of a global oncology leader. Our mission is to develop transformative radiopharmaceutical therapies that bring new hope to people living with cancer. You will join a multidisciplinary team that values your ideas, strengthens your expertise, and puts collaboration at the center of our work. From day one, you can make an immediate impact on our science, our teams, and, most importantly, patients. Learn more about RayzeBio: <a href="https://careers.bms.com/rayzebio/" target="_blank">https://careers.bms.com/rayzebio/</a></p><p>RayzeBio, a Bristol Myers Squibb company headquartered in San Diego, California, is a biotechnology company focused on improving cancer survival through targeted radioisotopes. The company is developing innovative therapies for solid tumor targets and aims to become a global leader in radiopharmaceuticals.</p><p>We are seeking a Radiopharmaceutical Applications Liaison to serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products. In this role, you will advance clinical adoption, institutional readiness, and workflow optimization across imaging and treatment centers. You will also partner cross-functionally with Medical Affairs, Clinical Development, Clinical Operations, and Commercial teams to translate scientific innovation into safe, compliant, and scalable real-world practice.</p><div></div><p><b>Key Responsibilities</b></p><ul><li>Build and sustain strategic relationships with KOLs and institutional stakeholders, including Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Radiation Safety Officers, Health Physicists, Nursing Staff, and Advanced Practice Providers.</li></ul><ul><li>Lead site readiness and workflow integration efforts for approved agents and clinical trials, including product handling, administration, radiation safety, and radiopharmaceutical licensing considerations.</li><li>Deliver high-impact clinical and technical education to ensure safe, effective, and guideline-aligned product utilization.</li><li>Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications, maintaining deep expertise in imaging techniques, oncology practice patterns, and emerging therapeutic advances.</li><li>Support clinical trial execution through site training, protocol education, and alignment with Clinical Development and Operations.</li><li>Respond to unsolicited scientific inquiries regarding approved and investigational products, ensuring accurate documentation and full regulatory compliance.</li><li>Generate actionable field insights on diagnostic imaging and radiopharmaceutical trends, institutional barriers, and adoption dynamics, informing launch strategy.</li><li>Provide medical and scientific congress support as requested, in compliance with company policies and industry regulations.</li><li>Ensure adherence to all SOPs and regulatory frameworks, including U.S. Compliance Code of Conduct, OIG Guidance, PhRMA Code, GCP, HIPAA, and applicable FDA regulations.</li><li>Applies AI to improve team execution and decision‑making</li></ul><div></div><p><b>Qualifications &amp; Experience</b></p><ul><li>Bachelor’s degree required. (CNMT preferred)</li><li>7&#43; years of experience in nuclear medicine, radiopharmaceutical clinical applications, oncology imaging, or related field.</li><li>Demonstrated experience leading complex site education and workflow implementation initiatives.</li><li>Advanced understanding of radiopharmaceutical science, nuclear medicine operations, and diagnostic imaging trends.</li><li>Ability to translate complex data into practical, site-level execution strategies.</li><li>Strong executive presence and ability to build institutional relationships.</li><li>Experience working cross-functionally within a matrixed biotech or pharmaceutical environment.</li><li>Excellent communication, presentation, and organizational skills.</li><li>Experience in oncology and radiopharmaceuticals is strongly preferred.</li></ul><p></p><p></p><p><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Remote - United States - US: $173,217 - $209,899&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p></p><p><b>RayzeBio and Bristol Myers Squibb</b></p><p>RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization.</p><p></p><p><b>Supporting People with Disabilities</b></p><p>BMS and RayzeBio are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable <span><span><span><span><span><span><span><span>workplace accommodations/adjustments and</span></span></span></span></span></span></span></span> ongoing support in their roles. Applicants can request a reasonable <span><span><span><span><span><span><span><span>workplace accommodation/adjustment prior</span></span></span></span></span></span></span></span> to accepting a job offer. If you require <span><span><span><span><span><span><span><span>reasonable accommodations/adjustments in</span></span></span></span></span></span></span></span> completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span><span><span>adastaffingsupport&#64;bms.com</span></span></span></span></span></span></span></span></a>. Visit <a href="https://careers.bms.com/eeo-accessibility" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.</p><p></p><p><b>Candidate Rights</b></p><p>BMS and RayzeBio will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</p><p></p><p>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span><span><span>https://careers.bms.com/california-residents/</span></span></span></span></span></span></span></span></a></p><p></p><p><b>Data Protection</b></p><p>We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="https://careers.bms.com/fraud-protection/" target="_blank"><span><span><span><span><span><span><span><span>https://careers.bms.com/fraud-protection/</span></span></span></span></span></span></span></span></a></p><p></p><p>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response.</span></p><p></p>R1602432 : Radiopharmaceuticals Applications Liaison]]></description><link>http://biotechroles.com/radiopharmaceuticals-applications-liaison-bristol-myers-squibb/6a0899232f1861929d2533a8</link><guid isPermaLink="true">http://biotechroles.com/radiopharmaceuticals-applications-liaison-bristol-myers-squibb/6a0899232f1861929d2533a8</guid><pubDate>Sat, 16 May 2026 16:19:47 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Remote - United States - US</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[Regulatory Operation Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Key Responsibilities</b></p><ul><li><p><b>Regulatory Submission Support</b></p></li><li><p><b>GRS label and artwork coordination and facilitation</b></p></li><li><p><b>Internal and external system maintenance and Information management</b></p></li><li><p><b>Provide operational support for other assigned projects as needed.</b></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1600083 : Regulatory Operation Manager]]></description><link>http://biotechroles.com/regulatory-operation-manager-bristol-myers-squibb/6a0899222f1861929d2533a7</link><guid isPermaLink="true">http://biotechroles.com/regulatory-operation-manager-bristol-myers-squibb/6a0899222f1861929d2533a7</guid><pubDate>Sat, 16 May 2026 16:19:46 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Beijing - CN</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Executive Director, Data Sciences & Advanced Analytics]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b><i>Executive Director </i></b></p><p>As a senior strategic leader of the Data Science and Advance Analytics (DSAA) organization in drug development, this role provides enterprise-wide vision and direction as part of a cross-functional team of drug development scientists and data scientists. The Executive Director will set and drive the strategic vision of exploratory analysis for scientific considerations related to drug development and clinical study design, with primary focus in early to late-phase clinical programs in Neuroscience and digital health technologies across all disease areas.</p><p></p><p>Through strategic oversight and hands-on leadership, the Executive Director will define approaches, processes, algorithms, and tools that support the analytics, visualizations, and decision support needs of drug development scientists and projects. The Executive Director will play a pivotal role in building and scaling the organization, cultivating relationships with senior stakeholders, and championing the adoption of relevant tools and approaches. The Executive Director will collaborate with Biostatistics leadership and cross-functional leaders to ensure connectivity of exploratory analysis work in support of development, regulatory approval, and market acceptance of Bristol-Myers Squibb (BMS) products. This position includes functional management responsibilities.</p><p>  </p><p><b>What you’ll do:</b></p><ul><li>Lead a team of approximately 10 or more individuals with direct and indirect reports across diverse expertise.</li><li>Utilize clinical/medical and disease area expertise to generate novel insights from data and present them via rich and intuitive visualizations, including senior leadership and executive committees.</li><li>Define and drive the strategic vision for data science across early to late-phase drug development across multiple disease indications, with primary focus in <i>Neurology</i> portfolio.</li><li>Develop novel ways of integrating, mining, and visualizing diverse, clinical and high-dimensional data sets such as genomics, imaging, fluid biomarkers and digital measurements.</li><li>Oversee the development, validation, and implementation of predictive models for clinical trial use, and deploy automated processes for producing modeling results at scale.</li><li>Lead end-to-end digital health data science strategy and execution in Neurology and other disease areas, encompassing wearable/sensor signal processing pipelines through to advanced predictive modeling (including deep learning), with rigorous validation and clinical interpretability.</li><li>Builds and sustains high-impact, enterprise-level partnerships and seamless interfaces within the department and the broader research and development organization. Influences and aligns stakeholders at the VP/SVP level.</li><li>Ensures quality of deliverables by consistently applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs, and work practices.</li><li>Leads the vision and execution of innovative strategies and technologies across the DSAA enterprise.</li><li>Provides executive-level clinical and technical guidance and sets direction for complex clinical programs and utilities.</li><li>Provides clinical and technical guidance to external partners concerning clinical trial and data standards, and analysis practices to ensure efficient and integrated clinical project strategies.</li><li>Champions and governs software development methodologies across the organization.</li><li>Leads and sponsors increased efficiency and continuous improvement initiatives within and beyond DSAA.</li><li>Represents DSAA at the enterprise level, contributing to BMS R&amp;D strategy discussions with senior leadership, external regulatory bodies, and scientific conferences.</li><li>Responsible for workforce planning, talent strategy, and building a culture of innovation within the DSAA organization.</li></ul><p></p><p><b>Key Requirements:</b></p><p>Degree Requirements:</p><p>M.D. and/or PhD in a relevant clinical and quantitative field (i.e. Biostatistics, Neuroscience, Bioinformatics, etc.).</p><p>Experience Requirement:</p><ul><li>15&#43; years of relevant experience after receiving a graduate degree</li><li>5&#43; years of senior leadership experience managing large, cross-functional teams, with a preference for those with a background leading clinical programs in Neuroscience</li></ul><p></p><p>Key Competency Requirements:</p><ul><li>Strong expertise and experience in the medical field and disease areas, especially in Neurology, along with experience in quantitative modeling and applications clinical trials.</li><li>Mastery in data analysis with data generated from clinical trials, observational research or real-world cohorts, and modeling methods particularly in their application to clinical trials.</li><li>Expertise in quantitative modeling and AI/ML applied to clinical trials, underpinned by strong command of core statistical methods (e.g., mixed effects models, nonlinear models, survival analysis).</li><li>Broad clinical trial and medical experience across multiple disease areas, with particular depth in Neurology. Expertise with various types of multi-modal data and modeling in clinical trials.</li><li>Outstanding clinical, technical and analytic skills, proficient at understanding and conceptualizing business problems and implementing analytic or decision support solutions.</li><li>Exceptional communication, organizational, motivational, and executive leadership skills capable of influencing and aligning at the most senior levels within and across R&amp;D.</li><li>Demonstrated ability to build, scale, and lead large organizations with diverse experience and expertise.</li><li>Ability to explain technically complex information for a non-technical audience.</li><li>Proven ability to define and execute enterprise-wide strategic and long-range plans.</li><li>Strong positive attitude, thrives in a dynamic, fast paced environment with many simultaneous projects.</li><li>Expert knowledge of programming languages (R, Python) in high-performance computing environments.</li><li>Knowledge of industry practices and regulatory requirements.</li><li>Track record of driving organizational transformation and scaling data science functions</li></ul><p></p><p>Travel Requirements</p><ul><li>This position may require up to 20% travel for meetings and/or professional conferences/congresses </li></ul><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>$340,870 - $413,051<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. </p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602409 : Executive Director, Data Sciences &amp; Advanced Analytics]]></description><link>http://biotechroles.com/executive-director-data-sciences-and-advanced-analytics-bristol-myers-squibb/6a0899212f1861929d2533a6</link><guid isPermaLink="true">http://biotechroles.com/executive-director-data-sciences-and-advanced-analytics-bristol-myers-squibb/6a0899212f1861929d2533a6</guid><pubDate>Sat, 16 May 2026 16:19:45 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Cambridge Crossing - MA - US</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Medical Advisor]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p><b><span>Key Responsibilities:</span></b></p></div><ul><li><span>Develops medical science liaison focused slide decks and training modules with assessments on the disease state, therapeutic landscape and competitive intelligence.</span></li><li><span>Develops and maintains collaborations and relationships with relevant professional societies and patient organizations.</span></li><li><span>Delivers relevant scientific data tailored to healthcare professional needs.</span></li><li><span>Implements and evaluates a strategic territory plan prioritizing core medical science liaison activities.</span></li><li><span>Tracks insights and best practices to identify unmet needs and inform clinical development.</span></li><li><span>Ensures adherence to corporate and healthcare compliance guidance, including during clinical trials and scientific interactions with internal and external groups.</span></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602455 : Medical Advisor]]></description><link>http://biotechroles.com/medical-advisor-bristol-myers-squibb/6a08991f2f1861929d2533a5</link><guid isPermaLink="true">http://biotechroles.com/medical-advisor-bristol-myers-squibb/6a08991f2f1861929d2533a5</guid><pubDate>Sat, 16 May 2026 16:19:43 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Taipei - TW</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Director, Global Clinical Physician, Oncology]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a target="_blank" href="https://careers.bms.com/working-with-us"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><span>The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, and manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities. It has matrix management responsibilities across the internal and external network and the role provides medical and scientific expertise to cross-functional BMS colleagues.</span></p><p></p><p><b><u><span>Position responsibilities</span></u></b></p><p><span>Medical Monitoring:</span></p><ul><li><b><span>Team Leadership &amp; Collaboration</span></b><span> — Serve as a key contributor to the Study Delivery Team (SDT) and Clinical Development Team (CDT), partnering with Clinical Scientists to provide medical oversight on protocol development, including inclusion/exclusion criteria and safety considerations</span></li><li><b><span>Medical Monitoring &amp; Safety</span></b><span> — Lead medical and eligibility data reviews, assess safety-related serious adverse events in partnership with Worldwide Patient Safety, and oversee site interactions and safety narratives</span></li><li><b><span>GCP &amp; Compliance</span></b><span> — Uphold all GCP obligations for clinical conduct, safety management guidelines, and maintain up-to-date required training</span></li></ul><p><span> </span></p><p><span>Clinical Development Expertise &amp; Strategy:</span></p><ul><li><b><span>Clinical Strategy &amp; Protocol Design</span></b><span> — Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols, with a strategic focus on drug/asset knowledge, disease area science, and regulatory targets</span></li><li><b><span>Medical Oversight &amp; Accountability</span></b><span> — Provide medical accountability across a group of studies, leading benefit/risk analyses within a matrix team environment alongside Clinical Scientists</span></li><li><b><span>Study Execution &amp; Delivery</span></b><span> — Partner with Clinical Scientists to support all aspects of study delivery, including site activation, enrollment, and adjudication of protocol violations and deviations</span></li><li><b><span>Stakeholder Engagement &amp; Thought Leadership</span></b><span> — Build and maintain relationships with principal investigators and key opinion leaders to inform emerging science, biomarker research, and clinical program design</span></li><li><b><span>Scientific Expertise &amp; Education</span></b><span> — Maintain deep, up-to-date knowledge of the disease area through conference attendance and literature review, while staying informed on the competitive landscape and providing ongoing protocol-specific medical education to study teams and investigators</span></li></ul><p><span> </span></p><p><span>Health Authority Interactions &amp; Publications:</span></p><ul><li><b><span>Health Authority &amp; Advisory Engagement</span></b><span> — Serve as the medical point of expertise in key Health Authority interactions and advisory board meetings</span></li><li><b><span>Regulatory Writing &amp; Submissions</span></b><span> — Author and draft clinical content for CSRs, regulatory reports, briefing books, and submission documents, including clinical narratives, in partnership with Clinical Scientists</span></li></ul><p></p><p><b><u><span>Qualifications and experience</span></u></b></p><ul><li><span>MD required (or equivalent)</span></li><li><span>5 or more years of Industry experience and/or clinical trials experience is required</span></li><li><span>Ability to communicate information clearly and lead presentations in scientific and clinical settings</span></li><li><span>Subspecialty training in applicable therapeutic area desired</span></li><li><span>Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation</span></li><li><span>Expertise in drug development process</span></li><li><span>Expertise in the components needed to execute an effective clinical plan and protocols</span></li><li><span>Strong leadership skills with proven ability to lead and work effectively in a team environment</span></li><li><span>Domestic and International travel may be required.</span></li></ul><p></p><p></p><p><b>#LI-Hybrid</b></p><p></p><p></p><p></p><p><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p></p><p><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation</span> in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p></p><p><b>On-site Protocol</b><br /><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p></p><p><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p></p><p><b>Supporting People with Disabilities</b></p><p><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span>accommodations/adjustments</span> and ongoing support in their roles. Applicants can request a reasonable workplace <span>accommodation/adjustment</span> prior to accepting a job offer. If you require reasonable <span>accommodations/adjustments</span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span>adastaffingsupport&#64;bms.com</span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p></p><p>Bristol Myers Squibb is Disability Confident – Employer</p><p></p><p>A UK Government scheme</p><p></p><p><b>Candidate Rights</b></p><p>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</p><p></p><p><b>Data Protection</b></p><p>We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank">https://careers.bms.com/fraud-protection</a>.</p><p></p><p>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602278 : Director, Global Clinical Physician, Oncology]]></description><link>http://biotechroles.com/director-global-clinical-physician-oncology-bristol-myers-squibb/6a08991e2f1861929d2533a4</link><guid isPermaLink="true">http://biotechroles.com/director-global-clinical-physician-oncology-bristol-myers-squibb/6a08991e2f1861929d2533a4</guid><pubDate>Sat, 16 May 2026 16:19:42 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Uxbridge - GB</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Senior Specialist, QC Systems and Support]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p></p><p>The Senior Specialist QC Systems and Support is responsible for maintaining QC laboratory equipment in a cGMP-compliant state and ensuring the integrity of equipment-related data, systems, and processes throughout the equipment lifecycle. This function is the Subject matter expert (SME) for QC equipment qualification, computerized systems, and data integrity, supporting first-line troubleshooting and regulatory inspections. Responsibilities include tracking, trending, and reporting QC equipment key performance metrics and leading continuous improvement initiatives. This role interfaces cross-functionally with QC laboratories, Facilities &amp; Engineering and Quality Assurance to drive operational excellence in a fast-paced, highly regulated cell therapy manufacturing environment.</p><p></p><p><b>Duties/Responsibilities</b></p><ul><li><p>As system owner, accountable for the full QC equipment lifecycle (including validation, qualification, calibration, preventive maintenance, and repairs) ensuring equipment remains in a cGMP-compliant state in accordance with GMP requirements and written procedures, in collaboration with Facilities &amp; Engineering</p></li><li><p>Own and oversee processes associated with QC equipment in computerized systems (e.g. VLMS, EAM), ensuring alignment with GMP and data integrity requirements in partnership with relevant system stakeholders</p></li><li><p>Manage QC Alarm processes, ensuring timely review, escalation, and resolution of equipment and system alarms in accordance with GMP requirements</p></li><li><p>Track, trend, and report KPIs related to QC equipment reliability, availability, and compliance, driving accountability and performance visibility across stakeholders</p></li><li><p>Accountable for data integrity (DI) compliance for QC laboratory equipment and processes, ensuring adherence to ALCOA&#43; principles across all equipment-generated data</p></li><li><p>Lead continuous improvement initiatives associated with QC equipment</p></li><li><p>Author, review, and approve technical documents, SOPs, qualification protocols/reports, and GMP records</p></li><li><p>Own, lead, and manage Change Controls, Deviations, Investigations, and CAPAs related to QC equipment and systems</p></li><li><p>Support first-line troubleshooting for equipment issues</p></li><li><p>Support internal and external GMP inspections as SME for QC systems, equipment, and data integrity</p></li><li><p>Train and mentor peers on equipment processes, data integrity principles, and QC systems operations</p></li><li><p>Perform additional tasks as required to support QC laboratory operations</p></li></ul><p></p><p><span><b>Qualifications</b></span></p><p></p><p><b><u>Specific Knowledge, Skills, Abilities</u></b><u>:</u></p><ul><li><p>Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.</p></li><li><p>Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.</p></li><li><p>Attention to detail and demonstrated organizational skills.</p></li><li><p>Ability to work in a fast-paced team environment, meet deadlines and changing priorities.</p></li><li><p>Problem-solving ability/mentality, technically adept and logical</p></li><li><p>Ability to apply Lean, Six Sigma and Risk Management concepts and tools preferred.</p></li></ul><p></p><p></p><p><b><u>Education/Experience/ Licenses/Certifications</u></b><u>:</u></p><ul><li><p>Bachelor&#39;s degree (BSc) in a life science, chemistry, or related scientific discipline preferred, MLO Level 4 or equivalent combination of relevant education and professional experience will be considered</p></li><li><p>4&#43; years of relevant laboratory experience in a GMP-regulated environment, preferably within pharmaceutical, biotech, or cell/gene therapy manufacturing</p></li><li><p>Demonstrated hands-on experience with:</p></li><li><p>Equipment qualification and validation (IQ/OQ/PQ)</p></li><li><p>Data integrity principles and implementation (ALCOA&#43;, 21 CFR Part 11, EU Annex 11)</p></li><li><p>Quality Management Systems (QMS), including CAPA, deviation, and change control management</p></li><li><p>Working knowledge and practical application of data integrity regulations and guidelines</p></li><li><p>Advanced proficiency with computerized systems and enterprise applications (VLMS, LIMS, EAM or equivalent)</p></li></ul><p></p><p>#LI-Onsite</p><p></p><p></p><p></p><p>Disclaimer: For any third parties or external agencies, please, be informed we do not accept unsolicited requests, proposals, applications or profiles for any of our roles at BMS.</p><p></p><p></p><p></p><p>Why You Should Apply</p><p></p><p>Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p></p><p>Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.</p><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602402 : Senior Specialist, QC Systems and Support]]></description><link>http://biotechroles.com/senior-specialist-qc-systems-and-support-bristol-myers-squibb/6a08991e2f1861929d2533a3</link><guid isPermaLink="true">http://biotechroles.com/senior-specialist-qc-systems-and-support-bristol-myers-squibb/6a08991e2f1861929d2533a3</guid><pubDate>Sat, 16 May 2026 16:19:42 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Leiden – NL</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[HR Advisor - AI enabled]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary: </b></p><p></p><p>The HR Advisor provides timely, accurate and pragmatic advice to employees and leaders across the employee lifecycle, ensuring a positive and employee-centric experience.HR Advisors use AI-enabled tools to triage and resolve enquiries, draft and quality-check responses, and surface insights that improve service delivery. They also play an active role in knowledge management by creating, maintaining and continuously improving HR knowledge content, ensuring information is easy to find, accurate, and optimised for use in AI-driven and self-service channels.</p><p></p><p><b>Key Accountabilities:</b></p><p><b>HR Advisory &amp; Case Management:</b></p><ul><li>Provide expert guidance to employees and leaders on HR policies, processes and employee matters, applying sound judgement and a customer-first approach.</li></ul><ul><li>Manage HR enquiries and cases end-to-end, coordinating and aligning actions across cross-functional teams ensuring quality documentation, appropriate escalation and timely resolution in line with service standards, and delivering a seamless, consistent employee experience.</li><li>Maintain strong understanding of market-specific employment legislation and partner with specialist teams (e.g., ER/Legal, Talent, Reward, Payroll) to deliver compliant and practical outcomes.</li><li>Provide proactive advice and support to customers for “Moments That Matter”.</li></ul><p><b>AI-enabled Service Delivery:</b></p><ul><li>Use BMS approved AI tools to triage enquiries, retrieve knowledge, draft responses and summarise case notes, while applying critical thinking and verifying accuracy before sharing or acting on the output.</li></ul><ul><li>Apply safe and responsible AI practices, including appropriate handling of confidential information, privacy requirements and data minimisation.</li></ul><ul><li>Identify and reduce avoidable contacts by improving knowledge content, self-service pathways and first-contact resolution. Analyse enquiry drivers and service data to address root causes and streamline the employee experience.</li></ul><ul><li>Analyse approved AI tools from a frontline user perspective, identifying usability gaps and providing structured feedback and recommendations to product owners to drive continuous enhancement.Coach peers on effective use of AI tools (e.g., prompting, validation and tone), contributing to capability uplift across HR Services.</li></ul><p><b>Process &amp; Knowledge Optimisation:</b></p><ul><li>Take a proactive approach to improving end-user guidance (knowledge articles, templates, FAQs and process documentation) based on enquiry trends and data-driven analysis.</li></ul><ul><li>Conduct root-cause analysis on recurring enquiries and service failures; recommend and implement sustainable improvements across policy, process, knowledge and tooling.</li><li>Partner with People Services leaders to address service issues, proposing and implementing improvements that enhance employee experience and compliance.</li></ul><p><b>Stakeholder Engagement:</b></p><ul><li>Communicate complex information clearly and professionally, tailoring detail and tone to the audience across verbal and written channels.</li><li>Influence subject matter experts to validate and maintain knowledge content, and ensure updates are reflected across interconnected systems and processes.</li><li>Engage with external vendors and third-party service providers as required, raising issues, sharing frontline user insights, and collaborating to ensure tools and services continue to meet operational and employee experience standards.</li></ul><p><b>Desired Experience &amp; Skills:</b></p><p><b>Digital, AI &amp; Knowledge Management Capability:</b></p><ul><li>Highly computer literate with knowledge of HR systems (e.g., HCM/Workday), case management tools and knowledge bases, and confident using approved genAI-enabled tools (e.g., copilots/assistants) to support day-to-day service delivery.</li></ul><ul><li>Demonstrated ability to use genAI effectively (e.g., prompting, summarisation and drafting) and to apply human review to validate outputs for accuracy, completeness, tone, bias and policy/legislative alignment before use.</li><li>Understanding of digital knowledge management practices, including content lifecycle management (create, review, publish, retire and version), content governance and quality standards, and findability (plain-language writing, taxonomy/metadata and search optimisation). Able to maintain an authoritative “single source of truth” so knowledge supports self-service and improves AI-assisted retrieval.</li><li>Awareness of privacy, confidentiality and information security obligations when using HR systems, knowledge platforms and AI tools, including appropriate handling of sensitive data and data minimisation.</li><li><b>Experience using GenAI (human-in-the-loop):</b> prompting, summarisation, drafting, and <b>validation</b> of AI outputs for accuracy, tone, bias, and policy/legislative alignment.</li></ul><p></p><p><b>HR Expertise:</b></p><ul><li>Bachelor&#39;s degree in HR or a recognised HR certification (or equivalent experience).</li></ul><ul><li>Minimum of 4 years’ HR advisory/HR Services experience, with strong understanding of HR policies, processes and relevant employment legislation.</li><li>Demonstrated experience handling complex cases and providing practical, risk-aware advice in a fast-paced environment.</li><li>Thinks globally while operating locally, applying enterprise-wide HR frameworks with the cultural and legislative nuance needed to deliver consistent, market-relevant outcomes.</li></ul><p></p><p><b>Analytical and Problem-Solving Skills:</b></p><ul><li>Demonstrated analytical abilities and a continuous improvement mindset.</li><li>Proven track record of using sound judgment to identify solutions that meet business needs.</li><li>Experience analysing service and customer data and feedback and translating analysis into actions or improvements, working with partners to redesign the employee experience</li><li>Strong ability to independently research, evaluate and synthesise information from multiple sources, building end-to-end understanding of complex situations to deliver accurate, well-informed outcomes</li></ul><p><b>Communication and Leadership:</b></p><ul><li>Excellent presentation skills for conveying complex information in a structured manner.</li><li>Ability to coach others to build capabilities and enhance professional depth.</li></ul><p><b>Cultural Competence:</b></p><ul><li>Experience working in a multicultural/multi-country environment.</li><li>Language proficiency beyond English is desirable.</li></ul><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Warsaw - PL: zł112,350 - zł136,145&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602487 : HR Advisor - AI enabled]]></description><link>http://biotechroles.com/hr-advisor-ai-enabled-bristol-myers-squibb/6a08991d2f1861929d2533a2</link><guid isPermaLink="true">http://biotechroles.com/hr-advisor-ai-enabled-bristol-myers-squibb/6a08991d2f1861929d2533a2</guid><pubDate>Sat, 16 May 2026 16:19:41 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Warsaw - PL</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Cell Therapy Manufacturing in Devens, MA]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>At <b>Bristol Myers Squibb</b> we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.</p><p></p><p>The <b>Senior Manager, Cell Therapy Manufacturing</b> supports the clinical and commercial operations of the facility. The Senior Manager will be responsible for the people manufacturing both clinical and commercial product with oversight of shifts that cover 24/7 cell therapy manufacturing unit operations such as media preparation, cell selection, cell processing, or product fill, all of which are executed in accordance with Current Good Manufacturing Practices (cGMP’s).</p><p></p><p><b>Shifts Available:</b></p><p>Monday – Friday, 2pm – 11pm</p><p></p><p><b>Responsibilities will include, but are not limited to the following:</b></p><p><span>Serves as manufacturing functional area owner and manages commercial and clinical manufacturing teams and areas. This includes:</span></p><ul><li><span>Hiring, mentoring and developing exceptional people</span></li><li><span>Conducting performance reviews and identifying opportunities for career growth for supervisors and associates.</span></li><li><span>Championing a culture of exceptional teamwork and communication across the organization.</span></li><li><span>Ensuring people have and maintain the appropriate level of training necessary for CAR-T GMP manufacturing in a multi-product commercial facility.</span></li><li><span>Building effective cross-functional relationships with Quality, Supply Chain, MS&amp;T, EHS and F&amp;E.</span></li><li><span>Ensuring a culture that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements. Models these behaviors every day. </span></li></ul><p></p><p><span>Plans for and executes commercial and clinical operations for a licensed CAR-T</span></p><p><span>product in the Devens CTF Manufacturing Plant. This includes:</span></p><ul><li><span>Establishing department goals, tracking and reporting KPIs, and driving a culture continuous improvement through innovation and implementing lean manufacturing initiatives.</span></li><li><span>Authoring, reviewing and approving documents, including standard operating procedures, batch records, material specifications, training materials and validation protocols / reports.</span></li><li><span>Developing and communicating project goals, strategy and timeline with manufacturing management</span></li><li><span>Implementing and operating manufacturing systems that are technically sound, promote effective and efficient operations, and comply with cGMP requirements.</span></li><li><span>Ensuring schedules of the people, facility, equipment, materials, and documents are established and maintained to support the expected capacity of the facility for multiple CAR-T products.</span></li><li><span>Identifying and mitigating risks in manufacturing operations that could negatively impact delivery of safe and effective therapies to patients.</span></li><li><span>Championing inspection readiness efforts and initiatives for Right First- Time manufacturing.</span></li><li><span>Establishing team policies, organizational structure, shift structure, and career ladders for Associates, Team Leaders, Supervisors and Managers.</span></li></ul><p></p><p><b><span>Minimum Requirements:</span></b></p><ul><li>Bachelor’s degree in relevant science or engineering discipline, or equivalent in work experience.</li><li>Knowledge of Lean Manufacturing principles required.</li><li>Cleanroom garments and personal protective equipment will be required in designated areas which cover head, parts of the face, core body, and legs/feet.</li><li>Ability to work in the vicinity of strong magnets.</li><li>8&#43; years of relevant work experience within pharmaceutical or a similarly regulated industry</li><li>6&#43; years supervising staff in a management role</li></ul><p></p><p><b>BMSCART</b></p><p><b>#LI-ONSITE</b></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Devens - MA - US: $131,750 - $159,650&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602447 : Senior Manager, Cell Therapy Manufacturing in Devens, MA]]></description><link>http://biotechroles.com/senior-manager-cell-therapy-manufacturing-in-devens-ma-bristol-myers-squibb/6a08991d2f1861929d2533a1</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-cell-therapy-manufacturing-in-devens-ma-bristol-myers-squibb/6a08991d2f1861929d2533a1</guid><pubDate>Sat, 16 May 2026 16:19:41 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Devens - MA - US</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Full Stack Software Engineering & Operations Regulatory BI&T]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary:</b></p><p>We are seeking a Senior Manager, Full Stack Software Engineer, to serve as a technical leader in an AI first, agile product environment supporting Global Regulatory Sciences (GRS) technologies. This role is accountable for the end-to-end build and run of AI-native technology assets supporting Global Regulatory Sciences, ensuring solutions are reliable, accessible, secure, compliant, and cost-effective.</p><p>The Senior Manager designs, builds, and operates AI native products where large language models, agentic workflows, and data-driven intelligence are the default paradigm—not an addon. The role blends hands-on full-stack engineering, AI product thinking, and operational ownership, with responsibility for both delivery and long-term‑ sustainability of platforms in a regulated BioPharma environment.</p><p></p><p>This position provides cross-product technical leadership without direct line management, influencing architecture, shared capabilities, vendor direction, and long-term technical strategy through expertise, collaboration, and hands-on contribution.</p><p></p><p><u><b>Key Responsibilities:</b></u></p><p><b>AI Native‑ Product &amp; Platform Ownership:</b></p><ul><li><p>Own the build, operation, and continuous improvement of AI native Regulatory applications and platforms, including bespoke solutions and AI-enabled SaaS.</p></li><li><p>Ensure Regulatory technology assets are stable, secure, compliant, and operationally sound across their lifecycle.</p></li><li><p>Remain sufficiently hands-on‑ to design, build, review, and troubleshoot critical components.</p></li></ul><p></p><p><b>Technical Strategy, Architecture &amp; Roadmap:</b></p><ul><li><p>Develop and maintain an AI-first‑ Regulatory technology roadmap, guiding build vs. buy decisions, model selection, and platform capabilities aligned to business outcomes.</p></li><li><p>Define and enforce reference architectures, reusable patterns, and technical guardrails to ensure consistency and quality across products.</p></li><li><p>Evaluate emerging technologies and delivery models (SaaS / PaaS / IaaS) and influence vendor roadmaps and negotiations to align with enterprise strategy.</p></li></ul><p></p><p><b>Engineering Execution &amp; Operations:</b></p><ul><li><p>Design, develop, and operate scalable, secure full stack solutions using Python, Java / Node.js, React, REST APIs, and modern cloud-native architectures.</p></li><li><p>Design and operate Large Language Model LLM native and agentic systems as long-lived products, incorporating human‑ in‑ the-loop, monitoring, governance, and continuous improvement.</p></li><li><p>Build and maintain ML and data pipelines for training, validation, deployment, monitoring, retraining, and rollback.</p></li><li><p>Implement CI/CD practices and automate workflows across data ingestion, feature engineering, model versioning, and deployment.</p></li><li><p>Diagnose and resolve complex technical issues, balancing short-term remediation with long-term‑ architectural strategy.</p></li></ul><p></p><p><b>Product, Stakeholder &amp; Vendor Partnership:</b></p><ul><li><p>Partner closely with IT Product Managers and GRS stakeholders to plan, prioritize, deliver, and support strategic digital capabilities.</p></li><li><p>Translate business needs into well designed technical solutions that drive measurable impact in regulatory and operational workflows.</p></li><li><p>Operate effectively in a highly matrixed organization, aligning stakeholders with differing priorities.</p></li></ul><p></p><p><b>Financial &amp; Operational Stewardship:</b></p><ul><li><p>Manage and optimize Total Cost of Ownership (build and run) for technology assets, understanding and influencing key cost drivers.</p></li><li><p>Ensure solutions are cost efficient‑, scalable, and sustainable over time.</p></li></ul><p></p><p><b>Required Qualifications &amp; Experience:</b></p><ul><li><p>6&#43; years of software engineering experience; BioPharma / Life Sciences experience strongly preferred.</p></li><li><p>Bachelor’s degree in Computer Science, Software Engineering, Engineering, Life Sciences, or a related quantitative field; advanced degree preferred.</p></li><li><p>Proven track record delivering complex, production grade‑ solutions using structured SDLC and Agile product models in regulated environments.</p></li><li><p>Hands-on experience with developing software and applications that use Large Language Models (LLM) and hands on AI coding with tools such as Codex, Claude Code, OpenAI, etc.</p></li><li><p>Hands‑on experience building Generative and Agentic AI systems using frameworks such as LangChain, LlamaIndex, and enterprise LLM platforms (e.g., OpenAI, AWS Bedrock).</p></li><li><p>Strong proficiency in Python and React; familiarity with Java, TypeScript, and backend frameworks such as FastAPI.</p></li><li><p>Experience with AWS cloud services (Lambda, S3, DynamoDB, Bedrock, SageMaker) and event driven, microservices‑ based‑ architectures.</p></li><li><p>Knowledge of Github and source control version management.</p></li><li><p>Strong data engineering and analytics skills (SQL / NoSQL).</p></li><li><p>Experience working with vendor partners and offshore development models.</p></li><li><p>Experience in Regulatory Affairs technologies such as Veeva RIM, Lorenz DocuBridge, Health Authorities Queries (HAQ), or Labeling preferred.</p></li></ul><p></p><p><b>Core Competencies:</b></p><ul><li><p>Strong technical judgment with the ability to link architecture decisions to business outcomes.</p></li><li><p>Excellent communication skills across engineering, product, business, and executive audiences.</p></li><li><p>Ability to execute multiple large initiatives concurrently in an Agile, product centric‑ model.</p></li><li><p>Collaborative, pragmatic, and comfortable operating in ambiguity and change.</p></li><li><p>Innovative mindset with the discipline to deliver reliable, compliant, enterprise ‑grade solutions.</p></li></ul><p></p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Madison - Giralda - NJ - US: $135,320 - $163,976&amp;#xa;Princeton - NJ - US: $135,320 - $163,976 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1599885 : Senior Manager, Full Stack Software Engineering &amp; Operations Regulatory BI&amp;T]]></description><link>http://biotechroles.com/senior-manager-full-stack-software-engineering-and-operations-regulatory-biandt-bristol-myers-squibb/6a08991c2f1861929d2533a0</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-full-stack-software-engineering-and-operations-regulatory-biandt-bristol-myers-squibb/6a08991c2f1861929d2533a0</guid><pubDate>Sat, 16 May 2026 16:19:40 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Madison - Giralda - NJ - US</location><salary>$150000-210000</salary><type>Full time</type></item><item><title><![CDATA[Associate Specialist, Value Stream Cryo Operations]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><span>At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.</span></p><p></p><p>The Associate Specialist, Value Steam Cryo Operations is responsible for the Cryopreservation, movement, storage, control of manufacturing patient materials, and support of Liquid Nitrogen storage tanks and equipment at the CAR T manufacturing facility in Summit, NJ. This includes but is not limited to, cryopreservation, storage, inventory control, chain of custody, and material tracking.</p><p></p><p><b>Shift Available: </b></p><ul><li><p>Wednesday - Saturday (with e/o Wednesday off), Onsite Day Shift, 5 a.m. - 5:30 p.m.</p></li></ul><p></p><p><b>Responsibilities:</b></p><ul><li><p>Handling patient material throughout the material Cryopreservation, storage, distribution, transfer, and disposal.</p></li><li><p>Maintaining sample tracking and chain of custody records in accordance with GMP requirements and written procedures.</p></li><li><p>Ensuring that obsolete or expired samples and materials are destroyed and disposed of according to written procedures.</p></li><li><p>Performing sample queries and periodic storage reports, as required.</p></li><li><p>Assisting management with investigations and deviations related to sample management.</p></li><li><p>Collaborating with other departments to identity and implement process efficiencies.</p></li><li><p>Maintaining metrics for the Value Stream Cryo Operations group.</p></li><li><p>Facilitating cold chain transfers of material, as required.</p></li><li><p>Performs tasks for Cell Therapy products to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP’s) following the current, approved Standard Operating Procedures (SOPs) and Work Instructions (WIs).</p></li><li><p>Maintains timing according to the production schedule to ensure on-time</p></li><li><p>Cryopreservation support.</p></li><li><p>Cryopreserve Patient material daily, store and manage Inventory of material in LN2 storage locations.</p></li><li><p>Supports manual and electronic batch record executions, deviation investigations, and closure of CAPAs.</p></li><li><p>Maintains timing according to the production schedule to ensure on-time logistics.</p></li><li><p>Ensures all documentation is correct and addresses procedural/documentation errors expeditiously and effectively.</p></li><li><p>Work with management to ensure adequately trained personnel are available to perform all Value Stream Cryo Operations activities.</p></li><li><p>Records patient material handling data and information in a clear, concise, format according to proper GDPs.</p></li><li><p>Able to problem solve with minimal supervision.</p></li><li><p>Works in a team based, cross-functional environment to complete tasks required by shift schedule.</p></li><li><p>Other duties may be assigned, as necessary.</p></li></ul><p></p><p><b>Knowledge &amp; Skills:</b></p><ul><li><p>Experience with cold chain sample storage and transfer.</p></li><li><p>Knowledge of cGMP/FDA regulated industry.</p></li><li><p>Basic mathematical skills.</p></li><li><p>General understanding of cGMPs.</p></li><li><p>Technical writing capability.</p></li><li><p>Proficient in MS Office applications.</p></li><li><p>Inventory control and/or management.</p></li><li><p>Background to include an understanding of biology, chemistry, medical or clinical practices is a plus.</p></li><li><p>Available to work OT when business requires.</p></li><li><p>Willing to work staggered day shift hours.</p></li></ul><p></p><p><b>Minimum Requirements: </b></p><ul><li><p>High School Diploma required. Bachelor&#39;s or associate degree preferred.</p></li><li><p>0-1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience.</p></li></ul><p>BMSCART, #LI-Onsite</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Summit West - NJ - US: $34.66 - $42.00per hour&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601903 : Associate Specialist, Value Stream Cryo Operations]]></description><link>http://biotechroles.com/associate-specialist-value-stream-cryo-operations-bristol-myers-squibb/6a08991b2f1861929d25339f</link><guid isPermaLink="true">http://biotechroles.com/associate-specialist-value-stream-cryo-operations-bristol-myers-squibb/6a08991b2f1861929d25339f</guid><pubDate>Sat, 16 May 2026 16:19:39 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Summit West - NJ - US</location><salary>$75000-95000</salary><type>Full time</type></item><item><title><![CDATA[Drug Product Associate, Sterile Drug Product]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p>BMS Cruiserath Sterile Drug Product is seeking an experienced individual with manufacturing experience to provide on the floor technical support to our manufacturing teams within our new Sterile Drug Product (SDP) facility.  </p><p>Reporting to the Senior Manager, Manufacturing Shift Lead, the Drug Product Associate will play a key role in the establishing our multi-product commercial Drug Product Facility with both vial and syringe fill finish technology. The <b>Drug Product Associate</b> will provide input and support all phases of the SDP project, such as, CQV, Site Operational Readiness, Technical Transfer, new product introduction and commercialization activities.  Post start-up this role will be embedded within the shift teams charged with delivering the manufacturing plan for the facility. </p><p>The start-up nature of this project will require adaptability &amp; innovation due to the multiple project phases and multiple products onsite. The role will be both challenging &amp; rewarding and will thus ensure that the successful candidate can seize a wide range of development opportunities within BMS. </p><p></p><ul><li><p><i>The position will commence on a day schedule, with a planned transition to shift work in the future</i></p></li></ul><p></p><p><b>Key Responsibilities</b> </p><ul><li>Support the execution of one or more processes that include Formulation, Filling (vial &amp; syringe), Lyophilization, Capping, Visual Inspection &amp; Primary Packaging </li></ul><ul><li>Support technical issue troubleshooting, resolution both during and post facility start-up.  </li></ul><ul><li>Work with the cross functional departments to facilitate the implementation of the project design and validation of the SDP manufacturing facility. </li></ul><ul><li>Support all phases of Commissioning / Qualification and Validation during Start-up phase of state-of-the-art Drug Product Facility  </li></ul><ul><li>Support all Capital / Tech Transfer / Operational Readiness activities to support Commercial Readiness </li></ul><ul><li>Support delivery of training to SDP team on day-to-day operations within area of responsibility </li></ul><ul><li> Right First-Time execution of commercial manufacturing processes according to established work instructions </li></ul><ul><li>Support the implementation of all key Operational Excellence initiatives (5S / Std Work / LSW / Kaizen / Problem Solving etc.) </li></ul><ul><li>Taking part in investigations and optimization of processes using scientific, engineering and lean principles </li></ul><ul><li>Proficient use of process automation systems  </li></ul><ul><li>Assisting with review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative  </li></ul><ul><li>Engages in and supports culture of continuous improvement initiatives and safe working practices. </li></ul><ul><li>Designee for Senior DPA as required. </li></ul><ul><li>Support any other business deliverables as needed. </li></ul><p></p><p><b>Qualifications &amp; Experience</b> </p><ul><li>Experience in a high-speed manufacturing / regulated environment essential </li></ul><ul><li>Qualification in science, engineering, or related subject desirable. </li></ul><ul><li>Expertise in sterile drug product manufacturing along with demonstrated proficiency in technical troubleshooting and resolution is advantageous but not essential. </li></ul><ul><li>Ability to flexibly adapt to changing business needs in a start-up environment. </li></ul><p></p><p><b>Why you should apply</b></p><p></p><ul><li><span>You will help patients in their fight against serious diseases </span></li><li><span>You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees. </span></li><li><span>You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym </span></li></ul><p></p><p><b>#LI-Onsite</b></p></div><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602498 : Drug Product Associate, Sterile Drug Product]]></description><link>http://biotechroles.com/drug-product-associate-sterile-drug-product-bristol-myers-squibb/6a08991a2f1861929d25339e</link><guid isPermaLink="true">http://biotechroles.com/drug-product-associate-sterile-drug-product-bristol-myers-squibb/6a08991a2f1861929d25339e</guid><pubDate>Sat, 16 May 2026 16:19:38 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Cruiserath - IE</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Occupational Health Advanced Practice Nurse]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>OCCUPATIONAL HEALTH NURSE PRACTITIONER-New Brunswick, NJ</b></p><p></p><p>The Occupational Health Nurse Practitioner will provide advance practice nursing services</p><p>including BMS specified, medical surveillance, travel health programs, occupational injury/illness</p><p>care, case management, medical accommodation, and acute care of episodic non-occupational</p><p>injuries/illnesses.</p><p></p><p>This position is responsible for supporting a comprehensive occupational health program for the</p><p>BMS New Brunswick site. This program complies with BMS corporate standards as well as</p><p>federal and state occupational health and safety regulations and laws.</p><p>The position will be in the Occupational Health medical clinic at BMS New Brunswick, N.J. with</p><p>flexibility to cover as needed at other BMS central New Jersy sites.</p><p>This position will report directly to the Bristol Myers Squibb Occupational Health Senior Manager</p><p>in New Brunswick. The Nurse Practitioner is expected to work closely with the BMS New</p><p>Brunswick Environmental, Safety and Sustainability, Human Resources, and site management</p><p>teams.</p><p></p><p><b>RESPONSIBILITIES</b></p><p> Develop and implement objectives for BMS New Brunswick site Occupational Health</p><p>services that are aligned with the company corporate and occupational health goals and</p><p>objectives.</p><p> Collaborate directly with the Occupational Health Senior Manager, Associate Director of</p><p>Occupational Health, NJ, and the Global Medical Director as needed on case</p><p>management, employment issues and standard compliance, including work restrictions</p><p>and job accommodations.</p><p> Collaborate with management, EHSS, and other teams to develop occupational health</p><p>and safety standards for BMS New Brunswick, including risk assessments for safety</p><p>sensitive positions with development of appropriate medical surveillance programs.</p><p> Provide clinical occupational health services to the employees at BMS New Brunswick.</p><p>This includes examination, diagnosis, and treatment where appropriate, including</p><p>prescriptions when indicated.</p><p> Provide medical surveillance exams and testing when needed, including ECG, audiometry,</p><p>vision, spirometry, and phlebotomy.</p><p> Work with BMS disability and worker’s compensation insurance providers in case</p><p>managing occupational and non-occupational injuries and illnesses, and short- and longterm</p><p>disability claims.</p><p> Investigate, monitor, and analyze illness and injury episodes and trends; develop</p><p>strategies to promote and protect employee health and safety and prevent injury,</p><p>including ergonomic programs.</p><p> Plan and promote company-wide and site-based health and wellbeing programs in</p><p>collaboration with other Occupational Health and Wellbeing team members.</p><p> Support onsite medical emergency response during normal operating hours.</p><p><b>POSITION REQUIREMENTS</b></p><p> Licensed as RN and ANP-C in New Jersey</p><p> Hold certification as Family Nurse Practitioner or Adult Nurse Practitioner</p><p> DNP or MSN degree</p><p> Eligibility to practice as a nurse practitioner independently (at least 5 years of full time NP</p><p>practice)</p><p> COHN preferred</p><p> Basic Life Support (BLS) or equivalent.</p><p> Good interpersonal/communication skills</p><p> Computer skill proficiency, including experience using electronic medical record</p><p>programs.</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>New Brunswick - NJ - US: $125,460 - $152,028&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602497 : Occupational Health Advanced Practice Nurse]]></description><link>http://biotechroles.com/occupational-health-advanced-practice-nurse-bristol-myers-squibb/6a0899192f1861929d25339d</link><guid isPermaLink="true">http://biotechroles.com/occupational-health-advanced-practice-nurse-bristol-myers-squibb/6a0899192f1861929d25339d</guid><pubDate>Sat, 16 May 2026 16:19:37 GMT</pubDate><company>Bristol-Myers Squibb</company><location>New Brunswick - NJ - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Statistical Programming]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a target="_blank" href="https://careers.bms.com/working-with-us"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><h1><b>Position Summary </b></h1><p>The Manager, Statistical programming provides comprehensive programming expertise to clinical project teams to support the development, regulatory approval and market acceptance of  Bristol Myers Squibb (BMS) products.</p><p></p><p>This position is primarily responsible for the design, development and implementation of technical solutions for integrating, analyzing and reporting clinical data.  </p><p></p><p>The Manager, Statistical Programming  develops collaborative relationships and works effectively within  Global Biometrics &amp; Data Sciences (GBDS), with external vendors and members of cross-functional development teams.</p><p></p><h1><b>Key Responsibilities</b></h1><ul><li><p>Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs</p></li><li><p>Provides comprehensive programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis</p></li><li><p>Support the electronic submission preparation and review</p></li><li><p>Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities</p></li><li><p>Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers</p></li><li><p>Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS)  deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices</p></li><li><p>Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors</p></li><li><p>Independently leads and / or performs programming assignments across multiple projects with minimal supervision</p></li><li><p>Support improvement initiatives</p></li></ul><p></p><h1><b>Required Education &amp; Experience </b></h1><ul><li><p>Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required.</p></li><li><p>Demonstrated experience of programming in industry.</p></li></ul><p></p><h1><b>Required Knowledge, Skills &amp; Competences</b></h1><ul><li><p>Demonstrated proficiency in using SAS to produce derived analysis datasets and TFLs.</p></li><li><p>Have in-depth understanding of clinical data structure (e.g. CDISC standards) and relational database.</p></li><li><p>Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21.</p></li><li><p>Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.</p></li><li><p>Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.</p></li><li><p>Have good understanding of regulatory, industry, and technology standards and requirements.</p></li><li><p>Have good knowledge of statistical terminology, clinical tests, medical terminology and protocol designs.</p></li><li><p>Demonstrated ability to work in a team environment with clinical team members.</p></li></ul><p></p><h1><b>Preferred Requirements</b></h1><ul><li><p>Extensive Clinical / statistical programming experience within pharmaceutical clinical development - Supporting regulatory filings (e.g. NDA, BLA, MAA)</p></li><li><p>Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements</p></li><li><p>Experience in other software packages (e.g. R)</p></li><li><p>Experience with the Linux operating system</p></li></ul><p>#LI-Hybrid</p><p></p><p><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p></p><p><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation</span> in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p></p><p><b>On-site Protocol</b><br /><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p></p><p><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p></p><p><b>Supporting People with Disabilities</b></p><p><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span>accommodations/adjustments</span> and ongoing support in their roles. Applicants can request a reasonable workplace <span>accommodation/adjustment</span> prior to accepting a job offer. If you require reasonable <span>accommodations/adjustments</span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span>adastaffingsupport&#64;bms.com</span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p></p><p>Bristol Myers Squibb is Disability Confident – Employer</p><p></p><p>A UK Government scheme</p><p></p><p><b>Candidate Rights</b></p><p>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</p><p></p><p><b>Data Protection</b></p><p>We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank">https://careers.bms.com/fraud-protection</a>.</p><p></p><p>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602503 : Manager, Statistical Programming]]></description><link>http://biotechroles.com/manager-statistical-programming-bristol-myers-squibb/6a0899182f1861929d25339c</link><guid isPermaLink="true">http://biotechroles.com/manager-statistical-programming-bristol-myers-squibb/6a0899182f1861929d25339c</guid><pubDate>Sat, 16 May 2026 16:19:36 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Uxbridge - GB</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[Senior Drug Product Associate, Sterile Drug Product]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p>BMS Cruiserath Sterile Drug Product is seeking an experienced individual with aseptic manufacturing experience to provide on the floor technical leadership to our manufacturing teams within our new Sterile Drug Product (SDP) facility.  </p><p>Reporting to the Senior Manager, Manufacturing Shift Lead, the <b>Senior Drug Product Associate</b> will play a key role in the establishing our multi-product commercial Drug Product Facility with both vial and syringe fill finish technology. The Senior Drug Product Associate will provide input and support all phases of the SDP project, such as, CQV, Site Operational Readiness, Technical Transfer, new product introduction and commercialization activities.  Post start-up this role will be embedded within the shift teams charged with delivering the manufacturing plan for the facility. </p><p>The start-up nature of this project will require adaptability &amp; innovation due to the multiple project phases and multiple products onsite. The role will be both challenging &amp; rewarding and will thus ensure that the successful candidate can seize a wide range of development opportunities within BMS. </p><p></p><ul><li><p>The position will commence on a day schedule, with a planned transition to shift work in the future.</p></li></ul><p></p><p></p><p><b>Key Responsibilities</b> </p><ul><li>Manufacturing SME in one or more processes that include Formulation, Filling (vial &amp; syringe), Lyophilization, Capping, Visual Inspection &amp; Primary Packaging </li></ul><ul><li>Lead technical issue troubleshooting, resolution both during and post facility start-up.  </li></ul><ul><li>Work with the cross functional departments to facilitate the implementation of the project design and validation of the SDP manufacturing facility. </li></ul><ul><li>Support all phases of Commissioning / Qualification and Validation during Start-up phase of state-of-the-art Drug Product Facility  </li></ul><ul><li>Support all Capital / Tech Transfer / Operational Readiness activities including but not limited to: </li></ul><ul><li>Vendor site Factory Acceptance Tests  </li></ul><ul><li>MES / MBR Design  </li></ul><ul><li>SOP Development and Implementation </li></ul><ul><li>Training Material development </li></ul><ul><li>Room layouts and Ways of Working </li></ul><ul><li>Support delivery of training to SDP team on day-to-day operations within area of responsibility </li></ul><ul><li>Work in conjunction with the Shift Lead/Technical Lead to build the SDP Manufacturing teams technical competencies across a given area. </li></ul><ul><li>Lead the Right First-Time execution of commercial manufacturing processes within areas of responsibility. </li></ul><ul><li>Support key meetings on behalf of Manufacturing. </li></ul><ul><li>Support and Lead key Operational Excellence initiatives (5S / Std Work / LSW / Kaizen / Problem Solving etc.) </li></ul><ul><li>Support Operational related investigations and bey the key point of contact for all other functional investigations </li></ul><ul><li>SME in use of process automation systems (i.e., Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.). </li></ul><ul><li>Co-ordinating delivery review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative for area of responsibility </li></ul><ul><li>Drives and supports culture of continuous improvement initiatives and safe working practices. </li></ul><ul><li>Designee for Tech Lead, when required. </li></ul><p>Support any other business deliverables as needed. </p><p></p><p><b>Qualifications &amp; Experience</b> </p><ul><li>A Bachelors in a science, engineering, or related subject is desirable. </li></ul><ul><li>Minimum 3 years’ experience in a GMP environment with a minimum of 1 years’ biopharma manufacturing experience </li></ul><ul><li>Expertise in sterile drug product manufacturing along with demonstrated proficiency in technical troubleshooting and resolution is highly desirable. </li></ul><ul><li>Ability to flexibly adapt to changing business needs in a start-up environment. </li></ul><ul><li>Experience in lean manufacturing techniques and tools advantageous </li></ul><p></p><p></p><p><b>Why you should apply</b></p><p></p><ul><li>You will help patients in their fight against serious diseases</li><li>You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.</li><li>You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym</li></ul><p></p><p><b>#LI-Onsite</b></p></div><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602499 : Senior Drug Product Associate, Sterile Drug Product]]></description><link>http://biotechroles.com/senior-drug-product-associate-sterile-drug-product-bristol-myers-squibb/6a0899182f1861929d25339b</link><guid isPermaLink="true">http://biotechroles.com/senior-drug-product-associate-sterile-drug-product-bristol-myers-squibb/6a0899182f1861929d25339b</guid><pubDate>Sat, 16 May 2026 16:19:36 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Cruiserath - IE</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Senior Specialist, Label Operations]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.</p><p>Specialist, Label Operations at the S12 Cell Therapy manufacturing facility is responsible for supporting site Label Control activities at S12 in accordance with BMS policies, standards, procedures and Global cGMPs.  Functional responsibilities include performing in-process and drug product label printing activities, ensuring accurate and timely issuance of labels for manufacturing and packaging labeling activities for Cell Therapy Development and Operations (CTDO).</p><p></p><p><b>Shift Available:</b></p><ul><li>Sunday - Wednesday (with e/o Wednesday off), 2nd Shift, 6:00pm-6:30am.</li></ul><p></p><p><b>Responsibilities:</b></p><ul><li>Supports all activities for the Label Operations group.</li><li>Responsible for issuing clinical and commercial in-process and final product labels for labeling operations.</li><li>Responsible for ensuring accurate printed information on labels in compliance with health authority requirements.</li><li>Coordinates with production teams to ensure timely issuance of labels.</li><li>Performs training of label operations and issuance requirements for internal personnel as needed.</li><li>Ensures standard operating procedures (SOPs) related to job responsibilities define the steps necessary to complete tasks, etc. Writes, reviews and updates SOPs as required.</li><li>Carries out plans and actions to support new drug product launches, new market and other quality management activities as assigned.</li><li>Provides support during internal and health authority inspections and audits of facility.</li><li>Knowledge of quality processes, including label control and issuance, change control, product complaints, deviations, investigations and CAPA management.</li><li>Performs supplemental investigations/projects as required by Management.</li><li>Maintains knowledge of current GMPs and regulatory guidelines.</li></ul><p></p><p><b>Knowledge &amp; Skills: </b></p><ul><li>Preferred knowledge and experience with GMP, Quality, and compliance.</li><li>Able to write and review technical reports with clarity and brevity; provides guidance to other team members in technical writing skills.</li><li>Must have knowledge and experience with GMP, Quality, and compliance.</li><li>Able to write and review technical reports with clarity and brevity; provides guidance to other team members in technical writing skills.</li><li>Requires moderate direction to complete more complex tasks; completes routing tasks with little or no supervision.</li><li>Must be time organized and possess an independent mindset.</li><li>Good understanding of electronic document management and manufacturing execution systems.</li><li>Has advanced computer skills to increase department’s productivity, as well as broadening technical and scientific knowledge.</li><li>Confident in making decisions for non-routine issues.</li><li>Routinely recognizes and addresses quality opportunities to improve overall process/project efficiencies.</li><li>Proposes solutions for complex issues and works with management to resolve. Follows established procedures and performs work as assigned.</li><li>Builds relationships and effectively communicates internally within the function and with internal and external cross-functional teams. Interacts with internal and external cross-functional teams. Represents department in internal and external cross-functional teams.</li><li>Contributes to goals within the work group.</li><li>Able to recognize conflict and notify management with proposed recommendations for resolution.</li><li>Able to prepare written communications and communicate problems to management with clarity and accuracy.</li><li>Able to produce data reports with precision.</li><li>Able to muti-task.</li><li>Able to support internal and health authority inspections of facility</li></ul><p></p><p><b>Minimum Requirements: </b></p><ul><li>B.S. Degree required, minimum 2 years relevant work experience.</li><li>Equivalent combination of education and experience is acceptable.</li></ul><p></p><p><b>Working Conditions: (If applicable)</b></p><ul><li>Work is performed in a typical office environment, with standard office equipment available and used. Work is generally performed seated but may require standing and walking for up to 10% of the time. Lighting and temperature are adequate and there are no abnormal conditions caused by noise, dust, etc.</li><li>Required to carry and/or lift up to 30 pounds / 15 kg, several times a day, while handling production equipment and/or materials.</li><li>Must be able to work assigned shift (Day, Evening, Night, Weekends and/or Holidays).</li><li>Employees holding this position will be required to perform any other job-related duties as requested by management.</li></ul><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Summit West - NJ - US: $40.34 - $48.88per hour&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602383 : Senior Specialist, Label Operations]]></description><link>http://biotechroles.com/senior-specialist-label-operations-bristol-myers-squibb/6a0899172f1861929d25339a</link><guid isPermaLink="true">http://biotechroles.com/senior-specialist-label-operations-bristol-myers-squibb/6a0899172f1861929d25339a</guid><pubDate>Sat, 16 May 2026 16:19:35 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Summit West - NJ - US</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Bothell Materials Management]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p>The Associate Director, Materials Management provides strategic and operational leadership for all materials planning, purchasing, and raw materials inventory governance activities supporting the Bothell manufacturing site, encompassing both commercial and clinical production and New Product Introduction (NPI) activities within a GMP regulated biopharmaceutical environment.</p><p></p><p>As the site Materials Management leader, this role sets strategy and standards while ensuring compliant, consistent execution across all materials portfolios. The Associate Director provides people leadership and technical oversight to enable uninterrupted manufacturing and successful clinical and commercial launches, while serving as a key interface to Global Supply Chain and Strategic Sourcing to translate enterprise strategy into executable site plans, proactively manage risk, and drive cross‑functional resolution.</p><p><b>Duties/Responsibilities </b></p><p><b>Materials Management Strategy &amp; Site Accountability</b></p><ul><li>Own end-to-end site material availability across Operations, Quality Control, and Facilities, ensuring alignment between materials strategy, execution priorities, and manufacturing readiness.</li><li>Define and maintain site Materials Management standards, governance, and operating models to ensure consistent, compliant execution across all materials portfolios.</li><li>Serve as the senior site authority for Materials Management performance, risk posture, and decision making.</li></ul><p><b>Clinical Development, NPI &amp; Launch Enablement</b></p><ul><li>Serve as the site level functional owner for Materials Management strategy and risk posture across clinical programs, tech transfers, and new product introductions.</li><li>Define and approve site materials strategies for clinical development and launches, ensuring alignment across planning approaches, supplier readiness expectations, planning BOM governance, and inventory positioning.</li><li>Own escalation, prioritization, and decision making for materials related risks impacting clinical supply continuity and launch readiness, ensuring timely cross functional resolution.</li></ul><p><b>Materials Planning, Inventory Governance &amp; Risk Management</b></p><ul><li>Own site‑level inventory health strategy and risk posture for raw materials, including expiration risk, excess, obsolescence, and scrap.</li><li>Establish and oversee site material status governance, ensuring clear, real‑time visibility to material disposition, release readiness, constraints, shortages, and disruptions, with defined escalation and decision‑making accountability.</li><li>Define expectations for inventory accuracy, constraint recovery planning, and escalation pathways to protect manufacturing continuity.</li><li>Sponsor and prioritize site‑level continuous improvement initiatives to strengthen supply resilience, reduce waste, and improve long‑term inventory performance.</li></ul><p><b>Supplier, Quality &amp; Compliance Leadership</b></p><ul><li>Serve as the primary site interface with Global Supply Chain, Strategic Sourcing, and Quality to coordinate continuity, escalation, and supply‑risk mitigation.</li><li>Ensure appropriate investigation, root cause analysis, and CAPA ownership for material‑related issues through partnership with cross-functional stakeholders and suppliers.</li><li>Promote a culture of compliance, environmental health &amp; safety, and operational excellence through strong cross‑functional partnership and leadership.</li></ul><p><b>People Leadership &amp; Organizational Capability</b></p><ul><li>Lead, coach, and develop a team of Materials Management planners and buyers (people managers and/or individual contributors); set priorities, build technical and leadership capability, and ensure training and qualification aligned with cGMP requirements.</li><li>Establish clear performance expectations and accountability across the organization.</li></ul><p><b>Performance Management, Systems &amp; Change Enablement</b></p><ul><li>Define, monitor, and communicate Materials Management KPIs (e.g., service level, shortages, inventory health, supplier performance) to drive accountability and continuous improvement.</li><li>Serve as the site Materials Management SME for new processes, systems, and planning models, ensuring effective adoption, sustained performance, and alignment with global strategy.</li><li>Support additional site and enterprise initiatives as required.</li></ul><p><b>Reporting Relationship</b></p><p>This position reports to the Director, Site Supply Chain and Logistics.</p><p><b>Qualifications</b></p><p><b>Education</b></p><ul><li>Bachelor’s degree required in Supply Chain, Engineering, Life Sciences, Business, or a related field.</li><li>Advanced education or professional certification in supply chain management, product lifecycle management, or related disciplines (e.g., MBA, MS, graduate certificate, APICS CPIM/CSCP/CLTD) a plus.</li></ul><p><b>Experience</b></p><ul><li>8–12&#43; years of progressive experience in materials management or supply chain roles supporting manufacturing operations within a regulated biopharmaceutical or pharmaceutical environment.</li><li>Demonstrated experience leading materials planning, purchasing, and inventory governance activities in support of clinical development, tech transfer, new product introductions and commercial manufacturing.</li><li>Experience leading and developing teams and/or providing functional leadership within matrixed organizations.</li><li>Strong working knowledge of cGMP requirements and regulatory expectations as they apply to materials planning, purchasing, inventory control, and manufacturing readiness across clinical, launch, and commercial operations.</li><li>Hands‑on experience with ERP and planning systems, preferably SAP S/4 and SAP IBP, including sustained, regular use in materials planning, purchasing, and inventory management to support manufacturing operations.</li><li>Experience operating within global supply planning and purchasing models, including coordination across network strategies, Global Supply Chain organizations, and broader enterprise stakeholders.</li></ul><p><b>Technical &amp; Professional Competencies</b></p><ul><li>Deep expertise in materials planning and purchasing processes, including MRP‑based planning, Planning Bill of Materials (BOM) governance, consumption‑based planning models, inventory optimization and risk mitigation strategies.</li><li>Demonstrated experience establishing and governing planning BOM structures to support clinical programs, tech transfers, and new product introductions.</li><li>Proven ability to assess and manage complex supply risks, anticipate downstream impacts, and protect continuity in patient‑critical manufacturing environments.</li><li>Strong working knowledge of quality systems, material disposition and release readiness processes, and audit expectations.</li><li>Ability to define performance metrics, interpret data across systems, and drive risk‑based, data‑driven decision making.</li><li>Experience interpreting demand signals and scenario changes to inform materials planning, purchasing, and inventory strategies in clinical, launch, and commercial environments.</li></ul><p><b>Leadership &amp; Behavioral Competencies</b></p><ul><li>Demonstrated ability to lead, coach, and develop teams while building organizational capability.</li><li>Strong cross‑functional leadership and influence skills, with the ability to engage site, network, and enterprise stakeholders.</li><li>Ability to balance strategic leadership with hands‑on operational engagement in fast‑paced, high‑complexity manufacturing environments.</li><li>Resilient, adaptable, and solutions‑oriented approach to ambiguity, competing priorities, and change.</li></ul><p><b>Travel</b></p><ul><li>Occasional domestic travel may be required.</li></ul><p></p><p>BMSCART</p><p>#LI-HYBRID</p><p></p><div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Bothell - WA - US: $174,520 - $211,480&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602390 : Associate Director, Bothell Materials Management]]></description><link>http://biotechroles.com/associate-director-bothell-materials-management-bristol-myers-squibb/6a0899162f1861929d253399</link><guid isPermaLink="true">http://biotechroles.com/associate-director-bothell-materials-management-bristol-myers-squibb/6a0899162f1861929d253399</guid><pubDate>Sat, 16 May 2026 16:19:34 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Bothell - WA - US</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Oncology/ Hematology- Cleveland/ NE, OH]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>This territory includes: <span>Cleveland and Northeastern Ohio with responsibility </span><span>across<span> </span></span>major academic institutions and community-based accounts<span>.</span></p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602385 : Senior Therapeutic Area Specialist, Oncology/ Hematology- Cleveland/ NE, OH]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-oncology-hematology-cleveland-ne-oh-bristol-myers-squibb/6a0899152f1861929d253398</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-oncology-hematology-cleveland-ne-oh-bristol-myers-squibb/6a0899152f1861929d253398</guid><pubDate>Sat, 16 May 2026 16:19:33 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Cleveland - OH - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Specialist, Patient & Site Engagement Products, GDO BI&T]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p><b>Summary:</b></p><p>The Senior Specialist in the Patient &amp; Site Engagement Product Line in Global Development Operations IT (GDO IT) will play a key role in bridging the gap between Clinical operations needs and IT solutions, primarily focusing on Patient Engagement. This is a hands-on role where the successful candidate will work closely with Global Patient Recruitment, Study and Patient Experience teams to gather requirements, design prototypes, work with Product Manager to develop and support the technology solutions throughout its lifecycle.</p><p></p><p><b>Skills:</b></p><ul><li><p>Proven ability to use AI for solution prototyping, data analysis, and building solutions.</p></li><li><p>Have a commitment to a career in technology with a passion for healthcare.  </p></li><li><p>Able to collaborate across multiple teams and challenge the status quo.</p></li><li><p>Excellent communication skills.  </p></li><li><p>Able to learn new tools and processes quickly.</p></li></ul><p></p><p><b>Key Responsibilities:</b></p><ul><li><p>Serve as the system/business analyst on assigned initiatives in Patient &amp; Site Engagement product line within Global Development Operations IT organization.</p></li><li><p>Develop effective business relationships with stakeholders to ensure successful delivery of technology initiatives <i>and bring creative ideas to help solve pain points and business challenges</i></p></li><li><p>Work closely with product managers and business stakeholders to solve business problems using AI first approach.</p></li><li><p>Create IT documentation artifacts in support of an agile technology implementations, including but not limited to requirements specifications, process diagrams, user acceptance test plans, traceability matrices, wireframes, training documents, and change management artifacts.</p></li><li><p>Prototype technology solutions using tools such as python, Jupyter Notebook, and Figma.</p></li><li><p>Use AI to generate SQL scripts to analyze data, identify gaps, trends and improvement opportunities to analyze data, identify gaps, trends, and improvement opportunities</p></li><li><p>Generate relevant reports and visualizations.</p></li><li><p>Be the ‘Human in the Loop’ for AI products and Configure, test, and validate applications with engineering team</p></li><li><p>Coordinate and execute user acceptance testing, validate requirements, and manage traceability matrices.</p></li><li><p>Participate in retrospectives, collect user feedback, and propose improvements to business capabilities.</p></li><li><p>Develop effective business relationships with stakeholders to ensure successful delivery of technology initiatives</p></li></ul><p><br /><b>Qualifications &amp; Experience:</b></p><ul><li><p>Must have knowledge of the Software Development Lifecycle (SDLC) and have a working knowledge of the Business Analysis Body of Knowledge (BABOK).</p></li><li><p>Bachelor’s degree in computer science, Computer Engineering, Life Sciences, or related discipline.</p></li><li><p>2-4 years of experience as a technical business analyst, preferably in pharmaceutical, clinical research, or healthcare settings.</p></li><li><p>Experience using Python, SQL or similar tools for scripting, automation, and analytics.</p></li><li><p>Proficient in clear and concise requirements documentation, process modeling (e.g., BPMN, Visio, Lucidchart), and drafting user acceptance criteria.</p></li><li><p>Experience using business analysis tools (Figma, JIRA, Confluence, MS Office, or comparable platforms).</p></li><li><p>Effective communicator with ability to drive conversations with technical and non-technical stakeholders.</p></li><li><p>Detail-oriented, organized, and able to manage multiple priorities in a fast-paced environment.</p></li><li><p>Collaborative team player with willingness to learn and adapt in a dynamic product ecosystem.</p></li></ul><p></p><p></p></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $76,080 - $92,185 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602508 : Senior Specialist, Patient &amp; Site Engagement Products, GDO BI&amp;T]]></description><link>http://biotechroles.com/senior-specialist-patient-and-site-engagement-products-gdo-biandt-bristol-myers-squibb/6a0899152f1861929d253397</link><guid isPermaLink="true">http://biotechroles.com/senior-specialist-patient-and-site-engagement-products-gdo-biandt-bristol-myers-squibb/6a0899152f1861929d253397</guid><pubDate>Sat, 16 May 2026 16:19:33 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Data Sciences]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a target="_blank" href="https://careers.bms.com/working-with-us"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>please see attached</p><p></p><p><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p></p><p><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation</span> in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p></p><p><b>On-site Protocol</b><br /><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p></p><p><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p></p><p><b>Supporting People with Disabilities</b></p><p><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span>accommodations/adjustments</span> and ongoing support in their roles. Applicants can request a reasonable workplace <span>accommodation/adjustment</span> prior to accepting a job offer. If you require reasonable <span>accommodations/adjustments</span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span>adastaffingsupport&#64;bms.com</span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p></p><p>Bristol Myers Squibb is Disability Confident – Employer</p><p></p><p>A UK Government scheme</p><p></p><p><b>Candidate Rights</b></p><p>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</p><p></p><p><b>Data Protection</b></p><p>We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank">https://careers.bms.com/fraud-protection</a>.</p><p></p><p>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1600845 : Senior Manager, Data Sciences]]></description><link>http://biotechroles.com/senior-manager-data-sciences-bristol-myers-squibb/6a0899142f1861929d253396</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-data-sciences-bristol-myers-squibb/6a0899142f1861929d253396</guid><pubDate>Sat, 16 May 2026 16:19:32 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Uxbridge - GB</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Hematology- Greenville, NC]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>This territory includes: <span>Norfolk, VA , Greenville NC, Wilmington, NC</span></p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602423 : Senior Therapeutic Area Specialist, Hematology- Greenville, NC]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-hematology-greenville-nc-bristol-myers-squibb/6a0899142f1861929d253395</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-hematology-greenville-nc-bristol-myers-squibb/6a0899142f1861929d253395</guid><pubDate>Sat, 16 May 2026 16:19:32 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Greenville - NC - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Technical Product Manager – Commercial Operations]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b> </p><p>Bristol Myers Squibb is seeking an experienced Technical Product Manager to join the Commercial Operations Team.  </p><p>In this role, you will serve as a key functional expert on our applications supporting Commercial Operations (US &amp; Ex-US) and Global Patient Services (GPS), bridging the gap between business stakeholders and technical delivery teams. You will lead requirements management, ensuring compliance with GxP standards and enterprise best practices. </p><p>This high-impact position demands deep business acumen, strong analytical thinking, and the ability to partner seamlessly with global, cross-functional business and technical teams in a dynamic Agile environment. </p><p></p><p><b>Key Responsibilities</b> </p><p><b>Requirements &amp; Functional Analysis</b> </p><ul><li>Own and create <b>epics, features, and user stories</b> by translating business requirements, and design outcomes, into clear, actionable backlog items. </li></ul><ul><li>Partner <b>closely with Product Owners</b> to define scope, prioritize the backlog, and align deliverables for system <b>major and minor releases</b>. </li></ul><ul><li>Lead and actively participate in <b>backlog refinement and grooming</b>, conduct requirement gap and impact analysis, and functional risk assessments, ensuring stories are well‑defined, appropriately sized, and ready for sprint execution. </li></ul><ul><li>Collaborate with cross functional teams to incorporate <b>technical design considerations, dependencies, and acceptance criteria</b> into user stories. </li></ul><ul><li>Ensure user stories align with <b>Salesforce platform standards, system architecture, and GxP/CSV compliance requirements</b>. </li></ul><ul><li>Support <b>defect triage and production issue management</b> by translating defects and incidents into prioritized backlog items and tracking them to closure. </li></ul><ul><li>Coordinate with <b>BMS HYD teams, Product Owners, and business stakeholders</b> to ensure cross‑team alignment, dependency management, and transparent communication. </li></ul><ul><li>Mentor and guide team members on requirement management best practices, sprint delivery, and release demos </li></ul><ul><li>Identify opportunities where AI-based capabilities can enhance business workflows, translation processes, release demo development, and other operational efficiencies.  </li></ul><ul><li>Drive continuous improvement and process efficiencies across releases and enhancements, including the thoughtful adoption of automation and AI-enabled capabilities </li></ul><ul><li>Support release readiness and post‑release activities by ensuring <b>deployment coordination, documentation alignment, and operational stability</b>. </li></ul><ul><li>Author and maintain GxP documentation and SDLC artifacts in adherence to pharmaceutical industry compliance standards </li></ul><p></p><p><b>Qualifications</b> </p><p><b>Education</b> </p><ul><li>Bachelor&#39;s degree in computer science, Management Information Systems, or a related field <i>(required)</i> </li></ul><p><b>Experience</b> </p><ul><li>5–7 years of experience in technical product management, enterprise application delivery, and cross-functional leadership on large enterprise implementations </li></ul><ul><li>3&#43; years of experience with Salesforce technology </li></ul><ul><li>3&#43; years of experience working in JIRA, Confluence, Figma (Wireframes) </li></ul><ul><li>2&#43; years of experience in the pharmaceutical industry <i>(preferred)</i> </li></ul><ul><li>Cell Therapy domain knowledge (<i>a plus)</i> </li></ul><ul><li>Proven experience working with onsite and offshore delivery teams; systems supporting multi-product, multi-region environments <i>(preferred)</i> </li></ul><ul><li>Experience leveraging AI-enabled tools to support business analysis activities <i>(preferred)</i> </li></ul><p></p><p><b>Certifications</b> <i>(a plus)</i> </p><ul><li>Salesforce Certifications <i>(preferred)</i>  </li></ul><p></p><p><b>Skills &amp; Competencies</b> </p><ul><li>Excellent written and verbal communication skills, with the ability to convey complex information to both business and technical audiences at all levels </li></ul><ul><li>Strong interpersonal and collaborative skills; ability to build relationships across a matrixed, global organization </li></ul><ul><li>Demonstrated ability to manage a complex vendor environment </li></ul><ul><li>Experience with Agile/Scrum methodologies and release management processes </li></ul><ul><li>Ability to evaluate, adopt, and responsibly use AI-powered tools to enhance analysis, documentation quality, and team productivity </li></ul><ul><li>Self-motivated with a continuous improvement mindset </li></ul><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>New Brunswick - NJ - US: $94,180 - $114,124&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601305 : Technical Product Manager – Commercial Operations]]></description><link>http://biotechroles.com/technical-product-manager-commercial-operations-bristol-myers-squibb/6a0899132f1861929d253394</link><guid isPermaLink="true">http://biotechroles.com/technical-product-manager-commercial-operations-bristol-myers-squibb/6a0899132f1861929d253394</guid><pubDate>Sat, 16 May 2026 16:19:31 GMT</pubDate><company>Bristol-Myers Squibb</company><location>New Brunswick - NJ - US</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Hematology- Charleston, SC]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p>This territory includes: <span>Myrtle Beach, SC, Charleston, SC and Savannah GA</span></p><p></p><p><b><span>Position Summary</span></b><span> </span></p></div><div><p><span><span>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for<span> </span></span><span>appropriate patients</span><span>. </span></span><span> </span></p></div><div><p><span><span>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the<span> </span></span><span>appropriate patients</span><span>. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (</span><span>Cx</span><span>) through deeper scientific dialogue on and consistent with label,<span> </span></span><span>leveraging</span><span><span> </span>new ways of working and CE^3.</span></span><span> </span></p><p></p></div><div><p><span><span>The role builds and<span> </span></span><span>maintains</span><span><span> </span>strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact.</span></span><span> </span></p><p></p></div><div><p><span><span>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (</span><span>Cx</span><span>) – by meeting HCP needs in<span> </span></span><span>a timely</span><span><span> </span>and scientific manner. This role will prioritize the safe and<span> </span></span><span>appropriate use</span><span><span> </span>of BMS products while also focusing on overall business results and performance<span> </span></span><span>objectives</span><span><span> </span>while exemplifying BMS values. </span></span><span> </span></p><p></p></div><div><p><span><span>The TAS role is<span> </span></span><span>field-based</span><span>. A TAS is<span> </span></span><span>anticipated</span><span><span> </span>to spend 100% of their time in the field with external customers.</span></span><span> </span></p><p></p></div><div><p><b><span>Key Responsibilities:</span></b><span> </span></p></div><div><p><b><span>Portfolio Promotion</span></b><span> </span></p></div><div><ul><li><p><span><span>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in<span> </span></span><span>appropriate patients</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages with and continuously<span> </span></span><span>maintains</span><span>/grows<span> </span></span><span>a high level</span><span><span> </span>of scientific<span> </span></span><span>expertise</span><span><span> </span>in all assigned products and therapeutic areas.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Prepares and successfully implements comprehensive territory and account plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement.</span></span><span> </span></p></li></ul></div><div><p><b><span>Fair &amp; Balanced Scientific Dialogue</span></b><span> </span></p></div><div><ul><li><p><span><span>Demonstrates scientific<span> </span></span><span>expertise</span><span><span> </span>and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with<span> </span></span><span>label</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and<span> </span></span><span>facilitating</span><span><span> </span>scheduling and<span> </span></span><span>logistics</span><span>.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Maintains<span> </span></span><span>a high level</span><span><span> </span>of working<span> </span></span><span>expertise</span><span><span> </span>on emerging data for approved indications.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages real-time medical support through<span> </span></span><span>Medical on</span><span><span> </span>Call to reactively answer unsolicited questions and complex technical inquiries.</span></span><span> </span></p></li></ul></div><div><p><b><span>Cross-functional collaboration</span></b><span> </span></p></div><div><ul><li><p><span><span>Proactively collaborates with other field teams to ensure the best Customer Experience (</span><span>Cx</span><span>) for HCPs. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Gathers and shares relevant insights and information internally with the<span> </span></span><span>appropriate stakeholders</span><span><span> </span>to enable BMS to better serve its customers.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Complies with</span><span><span> </span>all laws, regulations, and policies that govern the conduct of BMS.</span></b><span> </span></p></li></ul></div><div><p><b><span>Required Qualifications &amp; Experience</span></b><span> </span></p></div><div><ul><li><p><span><span>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated experience building and<span> </span></span><span>maintaining</span><span><span> </span>strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (</span><span>Cx</span><span>).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in Hematology/Oncology<span> </span></span><span>required</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance<span> </span></span><span>track record</span><span><span> </span>of meeting or exceeding goals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong selling and promotional skills proven through<span> </span></span><span>a track record</span><span><span> </span>of performance.</span></span><span> </span></p></li></ul></div><div><p><b><span>Key Competencies Desired</span></b><span> </span></p></div><div><p><b><span>Customer/commercial mindset</span></b><span> </span></p></div><div><ul><li><p><span><span>Demonstrated ability to drive business results.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience<span> </span></span><span>identifying</span><span>, engaging, and cultivating credibility with customers across the patient care journey.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated resourcefulness and ability to connect with customers.</span></span><span> </span></p></li></ul></div></div><div><div><p><b><span>Patient centricity </span></b><span> </span></p></div><div><ul><li><p><span><span>Understands the<span> </span></span><span>patient</span><span><span> </span>journey and experience.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a patient-focused mindset.</span></span><span> </span></p></li></ul></div><div><p><b><span>Scientific Agility </span></b><span> </span></p></div><div><ul><li><p><span><span>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data.</span></span><span> </span></p></li></ul></div><div><p><b><span>Analytical Capability:</span></b><span> </span></p></div><div><ul><li><p><span><span>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understanding how to interpret and analyze data related to BMS products, customer preferences</span><span>, clinical</span><span><span> </span>data.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use CE^3 to generate insights<span> </span></span><span>and do</span><span><span> </span>dynamic call planning.</span></span><span> </span></p></li></ul></div><div><p><b><span>Technological Agility:</span></b><span> </span></p></div><div><ul><li><p><span><span>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and<span> </span></span><span>maintain</span><span><span> </span>effective communication.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in<span> </span></span><span>a timely</span><span><span> </span>and compliant manner, track interactions, and plan future engagements with healthcare professionals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use the Medical on Call technology effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Keeping up to date with technological advancements and changes.</span></span><span> </span></p></li></ul></div><div><p><b><span>Teamwork/Enterprise mindset</span></b><span> </span></p></div><div><ul><li><p><span><span>Strong business acumen to understand and<span> </span></span><span>analyze business and market drivers</span><span><span> </span>and develop, execute, and adjust business plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrates<span> </span></span><span>a strong sense</span><span><span> </span>of learning agility. Seeks out and learns from unfamiliar<span> </span></span><span>experiences, and</span><span><span> </span>then applies those lessons to achieve better results in<span> </span></span><span>subsequent</span><span><span> </span>situations.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Track record</span><span><span> </span>of balancing individual drive and collaborative attitude.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Holds<span> </span></span><span>a high level</span><span><span> </span>of integrity and good judgment,<span> </span></span><span>in order to</span><span><span> </span>navigate the requirements of the role effectively and compliantly<span> </span></span><span>in accordance with</span><span><span> </span>BMS policies and procedures.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company.</span></span><span> </span></p></li></ul></div><div><p><span><span>#LI-Remote</span></span><span> </span></p></div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602421 : Senior Therapeutic Area Specialist, Hematology- Charleston, SC]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-hematology-charleston-sc-bristol-myers-squibb/6a0899132f1861929d253393</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-hematology-charleston-sc-bristol-myers-squibb/6a0899132f1861929d253393</guid><pubDate>Sat, 16 May 2026 16:19:31 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Charleston - SC - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Oncology/ Hematology- San Diego, CA]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>This territory includes: <span>San Diego, Oceanside, Chula Vista, Murrieta, and Escondido</span></p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602405 : Senior Therapeutic Area Specialist, Oncology/ Hematology- San Diego, CA]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-oncology-hematology-san-diego-ca-bristol-myers-squibb/6a0899122f1861929d253392</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-oncology-hematology-san-diego-ca-bristol-myers-squibb/6a0899122f1861929d253392</guid><pubDate>Sat, 16 May 2026 16:19:30 GMT</pubDate><company>Bristol-Myers Squibb</company><location>San Diego - CA - US</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Oncology - Hawaii]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>The territory includes: Hawaii</p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602406 : Senior Therapeutic Area Specialist, Oncology - Hawaii]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-oncology-hawaii-bristol-myers-squibb/6a0899122f1861929d253391</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-oncology-hawaii-bristol-myers-squibb/6a0899122f1861929d253391</guid><pubDate>Sat, 16 May 2026 16:19:30 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Honolulu - HI - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Director, CEO Communications]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><u><b>Position Summary</b></u></p><p>Working in close partnership with the VP, Corporate Communications, the Senior Director, CEO Communications serves as a strategic parter on shaping and executing an integrated CEO communications approach.  This role helps translate enterprise priorities into clear, compelling messaging and ensures the CEO’s voice is consistently reflected across key internal and external engagements.</p><p>While the VP sets overall direction and positioning, this role plays a critical part in advancing that strategy, bringing forward ideas, pressure-testing messaging and leading execution of high-impact communications initiatives.  The Senior Director operates at the center of the enterprise, collaborating closely with the CEO, Chief of Staff and Leadership Team.</p><p>This role focuses on CEO communications for prepared remarks and engagements; media strategy and interview messaging remain within Media Relations.</p><div></div><div><p></p><p><u><b>Key Responsibilities</b></u></p><p></p><p><b>CEO Communications Strategy &amp; Execution</b></p><ul><li>Partner with the VP to shape CEO communications strategy, bringing forward insights, recommendations and draft approaches aligned to enterprise priorities.</li><li>As the lead writer for the CEO, responsible for translating strategic direction into clear, actionable communications plans and ensure consistent execution across CEO engagements.</li><li>Lead end-to-end planning and delivery of CEO communications across internal and external platforms, ensuring alignment, quality and impact.</li><li>Independently drive select CEO communications initiatives (e.g., thought leadership platforms, internal engagement moments) from concept through execution.</li></ul><p></p><p><b>Content &amp; Narrative Leadership</b></p><ul><li>Develop and/or oversee high-impact CEO content, including speeches, town halls, and prepared remarks for external engagements (e.g., conference, panels, leadership forums), stepping in directly for critical moments as needed.</li><li>Shape and refine messaging to ensure clarity, consistency and alignment with enterprise narrative and priorities.</li><li>Ensure all CEO communications reflect a cohesive voice, tone and positioning across channels and audiences.</li></ul><p></p><p><b>Executive Engagement &amp; Media Alignment</b></p><ul><li>Support preparation for CEO external engagement, including development of speeches and talking points for non-media settings.</li><li>Partner closely with Media Relations to ensure alignment between CEO prepared remarks and broader external communications strategy.</li><li>Media interview preparation, media strategy and reactive messaging are led by Media Relations; this role contributes input as needed to ensure consistency.</li></ul><p></p><p><b>Executive Alignment &amp; Stakeholder Engagement</b></p><ul><li>Partner closely with the Chief of Staff and senior leaders to align CEO communications with business priorities and leadership agendas.</li><li>Act as a central connector across Corporate Affairs and key functions to ensure integrated, enterprise-wide messaging.</li><li>Build strong relationships with senior stakeholders to inform messaging and support effective storytelling</li></ul><p></p><p><u><b>Qualifications Required</b></u></p><ul><li>Significant experience supporting and advising senior executives; experience working with C-suite leaders required.</li><li>Proven ability to operate as a strategic partner, bringing forward ideas, shaping messaging and influencing senior stakeholders.</li><li>Strong executive presence and judgement, with the ability to navigate complex, high-visibility environments.</li><li>Exceptional writing and storytelling skills with experience developing executive-level communications for high-impact moments.</li><li>Bachelor’s degree in communications, Journalism, Public Relations, English, or a related field</li><li><b>15&#43; years</b> of progressive experience in corporate communications, executive communications, or a related discipline, with significant experience in a large, complex, matrixed organization</li><li>At least<b> 4&#43; years</b> of senior leadership experience, including direct advisory responsibilities at the executive or C-suite level.</li><li>Demonstrated expertise in developing and executing CEO or C-suite communications strategies across internal and external audiences.</li><li>Proven experience crafting high-impact executive content including speeches, talking points, town halls, and written leadership communications.</li><li>Strong track record of managing sensitive and high-stakes communications with sound judgment and discretion.</li><li>Exceptional written and verbal communications skills, with the ability to capture and reflect executive voice authentically and consistently.</li><li>Experience collaborating cross-functionally with Media Relations, Legal, Government Affairs, and other key enterprise partners.</li></ul><p></p><p><b>Preferred</b></p><ul><li>Advanced degree (MBA, master’s in communications, or a related field).</li><li>Experience in the biopharmaceutical, life sciences, or healthcare industry.</li><li>Familiarity with global communications environments and diverse stakeholder audiences.</li><li>Experience supporting CEO or enterprise-level thought leadership and external positioning strategies.</li></ul><div></div><p></p><p><b>Core Competencies</b></p><ul><li><b>Strategic Vision:</b> Ability to develop a clear, forward-thinking CEO communications strategy that serves both immediate needs and long-term enterprise goals</li><li><b>Executive Presence &amp; Influence:</b> Trusted, credible, and composed at the most senior levels of the organization; capable of earning and maintaining the confidence of the CEO and Leadership Team</li><li><b>Exceptional Writing &amp; Storytelling:</b> Masters the art of executive voice — creating content that is compelling, clear, and authentically reflective of the CEO&#39;s perspective and the BMS enterprise narrative</li><li><b>Sound Judgment &amp; Discretion:</b> Demonstrates the highest level of confidentiality, professionalism, and integrity in all aspects of the role</li><li><b>Cross-Functional Collaboration:</b> Builds strong, productive relationships across the enterprise and operates effectively in a highly matrixed environment</li><li><b>Operational Excellence:</b> Detail-oriented, organized, and disciplined in planning, execution, and quality management across all communications deliverables</li><li><b>Agility &amp; Resilience:</b> Thrives in a fast-paced, dynamic environment and adapts quickly to shifting priorities, emerging issues, and evolving leadership needs</li></ul><p></p><p></p></div><div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $213,690 - $258,942 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602510 : Senior Director, CEO Communications]]></description><link>http://biotechroles.com/senior-director-ceo-communications-bristol-myers-squibb/6a0899112f1861929d253390</link><guid isPermaLink="true">http://biotechroles.com/senior-director-ceo-communications-bristol-myers-squibb/6a0899112f1861929d253390</guid><pubDate>Sat, 16 May 2026 16:19:29 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Specialist, QC Analytical, B2 Shift, Cell Therapy]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>Position Summary</p><p>Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts. The shift for this position is B2 (2pm-12am, Wednesday-Saturday).</p><p>Duties/Responsibilities</p><p>• Perform routine testing of in-process, final product, and stability samples.</p><p>• Perform testing for method transfer/validation/verification.</p><p>• Perform data verification, data review and review of GMP documentation for general methods.</p><p>• May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.</p><p>• Train analysts on general job duties.</p><p>• Perform other tasks as assigned.</p><p>Reporting Relationship</p><p>• This position will report to QC management.</p><p>Qualifications</p><p>Specific Knowledge, Skills, Abilities:</p><p>• Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.</p><p>• Knowledge of LIMS, ELN and laboratory data analysis systems preferred.</p><p>• Problem-solving ability/mentality, technically adept and logical.</p><p>• Ability to communicate effectively with peers, department management and cross-functional peers.</p><p>• Experience with writing technical documents preferred.</p><p>• Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.</p><p>Education/Experience/ Licenses/Certifications:</p><p>• Bachelor&#39;s degree or equivalent required, preferably in science. Netherlands: Bachelor&#39;s degree / HLO in (bioanalytical) science preferred. MLO level 4 with equivalent combination of work experience may be considered.</p><p>• 2&#43; years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.</p><p>• Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).</p><p>#LI-ONSITE</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Devens - MA - US: $40.04 - $48.52per hour&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601929 : Specialist, QC Analytical, B2 Shift, Cell Therapy]]></description><link>http://biotechroles.com/specialist-qc-analytical-b2-shift-cell-therapy-bristol-myers-squibb/6a0899112f1861929d25338f</link><guid isPermaLink="true">http://biotechroles.com/specialist-qc-analytical-b2-shift-cell-therapy-bristol-myers-squibb/6a0899112f1861929d25338f</guid><pubDate>Sat, 16 May 2026 16:19:29 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Devens - MA - US</location><salary>$85000-115000</salary><type>Full time</type></item><item><title><![CDATA[Associate, QC Microbiology, (A1), Cell Therapy]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><span>At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.</span></p><p></p><p><b>Job Summary</b></p><p></p><p><span>Bristol Myers Squibb is seeking a QC Associate to join our QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA.  The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product.  Additionally, the QC Associate will support clean utilities systems testing, environmental monitoring within the manufacturing environment, and may assist with investigations and continuous improvement efforts.  The QC Associate role is stationed in Devens, MA and reports to the Manager, QC Microbiology for the Devens CTF.</span></p><p></p><p></p><p><b>Job Responsibilities</b></p><ul><li>Perform microbiological testing and data review of in-process, batch release, and stability samples of cell therapy drug product in accordance with applicable procedures and cGMP requirements.</li><li>Perform environmental and clean utilities monitoring within the manufacturing environment.</li><li>Ensure timely completion of testing and tasks as assigned.</li><li>May train on additional test methods and provide support to a broader spectrum of testing responsibilities.</li><li>Support investigations through data gathering or interview process.</li><li>Apply scientific principles to testing and the proper use of laboratory equipment.</li><li>Communicate effectively with management regarding task completion, roadblocks, and needs.</li><li>May participate in projects and continuous improvement efforts.</li><li>Perform other tasks as assigned.</li><li>Support for QC and manufacturing operations requires shift coverage consisting of weekdays, weekends, holidays, and during adverse weather conditions.  This position works the following shift schedule:<ul><li>AM Shift: Sunday to Wednesday 6AM – 4PM</li></ul></li></ul><p></p><p><b>Qualifications and Education Requirements</b></p><ul><li>Bachelor’s degree required, preferably in the life sciences.</li><li>0-2&#43; years of relevant microbiological testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.</li><li>Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.</li><li>Prior experience in microbiology techniques (endotoxin, sterility, environmental monitoring, process gas &amp; water testing, aseptic technique) is preferred.</li><li>Knowledge of regulatory standards as they apply to GMP laboratories is preferred. </li><li>Attention to detail and demonstrated organizational skills.</li><li>Knowledge of basic electronic systems (email, MS Office, etc.) required.</li><li>Experience with LIMS and ELN computer applications preferred.</li><li>Ability to work in a high-paced team environment, meet deadlines, and prioritize work.</li><li>Ability to communicate effectively with peers and department management.</li></ul><p></p><p><span>If you want to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients’ lives through science. From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today.</span></p><p></p><p>Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p></p><p>Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.</p><p>#LI-ONSITE</p><p></p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Devens - MA - US: $35.03 - $42.45per hour&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602319 : Associate, QC Microbiology, (A1), Cell Therapy]]></description><link>http://biotechroles.com/associate-qc-microbiology-a1-cell-therapy-bristol-myers-squibb/6a0899102f1861929d25338e</link><guid isPermaLink="true">http://biotechroles.com/associate-qc-microbiology-a1-cell-therapy-bristol-myers-squibb/6a0899102f1861929d25338e</guid><pubDate>Sat, 16 May 2026 16:19:28 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Devens - MA - US</location><salary>$65000-85000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Specialist, Content & Digital Experience Capabilities - Web Product and Analytics Engineer]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p>This role serves as a Senior Specialist within the Content &amp; Digital Experience Capabilities team, bringing deep expertise in Web-based Product Builds, Web Content Management &amp; Analytics leveraging emerging AI/ML technologies to power modern, scalable digital experiences.</p><p></p><p>The individual will operate in a product-centric, agile environment, owning capabilities end-to-end from design through development &amp; deployment and ongoing/continuous optimization &amp; improvement. This role plays a critical part in shaping and delivering enterprise digital experience solutions, supporting global marketing objectives, and enhancing customer and patient engagement across channels.</p><p></p><p><b>Key Responsibilities</b></p><ul><li><p>Contributes to the evolution of the Web-based digital experience platform/products.</p></li><li><p>Design and deliver headless, API-first solutions to enable omnichannel experiences.</p></li><li><p>Integrate AI/ML-driven capabilities, including:</p></li></ul><p>o   Content personalization</p><p>o   Intelligent search and recommendations</p><p>o   Automated content generation, tagging, and metadata enrichment</p><ul><li><p>Partner with product managers to translate business needs into scalable, high-quality technical solutions.</p></li><li><p>Own features end-to-end, including development, testing, deployment, monitoring, and optimization.</p></li><li><p>Collaborate with data and AI teams to operationalize ML models within AEM workflows.</p></li><li><p>Continuously improve platform performance, scalability, security, and authoring experience.</p></li><li><p>Implement and maintain CI/CD pipelines and DevOps best practices.</p></li><li><p>Provide strategic input into the product roadmap, identifying high-value and differentiating capabilities.</p></li><li><p>Work closely with cross-functional teams (marketing, platform, delivery, analytics) to ensure alignment with business goals.</p></li><li><p>Develop and maintain a comprehensive product knowledge base, including documentation, training, roadmaps, and feature inventories.</p></li><li><p>Support product launches, experimentation, and testing initiatives.</p></li><li><p>Prototype and validate concepts using AI-powered tools to accelerate innovation.</p></li><li><p>Track and report on product performance, adoption of metrics, and business impact.</p></li><li><p>Drive product adoption through effective operating models, change management, and user enablement.</p></li><li><p>Identify opportunities for continuous improvement, cost optimization, and operational efficiency.</p></li></ul><p></p><p><b>Required Qualifications</b></p><ul><li><p>Bachelor’s or Master’s degree in Computer Science, Engineering, or a related field.</p></li><li><p>2-4 years of software development experience in an agile environment.</p></li><li><p>Strong hands-on expertise with:</p></li></ul><p>o   AEM stack: Java, OSGi, Apache Sling, JCR</p><p>o   Frontend: HTL (Sightly), HTML, CSS, JavaScript</p><p>o   Modern frontend frameworks (React, Angular, or Vue)</p><ul><li><p>Product mindset with a strong focus on user experience and business impact.</p></li><li><p>At least 1 year of experience contributing to product planning or product management.</p></li><li><p>Strong analytical, strategic, and problem-solving skills.</p></li><li><p>Ability to work effectively in a fast-paced, matrixed organization</p></li></ul><p></p><p><b>Desired Experience</b></p><ul><li><p> Deep knowledge and understanding of Adobe Experience Cloud Capabilities (i.e. AEM, Adobe Analytics)</p></li><li><p>Digital marketing or pharmaceutical industry experience.</p></li><li><p>Experience planning and delivering enterprise product capabilities with measurable KPIs.</p></li><li><p>Ability to evaluate emerging technologies and support building business cases for new investments.</p></li><li><p>Basic knowledge of CDN, DNS, Web Application Firewall</p></li><li><p>AI-powered content generation and summarization</p></li><li><p>Smart tagging in digital asset management (AEM Assets)</p></li><li><p>Chatbots or conversational interfaces integrated with AEM</p></li><li><p>Headless CMS and GraphQL in AEM and Cloud platforms (AWS, Azure, or GCP)</p></li><li><p>DevOps tooling including CI/CD pipelines, Docker, and Kubernetes.</p></li><li><p>NLP, recommendation systems, and personalization algorithms</p></li><li><p>Vector databases and semantic search (preferred)</p></li></ul><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $78,200 - $94,760 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602482 : Sr. Specialist, Content &amp; Digital Experience Capabilities - Web Product and Analytics Engineer]]></description><link>http://biotechroles.com/sr-specialist-content-and-digital-experience-capabilities-web-product-and-analytics-engineer-bristol-myers-squibb/6a0899102f1861929d25338d</link><guid isPermaLink="true">http://biotechroles.com/sr-specialist-content-and-digital-experience-capabilities-web-product-and-analytics-engineer-bristol-myers-squibb/6a0899102f1861929d25338d</guid><pubDate>Sat, 16 May 2026 16:19:28 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Technician I, QC Sample Management]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><span style="color:#4b4b4b">The QC Sample Management Technician is responsible for the movement and control of QC samples and materials, including in-process, finished drug product, characterization, retain, and stability samples processed through the QC laboratories. This includes, but is not limited to, sample collection and distribution, inventory control, chain of custody, sample tracking, and sample delivery. </span></p><p style="color:!important"><span style="color:#4b4b4b">This role works from 6AM to 6PM following a 12-hour rotating shift (36/48 hours over a 2-week period) which includes working every other weekend, holidays falling on scheduled workdays, and during adverse weather conditions in support of QC and the manufacturing facility. Flexibility to work irregular hours and short notice overtime may be required. </span></p><p style="color:!important"><span style="color:#4b4b4b"><span></span> </span></p><p style="color:!important"><span style="color:#4b4b4b">Education: </span></p><p style="color:!important"><span style="color:#4b4b4b">Associate’s degree in chemistry, Microbiology or related science; or a high school diploma/GED with 2&#43; years of relevant work experience, preferably in a regulated environment. An equivalent combination of education and experience may substitute. </span></p><p style="color:!important"><span style="color:#4b4b4b"><span></span> </span></p><p style="color:!important"><span style="color:#4b4b4b">Experience: </span></p><p style="color:!important"><span style="color:#4b4b4b">• Experience with cold chain sample storage and transfer in a GMP regulated environment is desirable. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Knowledge of basic electronic systems (email, MS Office, etc.). </span></p><p style="color:!important"><span style="color:#4b4b4b">• Experience with LIMS and ELN computer applications preferred. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Able to perform light to moderate lifting and carrying objects up to 20 lbs. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Knowledge of regulatory standards as they apply to GMP laboratories is preferred. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Attention to detail and demonstrated organizational skills. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Ability to adapt and adjust to changing priorities and to manage assignments with challenging/conflicting deadlines. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Ability to work in a high-paced team environment and meet deadlines. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Ability to communicate effectively with peers and department management. </span></p><p style="color:!important"><span style="color:#4b4b4b"><span></span> </span></p><p style="color:!important"><span style="color:#4b4b4b"><span></span> </span></p><p style="color:!important"><span style="color:#4b4b4b">DUTIES AND RESPONSIBILITIES: </span></p><p style="color:!important"><span style="color:#4b4b4b">• Handle test samples throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal. Facilitate cold chain transfers of samples. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records in accordance with regulatory requirements and written procedures. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Maintain inventory and distribution of QC samples and materials to functional groups as scheduled or requested. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Record performance metrics for the sample management group. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Support identification and implementation of process efficiencies. </span></p><p style="color:!important"><span style="color:#4b4b4b">• Communicate effectively with management regarding task completion, roadblocks, and needs. </span></p><p style="color:!important"><span style="color:#4b4b4b"><span></span> </span></p><p style="color:!important"><span style="color:#4b4b4b">WORKING CONDITIONS (US Only): </span></p><p style="color:!important"><span style="color:#4b4b4b">• The incumbent will be working around biohazardous materials and may be exposed to fluctuating and/or extreme temperatures on occasion. </span></p><p style="color:!important"><span style="color:#4b4b4b"><span></span> </span></p><p style="color:!important"><span style="color:#4b4b4b">This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. </span></p><p style="color:!important"><span style="color:#4b4b4b"><span></span> </span></p><p style="color:!important"><span style="color:#4b4b4b">This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position may be required to perform any other job-related duties as requested by management. </span></p><p style="color:!important"><span style="color:#4b4b4b">Additional Job Requirements:</span> <span style="color:#4b4b4b"> </span></p><p style="color:!important"><span style="color:#4b4b4b">Position Handles Hazardous Materials </span></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Devens - MA - US: $27.35 - $33.14per hour&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602339 : Technician I, QC Sample Management]]></description><link>http://biotechroles.com/technician-i-qc-sample-management-bristol-myers-squibb/6a08990f2f1861929d25338c</link><guid isPermaLink="true">http://biotechroles.com/technician-i-qc-sample-management-bristol-myers-squibb/6a08990f2f1861929d25338c</guid><pubDate>Sat, 16 May 2026 16:19:27 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Devens - MA - US</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Analyst, Compensation]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p>With a strong emphasis on analytical support, operational excellence, and customer-focused service delivery, the Compensation Analyst supports the administration and execution of compensation programs and processes. This role contributes to job architecture activities, market benchmarking, salary survey participation, compensation operations, and annual compensation cycle support.</p><p>Operating within a collaborative HR and Total Rewards environment, this position partners with Compensation, HR Operations, Payroll, and HRIT teams to support accurate, compliant, and efficient compensation administration. The Compensation Analyst helps ensure compensation programs and practices align with organizational guidelines, market competitiveness, and operational standards.</p><p><b>Key Responsibilities</b></p><p>• Support the administration and execution of annual compensation processes, including merit planning and incentive cycle activities.</p><p>• Prepare benchmarking data to support compensation recommendations, market competitiveness assessments, and business decision-making.</p><p>• Participate in compensation surveys, including data gathering, validation, submission, and analysis of market trends and salary positioning.</p><p>• Support job architecture activities, including job documentation, job matching and maintenance of compensation-related job data.</p><p>• Assist in maintaining salary structures, compensation records, and market pricing data to support compensation program administration.</p><p>• Participate in the implementation, and enhancement of compensation tools, systems upgrades, and operational processes that improve efficiency, data quality, and user experience.</p><p>• Support compensation operations activities including audits, data validation, and process documentation.</p><p>• Partner with HRIS, Payroll, HR Operations, and Compensation team members to ensure accurate and timely compensation administration.</p><p>• Contribute to compensation-related projects and continuous improvement initiatives across Total Rewards programs and processes.</p><p>• Support a customer-focused approach that balances operational accuracy, responsiveness, and high-quality service delivery.</p><p><b>Qualifications &amp; Experience</b></p><p>Bachelor’s degree in Human Resources, Business Administration, Finance, Economics, or related field preferred.</p><p>Typically requires 1–3 years of experience in Compensation, Total Rewards, HR Analytics, Finance, or related analytical function.</p><p>Experience supporting compensation analysis, market benchmarking, salary surveys, or HR operations activities preferred.</p><p>Strong analytical and quantitative skills with high attention to detail and data accuracy.</p><p>Proficiency in Microsoft Excel and familiarity with HR systems, preferably Workday and compensation tools.</p><p>Ability to manage multiple priorities and work effectively in a fast-paced, collaborative environment.</p><p>Strong written and verbal communication skills with the ability to present information clearly and professionally.</p><p>Demonstrated ability to work collaboratively and build strong partnerships across HR and business functions.</p><p><b>Minimum Requirement / Knowledge Desired:</b></p><p>Bachelor’s Degree or equivalent progressive work experience required.</p><p>Basic knowledge of compensation principles, market benchmarking, salary surveys, and compensation administration practices.</p><p>Strong analytical, organizational, and problem-solving skills.</p><p>Experience working with HRIS systems, reporting tools, or compensation platforms preferred.</p><p>Familiar knowledge of AI tools and technology and their application in HR, analytics, and compensation processes.</p><p>Ability to handle sensitive and confidential information with discretion.</p><p>Strong customer service orientation and attention to detail.</p><p></p><p><b>Direct Reports</b></p><p>None</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Tampa - FL - US: $64,940 - $78,692&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602505 : Analyst, Compensation]]></description><link>http://biotechroles.com/analyst-compensation-bristol-myers-squibb/6a08990f2f1861929d25338b</link><guid isPermaLink="true">http://biotechroles.com/analyst-compensation-bristol-myers-squibb/6a08990f2f1861929d25338b</guid><pubDate>Sat, 16 May 2026 16:19:27 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Tampa - FL - US</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Hematology - Buffalo, NY]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p>This territory includes: <span>Buffalo, Amherst, Williamsville, Batavia, Rochester, Pittsford, Brighton, Fairport</span></p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p></div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602466 : Senior Therapeutic Area Specialist, Hematology - Buffalo, NY]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-hematology-buffalo-ny-bristol-myers-squibb/6a08990e2f1861929d25338a</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-hematology-buffalo-ny-bristol-myers-squibb/6a08990e2f1861929d25338a</guid><pubDate>Sat, 16 May 2026 16:19:26 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Field - United States - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison, Cardiovascular - Milvexian (Pacific Northwest)]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p></p><p><b><span>Position:</span><span> Medical Science Liaison, Cardiovascular - Milvexian</span><br /><span><span>Location</span><span>: Field - Pacific Northwest (Seattle/Portland)</span></span></b></p><p><br /><span><span>The MSL role embodies our medical mission to be recognized as the trusted partner for internal stakeholders and </span>the</span> <span>healthcare community, driving scientific exchange to enhance medical education, data generation, insight generation </span><span><span>and patients’ access to medicine.  </span></span></p><p><br /><span><span>The Medical Science Liaison (MSL) is responsible for identifying disease and product related medical needs in a defined </span>geography. The primary role of the MSL is to develop and maintain relationships with Thought Leaders (TL) and </span><span><span>Healthcare Providers (HCP) within their healthcare system. The purpose of their interactions is to engage in meaningful </span>scientific exchange that will ensure patients have access to BMS medicines, to ensure their safe and appropriate use </span><span><span>through peer to peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to </span>facilitate research. The MSL also serves as the medical resource for external stakeholders in the community.</span><br /> </p><p><span><b><span>Key Responsibilities</span>:</b></span></p><p></p><p><u><span>External Environment and Customer Focus</span></u></p><ul><li><span>Develop and maintain relationships with academic and community research thought leaders, appropriate </span>HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product, and HEOR related questions.</li><li>The MSL will use various channels for interactions (1:1, group presentations, remote, etc.)</li><li><span>Demonstrate proficiency in using available scientific resources and presentations. </span></li><li><span>Effectively present </span>information to TL/HCPs and be able to respond to questions, ensuring medical accuracy and compliance <span><span>with local procedures, ethical and legal guidelines and directives. </span></span></li><li><span>Actively assess the medical landscape by meeting with TL/HCPs/Access Stakeholders to understand </span>their needs and expertise.</li><li>Continuously update own knowledge in treatment strategies, products, unmet medical needs, clinical trials, health economics outcomes research and scientific activities.</li><li>Understand the competitive landscape and evolving healthcare models and actively prepare to address informational needs of customers</li><li><span>Identify opportunities to partner with HCPs on disease state initiatives, collaborative research projects, </span>and investigator sponsored research (ISR) of interest and in alignment with BMS strategic objectives</li><li><span>Attend medical congresses and local/regional meetings. </span></li><li><span>Collect and provide meaningful medical insights </span>and/or impact by communicating these back to the medical and commercial organizations to support strategy development and business decisions</li></ul><p></p><p><u><span>Contribute to the Medical Plan</span></u></p><ul><li><span>Develop geography-specific Field Medical and TL Interaction plans based on therapeutic area objectives </span>and TLs needs</li><li><span>Adopt institution/account planning approach and contribute to cross-functional institution/account plans </span></li><li><span>Contribute to development and delivery of scientifically meaningful medical programs/projects in line with </span>the local Medical and Field Medical plan</li></ul><p></p><p><u><span>Provide Medical Support</span></u></p><ul><li><span>Establish a customer-centric, compliant collaboration with cross-matrix field teams within assigned </span>geography</li><li><span>As necessary and appropriate, support the initial and ongoing medical /scientific area and product specific </span>training and provide key scientific updates to internal stakeholders (e.g. Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Value Access &amp; Payment)</li><li><span>Provide scientific support at promotional meetings by presenting scientific and clinical data, by evaluating </span>speakers and by giving support to BMS-contracted speakers (if applicable)</li><li><span>Participate in assigned Congress activities </span></li></ul><p></p><p><u><span><span>Support Clinical Trial Activities</span></span></u></p><ul><li><span>Support Interventional and Non Interventional Research (NIR) studies (e.g. identification and assessment </span>of potential study sites) to facilitate patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with home office medical and Global Development Operations (GDO) and as defined by the study scope document</li><li><span>Provide recommendations and insights to clinical development team on study and site feasibilities within </span>the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with home office medical and GDO</li><li><span>Support HCPs in the ISR submission and execution process and study follow-up as agreed upon with </span>home office medical and GDO</li><li><span>Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators </span>of local studies, and alert appropriate BMS personnel to any identified Adverse Events</li><li><span>Actively support CRO sponsored studies as agreed with home office medical and GDO and as defined by </span>the study scope document</li></ul><p></p><p><b><span>Position Requirements:</span></b></p><ul><li><span>MD, PharmD, PhD, APP, PA, NP with experience in a specific Disease Area or with a broad medical background </span>and relevant pharmaceutical experience</li><li><span>Disease area knowledge and an understanding of scientific publications</span></li><li><span>Knowledge of a scientific or clinical area, competitive landscape and patient treatment trends </span></li><li><span>Knowledge of clinical trial design and process </span></li><li><span>Knowledge of the national healthcare and access environment </span></li><li><span>Knowledge of HEOR core concepts </span></li><li><span>Excellent English language skills, spoken and written</span></li></ul><p></p><p><u><span>Experience Desired</span></u></p><ul><li><span>A minimum of 2 years working in a clinical and/or pharmaceutical environment</span></li><li><span>Prior MSL experience</span></li><li><span>Ability to work independently and act as a team player </span></li><li><span>Translating scientific or clinical data into an understandable and valuable form to help physicians best serve their </span>patients</li><li><span>Good communication and presentation skills to present scientific and/or clinical data to research or healthcare </span>professionals</li><li><span>Developing peer-to-peer relationships with TLs, scientists and other healthcare professionals </span></li><li><span>Ability to quickly and comprehensively learn about new subject areas and environments</span></li><li><span>Demonstration of the BMS Values</span></li></ul><p></p><p><u><span>Essential Qualification</span></u></p><ul><li><span>Ability to drive a company-provided car is an essential qualification of this position. </span></li><li><span>Candidates must be </span>able to drive a BMS-provided vehicle between locations (often great distances apart) and arrive at each location ready and able to enthusiastically and efficiently demonstrate an applied knowledge of pertinent health care industry trends.</li><li>Candidates must possess a high level of ethics, integrity, and a responsible and safe driving history</li></ul><p></p><p><u><span>Travel Requirement</span></u></p><ul><li><span>Travel required. </span></li><li><span>Position is field based, MSL will be required to live in the territory which they manage or </span>within 50 miles of the territory borders</li><li><span>The MSL</span> <span>will spend the majority of their time in the field with their external customers. </span></li><li><span>Further requirements </span>based on territory assignment and team needs</li></ul><p></p><p><b><span>#LI-Remote</span></b></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $166,090 - $201,262&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1599253 : Medical Science Liaison, Cardiovascular - Milvexian (Pacific Northwest)]]></description><link>http://biotechroles.com/medical-science-liaison-cardiovascular-milvexian-pacific-northwest-bristol-myers-squibb/6a08990e2f1861929d253389</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-cardiovascular-milvexian-pacific-northwest-bristol-myers-squibb/6a08990e2f1861929d253389</guid><pubDate>Sat, 16 May 2026 16:19:26 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Seattle - WA - US</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Director, Global Pricing and Market Access Strategy Lead Immunology]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Summary:</b></p><p><span>The Director, Pricing and Market Access Strategy Lead (PASL) – Immunology will shape and drive the Global Market Access (GMAx) strategy for admilparant, a late-stage immunology asset. This is a highly strategic, high-visibility role with direct impact on how BMS positions a priority immunology asset for access success across the US and international markets.</span></p><p></p><p><span>Reporting to the Senior Director, GMAx Global Launch Strategy – Cardiovascular and Immunology, the PASL will represent integrated Market Access on the Global Product Team and partner closely with cross-functional stakeholders across Commercial, Medical, Regulatory, Clinical, Advocacy, Policy, and Business Insights &amp; Analytics, as well as with market leads worldwide. The role also includes active participation in all market access and pricing governance aspects.</span></p><p></p><p><span>Success in this position requires a motivated, inclusive, and decisive leader with deep expertise in global pricing and access, a proven track record of complex strategic decision-making, and the ability to communicate clearly and persuasively with senior leaders in an increasingly challenging global access environment.</span></p><div><p></p><p><b>Responsibilities:</b></p><p></p></div><ul><li><p><span>Lead the integrated Global Market Access strategy for admilparant in partnership with HEOR, anchored by bold and differentiated payer value propositions across clinical, humanistic, and economic dimensions.</span></p></li><li><p><span>Ensure value propositions are supported by a robust evidence base — spanning interventional, non-interventional, and real-world data.</span></p></li><li><p><span>Lead GMAx input to the Global Product Team to ensure the Market Access perspective is incorporated into development plans to optimize our registrational trial designs. Ensure study designs are supported by full evidence generation plans to meet payer needs and requirements.</span></p></li><li><p><span>Monitor the competitive access environment for immunology in partnership with Business Insights &amp; Analytics, proactively identifying pricing, reimbursement, and policy developments, and ensuring cross-functional teams are informed of the implications for admilparant and the broader portfolio</span></p></li><li><p><span>Influence brand and commercialization strategy by embedding access and pricing insights into Global Product Team decision-making, ensuring strategic choices reflect payer realities across US and international markets </span></p></li><li><p><span>Partner with HEOR and Regulatory to shape evidence generation and pursue optimal label and PRO claims that strengthen payer value propositions and maximize the long-term economic value of the asset.</span></p></li><li><p><span>Lead the Global MAx Core Value Team for admilparant</span></p></li><li><p><span>Drive the end-to-end management and execution of Market Access projects, ensuring timely delivery of key milestones and deliverables. Partner across the cross-functional matrix to align priorities, resolve dependencies, and embed access and pricing insights into brand strategy, while promoting consistency and best practice sharing across the portfolio.</span></p></li></ul><div><p></p><p><b>Qualifications:</b></p><p></p></div><ul><li><p><span>Undergraduate degree required, MBA and/or post graduate degree desired</span></p></li><li><p><span>Ideally the candidate should have a minimum of 5 years in Global Market Access, Pricing, and/or HEOR, ideally within pharma/biotech.</span></p></li><li><p><span>Understanding of the current and evolving global market access environment for Immunology products; including latest pricing, reimbursement and approaches in the marketplace and how they can be employed to advance product value propositions. </span></p></li><li><p><span>Knowledge of the product development and commercialization process including but not limited to solid scientific background or appropriate experience enabling assessment of trial design impact on payer strategies. Should also be able to interpret and critique clinical study protocols, as well as identify relevant clinical endpoints. Launch and commercialization experience desired.</span></p></li><li><p><span>Displays excellent business &amp; financial acumen, with awareness of the key issues and able to distil multiple perspectives and positions into a single set of recommendations for decision-making. </span></p></li><li><p><span>Proven ability to efficiently craft and accurately articulate access strategy to senior, cross functional, stakeholders with potentially limited understanding of the access environment in a particular disease area or region.</span></p></li><li><p><span>Demonstrated ability to lead cross-functional teams and constructively challenge cross functional partners, when needed. </span></p></li><li><p><span>Adept at navigating international, multi-lingual, and cross-functional organizational matrices within a diverse and cross-cultural work environment.</span></p></li><li><p><span>Experienced in prioritizing and managing multiple projects simultaneously and delivering results in a timely manner.</span></p></li><li><p><span>Comfortable working in a rapidly evolving landscape with a high degree of ambiguity.</span></p></li><li><p><span>Ability to travel to international congresses and BMS internal meetings.</span></p></li><li><p><span>Demonstration of all BMS Behaviors: Integrity, Inclusion, Accountability, Innovation, Passion &amp; Speed.</span></p></li></ul><p></p><p><span>#LI-Hybrid</span></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $196,390 - $237,982 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602480 : Director, Global Pricing and Market Access Strategy Lead Immunology]]></description><link>http://biotechroles.com/director-global-pricing-and-market-access-strategy-lead-immunology-bristol-myers-squibb/6a08990d2f1861929d253388</link><guid isPermaLink="true">http://biotechroles.com/director-global-pricing-and-market-access-strategy-lead-immunology-bristol-myers-squibb/6a08990d2f1861929d253388</guid><pubDate>Sat, 16 May 2026 16:19:25 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Senior Scientific Data Engineer]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>When you join BMS, you are joining a diverse, high-achieving team united by a common mission. </p><p></p><p>The Informatics and Predictive Sciences (IPS) mission is to Pioneer, Partner and Predict to drive transformative insights for patient benefit.  IPS conducts applied computational research in areas that include genomic, structural and molecular informatics, computational and systems biology, patient selection and translational biomarker research, and broader fields including knowledge science, epidemiology and machine learning—across the full lifecycle of drug discovery and development and across all therapeutic areas at BMS.   We do this in close partnership with scientific and clinical experts in the field, both inside and outside the company.   We perform innovative science to empower key data-driven decisions across a rich pipeline of next-generation medicines. In doing so, our work transforms the lives of patients, as well as our own lives and careers.</p><p></p><p>Here, you’ll get the chance to grow and thrive through opportunities that are uncommon in scale and scope. You’ll pursue innovative ideas while advancing professionally alongside some of the brightest minds in biopharma.</p><p></p><p><b>Position Summary</b></p><div><div><p></p><p><span><span>We are seeking a<span> </span></span></span><b><span>Senior Research AI Scientist</span></b><span><span><span> </span>to partner directly with discovery, translational, clinical, computational, and portfolio research teams to design, evaluate, and operationalize reusable AI-enabled capabilities for high-priority scientific needs.</span></span><span> </span></p><p></p></div><div><p><span><span>This role sits at the intersection of scientific<span> </span></span><span>expertise</span><span>, applied AI, research informatics, and platform-aligned engineering. The successful candidate will translate complex scientific questions into defensible AI workflows, reusable research tools, rigorous evaluation frameworks, and scientifically grounded agentic systems supporting use cases such as target evidence assembly,<span> </span></span><span>indication</span><span><span> </span>rationale, biomarker interpretation, translational synthesis, and decision support.</span></span><span> </span></p><p></p></div><div><p><span><span>This role calls for a scientist</span><span>-builder</span><span><span> </span>with deep AI fluency and an operating mode characterized by urgency, disciplined iteration, and tight scientific feedback loops.<span> </span></span><span>Impact will be measured by the rigor, adoption, reusability, and scientific value of delivered capabilities, including faster and better-evidenced research decisions, validated benchmarks, and patterns that scale across teams and use cases.</span></span><span> </span></p></div><div><p></p><p><b><span>Key Responsibilities</span></b><span> </span></p></div><div><ul><li><p><b><span>Partner</span></b><span><span><span> </span></span></span><b><span>with discovery, translational, clinical, computational, and<span> </span></span><span>portfolio</span><span><span> </span>scientists<span> </span></span></b><span><span>to<span> </span></span><span>identify</span><span><span> </span>high-value research opportunities for AI and translate them into AI-tractable specifications with measurable scientific success criteria.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Architect</span></b><span><span>, build, and operationalize<span> </span></span></span><b><span>agentic and multi-agent workflows for</span></b><span><span><span> </span>complex scientific tasks such as target evidence assembly,<span> </span></span><span>indication</span><span><span> </span>rationale construction, biomarker interpretation, translational synthesis, literature and evidence triangulation, and decision support.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Design reusable AI capabilities</span></b><span><span>, including agentic frameworks, evaluation harnesses, MCP-enabled tool integrations, prompt and policy libraries, and research workflows intended for adoption across multiple programs rather than single-use deployments.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Establish rigorous evaluation methodologies</span></b><span><span><span> </span>for AI-enabled research outputs and upstream data/tool quality, including expert-reviewed benchmarks, rubric-based assessments, grounding checks, uncertainty characterization, provenance review, reproducibility criteria, longitudinal monitoring, and failure-mode analysis.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Operate with urgency</span></b><span><span><span> </span>and tight scientific feedback loops, converging with scientists on working artifacts quickly and pivoting based on direct evidence, evaluation results, and stakeholder input.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Collaborate with engineering, data, IT,</span></b><span><span><span> </span>security, legal, vendor, and platform teams to ensure AI capabilities are designed with<span> </span></span><span>appropriate governance</span><span>, integration paths,<span> </span></span><span>productionization</span><span><span> </span>patterns, and credible scaling plans from<span> </span></span><span>inception</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Communicate AI opportunities</span></b><span><span>, risks, limitations, evaluation outcomes, and recommended decisions clearly to scientific, technical, and executive audiences; contribute to internal standards, reference implementations, and documentation.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Stay current</span></b><span><span><span> </span>with developments in agentic systems, evaluation<span> </span></span><span>methodology</span><span>, reasoning models, retrieval, grounding, biomedical AI tooling, and research informatics, and assess where they create practical value for Research.</span></span><span> </span></p></li></ul></div></div><div><div><p></p><p><b><span>Basic Qualifications</span></b><span> </span></p></div><div><ul><li><p>Bachelor&#39;s Degree <span><span>in computational biology, bioinformatics, genetics, biology, chemistry, pharmaceutical sciences, data science, scientific computing, or a closely related field and </span></span>7&#43; years of academic / industry experience</p></li><li><p>Or Master&#39;s Degree <span><span>in computational biology, bioinformatics, genetics, biology, chemistry, pharmaceutical sciences, data science, scientific computing, or a closely related field and</span></span> 5&#43; years of academic / industry experience</p></li><li><p>Or PhD <span><span>in computational biology, bioinformatics, genetics, biology, chemistry, pharmaceutical sciences, data science, scientific computing, or a closely related field</span></span> and 2&#43; years of academic / industry experience <span> </span></p></li></ul></div><div><p></p><p><b><span>Preferred Qualifications</span></b><span> </span></p></div><div><ul><li><p><span><span>Demonstrated track record translating complex scientific questions into AI-enabled workflows, reusable tools, evaluation frameworks, data products, or decision-support capabilities that scientists can evaluate, trust, and defend.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Substantive hands-on experience with<span> </span></span></span><b><span>modern AI and large language model methods</span></b><span><span>, including agentic workflows, multi-agent orchestration,<span> </span></span><span>GraphRAG</span><span>, scaled tool use, and MCP patterns.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated experience designing and operating scientifically rigorous<span> </span></span></span><b><span>evaluation frameworks for AI systems</span></b><span><span>, including curated benchmark datasets, expert-reviewed reference standards, rubric-based assessments, calibration and uncertainty metrics, and regression gating that has prevented quality drift in production.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Working fluency in at least one<span> </span></span></span><b><span>scientific domain relevant to drug research and development</span></b><span><span><span> </span>- including target biology, translational science, computational biology, clinical development, molecular invention, and biomarker science - sufficient to engage scientists as a peer on questions of evidence and interpretation.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Experience with knowledge graphs,</span></b><span><span><span> </span>biomedical ontologies, evidence models, disease models, gene/target models, and graph-based reasoning over heterogeneous biomedical evidence, including genetic associations, clinical outcomes, literature, omics data, assay data, and real-world data.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>A demonstrated bias toward urgency and tight iteration</span></b><span><span>: a track record of converging on working artifacts in days, iterating directly with scientific stakeholders, and pivoting decisively based on scientific feedback.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Sound engineering judgment</span></b><span><span><span> </span>regarding when to reuse existing platform components, when to extend them, when to maintain a prototype, and when to transition a capability to platform engineering for<span> </span></span><span>productionization</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Excellent written and verbal communication skills and a demonstrated ability to align scientific, technical, and executive audiences around practical AI opportunities and evaluation results.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Remote - United States - US: $128,890 - $156,179&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602118 : Senior Scientific Data Engineer]]></description><link>http://biotechroles.com/senior-scientific-data-engineer-bristol-myers-squibb/6a08990d2f1861929d253387</link><guid isPermaLink="true">http://biotechroles.com/senior-scientific-data-engineer-bristol-myers-squibb/6a08990d2f1861929d253387</guid><pubDate>Sat, 16 May 2026 16:19:25 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Remote - United States - US</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison, NMOSD & gMG-Rare Disease -  W. NC, SC]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Medical Affairs<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Medical Science Liaison, <span>NMOSD &amp; gMG-Rare Disease</span></b></p><p><b><span>Territory: </span> <span> </span></b> <span>W. NC, SC</span></p><p></p><p><b>What you will do</b></p><p>In this vital role you will support the MSL TA head and local TA lead in developing local territory R&amp;D tactics. The MSL plays an integral role in communicating accurate, clear, and valued information regarding Amgen science and products to multiple levels within the medical community and is responsible for providing field observations to internal collaborators.</p><ul><li><p>This role will support the territory of <span>W. NC, SC</span></p></li><li><p>Engage with healthcare partners to educate and communicate clinical and scientific data to advance the scientific platform as aligned with Amgen’s company goals and objectives</p></li><li><p>Educate and communicate clinical value, outcomes, and economic data to payers, providers, key partners, advocacy, and access enablers</p></li><li><p>Respond to unsolicited inquiries consistent with the MSL compliance standards</p></li><li><p>Provide and/or present field observations and insights to internal collaborators</p></li><li><p>Implement a scientific engagement plan according to annual MSL goals and metrics</p></li><li><p>Develop and implement local OL plans in line with the scientific engagement plan</p></li><li><p>Support speaker training as requested and ensure the speakers are updated on new data</p></li><li><p>Support Amgen-sponsored research and may serve as a study lead</p></li><li><p>Liaise with potential investigators in non-sponsored clinical research</p></li><li><p>Lead and/or participate on project teams that support MSL strategies and tactics as delegated by MSL leadership</p></li><li><p>Advance the MSL value proposition, identify gaps, achieve results, and set an example for others to follow by consistently demonstrating Amgen&#39;s values and leadership attributes. Demonstrate tact and integrity when communicating and interacting with others.</p></li><li><p>Lead and support congress activities as aligned with strategy</p></li><li><p>Compliantly collaborate with cross-functional colleagues. May serve as the main point of contact</p></li><li><p>Maintain clinical acuity and expertise and ensure timely completion of assigned training. May serve as a training lead, New Hire Mentor, and/or International MSL mentor or trainer</p></li></ul><h2></h2><p><b>What we expect of you</b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a self-starter with these qualifications.</p><h2></h2><h2></h2><h2><b>Basic Qualifications:</b></h2><ul><li><p>Doctorate degree</p></li></ul><p>Or</p><ul><li><p>Master’s degree and 3 years of Medical Affairs experience</p></li></ul><p>Or</p><ul><li><p>Bachelor’s degree and 5 years of Medical Affairs experience</p></li></ul><h2></h2><h2><b>Preferred Qualifications:</b></h2><ul><li><p>PharmD, PhD, MD, or DO (Other Doctoral degrees are considered.)</p></li><li><p>Two years of proven experience in scientific or medical affairs at a biotech or pharmaceutical company</p></li><li><p>Three or more years of clinical practice, clinical research, or medical research. Experience in a medically related field can include post-doctoral training (i.e., residencies and/or fellowships)</p></li><li><p>Rare Disease therapeutic area expertise</p></li></ul><h2></h2><h2></h2><p><b>What you can expect of us</b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models, including remote and hybrid work arrangements, where possible</p></li></ul><h2></h2><h2><b>Apply now</b></h2><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><h2><b>careers.amgen.com</b></h2><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2></h2><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p></p><h2>Sponsorship</h2><p></p><p>Sponsorship for this role is not guarantee.</p><p></p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p></p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>156,998.40USD -212,409.60 USD]]></description><link>http://biotechroles.com/medical-science-liaison-nmosd-and-gmg-rare-disease-w-nc-sc-amgen/6a08984a2f1861929d253386</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-nmosd-and-gmg-rare-disease-w-nc-sc-amgen/6a08984a2f1861929d253386</guid><pubDate>Sat, 16 May 2026 16:16:10 GMT</pubDate><company>Amgen</company><location>US - North Carolina - Charlotte</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Medical Science Liaison - Uncontrolled Gout - Rare Disease - WA, OR, AK, HI, Northern CA]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Medical Affairs<h2></h2><h2><b>Job Description</b></h2><div></div><div><p><b>Join Amgen’s Mission of Serving Patients</b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Medical Science Liaison, Uncontrolled Gout - Rare Disease - WA, OR, AK, HI, Northern CA </b></p><p><b>Territory to include WA, OR, AK, HI, Northern CA (San Francisco, San Jose, Sacramento)</b></p><p></p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will serve as a scientific liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with prominent experts and clinicians throughout the US.</p><ul><li><p>Network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors, managed care decision makers, and pharmacy directors in alignment with applicable compliance, legal, and regulatory guidelines.</p></li><li><p>Understand, integrate and effectively communicate scientific/medical information and commercial value of products to the medical community and other key internal and external audiences.</p></li><li><p>Prioritize and work effectively in a self-directed manner in a constantly changing environment, including ability to obtain, integrate, and communicate customer feedback.</p></li><li><p>Pair customers’ unmet needs with available internal resources.</p></li><li><p>Collaborate effectively with all functional areas to identify opportunities and needs that can be addressed via communication of scientific, medical, and health economic information.</p></li><li><p>Identify potential new speakers and train on scientific content for sponsored external speaker programs.</p></li><li><p>Participate in national and regional conferences, meetings, and other scientific venues as appropriate to support the Medical/Clinical strategy and to obtain new competitive information, keep abreast of clinical trends, and support and maintain relationships with key investigators and scientific research.</p></li><li><p>Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.</p></li><li><p>Monitor the competitive environment for advances and trends in our therapeutic areas, including new treatment management and new therapies, as well as competitive products and features and provide feedback to the senior leadership team on specific initiatives of competitors.</p></li></ul><p></p><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a self starter with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree &amp; 2 years of Medical Affairs experience</p></li></ul><p>OR</p><ul><li><p>Master’s degree &amp; 6 years of Medical Affairs experience</p></li></ul><p>OR</p><ul><li><p>Bachelor’s degree &amp; 8 years of Medical Affairs experience</p></li></ul><p></p><p></p><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered)</p></li><li><p>2 &#43; years in a medical science liaison role in a biotech or pharmaceutical company</p></li><li><p>Exceptional oral and written communication and interpersonal skills (including strong demonstration of ability to network) required.</p></li><li><p>Ability to travel up to 60% for territory management, attendance at regional and national conferences/workshops, and attendance at company meetings.</p></li><li><p>There may be a need to work up to 15-hour days due to travel</p></li><li><p>Must have ability to learn to use new business applications across hardware tools (e.g., PC, iPad).</p></li><li><p>Proficient in Microsoft Office.</p></li><li><p>Professional, proactive demeanor.</p></li><li><p>Strong interpersonal skills.</p></li><li><p>Excellent written and verbal communication skills.</p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models, including remote and hybrid work arrangements, where possible</p></li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p></p><p><b>Application deadline</b></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>172,344.30USD -233,171.70 USD]]></description><link>http://biotechroles.com/sr-medical-science-liaison-uncontrolled-gout-rare-disease-wa-or-ak-hi-northern-ca-amgen/6a08984a2f1861929d253385</link><guid isPermaLink="true">http://biotechroles.com/sr-medical-science-liaison-uncontrolled-gout-rare-disease-wa-or-ak-hi-northern-ca-amgen/6a08984a2f1861929d253385</guid><pubDate>Sat, 16 May 2026 16:16:10 GMT</pubDate><company>Amgen</company><location>US - Washington - Seattle</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison, IgG4 - Rare Disease - Mississippi/Alabama/FL Panhandle]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Medical Affairs<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Medical Science Liaison, IgG4 - Rare Disease </b></p><p><b>Territory to include Mississippi/Alabama/FL Panhandle</b></p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will serve as a scientific liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with prominent experts and clinicians throughout the US.</p><ul><li><p>Network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors, managed care decision makers, and pharmacy directors in alignment with applicable compliance, legal, and regulatory guidelines.</p></li><li><p>Understand, integrate and effectively communicate scientific/medical information and commercial value of products to the medical community and other key internal and external audiences.</p></li><li><p>Prioritize and work effectively in a self-directed manner in a constantly changing environment, including ability to obtain, integrate, and communicate customer feedback.</p></li><li><p>Pair customers’ unmet needs with available internal resources.</p></li><li><p>Collaborate effectively with all functional areas to identify opportunities and needs that can be addressed via communication of scientific, medical, and health economic information.</p></li><li><p>Identify potential new speakers and train on scientific content for sponsored external speaker programs.</p></li><li><p>Participate in national and regional conferences, meetings, and other scientific venues as appropriate to support the Medical/Clinical strategy and to obtain new competitive information, keep abreast of clinical trends, and support and maintain relationships with key investigators and scientific research.</p></li><li><p>Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.</p></li><li><p>Monitor the competitive environment for advances and trends in our therapeutic areas, including new treatment management and new therapies, as well as competitive products and features and provide feedback to the senior leadership team on specific initiatives of competitors.</p></li></ul><p></p><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a self starter with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree</p></li></ul><p>OR</p><ul><li><p>Master’s degree &amp; 3 years of Medical Affairs experience</p></li></ul><p>OR</p><ul><li><p>Bachelor’s degree &amp; 5 years of Medical Affairs experience</p></li></ul><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li>Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered)</li><li>2 years of proven experience in scientific or medical affairs at a biotech or pharmaceutical company</li><li>Exceptional oral and written communication and interpersonal skills (including strong demonstration of ability to network) required.</li><li>Ability to travel up to 60% for territory management, attendance at regional and national conferences/workshops, and attendance at company meetings.</li><li>There may be a need to work up to 15-hour days due to travel</li><li>Must have ability to learn to use new business applications across hardware tools (e.g., PC, iPad).</li><li>Proficient in Microsoft Office.</li><li>Professional, proactive demeanor.</li><li>Strong interpersonal skills.</li><li>Excellent written and verbal communication skills.</li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models, including remote and hybrid work arrangements, where possible</li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p></p><p><b>Application deadline</b></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>156,998.40USD -212,409.60 USD]]></description><link>http://biotechroles.com/medical-science-liaison-igg4-rare-disease-mississippialabamafl-panhandle-amgen/6a08984a2f1861929d253384</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-igg4-rare-disease-mississippialabamafl-panhandle-amgen/6a08984a2f1861929d253384</guid><pubDate>Sat, 16 May 2026 16:16:10 GMT</pubDate><company>Amgen</company><location>US - Alabama - Birmingham</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Director Observational Research]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Clinical<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><h2><b>Dir Observational Research</b></h2><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will leads the company&#39;s strategic planning initiatives and oversees its operational performance, working with leaders across the organization to implement the strategic vision.</p><p>Do you want an exciting position working with multiple teams to generate real-world evidence supporting a wide variety of business needs?</p><p>The growing demand for real-world evidence (RWE) from regulatory and reimbursement authorities makes observational research a key component of drug development and commercialization. Amgen&#39;s Center for Observational Research (CfOR) is a global organization with an industry-leading analytical capability that generates RWE to support business needs across a product’s lifecycle. CfOR scientists partner with internal collaborators and industry experts to craft, conduct, interpret, and publish observational research that advises decision-making from the early development of a molecule to the design of clinical trials and the safety and efficacy of Amgen medicines. CfOR studies include but are not limited to evidence generation regarding the frequency and distribution of disease, the clinical burden of disease, the natural history or clinical course of the disease, the design of clinical trials, treatment cost, and utilization patterns, and the safety and efficiency of therapeutic interventions.</p><p><b>Job Description</b></p><p>Amgen is searching for a Director of Observational Research, who will lead an asset in the Oncology therapeutic area. A CfOR director is recognized as a strong scientific contributor and is a first or contributing author for papers in peer-reviewed journals or for internal reports that enhance the company’s mission. Working with the cross-functional teams, the Director will be responsible for establishing strategic direction, and providing technical and managerial leadership through:</p><ul><li>Designing and executing studies to support evidence generation such as identifying appropriate patient populations, assessing disease burden and resource utilization, obtaining product registrations and label-expansions, meeting post-marketing requirements/commitments and product differentiation.</li><li>Finding opportunities to substitute for and/or complement interventional studies to reduce time and cost of drug development.</li><li>Influencing cross-functional stakeholders in the utilization and timing of non-interventional research to answer high-priority strategic business questions.</li><li>Leveraging real-world data and CfOR analytic approaches to inform high-value business decisions for multiple partners.</li><li>Tracking business and functional priorities and aligning resources for those priorities.</li><li>Contributing to the mission of the CfOR including progressing innovative epidemiological methods and analytical capabilities to support the CfOR’s leadership role within Amgen and the industry.</li><li>Effectively leading, developing and mentoring staff and teams.</li><li>Participating in initiatives to improve capabilities within the CfOR and providing input.</li><li>Supporting the development of product and CfOR strategies.</li><li>Developing and maintaining relationships with organizational leaders.</li></ul><p></p><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a leader with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 4 years of scientific experience OR</p><p>Master&#39;s degree and 7 years of scientific experience  OR</p><p>Bachelor&#39;s Degree and 9 years of scientific experience OR</p><p>Associate’s degree and 10 years of scientific experience OR</p><p>High school diploma / GED &amp; 12 years of scientific experience</p><p><b>Preferred Qualifications:</b></p><h2>•Doctorate in Epidemiology or other subject with high observational research content</h2><h2>•Experience in the design, execution, and analysis of observational research studies within Pharmaceutical or Public Health setting</h2><h2>•Experience in research to support drug development</h2><h2>•Experience in observational research project planning and management</h2><h2>•Excellent verbal and writing communication and interpersonal skills</h2><h2>•Experience working in multi-disciplinary teams</h2><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>202,250.70USD -273,633.30 USD]]></description><link>http://biotechroles.com/director-observational-research-amgen/6a0898492f1861929d253383</link><guid isPermaLink="true">http://biotechroles.com/director-observational-research-amgen/6a0898492f1861929d253383</guid><pubDate>Sat, 16 May 2026 16:16:09 GMT</pubDate><company>Amgen</company><location>United States - Remote</location><salary>$160000-240000</salary><type>Full time</type></item><item><title><![CDATA[Specialty Account Manager - Tepezza - Ocular - Dallas, TX (East) (Rare Disease)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p>Territory: Dallas, Plano, McKinney, Richardson, Sherman-Denison, Tyler and Longview.</p><p></p><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p><b>Account Manager/Specialty Account Manager - TEPEZZA</b></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will be responsible for representing TEPEZZA to physicians and health care professionals, establishing product sales, and performing total territory account management.</p><p>The Specialty Account Manager is responsible for providing account management support to accounts within a specific geography in the designated marketplace with a focus on issues specific to their designated accounts. The SAM acts as central account manager; responsible for driving product demand and coordinating relevant field teams to address account needs.</p><p><b>Responsibilities</b></p><ul><li><p>Develops a comprehensive and effective territory business plan aimed at achieving and exceeding annual sales goals established by sales and business unit leadership.</p></li><li><p>Promotes TEPEZZA within approved labeling in a comprehensive, fair and ethical manner that is consistent with industry specific and corporate legal and regulatory guidelines.</p></li><li><p>Addresses issues related to access, pull-through, and reimbursement by coordinating with key stakeholders and matrix team members.</p></li><li><p>Develops strong customer relationships by better understanding the customer’s needs and goals and communicating those needs and goals to other team members.</p></li><li><p>Consistently meets or exceeds corporate sales goals.</p></li><li><p>Communicates territory activity in an accurate and timely manner as directed by management.</p></li><li><p>Drive product demand among targets through education on disease state and product information.</p></li><li><p>Provides feedback to sales and business unit leadership, colleagues, and other internal departments about changing environment and results.</p></li><li><p>Adheres to the Company’s compliance policies and guidelines as well as any other applicable guidelines, including but not limited to the PhRMA code.</p></li><li><p>Must be able to work closely with patient services and market access team members, and understand their roles, to achieve overall business goals,</p></li><li><p>Coordinate between accounts and relevant Amgen field teams to support full range of account needs,</p></li><li><p>Educate healthcare professionals and office staff on site of care options.</p></li><li><p>Attends medical congresses and society meetings as needed.</p></li><li><p>Manages efforts within assigned promotional and operational budget.</p></li><li><p>Maximizes use of approved resources to achieve territory and account level goals</p></li><li><p>Successfully completes all Company training classes.</p></li><li><p>Completes administrative duties in an accurate and timely fashion.</p></li><li><p>Functions as a contributing member of a high-performance team.</p></li><li><p>Perform such other tasks and responsibilities as requested by the Company.</p></li></ul><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The Specialty Account Manager we seek is a motivated professional with these qualifications.</p><p><b>Basic Qualifications (Account Manager – Level 4)</b></p><p>Bachelor&#39;s Degree and 3 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />Associate degree and 6 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />High school diploma/GED and 8 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience</p><p><b>Basic Qualifications (Specialty Account Manager – Level 5)</b></p><p>Doctorate degree &amp; 2 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Master’s degree &amp; 6 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Bachelor’s degree &amp; 8 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Associate degree &amp; 10 years of collective account management experience, sales, &amp; commercial experience</p><p><b>Preferred Qualifications:</b></p><ul><li><p>Buy-and-bill experience with documented success and/or biologic/infusion experience strongly preferred.</p></li><li><p>Sales experience in Endocrinology, Ophthalmology, and/or rare/specialty disease states preferred.</p></li><li><p>Site of care and reimbursement experience strongly preferred.</p></li><li><p>Experience working with institutions and integrated delivery networks preferred.</p></li><li><p>Pharma account management selling experience essential; must be able to coordinate across field teams to address full range of account needs.</p></li><li><p>Approximately 80% travel (may vary by territory), including some overnight and weekend commitments.</p></li><li><p>Proficient in Microsoft Office.</p></li><li><p>Professional, proactive demeanor.</p></li><li><p>Strong interpersonal skills.</p></li><li><p>Excellent written and verbal communication skills.</p></li></ul><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.</p><p><i>The annual base salary range for the Account Manager opportunity in the U.S. is $ 154,736 to $ 183,900. This range is also referenced below.</i></p><p><i>The annual base salary range for the Specialty Account Manager opportunity is the U.S. is  $160,397 to  $190,628.</i></p><p>Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models, including remote work arrangements, where possible</p></li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>Application deadline</p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/specialty-account-manager-tepezza-ocular-dallas-tx-east-rare-disease-amgen/6a0898492f1861929d253382</link><guid isPermaLink="true">http://biotechroles.com/specialty-account-manager-tepezza-ocular-dallas-tx-east-rare-disease-amgen/6a0898492f1861929d253382</guid><pubDate>Sat, 16 May 2026 16:16:09 GMT</pubDate><company>Amgen</company><location>US - Texas - Dallas</location><salary>$110000-160000</salary><type>Full time</type></item><item><title><![CDATA[Project Coordinator, Senior Manager, Obesity]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Project Management<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><h2><b>Project Coordinator, Senior Manager, Obesity</b></h2><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. The Project Coordinator, Senior Manager, Obesity will be embedded in the Obesity Intelligence &amp; Analytics team, helping the team stay focused, organized, and connected to the market research and analytics that inform strategy. This role will partner closely with the Obesity Intelligence &amp; Analytics Executive Director to translate priorities across Amgen global offices into clear workplans, decision-ready deliverables, and timely cross-functional execution.</p><p>This individual must bring a consulting mindset, commercial judgment, digital curiosity, and strong organizational agility as part of a global commercial insights and analytics team. They will connect primary market research, competitive intelligence, secondary analytics, internal knowledge, and approved AI-enabled ways of working to align stakeholders, strengthen team culture, and deliver high-quality insights for product strategy, brand building, and governance milestones.</p><p></p><p><b>Flexible Commuter role to the Thousand Oaks, CA office. You will work on-site a minimum of 2-3 days a week</b></p><ul><li>Partner closely with the Obesity Intelligence &amp; Analytics Executive Director as an embedded extension of the team, translating priorities into workstreams, decision points, timelines, owners, and follow-through</li><li>Coordinate inputs and handoffs across Amgen offices located globally, market research, analytics, competitive intelligence, brand, medical, access, governance, and other partners to keep priority work connected and on track</li><li>Help frame business questions, connect them to research and analytics approaches, and ensure deliverables are decision-ready and grounded in clear implications</li><li>Maintain practical team operating rhythms, leadership and decision forums, timelines, onboarding/training resources, and knowledge management routines</li><li>Champion responsible adoption and evolution of approved AI use, identifying practical use cases for insight synthesis, planning, communications, and workflow efficiency</li><li>Identify dependencies, risks, and trade-offs; flex across insight synthesis, leadership communications, vendor coordination, team culture development, and ad hoc problem solving as needed</li></ul><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a project coordinator with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 2 years of project coordination/management, forecasting, analytics, market insights, finance, strategy, or commercial planning experience</p><p>OR</p><p>Master’s degree and 4 years of project coordination/management, forecasting, analytics, market insights, finance, strategy, or commercial planning experience</p><p>OR</p><p>Bachelor’s degree and 6 years of project coordination/management, forecasting, analytics, market insights, finance, strategy, or commercial planning experience</p><p>OR</p><p>Associate’s degree and 10 years of project coordination/management, forecasting, analytics, market insights, finance, strategy, or commercial planning experience</p><p>OR</p><p>High school diploma / GED and 12 years of project coordination/management, forecasting, analytics, market insights, finance, strategy, or commercial planning experience</p><p><b>Preferred Qualifications:</b></p><ul><li>Experience in commercial insights, analytics, market research, or strategy roles within pharma, biotech, or related healthcare</li><li>Ability to translate ambiguous business questions into structured workplans, research or analytics approaches, and decision-ready outputs</li><li>Demonstrated success driving cross-functional alignment across matrixed or multi-office teams and keeping complex insight workstreams on track</li><li>Ability to synthesize primary market research, secondary analytics, competitive intelligence, and internal knowledge into clear implications</li><li>Comfort exploring approved AI-enabled tools, automation, and knowledge management approaches to improve team effectiveness with sound judgment and appropriate governance</li><li>Experience supporting onboarding, training, ways of working, communication routines, or team culture-building activities</li><li>High ownership, judgment, discretion, and follow-through; collaborative communicator able to anticipate needs, simplify complex information, and flex between strategic thinking and hands-on execution</li></ul><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>137,340.45USD -185,813.55 USD]]></description><link>http://biotechroles.com/project-coordinator-senior-manager-obesity-amgen/6a0898492f1861929d253381</link><guid isPermaLink="true">http://biotechroles.com/project-coordinator-senior-manager-obesity-amgen/6a0898492f1861929d253381</guid><pubDate>Sat, 16 May 2026 16:16:09 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Coordinador Administrativo]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Administrative<h2></h2><h2><b>Job Description</b></h2><p><b>ÚNETE A LA MISIÓN DE AMGEN DE SERVIR A LOS PACIENTES </b></p><p></p><p>En Amgen si te sientes parte de algo más grande es porque lo eres. Nuestra misión compartida: servir a pacientes que viven con enfermedades graves, impulsa todo lo que hacemos. Desde 1980, hemos ayudado a ser pioneros en el mundo de la biotecnología en nuestra lucha contra las enfermedades más graves del mundo. Con nuestro enfoque en cuatro áreas terapéuticas –Oncología, Inflamación, Medicina General y Enfermedades Raras– llegamos a millones de pacientes cada año. Como miembro del equipo de Amgen, ayudará a generar un impacto duradero en las vidas de los pacientes mientras investigamos, fabricamos y entregamos medicamentos innovadores para ayudar a las personas a vivir vidas más largas y felices. Nuestra cultura galardonada es colaborativa, innovadora y basada en la ciencia. Si te apasionan los desafíos y las oportunidades que se presentan en ellos, prosperará como parte del equipo de Amgen. Únete a nosotros y transforma las vidas de los pacientes mientras transformas tu carrera.</p><p></p><p>Es momento de que tengas esa carrera de la que puedas estar orgulloso. ¡Únete a la familia Amgen!</p><h1></h1><h1><b>Coordinador Administrativo</b></h1><p></p><p>El Coordinador Administrativo será responsable de brindar soporte integral a la unidad de Medicina General, asegurando la correcta gestión administrativa, logística y presupuestal de las actividades promocionales. El rol contribuye al cumplimiento de los procesos internos, las políticas corporativas y el uso eficiente de los recursos, apoyando de manera transversal a los equipos comerciales y a las áreas internas involucradas.</p><p></p><p><b>Responsabilidades Principales</b></p><p></p><p><b>Gestión de material promocional</b></p><ul><li>Coordinar el envío, revisión, aprobación y seguimiento de materiales promocionales a través de la plataforma corporativa de aprobaciones globales.</li><li>Elaborar reportes bimestrales junto con los responsables de asuntos regulatorios para gestionar la correcta vigencia y destrucción de materiales promocionales físicos y digitales.</li><li>Coordinar despachos y recolecciones de material necesarios para actividades promocionales y eventos de la unidad.</li></ul><p></p><p><b>Gestión de órdenes de compra</b></p><ul><li>Someter a aprobación todas las órdenes de compra de la unidad, garantizando que cuenten con aprobación previa al inicio de cada servicio o entrega de material.</li><li>Enviar reportes de facturación pendiente de radicación al equipo de Medicina General, según sea requerido.</li></ul><p></p><p><b>Creación y gestión de proveedores</b></p><ul><li>Revisar la documentación de personas naturales y jurídicas, asegurando el cumplimiento de los requisitos mínimos para la creación de proveedores en el sistema corporativo correspondiente.</li><li>Gestionar el registro y seguimiento de proveedores de la unidad.</li></ul><p></p><p><b>Apoyo presupuestal</b></p><ul><li>Mantener actualizado el control de órdenes de compra para apoyar la revisión de ejecución presupuestal, provisiones y carga de información en la herramienta corporativa de planeación.</li><li>Garantizar la optimización del presupuesto destinado al almacenamiento y distribución de material promocional.</li></ul><p></p><p><b>Gestión de actividades promocionales y patrocinios</b></p><ul><li>Asegurar la correcta apertura y cierre de actividades promocionales y patrocinios a terceros, incluyendo los soportes correspondientes y el cumplimiento de los tiempos establecidos por las políticas internas.</li><li>Dar seguimiento a la fuerza de ventas para garantizar la entrega oportuna de evidencias requeridas para el cierre administrativo de actividades y eventos.</li></ul><p></p><p><b>Desarrollo del equipo y soporte transversal</b></p><ul><li>Capacitarse de manera continua en la herramienta de gestión comercial para brindar un soporte efectivo al equipo.</li><li>Brindar soporte a las áreas transversales en el uso de herramientas corporativas administrativas y comerciales.</li><li>Diseñar e implementar iniciativas de comunicación interna con recomendaciones prácticas para el uso correcto de las herramientas disponibles.</li></ul><p></p><p><b>Lo que esperamos de ti</b></p><p></p><p>Todos somos diferentes, sin embargo, podemos contribuir con nuestras singularidades a nuestra misión, servir a los pacientes. El profesional que buscamos deberá haber adquirido los conocimientos y habilidades vitales para desempeñar las funciones de este puesto mediante la siguiente combinación de educación, experiencia y conocimientos o su equivalente.</p><p></p><p><b>Requisitos básicos:</b></p><ul><li>Experiencia previa en roles administrativos o de coordinación, idealmente en el sector farmacéutico.</li><li>Experiencia en gestión de órdenes de compra, proveedores y seguimiento presupuestal.</li><li>Manejo de herramientas corporativas y sistemas administrativos.</li><li>Alto nivel de organización, atención al detalle y capacidad de seguimiento.</li><li>Habilidades de comunicación, trabajo en equipo y orientación al cumplimiento de procesos.</li><li>Capacidad para trabajar con múltiples actores y gestionar prioridades de manera efectiva.</li></ul><p></p><p><b>Lo que puedes esperar de nosotros</b></p><p></p><p>Así como trabajamos para desarrollar tratamientos para cuidar a nuestros pacientes, también trabajamos para cuidar la carrera profesional y crecimiento personal de nuestros colaboradores.</p><ul><li>Oportunidades para aprender y crecer en la organización a nivel global.</li><li>Una comunidad de diversidad e inclusión donde los colaboradores son empoderados para poner sus ideas en la mesa y desarrollarlas.</li><li>Beneficios competitivos</li></ul><p></p><p>Únete a nosotros. careers.amgen.com</p><p></p><p>Amgen es un empleador de Igualdad de Oportunidades y te considerará sin importar tu raza, color, religión, sexo, orientación sexual, identidad de género, origen nacional o estatus de discapacidad, asegurando que nuestros procesos sean transparentes y accesibles para todos.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/coordinador-administrativo-amgen/6a0898472f1861929d253380</link><guid isPermaLink="true">http://biotechroles.com/coordinador-administrativo-amgen/6a0898472f1861929d253380</guid><pubDate>Sat, 16 May 2026 16:16:07 GMT</pubDate><company>Amgen</company><location>Colombia - Bogota</location><salary>$18000-30000</salary><type>Full time</type></item><item><title><![CDATA[Sr Mgr Local Study Operations]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Clinical Development<h2></h2><h2><b>Job Description</b></h2><p> <b>Join Amgen’s Mission of Serving Patients </b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><h1></h1><h1><b>Sr Mgr Local Study Operations </b></h1><p></p><p><b>What you will do </b></p><p></p><p>Let’s do this. Let’s change the world. In this role, you will lead the skill development of Local Study Operations Managers (LSOM), ensuring effective trial implementation within the country and strong alignment with global strategies. You will oversee the delivery of the country’s study portfolio—managing scope, timelines, and budgets—through the leadership of LSOM. Working in close partnership with the Country GSSO Head, you will help foster, enhance, and sustain an optimal clinical research environment that supports global R&amp;D objectives. Additionally, you will drive alignment and continuous improvement in LSOM execution by integrating best practices, promoting digital innovation, and facilitating robust knowledge sharing across the team.</p><p></p><p><span class="emphasis"><b>IMPORTANT PLEASE READ! PLEASE SUBMIT YOUR CV IN ENGLISH</b></span></p><p></p><p><b>Key accountabilities</b></p><ul><li>Ensure the successful delivery of the study portfolio assigned to LSOMs.</li><li>Oversee LSOMs’ fulfillment of responsibilities throughout the assigned country portfolio, from feasibility through to study close-out.</li><li>Monitor portfolio progress, provide risk and quality oversight, and support issue escalation and resolution for LSOMs.</li><li>Manage LSOM and LSOM vendor performance to guarantee high-quality study execution, serving as the primary escalation point for local study challenges, driving solutions, and ensuring portfolio targets are met within the country.</li><li>Mentor, train, and support the professional development of LSOMs to prepare them for managing complex trials.</li><li>Build and maintain a high-performing team.</li><li>Facilitate close collaboration between the study strategy team and local study teams to effectively manage the assigned portfolio.</li><li>Promote cross-functional collaboration among country teams to ensure successful delivery of the country portfolio.</li><li>Support discussions regarding study placement decisions based on country capabilities and growth potential.</li><li>Proactively evaluate risks, quality trends, and resource requirements; implement mitigation strategies and drive continuous improvement in country operations.</li><li>Lead initiatives to enhance operational efficiency and encourage sharing of best practices.</li><li>Manage resource allocation and workload distribution across LSOMs, including both FSP and FTE personnel, to optimize trial execution and align with global priorities.</li><li>Ensure adherence to regulatory and quality standards where applicable.</li><li>Collaborate with and support the country head in engaging cross-functional stakeholders, aligning on trial deliverables, and managing escalations.</li></ul><p></p><p><b>What we expect of you </b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.</p><p></p><p><b>Basic Qualifications: </b></p><ul><li>Doctorate degree &amp; 2 years of clinical execution experience OR</li><li>Master’s degree &amp; 6 years of clinical execution experience OR</li><li>Bachelor’s degree &amp; 8 years of clinical execution experience OR</li><li>Associate’s degree &amp; 10 years of clinical execution experience OR</li><li>High school diploma / GED &amp; 12 years of clinical execution experience</li><li>In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced above</li><li>Advanced English proficiency</li></ul><p></p><p><b>Preferred Qualifications: </b></p><ul><li>7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company</li><li>Experience managing multiple teams / direct reports across multiple clinical functions / trials</li><li>Experience at, or oversight of, clinical research vendors (CRO’s, central labs, imaging vendors, etc.)</li><li>Experience managing clinical operations across relevant geography / region, including strong understanding of local regulatory requirements around global clinical trials</li></ul><p></p><p><b>What you can expect of us </b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities.</p><p></p><p><b>Apply now  for a career that defies imagination </b></p><p></p><p>Objects in your future are closer than they appear. Join us. <b>careers.amgen.com </b></p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-mgr-local-study-operations-amgen/6a0898472f1861929d25337f</link><guid isPermaLink="true">http://biotechroles.com/sr-mgr-local-study-operations-amgen/6a0898472f1861929d25337f</guid><pubDate>Sat, 16 May 2026 16:16:07 GMT</pubDate><company>Amgen</company><location>Brazil - São Paulo</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[District Sales Manager - Dermatology - Chicago, IL]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p><b>District Covers: </b>Illinois, Wisconsin, Grand Rapids, MI</p><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b> </p><p>If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.</p><p><b>District Sales Manager </b></p><p><b>Live</b> </p><p><b>What you will do</b> </p><p>Let’s do this. Let’s change the world. In this vital role you will be the connection to our customers by providing clinical knowledge of our products to medical professionals and helping them navigate the complex payer environment. </p><p>Amgen is a values-based organization with a powerful sense of shared purpose toward our mission: to serve patients. Within our US Commercial Operations (USCO), we provide the capabilities, resources, and rewards of a global enterprise, while maintaining the entrepreneurialism and verve that marked our early days as a biotechnology pioneer. We encourage our team members to have fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this District Sales Manager opportunity. </p><p>This position will require strong ability to collaborate cross-functionally with other Amgen business units including District Sales Mangers, Regional Sales Directors and Corporate Account Managers.</p><p></p><p>Additional Responsibilities and Duties Include:</p><ul><li><p>Track the progress of marketing messages and programs</p></li><li><p>Provide feedback to district teams on the marketing, allocating, monitoring, and leveraging of internal and external resources (e.g., discretionary spend)</p></li><li><p>Manage district teams to maximize their performance and help achieve/exceed sales and budget targets</p></li><li><p>Screen, interview, and hire candidates</p></li><li><p>Ensure compliance with training</p></li><li><p>Demonstrate the appropriate coaching and counseling to prepare individuals for future development</p></li><li><p>Conduct annual and on-going performance reviews and competency assessments</p></li><li><p>Communicate and coordinate with both district and cross-functional teams (e.g., Marketing, Finance, other Business Units)</p></li><li><p>Share best practices with direct reports and peers</p></li><li><p>Coordinate and/or participate in cluster teams</p></li><li><p>Conduct district sales meetings to guide districts</p></li><li><p>Develop local Opinion Leader relationships to achieve aligned objectives</p></li></ul><p></p><p><b>Win</b> </p><p><b>What we expect of you</b> </p><p>We are all different, yet we all use our unique contributions to serve patients. The sales professional we seek is a motivated individual with these qualifications.  </p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 2 years of Sales/Marketing experience</p><p>OR</p><p>Master’s degree and 6 years of Sales/Marketing experience</p><p>OR</p><p>Bachelor’s degree or and 8 years of Sales/Marketing experience</p><p>OR</p><p>Associate’s degree and 10 years of Sales/Marketing experience</p><p>OR</p><p>High school diploma / GED and 12 years of Sales/Marketing experience</p><p><b>AND</b></p><p><b>2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources.</b></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Three &#43; years of specialty sales experience</p></li><li><p>Experience in biologics</p></li><li><p>Buy and bill model experience</p></li><li><p>Ability to consistently and objectively recognize and promote success behaviors, as well as diagnose and change unsatisfactory behaviors through effective coaching</p></li><li><p>Ability to leverage market &amp; customer knowledge to strategically target messages, resources, and activities within the territory</p></li><li><p>Demonstrates knowledge of local payor coverage</p></li><li><p>Ability to understand and articulate clinical concepts, data, and conclusions</p></li><li><p>Demonstrated ability to utilize clinical information to effectively address customer questions and objections</p></li><li><p>Ability to recruit candidates that meet the minimum job criteria</p></li><li><p>Interviews and hires sales representatives that are capable and committed to fulfilling the job requirements</p></li><li><p>Strong sense of responsibility and demonstrated self-discipline</p></li><li><p>Setting appropriate short term and long term objectives; demonstrated success in communicating &amp; collaborating with sales staff, peers, business unit counterparts in an effective and timely manner.</p></li></ul><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.</p><p>Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models, including remote work arrangements, where possible</p></li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>171,117.75USD -231,512.25 USD]]></description><link>http://biotechroles.com/district-sales-manager-dermatology-chicago-il-amgen/6a0898462f1861929d25337e</link><guid isPermaLink="true">http://biotechroles.com/district-sales-manager-dermatology-chicago-il-amgen/6a0898462f1861929d25337e</guid><pubDate>Sat, 16 May 2026 16:16:06 GMT</pubDate><company>Amgen</company><location>US - Illinois - Chicago</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison (Oncology - CDMX)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. We have proudly achieved certifications as <b>Great Place to Work and Equidad MX</b>. Join us and transform the lives of patients while transforming your career.</p><h2><b>Medical Science Liaison (Oncology - CDMX)</b></h2><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will be responsible for:</p><ul><li>Engage with healthcare customers to educate and communicate clinical and scientific data to advance the scientific platform as aligned with Amgen’s goals of the company and objectives.</li><li>Educate and communicate clinical value, outcomes, and economic data to payers, providers, key partners, advocacy, and access enablers.</li><li>Respond to unsolicited inquiries consistent with the MSL compliance standards.</li><li>Provide and/or present field observations and insights to internal partners.</li><li>Implement scientific engagement plan according to annual MSL goals and metrics.</li><li>Develop and implement local OL plans in line with scientific engagement plan.</li><li>Support speaker training as requested and ensure the speakers are updated on new data.</li><li>Support Amgen sponsored research and may serve as a study lead.</li><li>Liaise with potential investigators in non-sponsored clinical research.</li><li>Lead and/or participate on project teams that support MSL strategies and tactics as delegated by MSL leadership.</li><li>Advance MSL value proposition, identify gaps, achieve results, and set an example for others to follow by consistently demonstrating Amgen values and leadership attributes. Demonstrate tact and integrity when communicating and interacting with others.</li><li>Lead and support congress activities as aligned with strategy.</li><li>Compliantly collaborate with cross-functional colleagues. May serve as main of point of contact.</li><li>Maintain clinical competence and expertise and timely completion of assigned training. May serve as a training lead.</li><li>May serve as New Hire Mentor and/or International MSL mentor/trainer</li><li>Cultivate long term relationships.</li><li><div><b>Availability to travel is required for this role.</b></div></li></ul><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The vital attribute professional we seek is a type of person with these qualifications.</p><p><b>Basic Qualifications:</b></p><ul><li>Doctorate degree and experience in Scientific/Medical Affairs at a biotech or pharmaceutical company Or</li><li>Master’s degree and 3years of experience in Scientific/Medical Affairs at a biotech or pharmaceutical company Or</li><li>Bachelor’s degree and 5years of experience in Scientific/Medical Affairs at a biotech or pharmaceutical company Or</li><li>Proficiency in English and Spanish, both in written and verbal communication.</li></ul><p><b>Preferred Qualifications:</b></p><ul><li>Plans, coordinates, and prioritizes with a cross-functional and adaptive attitude, evolving plans with new circumstances.</li><li>Cultivating relationships: Collaborates with partners to promote learning, exchanged views, thought diversity, and valued-based engagement.</li><li>Technical knowledge: Maintains and applies science-based expertise to educate customers internally and externally.</li><li>Effective Problem Solving and Decision Making</li><li>Communicating with impact: Engages in effective scientific exchange through active listening, impactful questioning, and information sharing.</li><li>Business and industry knowledge: Applies knowledge of business and healthcare industry to advise strategy and build balanced value for patients.</li><li>Demonstrates Individual Leadership and Integrity.</li><li>Exemplifies Amgen Values.</li></ul><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/medical-science-liaison-oncology-cdmx-amgen/6a0898452f1861929d25337d</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-oncology-cdmx-amgen/6a0898452f1861929d25337d</guid><pubDate>Sat, 16 May 2026 16:16:05 GMT</pubDate><company>Amgen</company><location>Mexico - Mexico City</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Study Data Deliver Mgr]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Clinical<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients </b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p><b><span>Data Delivery Lead</span></b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. <span>In this vital role you are accountable for the management and oversight of data collected within a study/program, you will lead end-to-end data management and ensure high-quality, timely, and decision-ready data that enables successful clinical trial delivery.</span></p><ul><li><span>Serve as the single accountable leader for study-level data management, driving quality, delivery, and cross-functional alignment, locally and globally</span></li><li><span>Lead development and execution of the Data Management Plan and Integrated Data Review Plan (IDRP) aligned to protocol and program strategy</span></li><li><span>Drive database build, UAT, and go-live readiness in partnership with Database Design and Acquisition teams</span></li><li><span>Oversee study conduct activities including data cleaning, query management, reconciliation, and database lock preparation, ensuring we are ‘delivery ready’ at all times</span></li><li><span>Monitor study data metrics (e.g., eCRF entry, Non-CRF data collection, query aging, reconciliation backlog, KRIs) and proactively resolve issues to ensure on-time delivery</span></li><li><span>Lead data deliverables, proactive in follow up, ensuring issue resolution and high-quality outputs</span></li></ul><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.</p><p><b>Basic Qualifications:</b></p><ul><li><span>Doctorate Degree OR</span></li><li><span>Master’s Degree and 2 years of life science, computer sciences, business administration experience OR</span></li><li><span>Bachelor’s degree and 4 years of life science, computer science, business administration experience OR</span></li><li><span>Associate’s degree and 8 years of life science, computer science, business administration experience OR</span></li><li><span>High school diploma / GED and 10 years of life science, computer science, business administration experience</span></li></ul><p></p><p><b>Preferred Qualifications:</b></p><p></p><ul><li><span>5 years’ work experience in life sciences or medically related field, including 3 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company </span></li><li><span>Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials</span></li><li><span>Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)</span></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p><b>The annual base salary range for this opportunity in the U.S. is [Talent Acquisition to input market pay range].</b></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans and bi-annual company-wide shutdowns</li><li>Flexible work models, including remote work arrangements, where possible</li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/study-data-deliver-mgr-amgen/6a0898452f1861929d25337c</link><guid isPermaLink="true">http://biotechroles.com/study-data-deliver-mgr-amgen/6a0898452f1861929d25337c</guid><pubDate>Sat, 16 May 2026 16:16:05 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$65000-110000</salary><type>Full time</type></item><item><title><![CDATA[Sr Associate Accounting]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Finance<h2></h2><h2><b>Job Description</b></h2><div><p>Amgen is seeking a <b>Sr Associate – Accounting (Technical &amp; Digital Enablement)</b> within Global Accounting Automation. This role is suited for a finance professional who understands Record‑to‑Report (R2R) accounting processes and controls, and who can support automation initiatives and enterprise digital projects in partnership with IT and automation teams.</p><p>The role supports accounting close efficiency, controllership, and digital enablement through structured project delivery and strong technical fundamentals.</p><h3><b>KEY RESPONSIBILITIES</b></h3><p><b>1) Automation &amp; Digital Enablement</b></p><ul><li>Identify and support automation opportunities across accounting processes to reduce manual effort, improve cycle times, and strengthen controls.</li><li>Build and support automation initiatives using:<ul><li><b>Advanced Excel &#43; VBA/ Macros (Must‑Have):</b> macro automation, reusable templates, validations/controls, error handling, and audit‑friendly outputs.</li></ul></li><li>Partner with Technology, Automation CoE, and developers to design and deliver scalable solutions using tools such as UiPath, Power Automate, Power BI, Alteryx, Smartsheet, DocuSign, and similar platforms.</li><li>Apply controls‑by‑design principles including access management, approvals, audit trails, change control, documentation, and production support models.</li></ul><p><b>2) Project Delivery &amp; Coordination</b></p><ul><li>Support end‑to‑end delivery of automation initiatives (intake → requirements → build → testing → deployment → stabilization).</li><li>Assist with requirements gathering, documentation (BRDs, user stories, acceptance criteria), testing coordination, and go‑live readiness.</li><li>Track timelines, risks, dependencies, and provide regular status updates to stakeholders.</li></ul><p><b>3) Accounting Close, Controls &amp; Compliance</b></p><ul><li>Support accurate and timely month‑end and quarter‑end close activities, including journal entries, reconciliations, and analysis.</li><li>Apply knowledge of <b>US GAAP</b> and financial reporting requirements.</li><li>Support SOX/internal control execution, documentation, and audit readiness.</li><li>Assist with internal, external, and tax audit requests within defined timelines.</li></ul><p><b>4) Reporting &amp; Insights</b></p><ul><li>Support development and maintenance of automated reports and dashboards for:<ul><li>Close health and cycle time</li><li>Reconciliation status and exceptions</li><li>Controls compliance and evidence completeness</li></ul></li><li>Perform data validation, reconciliations, and variance analysis to ensure audit‑ready outputs.</li></ul><p><b>5) Cross‑Functional Collaboration</b></p><ul><li>Work closely with Finance teams (RTR, FP&amp;A, P2P, Tax, Treasury) and Technology partners.</li><li>Coordinate with third‑party vendors where applicable and ensure service quality and documentation.</li></ul><h3><b>BASIC QUALIFICATIONS</b></h3><ul><li>Bachelor’s degree &#43; 5 years of relevant experience <b>OR</b></li><li>Associate’s degree &#43; 6 years of relevant experience <b>OR</b></li><li>High school diploma/GED &#43; 8 years of relevant experience</li></ul><h3><b>REQUIRED SKILLS (MUST‑HAVE)</b></h3><p><b>Technical</b></p><ul><li><b>Advanced Excel &#43; VBA/ Macros (Must‑Have):</b> automation, reusable templates, validations/controls, robust error handling.</li><li>Experience working with ERP systems (preferably SAP) and accounting data used in close processes.</li></ul><p><b>Finance / Controllership</b></p><ul><li>Hands‑on experience with accounting close, reconciliations, and journal entries.</li><li>Understanding of US GAAP and SOX/internal control requirements.</li></ul><p><b>Delivery / Collaboration</b></p><ul><li>Ability to support work end‑to‑end from requirements through go‑live and stabilization.</li><li>Strong analytical, organizational, and communication skills.</li></ul><h3><b>GOOD‑TO‑HAVE SKILLS</b></h3><ul><li><b>Power BI and/or Tableau:</b> dashboard development, reporting, data modeling (Power Query/DAX preferred)</li><li>RPA / automation tools (UiPath, Automation Anywhere); analytics tools such as Alteryx.</li><li>Power Automate / Power Apps.</li><li>Jira, Confluence, Smartsheet; process mapping tools (Visio).</li></ul></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-associate-accounting-amgen/6a0898442f1861929d25337b</link><guid isPermaLink="true">http://biotechroles.com/sr-associate-accounting-amgen/6a0898442f1861929d25337b</guid><pubDate>Sat, 16 May 2026 16:16:04 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Lead Business Analyst]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Business Development<h2></h2><h2><b>Job Description</b></h2><div><p><u><span>ABOUT THE ROLE</span></u><br /> </p></div><div><p><u><span>Role Description:</span></u></p></div><div><p><span><span>This role work</span><span>s </span><span>at the intersection of clinical </span><span>trial </span><span>operations, technology, and external partnership </span><span>and is critical for </span><span>supporting </span><span>the successful delivery of Amgen’s global clinical trials.</span></span></p></div><p></p><div><p><span><span>As a Lead Business Analyst, you will act as a trusted technology partner to global clinical trial teams, enabling the effective use of </span><span>Amgen </span><span>technolo</span><span>gies </span><span>by </span><span>specialist </span><span>external suppliers. </span><span>Y</span><span>ou</span><span>’ll have </span><span>respon</span><span>sibility </span><span>for managing </span><span>B2B </span><span>solutions for one or more capability </span><span>area </span><span>and for overseeing activities of other Business Analysts. </span></span></p></div><p></p><div><p><span><span>Y</span><span>ou</span><span>’ll </span><span>partner closely </span><span>with clinical teams, product owners, technology partners, and external </span><span>supplier</span><span>s </span><span>to t</span><span>ranslate complex business needs </span><span>and problems </span><span>into compliant, scalable, and sustainable solutions</span><span>.</span></span></p></div><div><div><p><u><span>Roles &amp; Responsibilities:</span></u></p></div><div><ul><li><p><span><span>Building </span><span>and maintain</span><span>ing strong </span><span>relationships </span><span>a cross </span><span>an extensive network of internal and external stakeholders.</span></span></p></li></ul></div><div><ul><li><p><span><span>Lead </span><span>comprehensive </span><span>business analysis to identify</span><span>, </span><span>understand </span><span>and </span><span>prioritize </span><span>IT requirements in the product backlog.</span></span></p></li></ul></div><div><ul><li><p><span><span>Own </span><span>the </span><span>imple</span><span>mentation and </span><span>deliv</span><span>ery of </span><span>IT </span><span>solutions and services for </span><span>one or more </span><span>s</span><span>upplier </span><span>c</span><span>apability </span><span>area</span><span>s </span><span>with</span><span>in </span><span>product team</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Coordinating the activities of other analysts on the product team.  </span></span></p></li></ul></div><div><ul><li><p><span><span>Ensuring I</span><span>T </span><span>solutions </span><span>comply with regulations </span><span>and information security policies</span><span>.</span></span></p></li></ul></div></div><div><div><ul><li><p><span><span>Partnering with </span><span>technology </span><span>owner</span><span>s</span><span>to deliver </span><span>B2B connectiv</span><span>ity</span><span>, integrations and c</span><span>ollaboration solutions.</span></span></p></li></ul></div><div><ul><li><p><span><span>Assessing new suppliers against</span><span>Amgen</span><span>’s</span><span>IT requirements and</span><span>documenting gaps and</span><span>risks</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Supporting</span><span>change</span><span>management</span><span>and</span><span>end user communication for large</span><span>user groups</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Maintain</span><span>ing</span><span>accurate documentation of systems and processes.</span></span></p></li></ul></div><div><ul><li><p><span><span>Staying informed </span><span>on the changing internal a</span><span>nd </span><span>external IT landscape </span><span>and continue to evolve and adapt </span><span>the </span><span>IT solution</span><span>s </span><span>strategy </span><span>t</span><span>o </span><span>maximize </span><span>effectiveness.</span></span></p></li></ul></div></div><div><div><p><u><span>Basic Qualifications and Experience:</span></u></p></div><div><ul><li><p><span><span>Any degree with 5 - 8 years </span><span>of </span><span>experience </span><span>working in </span><span>Life Science</span><span>, </span><span>Biotechnology </span><span>or </span><span>Information </span><span>Systems</span></span></p></li></ul></div><div><p></p></div><div><p><u><span>Functional Skills:</span></u></p></div><div><p><b><span>Must-Have Skills</span><span>:</span></b></p></div><div><ul><li><p><span><span>A </span><span>detailed </span><span>understanding of the clinical trial process and the </span><span>systems </span><span>used </span><span>to execute study delivery</span><span>(EDC, CTMS, eTMF </span><span>etc</span><span>.)</span></span></p></li></ul></div><div><ul><li><p><span><span>Customer focused and </span><span>a proven </span><span>business r</span><span>elationship manag</span><span>er </span><span>who is confident when </span><span>working with </span><span>technical and non-technical </span><span>senior </span><span>stakeholders</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Collaborative team player with</span><span>excellent</span><span>verbal and written communication skills; able to</span><span>influence and lead</span><span>effectively across global, cross-functional and remote stakeholders.</span></span></p></li></ul></div><div><ul><li><p><span><span>Experience of overseeing and coordinating the work of other Business Analysts</span></span></p></li></ul></div><div><ul><li><p><span><span>A</span><span>bility to lead business analysis activities </span><span>to </span><span>capture and prioritize requirements through interviews and workshops</span><span>.</span></span></p></li></ul></div></div><div><div><ul><li><p><span><span>Knowledge </span><span>of </span><span>B2B and integration technologies, including APIs, secure file transfers</span><span>, VPN’s </span><span>and </span><span>Virtual desktops</span></span></p></li></ul></div><div><ul><li><p><span><span>Confident at </span><span>document</span><span>ing complex </span><span>testable business requirements </span><span>as </span><span>clear </span><span>user stories </span><span>and in formal specification documentation</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Ana</span><span>lytical, detail orientated </span><span>with </span><span>excellent </span><span>problem-solving skills</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Experience of working with or as an external </span><span>technical service supplier.</span></span></p></li></ul></div><div><ul><li><p><span><span>Practical experience and </span><span>understanding of Agile </span><span>methodologies, particularly the Scaled Agile Framework (</span><span>SAFe</span><span>)</span></span></p></li></ul></div><div><p></p></div><div><p><b><span>Good-to-Have Skills:</span></b></p></div><div><ul><li><p><span><span>Experience of working with or for a clinical trial supplier (CRO, Lab, Imaging,</span><span>e.t.c</span><span>.) </span></span></p></li></ul></div><div><ul><li><p><span><span>Working in</span><span>a</span><span>regulated</span><span>environment where compliance and information security is essential</span></span></p></li></ul></div><div><ul><li><p><span><span>Ability to</span><span>Project manag</span><span>e complex</span><span>longer term</span><span>deliverables</span><span>,</span></span></p></li></ul></div><div><ul><li><p><span><span>Proficien</span><span>cy</span><span>in</span><span>IT service</span><span>delivery</span><span>tools such as Jira, Jira Align, and Confluence</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>An advocate of</span><span>the use</span><span>of</span><span>DevOps</span><span>,</span><span>AI</span><span>and</span><span>Test Automation in delivery</span></span></p></li></ul></div><div><p><u><span>Professional Certifications</span></u><u><span>(please mention if the certification is preferred or mandatory for the role):</span></u></p></div><div><ul><li><p><span><span>Business Analysis certifications (IIBA</span><span>BABOK) or similar (</span><span>pr</span><span>ef</span><span>erred</span><span>)</span></span></p></li></ul></div><div><ul><li><p><span><span>Certified</span><span>SAFe</span><span>for Tea</span><span>ms</span><span>or similar (preferred)</span></span></p></li></ul></div><div><p><u><span>Soft Skills:</span></u></p></div><div><ul><li><p><span><span>Excellent written and spoke English.</span></span></p></li></ul></div><div><ul><li><p><span><span>A people person, with e</span><span>xcellent written and spoke English</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Highly a</span><span>ccountable</span><span>, reliable</span><span>and proactive</span><span>.</span></span></p></li></ul></div><div><ul><li><p><span><span>Ab</span><span>le</span><span>to</span><span>self-</span><span>manage</span><span>activities across</span><span>multiple priorities</span><span>.</span></span></p></li></ul></div></div><div><p></p></div><div><p><u><span>Shift Information:</span></u></p></div><div><p><span><span>This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required based on business requirements.</span></span></p></div><div><p><span><span>This role</span><span>has global responsibilities</span><span>which may require flexibility with work</span><span>ing</span><span>h</span><span>our</span><span>to align with key</span><span>global</span><span>stakehold</span><span>e</span><span>r</span><span>s</span></span></p></div><div><p><u><span>EQUAL OPPORTUNITY STATEMENT</span></u></p></div><div><p><span><span>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</span></span></p></div><div><p><span><span>We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request</span><span>an accommodation</span><span>.</span></span></p></div><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/lead-business-analyst-amgen/6a0898422f1861929d25337a</link><guid isPermaLink="true">http://biotechroles.com/lead-business-analyst-amgen/6a0898422f1861929d25337a</guid><pubDate>Sat, 16 May 2026 16:16:02 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Maintenance Technician - Inspection & Packaging (24/7 Shift)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Maintenance<h2></h2><h2><b>Job Description</b></h2><p>Primary Responsibilities:<br />The Senior Maintenance Technician will report to a Maintenance Manager and will work as part of one of the site maintenance teams (Process, Utilities, Lyophilisation, Inspection, Packaging) with the primary responsibilities laid out below. As the site expands, development opportunities may exist to transfer internally between teams and to gain experience with the equipment in each area of the plant mentioned above.</p><p></p><p>Equipment Maintenance<br />•    Execute advanced maintenance activities on process equipment in accordance with standard operating procedures across multiple production and support facilities.<br />•    Perform troubleshooting and equipment investigation works while assuring minimal impact to plant operations and in compliance with good maintenance practices, SOP’s and GMP requirements.<br />•    Ability to work independently and as part of a team, taking responsibility for completion and handover of work, GMP documentation and ongoing maintenance of personal system qualifications.<br />•    Demonstrated ability to participate in cross-functional teams to investigate non-conformances, deviations, and troubleshoot issues to establish root causes and corrective actions.<br />•    Proactively integrate evolving technology and tools deployed as part of predictive maintenance strategies. </p><p></p><p>Projects and Continuous Improvement<br />•    Support projects and start-up of new process plant and equipment.<br />•    Support process investigations, trials, machine upgrades and testing in conjunction with the wider engineering team.<br />•    Assist with the development, execution, and support of the CQV (Commissioning, Qualification, Validation) process.<br />•    Identify and implement local projects to enhance equipment operation, reliability, and the efficiency of maintenance programs.</p><p></p><p>GMP and Compliance<br />•    Maintain high levels of aseptic compliance and housekeeping standards in manufacturing areas, workshops and training areas whilst operating as part of a cross functional team to support the plant.<br />•    Demonstrated ability to self-maintain online and practical training or qualification status in compliance with site operating procedures and key area metrics.<br />•    Ensure activities are undertaken in a safe, compliant manner in accordance with legislative, site and corporate safety and quality procedures.<br />•    Adopt compliance driven industry changes to document and record GMP activities.</p><p></p><p>Documentation<br />•    Ensure that maintenance documentation and records are completed accurately and in accordance with applicable procedures such as ALCOA&#43; principles.<br />•    Develop, revise &amp; review relevant technical documents (Maintenance SOP’s, Job Plans, P&amp;IDs etc.) in conjunction with the broader Engineering support team.<br />•    Familiarity with the purpose and use of CMMS systems, Electronic Batch Records, and electronic logs or recording systems.</p><p></p><p>Primary Knowledge and Education:</p><p>•    Recognised apprenticeship in an electrical / mechanical craft.<br />•    Ability to read and understand mechanical drawings, technical manuals, electrical wiring schematics, layout drawings and P&amp;ID’s.</p><p></p><p>Preferred Qualifications and Experience:<br />•    Combined education, training and experience in mechanical / electrical maintenance, experience in a regulated manufacturing environment would be an advantage.<br />•    Knowledge and experience working in a pharmaceutical or aseptic manufacturing facility.<br />•    Understanding of pneumatic, mechanical, and hydraulic systems with the ability to effectively perform any associated maintenance or troubleshooting activities.<br />•    Working knowledge and experience of site utilities and electrical systems.<br />•    Relevant experience in an automated manufacturing and inspection environment would be an advantage.<br />•    Experience executing and documenting maintenance work in a computerised maintenance management system.<br />•    Ability to interpret P&amp;ID&#39;s, identify hazards, isolation points and inter-dependencies between services for LOTO purposes.<br />•    Ability to work with minimum direction, identify issues and effectively communicate the status of equipment or tasks in a timely manner.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-maintenance-technician-inspection-and-packaging-247-shift-amgen/6a0898422f1861929d253379</link><guid isPermaLink="true">http://biotechroles.com/sr-maintenance-technician-inspection-and-packaging-247-shift-amgen/6a0898422f1861929d253379</guid><pubDate>Sat, 16 May 2026 16:16:02 GMT</pubDate><company>Amgen</company><location>Ireland - Dun Laoghaire</location><salary>$65000-85000</salary><type>Full time</type></item><item><title><![CDATA[Sr Manager Access Strategy, HEOR, Pricing]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Value and Access<h2></h2><h2><b>Job Description</b></h2><p><b><u><span>POSITION SUMMARY</span></u></b></p><ul><li>Develop and implement robust pricing strategies for Amgen products to obtain optimal reimbursement price through leading Amgen cross functional pricing teams  </li><li>Develop price negotiation strategy in China</li><li>Evidence generation, value story development and delivery to experts/payors</li><li>Act as a critical link between VA&amp;P, strategic planning, medical and JAPAC/global cross-functional team in strategy, market access, evidence generation, etc.</li></ul><p><b><u><span>POSITION RESPONSIBILITIES</span></u></b></p><p><b><span>Core Activities:</span></b></p><p><u>1. NRDL accountabilities</u>&#xff1a;</p><ul><li>Provide in-depth insights on pricing, access, payer, and policy matters critical for product evaluation regarding:</li><li>Evolution of the reimbursement/funding system and what the environment will evolve to at launch and beyond</li><li>Magnitude of the opportunity in relation to pricing implications</li><li>Value evidence that is required to support optimal product pricing at NRDL negotiation</li><li>External engagement : Engage regularly with relevant reimbursement/HEOR authorities, experts to understand current landscape and anticipate future changes</li></ul><p><u>2. Pricing and reimbursement accountabilities</u><u>&#xff1a;</u></p><ul><li>Develop and implement robust pricing strategies including NRDL negotiation to obtain optimal reimbursement price</li><li>Explore innovative payment method, commercial health insurance for new product reimbursement before NRDL listing</li><li>Serve as local technical expert to regional and global teams</li><li>Effectively represent Amgen China positions and requirements at regional &amp; global planning and strategy meetings</li><li>Working with Marketing, Finance and other functions to ensure business plans and forecasts incorporate latest pricing and reimbursement assumptions</li></ul><p><u>3. Pricing protection accountabilities</u><u>&#xff1a;</u></p><ul><li>Develop and implement robust strategies on national and local volumed based procurement (VBP)</li></ul><p><b><span>Building organizational capability</span></b></p><ul><li>Build trust among team members and broader stakeholders by setting a highly visible example for colleagues within VA&amp;P in terms of professional excellence and commitment to demonstrating leader behaviors and values</li></ul><ul><li>Create and maintain a team culture that values, recognizes and generates high performance, supports innovation and challenges the status quo</li><li>Provide clear role responsibility, establishing a climate of continuous measurement and performance improvement</li><li>Create processes to share information and experiences, leverage initiatives across teams where appropriate, and enhance productivity of marketing efforts</li><li>Actively support development of direct reports and high-potential colleagues providing insights, direction and opportunities</li></ul><p><b><u><span>ORGANIZATIONAL RELATIONSHIPS</span></u></b></p><ul><li>Report to VA&amp;P Head</li><li>Cross-functional (strategic planning, medical, marketing, KA, commercial, JAPAC/Global VA&amp;P, etc.)</li></ul><p><b><u><span>EDUCATION AND EXPERIENCE </span></u></b></p><ul><li>Master’s Degree and 10 years of Experience with pharmaceutical pricing, HEOR and reimbursement in China</li><li>Strong knowledge of global payer systems and policies</li></ul><p><b><u><span>TECHNICAL SKILLS REQUIREMENTS</span></u></b></p><p>Basic Requirements</p><ul><li>Good understanding of China healthcare system including pricing &amp; reimbursement mechanism and system</li><li>Skillful in KOL engagement, and payor negotiation preferred</li><li>Clear, effective communication in Chinese and English both in oral and writing</li><li>Strong strategic thinking abilities, results oriented</li><li>Logical thinking, creative, willingness to bring forward new and different approaches</li><li>Enjoy new challenges and is comfortable with responsibilities</li></ul><p></p><p>Key Capabilities</p><ul><li>Manage uncertainties with focus on delivering results through Effective Team and Peer Leadership</li><li>Formulating Integrated, Cross-Functional Strategies through effective communicating with logical thinking approach</li></ul><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-manager-access-strategy-heor-pricing-amgen/6a0898412f1861929d253378</link><guid isPermaLink="true">http://biotechroles.com/sr-manager-access-strategy-heor-pricing-amgen/6a0898412f1861929d253378</guid><pubDate>Sat, 16 May 2026 16:16:01 GMT</pubDate><company>Amgen</company><location>China - Beijing</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Value & Access Transformation Initiatives]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Value and Access<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients </b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>What You Will Do</b></p><p>As Manager – V&amp;A Transformation Initiatives, you will be at the forefront of solving the US Value &amp; Access team’s biggest challenges using cutting edge technology. The AIN Transformation team will be viewed as an “innovation engine”, constantly testing and refining analytics solutions to address customer needs and opportunities alongside business partners. </p><p>In your role as a manager, you’ll be expected to combine a deep understanding of access data and analytics with experience in developing and deploying advanced machine learning, operational research, semantic analysis, and statistical methods to uncover structure in large data sets. Together with 2-4 associates you lead, you will be responsible for building and testing solutions for targeted business challenges. This will include application of advanced machine learning, operational research, semantic analysis, and statistical methods to uncover structure in large data sets.</p><p>The ideal candidate for this position will understand the business challenges that US Value &amp; Access teams face and will have with a track record of success in applying that knowledge to build, deploy, and refine high impact advanced analytics tools.</p><p></p><p>This role will report to the Senior Manager, V&amp;A Transformation Initiatives and will work in close collaboration with leaders of the Strategy &amp; Innovation Team in the United States Access Analytics &amp; Insights organization in India.</p><p>Roles &amp; Responsibilities:  </p><ul><li><p>Accountable to drive full lifecycle of data science projects delivery and ability to guide data scientists in shaping the developing the solution and act as a subject matter expert in solving development and commercial questions</p></li><li><p>Assume the role of business owner and manage the Proprietary AI engine built to optimize Copay</p></li><li><p>Ensure models are trained with the latest data and meet the SLA expectations </p></li><li><p>Manage AI tool’s road map, working with a global cross functional team  </p></li><li><p>Work in technical teams in development, deployment, and application of applied analytics, predictive analytics, and prescriptive analytics.</p></li><li><p>Utilize technical skills such as hypothesis testing, machine learning and retrieval processes to apply statistical and data mining techniques to identify trends, create figures, and analyze other relevant information.</p></li><li><p>Perform exploratory and targeted data analyses using descriptive statistics and other methods.</p></li><li><p>Model/analytics experiment and development pipeline leveraging MLOps.</p></li><li><p>Oversee efforts of 2-4 associates, including setting performance standards, managing their staffing, and monitoring performance</p></li><li><p>Collaborate with technical teams to translate the business needs into technical specifications, particularly focusing on AI-driven automation and insights.</p></li><li><p>Develop and integrate custom applications, intelligent dashboards, and automated workflows that incorporate AI capabilities to enhance decision-making and efficiency.</p></li></ul><p></p><p><b>What We Expect of You</b></p><p>We are all different, yet we all use our unique contributions to serve patients.</p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>8-13 years post degree in computer science, statistics or STEM majors with a minimum of 4 years of Information Systems experience</p></li><li><p>Foundational understanding of US pharmaceutical ecosystem and Patient support services offerings and other standard data sets including claims, prescription, EMR</p></li><li><p>Experience with one or more analytic software tools or languages like R and Python</p></li><li><p>Strong foundation in machine learning algorithms and techniques</p></li><li><p>Experience in statistical techniques and hypothesis testing, experience with regression analysis, clustering and classification</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Experience in MLOps practices and tools (e.g., MLflow, Kubeflow, Airflow); Experience in DevOps tools (e.g., Docker, Kubernetes, CI/CD) </p></li><li><p>Proficiency in Python and relevant ML libraries (e.g., TensorFlow, PyTorch, Scikit-learn) </p></li><li><p>Outstanding analytical and problem-solving skills; Ability to learn quickly; Excellent communication and interpersonal skills </p></li><li><p>Experience with data engineering and pipeline development </p></li><li><p>Knowledge of NLP techniques for text analysis and sentiment analysis </p></li><li><p>Experience in analyzing time-series data for forecasting and trend analysis </p></li><li><p>Experience with AWS, Azure, or Google Cloud </p></li><li><p>Experience with Databricks platform for data analytics and MLOps </p></li></ul><p></p><p><b>Professional Certifications</b></p><ul><li><p>Any AWS Developer certification (preferred) </p></li><li><p>Any Python and ML certification (preferred) </p></li></ul><p></p><p><b>Soft Skills: </b></p><ul><li><p>Initiative to explore alternate technology and approaches to solving problems. </p></li><li><p>Skilled in breaking down problems, documenting problem statements, and estimating efforts. </p></li><li><p>Excellent analytical and troubleshooting skills. </p></li><li><p>Strong verbal and written communication skills </p></li><li><p>Ability to work effectively with global, virtual teams </p></li><li><p>High degree of initiative and self-motivation. </p></li><li><p>Ability to manage multiple priorities successfully.  </p></li><li><p>Team-oriented, with a focus on achieving team goals </p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p><p></p><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/manager-value-and-access-transformation-initiatives-amgen/6a0898412f1861929d253377</link><guid isPermaLink="true">http://biotechroles.com/manager-value-and-access-transformation-initiatives-amgen/6a0898412f1861929d253377</guid><pubDate>Sat, 16 May 2026 16:16:01 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Associate DevOps Engineer]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p><b>Associate DevOps Engineer </b></p><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b></p><p>If you feel like you&#39;re part of something bigger, it&#39;s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to becoming one of the world&#39;s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It&#39;s time for a career you can be proud of. Join us!</p><p><b>DevOps Engineer</b></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let&#39;s do this! Let&#39;s change the world. Play a vital role and be part of the web team, which provides end-to-end digital solutions and hosting for global websites enabling Amgen brands to engage with healthcare professionals (HCPs) and our patients. The team offers an innovative web technology platform hosted in the cloud and ensures compliances and security features across our websites. You will be part of Amgen&#39;s Global Commercial Operations Digital Technology Innovation (GCO DTI) organization.</p><ul><li>Automate and improve development and release processes</li><li>Guide teams to build infrastructure-as-code that is scalable, performant, reliable, and secure</li><li>Analyse data to improve existing processes and to implement automation tools for digital deployment pipelines (CI/CD)</li><li>Document procedures for system troubleshooting and maintenance</li><li>Partner with the web team’s DevOps lead to automate regression testing</li><li>Partner with the web team’s DevOps lead for crafting integration toolkits to be used by other product and go-to-market teams</li><li>Able to manage various types of work assignments, which include ticket support work, small enhancements, and larger feature development</li></ul><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our outstanding contributions to serve patients. The professional we seek is a problem-solver with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Bachelor&#39;s degree and 2 –6 years of Information Science experience</p><p><b>Preferred Qualifications:</b></p><ul><li>Experience in programming languages such as Python, &amp; .Net</li><li>Experience in DevOps (CI/CD) and automation tools such as digital.ai, Jenkins, Docker, GitHub</li><li>Good written and verbal communication skills, with an ability to express yourself succinctly</li><li>Experience using Jira for releases notifications and practical understanding of Agile/SAFe is a plus</li><li>Basic knowledge of the software development lifecycle (SDLC)</li><li>Exposure to AI/ML-driven applications or generative AI technologies.</li><li>Knowledge of CMS tools like Sitecore and web technologies such as HTML CSS, JavaScript, ASP.NET, and SQL a plus</li><li>Familiarity with AWS concepts.</li></ul><p><b>Additional Requirements</b></p><ul><li>Must be able to work overlapping hours with US based team as needed (8 to 11 A.M. PST)</li><li>Able to work with offshore teams and act as a liaison as needed</li></ul><p><b>Soft Skills</b> </p><ul><li>Strong analytical and troubleshooting abilities. </li></ul><ul><li>Effective communication and collaboration skills. </li></ul><ul><li>Eagerness to learn and adapt to new technologies. </li></ul><ul><li>Ability to manage multiple tasks with minimal supervision. </li></ul><ul><li>Team-oriented mindset and commitment to shared goals. </li></ul><ul><li>Strong sense of ownership and accountability. </li></ul><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we work to care for our teammates&#39; professional and personal growth and well-being.</p><ul><li>Vast opportunities to learn and move up and across our global organization</li><li>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.</p><p><a href="http://careers.amgen.com/" target="_blank"><b>careers.amgen.com</b></a></p><p><b>Ready to Apply for the Job?</b></p><p>We highly recommend utilizing Workday&#39;s robust <b>Career Profile</b> feature to complete the application process. A link to update your profile is available when you click <b>Apply</b>. You can then complete your Workday profile in minutes with the &#34;Upload My Experience&#34; functionality to upload an updated copy of your resume or you can simply edit the individual sections of your Career Profile.</p><p>Please note that you should be in your current position for at least 18 months before applying to internal positions. Staff must notify their current manager if invited for an interview. In addition, Staff are ineligible to apply for open positions if (a) their performance is currently being managed on a performance improvement plan (PIP) or other locally utilized formal coaching document or (b) their most recent performance rating was not a &#34;Partially Meets Expectations&#34; or higher. Please visit our <a href="https://saml.alight.com/sp/startSSO.ping?PartnerIdpId&#61;http://www.okta.com/exkkrgnd0n5vXjqVt0x7&amp;TargetResource&#61;https%3A%2F%2Fsso.alight.com%2Fportal%3FpageCd%3DAGN_INT_GUIDE_LNK" target="_blank">Internal Transfer Guidelines</a> for more detailed information.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/associate-devops-engineer-amgen/6a0898402f1861929d253376</link><guid isPermaLink="true">http://biotechroles.com/associate-devops-engineer-amgen/6a0898402f1861929d253376</guid><pubDate>Sat, 16 May 2026 16:16:00 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$18000-30000</salary><type>Full time</type></item><item><title><![CDATA[Associate Cloud Engineer]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b></p><p>If you feel like you&#39;re part of something bigger, it&#39;s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to becoming one of the world&#39;s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It&#39;s time for a career you can be proud of. Join us!</p><p><b>Cloud Engineer</b></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let&#39;s do this! Let&#39;s change the world. Play a vital role and be part of the web team, which provides end-to-end digital solutions and hosting for global websites enabling Amgen brands to engage with healthcare professionals (HCPs) and our patients. The team offers an innovative web technology platform hosted in the cloud and ensures compliances and security features across our websites. You will be part of Amgen&#39;s Global Commercial Operations Digital Technology Innovation (GCO DTI) organization.</p><ul><li>Implement, and manage <b>highly available AWS cloud environments</b>.</li><li>Maintain <b>VPCs, Subnets, Security Groups, and IAM policies</b> to enforce security best practices.</li><li>Optimize AWS costs using <b>reserved instances, savings plans, and auto-scaling</b>.</li><li>Maintain, and enhance Terraform &amp; CloudFormation templates for cloud provisioning.</li><li>Automate deployment, scaling, and monitoring using AWS-native tools &amp; scripting.</li><li>Implement and manage CI/CD pipelines for infrastructure and application deployments.</li><li>Set up AWS CloudWatch and logging solutions for proactive monitoring.</li><li>Implement autoscaling, load balancing, and caching strategies for performance optimization.</li><li>Troubleshoot cloud infrastructure issues and conduct root cause analysis.</li><li>Work closely with software engineers, SREs, and DevOps teams to support deployments.</li><li>Maintain Git best practices for cloud infrastructure versioning.</li><li>Support on-call rotation for high-priority cloud incidents.</li></ul><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our outstanding contributions to serve patients. The professional we seek is a problem-solver with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Bachelor&#39;s degree and 2 - 6 years of Information Science experience</p><p><b>Preferred Qualifications:</b></p><ul><li>Experience in programming languages such as Python, &amp; .Net</li><li>Experience in DevOps (CI/CD) and automation tools such as digital.ai, Jenkins, Docker, GitHub</li><li>Hands-on experience with AWS (EC2, S3, RDS, CDN, Route 54, WAF, Lambda, VPC, IAM, ECS/EKS, API Gateway, etc.).</li><li>Expertise in Terraform &amp; CloudFormation for AWS infrastructure automation.</li><li>Experience with Kubernetes (EKS) and service mesh architectures.</li><li>Knowledge of AWS Lambda and event-driven architectures.</li><li>Good written and verbal communication skills, with an ability to express yourself succinctly</li><li>Experience using Jira for releases notifications and practical understanding of Agile/SAFe is a plus</li><li>Basic knowledge of the software development lifecycle (SDLC)</li><li>Exposure to AI/ML-driven applications or generative AI technologies.</li><li>Knowledge of CMS tools like Sitecore and web technologies such as HTML CSS, JavaScript, ASP.NET, and SQL a plus</li></ul><p><b>Additional Requirements</b></p><ul><li>Must be able to work overlapping hours with US based team (8 to 11 A.M. PST)</li><li>Able to work with offshore teams and act as a liaison as needed</li></ul><p><b>Soft Skills</b> </p><ul><li>Strong analytical and troubleshooting abilities. </li></ul><ul><li>Effective communication and collaboration skills. </li></ul><ul><li>Eagerness to learn and adapt to new technologies. </li></ul><ul><li>Ability to manage multiple tasks with minimal supervision. </li></ul><ul><li>Team-oriented mindset and commitment to shared goals. </li></ul><ul><li>Strong sense of ownership and accountability. </li></ul><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we work to care for our teammates&#39; professional and personal growth and well-being.</p><ul><li>Vast opportunities to learn and move up and across our global organization</li><li>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.</p><p><a href="http://careers.amgen.com/" target="_blank"><b>careers.amgen.com</b></a></p><p><b>Ready to Apply for the Job?</b></p><p>We highly recommend utilizing Workday&#39;s robust <b>Career Profile</b> feature to complete the application process. A link to update your profile is available when you click <b>Apply</b>. You can then complete your Workday profile in minutes with the &#34;Upload My Experience&#34; functionality to upload an updated copy of your resume or you can simply edit the individual sections of your Career Profile.</p><p>Please note that you should be in your current position for at least 18 months before applying to internal positions. Staff must notify their current manager if invited for an interview. In addition, Staff are ineligible to apply for open positions if (a) their performance is currently being managed on a performance improvement plan (PIP) or other locally utilized formal coaching document or (b) their most recent performance rating was not a &#34;Partially Meets Expectations&#34; or higher. Please visit our <a href="https://saml.alight.com/sp/startSSO.ping?PartnerIdpId&#61;http://www.okta.com/exkkrgnd0n5vXjqVt0x7&amp;TargetResource&#61;https%3A%2F%2Fsso.alight.com%2Fportal%3FpageCd%3DAGN_INT_GUIDE_LNK" target="_blank">Internal Transfer Guidelines</a> for more detailed information.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/associate-cloud-engineer-amgen/6a0898402f1861929d253375</link><guid isPermaLink="true">http://biotechroles.com/associate-cloud-engineer-amgen/6a0898402f1861929d253375</guid><pubDate>Sat, 16 May 2026 16:16:00 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$60000-90000</salary><type>Full time</type></item><item><title><![CDATA[Scrum Master, Commercial Data & Analytics]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><div><div><p>Join our team at AMGEN Capability Center Portugal, consistently recognized among the top companies in the Best Workplaces™ ranking by Great Place to Work® in Portugal. In 2026, we were once again distinguished as one of the top Best Workplaces in the country (category 201–500 employees), reinforcing our commitment to an exceptional employee experience and workplace culture.</p><p></p><p>We are a team of over 500 talented individuals, spanning more than 30 functions and areas of expertise, and representing over 40 nationalities. Together, we bring diverse perspectives and professional backgrounds to help shape the future of healthcare through innovation and technology.</p><p>This is your opportunity to explore a world of possibilities across areas such as Data &amp; Analytics, Digital, Technology &amp; Innovation, Cybersecurity, R&amp;D Operations, Global Distribution, Finance, Regulatory Affairs, General &amp; Administrative, Human Resources, and many more.</p><p></p><p>Located in the heart of Lisbon, our AMGEN office fosters a culture of innovation, excellence, and purpose. Come thrive with us at AMGEN, supporting our mission To Serve Patients.</p><p></p><p>What we do at AMGEN matters in people’s lives.</p><p></p><p></p><p><span class="emphasis-3"><b><b>Scrum Master, Commercial Data &amp; Analytics</b></b></span></p></div><div><p><span><span> </span></span><span> </span></p><p></p><p><span>At Amgen, Technology isn’t just a support function—it’s a catalyst for discovery, transformation, and real-world impact. Here, your ideas fuel innovation that improves and saves lives of patients in dire need of our medicines. Are you ready to do meaningful work that matters?</span></p><p></p><p></p><p></p><p><span class="emphasis-3"><b><b>LIVE</b></b></span></p><p><span class="emphasis-3"><b><b>WHAT YOU WILL DO</b></b></span></p></div><p></p><p></p><p></p><div><p><span><span>The </span><span>Scrum Master </span><span>is a leader and coach who </span><span>plays the scrum master role by </span><span>facilitat</span><span>ing</span><span> </span><span>team </span><span>events</span><span>, </span><span>processes</span><span>,</span><span> and</span><span> support</span><span>ing</span><span> teams in delivering value.</span><span> The role involves </span><span>facilitating</span><span> communication and collaboration among teams</span><span> that are geographically distributed</span><span>, ensuring alignment with the program vision, managing risks and dependencies</span><span>,</span><span> and driving relentless improvement.</span><span> </span></span><span> </span></p></div><div><p></p><p><u><span>Roles &amp; Responsibilities:</span></u><span><span> </span></span><span> </span></p><p></p></div><div><ul><li><p><span><span>Lead and manage product delivery using agile frameworks and techniques. Align with Agile values such as prioritizing individuals and interactions over processes and tools. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Lead and </span><span>facilitate</span><span> agile </span><span>events</span><span> including stand-ups, sprint</span><span> &amp; </span><span>PI</span><span> planning, reviews, retrospectives, </span><span>demos</span><span> </span><span>and backlog refinement meetings to promote team collaboration.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Advise</span><span> </span><span>SAFe</span><span> events, including PI Planning, Scrum of Scrums, and Inspect &amp; Adapt workshops.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Collaborate with cross-functional teams to </span><span>identify</span><span> business requirements and develop solutions that meet customer needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Work with Product Owners, Product and Solution Management, and stakeholders to ensure strategy and execution alignment</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Help the scrum teams achieve delivery acceleration focused on business outcomes by reaching higher levels of scrum maturity</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Identify</span><span>, escalate, and manage risks and dependencies across </span><span>Teams / ART to </span><span>ensur</span><span>e</span><span> </span><span>that </span><span>they are addressed </span><span>in a timely manner</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Coordinate with Services and support to schedule resolution of issues with released products </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Foster a culture of continuous improvement within the </span><span>Teams / ART </span><span>by leading retrospectives and encouraging innovation</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Monitor and report on the progress of the</span><span> Team / ART</span><span>, ensuring transparency and alignment with solution objectives</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Provide guidance and support to RTEs, Scrum Masters, and Product Management teams to help them deliver value</span><span> </span><span>effectively and adhere to Agile best practices</span></span><span> </span></p></li></ul></div><div><p></p><p></p><p></p><p><span class="emphasis-3"><b><b>WIN</b></b></span></p><p><span class="emphasis-3"><b><b>WHAT WE EXPECT OF YOU</b></b></span></p><p></p><p></p><p></p><p><b><span>Basic Qualifications and Experience: </span></b></p><p></p></div><div><ul><li><p><span><span>Doctorate Degree OR</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Master’s degree with 4 - 6 years of experience in </span><span>Computer Science, Business, Engineering, </span><span>IT</span><span> or related </span><span>field </span><span> OR</span><span> </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Bachelor’s degree with 6 - 8 years of experience in </span><span>Computer Science, Business, Engineering, </span><span>IT</span><span> or related </span><span>field </span><span> OR</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Diploma with 10 - 12 years of experience in </span><span>Computer Science, Business, Engineering, </span><span>IT</span><span> or related field </span><span> </span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p></p></div><div><p><b><span>Must-Have Skills</span><span>:</span></b><span> </span></p><p></p></div><div><ul><li><p><span><span>Strong understanding of Agile methodologies, particularly the Scaled Agile Framework (</span><span>SAFe</span><span>)</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Prior experience with Agile project management tools, such as Jira</span><span>, </span><span>Confluence</span><span> and Jira Align</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in guiding teams through Agile </span><span>events</span><span> and ensuring adherence to </span><span>S</span><span>AFe</span><span> practices</span><span> and behaviors</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Excellent problem-solving skills and a passion for tackling complex challenges </span><span>with data</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Collaborative spirit and effective communication skills to work seamlessly in a cross-functional team</span></span><span> </span></p></li></ul></div><div><p></p><p><b><span>Good-to-Have Skills:</span></b><span> </span></p><p></p></div><div><ul><li><p><span><span>Deep understanding of DevOps and Test Automation Processes in software delivery </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Workshop facilitation </span><span>and training experience</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Strong learning agility; ability to understand </span><span>data and analytics processes that this role will </span><span>play a leadership role on</span></span><span> </span></p></li></ul></div><div><p></p><p><b><span>Professional Certifications:</span><span> </span></b></p><p></p></div><div><ul><li><p><span><span>Certified </span><span>SAFe</span><span> Scrum Master or similar (preferred)</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Certified</span><span> </span><span>SAFe</span><span> RTE or similar</span><span> (</span><span>preferred</span><span>)</span></span><span> </span></p></li></ul></div><div><p></p><p><b><span>Soft Skills: </span></b></p><p></p></div><div><ul><li><p><span><span>Excellent people and project management skills</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to work collaboratively with cross-functional teams</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to manage multiple priorities successfully</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Team oriented with a focus on achieving </span><span>team goals</span></span><span> </span></p></li></ul></div><div><p><span> </span></p><p></p><p></p></div><div><p><span class="emphasis-3"><b><b>THRIVE</b></b></span></p><p><span class="emphasis-3"><b><b>WHAT YOU CAN EXPECT OF US</b></b></span></p><p></p><p></p><ul><li><p>Vast opportunities to learn, develop, and move up and across our global organization.</p></li><li><p>Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</p></li><li><p>Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits.</p></li><li><p>Flexible work arrangements.</p></li></ul><p></p><p></p><p><span class="emphasis-3"><b>APPLY NOW</b></span></p><p></p><p>Objects in your future are closer than they appear. Join us.</p><p></p><p></p><p><span class="emphasis-3"><b>CAREERS.AMGEN.COM</b></span></p><p></p><p></p><p><span class="emphasis-3"><b>EQUAL OPPORTUNITY STATEMENT</b></span></p><p></p><p></p><p>AMGEN is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/scrum-master-commercial-data-and-analytics-amgen/6a08983f2f1861929d253374</link><guid isPermaLink="true">http://biotechroles.com/scrum-master-commercial-data-and-analytics-amgen/6a08983f2f1861929d253374</guid><pubDate>Sat, 16 May 2026 16:15:59 GMT</pubDate><company>Amgen</company><location>Portugal - Lisbon</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Sr Congress & Events Coordinator, based in Egypt]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales &amp; Marketing Operations<h2></h2><h2><b>Job Description</b></h2><p></p><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b></p><p>You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.</p><p></p><p></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role, you will coordinate Amgen Events, local, regional and at various international congresses and implements international programs and events, managing the logistical elements of Congress and Events:</p><ul><li><p>Supports the different businesses in coordinating congresses related to their product launch</p></li><li><p>Coordinates all events ensuring onsite quality of services (corporate socials, KOL diners, hospitality suite etc.)</p></li><li><p>Identifies and coordinates locations (e.g., hotels, restaurants, social events, etc.)</p></li><li><p>Negotiates contracts with different suppliers (e.g., hotels, restaurants, etc.)</p></li><li><p>Updates, compiles and maintains appropriate databases for travel bookings, invoices, cancellation policies</p></li><li><p>Monitors and meets deadlines (e.g., invoices, cancellation policies)</p></li><li><p>Communicates with participants to disseminate information related to the congress and related events</p></li><li><p>Consistently evaluates existing procedures and congress tools, sources and implements new practices</p></li><li><p>Builds hotel &amp; invites request forms, send to affiliates, collect and consolidate data</p></li><li><p>Co-ordination with other country contacts throughout affiliates</p></li><li><p>Back charging of the appropriate expenses to the various affiliates and internal clients</p></li><li><p>Follows Amgen Compliance regulations and is able to train the team on the event requirements as per SOPs</p></li><li><p>Uses the company’s internal systems to submit, update and close all related events in a timely and compliant manner</p></li></ul><p></p><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The Sr Congress Events Coordinator professional we seek is a teammate with these qualifications:</p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Bachelor&#39;s Degree</p></li><li><p>Minimum 5 years of related industry experience</p></li><li><p>Experience in organization of congresses and events</p></li><li><p>Knowledge of travel and tourism industry</p></li><li><p>Fluency in English, both verbally and written</p></li><li><p>Experience with MS Office programs</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Knowledge of health regulations</p></li><li><p>Degree in Business or Marketing</p></li><li><p>Advanced knowledge of Marketing and Finance procedures</p></li><li><p>Fluency in additional languages</p></li><li><p>BA in Hotel management</p></li></ul><p></p><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.</p><p>In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p><p></p><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p></p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-congress-and-events-coordinator-based-in-egypt-amgen/6a08983f2f1861929d253373</link><guid isPermaLink="true">http://biotechroles.com/sr-congress-and-events-coordinator-based-in-egypt-amgen/6a08983f2f1861929d253373</guid><pubDate>Sat, 16 May 2026 16:15:59 GMT</pubDate><company>Amgen</company><location>Egypt - Cairo</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Quality Manager, Global Distribution Quality]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Quality<h2></h2><h2><b>Job Description</b></h2><div><div><div><div><div><div><div><div><div><p>At Amgen, our mission is simple: to serve patients. Every day, our teams ensure that critical manufacturing processes run safely, reliably, and compliantly — enabling the delivery of life-changing medicines to millions of patients worldwide. Join us as:</p><p></p></div></div></div></div></div></div></div></div></div><h1></h1><p><span class="emphasis-3">Quality Specialist, Global Distribution Quality</span></p><p></p><p><span class="emphasis-3"><b>LIVE</b></span></p><p><span class="emphasis-3"><b>What you will do</b></span></p><p>The Quality Specialist, Global Distribution Quality, will serve as a key member of Amgen&#39;s global quality organization, providing quality assurance oversight for global distribution operations, transportation quality systems, and distribution-related partners and service providers. This role will act as a subject matter expert for Good Distribution Practices, controlled temperature shipping, distribution documentation, quality systems, deviations, complaints, audits, inspections, and transportation lane assessments. The Quality Specialist will partner closely with Global Supply Chain, Regional Quality, Global Distribution Hubs, the Global Transportation Excellence Team, Thermal Engineering Systems, manufacturing sites, and external distribution partners to ensure Amgen products are transported and distributed in compliance with applicable regulations, internal standards, and patient-focused quality expectations. This role requires strong technical judgment, operational discipline, stakeholder influence, and the ability to work effectively in complex, global, and cross-functional environments.</p><p></p><p>Key Responsibilities:</p><ul><li><p>Provide quality assurance oversight for Amgen&#39;s Global Distribution Hubs, transportation processes, and distribution-related quality systems.</p></li><li><p>Serve as a subject matter expert for Good Distribution Practices, transportation quality requirements, distribution documentation, and applicable procedures.</p></li><li><p>Support the selection, qualification, approval, and ongoing quality oversight of distribution partners, suppliers, third-party service providers, and transportation-related vendors.</p></li><li><p>Provide QA support for distribution deviations, complaints, transportation lane assessments, change controls, and related investigations.</p></li><li><p>Partner with Supply Chain and cross-functional teams to assess and support productivity, transformation, and cost-saving initiatives while maintaining compliance and product quality.</p></li><li><p>Collaborate with Thermal Engineering Systems to implement, qualify, and continuously improve Controlled Temperature Shipping Systems.</p></li><li><p>Support audits and inspections of manufacturing sites, supply hubs, distribution partners, and third-party service providers.</p></li><li><p>Execute internal assessments and audits, develop clear reports, communicate findings, and support timely completion of corrective and preventive actions.</p></li><li><p>Apply risk-based and data-driven decision-making to identify quality risks, evaluate controls, and recommend preventive measures.</p></li><li><p>Represent Quality in cross-functional meetings, quality forums, management reviews, inspection readiness activities, and project teams.</p></li><li><p>Communicate complex quality issues clearly and effectively to stakeholders, including leadership, site teams, regional teams, and external partners.</p></li><li><p>Promote strict adherence to procedures, documentation standards, GDP expectations, and applicable regulatory requirements.</p></li><li><p>Contribute to global quality initiatives, continuous improvement efforts, and harmonization of distribution quality practices across the network.</p></li></ul><p></p><p><span class="emphasis-3"><b>WIN</b></span></p><p><span class="emphasis-3"><b>What we expect of you</b></span></p><p>Minimum Requirements:</p><ul><li><p>Doctorate degree and 2 years of Quality and Compliance experience; or</p></li><li><p>Master&#39;s degree and 6 years of Quality and Compliance experience; or</p></li><li><p>Bachelor&#39;s degree and 8 years of Quality and Compliance experience; or</p></li><li><p>Associate&#39;s degree and 10 years of Quality and Compliance experience; or</p></li><li><p>High school diploma / GED and 12 years of Quality and Compliance experience.</p></li></ul><p></p><p>Preferred Qualifications:</p><ul><li><p>Strong Experience in Quality Assurance, Distribution Quality, Supply Chain Quality, Manufacturing Quality, or Quality Compliance within a regulated pharmaceutical, biotechnology, or life sciences environment.</p></li><li><p>Knowledge of Good Distribution Practices, cGMP expectations, quality systems, documentation practices, deviations, distribution complaints, CAPA, change control, audits, and inspections.</p></li><li><p>Experience supporting global distribution, transportation, cold chain, controlled temperature shipping, logistics, supplier quality, or third-party service provider oversight.</p></li><li><p>Ability to interpret regulatory requirements, internal procedures, and quality standards and apply them to complex or ambiguous operational situations.</p></li><li><p>Demonstrated ability to make data-driven, risk-based decisions and translate technical information into clear recommendations.</p></li><li><p>Strong project execution skills, including planning, stakeholder alignment, risk management, issue escalation, and timely delivery of quality outcomes.</p></li><li><p>Proven ability to build effective partnerships across Quality, Supply Chain, Manufacturing, Engineering, Regional Quality, and external partners.</p></li><li><p>Strong written and verbal communication skills, including the ability to prepare reports, present findings, and influence stakeholders.</p></li><li><p>Ability to manage multiple priorities in a dynamic global environment while maintaining attention to detail and compliance.</p></li><li><p>Demonstrated commitment to continuous improvement, operational excellence, and Amgen&#39;s mission to serve patients.</p></li></ul><p></p><p>Core Competencies:</p><ul><li><p>Technical mastery in distribution quality, quality systems, GDP, documentation, and compliance expectations.</p></li><li><p>Precision and accountability in execution, documentation, and oversight of regulated processes.</p></li><li><p>Strong problem-solving capability, including root cause thinking, deviation support, risk identification, and prevention-focused decision-making.</p></li><li><p>Analytical thinking and ability to interpret data, trends, quality risks, and operational impacts.</p></li><li><p>Compliance leadership, including inspection readiness, audit support, and constructive challenge when standards are at risk.</p></li><li><p>Project and initiative execution with clear ownership, timely delivery, and proactive risk management.</p></li><li><p>Cross-functional partnership, stakeholder influence, and clear communication across sites, regions, functions, and external partners.</p></li><li><p>Commitment to high performance, continuous improvement, and development of others through coaching, knowledge-sharing, and collaboration.</p></li></ul><p></p><p>Location and Travel</p><p>This role may be based in ABR, with regional and global responsibilities across manufacturing sites, supply hubs, distribution partners, and cross-functional teams. Travel may be required.</p><p></p><p><span class="emphasis-3">THRIVE</span></p><p><span class="emphasis-3">WHAT YOU CAN EXPECT OF US</span></p><p>As we work to develop treatments that take care of others, we also care deeply for our teammates’ well-being and growth.</p><ul><li><p>Vast opportunities to learn, develop, and move up and across our global organization.</p></li><li><p>Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</p></li><li><p>Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits.</p></li><li><p>Flexible work arrangements.</p></li></ul><p></p><p><span class="emphasis-3">APPLY NOW</span></p><p>Objects in your future are closer than they appear. Join us.</p><p></p><p><span class="emphasis-3">CAREERS.AMGEN.COM</span></p><p><span class="emphasis-3">EQUAL OPPORTUNITY STATEMENT</span></p><p></p><p>AMGEN is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/quality-manager-global-distribution-quality-amgen/6a08983f2f1861929d253372</link><guid isPermaLink="true">http://biotechroles.com/quality-manager-global-distribution-quality-amgen/6a08983f2f1861929d253372</guid><pubDate>Sat, 16 May 2026 16:15:59 GMT</pubDate><company>Amgen</company><location>Netherlands - Breda</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Sr Workday Data Operation Analyst]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Human Resources<h2></h2><h2><b>Job Description</b></h2><p>Join our team at <b>AMGEN Capability Center Portugal</b>, consistently recognized among the top companies in the Best Workplaces™ ranking by Great Place to Work® in Portugal. In 2026, we were once again distinguished as one of the top Best Workplaces in the country (category 201–500 employees), reinforcing our commitment to an exceptional employee experience and workplace culture.</p><p></p><p>We are a team of over 500 talented individuals, spanning more than 30 functions and areas of expertise, and representing over 40 nationalities. Together, we bring diverse perspectives and professional backgrounds to help shape the future of healthcare through innovation and technology.</p><p></p><p>This is your opportunity to explore a world of possibilities across areas such as Data &amp; Analytics, Digital, Technology &amp; Innovation, Cybersecurity, R&amp;D Operations, Global Distribution, Finance, Regulatory Affairs, General &amp; Administrative, Human Resources, and many more.</p><p></p><p>Located in the heart of Lisbon, our AMGEN office fosters a culture of innovation, excellence, and purpose. Come thrive with us at AMGEN, supporting our mission To Serve Patients.</p><p></p><p>What we do at AMGEN matters in people’s lives.</p><p></p><p></p><p><span class="emphasis-3"><b>Sr Workday Data Operation Analyst</b></span></p><p></p><p></p><p><span class="emphasis-3"><b>LIVE</b></span></p><p><span class="emphasis-3"><b>WHAT YOU WILL DO</b></span></p><p></p><p></p><p>As part of the HR service delivery team, this role serves as a key point of contact and subject matter expert for Workday, ServiceNow, and core HR processes. The Sr Workday Data Operation Analyst will support and improve HR service delivery by providing business subject matter expertise, resolving escalated HR system and process issues, maintaining HR knowledge bases, monitoring HR data quality, and contributing to process and system improvements.</p><p></p><p></p><p><b>Let’s do this. Let’s change the world. In this vital role you will:</b></p><ul><li><p><b>Workday &amp; HR expertise</b> – Act as a subject matter expert for Workday and core HR processes, supporting workforce administration activities in alignment with global standards.</p></li><li><p><b>HR service delivery support</b> – Provide support to employees, managers, HR Associates, and local HR teams by resolving escalated Workday and HR process inquiries, ensuring adherence to service level agreements.</p></li><li><p><b>Data quality &amp; governance</b> – Monitor and ensure HR data accuracy through audits, reporting, mass uploads (EIBs), and data correction activities.</p></li><li><p><b>Process &amp; knowledge management</b> – Maintain internal and external HR knowledge bases, identifying opportunities for simplification and continuous improvement.</p></li><li><p><b>Security &amp; compliance</b> – Support Workday security role assignments, reviews, and documentation, ensuring alignment with SOX and compliance requirements.</p></li><li><p><b>Continuous improvement</b> – Contribute to system, process, and service enhancement initiatives across Workday, ServiceNow, and HR operations.</p></li><li><p><b>Business analysis</b> – Analyze business needs and translate them into effective HR system or process solutions.</p></li><li><p><b>Stakeholder collaboration</b> – Build strong relationships with global HR teams, employees, managers, and key stakeholders across regions.</p></li></ul><p></p><p></p><p><span class="emphasis-3"><b>WIN</b></span></p><p><span class="emphasis-3"><b>WHAT WE EXPECT OF YOU</b></span></p><p></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The HR professional we seek is detail-oriented and analytical with a strong ability to navigate systems and processes in a global environment.</p><p></p><p></p><p><b>Minimum requirements</b></p><p><br />• Minimum 4 years of experience in Human Resources and/or a corporate service center environment<br />• Minimum 3 years of experience supporting Workday in an HR service delivery environment<br />• Experience with Workday Core HCM processes and workforce administration<br />• Experience with EIBs, data audits, and data correction processes<br />• Proficiency in Microsoft Office 365, especially Excel<br />• Experience working with standard operating procedures<br />• Fluency in English</p><p></p><p></p><p><b>Preferred requirements</b></p><p>• Bachelor’s degree in Human Resources, Business Administration, Economics, or a related field<br />• Experience in a multinational or shared service center environment<br />• Experience with Workday security and SOX-related processes<br />• Project management experience<br />• Fluency in additional languages</p><p></p><p></p><p></p><p><span class="emphasis-3"><b>THRIVE</b></span></p><p><span class="emphasis-3"><b>WHAT YOU CAN EXPECT OF US</b></span></p><p></p><p></p><p>As we work to develop treatments that take care of others, we also care deeply for our teammates’ well-being and growth.</p><ul><li><p>Vast opportunities to learn, develop, and move up and across our global organization.</p></li><li><p>Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</p></li><li><p>Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits.</p></li><li><p>Flexible work arrangements.</p></li></ul><p></p><p></p><p><span class="emphasis-3"><b>APPLY NOW</b></span></p><p>Objects in your future are closer than they appear. Join us.</p><p></p><p></p><p></p><p><span class="emphasis-3"><b>CAREERS.AMGEN.COM</b></span></p><p></p><p></p><p></p><p><span class="emphasis-3"><b>EQUAL OPPORTUNITY STATEMENT</b></span></p><p>AMGEN is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-workday-data-operation-analyst-amgen/6a08983e2f1861929d253371</link><guid isPermaLink="true">http://biotechroles.com/sr-workday-data-operation-analyst-amgen/6a08983e2f1861929d253371</guid><pubDate>Sat, 16 May 2026 16:15:58 GMT</pubDate><company>Amgen</company><location>Portugal - Lisbon</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[SAP Transportation Technical Lead]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p></p><p>Join our team at <b>AMGEN Capability Center </b>, number 1 company in Best Workplaces TM. We have a team of over 500 talented people and more than 40 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data &amp; Analytics, Digital, Technology and Innovation, Finance, General &amp; Admin, Human Resources, Regulatory Affairs and many more. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives.</p><p></p><p><span class="emphasis-3"><b>SAP Transportation Technical Lead</b></span></p><p></p><p><span class="emphasis-3"><b>LIVE </b></span></p><p><span class="emphasis-3"><b>WHAT YOU WILL DO</b></span></p><p></p><p>Amgen is seeking an experienced SAP Transportation Management Technical Lead to join the product team responsible for delivering end-to-end SAP TM solutions within an Agile framework. This role focuses on designing, configuring, and supporting transportation management processes using SAP TM on S/4HANA and ECC platforms.</p><p><br />This architect will work hands-on within a collaborative Agile team, participating in all phases of solution delivery—from gathering functional requirements and managing transportation master data to configuration, testing, and deployment. The role includes demonstrating working solutions to the team, ensuring continuous feedback and alignment with product goals.</p><p><br />This position requires strong expertise in designing and configuring the TM solution in all areas including Package Building, Consolidation, Change Controller, Carrier Invoicing, Freight Settlement, TM Analytics and TM integration with EWM and BN4L (Business Network for Logistics).</p><p></p><p><b>Key Responsibilities:</b></p><ul><li><p>Design, Configure and Optimize transportation planning, execution, and freight cost management, etc.</p></li><li><p>Thorough understanding of BN4L platform and ability to integrate third party service providers using APIs and EDI capabilities on BN4L Freight Collaboration module</p></li><li><p>Thorough understanding of updates from BN4L to TM</p></li><li><p>Configure and support SAP TM solutions in both ECC and S/4HANA environments</p></li><li><p>Design and implement transportation lane-based transportation solutions for optimized routing and cost efficiency</p></li><li><p>Conduct architectural reviews and assessments to identify potential risks and recommend mitigation strategies</p></li><li><p>Oversee creation and maintenance of critical documentation such as functional designs, test cases, and user manuals. Ensure compliance with pharmaceutical industry standards and regulations.</p></li><li><p>Participate in ERP implementation projects, including blueprinting, gap analysis, testing, go-live, and post-production support.</p></li><li><p>Lead/Oversee and mentor other architects and team members to ensure the effective execution of the projects and services</p></li><li><p>Participate in sprint planning, reviews, and retrospectives to deliver and sustain Amgen&#39;s S/4HANA ecosystem utilizing the Scaled Agile Framework (SAFe)</p></li><li><p>Develop innovative solutions that drive speed to value via AI/ML and leading control practices</p></li></ul><p></p><p><span class="emphasis-3"><b>WIN</b></span></p><p><span class="emphasis-3"><b>WHAT WE EXPECT OF YOU</b></span></p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Any degree with 12 - 17 years of SAP implementation experience in SAP MM, PP-PI and QM modules</p></li><li><p>Proven understanding and application of BN4L best practices for Freight Collaboration</p></li><li><p>Strong knowledge of transportation execution, freight cost calculation, and carrier collaboration</p></li></ul><p></p><p><b>Must-Have Skills:</b></p><ul><li><p>Strong hands-on experience configuring and customizing SAP S/4 TM</p></li><li><p>Hands-on experience with configuring and onboarding 3rd party service providers on BN4l Freight Collaboration platform</p></li><li><p>Ability to design and implement solutions based on business requirements, including debugging and root cause analysis.</p></li><li><p>Experience in creating detailed documentation, including functional specifications, test cases, and compliance reports.</p></li></ul><p></p><p><b>Good-to-Have Skills:</b></p><ul><li><p>Knowledge of SAP S/4 Inbound logistics and warehouse management process, Transportation management.</p></li><li><p>Familiarity with Agile methodologies for software delivery and process improvement.</p></li></ul><p></p><p><b>Professional Certifications<i>:</i></b></p><ul><li><p>SAP S/4 TM (preferred) </p></li><li><p>Agile Certified Practitioner (preferred)</p></li></ul><p></p><p><b> Soft Skills:</b></p><ul><li><p>Experience in life sciences, biotech, or other regulated industries</p></li><li><p>SAP S/4HANA implementation or upgrade experience</p></li><li><p>Familiarity with freight settlement, lane planning, and third-party logistics integration</p></li><li><p>Working knowledge of JIRA, ALM, ServiceNow, and Solution Manager</p></li><li><p>Exposure to AI and automation in supply chain applications</p></li><li><p>Strong analytical and problem-solving abilities.</p></li><li><p>Excellent communication and collaboration skills.</p></li><li><p>Ability to work effectively with cross-functional teams and stakeholders.</p></li><li><p>Detail-oriented with a focus on accuracy and compliance.</p></li></ul><p></p><p><b><span>Shift Information:</span></b></p><p></p><p>This role may require occasional flexibility in working hours to meet evolving business needs.</p><p></p><p><span class="emphasis-3"><b>THRIVE<br />WHAT YOU CAN EXPECT OF US</b></span></p><ul><li><p>Vast opportunities to learn, develop, and move up and across our global organization. </p></li><li><p>A diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act. </p></li></ul><p></p><p><span class="emphasis-3"><b>APPLY NOW</b></span></p><p></p><p>Objects in your future are closer than they appear. Join us. <b> </b></p><p></p><p><span class="emphasis-3"><b>CAREERS.AMGEN.COM</b></span></p><p></p><p><span class="emphasis-3"><b>EQUAL OPPORTUNITY STATEMENT  </b></span></p><p></p><p></p><p>AMGEN is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.  </p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sap-transportation-technical-lead-amgen/6a08983e2f1861929d253370</link><guid isPermaLink="true">http://biotechroles.com/sap-transportation-technical-lead-amgen/6a08983e2f1861929d253370</guid><pubDate>Sat, 16 May 2026 16:15:58 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Web Strategy & Operations Senior Associate]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Marketing<h2></h2><h2><b>Job Description</b></h2><div><div><p>Join our team at AMGEN Capability Center Portugal, consistently recognized among the top companies in the Best Workplaces™ ranking by Great Place to Work® in Portugal. In 2026, we were once again distinguished as one of the top Best Workplaces in the country (category 201–500 employees), reinforcing our commitment to an exceptional employee experience and workplace culture.</p><p></p><p>We are a team of over 500 talented individuals, spanning more than 30 functions and areas of expertise, and representing over 40 nationalities. Together, we bring diverse perspectives and professional backgrounds to help shape the future of healthcare through innovation and technology.</p><p>This is your opportunity to explore a world of possibilities across areas such as Data &amp; Analytics, Digital, Technology &amp; Innovation, Cybersecurity, R&amp;D Operations, Global Distribution, Finance, Regulatory Affairs, General &amp; Administrative, Human Resources, and many more.</p><p></p><p>Located in the heart of Lisbon, our AMGEN office fosters a culture of innovation, excellence, and purpose. Come thrive with us at AMGEN, supporting our mission To Serve Patients.</p><p></p><p>What we do at AMGEN matters in people’s lives.</p></div><div><p><span> </span></p><p></p><p></p></div><div><p><span class="emphasis-3"><b>Sr Associate, Web Strategy &amp; Operations</b></span></p><p></p><p></p><p></p><p><span class="emphasis-3"><b>LIVE</b></span></p></div><div><p><span class="emphasis-3"><b>WHAT YOU WILL DO</b></span></p><p></p><p></p><p></p></div><div><p><span><span>The<span>  </span></span><span>Global Customer Capabilities &amp; Innovation (GCCI) team</span><span><span>  </span>is looking for an experienced <span> </span></span><span>S</span><span>enio</span><span>r Associate, Web Strategy &amp; Op</span><span>eration</span><span>s</span><span><span> </span></span><span>(WSO)</span><span>. GCC</span><span>I</span><span><span>  </span>delivers efficient and consistent quality global marketing assets<span>  </span></span><span>that </span><span><span> </span>scale across multiple channels &amp; markets. As part of the GCC</span><span>I</span><span>, the <span> </span></span><span>S</span><span>enior</span><span><span>  </span>Associate</span><span><span>  </span></span><span>provides integrated end-to-end<span>  </span></span><span>program and<span>  </span></span><span>project management to ensure successful delivery of websites and bring thought leadership and drive delivery.</span></span></p><p></p><p></p></div><div><p><b><span>Key Responsibilities:</span></b></p><p></p></div><div><ul><li><p><b><span>Strategic Web <span> </span></span><span>Project</span><span><span>  </span>Lead</span><span>: <span> </span></span></b><span><span>Support the coordination and execution of cross-functional web programs across GCCI WSO, helping to ensure alignment on timelines, resources, and budgets for website launches, enhancements, and optimization initiatives. Partner with program leads to track progress, <span> </span></span><span>maintain</span><span><span>  </span>alignment across initiatives, and <span> </span></span><span>identify</span><span><span>  </span>potential risks, escalating as needed.</span></span></p></li></ul><p></p></div><div><ul><li><p><b><span>Portfolio Prioritization &amp; Planning:</span></b><span><span><span>  </span></span><span>Own<span>  </span></span><span>quarterly portfolio intake and prioritization across web initiatives in partnership with Technology and business stakeholders, ensuring alignment to enterprise strategy and value realization goals. Operationalize governance frameworks to evaluate demand,<span>  </span></span><span>clarify</span><span><span>  </span>requirements at a program level, assess cross-project dependencies, and align on delivery.</span></span></p></li></ul><p></p></div><div><ul><li><p><b><span>Cross-Functional<span> </span></span><span>Coordination</span><span>:</span></b><span><span><span>  </span></span><span>Assist in<span> </span></span><span>alignment and day-to-day coordination across cross-functional teams, including content, design, development, SEO, analytics, project owners, and platform stakeholders, to enable effective planning and execution of web initiatives.</span></span></p></li></ul><p></p></div><div><ul><li><p><b><span>Program Governance &amp; Risk<span> </span></span><span>Management</span><span>:</span></b><span><span><span>  </span></span><span>Oversee program health across initiatives by monitoring delivery progress, governance adherence, documentation standards, cross-project risks, issues, and change impacts throughout launch and hypercare. </span></span><span> </span></p></li></ul><p></p></div><div><ul><li><p><b><span>Website Performance &amp; Analytics: </span></b><span><span><span> </span></span><span>Support the </span><span><span> </span>track</span><span>ing </span><span><span> </span>and report</span><span>ing of</span><span><span>  </span>KPIs by analyzing web traffic, user behavior, and SEO metrics. <span> </span></span><span>Contribute insights to help improve site performance and inform operational reviews.</span></span></p></li></ul><p></p></div><div><ul><li><p><b><span>Quality Assurance &amp; Testing:</span></b><span><span><span>  </span></span><span>Partner with stakeholders to conduct functional testing and ensure adherence to agile web development processes, industry best practices, and high-quality standards</span><span>.</span></span></p></li></ul><p></p></div></div><div><div><ul><li><p><b><span>Continuous Improvement &amp; Operational Excellence:</span></b><span><span><span>  </span></span><span>Lead structured retrospectives,<span>  </span></span><span>identifying</span><span><span>  </span>improvement opportunities.</span><span><span>  </span></span><span>Support the adoption of governance frameworks, templates, and delivery processes to improve efficiency and speed-to-market.</span></span><span> </span></p></li></ul><p></p></div><div><ul><li><p><b><span>Capability Enablement &amp; Portfolio<span>  </span></span><span>Optimization</span><span>:</span></b><span><span><span>  </span></span><span>Continuously assess and<span>  </span></span><span>optimize</span><span><span>  </span>the web portfolio to ensure alignment with evolving business priorities, resource capacity, and long-term digital strategy.</span></span><span> </span></p></li></ul><p></p></div><div><ul><li><p><b><span>Compliance, Risk &amp; Operational Resilience:</span></b><span><span><span>  </span></span><span>Ensure compliance</span><span><span>  </span>with regulatory, legal, and brand standards across all web initiatives. Embed risk management into program governance to support sustainable digital operations.</span></span></p></li></ul><p>​<span> </span></p><p></p><p></p><p><span class="emphasis-3"><b>WIN</b></span></p></div><div><p><span class="emphasis-3"><b>WHAT WE EXPECT OF YOU</b> </span></p><p></p><p></p><p></p></div><div><p><span><span>We are all different, yet we all use our unique contributions to serve patients. The Web Project<span> </span></span><span>Manager</span><span><span> </span>professional we<span> </span></span><span>seek</span><span><span> </span>is a collaborator with these qualifications.</span></span></p><p></p></div><div><p><b><span>Basic Qualifications:</span></b><span> </span></p><p></p></div><div><p><span><span>Doctorate degree</span></span></p></div><div><p><span><span>O</span><span>r</span></span></p></div><div><p><span><span>Master’s degree and 2 years of digital or web project management experience</span></span></p></div><div><p><span><span>Or</span></span></p></div><div><p><span><span>Bachelor’s degree and<span> </span></span><span>4</span><span><span> </span>years of digital or web project management experience</span></span></p></div><div><p><span><span>Or</span></span></p></div><div><p><span><span>Associate’s degree and 10 years of digital or web project management experience</span></span></p></div><div><p><span><span>Or</span></span></p></div><div><p><span><span>High school diploma / GED and 12 years of digital or web project management experience</span></span></p><p></p><p></p></div><div><p><b><span>Preferred<span> </span></span><span>Experience</span><span>:</span></b><span> </span></p><p></p></div><div><ul><li><p><b><span>Digital<span> </span></span><span>Program /<span> </span></span><span>Project Management Expertise:</span></b><span><span> </span></span><br /><span><span>3</span><span>&#43; years of experience managing end-to-end digital and website lifecycle projects in fast-paced, multi-stakeholder environments, including complex, cross-country, and high-impact initiatives.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Agile &amp; Program Management:</span></b><span><span> </span></span><br /><span><span>Strong knowledge of Agile methodologies (preferably<span> </span></span><span>SAFe</span><span>) with experience managing website roadmaps and continuous improvement initiatives. Proficient in<span> </span></span><span>Program / Project Management<span> </span></span><span>tools such as JIRA, ServiceNow, Confluence, and Google Analytics.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Stakeholder &amp; Vendor Management:</span></b><span><span> </span></span><br /><span><span>Proven ability to negotiate priorities, manage expectations, and build productive relationships across diverse, cross-functional teams and external partners.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><b><span>Regulatory &amp; Technical Acumen:</span></b><span><span> </span></span><br /><span><span>Experience <span> </span></span><span>operating</span><span><span> </span>in regulated industries (preferably pharma) with understanding of compliance requirements. Familiarity with accessibility standards (WCAG), privacy regulations (GDPR,<span> </span></span><span>CCPA</span><span>), web technologies (</span><span>e.g.</span><span><span> </span>HTML</span><span>,<span> </span></span><span>CSS), and industry best practices is a plus.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Documentation &amp; Governance:</span></b><span><span> </span></span><br /><span><span>Experience developing detailed project documentation and translating business requirements into technical specifications.</span></span><span> </span></p></li></ul><p></p><p></p></div><div><p><b><span>Preferred<span> </span></span><span>Competencies:</span></b><span> </span></p><p></p></div><div><ul><li><p><b><span>Customer Relationship</span><span><span> </span>&amp; Collaboration:</span></b><br /><span><span>Effective communication</span><span>, relationship management, and cross-functional collaboration skills; able to convey complex technical concepts clearly to non-technical stakeholders.</span></span></p></li></ul></div><div><ul><li><p><b><span>Analytical &amp; Digital Expertise:</span></b><br /><span><span>Proficiency in web analytics, SEO, and UX/UI principles, with the ability to interpret data and drive actionable insights using digital marketing tools.</span></span></p></li></ul></div><div><ul><li><p><b><span>Problem-Solving &amp; Quality Focus:</span></b><br /><span><span>Advanced problem-solving capabilities, attention to detail, and commitment to delivering high-quality outcomes while incorporating feedback.</span></span></p></li></ul></div><div><ul><li><p><b><span>Adaptability &amp; Growth Mindset:</span></b><br /><span><span>Proactive, inclusive, and flexible approach with a willingness to learn, experiment, and continuously improve. Comfortable working across time zones when<span> </span></span><span>required</span><span>.</span></span></p></li></ul><p></p><p></p><p></p></div><div><p><span class="emphasis-3"><b>THRIVE</b></span></p><p><span class="emphasis-3"><b>WHAT YOU CAN EXPECT OF US</b></span></p><p></p><ul><li><p>Vast opportunities to learn, develop, and move up and across our global organization.</p></li><li><p>Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</p></li><li><p>Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits.</p></li><li><p>Flexible work arrangements.</p></li></ul><p></p><p></p><p><span class="emphasis-3"><b>APPLY NOW</b></span></p><p></p><p>Objects in your future are closer than they appear. Join us.</p><p></p><p></p><p><span class="emphasis-3"><b>CAREERS.AMGEN.COM</b></span></p><p></p><p></p><p><span class="emphasis-3"><b>EQUAL OPPORTUNITY STATEMENT</b></span></p><p></p><p></p><p>AMGEN is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/web-strategy-and-operations-senior-associate-amgen/6a08983d2f1861929d25336f</link><guid isPermaLink="true">http://biotechroles.com/web-strategy-and-operations-senior-associate-amgen/6a08983d2f1861929d25336f</guid><pubDate>Sat, 16 May 2026 16:15:57 GMT</pubDate><company>Amgen</company><location>Portugal - Lisbon</location><salary>$55000-80000</salary><type>Full time</type></item><item><title><![CDATA[Senior Packaging Engineer]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Process Development<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Senior Packaging Engineer</b></p><p></p><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. The Packaging Engineering department is a key partner to commercial manufacturing, providing direct technical support to ensure reliable, compliant, and efficient packaging operations. In this role, you will work closely with manufacturing teams on the shop floor to sustain packaging line performance, resolve issues in real time, and drive continuous improvement. The position focuses on lifecycle management of packaging systems within a GMP environment, ensuring consistent product supply and operational excellence across commercial production.</p><p></p><p>This role is highly hands-on and requires applying engineering, physics, and materials science principles to troubleshoot and resolve packaging and material-related challenges in a fast-paced manufacturing setting. You will also play an important role in mentoring junior engineers and supporting the development of technical capabilities within the team.</p><p></p><p><b>Key Responsibilities:</b></p><ul><li>Provide day-to-day technical support to commercial packaging operations, including on-the-floor troubleshooting and issue resolution</li><li>Investigate and resolve deviations, non-conformances, and packaging-related events, including root cause analysis and implementation of effective CAPAs</li><li>Support packaging line performance by identifying and implementing improvements to enhance efficiency, reduce downtime, and minimize waste</li><li>Evaluate and qualify packaging materials to ensure suitability for commercial manufacturing, including managing material changes and supplier issues</li><li>Develop and execute test protocols, generate technical assessments, and support documentation required for material and process changes</li><li>Collaborate closely with Manufacturing, QA, Supply Chain, Maintenance, and Regulatory teams to ensure alignment and rapid issue resolution</li><li>Manage and prioritize multiple operational and project-based activities to meet production schedules and business needs</li></ul><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The packaging professional we seek will possess these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><p>Doctorate degree</p><p>OR</p><p>Master’s degree and 2 years of Engineering, Materials Science, or Industrial Design experience</p><p>OR</p><p>Bachelor’s degree and 4 years of Engineering, Materials Science, or Industrial Design experience</p><p>OR</p><p>Associate’s degree and 8 years of Engineering, Materials Science, or Industrial Design experience</p><p>OR</p><p>High school diploma / GED and 10 years of Engineering, Materials Science, or Industrial Design experience</p><p></p><p><b>Preferred Qualifications:</b></p><ul><li>·Bachelor’s or Master’s degree in Engineering, Materials Science, or Industrial Design</li><li>·Minimum of 5 years of experience in pharmaceutical packaging, with strong exposure to commercial manufacturing support</li><li>·Hands-on experience in a GMP manufacturing environment, including deviation management and root cause analysis</li><li>·Demonstrated ability to work effectively in a fast-paced, operations-driven setting</li><li>·Experience leading or mentoring team members is preferred</li><li>·Strong problem-solving, communication, and cross-functional collaboration skills</li></ul><p></p><p>A strong understanding of materials commonly used in pharmaceutical packaging is essential. Familiarity with the structural and chemical properties of glass, polymers, adhesives, inks, varnishes, and paper is critical to effectively support manufacturing operations.</p><p></p><p>If you are motivated by solving real-time challenges on the production floor and ensuring consistent, high-quality product supply, this role offers an excellent opportunity to make a direct impact.</p><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>115,494.60USD -156,257.40 USD]]></description><link>http://biotechroles.com/senior-packaging-engineer-amgen/6a08983d2f1861929d25336e</link><guid isPermaLink="true">http://biotechroles.com/senior-packaging-engineer-amgen/6a08983d2f1861929d25336e</guid><pubDate>Sat, 16 May 2026 16:15:57 GMT</pubDate><company>Amgen</company><location>US - Ohio - New Albany</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[FP&A Process & Technology Manager]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Finance<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Finance Manager</b></p><p></p><h2><b>What you will do</b></h2><p><span>Let’s do this. Let’s change the world. In this vital role you will </span></p><div><p><span><span>rives</span><span><span> </span>improvements in financial planning and reporting through global process mapping,<span> </span></span><span>standardization,<span> </span></span><span>and technology enablement. This role leads initiatives to streamline workflows, enhance planning models, and implement scalable, automated solutions.</span></span><span> </span></p><p><br /><b><span>FP&amp;A Transformation &amp; Process Improvement</span></b><span> </span></p></div><div><ul><li><p><span><span>Lead or support FP&amp;A transformation initiatives across budgeting, forecasting, long-range planning, management reporting, and performance management </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Conduct stakeholder interviews across functions and regions; develop process maps, perform fit-gap analyses, and design standardized, scalable FP&amp;A processes </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Drive process standardization and simplification,<span> </span></span><span>identifying</span><span><span> </span>opportunities for automation and efficiency </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Prepare and execute change management plans, including training and communications, to ensure adoption of standardized processes, templates, metrics, and ways of working </span></span><span> </span></p></li></ul><p></p></div><div><p><b><span>Technology &amp; Enablement</span></b><span> </span></p></div><div><ul><li><p><span><span>Partner with Finance<span> </span></span><span>and Technology<span> </span></span><span>to implement and enhance planning systems, data models,<span> </span></span><span>AI agent use,<span> </span></span><span>and reporting tools </span></span><span> </span></p></li></ul></div><div><p><b><span>Project Management &amp; Governance</span></b><span> </span></p></div><div><ul><li><p><span><span>Manage end-to-end project delivery, including timelines, milestones, risks, and stakeholder alignment </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Track progress, adoption, and benefits realization of transformation initiatives</span></span><span> </span></p></li></ul><p></p><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a person with these qualifications.</p><p></p><div><p><b><span>Basic Qualifications</span></b><span> </span></p></div><div><p><span><span>Master’s degree AND 2 years of Finance experience</span></span><span> </span></p></div><div><div><p><span><span>OR</span></span><span> </span></p></div><div><p><span><span>Bachelor’s degree AND 4 years of Finance experience</span></span><span> </span></p></div><div><p><span><span>OR</span></span><span> </span></p></div><div><p><span><span>Associate’s degree AND 8 years of Finance experience</span></span><span> </span></p></div><div><p><span><span>OR</span></span><span> </span></p></div><div><p><span><span>High school diploma / GED AND 10 years of Finance experience</span></span><span> </span></p></div><div><p><span><span> </span></span><span> </span></p></div><div><p><b><span>Preferred Qualifications</span></b><span> </span></p></div><div><ul><li><p><span><span>Experience in FP&amp;A, finance transformation, or process improvement </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong<span> </span></span></span><b><span>project management and<span> </span></span><span>change</span><span><span> </span>management</span></b><span><span><span> </span>skills </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience with<span> </span></span></span><b><span>financial systems, data tools, or automation solutions</span></b><span><span><span> </span>(e.g., Anaplan, SAP, Power BI) </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to map processes, manage stakeholders, and deliver scalable solutions </span></span><span> </span></p></li></ul></div><div><p><span> </span></p><p></p><h2>What you can expect from us</h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><p><b>careers.amgen.com</b></p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p></p></div></div><p></p></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>100,629.80USD -136,146.20 USD]]></description><link>http://biotechroles.com/fpanda-process-and-technology-manager-amgen/6a08983c2f1861929d25336d</link><guid isPermaLink="true">http://biotechroles.com/fpanda-process-and-technology-manager-amgen/6a08983c2f1861929d25336d</guid><pubDate>Sat, 16 May 2026 16:15:56 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$130000-170000</salary><type>Full time</type></item><item><title><![CDATA[Specialist Software Engineer(AI/ML)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p>As a Full Stack Developer at Amgen India, you will be responsible for developing and integrating user-facing applications that enable Amgen’s AI/ML and GenAI initiatives.</p><p><br />You’ll work across the frontend and backend stack to create performant, secure, and compliant digital solutions, collaborating closely with UX designers, AI/ML engineers, and Amgen stakeholders.</p><p><br /><b>Key Responsibilities</b></p><ul><li>Build and maintain end-to-end web and data applications that visualize AI/ML outputs.</li><li>Design and develop frontend (React JS) and backend (Python / Node / Java) components.</li><li>Integrate APIs and machine learning models developed within the lab.</li><li>Work with Amgen’s UX team to ensure alignment with brand and usability standards.</li><li>Collaborate with data engineers for API design, data flow, and pipeline integration.</li><li>Implement CI/CD pipelines, containerized deployments, and automated testing.</li><li>Maintain documentation, reusable components, and version control practices.</li></ul><p><br /><b>Required Qualifications</b></p><ul><li>7–10 years of full-stack development experience.</li><li>Strong proficiency in JavaScript / TypeScript, React JS, Node JS, Python / Java.</li><li>Experience with RESTful APIs, GraphQL, and microservices architectures.</li><li>Hands-on experience with cloud-native development (AWS preferred).</li><li>Understanding of secure coding and performance optimization.</li><li>Proficiency in version control (Git) and DevOps practices.</li></ul><p><br /><b>Preferred Skills</b></p><ul><li>Experience building GenAI or data-driven applications integrating ML models.</li><li>Knowledge of Docker, Kubernetes, and Terraform.</li><li>Exposure to MLOps pipelines and model-serving frameworks.</li><li>Familiarity with regulated environments (life sciences / healthcare).</li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/specialist-software-engineeraiml-amgen/6a08983c2f1861929d25336c</link><guid isPermaLink="true">http://biotechroles.com/specialist-software-engineeraiml-amgen/6a08983c2f1861929d25336c</guid><pubDate>Sat, 16 May 2026 16:15:56 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Specialist Cloud DevOps(Amazon Bedrock)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p><b><u>About Amgen</u></b></p><p>Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller, and longer. We discover, develop, manufacture, and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.</p><p></p><p><b><u>ABOUT THE ROLE</u></b></p><p><b><u>Role Description: </u></b></p><p></p><p>The Cloud Lead will own and manage the cloud infrastructure supporting Amgen’s AI/ML Innovation Lab.</p><p></p><p>This position will ensure that all environments—development, testing, and production—are secure, compliant, and scalable.</p><p></p><p>This role combines technical cloud expertise with strong governance and compliance oversight, enabling seamless collaboration between Amgen’s internal IT teams and delivery engineers.<br /> </p><p><b>Key Responsibilities</b></p><ul><li>Lead the cloud governance and provisioning for AI/ML lab environments hosted on AWS.</li><li>Define and enforce cloud security, access control, and compliance policies (GxP, HIPAA, GDPR).</li><li>Collaborate with Amgen’s enterprise IT to align infrastructure with corporate standards.</li><li>Automate environment provisioning using Infrastructure-as-Code (Terraform, CloudFormation).</li><li>Enable CI/CD, containerization, and MLOps pipelines in collaboration with vendor team.</li><li>Monitor system performance, cost efficiency, and reliability across projects.</li><li>Manage network configurations, VPN access, and IAM roles for lab participants.</li><li>Maintain disaster recovery, backup, and audit readiness documentation.<br /> </li></ul><p><b>Required Qualifications</b></p><ul><li>7–10 years of experience in Cloud / DevOps / IT Infrastructure roles.</li><li>Deep expertise in AWS (S3, EC2, EKS, Lambda, SageMaker, IAM, CloudWatch) and Amazon BedRock</li><li>Proven experience with infrastructure automation and CI/CD pipelines.</li><li>Strong understanding of network security, identity, and data privacy controls.</li><li>Prior exposure to regulated industries (life sciences, healthcare) preferred.</li><li>Excellent collaboration and documentation skills.</li></ul><ul><li>Hands-on experience with MLOps, Databricks, or model deployment pipelines.</li><li>Certification in AWS Solutions Architect / DevOps Engineer.</li><li>Familiarity with multi-cloud or hybrid architecture models.</li><li>Knowledge of cost optimization and cloud governance frameworks.<p><b><u>EQUAL OPPORTUNITY STATEMENT</u></b></p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/specialist-cloud-devopsamazon-bedrock-amgen/6a08983c2f1861929d25336b</link><guid isPermaLink="true">http://biotechroles.com/specialist-cloud-devopsamazon-bedrock-amgen/6a08983c2f1861929d25336b</guid><pubDate>Sat, 16 May 2026 16:15:56 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Patient Access Liaison, Manager - Krystexxa - New Orleans, LA (Rare Disease)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p>Join Amgen’s Mission of Serving Patients</p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p>Patient Access Liaison, Manager - KRYSTEXXA</p><p></p><p>What you will do</p><p></p><p>Let’s do this. Let’s change the world. The Patient Access Liaison, Manager is a field-based patient access and reimbursement specialist responsible for supporting patients, caregivers, healthcare providers, and sites of care in navigating insurance coverage and reimbursement pathways for Amgen therapies.</p><p></p><p>The PAL Manager serves as a key resource in helping stakeholders understand payer requirements, prior authorization processes, reimbursement considerations, and available patient support resources. The role focuses on ensuring timely and sustained access to therapy by addressing reimbursement barriers and providing education to patients and providers on coverage and financial assistance programs.</p><p></p><p>Working within a collaborative field environment, the PAL Manager partners with internal teams including Market Access, Medical Affairs, Advocacy, Marketing, Case Management, and Site of Care teams to support the patient journey. The role operates with independence in managing assigned patient cases and contributes field insights that inform broader access strategies.</p><p></p><p>Key Responsibilities</p><p></p><p></p><p>Patient Access and Reimbursement Support</p><ul><li><p>Serve as a resource on patient access and reimbursement for infused and specialty therapies.</p></li><li><p>Assist patients, caregivers, and healthcare providers in navigating insurance benefits, prior authorization requirements, and reimbursement processes.</p></li><li><p>Support the identification and resolution of access challenges, including coverage questions, prior authorization barriers, and denied claims.</p></li><li><p>Provide education regarding coding and billing considerations relevant to therapy access.</p></li></ul><p></p><p>Patient and Caregiver Engagement</p><ul><li><p>Develop relationships with patients and caregivers through phone, virtual, and in-person engagement.</p></li><li><p>Secure written or electronic patient HIPAA authorization within assigned geography.</p></li><li><p>Assess individual patient needs and provide education and resources that support access to therapy.</p></li><li><p>Educate patients on coverage considerations and the steps required to obtain prior authorization.</p></li><li><p>Provide information regarding co-pay assistance programs, national foundations, and free drug programs when appropriate.</p></li></ul><p></p><p>Provider and Site-of-Care Education</p><ul><li><p>Educate physician offices and sites of care on therapy coverage pathways and reimbursement processes.</p></li><li><p>Provide information regarding common prior authorization requirements, coding considerations, and billing practices.</p></li><li><p>Support healthcare providers and infusion centers in navigating reimbursement questions related to patient cases.</p></li></ul><p></p><p>Access Issue Resolution</p><ul><li><p>Investigate patient access challenges before and after infusion.</p></li><li><p>Support physician offices and sites of care in reviewing denied claims and identifying potential next steps.</p></li><li><p>Escalate complex or systemic reimbursement issues to appropriate internal stakeholders.</p></li></ul><p></p><p>Cross-Functional Collaboration</p><ul><li><p>Partner with internal stakeholders including Market Access, Medical Affairs, Advocacy, Case Managers, and Site of Care teams to support patient access initiatives.</p></li><li><p>Coordinate with internal and external partners to ensure appropriate resources are available to support patient access.</p></li><li><p>Share field insights regarding payer policies and reimbursement challenges.</p></li></ul><p></p><p>Compliance, Safety, and Operational Excellence</p><ul><li><p>Adhere to company policies, compliance guidance, and applicable to federal, state, and local regulations.</p></li><li><p>Ensure activities align with HIPAA privacy requirements and internal compliance guidelines.</p></li><li><p>Report adverse events and product complaints through established pharmacovigilance processes.</p></li><li><p>Maintain accurate documentation of activities and interactions in Amgen’s internal system.</p></li></ul><p></p><p><b>What we expect of you</b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is someone with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications</b></p><p></p><p>Doctorate degree</p><p>OR</p><p>Master’s degree and 2 years of patient services and/or access and reimbursement experience</p><p>OR</p><p>Bachelor’s degree and 4 years of patient services and/or access and reimbursement experience</p><p>OR</p><p>Associate’s degree and 8 years of patient services and/or access and reimbursement experience</p><p>OR</p><p>High school diploma / GED and 10 years of patient services and/or access and reimbursement experience</p><p></p><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>Experience supporting buy-and-bill or infused pharmaceutical therapies</p></li><li><p>Rare disease or orphan drug experience</p></li><li><p>Clinical background such as nursing or allied health</p></li><li><p>Understanding of reimbursement processes including prior authorization, appeals, and denied claims management</p></li><li><p>Knowledge of HIPAA guidelines and FDA regulatory requirements</p></li><li><p>Familiarity with internal and OIG compliance guidelines</p></li><li><p>Strong analytical and problem-solving skills</p></li><li><p>Excellent written and verbal communication skills</p></li><li><p>Ability to manage complex patient situations and resolve access barriers</p></li><li><p>Experience working in cross-functional field teams</p></li><li><p>Proficiency in Microsoft Office, CRM, AI and relevant systems</p></li></ul><ul><li><p>Access and reimbursement knowledge</p></li><li><p>Prior authorization processes</p></li><li><p>Healthcare reimbursement systems</p></li><li><p>Coding and billing awareness</p></li><li><p>Patient support program knowledge</p></li><li><p>Compliance and privacy requirements</p></li></ul><ul><li><p>Learning agility</p></li><li><p>Decision quality</p></li><li><p>Stakeholder engagement</p></li></ul><ul><li><p>Ability to respond rapidly to urgent access needs to prevent treatment delays or lapses</p></li><li><p>Ability to operate effectively in matrix field environments</p></li><li><p>Travel up to 50%, including occasional overnight and weekend commitments</p></li></ul><p></p><p><b>What you can expect of us</b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><p></p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><p></p><p>Apply now and make a lasting impact with the Amgen team.</p><p></p><p>careers.amgen.com</p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p>Application deadline</p><p></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p>Sponsorship</p><p></p><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><div><p></p></div><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/patient-access-liaison-manager-krystexxa-new-orleans-la-rare-disease-amgen/6a08983b2f1861929d25336a</link><guid isPermaLink="true">http://biotechroles.com/patient-access-liaison-manager-krystexxa-new-orleans-la-rare-disease-amgen/6a08983b2f1861929d25336a</guid><pubDate>Sat, 16 May 2026 16:15:55 GMT</pubDate><company>Amgen</company><location>US - Louisiana - New Orleans</location><salary>$95000-135000</salary><type>Full time</type></item><item><title><![CDATA[Clinical Development Director - Oncology]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Clinical<h2></h2><h2><b>Job Description</b></h2><div></div><div><div><div><div><div><div><div><div><div><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><h2><span>Clinical Development Director - Oncology </span></h2><p></p><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will support Clinical Development in Prostate cancer.</p><ul><li><p>Supporting the development, execution and communication of the global scientific/medical evidence plan</p></li><li><p>Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program</p></li><li><p>Supporting the development of key scientific external relationships with opinion leaders</p></li><li><p>Participating and providing clinical input into safety and regulatory interactions</p></li><li><p>Provide clinical/scientific input during the development and execution of clinical trials</p></li><li><p>Interpret clinical trial data</p></li><li><p>Participate in safety assessments</p></li><li><p>Participate in interactions with regulatory agencies</p></li><li><p>Author CSRs, publications and regulatory submissions</p></li><li><p>Develop key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by Global Development Leader</p></li><li><p>Identify new clinical research opportunities</p></li><li><p>Support in-licensing and out-licensing activities and partner relationships</p></li><li><p>Support product lifecycle management for new indications as directed by Global Development Leader</p></li><li><p>Provide clinical content input to:</p><ul><li><p>Regulatory interactions and documents</p></li><li><p>Safety interactions and documents</p></li><li><p>Materials to be used in Scientific Affairs</p></li><li><p>Materials to be used by the Commercial Organization</p></li></ul></li></ul><p></p><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The clinical development professional we seek has these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><p>MD or DO degree from an accredited medical school<br />AND<br />2 years of clinical research experience and/or basic science research</p><p></p><p><b>Preferred Qualifications:</b></p><p>·5&#43; years of clinical research experience and/or basic science research combined with clinical teaching and patient care activities, particularly in GU Oncology (prostate cancer)</p><p>·Clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company)</p><p>·In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale</p><p>·Familiarity with concepts of clinical research and clinical trial design, including biostatistics</p><p>·Sound scientific and clinical judgment</p><p>·Knowledge of Good Clinical Practices (GCP), FDA and EMEA/CHMP regulations and guidelines, and applicable international regulatory requirements</p><p>·Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication</p><p>·Demonstrated ability as a medical expert in a complex matrix environment</p><p>·History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues</p><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>274,788.85USD -371,773.15 USD]]></description><link>http://biotechroles.com/clinical-development-director-oncology-amgen/6a08983b2f1861929d253369</link><guid isPermaLink="true">http://biotechroles.com/clinical-development-director-oncology-amgen/6a08983b2f1861929d253369</guid><pubDate>Sat, 16 May 2026 16:15:55 GMT</pubDate><company>Amgen</company><location>United States - Remote</location><salary>$180000-280000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director Process Development]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients </b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p><b>Associate Director, Commercial Drug Products &amp; Life Cycle Management</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will be part of Amgen’s Process Development organization, Drug Product Technologies unit that continuously strives to be a technical leader in delivering superior, robust drug product manufacturing processes, high-quality CMC sections, and ensuring supply of commercial products. Drug Product Team leaders (DPTLs) play a central role in this process by serving as single point of accountability for individual drug product programs for technical activities specific to formulation, aseptic drug product process design and validation, integrated development of combination products, process improvements, life cycle changes, regulatory submissions, annual product reviews, etc. DPTLs are part of an integrated operations team and lead a technical team responsible for delivering drug product process transfers, process optimization, process trouble shooting, timely closure of non-conformance investigations and change control assessments to ensure supply of commercial drug products. We are seeking an Associate Director to lead commercial drug product programs as DPTL and lead a scientific team that supports advancing the commercial drug product programs in our portfolio.</p><ul><li><p>Serve as a leader on Drug Product Commercialization Teams responsible for planning, designing, executing, and documenting laboratory studies related to drug product design, formulation, and process development in support of commercialization and lifecycle management of parenteral and/or oral solid dosage presentations.</p></li><li><p>Lead a team of scientists focused on late-stage drug product process development and tech transfer and coach staff with emphasis on people-centered leadership.</p></li><li><p>Provide support, as needed, to clinical and commercial fill/finish manufacturing operations through process capability analysis, troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements.</p></li><li><p>Drive continuous improvement in the drug product development process through technological innovation and application of first principles in process engineering.</p></li><li><p>Participate and lead global cross-functional teams working effectively in a highly matrixed team environment to influence and drive change, efficiency, and foster strong relationships.</p></li><li><p>Author and review guideline documents, technical protocols, reports, product impact assessments, regulatory submissions, and developing responses to regulatory questions.</p></li><li><p>Deliver progress reports and presentations to ensure management awareness and engagement of the status, progress, and future program and functional needs.</p></li><li><p>Actively utilize advanced IS systems to improve drug product design through faster data availability, leveraging historical information, analyzing large data sets, and statistical analysis.</p></li><li><p>Ability to travel domestically and internationally up to 10% of the time.</p></li></ul><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 3 years of experience in engineering or science <b>OR</b></p><p>Masters degree and 7 years of experience in engineering or science <b>OR</b></p><p>Bachelors degree and 9 years of experience in engineering or science <b>OR</b></p><p>Associate’s degree and 12 years of experience in engineering or science <b>OR</b><br />High school diploma / GED and 14 years of experience in engineering or science</p><p><b>And</b></p><p>In addition to meeting at least one of the above requirements, you must have a minimum of 3 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.  Your managerial experience may run concurrently with the required technical experience referenced above </p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>PhD from an accredited college or university in one of the following areas Biotechnology, Pharmaceutical Sciences, Pharmaceutical Chemistry, Chemical Engineering, Biomedical Engineering or a related scientific subject area</p></li><li><p>8&#43; years of pharmaceutical development and management experience</p></li><li><p>8&#43; years of relevant formulation and process development experience within a major biopharmaceutical or pharmaceutical organization</p></li><li><p>Demonstrated knowledge of drug product commercialization and integrated combination product development with hands-on experience with end-to-end development for liquid, lyophilized and/or oral solid dosage drug products in various presentations</p></li><li><p>Demonstrated experience in process transfers, control strategy, authoring MAs, developing robust responses to regulatory questions, supporting validation activities and PAIs at commercial sites</p></li><li><p>Understanding of physical/chemical stability of proteins and how process related stress impacts product quality, specifically, the impact of freezing and drying to short- and long-term stability</p></li><li><p>Strong knowledge about developing processes with single-use manufacturing equipment</p></li><li><p>Aseptic processing experience and familiarity with cGMPs, ICH guidelines</p></li><li><p>Experience that includes elements of new product development, process characterization, equipment design and implementation, technical transfers to global manufacturing sites, statistical process control (SPC), and statistical design and analysis of experiments</p></li><li><p>Strong problem solving and effective cross-functional communication skills</p></li><li><p>Proven ability to learn and act on dynamic information at a rapid pace</p></li><li><p>Ability to participate in global cross-functional teams and work effectively in a highly matrixed environment to lead change, efficiency, and strong cross functional relationships</p></li></ul><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><h2></h2><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2></h2><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2></h2><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>164,021.95USD -221,912.05 USD]]></description><link>http://biotechroles.com/associate-director-process-development-amgen/6a0898382f1861929d253368</link><guid isPermaLink="true">http://biotechroles.com/associate-director-process-development-amgen/6a0898382f1861929d253368</guid><pubDate>Sat, 16 May 2026 16:15:52 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Salesforce Data Cloud Specialist]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p>Join Amgen’s Mission of Serving Patients </p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. </p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas – Oncology, Inflammation, General Medicine, and Rare Disease – we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. </p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. </p><p></p><p><b>Salesforce Data Cloud Specialist</b></p><p><b>What you will do</b> </p><p>Let’s do this. Let’s change the world. In this vital role you will design, develop, configure, test, deploy, and maintain Salesforce applications and solutions that meet business needs, while ensuring the availability, reliability, and performance of critical systems and applications. This role involves working closely with product managers, architects, designers, business stakeholders, and other engineers to create high-quality, scalable solutions across Salesforce Platform, Salesforce Data Cloud, and Salesforce Marketing Cloud. </p><p>You will be part of a team specifically focusing on enterprise CRM, customer data, and omnichannel marketing capabilities. Amgen is using fully integrated and best-in-class technologies, having various enterprise platforms such as SAP, Salesforce, Workday, Veeva, Planisware, or Anaplan; enterprise collaboration platforms such as O365, SharePoint Online and MS Teams, as well as vertical-specific platforms in R&amp;D, Operations, Process Development and Commercial/Marketing areas. </p><p><b>Roles &amp; Responsibilities:</b> </p><ul><li>Design, develop, configure, and implement scalable enterprise applications and integrated solutions across Salesforce Platform, Salesforce Data Cloud, and Salesforce Marketing Cloud ecosystems. </li></ul><ul><li>Own development and configuration of user stories in collaboration with product managers, architects, business stakeholders, and experienced engineers  </li></ul><ul><li>Develop Salesforce solutions using Apex, Lightning Web Components, Flows, Visualforce, SOQL, SOSL, and Salesforce APIs  </li></ul><ul><li>Develop and maintain Salesforce Data Cloud capabilities including data streams, data model objects, identity resolution, calculated insights, segmentation, and activations  </li></ul><ul><li>Develop and maintain Salesforce Marketing Cloud capabilities using Journey Builder, Automation Studio, Email Studio, Mobile Studio, AMPscript, SSJS, and SQL  </li></ul><ul><li>Build and maintain integrations between Salesforce applications, Data Cloud, Marketing Cloud, and enterprise systems using APIs and integration patterns  </li></ul><ul><li>Create and maintain documentation on software design, configuration, integrations, data flows, and deployment processes  </li></ul><ul><li>Turn business ideas and requirements into working solutions through prototypes, proof-of-concepts, and production-ready development  </li></ul><ul><li>Perform front-end and back-end development tasks using Salesforce technologies and Amgen preferred platforms/tools  </li></ul><ul><li>Work with the team to troubleshoot and resolve technical issues, escalating complex issues when needed  </li></ul><ul><li>Analyse business and technical requirements and translate them into clear development tasks  </li></ul><ul><li>Execute unit testing, integration testing, deployment validation, and defect resolution activities  </li></ul><ul><li>Identify and fix bugs and defects during development, testing, and production validation phases  </li></ul><ul><li>Own application maintenance activities by monitoring performance, reviewing issues, and improving reliability  </li></ul><ul><li>Develop and maintain CI/CD pipelines as part of DevOps practices and participate in release management activities  </li></ul><ul><li>Work effectively with global teams to deliver scalable, secure, and compliant enterprise solutions  </li></ul><p><b>What we expect of you</b> </p><p>We are all different, yet we all use our unique contributions to serve patients. </p><p><b>Basic Qualifications:</b> </p><p>Doctorate degree / Master&#39;s degree / Bachelor&#39;s degree and 5 to 9 years of experience in Computer Science, Information Technology, or a related field </p><p><b>Must-Have Skills</b> </p><ul><li>Proficient experience in Agile or Scrum methodologies  </li></ul><ul><li>Professional software development experience in Salesforce  </li></ul><ul><li>Hands-on experience as a Salesforce Developer with Apex, Lightning Web Components, Flows, Visualforce, SOQL, SOSL, and Salesforce APIs  </li></ul><ul><li>Hands-on development experience with Salesforce Data Cloud capabilities including data streams, data model objects, identity resolution, calculated insights, segmentation, and activations  </li></ul><ul><li>Hands-on experience with Salesforce Marketing Cloud technologies including Journey Builder, Automation Studio, Email Studio, AMPscript, SSJS, and SQL  </li></ul><ul><li>Proficient with cloud-based platforms and system integration  </li></ul><ul><li>Proficient version control systems like Git &amp; Release management tools  </li></ul><ul><li>Experience with CI/CD pipelines and DevOps practices  </li></ul><ul><li>Fluent in enterprise collaboration platforms such as O365, SharePoint Online and MS Teams  </li></ul><ul><li>Proficiency in incorporating AI tools in daily activities as well as proactively seeking opportunities to utilize and extend AI toolsets into development work  </li></ul><ul><li>Direct experience in working in global teams  </li></ul><ul><li>Strong understanding of CRM, customer data, digital marketing, and omnichannel engagement capabilities  </li></ul><ul><li>Mastery with at least one programming language such as Python, JavaScript, or similar  </li></ul><ul><li>Experience with vibe coding using large language models for production systems  </li></ul><ul><li>Broad interest in various Amgen preferred platforms/tools  </li></ul><ul><li>Eagerness to learn and grow in a software development environment  </li></ul><ul><li>Ability to work well within a team and communicate effectively  </li></ul><p><b>Preferred Qualifications:</b> </p><p><b>Good-to-Have Skills:</b> </p><ul><li>Salesforce certifications such as Salesforce Platform Developer I, Platform Developer II, Data Cloud Consultant, Marketing Cloud Developer, or Marketing Cloud Consultant  </li></ul><ul><li>Direct experience with one or more Salesforce clouds such as Sales Cloud, Service Cloud, Experience Cloud, Data Cloud, or Marketing Cloud  </li></ul><ul><li>Direct experience with enterprise integration tools or middleware platforms such as MuleSoft  </li></ul><ul><li>Direct experience in one or more enterprise platforms such as AWS, Databricks, Posit, SAP, Salesforce, Workday, Veeva, Planisware, or Anaplan  </li></ul><ul><li>Working understanding in one or more vertical-specific platforms in R&amp;D, Operations, Process Development and Commercial/Marketing areas  </li></ul><ul><li>Experience working with customer data platforms, marketing automation platforms, or personalization solutions  </li></ul><ul><li>Certifications related to Agile or any software or cloud platform are advantageous  </li></ul><p><b>Soft Skills:</b> </p><ul><li>Excellent analytical and troubleshooting skills  </li></ul><ul><li>Comfortable to work effectively with global, virtual teams  </li></ul><ul><li>High degree of initiative and self-motivation  </li></ul><ul><li>Strong collaboration and communication skills  </li></ul><ul><li>Ability to work independently while partnering effectively with cross-functional teams  </li></ul><p><b>What you can expect of us</b> </p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. </p><p>In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. </p><p><b>Apply now and make a lasting impact with the Amgen team.</b> </p><p><b>careers.amgen.com</b> </p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. </p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. </p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. </p><p></p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/salesforce-data-cloud-specialist-amgen/6a0898372f1861929d253367</link><guid isPermaLink="true">http://biotechroles.com/salesforce-data-cloud-specialist-amgen/6a0898372f1861929d253367</guid><pubDate>Sat, 16 May 2026 16:15:51 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Executive Director, Global Insights]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales &amp; Marketing Operations<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients </b></p><p>At Amgen, if you feel like you are a part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. The Executive Director, Global Insights is responsible for leading a best-in-class insights organization that delivers integrated market, customer, and business understanding to inform asset, brand, and portfolio strategy across Amgen’s Global business (excluding Obesity). This role provides strategic leadership across multiple therapeutic areas, including Inflammation, General Medicine, Oncology, and Rare Disease, ensuring that actionable insights shape key decisions across both pipeline and in-line assets. The Executive Director synthesizes complex data, customer perspectives, and market dynamics into clear, compelling, and executive-level recommendations that drive strategic choices and maximize business impact. Business Analytics &amp; Insights (BAI) at Amgen serves as a strategic partner to Global and Regional leadership, enabling data-driven decision-making across the enterprise. BAI integrates a diverse set of capabilities including forecasting, market research and insights, competitive intelligence, and advanced analytics to provide a comprehensive understanding of markets, customers, and portfolio performance. By translating complex data and market dynamics into actionable insights, BAI helps shape commercial strategy, inform investment decisions, and maximize the value of Amgen’s portfolio across therapeutic areas and geographies.This role reports to the Vice President of Business Analytics and Insights (BAI) and works closely with the SVP of Global Marketing &amp; Access and other cross-functional leaders across Forecasting, Competitive Intelligence, Global Marketing, Global Value &amp; Access, as well as regional US and OUS leaders. The Executive Director leads a global organization of insights professionals across multiple global sites and is responsible for advancing insights capabilities through the adoption of automation, artificial intelligence, and advanced analytics to strengthen predictive capabilities, accelerate insight generation, and improve analytical rigor.</p><p></p><p><b>Responsibilities</b></p><ul><li><p>Lead the Global Insights organization, overseeing Directors and their teams responsible for delivering market and customer insights across multiple therapeutic areas, pipeline assets and in-line brands</p></li><li><p>Serve as a strategic thought partner to senior commercial leadership, including Therapeutic Area Heads and the SVP of Global Market Access, providing insights and recommendations that inform brand and portfolio strategy</p></li><li><p>Ensure portfolio-based operating model that enables prioritization, standardization of best practices, and scalable insight generation </p></li><li><p>Partner with Global Marketing, Global Value &amp; Access, Forecasting, Competitive Intelligence, Analytics, and regional teams to ensure insights are integrated and connected across functions</p></li><li><p>Advance insights capabilities through adoption of automation, artificial intelligence, and advanced analytics to strengthen predictive capabilities, accelerate insight generation, and improve analytical rigor</p></li><li><p>Drive collaboration across analytics, market research, forecasting, and competitive intelligence to deliver comprehensive perspectives that inform enterprise decisions and avoid fragmented insights</p></li><li><p>Provide strategic guidance on key initiatives including market opportunity assessments, brand strategy development, lifecycle planning, and clinical development support</p></li><li><p>Build and lead a high performing, interconnected global workforce across multiple global sites, fostering strong talent development and collaboration</p></li><li><p>Ensure insights activities are delivered with high standards for quality, timeliness, and budget management and comply with Amgen SOPs</p></li></ul><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree &amp; 6 years of market research, analytics, competitive intelligence, sales, and/or marketing operations experience OR</p></li><li><p>Master’s degree &amp; 10 years of market research, analytics, competitive intelligence, sales, and/or marketing operations insights experience OR</p></li><li><p>Bachelor’s degree &amp; 12 years of market research, analytics, competitive intelligence, sales, and/or marketing operations insights experience AND</p></li><li><p>6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Ability to influence senior leadership and shape strategic decisions through insights and analytics</p></li><li><p>Strategic thinking and business acumen with deep understanding of commercial drivers in the biopharmaceutical industry</p></li><li><p>Experience leading insights, analytics, or market research organizations supporting multiple brands or therapeutic areas</p></li><li><p>Experience integrating multiple insights capabilities including market research, analytics, forecasting, and competitive intelligence</p></li><li><p>Executive communication and storytelling skills with experience presenting to senior leadership</p></li><li><p>Experience building and leading global teams across multiple geographies</p></li><li><p>Knowledge of drug development, commercialization, and the broader healthcare ecosystem including patients, healthcare providers, and payers</p></li><li><p>Experience leveraging advanced analytics, automation, and AI-enabled insights capabilities</p></li><li><p>Ability to build and develop high-performing teams</p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is <span>$</span>252,756.85 to $341,965.15. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p>Sponsorship for this role is not guaranteed.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>252,756.85USD -341,965.15 USD]]></description><link>http://biotechroles.com/executive-director-global-insights-amgen/6a0898372f1861929d253366</link><guid isPermaLink="true">http://biotechroles.com/executive-director-global-insights-amgen/6a0898372f1861929d253366</guid><pubDate>Sat, 16 May 2026 16:15:51 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Specialty Representative / Senior Specialty Representative - Primary Care - Lexington West]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><h2><b>Territory covers:</b> <span>Lexington West, will cover&gt; Lexington, Bardstown, Campbellsville, Columbia, Greensburg, Russell Springs</span></h2><p><b>Relocation is not offered for this role.</b></p><p></p><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b></p><p><b>Join Amgen’s Mission of Serving Patients</b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p><b>Specialty Representative/Senior Specialty Representative - Repatha.</b></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will be the connection to our customers by providing clinical knowledge of our products to medical professionals and helping them navigate the complex payer environment.</p><p>We are actively searching for a <b>Specialty Representative or Senior Specialty Representative</b> to deliver on our commitment to serve patients. The Specialty Representative/Senior Specialty Representative acts as the primary customer contact and is responsible for implementing marketing strategy and promoting Amgen products as led by the District Manager.</p><p>Amgen supports and encourages our team members to have long term, fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this opportunity to craft a long-term career with Amgen. The Specialty/Senior Specialty Representative acts as the primary customer contact and is responsible for implementing marketing strategy and promoting Amgen products as led by the District Manager.</p><p>Responsibilities include:</p><ul><li><p>Provide current and comprehensive knowledge of Amgen’s products and effectively communicate the clinical benefits to medical professionals to drive appropriate utilization of the products.</p></li><li><p>Perform as a sales leader to achieve territory sales by delivering branded sales messages, conducting planned programs, scheduling and following up on medical educational programs, and achieving or exceeding sales targets through both in-person and virtual engagement.</p></li><li><p>Develop relationships to service and manage accounts, including customizing discussions and customer interactions based on an understanding of customer needs, ensuring product access, resolving or triaging reimbursement issues, and maintaining product contracts.</p></li><li><p>Provide feedback on marketing strategy, analyze the business effectiveness of sales activities and territory performance, and develop territory plans in partnership with the District Manager.</p></li><li><p>Partner with other colleagues to share best practices and continuously learn and grow as a Specialty Representative or Senior Specialty Representative.</p></li><li><p>Demonstrate passion for Amgen’s products and sustain that passion throughout the entire sales cycle, consistently building the brand while keeping patient impact at the forefront.</p></li><li><p>Uphold Amgen values by being science-based, competing intensely to win, creating value for patients, staff, and stockholders, acting ethically, fostering trust and respect, ensuring quality, working in teams, and collaborating, communicating, and remaining accountable.</p></li></ul><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The sales professional we seek is a go-getter with these qualifications. </p><p><b>Basic Qualifications Specialty Representative: </b></p><ul><li><p>Bachelor&#39;s Degree OR</p></li><li><p>Associate&#39;s degree and 4 years of Sales experience OR</p></li><li><p>High school diploma/GED and 6 years of Sales experience</p></li></ul><p><b>Basic Qualifications Senior Specialty Representative: </b></p><ul><li><p>Bachelor’s degree and 3 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related OR  </p></li><li><p>Associate degree and 6 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related OR  </p></li><li><p>High school diploma / GED and 8 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related</p></li></ul><p><b>Preferred Qualifications:</b></p><ul><li><p>Three or more years of sales experience within pharmaceutical, biotech or medical device industry Product or hospital sales experience in the areas of oncology, nephrology, dermatology, rheumatology, inflammation, cardiology, neurology, endocrinology, hepatology, gastroenterology or infectious diseases; and the diseases and treatments involved with these specialties</p></li><li><p>Local market knowledge</p></li><li><p>Established relationships in the territory</p></li><li><p>A Bachelor&#39;s degree in Life Sciences or Business Administration</p></li><li><p>Adaptability with our Core Competencies: Planning and Organizing; Leveraging Business, Industry, and Technical Knowledge; Communicating with Impact; Driving for Results; and Cultivating Internal and External Relationships.</p></li></ul><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for <b>Specialty Representative</b> in the U.S. (excluding Puerto Rico) is $89,880- $121,602. The expected annual salary range for <b>Senior Specialty Representative</b> in the U.S. (excluding Puerto Rico) is $115,036- $155,638. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications. </p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models, including remote and hybrid work arrangements, where possible</p></li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/specialty-representative-senior-specialty-representative-primary-care-lexington-west-amgen/6a0898362f1861929d253365</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-senior-specialty-representative-primary-care-lexington-west-amgen/6a0898362f1861929d253365</guid><pubDate>Sat, 16 May 2026 16:15:50 GMT</pubDate><company>Amgen</company><location>US - Kentucky - Lexington-Fayette</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Senior Oncology Specialist - Sapphire - Jacksonville, FL]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p><b>Territory covers: </b><span>Jacksonville, Tallahassee Gainesville and Daytona, FL</span></p><p>Relocation is not offered for this role.</p><p><b>Join Amgen’s Mission of Serving Patients</b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p><b>Senior Oncology Specialist</b></p><p><b>What you will do</b> </p><p>Let’s do this. Let’s change the world. In this vital role you will be the liaison to our customers by providing clinical knowledge of our products to medical professionals. </p><p>Amgen&#39;s medicines treat serious illnesses and our research address diseases with a limited number of treatment options. With a robust and differentiated pipeline, Amgen remains committed to advancing science to dramatically improve people&#39;s lives. As a values-based organization with a powerful sense of shared purpose toward our mission: to serve patients, we are actively searching for a Senior Oncology Specialist to deliver on this commitment to patients. </p><p>Amgen Oncology is committed to helping patients take on some of the toughest cancers, such as those that have been resistant to drugs, those that progress rapidly through the body and those where limited treatment options exist.</p><p>Amgen&#39;s supportive care treatments help patients combat certain side effects of strong chemotherapy, and our targeted medicines and immunotherapies focus on more than a dozen different malignancies, ranging from blood cancers to solid tumors. With decades of experience providing therapies for cancer patients, Amgen continues to grow its portfolio of innovative and biosimilar oncology medicines.  Amgen is a values-based organization with a powerful sense of shared purpose.  Our mission is to serve patients. </p><p>Amgen supports and encourages our team members to have long term, fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this Senior Oncology Specialist opportunity in the territory</p><p>You will act as the primary customer contact to provide current and comprehensive clinical knowledge of Amgen&#39;s products and effectively communicate the clinical and economic benefits of the products to medical professionals. </p><p>Our Senior Oncology Specialists achieve territory sales by utilizing their Oncology background and experience to: </p><ul><li><p>Create and execute on a comprehensive territory plan, which includes delivering branded sales messages, executing planned programs, scheduling and following-up with medical educational programs, and achieving or exceeding sales targets. </p></li><li><p>Utilize your internal and external relationships to service and manage accounts, including ensuring product access, resolving/triage reimbursement issues, and maintaining product contracts. </p></li><li><p>Craft an effective marketing strategy to aid in driving sales </p></li><li><p>Analyze your business effectiveness of sales activities and territory analysis, as well as develop territory plans with your District Manager </p></li><li><p>Have the passion for our products to sustain that passion through the entire sales cycle while always building our brand and never losing sight of how we serve patients </p></li><li><p>Partner with other colleagues to share best practices and be in a state of continuous curiosity and learning to help you grow as a Sr. Oncology Specialist </p></li><li><p>Leverage your passion for Oncology and disease state awareness, Industry, regulatory and competitive changes to deliver agreed results </p></li></ul><p></p><p><b>What we expect of you</b> </p><p>We are all different, yet we all use our unique contributions to serve patients. The sales professional we seek is a go-getter with these qualifications. </p><ul><li><p>Bachelor’s degree and 3 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related </p></li><li><p>OR  </p></li><li><p>Associate degree and 6 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related </p></li><li><p>OR  </p></li><li><p>High school diploma / GED and 8 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related </p></li></ul><p></p><p><b>Preferred Qualifications:</b> </p><ul><li><p>Preferred experience in Oncology</p></li><li><p>Three or more years of sales and/or marketing experience within pharmaceutical, biotech, healthcare, or medical device industries. </p></li><li><p>Product or hospital sales experience in the areas of oncology, nephrology, dermatology, rheumatology and inflammation. Neurology, endocrinology, hepatology, gastroenterology, or infectious diseases, and the diseases and treatments involved with these specialties. </p></li><li><p>Local Market knowledge. </p></li><li><p>A Bachelor&#39;s degree in Life Sciences or Business Administration. </p></li><li><p>Adaptability with our Core Competencies: Planning and Organizing; Leveraging Business, Industry, and Technical Knowledge; Communicating with Impact; Driving for Results; and Cultivating Internal and External Relationships. </p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $140,465 to $190,041. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models, including remote and hybrid work arrangements, where possible</p></li></ul><p></p><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/senior-oncology-specialist-sapphire-jacksonville-fl-amgen/6a0898352f1861929d253364</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-specialist-sapphire-jacksonville-fl-amgen/6a0898352f1861929d253364</guid><pubDate>Sat, 16 May 2026 16:15:49 GMT</pubDate><company>Amgen</company><location>US - Florida - Jacksonville</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Scientist - Target Discovery & Validation – Induced Proximity Platform (IPP)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><span><b>Role: Senior Scientist - Target Discovery &amp; Validation – Induced Proximity Platform (IPP)</b></span></p><p><span>Reports to: Principal Scientist</span></p><p><span>Location: Burnaby, BC<br /><br /><b>What You Will Do</b><br /><br />Let’s do this. Let’s change the world. Amgen is seeking a passionate and innovative Scientist to join the <b>Induced Proximity Platform</b> team in Burnaby. This role is at the frontier of <b>discovery biology, combining induced proximity technologies to uncover novel therapeutic targets across Amgen’s key therapeutic areas</b> including Oncology, Inflammation, and Cardiometabolic diseases<br /><br />The successful candidate will lead and support cell surface target discovery, validation, and functionalization efforts by developing and applying innovative in vitro assays, proteomics workflows, and flow cytometry based approaches. This role will contribute to large molecule multispecific therapeutic development through target validation, model development, and MOA studies, while collaborating across multidisciplinary teams to analyze data, communicate findings, and maintain high-quality experimental documentation</span><br /> </p><ul><li><span>Design, implement, and execute complex experimental workflows to profile and validate cell surface proteins.</span></li><li><span>Lead and support cell surface-based target discovery and validation projects using in vitro models (cell lines, primary cells, tissues, etc.).</span></li><li><span>Apply proximity labeling, cell surface enrichment, and related proteomics efforts for target validation and nomination studies.</span></li><li><span>Support target functionalization efforts toward developing multispecific antibody therapeutics, and perform efficacy, mechanism of action (MoA) and drug response studies for these therapeutics.</span></li><li><span>Use cutting-edge software tools and collaborate with bioinformatics to analyze and interpret target discovery proteomics datasets.</span></li><li><span>Collaborate across multidisciplinary teams to drive integrated target discovery, validation and functionalization efforts.</span></li><li><span>Present findings internally and externally through team meetings, conferences, and peer-reviewed publications.</span></li><li><span>Maintain detailed electronic lab notebooks and experimental records.</span></li></ul><p></p><p><span><b>What We Expect of You</b><br /><br />We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a Scientist with these qualifications.<br /><br /><b>Basic Qualifications:</b></span></p><ul><li><span>Doctorate degree or</span></li><li><span>Master’s degree and 2 years of relevant scientific experience or</span></li><li><span>Bachelor’s degree and 4 years of relevant scientific experience</span></li></ul><p></p><p><span><b>Preferred Qualifications:</b></span></p><ul><li><span>Expertise in proximity labeling proteomics platforms and target validation using flow cytometry, biochemical and imaging-based techniques.</span></li><li><span>Experience in cell line generation and overexpression systems (e.g., lentiviral delivery).</span></li><li><span>Experience with antibody therapeutics and functional validation of targets using cell-based assays.</span></li><li><span>Hands on experience with cloning, expression and purification analysis is a plus.</span></li><li><span>Familiarity with high-throughput automation platforms (e.g., Agilent Bravo), high-content imaging platforms and analysis software.</span></li><li><span>Track record of scientific innovation, publications, and/or conference presentations.</span></li><li><span>Demonstrated ability to work collaboratively in fast-paced, multidisciplinary teams.</span></li><li><span>Excellent verbal, written, and organizational skills.</span></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>Amgen is proud to have been recognized as one of LinkedIn Top 25 Companies in Canada for career growth. Click <a href="https://lnkd.in/CATopCompanies25" target="_blank">HERE</a> for more details.  If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p>The salary range for this position is $115,503 - $156,269.</p><p>In addition to base salary, Amgen offers competitive and comprehensive total compensation programs aligned with local industry standards.</p><p></p><p><b>Apply now for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>115,503.10 CAD - 156,268.90 CAD]]></description><link>http://biotechroles.com/senior-scientist-target-discovery-and-validation-induced-proximity-platform-ipp-amgen/6a0898352f1861929d253363</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-target-discovery-and-validation-induced-proximity-platform-ipp-amgen/6a0898352f1861929d253363</guid><pubDate>Sat, 16 May 2026 16:15:49 GMT</pubDate><company>Amgen</company><location>Canada - Burnaby</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[EH&S Mgr]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Corporate Services<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><h1><b>EH&amp;S MGR </b></h1><p></p><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will be responsible for corporate policies, guidelines, and standards as well as related training programs and regulatory compliance. Provides leadership vital to implement Global EHSS programs. Develops, monitors, and coordinates Company EHSS programs in accordance with federal, state, and local regulations. Initiates and maintains extensive contacts with key managers and officials of other organizations and regulatory agencies, requiring skill in persuasion and negotiation of critical issues. Provides market/customer sensitivity and commits to talent development.</p><ul><li>Demonstrate functional expertise across high-risk EHSS programs including hot work, pressure safety, machine safety, lockout/tagout (LOTO), working at heights, cranes and lifting, MEWPs, PIVs, confined space, electrical safety, and fire prevention.</li><li>Drive continuous improvement of high-risk programs and work with clients to drive an actively caring safety culture.</li><li>Apply knowledge of OSHA, NFPA, and related regulations to ensure compliant and effective program implementation.</li><li>Identify hazards and apply practical, risk-based solutions to reduce exposure to serious injuries and high-consequence events.</li><li>Conduct periodic inspections and audits using established governance systems and keep EHSS management apprised of potential risks and liabilities. </li></ul><p></p><h2><b>Primary responsibilities include:</b></h2><ul><li>Own and drive the execution of site high-risk EHSS programs, ensuring effective implementation, compliance, and continuous improvement across operations.</li><li>Implement and maintain site-level EHSS programs for high-risk activities including LOTO, confined space, electrical safety, hot work, working at heights, lifting operations, MEWPs, PIVs, pressure safety, and fire prevention.</li><li>Support safe execution of work through participation in pre-task planning, hazard assessments, and permit reviews.</li><li>Participate in and facilitate job hazard analyses (JHAs), safe task analysis (STAs), and other risk assessments for high-risk tasks.</li><li>Support delivery and coordination of EHSS training programs related to high-risk work activities.</li><li>Provide EHSS input to small-to-medium site projects, including participation in design reviews and startup activities.</li></ul><h2></h2><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The EHS professional we seek is a collaborative leader with these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><ul><li>High school diploma / GED and 10 years of Environmental, Safety, Science, Engineering or EHS experience OR</li><li>Associate’s degree and 8 years of Environmental, Safety, Science, Engineering or EHS experience OR</li><li>Bachelor’s degree and 4 years of Environmental, Safety, Science, Engineering or EHS experience OR</li><li>Master’s degree and 2 years of Environmental, Safety, Science, Engineering or EHS experience OR</li><li>Doctorate degree<br /> </li></ul><p><b>Preferred Qualifications:</b></p><ul><li>Degree in Environmental Health &amp; Safety, Occupational Safety, Engineering, or a related Science discipline.</li><li>Experience in project EHS reviews, engineering design, Risk Management, including developing and implementing EHSS risk management programs in biotech/pharma.</li><li>Familiarity with typical project documents including process diagrams, P&amp;ID’s, equipment specifications, design drawings etc.</li><li>Experience managing high-risk safety programs such as LOTO, confined space, electrical safety, hot work, working at heights, and lifting operations. Knowledge of relevant OSHA, EPA, NFPA and Building regulations.</li><li>Applied knowledge and understanding of EHSS principles and practices, regulatory standards, and requirements in context of business activities.</li><li>Proficient in Microsoft Office and other computer software systems.</li><li>6 years of experience in the pharmaceutical/biotech industry managing EHSS programs.</li><li>Experience supporting commissioning, startup, or operational readiness activities.</li><li>Well-developed skills in leadership, communication, program development and project management.</li></ul><h2></h2><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2></h2><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>107,445.10USD -145,366.90 USD]]></description><link>http://biotechroles.com/ehands-mgr-amgen/6a0898342f1861929d253362</link><guid isPermaLink="true">http://biotechroles.com/ehands-mgr-amgen/6a0898342f1861929d253362</guid><pubDate>Sat, 16 May 2026 16:15:48 GMT</pubDate><company>Amgen</company><location>US - North Carolina - Holly Springs</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Medical Intern]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Medical Affairs<h2></h2><h2><b>Job Description</b></h2><p><b>ÚNETE A LA MISIÓN DE AMGEN DE SERVIR A LOS PACIENTES </b></p><p></p><p>En Amgen si te sientes parte de algo más grande es porque lo eres. Nuestra misión compartida (servir a pacientes que viven con enfermedades graves) impulsa todo lo que hacemos. Desde 1980, hemos ayudado a ser pioneros en el mundo de la biotecnología en nuestra lucha contra las enfermedades más graves del mundo. Con nuestro enfoque en cuatro áreas terapéuticas –Oncología, Inflamación, Medicina General y Enfermedades Raras– llegamos a millones de pacientes cada año. Como miembro del equipo de Amgen, ayudará a generar un impacto duradero en las vidas de los pacientes mientras investigamos, fabricamos y entregamos medicamentos innovadores para ayudar a las personas a vivir vidas más largas y felices. Nuestra cultura galardonada es colaborativa, innovadora y basada en la ciencia. Si te apasionan los desafíos y las oportunidades que se presentan en ellos, prosperará como parte del equipo de Amgen. Únete a nosotros y transforma las vidas de los pacientes mientras transformas tu carrera.</p><p></p><p>Es momento de que tengas esa carrera de la que puedas estar orgulloso. ¡Únete a la familia Amgen! Estamos buscando en el programa Amgen IDEA un&#64; <b>Pasante en Medical</b>.</p><p> Por esto te invitamos para que juntos ¡Cambiemos el mundo!</p><p></p><p><b>Funciones:</b></p><ul><li>Implementación de proyectos estratégicos.</li><li>Búsqueda y análisis de literatura científica.</li><li>Actualización documental de archivos y materiales.</li><li>Preparación de información en las áreas terapéuticas asignadas.</li><li>Análisis y uso de información.</li><li>Presentación de avances a los equipos médico y de farmacovigilancia.</li><li>Entrenamiento en diferentes políticas internas y habilidades.</li></ul><p></p><p><b>Lo que puedes esperar de nosotros</b></p><p></p><p>Así como trabajamos para desarrollar tratamientos para cuidar a nuestros pacientes, también trabajamos para cuidar la carrera profesional y crecimiento personal de nuestros colaboradores.</p><ul><li>Oportunidades para aprender y crecer en la organización a nivel global.</li><li>Una comunidad de diversidad e inclusión donde los colaboradores son empoderados para poner sus ideas en la mesa y desarrollarlas.</li><li>Plan de recompensas.</li></ul><p></p><p>Aplica ahora a una carrera que desafía la imaginación.</p><p></p><p>En nuestra búsqueda para servir a los pacientes por encima de todo, Amgen es el primero en imaginar, y el último en dudar. Únete a nosotros. careers.amgen.com</p><p></p><p>Amgen es un empleador de Igualdad de Oportunidades y te considerará sin importar tu raza, color, religión, sexo, orientación sexual, identidad de género, origen nacional o estatus de discapacidad, asegurando que nuestros procesos sean transparentes y accesibles para todos.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/medical-intern-amgen/6a0898342f1861929d253361</link><guid isPermaLink="true">http://biotechroles.com/medical-intern-amgen/6a0898342f1861929d253361</guid><pubDate>Sat, 16 May 2026 16:15:48 GMT</pubDate><company>Amgen</company><location>Colombia - Bogota</location><salary>$12000-18000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director Media - LVL]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Marketing<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Associate Director, Media - LVL</b></p><p></p><p>In this role, you will support the planning, execution, and optimization of Amgen’s U.S. commercial media strategy, with responsibility across Digital, Addressable, Video, TV, Search, and Point of Care channels within both HCP and DTC landscapes. You will translate brand and business objectives into integrated media plans and ensure strong execution across activation, operations, and performance optimization.</p><p></p><p>You will bring strong working expertise across the modern media ecosystem, with a clear understanding of how channels work together across the customer journey to drive commercial outcomes. You will manage day‑to‑day media execution, including activation workflows, trafficking, tagging, and tracking, and partner closely with agency teams to ensure accuracy, consistency, and scalability across campaigns.</p><p></p><p>You will work in close partnership with analytics, technology, and agency teams to support measurement frameworks, ensuring media is measurable by design and enabling performance optimization and reporting at the brand level.</p><p></p><p>As a key member of the media leadership team, you will manage agency relationships at the brand or portfolio level, support alignment with platform partners, and collaborate with Brand, Medical, Legal, and cross‑functional stakeholders to ensure compliant and effective execution. This role contributes to advancing Amgen’s media capabilities by applying enterprise standards, identifying optimization opportunities, and supporting test‑and‑learn initiatives that can scale across the portfolio.</p><p></p><p></p><p><b>Responsibilities include:</b></p><ul><li><p>Support the execution of media strategy across Digital, Addressable, Video, TV, Search, and Point of Care channels for both HCP and DTC audiences, ensuring alignment to brand and enterprise objectives.</p></li><li><p>Serve as a media subject‑matter expert at the brand or portfolio level, advising stakeholders on channel roles, audience strategy, investment mix, and optimization across the customer journey.</p></li><li><p>Manage day‑to‑day media activation and operations, including trafficking, tagging, tracking, and quality control, ensuring accurate and timely execution across all assigned campaigns.</p></li><li><p>Apply and reinforce enterprise media platform and operational standards (e.g., DCM, Prisma, MediaTools, Guidelines), ensuring consistency, compliance, and data integrity in execution.</p></li><li><p>Partner closely with Analytics and Technology teams to implement measurement frameworks, tagging standards, and tracking methodologies that enable performance reporting and optimization.</p></li><li><p>Manage brand‑level agency relationships, setting clear expectations for execution quality, measurement rigor, and operational discipline across planning, buying, and reporting.</p></li><li><p>Support coordination with media platform partners, staying informed on platform capabilities, policy updates, and compliance considerations relevant to pharmaceutical marketing.</p></li><li><p>Enable effective cross‑functional collaboration with Brand, Medical, Corporate Communications, Legal, Technology, and Analytics teams to ensure seamless, compliant execution.</p></li><li><p>Identify and support test‑and‑learn initiatives, including piloting new channels, platforms, data solutions, or activation models.</p></li><li><p>Evaluate pilot results and performance insights, providing recommendations to inform enterprise‑level scaling decisions.</p></li><li><p>Drive continuous improvement by applying learnings from campaign performance, pilots, and evolving media best practices.</p></li><li><p>Ensure all media activity is executed in compliance with regulatory, privacy, and security requirements, escalating risks or issues as appropriate.</p></li><li><p>Travel: Up to 20% domestic travel annually to visit agency partners and Amgen headquarters (Thousand Oaks).</p></li></ul><p></p><p><b>What we expect of you</b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a collaborative partner with these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><p></p><ul><li><p>Doctorate degree and 3 years of media and/or marketing experience OR</p></li><li><p>Master’s degree and 5 years of media and/or marketing experience OR</p></li><li><p>Bachelor’s degree and 7 years of media and/or marketing experience OR</p></li><li><p>Associate’s degree and 12 years of media and/or marketing experience OR</p></li><li><p>High school diploma / GED and 14 years of media and/or marketing experience</p></li></ul><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>7&#43; years of experience in paid media/marketing with a focus on planning, buying, execution and measurement</p></li><li><p>Technical competencies: expert in media targeting and segmentation (consumer and HCP), multi-channel media plan development, omnichannel orchestration and journey planning and execution, media measurement and optimization, agency leadership</p></li><li><p>Experienced leader of teams, both internal and external</p></li><li><p>Expertise in media planning and deliveries for traditional/linear/TV as well as digital channels and platforms</p></li><li><p>Strong analytical skills with an ability to uncover insights from performance/measurement tracking to drive action that increases brand impact.</p></li><li><p>Strong ability in both leading cross-functional teams, and in being a member of a cross-functional team</p></li><li><p>Skilled communication effectiveness: the ability to effectively engage, connect, and influence senior leadership and marketing organizations</p></li><li><p>Ability to translate and communicate complex information/strategies into simple and impactful carry out of plans</p></li><li><p>Desire and ability to find opportunities to work smarter and more efficiently, and implement with excellence</p></li><li><p>Ability to excel and navigate a fast-paced environment requiring excellent multi-tasking and instinctual decision-making skills</p></li><li><p>Comfortable with inspiring change and navigating internal and external impact accordingly</p></li><li><p>Preferred experience working within media agencies</p></li></ul><p></p><p><b>What you can expect of us</b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><p></p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><p></p><p>Apply now and make a lasting impact with the Amgen team.</p><p></p><p>careers.amgen.com</p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p>Application deadline</p><p></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p>Sponsorship</p><p></p><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>150,768.75USD -203,981.25 USD]]></description><link>http://biotechroles.com/associate-director-media-lvl-amgen/6a0898342f1861929d253360</link><guid isPermaLink="true">http://biotechroles.com/associate-director-media-lvl-amgen/6a0898342f1861929d253360</guid><pubDate>Sat, 16 May 2026 16:15:48 GMT</pubDate><company>Amgen</company><location>United States - Remote</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director Media - OBU]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Marketing<h2></h2><h2><b>Job Description</b></h2><p></p><div><div><div><div><div><div><div><div><div><p><b>Join Amgen’s Mission of Serving Patients</b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Associate Director, Media - OBU</b></p></div></div></div></div></div></div></div></div></div><p></p><p>In this role, you will support the planning, execution, and optimization of Amgen’s U.S. commercial media strategy, with responsibility across Digital, Addressable, Video, TV, Search, and Point of Care channels within both HCP and DTC landscapes. You will translate brand and business objectives into integrated media plans and ensure strong execution across activation, operations, and performance optimization.</p><p></p><p>You will bring strong working expertise across the modern media ecosystem, with a clear understanding of how channels work together across the customer journey to drive commercial outcomes. You will manage day‑to‑day media execution, including activation workflows, trafficking, tagging, and tracking, and partner closely with agency teams to ensure accuracy, consistency, and scalability across campaigns.</p><p></p><p>You will work in close partnership with analytics, technology, and agency teams to support measurement frameworks, ensuring media is measurable by design and enabling performance optimization and reporting at the brand level.</p><p></p><p>As a key member of the media leadership team, you will manage agency relationships at the brand or portfolio level, support alignment with platform partners, and collaborate with Brand, Medical, Legal, and cross‑functional stakeholders to ensure compliant and effective execution. This role contributes to advancing Amgen’s media capabilities by applying enterprise standards, identifying optimization opportunities, and supporting test‑and‑learn initiatives that can scale across the portfolio.</p><p></p><p></p><p><b>Responsibilities include:</b></p><ul><li><p>Support the execution of media strategy across Digital, Addressable, Video, TV, Search, and Point of Care channels for both HCP and DTC audiences, ensuring alignment to brand and enterprise objectives.</p></li><li><p>Serve as a media subject‑matter expert at the brand or portfolio level, advising stakeholders on channel roles, audience strategy, investment mix, and optimization across the customer journey.</p></li><li><p>Manage day‑to‑day media activation and operations, including trafficking, tagging, tracking, and quality control, ensuring accurate and timely execution across all assigned campaigns.</p></li><li><p>Apply and reinforce enterprise media platform and operational standards (e.g., DCM, Prisma, MediaTools, Guidelines), ensuring consistency, compliance, and data integrity in execution.</p></li><li><p>Partner closely with Analytics and Technology teams to implement measurement frameworks, tagging standards, and tracking methodologies that enable performance reporting and optimization.</p></li><li><p>Manage brand‑level agency relationships, setting clear expectations for execution quality, measurement rigor, and operational discipline across planning, buying, and reporting.</p></li><li><p>Support coordination with media platform partners, staying informed on platform capabilities, policy updates, and compliance considerations relevant to pharmaceutical marketing.</p></li><li><p>Enable effective cross‑functional collaboration with Brand, Medical, Corporate Communications, Legal, Technology, and Analytics teams to ensure seamless, compliant execution.</p></li><li><p>Identify and support test‑and‑learn initiatives, including piloting new channels, platforms, data solutions, or activation models.</p></li><li><p>Evaluate pilot results and performance insights, providing recommendations to inform enterprise‑level scaling decisions.</p></li><li><p>Drive continuous improvement by applying learnings from campaign performance, pilots, and evolving media best practices.</p></li><li><p>Ensure all media activity is executed in compliance with regulatory, privacy, and security requirements, escalating risks or issues as appropriate.</p></li><li><p>Travel: Up to 20% domestic travel annually to visit agency partners and Amgen headquarters (Thousand Oaks).</p></li></ul><p></p><p><b>What we expect of you</b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a collaborative partner with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications:</b></p><p></p><ul><li><p>Doctorate degree and 3 years of media and/or marketing experience OR</p></li><li><p>Master’s degree and 5 years of media and/or marketing experience OR</p></li><li><p>Bachelor’s degree and 7 years of media and/or marketing experience OR</p></li><li><p>Associate’s degree and 12 years of media and/or marketing experience OR</p></li><li><p>High school diploma / GED and 14 years of media and/or marketing experience</p></li></ul><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>7&#43; years of experience in paid media/marketing with a focus on planning, buying, execution and measurement</p></li><li><p>Technical competencies: expert in media targeting and segmentation (consumer and HCP), multi-channel media plan development, omnichannel orchestration and journey planning and execution, media measurement and optimization, agency leadership</p></li><li><p>Experienced leader of teams, both internal and external</p></li><li><p>Expertise in media planning and deliveries for traditional/linear/TV as well as digital channels and platforms</p></li><li><p>Strong analytical skills with an ability to uncover insights from performance/measurement tracking to drive action that increases brand impact.</p></li><li><p>Strong ability in both leading cross-functional teams, and in being a member of a cross-functional team</p></li><li><p>Skilled communication effectiveness: the ability to effectively engage, connect, and influence senior leadership and marketing organizations</p></li><li><p>Ability to translate and communicate complex information/strategies into simple and impactful carry out of plans</p></li><li><p>Desire and ability to find opportunities to work smarter and more efficiently, and implement with excellence</p></li><li><p>Ability to excel and navigate a fast-paced environment requiring excellent multi-tasking and instinctual decision-making skills</p></li><li><p>Comfortable with inspiring change and navigating internal and external impact accordingly</p></li><li><p>Preferred experience working within media agencies</p></li></ul><p></p><p></p><p><b>What you can expect of us</b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><p></p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><p></p><p>Apply now and make a lasting impact with the Amgen team.</p><p></p><p>careers.amgen.com</p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p>Application deadline</p><p></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p>Sponsorship</p><p></p><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>150,768.75USD -203,981.25 USD]]></description><link>http://biotechroles.com/associate-director-media-obu-amgen/6a0898332f1861929d25335f</link><guid isPermaLink="true">http://biotechroles.com/associate-director-media-obu-amgen/6a0898332f1861929d25335f</guid><pubDate>Sat, 16 May 2026 16:15:47 GMT</pubDate><company>Amgen</company><location>United States - Remote</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Executive Director of Regulatory Affairs - Obesity and Related Conditions]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Regulatory<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients </b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions.</p><p></p><p>As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Executive Director of Regulatory Affairs &amp; Obesity Related Conditions</b></p><p></p><p><b>What you will do</b></p><p></p><p>Let’s do this. Let’s change the world. In this vital role as Executive Director of Regulatory Affairs, you will direct regulatory affairs activities within an assigned disease area, ensuring compliance with applicable laws and regulations.   You will also provide strategic direction and leadership to the regulatory affairs team.</p><p></p><p>The Executive Director of Regulatory Affairs is a product facing cross-indication regulatory integration role that leads a designated part of the Obesity and Related Conditions Global Regulatory Therapeutic Area in the Global Regulatory Affairs organization.  This role ensures strategic coherence, alignment, and risk management across multiple products with concurrent indications and global filings.</p><p></p><p>This role will report into the Vice President, Global Regulatory Affairs.</p><p></p><p><b>Responsibilities:</b></p><ul><li><p>Lead, coach, and mentor staff to develop a high-performing regulatory organization grounded in continuous learning, with a strong focus on talent development, leadership capability, and a succession planning culture.</p></li><li><p>Build strong alignment across global and regional teams ensuring clarity of purpose, priorities and coordinated execution</p></li><li><p>Guide integrated cross-indication regulatory strategy across Obesity programs, ensuring alignment of development pathways, evidence generation, and global registration approaches</p></li><li><p>Provide strategic regulatory expertise and guidance to therapeutic area commercialization teams and other governance bodies</p></li><li><p>Act as a trusted strategic partner to Global Regulatory Leaders (GRLs) providing guidance on complex regulatory decisions, risk management, and long-term strategy</p></li><li><p>Conduct management review and approval of Global Regulatory Strategic Plans</p></li><li><p>Conduct review and approval of key documents for regulatory submissions</p></li><li><p>Anticipate and translate the evolving regulatory landscape within therapeutic area into forward looking regulatory strategies and opportunities</p></li><li><p>Work externally to influence regulatory legislative environment in line with Amgen policy priorities for the therapeutic area</p></li><li><p>Oversee and participate in licensing/acquisition due diligence and other activities in partnership with Amgen licensing groups</p></li><li><p>Communicate and ensure alignment of global functional and cross-functional goals and objectives</p></li></ul><p></p><p><b>Knowledge and skills include:</b></p><ul><li><p>Demonstrated experience leading complex, multi-indication regulatory strategy integration</p></li><li><p>Demonstrated ability to lead teams</p></li><li><p>Strong communication skills - both oral and written</p></li><li><p>Ability to understand and communicate scientific information</p></li><li><p>Comprehensive understanding of regulatory activities and how they affect projects and processes</p></li><li><p>Demonstrable ability to set organizational direction &amp; champion change and continuous improvement</p></li><li><p>Proven ability to anticipate and mitigate against future strategic issues &amp; uncertainties</p></li><li><p>Ability to resolve conflicts and develop a course of action leading to a beneficial outcome</p></li><li><p>Proven ability to drive enterprise-level alignment under high portfolio complexity</p></li></ul><p></p><p><b>What we expect of you</b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The executive candidate we seek is an experienced leader with the following qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree &amp; 6 years of regulatory affairs experience OR</p></li><li><p>Master’s degree &amp; 10 years of regulatory affairs experience OR</p></li><li><p>Bachelor’s degree &amp; 12 years of regulatory affairs experience AND</p></li><li><p>6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Demonstrated leadership of regulatory strategy for programs in obesity, metabolic disorders, endocrinology, cardiovascular risk, or related therapeutic areas.</p></li></ul><p></p><p>They will also embody the Amgen leadership attributes which are:</p><ul><li><p><b>Inspire:</b> Create a connected, inclusive, and inspiring work environment that empowers talent to thrive</p></li><li><p><b>Accelerate:</b> Enable speed that matches the urgency of patient needs by encouraging progress over perfection</p></li><li><p><b>Integrate:</b> Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholders</p></li><li><p><b>Adapt:</b> Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver results</p></li></ul><p></p><p><b>What you can expect of us</b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $255,302 - $345,408. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>255,301.75USD -345,408.25 USD]]></description><link>http://biotechroles.com/executive-director-of-regulatory-affairs-obesity-and-related-conditions-amgen/6a0898332f1861929d25335e</link><guid isPermaLink="true">http://biotechroles.com/executive-director-of-regulatory-affairs-obesity-and-related-conditions-amgen/6a0898332f1861929d25335e</guid><pubDate>Sat, 16 May 2026 16:15:47 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Global Insights, Senior Manager Rare Disease]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales &amp; Marketing Operations<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><h2><b>Global Insights, Sr. Mgr.</b></h2><p></p><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will be a strategic thought partner to brand and cross‑functional teams, responsible for generating rigorous, business‑relevant insights that inform brand strategy, execution, and decision‑making.</p><p>Amgen is seeking a Senior Manager, Global Commercial Insights to lead insights generation for the rare disease pipeline to support global commercialization planning. This role partners closely with global marketing, global value and access, competitive intelligence, forecasting, and other cross-functional teams to provide insights that inform global go-to-market strategy<span>,</span> early commercial planning, therapeutic area strategy, and advancement of the pipeline.</p><p></p><p><b><span>Responsibilities</span></b></p><div><ul><li>Synthesize information from a variety of sources (e.g., market research, competitive intelligence, secondary data, advisory boards) to develop strategic insights that address business needs</li><li>Integrate insights and knowledge to develop business cases and facilitate workshops to support clinical development plans, lifecycle management and other strategic decisions - supporting critical go/no-go decisions and senior leadership presentations</li><li>Plan, design, and lead primary market research with a research agency for assets across various phases of the product lifecycle to enable strategic decision making</li><li>Lead ad hoc strategic secondary analytics to inform strategic decisions</li><li>Be the subject matter expert on HCP, patient, and payer insights for the brand</li><li>Clearly communicate insights and recommendations to variety of audiences, including senior leadership (e.g., Therapeutic Area Heads, Disease Area Strategy Leads), and become a &#39;devil&#39;s advocate&#39; when needed</li><li>Partner with commercial leadership and cross-functional partners to define and prioritize objectives, budget and work plans to meet evolving business needs</li><li>Identify, evaluate, and manage relationships with best-in-class vendors and look for opportunities to innovate and advance capabilities</li><li>Support advancement of AI capabilities for insights generation</li><li>Support Amgen’s advancement in marketing excellence through aligned insights generation and deep brand-building knowledge</li><li>Ensure that both routine and ad-hoc projects are in compliance with all Amgen SOPs and meet service-level expectations for quality, timeliness, and budget</li></ul></div><h2></h2><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The insights professional we seek is a collaborator with these qualifications.</p><div><p>Doctorate degree and 2 years of <span><span> </span></span>market research, analytics, competitive intelligence, sales and/or marketing operations experience<br /><span>OR<br />Master’s degree and 6 years of </span>market research, analytics, competitive intelligence, sales and/or marketing operations experience<br /><span>OR<br />Bachelor’s degree and 8 years of<span>  </span></span>market research, analytics, competitive intelligence, sales and/or marketing operations experience<br /><span>OR<br />Associate’s degree and 10 years of </span>market research, analytics, competitive intelligence, sales and/or marketing operations experience<br /><span>OR<br />High school diploma / GED and 12 years of<span>  </span></span>market research, analytics, competitive intelligence, sales and/or marketing operations experience<br /><br /><span>In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.<span>  </span>Your managerial experience may run concurrently with the required technical experience referenced above<span> </span></span></p></div><p></p><p><b><span>Preferred Requirements</span></b></p><div><ul><li>Demonstrated exceptional business acumen, strategic / critical thinking skills, and ability to influence key decisions</li><li>Proven ability to build and evolve brands through strategic insight generation, including expertise in market research design, Jobs-to-Be-Done methodologies, identification of moments that matter, and translating deep human insights into compelling brand narratives and customer experiences</li><li>Strong understanding of marketing and marketing strategy</li><li>Ability to independently extract, analyze, treat, and consolidate data from sources in formats with rigor and high level of accuracy and translate into actionable recommendations</li><li>Excellent oral, written and presentation skills with ability to explain complex concepts clearly to a variety of audiences, including senior management</li><li>Ability to work collaboratively and adaptively in team-based, cross-functional environments</li><li>Ability to balance a multitude of stakeholders and projects in parallel</li><li>Strong knowledge of drug development, commercialization and the broader healthcare industry (patients, HCPs, payers)</li><li>Experience leading primary research</li></ul><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2></h2><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>155,747.20USD -210,716.80 USD]]></description><link>http://biotechroles.com/global-insights-senior-manager-rare-disease-amgen/6a0898322f1861929d25335d</link><guid isPermaLink="true">http://biotechroles.com/global-insights-senior-manager-rare-disease-amgen/6a0898322f1861929d25335d</guid><pubDate>Sat, 16 May 2026 16:15:46 GMT</pubDate><company>Amgen</company><location>US - Illinois - Chicago</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director - Marketing AI & Innovation]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Marketing<h2></h2><h2><b>Job Description</b></h2><p></p><div><div><div><div><div><div><div><div><div><p><b>Join Amgen’s Mission of Serving Patients</b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p></div></div></div></div></div></div></div></div></div><p></p><p><b>Associate Director - Marketing AI &amp; Innovation</b></p><p></p><p><b>What you will do</b></p><p></p><p>The Associate Director of Marketing AI and Innovation (GCCI) is responsible for activating and scaling AI-enabled marketing capabilities across Amgen’s brands, with a primary focus on operationalizing the Generative Engine Optimization (GEO) model and supporting enterprise AI partnerships. This role ensures that centrally developed capabilities, and partnerships are effectively translated into brand-level execution, driving measurable impact on brand strategy &amp; execution.</p><p></p><p>This individual will serve as a critical bridge between strategy and execution—orchestrating cross-functional teams to embed AI-driven insights and new ways of working into day-to-day marketing activities.</p><p></p><p><b>Key Responsibilities:</b></p><ul><li><p><b>GEO Activation Across Brands:</b> Drive adoption and execution of the GEO operating model across priority brands, embedding GEO principles into campaign planning, content strategy, and optimization workflows.</p></li><li><p><b>AI Partnership Management:</b> Oversee day-to-day engagement with key AI and data partners (e.g., GEO partner), ensuring capabilities translate into tangible brand use cases and outcomes</p></li><li><p><b>Pilot Execution &amp; Scaling:</b> Support implementation of pilot programs across brands, capturing learnings and enabling enterprise scaling solutions through structured playbooks and recommendations</p></li><li><p><b>Cross-Functional Orchestration:</b> Partner with Marketing, GCCI Media, GCCI WebOps, and BAI to ensure AI-driven insights are fully integrated into marketing execution, measurement, and optimization processes</p></li><li><p><b>Performance Tracking &amp; Optimization:</b> Monitor adoption, performance, and ROI of AI-enabled initiatives at the brand level, driving continuous improvement and scaling best practices</p></li><li><p><b>Future of Marketing:</b> Partner cross-functionally to define the future marketer experience, identify required capabilities, and drive their development and implementation.</p></li><li><p><b>Change Management &amp; Adoption:</b> Lead change management efforts to embed new AI-enabled ways of working, ensuring strong adoption and sustained behavioral change across marketing teams</p></li></ul><p></p><p><b>Key Activities</b></p><ul><li><p>Drive GEO implementation at the brand level, translating GEO insights into actionable optimizations across content &amp; media strategy.</p></li><li><p>Partner with brand teams to embed AI insights into creative development, messaging, and content strategies</p></li><li><p>Support execution of AI-driven pilots (e.g., patient identification, diagnosis, media scaling), ensuring effective coordination across stakeholders, and scaling plans across the enterprise</p></li><li><p>Manage day-to-day operations with external partners, ensuring alignment with internal objectives and seamless execution</p></li><li><p>Orchestrate cross-functional teams (Marketing, GCCI, Medical, Corp Affairs, BAI, etc) to deliver on AI enabled solutions</p></li><li><p>Identify, document, and scale best practices across brands to drive consistency and efficiency</p></li><li><p>Gather feedback from brand teams and stakeholders to refine tools, processes, and approaches</p></li><li><p>Track performance metrics and contribute to reporting on impact of AI-enabled marketing initiatives</p></li></ul><p></p><p><b>What we expect of you</b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is collaborative, execution-focused, and results-driven with these qualifications:</p><p></p><p><b><span>Basic Qualifications</span></b></p><p></p><p>Doctorate degree and 3 years of  Marketing experience<br />OR<br />Master’s degree and 5 years of  Marketing experience<br />OR<br />Bachelor’s degree and 7 years  Marketing experience<br />OR<br />Associate’s degree and 12 years of Marketing experience <br />OR<br />High school diploma / GED and 14 years of Marketing experience</p><p></p><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>Strong marketing and digital acumen, with experience in omnichannel, content, or performance marketing</p></li><li><p>Familiarity with SEO, analytics, or emerging AI-driven marketing approaches (e.g., GEO)</p></li><li><p>Experience translating strategy into execution across multiple brands or markets</p></li><li><p>Proven ability to manage external partners and vendors to deliver business outcomes.</p></li><li><p>Strong cross-functional collaboration skills within a matrixed organization</p></li><li><p>Experience in change management and driving adoption of new capabilities or ways of working</p></li><li><p>Ability to influence across levels and functions, including brand, media, analytics, and technology teams</p></li><li><p>Strong analytical mindset with ability to translate data into actionable insights</p></li><li><p>Excellent verbal and written communication skills</p></li><li><p>Track record of delivering complex initiatives that drive measurable business impact</p></li></ul><p></p><p><b>What you can expect of us</b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><p></p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><p></p><p>Apply now and make a lasting impact with the Amgen team.</p><p></p><p>careers.amgen.com</p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p>Application deadline</p><p></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p></p><p>Sponsorship</p><p></p><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>158,999.30USD -215,116.70 USD]]></description><link>http://biotechroles.com/associate-director-marketing-ai-and-innovation-amgen/6a0898322f1861929d25335c</link><guid isPermaLink="true">http://biotechroles.com/associate-director-marketing-ai-and-innovation-amgen/6a0898322f1861929d25335c</guid><pubDate>Sat, 16 May 2026 16:15:46 GMT</pubDate><company>Amgen</company><location>United States - Remote</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Senior Medical Science Liaison - Obesity - MN, IA, WI]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Medical Affairs<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Senior Medical Science Liaison - Obesity - MN, IA, WI</b></p><p><b>Territory to include MN, IA, WI</b></p><p></p><p></p><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will act as the primary scientific/clinical resource to Opinion Leaders (OLs), Population Heath Decision Makers (PHDMs) and other healthcare providers and is responsible for executing Amgen Medical function and product strategy as led by MSL Leadership, with the goal of giving accurate information to OLs, community healthcare providers and PHDMS to improve patient outcomes. The Obesity General Medicine Sr. MSL is a field-based position within the U.S. Medical team reporting to an Obesity MSL Field Director.</p><p></p><p>Responsibilities for the Sr. MSL include:</p><p></p><ul><li><p>Majority of time spent on peer-to-peer activities with Obesity and related conditions Opinion Leaders, community healthcare providers, and PHDMs to discuss and advance the scientific platform as aligned with Amgen’s corporate goals and objectives.</p></li><li><p>Engage with clinical investigators and sites in support of the obesity pipeline.</p></li><li><p>Engage with PHDMs within assigned IDNs and other institutions to communicate scientific based data of clinical value, outcomes, and economic data.</p></li><li><p>Connect external and internal stakeholders to amplify Amgen’s reach and access for patients.</p></li><li><p>Conduct in-depth scientific exchange to provide focused and balanced clinical and scientific information consistent with MSL compliance standards.</p></li><li><p>Support Amgen sponsored research and may serve as a study lead.</p></li><li><p>Liaise with potential investigators in non-sponsored clinical research.</p></li><li><p>Provide and/or present field observations and insights to internal stakeholders to inform Amgen strategies.</p></li><li><p>Lead and support congress activities as aligned with strategy.</p></li><li><p>Support speaker training as requested and ensure the speakers are updated on new data.</p></li><li><p>Lead and/or participate on project teams that support MSL strategies and tactics as delegated by MSL leadership.</p></li><li><p>Compliantly partner across all Amgen field roles who share customers to create an appropriately coordinated One Amgen experience.</p></li><li><p>MSLs instill passion and move HCPs to take action in improving patient care related to closing care gaps</p></li><li><p>Execute all administrative responsibilities and training (e.g., Veeva CRM, expense reports, compliance modules, etc.) in a timely manner.</p></li><li><p>Maintain and improve clinical/scientific acumen and expertise with current data/information and healthcare trends.</p></li><li><p>Ability to build and maintain strong relationships with external stakeholders and possess excellent communication skills to effectively communicate scientific data.</p></li></ul><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree &amp; 2 years of Medical Affairs experience</p></li></ul><p>OR</p><ul><li><p>Master’s degree &amp; 6 years of Medical Affairs experience</p></li></ul><p>OR</p><ul><li><p>Bachelor’s degree &amp; 8 years of Medical Affairs experience.</p></li></ul><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered)</p></li><li><p>Seven or more years in a medically related field, including 1 year focused on clinical practice, clinical research, or medical research. Experience in a medically related field can include post-doctoral training (i.e., residencies and/or fellowships)</p></li><li><p>2 &#43; years in a medical science liaison role in a biotech or pharmaceutical company. Current experience in Scientific Affairs or Medical Affairs at a biotech or pharmaceutical company</p></li><li><p>Cardiometabolic and/or Obesity expertise</p></li><li><p>Experience with designated territory</p></li></ul><p></p><h2></h2><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><h2></h2><h2></h2><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2></h2><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2></h2><h2></h2><h2></h2><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>172,344.30USD -233,171.70 USD]]></description><link>http://biotechroles.com/senior-medical-science-liaison-obesity-mn-ia-wi-amgen/6a0898322f1861929d25335b</link><guid isPermaLink="true">http://biotechroles.com/senior-medical-science-liaison-obesity-mn-ia-wi-amgen/6a0898322f1861929d25335b</guid><pubDate>Sat, 16 May 2026 16:15:46 GMT</pubDate><company>Amgen</company><location>US - Minnesota - Minneapolis</location><salary>$130000-170000</salary><type>Full time</type></item><item><title><![CDATA[Human Resources Director – U.S. Commercial & Global Customer Capabilities and Innovation]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Human Resources<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><h2><b>Human Resources Director – U.S. Commercial &amp; Global Customer Capabilities and Innovation</b></h2><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. The Human Resources Director is a senior leadership role that shapes and delivers people strategies that drive business performance, organizational effectiveness, and talent outcomes across Amgen’s Commercial organization.</p><p>Serving as a strategic HR Business Partner to senior leaders, this role supports both field-based and home-office staff. Reporting to the Executive Director, Human Resources (U.S. and Global Commercial), the HR Director works with executive leadership teams to drive transformation and strengthen leadership capability.</p><p>As Amgen advances an unprecedented number of innovative and biosimilar medicines, this role offers a unique opportunity to help evolve how the organization operates—so we can maximize our reach to patients worldwide and deliver on our mission.</p><p>In a fast-paced environment, the HR Director delivers practical solutions to complex business and talent challenges and helps leaders navigate growth and change.</p><p><b><u>Key Responsibilities</u></b></p><p><b>Strategic HR Partnership</b></p><ul><li>Serve as a trusted advisor to senior leaders across the U.S. Commercial organization, aligning people strategies to evolving business priorities and enterprise goals.</li><li>Develop and execute HR strategies that strengthen organizational effectiveness, leadership capability, employee engagement, and business performance.</li><li>Coach leaders on HR and business issues to accelerate change and improve team effectiveness.</li></ul><p><b>Workforce and Talent Development</b></p><ul><li>Work with senior leaders to assess workforce capabilities, identify talent needs, and build forward-looking workforce and succession strategies.</li><li>Lead talent management initiatives including leadership development, succession planning, organizational capability building, engagement, and retention.</li><li>Partner with HR Centers of Excellence on compensation, talent planning, culture, diversity and inclusion, and workforce strategy.</li><li>Drive the attraction, development, and retention of top talent in partnership with Talent Acquisition and business leaders.</li></ul><p><b>Organizational Transformation and Change Leadership</b></p><ul><li>Lead organizational design efforts with leadership teams to improve agility, scalability, and business effectiveness.</li><li>Lead and influence large-scale transformation and change management initiatives across therapeutic areas and commercial functions.</li><li>Use data, analytics, and organizational insights to inform decisions, surface trends, and drive continuous improvement.</li></ul><p><b>Employee Engagement and HR Excellence</b></p><ul><li>Foster a high-performing, engaged, and inclusive culture aligned with Amgen’s mission and values.</li><li>Ensure alignment with employment laws, HR policies, and business practices while balancing business objectives with a strong employee experience.</li><li>Stay current on external talent and organizational trends, bringing practical, innovative thought leadership to the business and HR organization.</li></ul><p><b>Cross-Functional Partnership and HR Leadership</b></p><ul><li>Align HR and business partners to deliver integrated, enterprise-level solutions.</li><li>This role will have one direct report and will actively invest in coaching, mentoring, and developing HR talent.</li><li>Contribute to the broader HR organization by sharing best practices, thought leadership, and innovative approaches that strengthen HR impact across the enterprise.</li></ul><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 4 years of Human Resources experience</p><p>OR</p><p>Master’s degree and 7 years of Human Resources experience</p><p>OR</p><p>Bachelor’s degree and 9 years of Human Resources experience</p><p><b>Preferred Qualifications:</b></p><ul><li>Experience coaching and influencing leaders to drive organizational effectiveness and change.</li><li>Experience partnering with HR Centers of Excellence on talent planning, leadership development, compensation, and workforce strategy.</li><li>Demonstrated ability to translate business priorities into strategic and practical HR solutions.</li><li>Strong knowledge of employment laws, HR regulations, and relevant business practices.</li><li>Strong business acumen, analytical/problem-solving skills, and project/program management capability.</li><li>Excellent communication and interpersonal skills; ability to build credibility and influence at senior levels.</li><li>Proven ability to collaborate across HR and business functions and manage competing priorities in a fast-paced environment.</li></ul><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>167,444.90USD -226,543.10 USD]]></description><link>http://biotechroles.com/human-resources-director-us-commercial-and-global-customer-capabilities-and-innovation-amgen/6a0898312f1861929d25335a</link><guid isPermaLink="true">http://biotechroles.com/human-resources-director-us-commercial-and-global-customer-capabilities-and-innovation-amgen/6a0898312f1861929d25335a</guid><pubDate>Sat, 16 May 2026 16:15:45 GMT</pubDate><company>Amgen</company><location>United States - Remote</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Strategic Account Manager]]></title><description><![CDATA[<p><b>Role Summary</b></p><p></p><p>As a Strategic Accounts Manager for GSK in the Philippines, you will lead and manage a team of strategic account representatives to deliver sales targets, strengthen key account relationships, and drive growth in your region.</p><p></p><p>You will execute sales strategy, coach and develop the team, and ensure alignment with GSK’s values and objectives.</p><p></p><p>Key Responsibilities</p><p>1. Leadership &amp; Management:</p><p>· Lead, coach, and motivate a team of strategic account representatives to meet or exceed targets.</p><p>· Conduct performance reviews, provide feedback, and address development needs.</p><p>· Build a collaborative culture aligned with GSK values.</p><p>· Drive integrated solutions across Commercial, Medical, and Market Access to improve patient and business outcomes</p><p>2. Business Performance &amp; Execution</p><p>· Develop and deliver a team operating plan aligned with national brand strategy.</p><p>· Deliver sales demand and access objectives for assigned region and accounts.</p><p>· Track sales performance KPIs and take corrective action as needed.</p><p>3. Customer Relationship &amp; Account Management</p><p>· Build and maintain relationships with key prescribers, hospital decision-makers, and payers.</p><p>· Address customer needs and issues promptly.</p><p>· Represent GSK at industry events and meetings.</p><p>4. Compliance &amp; Reporting:</p><p>· Ensure sales activities comply with GSK policies, ethical standards, and regulatory requirements.</p><p>· Report on sales performance, market trends, and competitor activity.</p><p>· Maintain accurate sales and customer records.</p><p>5. Training &amp; Development:</p><p>· Identify training needs and coordinate team training.</p><p>· Build key account management skills to uncover and act on growth opportunities.</p><p></p><p><span><span class="emphasis"><b><i>Why you?</i></b></span></span></p><p></p><p><span><span class="emphasis">Basic Qualifications:</span></span></p><p>We are looking for professionals with these required skills to achieve our goals:</p><ul><li><p>Qualifications &amp; Experience</p><p>· 5&#43; years in pharma sales/marketing, key account management, and/or medical affairs; 2&#43; years in a people-management role.</p><p>· Bachelor’s degree in science, business, or related field.</p><p>· Oncology, biologics/immunotherapy, or specialty therapy experience preferred.</p><p>· Proven record of meeting/exceeding targets; launch experience preferred.</p><p>· Strong leadership, coaching, and people development skills.</p></li><li><p>Competencies &amp; Capabilities</p><p>· Strong scientific knowledge and ability to discuss clinical topics.</p><p>· Strategic mindset and strong commercial acumen.</p><p>· Strong communication, presentation, and stakeholder management.</p><p>· Strong planning and execution with high accountability.</p><p>· Omnichannel mindset and ability to orchestrate cross-functional engagement.</p><p>· High integrity, compliance-focused, and patient-centric.</p></li></ul><p></p><p><span><span class="emphasis"><b>Preferred Qualifications:</b></span></span></p><p>If you have the following characteristics, it would be a plus:</p><ul><li><p>Additional Requirements</p><p>· Fluent in English and Filipino (written and spoken).</p><p>· Valid Philippine driver’s license; willing to travel.</p></li></ul><p></p><p><span><span class="emphasis"><b><i>Why GSK?</i></b></span></span></p><p></p><p><i>Our values and expectations</i><b><i> </i></b><i>are at the heart of everything we do and form an important part of our culture.</i></p><p><i>These include</i> <i>Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork.</i><i> As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: </i></p><p></p><ul><li>Operating at pace and agile decision-making – using evidence and applying judgement to balance pace, rigour and risk.</li><li>Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.</li><li>Continuously looking for opportunities to learn, build skills and share learning.</li><li>Sustaining energy and well-being</li><li>Building strong relationships and collaboration, honest and open conversations.</li><li>Budgeting and cost-consciousness</li></ul><p></p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact <a target="_blank" href="mailto:APACRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>APACRecruitment.Adjustments&#64;gsk.com</u></span></a>. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/strategic-account-manager-gsk/6a08981c2f1861929d253359</link><guid isPermaLink="true">http://biotechroles.com/strategic-account-manager-gsk/6a08981c2f1861929d253359</guid><pubDate>Sat, 16 May 2026 16:15:24 GMT</pubDate><company>GSK</company><location>Philippines - National Capital Region</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Product Owner]]></title><description><![CDATA[<p><span class="emphasis">Business Introduction</span><br />We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.<br />Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.<br />We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.<br /><br /><br /><span class="emphasis">Position Summary</span><br />The Product Owner provides technical leadership, guidance, oversight, and support for the associated product or product portfolio, through effective Product Lifecycle Management (PLM) and support for day-to-day operations, to ensure the ongoing manufacture and supply of our products in alignment with Regulatory and Quality standards and business objectives<br /><br /><span class="emphasis">Responsibilities</span><br />This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><ul><li><p>Provide technical input and support for product transfer, registration, validation and launch.</p></li><li><p>Ensure that all aspects of Product Lifecycle Management are in place, actively maintained, and ensure risks are identified and escalated as appropriate and mitigation plans are in place and agreed. The key components of the PLM process include: Development History, Material and Technical Risk Assessments, Product Specifications, Control Strategy, Performance Qualification and Continued Process Verification, Periodic Product Reviews, and Product Costing Standards.</p></li><li><p>Translate the Control Strategy to the production floor such that Critical Raw Materials attributes, Critical Process Parameters, Critical Quality Attributes and Manufacturing controls are understood, appropriately challenged, agreed, verified, controlled and communicated.</p></li><li><p>Perform GEMBAs in production and analytical testing to ensure that the relevant control and verification strategies are in place, in use and effective.</p></li><li><p>Lead product failure investigations, escalating significant issues to ensure appropriate support and expertise are provided.</p></li><li><p>Trend product performance data, identify and investigate trends and concerns, and communicate to key stakeholders. Present product performance data to the relevant governance meetings (e.g. Product Technical Review Team (PTRT), Communities of Practice and provide input to PPR for assigned products.</p></li><li><p>Lead cross-functional teams to evaluate and implement post-approval changes and drive improvements in product control and robustness.</p></li><li><p>Work with the supply chain (including primary, excipient and/or component suppliers) to manage inputs that impact the technical performance of allocated products within manufacturing, packaging and testing.</p></li><li><p>Provide technical input to regulatory submissions and responses to questions from regulatory agencies. Prepare technical documents, provide technical input and participate in regulatory inspections.</p></li><li><p>Contribute to major technology development projects aligned to allocated products</p></li></ul><p><br /><span class="emphasis">Why You?<br /><br />Basic Qualification</span><br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li><p>Bachelor’s degree in a scientific, engineering, or technical discipline.</p></li><li><p>5&#43; years’ experience in regulated manufacturing, technology transfer, or product lifecycle roles.</p></li><li><p>Required experience working with raw materials, equipment, unit operations and testing for sterile injectables, especially pre-filled syringe and auto injector formats.</p></li><li><p>Experienced with Product Lifecycle Management, including Control Strategies, Process Qualification, Change Control, and Technical Risk Assessment (L1 TRA Facilitator desired)</p></li><li><p>Demonstrable experience as a Product Owner or similar role in regulated environments.</p></li></ul><p></p><p><span class="emphasis">Preferred Qualification</span><br />If you have the following characteristics, it would be a plus:</p><ul><li><p>Master’s degree or advanced technical qualification.</p></li><li><p>Experience with technology transfer, scale-up, or commercial launch activities, with strong preference for experience supporting tech transfer for sterile injectables, pre-filled syringe, and auto injector products.</p></li><li><p>Working knowledge of product control strategies and technical risk assessment methods.</p></li><li><p>Familiarity with statistical tools for process capability and trend analysis.</p></li><li><p>Experience preparing technical documentation for regulatory submissions or inspections.</p></li><li><p>Demonstrated project management or cross-functional team leadership experience.</p></li><li><p>Practical experience with product performance monitoring and data trending.</p></li><li><p>Experience leading investigations and implementing corrective and preventive actions.</p></li><li><p>Familiarity with quality systems, regulatory expectations, and Good Manufacturing Practices.</p></li><li><p>Strong stakeholder engagement and communication skills.</p></li><li><p>Experience with assemblies and devices, especially pre-filled syringe and auto injector systems.</p></li><li><p>Basic understanding of the drug development process.</p></li><li><p>Experienced in scale-up and technology transfer.</p></li><li><p>Understanding of control strategy principles and application.</p></li><li><p>Working knowledge of FMEA techniques.</p></li><li><p>Knowledge of cGMPs related ICH guidance (specifically ICHQ8- 11).</p></li><li><p>Experienced with Product Lifecycle Management, including Control Strategies, Process Qualification, Change Control, and Technical Risk Assessment (L1 TRA Facilitator desired).</p></li><li><p>Statistical knowledge and use of Statistica, JMP, SAS, or other data analysis software. · Experience writing technical protocols and reports.</p></li><li><p>Experience preparing for and delivering technical presentations to key stakeholders.</p></li><li><p>Experience with investigation techniques and tools for process investigations.</p></li><li><p>Excellent technical writing and oral communication skills.</p></li><li><p>Excellent project management skills.</p></li><li><p>Ability to navigate critical business systems and databases (e.g. MERP, IP21) and mine relevant data for reporting, review and analysis.</p></li><li><p>Familiar with risk-based approach and use of data to design a process qualification strategy, including the selection of batches and development of sampling plans.</p></li><li><p>Familiar with cleaning validation approach as it relates to manufacturing operations and limitations.</p></li></ul><p><br /><span class="emphasis">Working Model</span><br />This role is hybrid, with an expectation to be onsite for key meetings and manufacturing support. Exact on-site frequency will be agreed at offer stage and may vary by location and business needs.<br /><br /><span class="emphasis">What we offer</span><br />You will join a team that values collaboration, learning, and purpose. You will find opportunities to grow professionally and to shape work that helps patients worldwide. We welcome applications from people who bring different perspectives and lived experience. If this role matches your skills and ambitions, we encourage you to apply and tell us how you can contribute.</p><p></p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/product-owner-gsk/6a08975d2f1861929d253358</link><guid isPermaLink="true">http://biotechroles.com/product-owner-gsk/6a08975d2f1861929d253358</guid><pubDate>Sat, 16 May 2026 16:12:13 GMT</pubDate><company>GSK</company><location>USA - North Carolina - Zebulon</location><salary>$105000-145000</salary><type>Full time</type></item><item><title><![CDATA[Pediatric Immunization Specialist]]></title><description><![CDATA[<p></p><p><span class="emphasis"><b>Territory to include, but not limited to, Great Neck, NY</b></span></p><p></p><p>For more than 140 years, GSK has pioneered novel research methods and technologies to help protect people from infectious diseases. Our vaccines portfolio of more than 20 marketed vaccines is the broadest in the industry, helping to protect people throughout their lives. We believe prevention, at scale and for impact, is the best health investment for society, patients, and the economy. Vaccine preventable diseases are a significant burden on society and healthcare systems; approximately $1 trillion in productivity is lost each year due to preventable conditions. This includes the impact from the 330,000 older adults hospitalized globally each year with RSV, approximately 1 in 3 people who will develop shingles in their lifetime and the 3-11% of people infected with seasonal influenza each year. Our Vaccines portfolio will reach over 1 billion people globally this decade. Each year, around 40% of children globally receive a GSK vaccine and GSK is well-placed to lead in the growing adult immunization market. </p><p></p><p>GSK’s US vaccines business and Sales team is designed to support the unique needs of the customer base in the given geography. In a local market, there are multiple customer-facing roles, each with unique customers/call points, but all dependent upon a high degree of collaboration.</p><p><br />The <span class="emphasis"><b>Pediatric Immunization Specialist, or ISP</b></span>, is a pivotal role, responsible for engaging health care providers (HCPs) to drive uptake of GSK vaccines. The role of the ISP is to educate HCPs on both disease state and the approved GSK vaccine solutions. The ISP must possess strong customer engagement skills, along with a strong knowledge of GSK vaccines, competitor vaccines, and public health guidelines in order to represent GSK vaccines product and portfolio value proposition. The ISP must also collaborate closely with first line leaders and other field teams, including Account Management and Contracting Specialists.</p><p><br /><b>Responsibilities:</b></p><ul><li><p>The Immunization Specialist will develop and maintain specialized expertise in vaccine therapeutic areas, products and markets.</p></li><li><p>Demonstrate knowledge of GSK pediatric and adolescent vaccines, competitive products and GSK promotional strategies and objectives to meet customer needs. This includes knowledge of contracting structures for GSK and competitor portfolios.</p></li><li><p>Demonstrate high-level selling skills, including account-based selling, strategic thinking, drive for results, and the ability to ask for the business.</p></li><li><p>Demonstrate the ability to provide value to each targeted account through proper blending of science &amp; service based upon each account’s individual needs.</p></li><li><p>Demonstrate the ability to effectively follow public health guidelines and use the vaccines sales process in a way that engages customers and supports them in their effort to vaccinate or refer their patients.</p></li><li><p>Demonstrate ability to drive vaccination uptake in both Private (e.g. Health systems and independent) and public sector (e.g. Vaccines for Children, Health Department, Federally Qualified Health Centers) providers</p></li><li><p>Collaborate with the broader field-based teams, including Account Managers and Contract Specialists, to help pull through GSK vaccine business.</p></li><li><p>Effectively utilize and provide feedback on marketing content and digital tools to help optimize and evolve them.</p></li></ul><p></p><p><b>Why You?</b><br /><b>Basic Qualifications:</b></p><ul><li><p>Bachelor’s Degree </p></li><li><p>2&#43; years of business-to-business or pharmaceutical sales experience </p></li><li><p>Ability to travel domestically as necessary </p></li><li><p>Valid driver’s license and willingness to drive (essential function of this role) </p></li><li><p>The selected candidate will be hired at the appropriate level based on experience</p><ul><li><p><b>Immunization Specialist (grade 8)</b>: 2&#43; years business-to-business or pharmaceutical sales experience</p></li><li><p><b>Senior Immunization Specialist (grade 7)</b>: 5&#43; years business-to-business or pharmaceutical sales experience</p></li></ul></li></ul><p></p><p><b>Preferred Qualifications:</b> </p><ul><li><p>Vaccines sales experience </p></li><li><p>Strong track record of high-level performance and consistent achievements</p></li><li><p>Strong account-selling skills, including business-to-business experience in a healthcare setting  </p></li><li><p>Demonstrated competency of science, business acumen, and customer engagement </p></li><li><p>Knowledge and experience in a healthcare setting </p></li><li><p>Demonstrated learning agility </p></li></ul><p></p><p><b>Key Skills/Competencies:</b>  </p><ul><li><p>Advanced business acumen and analytical skills to diagnose opportunities  </p></li><li><p>Self-directed and organized with the ability to adapt and change in a shifting environment  </p></li><li><p>Impact and influence with customers to mobilize action plans  </p></li><li><p>Ability to quickly identify issues and develop recommendations for timely, compliant resolution  </p></li></ul><p></p><p><b>Location: </b>This is a field-based position. The percentage of travel will be determined by customer location in relation to the geographic location of the successful candidate. </p><p></p><p>#GSKCommercial</p><p></p>The US annual base salary for new hires in this position ranges from $119,250 to $198,750.  The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.&amp;#xa;&amp;#xa;If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pediatric-immunization-specialist-gsk/6a08975d2f1861929d253357</link><guid isPermaLink="true">http://biotechroles.com/pediatric-immunization-specialist-gsk/6a08975d2f1861929d253357</guid><pubDate>Sat, 16 May 2026 16:12:13 GMT</pubDate><company>GSK</company><location>USA - New York - Bronx</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Lab Analyst]]></title><description><![CDATA[<p><b>Role Summary</b><br />You will support analytical testing activities at our Pakistan laboratory to help ensure product quality and safety. You will work closely with laboratory colleagues, production and quality teams. We value practical laboratory skills, clear communication, and a commitment to continuous learning. This role offers hands-on experience, clear career growth, and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.<br /><br /><b>Key Responsibilities</b></p><ul><li><p>Perform testing of raw materials, intermediates, and finished products as per effective IFS and TM, including data reporting in LIMS and SAP transactions, and sample disposal after release</p></li><li><p>Generate and maintain raw data sheets (logbooks), calculation sheets, summary sheets, and electronically signed reports in LIMS</p></li><li><p>Operate analytical instruments and related software, calibrate analytical balances, and prepare laboratory solutions</p></li><li><p>Maintain reference samples, support standardization of materials, and perform testing for cleaning and cross-contamination studies</p></li><li><p>Report LIRs including OOS, atypical results, and errors in line with quality procedures</p></li><li><p>Actively participate in EHS, fire safety, and learning activities, report EHS incidents/adverse events, and ensure daily GMP-compliant housekeeping</p></li><li><p>Maintain departmental document lists and repositories as per SOP (VQD-SOP-051700)</p></li><li><p>Manage document inventory and issuance across the department</p></li><li><p>Coordinate with document owners for document preparation and revisions (e.g. SOPs, impact assessments)</p></li><li><p>Liaise with the documentation SME/record champion at site for timely and compliant document destruction</p></li></ul><p></p><p><b>Education, Experience &amp; Skills</b></p><ul><li><p>Master’s degree in Chemistry, Pharm-D or a related life sciences field (16 years of education).</p></li><li><p>At least 2 years of laboratory experience in quality control, analytical testing, or a similar environment. Fresh graduates with practical laboratory experience are welcome to apply.</p></li><li><p>Practical knowledge of common lab techniques and instruments such as titration, spectrophotometry, HPLC, GC or basic microbiology methods.</p></li><li><p>Prior use of LIMS, SAP or other enterprise systems for sample tracking and reporting.</p></li><li><p>Basic understanding of good manufacturing practices, quality systems and data integrity principles.</p></li><li><p>Experience in investigations, root cause analysis and CAPA processes.</p></li><li><p>Exposure to continuous improvement approaches such as Lean or Six Sigma.</p></li><li><p>This role is on-site in Pakistan and requires full-time presence at the laboratory.</p></li></ul>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?<br />Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Contact information:</b><br />You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/lab-analyst-gsk/6a08975c2f1861929d253356</link><guid isPermaLink="true">http://biotechroles.com/lab-analyst-gsk/6a08975c2f1861929d253356</guid><pubDate>Sat, 16 May 2026 16:12:12 GMT</pubDate><company>GSK</company><location>Pakistan - Sindh - Karachi</location><salary>$8000-15000</salary><type>Full time</type></item><item><title><![CDATA[Beca Ensayos Clínicos]]></title><description><![CDATA[<p><b>IMPORTANTE: </b>Por favor, todas aquellas personas que estén interesadas en aplicar a esta beca, <b>deberán completar 2 solicitudes para poder ser considerados:</b></p><p></p><p><b>1)</b> A través del enlace de LinkedIn<b> (Plataforma de GSK/ViiV Healthcare)</b></p><p><b>2)</b> A través del siguiente enlace de <b>Talentoteca: </b> <a href="https://www.talentoteca.es/finder/details/00586011/practicas-ensayos-clinicos" target="_blank">Prácticas Ensayos clinicos | GLAXOSMITHKLINE, S.A. | T/2026/50001</a></p><p></p><p><b>Sobre la beca:</b></p><p></p><p>En el área de <b>Operaciones Clínicas</b>, se focaliza en la gestión y monitorización de ensayos clínicos, asegurando cumplimiento normativo con CEIC, AEMPS y buenas prácticas clínicas.</p><p></p><p><b>Programa formativo:</b></p><p></p><ul><li><b>Elaboración de documentación clínica reglada</b></li><li>Aprendizaje en la preparación y presentación de documentación regulatoria, comprendiendo los procesos ante CEIC/AEMPS. <b>Gestión documental física y digital</b></li><li>Formación en métodos de organización, archivo y actualización de expedientes clínicos.</li><li><b>Seguimiento logístico de productos de investigación</b></li><li>Integración de teoría y práctica en sistemas de gestión y control de suministros de investigación.</li><li><b>Actualización de bases de datos clínico-epidemiológicas</b></li><li>Aplicación de metodologías y conocimientos técnicos adquiridos en la carrera al mantenimiento de registros y bases de datos.</li><li><b>Monitorización y visitas a centros</b></li><li>Trabajo conjunto con un Clinical Research Associate: preparación de visitas, informes de seguimiento, formación en calidad y estándares.</li><li><b>Formación jurídica y normativa</b></li></ul><p></p><p><b>Requisitos Básicos:</b></p><ul><li>Grado Biotecnología, Farmacia, Veterinaria o Biología o carreras similares</li><li>Nivel de inglés C1 (preferible para manejo de documentos clínicos internacionales).</li><li>Valorables competencias en gestión documental, bases de datos y habilidades interpersonales.</li></ul><p></p><p><b><u>Qué ofrecemos?</u></b></p><ul><li><p>Bolsa de ayuda de <b>900,00€</b> brutos mensuales</p></li><li><p>8h. diarias en Jornada completa</p></li><li><p>Modelo híbrido de teletrabajo</p></li><li><p>Beca de 1 año de duración</p></li><li><p>25 días de vacaciones durante todo el año</p></li><li><p>Comedor gratuito en las instalaciones</p></li><li><p>Centro de prácticas en Tres Cantos (Madrid)</p></li><li><p>La beca incluye matrícula en Programa CITIUS de Iniciación profesional en la Empresa (Universidad Autónoma de Madrid)</p></li></ul><p></p><p><i><b>#LI-Hybrid</b></i></p><p></p>&amp;#xa;&amp;#xa;This is a temporary internship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process.&amp;#xa;&amp;#xa;Se trata de una oportunidad de prácticas de carácter temporal, orientada al desarrollo profesional. Los gastos elegibles, así como las becas o tasas podrán ser reembolsados de acuerdo con la legislación local aplicable, la normativa vigente o la política del centro de GSK. Se proporcionará información más detallada durante el proceso de selección.<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any reasonable adjustments or arrangements to support you during the recruitment process, specific to your individual needs, please contact us on <a target="_blank" href="mailto:esp-inclusion.recruitment&#64;gsk.com"><span style="color:#0000ff"><u>esp-inclusion.recruitment&#64;gsk.com</u></span></a>.</p><p></p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/ </u></span></a></p>]]></description><link>http://biotechroles.com/beca-ensayos-clinicos-gsk/6a08975c2f1861929d253355</link><guid isPermaLink="true">http://biotechroles.com/beca-ensayos-clinicos-gsk/6a08975c2f1861929d253355</guid><pubDate>Sat, 16 May 2026 16:12:12 GMT</pubDate><company>GSK</company><location>GSK Tres Cantos, Madrid</location><salary>$12000-18000</salary><type>Full time</type></item><item><title><![CDATA[Beca Datos, Insights & Analytics]]></title><description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><b>IMPORTANTE: </b>Por favor, todas aquellas personas que estén interesadas en aplicar a esta beca, <b>deberán completar 2 solicitudes para poder ser considerados:</b></p><p></p><p><b>1)</b> A través del enlace de LinkedIn<b> (Plataforma de GSK/ViiV Healthcare)</b></p><p><b>2)</b> A través del siguiente enlace de <b>Talentoteca: </b> <a href="https://www.talentoteca.es/finder/details/42898517/practicas-datos-insights-analytics" target="_blank">Prácticas Datos, Insights &amp; Analytics | GLAXOSMITHKLINE, S.A. | T/2026/50000</a></p><p></p></div></div></div></div></div></div></div></div></div><p><b>Descripción del Puesto</b></p><p></p><p>Únete al equipo Comercial con la <b>beca del Departamento de Datos, Insights &amp; Analytics</b> y transforma datos comerciales complejos en historias claras y accionables que impulsen el crecimiento. Ayudarás a impulsar la transformación de datos en la nube, evolucionando nuestro data lake corporativo hacia conjuntos de datos confiables listos para Analytics/IA, mientras colaboras para perfeccionar el seguimiento de performance e incorporar analítica avanzada e IA en la toma de decisiones del día a día.</p><p></p><p><b>Objetivos Formativos y responsabilidades:</b><br />Acorde con el <b>Programa CITIUS </b>de Iniciación Profesional en la Empresa, que fomenta la combinación de formación académica con prácticas empresariales adaptativas, el becario:</p><ul><li>Desarrollará competencias en el uso de herramientas tecnológicas avanzadas como Azure, Databricks, SQL Server, GitHub, Power BI, además de aprender lenguajes de programación como SQL, Python-pySpark, DAX, en línea con la personalización y adaptabilidad del <b>itinerario formativo</b> promovido por el Programa <b>CITIUS</b>.</li><li>Transformará datos comerciales en conjuntos de datos confiables y generar insights precisos para la toma de decisiones.</li><li>Creará dashboards y reports de rendimiento que destaquen los factores que impulsan las ventas, los cambios en el mercado y el comportamiento del cliente.</li><li>Respaldará decisiones de lanzamiento, ventas y marketing con análisis rápidos, bien planteados y presentaciones concisas para stakeholders.</li><li>Colaborará con las partes interesadas para alinear definiciones y mejorar la calidad de los datos, asegurando que los insights sean confiables y reutilizables.</li><li>Usará Machine Learning (ML) e IA generativa para prototipar formas de trabajo más inteligentes (por ejemplo, pronósticos, segmentación, personalización).</li><li>Contribuirá a la transformación del data lake en la nube moldeando conjuntos de datos aptos para análisis (por ejemplo, pipelines de datos ELT, controles de calidad de datos, y modelos reutilizables de datos).</li></ul><p></p><p><b>Oportunidades de Desarrollo Profesional:</b></p><p></p><ul><li>Aprender haciendo: mentoría, exposición transversal y proyectos de alto impacto que puedas presentar.</li><li>Desarrollar una visión estratégica del negocio conectando rendimiento, señales de mercado e insights de clientes en recomendaciones claras.</li><li>Liderar un proyecto de principio a fin (desde la formulación de la pregunta hasta las conclusiones y narrativa) y presentar resultados a stakeholders comerciales.</li></ul><p></p><p><b>Requisitos básicos:</b></p><ul><li>Grado en Administración y Dirección de Empresas (ADE), Grado en Estadística, Grado en Ingeniería de Datos, Grado en Matemáticas, Grado en Ingeniería Informática, Grado en Ingeniería Biomédica, Grado en Biotecnología o similares...</li><li>Nivel C1 de inglés</li><li>Dominio avanzado de Excel y al menos una herramienta analítica/de programación (Power BI/Tableau, Python o R).</li><li>Curiosidad por la IA/ML y entusiasmo por explorar casos prácticos de uso de Analytics/IA.</li><li>Pensador estructurado con una sólida mentalidad analítica y atención a los detalles.</li><li>Comunicador claro capaz de traducir números en narrativas y trabajar eficazmente en equipo.</li><li>Interés en el sector farmacéutico y en cómo las estrategias comerciales mejoran el acceso de los pacientes y los resultados del negocio.</li></ul><p></p><p><b>Requisitos valorables:</b></p><ul><li>Máster en Big Data o análisis de datos.</li><li>Valorable proficiencia en herramientas de Microsoft Office, Azure, Databricks, GitHub.</li><li>Buen expediente académico.</li></ul><p></p><p><b><u>Qué ofrecemos?</u></b></p><ul><li><p>Bolsa de ayuda de <b>900,00€</b> brutos mensuales</p></li><li><p>8h. diarias en Jornada completa</p></li><li><p>Modelo híbrido de teletrabajo</p></li><li><p>Beca de 1 año de duración</p></li><li><p>25 días de vacaciones durante todo el año</p></li><li><p>Comedor gratuito en las instalaciones</p></li><li><p>Centro de prácticas en Tres Cantos (Madrid)</p></li><li><p>La beca incluye matrícula en Programa CITIUS de Iniciación profesional en la Empresa (Universidad Autónoma de Madrid)</p></li></ul><p></p><p><i><b>#LI-Hybrid</b></i></p>&amp;#xa;&amp;#xa;This is a temporary internship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process.&amp;#xa;&amp;#xa;Se trata de una oportunidad de prácticas de carácter temporal, orientada al desarrollo profesional. Los gastos elegibles, así como las becas o tasas podrán ser reembolsados de acuerdo con la legislación local aplicable, la normativa vigente o la política del centro de GSK. Se proporcionará información más detallada durante el proceso de selección.<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any reasonable adjustments or arrangements to support you during the recruitment process, specific to your individual needs, please contact us on <a target="_blank" href="mailto:esp-inclusion.recruitment&#64;gsk.com"><span style="color:#0000ff"><u>esp-inclusion.recruitment&#64;gsk.com</u></span></a>.</p><p></p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/ </u></span></a></p>]]></description><link>http://biotechroles.com/beca-datos-insights-and-analytics-gsk/6a08975c2f1861929d253354</link><guid isPermaLink="true">http://biotechroles.com/beca-datos-insights-and-analytics-gsk/6a08975c2f1861929d253354</guid><pubDate>Sat, 16 May 2026 16:12:12 GMT</pubDate><company>GSK</company><location>GSK Tres Cantos, Madrid</location><salary>$12000-18000</salary><type>Full time</type></item><item><title><![CDATA[ViiV Medical Science Liaison, Pacific Northwest (OR/WA/ID/AK)]]></title><description><![CDATA[<div><h2><b><span class="emphasis">Pacific Northwest Region: OR, WA, ID &amp; AK</span></b></h2></div><div><div><div><div><div><div><div><div><div><p></p><p>ViiV Healthcare is a global specialty HIV company, the only one that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV Healthcare is highly mission-driven in our unrelenting commitment to being a trusted partner for all people living with and affected by HIV. Our aim is to think, act, and connect differently through a focus on education on for the prevention and treatment for HIV.  We go to extraordinary lengths to deliver the sorts of breakthroughs, both in prevention, treatments, care solutions and communities, that really count. We go beyond the boundaries of medicine by taking a holistic approach to HIV through developing and supporting sustainable community programs and improving access to care.  We are fully committed to push through every challenge until HIV/AIDS is eradicated. ViiV Healthcare has played a significant part in delivering breakthroughs that have turned HIV into a manageable health condition. We offer the largest portfolio of HIV medicines available anywhere, and we continue our work to cater for the widest possible range of needs in response to the HIV epidemic.</p><p></p><p>We are aware of how much is at stake for those at-risk or affected by HIV and we show up every day 100% committed to the patients. Our work culture is fast-paced, diverse, inclusive, competitive, and caring. But ViiV Healthcare isn’t just somewhere to work – it’s a place to belong, an invitation to bring your very best, and a team full of impact-driven team members who are hungry to make a difference.</p><p></p><p>The <b>Medical Science Liaison (MSL)</b> role is a field based, customer-facing, non-promotional medical and scientific position within the <b>Pacific Northwest (PNW)</b><b> </b>area. The MSL’s key objective is to create impact through advancing clinical practice within the assigned territory that leads to improved patient outcomes. The MSL serves as a scientific expert in HIV treatment and prevention, understands territory and market influences, engages scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop their territory and execute all relevant activities in alignment with the medical strategic plan. The MSL will Inform and shape medical strategy through application of a curious mindset to collect impactful and actionable insights to drive the development and commercialization of our products.</p><p></p><p></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following</p><ul><li><p><b>Scientific Expertise:</b> Build strong scientific acumen and serve as a primary point of contact for medical and scientific inquiries in HIV treatment and prevention supporting scientific engagement for territory. Provide advanced scientific and clinical knowledge to internal teams and external stakeholders.</p></li><li><p><b>Stakeholder Engagement:</b> Identify, develop, and maintain relationships with external experts, researchers, and healthcare professionals. Maintain a strategic plan to provide support to external experts in order to facilitate scientific discussions and collaborations to support ViiV Medical’s scientific and clinical objectives. Engagements may include but not limited to emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within their territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle.</p></li><li><p><b>Clinical Insights:</b> Gather and relay insights from the field to inform product development, clinical trial design, and market strategies. Provide feedback on ViiV products and services.</p></li><li><p><b>Education and Training:</b> Develop and deliver scientific presentations and training sessions for healthcare professionals and internal teams. Support the creation of educational materials and provide scientific training to colleagues.</p></li><li><p><b>Compliance and Documentation:</b> Ensure all activities comply with regulatory guidelines and company policies. Maintain accurate records of interactions and outcomes.</p></li><li><p><b>Leadership and Mentorship:</b> Act as a role model of ViiV’s culture and values. Mentor and coach new or less experienced MSLs and lead scientific or strategic projects to elevate team acumen.</p></li><li><p><b>Safety Communication:</b> Disseminate important safety information to healthcare professionals as directed by Medical Affairs or Research and Development teams.</p></li><li><p><b>Agility and Adaptability:</b> Interface with a wide range of internal and external stakeholders, including external experts, healthcare professionals, investigators, professional societies, advocacy groups, and formulary decision-makers.</p></li><li><p><b>Clinical Development Support:</b> Assist in clinical development activities, including GSK and Investigator Sponsored Studies (ISS). Work with Clinical Teams to improve site performance and provide insights into GSK research interests.</p></li></ul><ul><li><p><b>National Meetings</b>: Attend both national and regional scientific/medical meetings to gain medical voice of the customer on recent data being presented on products and disease states of interest to ViiV.</p></li><li><p><b>Matrix Collaboration</b>: Conducts business with a One-ViiV mindset compliantly and regularly engaging across matrix stakeholders.</p></li><li><p><b>Administration</b>: Execute all responsibilities and training (i.e., Veeva CRM, email, expense report mylearnings) in a timely manner, including profiling of core customers and ensuring up-to-date information in the CRM</p></li></ul><p></p><h1><span class="emphasis"><i><b>Why you?</b></i></span></h1><p></p><p><b>Basic Qualifications: </b></p><p><i>We are looking for professionals with these required skills to achieve our goals:</i></p><ul><li><p>Advanced degree (MD or DO or PharmD or PhD or APP)</p></li><li><p>3&#43; years of clinical experience in HIV OR Infectious Disease</p></li><li><p>Stakeholder management experience</p></li><li><p>Valid Driver’s License</p></li><li><p>Ability to travel 40-60%</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><p><i>If you have the following characteristics, it would be a plus:</i></p><ul><li><p>HIV field medical experience in the US</p></li><li><p>Proven track record of consistent, high performance within Field-Based Medical Affairs</p></li><li><p>Solid grounding in clinical, medical, and pharmaceutical science with demonstrated ability to rapidly assimilate specific and detailed knowledge in these areas.</p></li><li><p>Experience evaluating and effectively communicating evidence-based medicine with strong scientific communication and presentation skills</p></li><li><p>Leadership skills and experience, including high business acumen, stakeholder management, as well as successful project participation and completion</p></li><li><p>Demonstrated excellence in mentoring fellow MSLs, leading complex field based medical team initiatives, participating in and representing field-based medical on internal cross-functional team, and contributing to strategic planning and development of team’s objectives.</p></li><li><p>Experience engaging effectively one on one and in group settings</p></li><li><p>Effective communication skills</p></li></ul><p></p><p>#LI-ViiV</p><p>#LI-GSK</p><p>#LI-Remote</p></div></div></div></div></div></div></div></div></div>The US annual base salary for new hires in this position ranges from $168,750 to $281,250.  The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.&amp;#xa;&amp;#xa;If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit <a target="_blank" href="https://us.gsk.com/media/7963/ustrataglance-jobpostings.pdf">GSK US Benefits Summary</a><a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"> </a>to learn more about the comprehensive benefits program ViiV offers US employees. All ViiV employees receive the same benefits options and plans as GSK employee.</p><p></p><p><b>Why Us?</b></p><p>At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. </p><p></p><p>We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>GSK</u></span></a> and <a target="_blank" href="http://www.Pfizer.com"><span style="color:#0000ff"><u>Pfizer</u></span></a> in 2009, with <a target="_blank" href="http://www.Shionogi.com"><span style="color:#0000ff"><u>Shionogi</u></span></a> joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.</p><p></p><p>Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. </p><p></p><p>Having a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a></p><p></p><p>ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/viiv-medical-science-liaison-pacific-northwest-orwaidak-gsk/6a08975b2f1861929d253353</link><guid isPermaLink="true">http://biotechroles.com/viiv-medical-science-liaison-pacific-northwest-orwaidak-gsk/6a08975b2f1861929d253353</guid><pubDate>Sat, 16 May 2026 16:12:11 GMT</pubDate><company>GSK</company><location>Field Worker - USA</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Practicante Pre Profesional, Comunicación, Perú, 2026]]></title><description><![CDATA[<p><b>Ayúdanos a adelantarnos a las enfermedades junto con nuestra Área de Comunicación.</b></p><p><b>Formación requerida: </b>Actualmente estudiante activo de Diseño Gráfico, Comunicación, Administración o afines (al menos 1 año para graduarte).</p><p><b>Otros requisitos:</b> Debe estar matriculado/a en una universidad de Perú durante toda la duración de las prácticas.</p><p>Buen manejo de Microsoft Office y de programas de diseño.</p><p><b>Requisitos de idioma</b>: Inglés intermedio (lectura y comunicación básica)</p><p><b>Fecha de inicio prevista:</b> Junio 2026</p><p><b>Periodo de prácticas</b>: 1 año</p><p><i>Modelo híbrido: 2 días onsite</i></p><p><b>Fecha límite de solicitud:</b> Recomendamos postular lo antes posible. Cerraremos esta vacante cuando tengamos suficientes solicitudes, así que aplica cuanto antes para que tu candidatura pueda ser considerada.</p><p></p><p><b>¿Buscas adquirir una valiosa experiencia laboral a nivel mundial y ayudar a impactar positivamente en la salud de miles de millones de personas? ¡Solicita hoy una práctica en GSK!</b></p><p></p><p>Una práctica en GSK te ofrece la oportunidad de impulsar tu carrera: ¡asumirás un puesto real con un impacto genuino! Realizarás un trabajo exigente y significativo en proyectos o asignaciones reales. También aprenderás con nosotros, desarrollarás tus habilidades y adquirirás una experiencia valiosa para dondequiera que te lleve el futuro.</p><p><br /><b>¿Qué harás? </b></p><ul><li>Diseño de materiales de comunicación interna</li><li>Soporte al equipo de comunicaciones</li><li>Coordinación de contenidos con el área de Marketing</li><li>Generación de contenidos para RRSS y Workplace</li><li>Asegurar las aprobaciones de materiales en Content Lab de manera oportuna.</li><li>Hacer solicitudes de órdenes de compra</li></ul><p></p><p><b>¿Qué aprenderás?</b></p><p>Serás parte de un equipo que aporta apoyo operativo y administrativo en un entorno global. Trabajarás de cerca con líderes y colegas de varias áreas para ejecutar tareas diarias, proyectos y eventos.</p><p></p><p><b>¿Qué estamos buscando?</b></p><ul><li>Contacto de proveedores externos e internos.</li><li>Gestión y carga de órdenes de compra.</li><li>Estudiante de Diseño gráfico, Comunicaciones o afines.</li><li>Manejo de MS Office, Adobe, Illustrator, Photoshop</li><li>Conocimientos en edición de audio y video.</li><li>Inglés intermedio</li><li>Horario por la mañana o tarde (remoto y presencial on site).</li></ul><p></p><p><b>¿Qué te ofrecemos? </b></p><ul><li>Una práctica remunerada con formación práctica y mentoría.</li><li>Entorno de trabajo inclusivo que apoya tu desarrollo y bienestar.</li><li>Oportunidad de aprender de equipos multidisciplinarios y aportar en proyectos reales.</li><li>Flexibilidad híbrida según la área y necesidades del puesto.</li></ul><p></p><p><b>¡Hagámoslo realidad!</b></p><p>Encontrarás consejos, sugerencias y orientación sobre nuestro proceso de selección en nuestro sitio web.</p><p>Obtén más información sobre el proceso de solicitud en gsk.to/ECprocess (opcional).</p><p>Puedes aprender más sobre GSK y nuestras carreras aquí: <a href="https://www.gsk.com/en-gb/careers/" target="_blank">https://www.gsk.com/en-gb/careers/</a></p><p></p><p><b>¡Postúlate ahora!</b></p><p><b><i>¿Necesitas ayuda con tu solicitud?</i></b></p><p><i>Por favor escríbenos a</i> <a href="mailto:AM.EarlyTalentRecruitment&#64;gsk.com" target="_blank">AM.EarlyTalentRecruitment&#64;gsk.com</a> <i>y dinos cómo podemos ayudarte.</i></p><p>#EarlyCareers</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>If you require any adjustments or accommodation during the selection process to better showcase your abilities, please let our team know as soon as we contact you. We&#39;re here to support you.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Our inclusive workplace makes our employees feel engaged by the contribution they make, by affording them equal treatment regardless of actual or perceived characteristics. As so, when you apply for a job at GSK, it is not necessary to include on your resume information such as: race, color, ethnicity, age, gender, sexual orientation, marital status, religion, origin, photographs or any other personal characteristics.</p><p> </p><p>Find out what life at GSK is really like <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>www.gsk.com</u></span></a></p>]]></description><link>http://biotechroles.com/practicante-pre-profesional-comunicacion-peru-2026-gsk/6a08975b2f1861929d253352</link><guid isPermaLink="true">http://biotechroles.com/practicante-pre-profesional-comunicacion-peru-2026-gsk/6a08975b2f1861929d253352</guid><pubDate>Sat, 16 May 2026 16:12:11 GMT</pubDate><company>GSK</company><location>Lima Avenida Belaunde</location><salary>$0-0</salary><type>Part time</type></item><item><title><![CDATA[Senior Legal Counsel, Corporate]]></title><description><![CDATA[<p><br /> </p><h1><span class="emphasis"><b>Senior Legal Counsel, Corporate</b></span></h1><h2></h2><h2><br /><br /><span class="emphasis"><b>Business Introduction</b></span></h2><h2></h2><p><br />GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.</p><p><br />Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.<br />Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.<br /><br /> </p><h2><span class="emphasis"><b>Position Summary</b></span></h2><p><br />This is an exceptional opportunity for an experienced corporate lawyer to take on a pivotal role at the centre of a UK and US listed company. Sitting within a high-performing and collaborative Legal function, you will serve as a legal expert on the company’s obligations as a listed entity, including governance, and investor and market disclosures. You will act as trusted counsel on the execution of strategically significant corporate transactions and provide legal support on the group’s equity investments. You will also provide legal support to many of the group’s corporate functions.</p><p></p><p></p><h2><span class="emphasis"><b>Responsibilities</b></span></h2><p></p><ul><li><p>Provide legal support on UK-listed company governance and public disclosure obligations, including external reporting, investor disclosures and other market-facing communications.</p></li><li><p>Lead the legal aspects of complex corporate transactions and investments, including M&amp;A, joint ventures, bond issuances and share buy-backs, from initial structuring and due diligence through signing, closing and post-completion matters.</p></li><li><p>Coordinate the legal review of the Annual Report, Form 20-F, quarterly results and related filings, coordinating across functions and with external counsel to ensure regulatory compliance.</p></li><li><p>Provide legal support on corporate group governance matters, including the review of delegations of authority and corporate powers, ensuring changes to GSK group legal entities are compliant, and conducting legal review of documents before execution by authorised signatories.</p></li><li><p>Provide legal support on intra-group arrangements, including transfer pricing matters and the intra-group movement of goods, in collaboration with Finance and GSK trading entities.</p></li><li><p>Provide corporate law advice in relation to GSK’s equity investment portfolio, reviewing and approving investor‑side documentation, supporting governance and information rights, and advising on ongoing portfolio company matters from a corporate law perspective.</p></li><li><p>Provide legal support to corporate-led programmes and corporate functions, including to Communications and Government Affairs.</p></li><li><p>Manage and improve legal processes, templates and know-how in your areas of accountability, with a focus on simplification and efficiency.</p></li><li><p>Act as legal reviewer and approver for designated corporate policies, providing advice on legal risk, consistency with applicable law and group governance standards, and supporting periodic reviews and updates.</p></li><li><p>Oversee external counsel on corporate matters, managing quality, cost and delivery.</p></li><li><p>Provide periodic legal support on a range of adjacent legal matters as required, including advising on the management of legal risks (particularly anti-bribery and corruption and related matters) and providing legal support on broader business development activities, in collaboration with specialist legal teams.</p></li></ul><p></p><p></p><h2><span class="emphasis"><b>Qualifications/Skills</b></span></h2><h2><span class="emphasis"><b>Basic Qualifications:</b></span></h2><p></p><ul><li><p>UK-qualified solicitor with significant &amp; demonstrable post-qualification experience, ideally gained at a top-tier law firm and/or in-house within a UK-listed company environment.</p></li><li><p>Significant experience leading complex, high-value transactions.</p></li><li><p>Deep understanding of UK corporate law, particularly as it relates to publicly listed companies and intra-group arrangements.</p></li><li><p>Strong business acumen, with the ability to balance legal risk and commercial opportunity.</p></li><li><p>Proven ability to communicate complex legal issues with clarity and precision, delivering focused, actionable advice to senior leaders.</p></li><li><p>Excellent interpersonal and communication skills, with the ability to collaborate effectively across diverse teams and align stakeholders to achieve strategic outcomes.</p></li><li><p>Proactive, detail-oriented and adaptable.</p></li></ul><p></p><p></p><h2><span class="emphasis"><b>Preferred Qualifications:</b></span></h2><p></p><ul><li><p>Experience in the life sciences, pharmaceutical or healthcare sector or other regulated industry.</p></li><li><p>Knowledge of laws relevant to our business such as competition, advertising/communications, procurement, data privacy and anti-bribery.</p></li><li><p>Experience managing multi-jurisdictional matters and working with external counsel internationally.</p></li></ul><p></p><p></p><h2><span class="emphasis"><b>Work Location:</b></span><br /><br />This role is based in the United Kingdom (GSK HQ, London) and offers a hybrid working model, combining on-site and remote work.</h2><p></p><p></p><p><span class="emphasis"><b>Closing Date for Applications:</b></span> 27th May 2026</p><p></p><p></p><p>Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.</p><p></p><p></p><p><b>#Li-Hybrid</b></p><p><br /><br /><span class="emphasis">What we offer</span><br /><br />You will join a team that values respect, transparency and development. You will have access to learning and career development opportunities. You will work on meaningful matters that support the company mission to unite science, technology and talent to get ahead of disease together.<br /><br /><span class="emphasis">Ready to apply?</span><br /><br />If this role matches your experience and ambitions, we would like to hear from you. Please submit your CV and a short cover letter that explains how you meet the basics of the role and what impact you hope to make. We welcome applications from people at different career stages and from all backgrounds.</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/senior-legal-counsel-corporate-gsk/6a08975a2f1861929d253351</link><guid isPermaLink="true">http://biotechroles.com/senior-legal-counsel-corporate-gsk/6a08975a2f1861929d253351</guid><pubDate>Sat, 16 May 2026 16:12:10 GMT</pubDate><company>GSK</company><location>UK – London – New Oxford Street</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Sales Representative - Lower Manhattan, NY]]></title><description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><b>Territory: </b>Includes but is not limited to:<b> Lower Manhattan, NY</b></p><p></p><p>At GSK we unite science, talent and technology to get ahead of disease together. We’ve transformed R&amp;D and commercial execution to deliver life‑changing vaccines and specialty medicines. If you’re ready to improve the lives of billions and grow your career in a purpose‑driven company, join us. </p><p></p><p><span class="emphasis"><b>About the Role</b></span> </p><p></p><p>The GSK <i>US Respiratory &amp; Anti-Infectives </i><b>Sales</b> Professional is responsible for engaging physicians and allied health professionals across independent practices, physician groups, and hospital systems to drive appropriate prescribing of GSK products. This includes influencing prescribing decisions versus competitive therapies for relevant disease states through compliant, face-to-face interactions, in alignment with approved product indications and prescribing information. </p><p></p><p>This role gives you the opportunity to build your skills and grow your career. Key responsibilities include: </p><p></p><p><span class="emphasis"><b>Key Responsibilities</b> </span></p><ul><li><p>Drive territory sales and market share growth across promoted COPD, asthma, and anti-infective products through targeted, compliant, evidence-based customer engagement. </p></li></ul><ul><li><p>Own territory business planning; analyze sales data and execute actions to meet goals. </p></li></ul><ul><li><p>Develop dynamic call plans and collaborate with local territory colleagues to maximize reach and frequency. </p></li></ul><ul><li><p>Build strong partnerships with Marketing, Payer Relations, Medical (MSLs), and other internal stakeholders to align strategy and resources. </p></li></ul><ul><li><p>Plan and deliver in-services, educational programs, and sample distribution in accordance with FDA regulations and company policy. </p></li></ul><ul><li><p>Complete administrative responsibilities accurately and on time (e.g., sample accountability, call reporting, eLearning, and expense reporting). </p></li></ul><ul><li><p>Comply with GSK policies, ethical standards, and all applicable regulatory requirements. </p></li></ul><p></p><p><span class="emphasis"><b>Why You? </b></span></p><p></p><p><span class="emphasis"><b>Basic Qualifications </b></span></p><ul><li><p>BA/BS from an accredited institution </p></li></ul><ul><li><p>Valid driver’s license; driving is an essential function of this role </p></li></ul><ul><li><p>Willingness to travel within the territory, including occasional overnight and weekend travel, based on business needs </p></li></ul><ul><li><p>The selected candidate will be hired at the appropriate level based on experience: </p></li></ul><ul><li><p><b>Grade 8</b>: Minimum of 2 years of pharmaceutical or business-to-business sales experience </p></li></ul><ul><li><p><b>Grade 7</b>: Minimum of 5 years of pharmaceutical or business-to-business sales experience </p></li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications</b></span> </p><ul><li><p>Bilingual preferred based on location </p></li></ul><ul><li><p>Account management experience within local IDNs/large hospital systems </p></li></ul><ul><li><p>Experience in respiratory/allergy or other healthcare sales </p></li></ul><ul><li><p>Familiarity with managed care, formularies, retail pharmacy operations, prior authorization processes </p></li></ul><ul><li><p>Strong presentation, influencing and business planning skills </p></li></ul><ul><li><p>Self‑starter with attention to detail and ability to manage multiple priorities </p></li></ul><p></p><p><span class="emphasis"><b>Core Capabilities</b> </span></p><ul><li><p>Winning mindset and results orientation </p></li></ul><ul><li><p>Ambitious goal setting and performance discipline </p></li></ul><ul><li><p>Courage to challenge constructively and resilience to overcome setbacks </p></li></ul><ul><li><p>Change leadership and continuous improvement mindset </p></li></ul><ul><li><p>Accountability, team inspiration and influential communication </p></li></ul><p></p><p>We invest in development and transparent talent management. Grow your career with meaningful work that impacts patients and communities. Join our challenge to get Ahead Together. </p><p></p><p>#LI-GSK </p><p>#LI-Remote </p><p>#GSKCommercial </p></div></div></div></div></div></div></div></div></div>The US annual base salary for new hires in this position ranges from $99,000 to $165,000.  The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.&amp;#xa;&amp;#xa;If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pharmaceutical-sales-representative-lower-manhattan-ny-gsk/6a08975a2f1861929d253350</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-sales-representative-lower-manhattan-ny-gsk/6a08975a2f1861929d253350</guid><pubDate>Sat, 16 May 2026 16:12:10 GMT</pubDate><company>GSK</company><location>USA - New York - Lower Manhattan</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Sales Representative - Pittsburgh, PA]]></title><description><![CDATA[<div><b>Territory: </b>Includes but is not limited to: <b>Pittsburgh, PA</b></div><div><div><div><div><div><div><div><div><div><p></p><p>At GSK we unite science, talent and technology to get ahead of disease together. We’ve transformed R&amp;D and commercial execution to deliver life‑changing vaccines and specialty medicines. If you’re ready to improve the lives of billions and grow your career in a purpose‑driven company, join us. </p><p></p><p><span class="emphasis"><b>About the Role</b></span> </p><p></p><p>The GSK <i>US Respiratory &amp; Anti-Infectives </i><b>Sales</b> Professional is responsible for engaging physicians and allied health professionals across independent practices, physician groups, and hospital systems to drive appropriate prescribing of GSK products. This includes influencing prescribing decisions versus competitive therapies for relevant disease states through compliant, face-to-face interactions, in alignment with approved product indications and prescribing information. </p><p></p><p>This role gives you the opportunity to build your skills and grow your career. Key responsibilities include: </p><p></p><p><span class="emphasis"><b>Key Responsibilities</b> </span></p><ul><li><p>Drive territory sales and market share growth across promoted COPD, asthma, and anti-infective products through targeted, compliant, evidence-based customer engagement. </p></li></ul><ul><li><p>Own territory business planning; analyze sales data and execute actions to meet goals. </p></li></ul><ul><li><p>Develop dynamic call plans and collaborate with local territory colleagues to maximize reach and frequency. </p></li></ul><ul><li><p>Build strong partnerships with Marketing, Payer Relations, Medical (MSLs), and other internal stakeholders to align strategy and resources. </p></li></ul><ul><li><p>Plan and deliver in-services, educational programs, and sample distribution in accordance with FDA regulations and company policy. </p></li></ul><ul><li><p>Complete administrative responsibilities accurately and on time (e.g., sample accountability, call reporting, eLearning, and expense reporting). </p></li></ul><ul><li><p>Comply with GSK policies, ethical standards, and all applicable regulatory requirements. </p></li></ul><p></p><p><span class="emphasis"><b>Why You? </b></span></p><p></p><p><span class="emphasis"><b>Basic Qualifications </b></span></p><ul><li><p>BA/BS from an accredited institution </p></li></ul><ul><li><p>Valid driver’s license; driving is an essential function of this role </p></li></ul><ul><li><p>Willingness to travel within the territory, including occasional overnight and weekend travel, based on business needs </p></li></ul><ul><li><p>The selected candidate will be hired at the appropriate level based on experience: </p></li></ul><ul><li><p><b>Grade 8</b>: Minimum of 2 years of pharmaceutical or business-to-business sales experience </p></li></ul><ul><li><p><b>Grade 7</b>: Minimum of 5 years of pharmaceutical or business-to-business sales experience </p></li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications</b></span> </p><ul><li><p>Bilingual preferred based on location </p></li></ul><ul><li><p>Account management experience within local IDNs/large hospital systems </p></li></ul><ul><li><p>Experience in respiratory/allergy or other healthcare sales </p></li></ul><ul><li><p>Familiarity with managed care, formularies, retail pharmacy operations, prior authorization processes </p></li></ul><ul><li><p>Strong presentation, influencing and business planning skills </p></li></ul><ul><li><p>Self‑starter with attention to detail and ability to manage multiple priorities </p></li></ul><p></p><p><span class="emphasis"><b>Core Capabilities</b> </span></p><ul><li><p>Winning mindset and results orientation </p></li></ul><ul><li><p>Ambitious goal setting and performance discipline </p></li></ul><ul><li><p>Courage to challenge constructively and resilience to overcome setbacks </p></li></ul><ul><li><p>Change leadership and continuous improvement mindset </p></li></ul><ul><li><p>Accountability, team inspiration and influential communication </p></li></ul><p></p><p>We invest in development and transparent talent management. Grow your career with meaningful work that impacts patients and communities. Join our challenge to get Ahead Together. </p><p></p><p>#LI-GSK </p><p>#LI-Remote </p><p>#GSKCommercial </p></div></div></div></div></div></div></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pharmaceutical-sales-representative-pittsburgh-pa-gsk/6a0897592f1861929d25334f</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-sales-representative-pittsburgh-pa-gsk/6a0897592f1861929d25334f</guid><pubDate>Sat, 16 May 2026 16:12:09 GMT</pubDate><company>GSK</company><location>USA - Pennsylvania - Pittsburgh</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Sales Representative - New Haven, CT]]></title><description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><b>Territory: </b>Includes but is not limited to: <b>New Haven, CT</b></p><p></p><p>At GSK we unite science, talent and technology to get ahead of disease together. We’ve transformed R&amp;D and commercial execution to deliver life‑changing vaccines and specialty medicines. If you’re ready to improve the lives of billions and grow your career in a purpose‑driven company, join us. </p><p></p><p><span class="emphasis"><b>About the Role</b></span> </p><p></p><p>The GSK <i>US Respiratory &amp; Anti-Infectives </i><b>Sales</b> Professional is responsible for engaging physicians and allied health professionals across independent practices, physician groups, and hospital systems to drive appropriate prescribing of GSK products. This includes influencing prescribing decisions versus competitive therapies for relevant disease states through compliant, face-to-face interactions, in alignment with approved product indications and prescribing information. </p><p></p><p>This role gives you the opportunity to build your skills and grow your career. Key responsibilities include: </p><p></p><p><span class="emphasis"><b>Key Responsibilities</b> </span></p><ul><li><p>Drive territory sales and market share growth across promoted COPD, asthma, and anti-infective products through targeted, compliant, evidence-based customer engagement. </p></li></ul><ul><li><p>Own territory business planning; analyze sales data and execute actions to meet goals. </p></li></ul><ul><li><p>Develop dynamic call plans and collaborate with local territory colleagues to maximize reach and frequency. </p></li></ul><ul><li><p>Build strong partnerships with Marketing, Payer Relations, Medical (MSLs), and other internal stakeholders to align strategy and resources. </p></li></ul><ul><li><p>Plan and deliver in-services, educational programs, and sample distribution in accordance with FDA regulations and company policy. </p></li></ul><ul><li><p>Complete administrative responsibilities accurately and on time (e.g., sample accountability, call reporting, eLearning, and expense reporting). </p></li></ul><ul><li><p>Comply with GSK policies, ethical standards, and all applicable regulatory requirements. </p></li></ul><p></p><p><span class="emphasis"><b>Why You? </b></span></p><p></p><p><span class="emphasis"><b>Basic Qualifications </b></span></p><ul><li><p>BA/BS from an accredited institution </p></li></ul><ul><li><p>Valid driver’s license; driving is an essential function of this role </p></li></ul><ul><li><p>Willingness to travel within the territory, including occasional overnight and weekend travel, based on business needs </p></li></ul><ul><li><p>The selected candidate will be hired at the appropriate level based on experience: </p></li></ul><ul><li><p><b>Grade 8</b>: Minimum of 2 years of pharmaceutical or business-to-business sales experience </p></li></ul><ul><li><p><b>Grade 7</b>: Minimum of 5 years of pharmaceutical or business-to-business sales experience </p></li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications</b></span> </p><ul><li><p>Bilingual preferred based on location </p></li></ul><ul><li><p>Account management experience within local IDNs/large hospital systems </p></li></ul><ul><li><p>Experience in respiratory/allergy or other healthcare sales </p></li></ul><ul><li><p>Familiarity with managed care, formularies, retail pharmacy operations, prior authorization processes </p></li></ul><ul><li><p>Strong presentation, influencing and business planning skills </p></li></ul><ul><li><p>Self‑starter with attention to detail and ability to manage multiple priorities </p></li></ul><p></p><p><span class="emphasis"><b>Core Capabilities</b> </span></p><ul><li><p>Winning mindset and results orientation </p></li></ul><ul><li><p>Ambitious goal setting and performance discipline </p></li></ul><ul><li><p>Courage to challenge constructively and resilience to overcome setbacks </p></li></ul><ul><li><p>Change leadership and continuous improvement mindset </p></li></ul><ul><li><p>Accountability, team inspiration and influential communication </p></li></ul><p></p><p>We invest in development and transparent talent management. Grow your career with meaningful work that impacts patients and communities. Join our challenge to get Ahead Together. </p><p></p><p>#LI-GSK </p><p>#LI-Remote </p><p>#GSKCommercial </p></div></div></div></div></div></div></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pharmaceutical-sales-representative-new-haven-ct-gsk/6a0897592f1861929d25334e</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-sales-representative-new-haven-ct-gsk/6a0897592f1861929d25334e</guid><pubDate>Sat, 16 May 2026 16:12:09 GMT</pubDate><company>GSK</company><location>USA - Connecticut - New Haven</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Sales Representative- Glendale,CA]]></title><description><![CDATA[<div><div></div></div><div><div><div><div><div><div><div><div><div><p><b>Territory: </b>Includes but is not limited to: <b>Glendale,CA </b></p><p></p><p>At GSK we unite science, talent and technology to get ahead of disease together. We’ve transformed R&amp;D and commercial execution to deliver life‑changing vaccines and specialty medicines. If you’re ready to improve the lives of billions and grow your career in a purpose‑driven company, join us. </p><p></p><p><span class="emphasis"><b>About the Role</b></span> </p><p></p><p>The GSK <i>US Respiratory &amp; Anti-Infectives </i><b>Sales</b> Professional is responsible for engaging physicians and allied health professionals across independent practices, physician groups, and hospital systems to drive appropriate prescribing of GSK products. This includes influencing prescribing decisions versus competitive therapies for relevant disease states through compliant, face-to-face interactions, in alignment with approved product indications and prescribing information. </p><p></p><p>This role gives you the opportunity to build your skills and grow your career. Key responsibilities include: </p><p></p><p><span class="emphasis"><b>Key Responsibilities</b> </span></p><ul><li><p>Drive territory sales and market share growth across promoted COPD, asthma, and anti-infective products through targeted, compliant, evidence-based customer engagement. </p></li></ul><ul><li><p>Own territory business planning; analyze sales data and execute actions to meet goals. </p></li></ul><ul><li><p>Develop dynamic call plans and collaborate with local territory colleagues to maximize reach and frequency. </p></li></ul><ul><li><p>Build strong partnerships with Marketing, Payer Relations, Medical (MSLs), and other internal stakeholders to align strategy and resources. </p></li></ul><ul><li><p>Plan and deliver in-services, educational programs, and sample distribution in accordance with FDA regulations and company policy. </p></li></ul><ul><li><p>Complete administrative responsibilities accurately and on time (e.g., sample accountability, call reporting, eLearning, and expense reporting). </p></li></ul><ul><li><p>Comply with GSK policies, ethical standards, and all applicable regulatory requirements. </p></li></ul><p></p><p><span class="emphasis"><b>Why You? </b></span></p><p></p><p><span class="emphasis"><b>Basic Qualifications </b></span></p><ul><li><p>BA/BS from an accredited institution </p></li></ul><ul><li><p>Valid driver’s license; driving is an essential function of this role </p></li></ul><ul><li><p>Willingness to travel within the territory, including occasional overnight and weekend travel, based on business needs </p></li></ul><ul><li><p>The selected candidate will be hired at the appropriate level based on experience: </p></li></ul><ul><li><p><b>Grade 8</b>: Minimum of 2 years of pharmaceutical or business-to-business sales experience </p></li></ul><ul><li><p><b>Grade 7</b>: Minimum of 5 years of pharmaceutical or business-to-business sales experience </p></li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications</b></span> </p><ul><li><p>Bilingual preferred based on location </p></li></ul><ul><li><p>Account management experience within local IDNs/large hospital systems </p></li></ul><ul><li><p>Experience in respiratory/allergy or other healthcare sales </p></li></ul><ul><li><p>Familiarity with managed care, formularies, retail pharmacy operations, prior authorization processes </p></li></ul><ul><li><p>Strong presentation, influencing and business planning skills </p></li></ul><ul><li><p>Self‑starter with attention to detail and ability to manage multiple priorities </p></li></ul><p></p><p><span class="emphasis"><b>Core Capabilities</b> </span></p><ul><li><p>Winning mindset and results orientation </p></li></ul><ul><li><p>Ambitious goal setting and performance discipline </p></li></ul><ul><li><p>Courage to challenge constructively and resilience to overcome setbacks </p></li></ul><ul><li><p>Change leadership and continuous improvement mindset </p></li></ul><ul><li><p>Accountability, team inspiration and influential communication </p></li></ul><p></p><p>We invest in development and transparent talent management. Grow your career with meaningful work that impacts patients and communities. Join our challenge to get Ahead Together. </p><p></p><p>#LI-GSK </p><p>#LI-Remote </p><p>#GSKCommercial </p></div></div></div></div></div></div></div></div></div>The US annual base salary for new hires in this position ranges from $99,000 to $165,000.  The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.&amp;#xa;&amp;#xa;If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pharmaceutical-sales-representative-glendaleca-gsk/6a0897592f1861929d25334d</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-sales-representative-glendaleca-gsk/6a0897592f1861929d25334d</guid><pubDate>Sat, 16 May 2026 16:12:09 GMT</pubDate><company>GSK</company><location>USA - California - California Central Valley</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Sales Representative - Petoskey, Michigan]]></title><description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><b>Territory: </b>Includes but is not limited to: <b>Petoskey, Michigan</b></p><p></p><p>At GSK we unite science, talent and technology to get ahead of disease together. We’ve transformed R&amp;D and commercial execution to deliver life‑changing vaccines and specialty medicines. If you’re ready to improve the lives of billions and grow your career in a purpose‑driven company, join us. </p><p></p><p><span class="emphasis"><b>About the Role</b></span> </p><p></p><p>The GSK <i>US Respiratory &amp; Anti-Infectives </i><b>Sales</b> Professional is responsible for engaging physicians and allied health professionals across independent practices, physician groups, and hospital systems to drive appropriate prescribing of GSK products. This includes influencing prescribing decisions versus competitive therapies for relevant disease states through compliant, face-to-face interactions, in alignment with approved product indications and prescribing information. </p><p></p><p>This role gives you the opportunity to build your skills and grow your career. Key responsibilities include: </p><p></p><p><span class="emphasis"><b>Key Responsibilities</b> </span></p><ul><li><p>Drive territory sales and market share growth across promoted COPD, asthma, and anti-infective products through targeted, compliant, evidence-based customer engagement. </p></li></ul><ul><li><p>Own territory business planning; analyze sales data and execute actions to meet goals. </p></li></ul><ul><li><p>Develop dynamic call plans and collaborate with local territory colleagues to maximize reach and frequency. </p></li></ul><ul><li><p>Build strong partnerships with Marketing, Payer Relations, Medical (MSLs), and other internal stakeholders to align strategy and resources. </p></li></ul><ul><li><p>Plan and deliver in-services, educational programs, and sample distribution in accordance with FDA regulations and company policy. </p></li></ul><ul><li><p>Complete administrative responsibilities accurately and on time (e.g., sample accountability, call reporting, eLearning, and expense reporting). </p></li></ul><ul><li><p>Comply with GSK policies, ethical standards, and all applicable regulatory requirements. </p></li></ul><p></p><p><span class="emphasis"><b>Why You? </b></span></p><p></p><p><span class="emphasis"><b>Basic Qualifications </b></span></p><ul><li><p>BA/BS from an accredited institution </p></li></ul><ul><li><p>Valid driver’s license; driving is an essential function of this role </p></li></ul><ul><li><p>Willingness to travel within the territory, including occasional overnight and weekend travel, based on business needs </p></li></ul><ul><li><p>The selected candidate will be hired at the appropriate level based on experience: </p></li></ul><ul><li><p><b>Grade 8</b>: Minimum of 2 years of pharmaceutical or business-to-business sales experience </p></li></ul><ul><li><p><b>Grade 7</b>: Minimum of 5 years of pharmaceutical or business-to-business sales experience </p></li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications</b></span> </p><ul><li><p>Bilingual preferred based on location </p></li></ul><ul><li><p>Account management experience within local IDNs/large hospital systems </p></li></ul><ul><li><p>Experience in respiratory/allergy or other healthcare sales </p></li></ul><ul><li><p>Familiarity with managed care, formularies, retail pharmacy operations, prior authorization processes </p></li></ul><ul><li><p>Strong presentation, influencing and business planning skills </p></li></ul><ul><li><p>Self‑starter with attention to detail and ability to manage multiple priorities </p></li></ul><p></p><p><span class="emphasis"><b>Core Capabilities</b> </span></p><ul><li><p>Winning mindset and results orientation </p></li></ul><ul><li><p>Ambitious goal setting and performance discipline </p></li></ul><ul><li><p>Courage to challenge constructively and resilience to overcome setbacks </p></li></ul><ul><li><p>Change leadership and continuous improvement mindset </p></li></ul><ul><li><p>Accountability, team inspiration and influential communication </p></li></ul><p></p><p>We invest in development and transparent talent management. Grow your career with meaningful work that impacts patients and communities. Join our challenge to get Ahead Together. </p><p></p><p>#LI-GSK </p><p>#LI-Remote </p><p>#GSKCommercial </p></div></div></div></div></div></div></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pharmaceutical-sales-representative-petoskey-michigan-gsk/6a0897572f1861929d25334c</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-sales-representative-petoskey-michigan-gsk/6a0897572f1861929d25334c</guid><pubDate>Sat, 16 May 2026 16:12:07 GMT</pubDate><company>GSK</company><location>USA - Michigan - Petoskey</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[ViiV Healthcare (GSK) Consumer Marketing Director, HIV Treatment, Long-Acting Injectable]]></title><description><![CDATA[<h2>ViiV Healthcare is a global specialty HIV company, the only one that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV is highly mission-driven in its unrelenting commitment to be a trusted partner for all people living with and affected by HIV.  ViiV has played a significant part in delivering breakthroughs that have turned HIV into a manageable health condition.  Our work culture is fast-paced, diverse, inclusive, competitive, and caring. But ViiV isn’t just somewhere to work – it’s a place to belong, an invitation to bring your very best, and a team full of impact-driven team members who are hungry to make a difference</h2><h2></h2><h2><span>As <b>Consumer Marketing Director, HIV Treatment, Long-Acting Injectable, </b>you will lead DTC creative and media strategy, execution, and measurement.  Our candidate should have a passion for marketing and the ability to work across multiple stakeholders and external agency partners. We are looking for a strong business owner to leverage data to make smart strategic choices and media allocations that will generate results. You will manage a team of 3 marketing managers, and a large budget. The role reports to the Sr Director Consumer Marketing ViiV Healthcare.</span></h2><p></p><p><span class="emphasis"><b>This role will be based out of Durham, NC is eligible for a domestic relocation package. Check out this link to learn more about the thriving, diverse, and cutting edge RTP area!</b></span></p><p><a href="https://www.rtp.org/" target="_blank"><span class="emphasis">Research Triangle Park | Where People &#43; Ideas Converge (rtp.org)</span></a></p><p></p><h2><i>This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following…</i></h2><ul><li><h2>Effectively partner with brand teams and matrix partners to help meet brand objectives</h2></li><li><h2>Develop effective consumer/patient strategies, campaigns and tactics to drive brand growth throughout the patient journey</h2></li><li><h2>Manage media plans to ensure effective and efficient investment</h2></li><li><h2>Measure and continually optimize all investments; effectively manage large budget</h2></li><li><h2>Ensure effective relationships with multiple agencies (creative, media, and patient ambassadors), and build collaboration and integration across agency teams</h2></li><li><h2>Lead and develop team of Marketing Managers</h2></li></ul><h2></h2><h1><span class="emphasis"><b><i>Why you?</i></b></span></h1><p></p><p><b>Basic Qualifications: </b></p><p><i>We are looking for professionals with these required skills to achieve our goals:</i></p><p></p><ul><li><h2>Bachelor’s Degree &amp; 4 plus years of pharmaceutical experience to include Marketing OR Commercial roles</h2></li><li><h2>Experience managing and leading campaigns, media plans, and marketing budget</h2></li><li><h2>Experience leading direct reports, matrix teams, and agencies</h2></li><li><h2>Experience navigating within promotional review processes</h2></li></ul><h2></h2><h2><b><span>Preferred Qualifications: </span></b></h2><h2><i>If you have the following characteristics, it would be a plus:</i></h2><ul><li><h2>Direct to Consumer Pharma Marketing experience; experience with specialty pharmaceuticals/ injectables a plus</h2></li><li><h2>Graduate Degree level (e.g., MBA) or equivalent experience</h2></li><li><h2>Marketing competencies including insights, positioning, segmentation, consumer journey, competitive understanding, positioning, strategy, brief development, media/campaign planning and orchestration, measurement and optimization</h2></li><li><h2>Experience building consensus and influencing others, presenting to senior leadership, prioritization, and proactive risk management</h2></li></ul><h2></h2><h2>#LI-ViiV</h2><h2>#LI-GSK</h2>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit <a target="_blank" href="https://us.gsk.com/media/7963/ustrataglance-jobpostings.pdf">GSK US Benefits Summary</a><a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"> </a>to learn more about the comprehensive benefits program ViiV offers US employees. All ViiV employees receive the same benefits options and plans as GSK employee.</p><p></p><p><b>Why Us?</b></p><p>At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. </p><p></p><p>We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>GSK</u></span></a> and <a target="_blank" href="http://www.Pfizer.com"><span style="color:#0000ff"><u>Pfizer</u></span></a> in 2009, with <a target="_blank" href="http://www.Shionogi.com"><span style="color:#0000ff"><u>Shionogi</u></span></a> joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.</p><p></p><p>Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. </p><p></p><p>Having a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a></p><p></p><p>ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/viiv-healthcare-gsk-consumer-marketing-director-hiv-treatment-long-acting-injectable-gsk/6a0897572f1861929d25334b</link><guid isPermaLink="true">http://biotechroles.com/viiv-healthcare-gsk-consumer-marketing-director-hiv-treatment-long-acting-injectable-gsk/6a0897572f1861929d25334b</guid><pubDate>Sat, 16 May 2026 16:12:07 GMT</pubDate><company>GSK</company><location>Durham Blackwell Street</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Principal Scientist]]></title><description><![CDATA[<p>We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.</p><p></p><p>We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.</p><p></p><p>Discover more about our company wide benefits and life at GSK on our webpage <a href="https://www.gsk.com/en-gb/careers/life-at-gsk/" target="_blank">Life at GSK | GSK</a></p><p></p><p><b>Principal Scientist, Oncology Data Science</b></p><p>Are you passionate about leveraging cutting-edge computational approaches to revolutionize our understanding and treatment of cancer? If so, this is an exciting opportunity to join GSK&#39;s Oncology team and contribute to our mission of getting ahead of disease together.</p><p></p><p><b>Overview</b> </p><p>The GSK Oncology team is seeking a highly motivated computational biologist to play a pivotal role in shifting our understanding of cancer. While many models in oncology focus solely on predicting outcomes, we are dedicated to developing new approaches that understand disease not as static labels or endpoints, but as dynamic, evolving biological states.</p><p></p><p>By integrating (bulk, single cell and spatial) multi-omics and clinical data, you will characterize disease heterogeneity, model how disease changes over time and under treatment, and investigate how biological context influences treatment response and resistance. This work focuses on understanding, and ultimately shaping, disease trajectories in a biologically meaningful way, directly supporting GSK&#39;s ambitious goal to deliver transformative oncology therapeutics to patients. You will work at the interface of data, biology, and experimentation, tackling real questions in close collaboration with experimental and clinical teams, with the goal of making data-driven approaches more interpretable, robust, and actionable.</p><p></p><p><b>In this role you will</b></p><ul><li>Analyze and integrate complex multi-omics and clinical data to characterize disease heterogeneity and drive decision-making insights.</li><li>Develop and apply advanced models that capture disease states and their evolution, to predict and influence disease trajectories.</li><li>Investigate how biological context and underlying mechanisms influence treatment response and resistance.</li><li>Collaborate closely with experimental scientists to generate and test mechanistic hypotheses, translating complex data into actionable insights for drug discovery.</li><li>Contribute to the development of frameworks and computational tools that support better therapeutic decision-making and advance our oncology portfolio.</li><li>Communicate complex scientific findings clearly to both technical and non-technical audiences, acting as a subject matter expert within interdisciplinary teams.</li><li>Maintain current knowledge of advancements in cancer research, computational biology, and AI/ML methods.</li></ul><p><br /> </p><p><b><i>Why you?</i></b></p><p><b>Basic Qualifications &amp; Skills:</b></p><p><b>We are looking for professionals with these required skills to achieve our goals:</b></p><ul><li>PhD (or equivalent experience) with postdoc/industry experience in Computational Biology, Bioinformatics, Systems Biology, or a related field.</li><li>Strong understanding of biological mechanisms and disease processes, particularly within oncology.</li><li>Proven experience working with high-dimensional biological data.</li><li>Strong analytical and modeling skills, including expertise in statistical or machine learning approaches.</li><li>Experience in systems biology and/or network analysis.</li><li>Ability to work effectively in interdisciplinary and collaborative teams.</li><li>Proficiency in programming languages such as Python or R for data analysis and model development.  </li></ul><p></p><p><b>Preferred Qualifications &amp; Skills:</b></p><p><b>Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:</b></p><ul><li>Experience with spatial transcriptomics and/or proteomics analysis</li><li>Experience with multi-omics integration or trajectory inference methods.</li><li>Familiarity with advanced machine learning methods, including deep learning.</li><li>Experience working with perturbation or longitudinal data.</li><li>Highly independent, eager to learn new areas, and build expertise, with a sense of accountability.</li><li>Excellent written and oral communication skills, with the ability to present complex data to varied audiences.</li></ul><p><br /><br /> </p><p><b>Closing Date for Applications – (COB) 29/05/2026</b></p><p>#LI-GSK</p><p></p><p>Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.</p><p></p><p>At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&amp;D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting‑edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.</p><p></p><p>Find out more:</p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/principal-scientist-gsk/6a0897572f1861929d25334a</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-gsk/6a0897572f1861929d25334a</guid><pubDate>Sat, 16 May 2026 16:12:07 GMT</pubDate><company>GSK</company><location>UK - Hertfordshire - Stevenage</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Principal Scientist, Innovation ETCT]]></title><description><![CDATA[<p>We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.</p><p></p><p>We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.</p><p></p><p>Discover more about our company wide benefits and life at GSK on our webpage <a href="https://www.gsk.com/en-gb/careers/life-at-gsk/" target="_blank">Life at GSK | GSK</a></p><p></p><p><b>Principal </b><b>Scientist</b><b> (Gd7), Innovation ETCT</b></p><p></p><p>The Extracellular Targeted Cancer Therapeutics (ETCT) Biology Unit within the Oncology Research Unit is seeking an experienced <b><span>Principal Scientist </span></b>to contribute to internal initiatives designed to accelerate the build of a targeted biologics portfolio in Oncology.</p><p></p><p>The candidate will collaborate with an experienced team of scientists in using bioinformatic data for target ID/validation and interface with key internal/external business partners to accelerate next generation biologics asset development. The successful applicant will have prior experience managing cross-functional biologics matrix teams with oversight of critical path biology in the preclinical development of novel biologics for cancer therapy.</p><p></p><p><b>In this role you will</b></p><ul><li>Lead target discovery screening and early biologics programs, specifically antibody drug conjugates (ADCs) and T cell engaging bispecific antibodies (TCEs).</li><li>Collaborate with internal platform groups to deliver success on externally partnered programs and/or technologies.</li><li>Contribute to analyses of external technology to build next generation ADCs and TCEs.</li></ul><p><br /> </p><p><b><i>Why you?</i></b></p><p><b>Basic Qualifications &amp; Skills:</b></p><p><b>We are looking for professionals with these required skills to achieve our goals:</b></p><ul><li>PhD or equivalent experience in Cancer Biology, Pharmacology, Cellular Biology, or related life science fields</li><li>Experience in progressing cancer therapies from target ID to candidate selection and supporting critical path mechanistic biology and/or in vivo translational studies.</li><li>Experience executing target discovery/validation and experimental medicine development of biologics assets for cancer therapy.</li><li>Experience leading cross-functional drug discovery project teams.</li><li>Scientific experience leading hybrid internal/external collaboration teams</li></ul><p></p><p><b>Preferred Qualifications &amp; Skills:</b></p><p><b>Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:</b></p><ul><li>Pharmaceutical or biotechnology industry research and leadership experience in preclinical oncology biologics drug discovery.</li><li>Strong organizational and interpersonal skills and the ability to work independently.</li><li>Excellent communication and collaboration skills, with a proven track record of working effectively in a multidisciplinary environment.</li></ul><p><br /><br /> </p><p><b>Closing Date for Applications – (COB) 21/05/26</b></p><p>#LI-GSK</p><p></p><p>Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.</p><p></p><p>At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&amp;D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting‑edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.</p><p></p><p>Find out more:</p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/principal-scientist-innovation-etct-gsk/6a0897562f1861929d253349</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-innovation-etct-gsk/6a0897562f1861929d253349</guid><pubDate>Sat, 16 May 2026 16:12:06 GMT</pubDate><company>GSK</company><location>UK - Hertfordshire - Stevenage</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Vaccine Sales, 兒科疫苗  高屏區]]></title><description><![CDATA[<p>Business Introduction<br />GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.<br />Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.<br />Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.</p><p></p><p>Position Summary<br />You will be a trusted professional sales representative covering an assigned territory in Taiwan. You will develop strong, professional relationships with healthcare teams across hospitals, clinics and community settings. You will share clear, evidence-based scientific information and deliver territory plans that improve patient access. You will work closely with commercial, medical and operations colleagues. We value curiosity, integrity, collaboration and a growth mindset. This role offers learning, career growth and a chance to join GSK in uniting science, technology and talent to get ahead of disease together.<br /><br />Responsibilities<br />This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><ul><li>Build and maintain trusted relationships with healthcare professionals and clinic staff across your assigned territory.</li><li>Present accurate, evidence-based scientific information and provide clear educational support to healthcare teams.</li><li>Create and execute territory plans to meet sales and patient access objectives.</li><li>Use local market insights and data to prioritise customers and identify opportunities.</li><li>Collaborate with internal colleagues to plan and deliver customer-facing initiatives and local events.</li><li>Keep clear records of activities, follow-up actions and progress using CRM and reporting tools.</li></ul><p><br />Why You?<br />This role is on-site with regular travel across your assigned territory in Taiwan. You will join a supportive and inclusive team that invests in learning and development. You will have clear opportunities to take on increasing responsibility through coaching, practical experience and structured training. We welcome applicants from all backgrounds. If you want to grow your career and make a meaningful impact on patient care, please apply.<br /><br />Basic Qualification<br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li>achelor’s degree in life sciences, healthcare, business or a related field.</li><li>Minimum 2 years’ experience in pharmaceutical, medical or healthcare sales.</li><li>Strong verbal and written communication skills in Mandarin. Functional English for written materials and training.</li><li>Proven ability to build relationships and work independently in the field.</li><li>Valid Taiwan driver’s license and willingness to travel regularly across the territory.</li><li>Commitment to ethical conduct and a patient-focused approach.</li></ul><p><br />Preferred Qualification<br />If you have the following characteristics, it would be a plus:<br />- Experience working with hospitals, clinics or public health teams.<br />- Familiarity with Taiwan’s healthcare system and vaccination or preventive programmes.</p><ul><li>Proven track record of meeting or exceeding sales or access targets.</li><li>Comfortable using CRM systems and digital tools for planning and reporting.</li><li>Strong planning and analytical skills to turn customer insight into action.</li><li>Collaborative mindset and openness to continuous learning.</li></ul><p><br />How to apply<br />Ready to grow your career and make a real difference in healthcare? Please apply now. Tell us briefly about your experience and why this role matters to you. We look forward to hearing from you.</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact <a target="_blank" href="mailto:APACRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>APACRecruitment.Adjustments&#64;gsk.com</u></span></a>. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/vaccine-sales-gsk/6a0897552f1861929d253348</link><guid isPermaLink="true">http://biotechroles.com/vaccine-sales-gsk/6a0897552f1861929d253348</guid><pubDate>Sat, 16 May 2026 16:12:05 GMT</pubDate><company>GSK</company><location>Field Worker - TWN</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Analyst – Cyber Design Assurance & Product Management (DA&PM)]]></title><description><![CDATA[<p><b>Analyst – Cyber Design Assurance &amp; Product Management (DA&amp;PM)</b></p><p></p><p>The Design Assurance &amp; Product Management (DA&amp;PM) function supports the integration of cybersecurity into products, platforms, cloud services, and enterprise infrastructure throughout their lifecycle. DA&amp;PM contributes to technical design assurance, governance activities, product assurance, and security enablement initiatives to help ensure secure-by-design implementation across enterprise technologies.</p><p></p><p>This role works closely with architecture, engineering, cloud, infrastructure, identity, and product teams to support secure delivery, operational alignment, and continuous improvement of cybersecurity controls and practices.</p><p></p><p><b>Key Responsibilities</b></p><ul><li><p>Support the integration of secure design principles into product, platform, infrastructure, and cloud environments during planning, design, and implementation phases.</p></li><li><p>Support security design reviews, technical assessments, control validations, threat modelling activities, and architecture assurance exercises across enterprise technologies and platforms.</p></li><li><p>Contribute to governance activities including control assessments, standards alignment, exception tracking, and lifecycle assurance across security and technology platforms.</p></li><li><p>Assist in evaluating, onboarding, operationalizing, and reviewing cybersecurity tools across cloud, identity, application security, infrastructure, and data protection domains.</p></li><li><p>Work with engineering, platform, cloud, hosting, and cyber defence teams to support secure implementation, remediation planning, telemetry enablement, and operational alignment.</p></li><li><p>Support identification of security risks, control gaps, configuration issues, and exposure scenarios across enterprise systems, cloud environments, and platforms.</p></li><li><p>Assist in preparing dashboards, assessment summaries, risk metrics, usage insights, and reporting related to security controls, product assurance, and governance activities.</p></li><li><p>Help maintain security guidance, reusable assessment templates, design assurance checklists, and secure-by-default implementation standards.</p></li><li><p>Contribute to initiatives related to Zero Trust, cloud security, identity security, API security, DevSecOps, and enterprise security transformation programs.</p></li><li><p>Collaborate with product owners, architecture teams, engineering teams, operations teams, and vendors to support delivery of secure and scalable enterprise solutions.</p></li></ul><p></p><p><b>Minimum Qualifications</b></p><ul><li><p>Bachelor’s degree in Computer Science, Information Security, Engineering, or a related technical field.</p></li><li><p>2–5 years of experience in cybersecurity, cloud security, infrastructure security, application security, or security engineering functions.</p></li><li><p>Working knowledge of cloud platforms such as Microsoft Azure and Google Cloud Platform (GCP), including security controls, identity and access management, networking, monitoring, and cloud-native security principles.</p></li><li><p>Familiarity with cybersecurity concepts including IAM, network security, endpoint security, application security, vulnerability management, and data protection principles.</p></li><li><p>Understanding of security standards and frameworks (e.g., NIST CSF, CIS Benchmarks, OWASP, MITRE ATT&amp;CK, Zero Trust).</p></li><li><p>Experience supporting security assessments, governance activities, engineering functions, or operational security processes.</p></li></ul><p></p><p><b>Preferred Skills</b></p><ul><li><p>Familiarity with DevSecOps practices and integrating security into CI/CD pipelines.</p></li><li><p>Exposure to security technologies across the stack (e.g., CNAPP, CSPM, SIEM/SOAR, EDR/XDR, PAM/PIM, SAST/DAST, API Security, Data Classification/Labeling).</p></li><li><p>Basic scripting or automation knowledge (e.g., PowerShell, Python, Bash) is beneficial.</p></li><li><p>Strong analytical, troubleshooting, and problem-solving capabilities.</p></li><li><p>Good communication and stakeholder collaboration skills.</p></li><li><p>Ability to work in a fast-paced, federated environment supporting secure delivery and operational alignment.</p></li><li><p>Interest in modern cybersecurity practices aligned to Zero Trust, secure-by-design, cloud-native security, and enterprise transformation initiatives.</p></li></ul><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/analyst-cyber-design-assurance-and-product-management-daandpm-gsk/6a0897552f1861929d253347</link><guid isPermaLink="true">http://biotechroles.com/analyst-cyber-design-assurance-and-product-management-daandpm-gsk/6a0897552f1861929d253347</guid><pubDate>Sat, 16 May 2026 16:12:05 GMT</pubDate><company>GSK</company><location>Bengaluru Luxor North Tower</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Product Specialist (Specialty) - Ho Chi Minh]]></title><description><![CDATA[<p><b>Location: </b>Ho Chi Minh</p><p><br /><b>Role Purpose:</b></p><p>As a Product Specialist, you will serve as a deep specialty field partner for priority healthcare organizations (HCOs) and healthcare professionals (HCPs). Leveraging your scientific expertise, stakeholder engagement skills, and patient-centric communication, you will execute account and territory plans aligned with product launch objectives, ensuring disciplined and compliant field activities. Collaborate cross-functionally to support account activation and hospital-level initiatives that aim to improve real-world patient outcomes.</p><p><b>Key Responsibilities:</b></p><ul><li>Develop and implement territory and account plans with a patient-focused approach, prioritizing key accounts.</li><li>Build and maintain strong relationships with treatment-specialty HCO stakeholders and key HCPs.</li><li>Deliver high-quality scientific information with compelling data storytelling to aid patient identification and treatment decisions.</li><li>Engage in patient-focused conversations to address practice gaps and enhance treatment effectiveness.</li><li>Coordinate integrated communication plans across functions for consistent messaging and activity goals.</li><li>Support account-level activation initiatives in compliance with governance and controls.</li><li>Provide timely field insights and feedback to Marketing and Medical teams.</li><li>Uphold strict adherence to Vietnamese laws, GSK policies, and the GSK Code of Conduct.</li></ul><p><b>Requirements:</b></p><p><b>Qualifications and Experience:</b></p><ul><li>University/college degree.</li><li>Minimum of 3–5 years of field roles experience, particularly in specialty, biologics, or respiratory segments.</li><li>Proven expertise in territory/account management and stakeholder engagement.</li><li>Strong experience in compliant scientific selling to treatment-specialty/respiratory HCPs and HCOs.</li></ul><p><b>Skills and Attributes:</b></p><ul><li>Decision making and strategic agility.</li><li>Priority setting and problem-solving ability.</li><li>Strong communication, presentation, and teamwork skills.</li><li>Adaptability to work in complex, cross-functional environments.</li><li>Focus on patient needs and outcomes.</li><li>Coaching and development of potential in others.</li></ul><p></p><p>*Li-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact <a target="_blank" href="mailto:APACRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>APACRecruitment.Adjustments&#64;gsk.com</u></span></a>. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/product-specialist-specialty-ho-chi-minh-gsk/6a0897542f1861929d253346</link><guid isPermaLink="true">http://biotechroles.com/product-specialist-specialty-ho-chi-minh-gsk/6a0897542f1861929d253346</guid><pubDate>Sat, 16 May 2026 16:12:04 GMT</pubDate><company>GSK</company><location>Vietnam - Ho Chi Minh City</location><salary>$18000-30000</salary><type>Full time</type></item><item><title><![CDATA[Product Specialist (Specialty) - Hanoi]]></title><description><![CDATA[<p><b>Location: </b>Hanoi<br /><b>Role Purpose:</b></p><p>As a Product Specialist, you will serve as a deep specialty field partner for priority healthcare organizations (HCOs) and healthcare professionals (HCPs). Leveraging your scientific expertise, stakeholder engagement skills, and patient-centric communication, you will execute account and territory plans aligned with product launch objectives, ensuring disciplined and compliant field activities. Collaborate cross-functionally to support account activation and hospital-level initiatives that aim to improve real-world patient outcomes.</p><p><b>Key Responsibilities:</b></p><ul><li>Develop and implement territory and account plans with a patient-focused approach, prioritizing key accounts.</li><li>Build and maintain strong relationships with treatment-specialty HCO stakeholders and key HCPs.</li><li>Deliver high-quality scientific information with compelling data storytelling to aid patient identification and treatment decisions.</li><li>Engage in patient-focused conversations to address practice gaps and enhance treatment effectiveness.</li><li>Coordinate integrated communication plans across functions for consistent messaging and activity goals.</li><li>Support account-level activation initiatives in compliance with governance and controls.</li><li>Provide timely field insights and feedback to Marketing and Medical teams.</li><li>Uphold strict adherence to Vietnamese laws, GSK policies, and the GSK Code of Conduct.</li></ul><p><b>Requirements:</b></p><p><b>Qualifications and Experience:</b></p><ul><li>University/college degree.</li><li>Minimum of 3–5 years of field roles experience, particularly in specialty, biologics, or respiratory segments.</li><li>Proven expertise in territory/account management and stakeholder engagement.</li><li>Strong experience in compliant scientific selling to treatment-specialty/respiratory HCPs and HCOs.</li></ul><p><b>Skills and Attributes:</b></p><ul><li>Decision making and strategic agility.</li><li>Priority setting and problem-solving ability.</li><li>Strong communication, presentation, and teamwork skills.</li><li>Adaptability to work in complex, cross-functional environments.</li><li>Focus on patient needs and outcomes.</li><li>Coaching and development of potential in others.</li></ul><p></p><p>*Li-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact <a target="_blank" href="mailto:APACRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>APACRecruitment.Adjustments&#64;gsk.com</u></span></a>. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/product-specialist-specialty-hanoi-gsk/6a0897542f1861929d253345</link><guid isPermaLink="true">http://biotechroles.com/product-specialist-specialty-hanoi-gsk/6a0897542f1861929d253345</guid><pubDate>Sat, 16 May 2026 16:12:04 GMT</pubDate><company>GSK</company><location>Vietnam - North Provinces</location><salary>$18000-32000</salary><type>Full time</type></item><item><title><![CDATA[Therapeutics Lead - Specialty]]></title><description><![CDATA[<p><b>Location:</b> Ho Chi Minh</p><p><b>Role Purpose:</b></p><p>The Therapeutics Lead – Specialty will take on a multifaceted leadership role, combining strategic marketing expertise with national fieldforce team management to ensure success across GSK’s specialty portfolio. This position is responsible for driving product strategy, market access, promotional activities, and cross-functional fieldforce leadership to maximize commercialization and patient impact.</p><p><b>Key Responsibilities:</b></p><p><b>Strategic Marketing and Commercial Execution:</b></p><ul><li>Lead the launch and lifecycle management plans for specialty portfolios, tailored to Vietnam’s regulatory and market environment.</li><li>Conduct in-depth market analyses to define product value propositions for payers, HCPs, and patients.</li><li>Develop marketing strategies focused on optimizing patient journeys, enhancing diagnosis, treatment, and disease monitoring pathways to ensure impactful specialty product utilization.</li><li>Implement omnichannel promotional campaigns, designing compliant marketing materials and patient support programs.</li></ul><p><b>Fieldforce Team Management:</b></p><ul><li>Manage the nationwide specialty fieldforce team, ensuring alignment with marketing strategies and exceptional execution of account plans.</li><li>Train and mentor fieldforce teams on product science, value messaging, and access strategies.</li><li>Set performance goals, monitor KPIs, and drive consistent achievement of commercial and patient-related objectives across the fieldforce.</li><li>Develop and implement leadership and training programs to strengthen fieldforce capabilities.</li></ul><p><b>Stakeholder Engagement &amp; Cross-Functional Leadership:</b></p><ul><li>Establish strong relationships with key HCOs, HCPs, and external partners to further disease awareness and support patient access initiatives.</li><li>Collaborate with Medical, Regulatory, Supply Chain, Commercial, and regional/global teams to align strategies and share best practices.</li><li>Ensure successful account activation and support hospital-level initiatives.</li></ul><p><b>Compliance &amp; Governance:</b></p><ul><li>Oversee adherence to GSK policies, Vietnamese regulations, HTA, and reimbursement protocols across all activities.</li><li>Stay updated on evolving regulatory and market requirements for specialty medicines.</li></ul><p><b>Requirements:</b></p><p><b>Qualifications and Experience:</b></p><ul><li>Bachelor’s degree in Life Sciences, Pharmacy, or Medicine; Master’s degree preferred.</li><li>Minimum of 7 years of progressive experience in specialty product management and pharmaceutical fieldforce leadership roles.</li><li>Strong successes in managing specialty/rare disease product launches and fostering market-building capabilities in Vietnam.</li></ul><p><b>Skills and Attributes:</b></p><ul><li>Leadership and team coaching capabilities.</li><li>Strategic agility and decision-making skills.</li><li>Effective stakeholder management and cross-functional collaboration skills.</li><li>Strong analytical, problem-solving, and presentation skills.</li><li>A patient-centered approach to account and territory management.</li><li>Proven ability to deliver outstanding results with compliance.</li></ul><p></p><p>*Li-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact <a target="_blank" href="mailto:APACRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>APACRecruitment.Adjustments&#64;gsk.com</u></span></a>. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/therapeutics-lead-specialty-gsk/6a0897532f1861929d253344</link><guid isPermaLink="true">http://biotechroles.com/therapeutics-lead-specialty-gsk/6a0897532f1861929d253344</guid><pubDate>Sat, 16 May 2026 16:12:03 GMT</pubDate><company>GSK</company><location>Vietnam - Ho Chi Minh City</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Brand Manager]]></title><description><![CDATA[<p>We are ViiV Healthcare – the only pharmaceutical company focused on solely on HIV therapeutic area.</p><p>Our mission is to leave no patient behind. We are looking for a creative and driven <b>Brand Manager </b>who is passionate about bringing our innovative portfolio to the Dutch market. This role is one of the most impactful and rewarding positions at ViiV Netherlands and includes:</p><ul><li>Drive and inspire a cross functional team towards meeting the business objectives and being accountable for the team delivery</li></ul><ul><li>Challenge the status quo. Exploring &amp; testing new activities to be impactful in making HCPs understand the benefits of ViiV innovative portfolio</li><li>Translat and implement global strategy into a strong local execution plan, maximising the number of eligible people living with HIV (per SmPC) who can benefit from the ViiV portfolio.</li><li>Own the development and execution of the omnichannel customer experience strategy and drive continuous improvement in omnichannel customer experience, leveraging digital innovations to create seamless and impactful interactions.</li></ul><p></p><p><span class="emphasis"><b>Your responsibilities:</b></span></p><p><b>Accelerate the adoption of an established, innovative brand in a complex and evolving HIV treatment landscape, including:</b></p><ul><li>Identify and address barriers to uptake, translating insights into targeted strategies to drive sustainable growth</li><li>Adapt global campaigns and value propositions to local market dynamics, ensuring relevance and impact</li><li>Develop and execute marketing strategies that shift clinical practice and support behaviour change among healthcare professionals</li><li>Collaborate cross-functionally (Medical, Sales, Patient Affairs) to align on priorities and deliver a consistent and compelling customer experience</li><li>Lead the continuous optimisation of in-line brand plans based on performance data, customer feedback, and market insights</li><li>Drive the localisation and implementation of EU best practices, ensuring strong execution in the Dutch market</li></ul><p></p><p><b>Brand Performance Governance &amp; Representation</b></p><ul><li>Act as the single point of accountability for brand performance in monthly performance meetings, forecast or other internal meetings.</li><li>Represent the brand with a clear, consistent and data‑backed narrative, covering performance, drivers, risks, opportunities and proposed corrective actions.</li><li>Ensure alignment of brand assumptions across Marketing, Sales, Medical, and Finance prior to meetings.</li><li>Manage brand budgets with a strong focus on prioritisation, ensuring optimal allocation of resources to maximise impact while maintaining strict financial discipline</li></ul><p></p><p><b>Lead NL Portfolio Multichannel activities:</b></p><ul><li>Own the development and execution of the omnichannel customer experience strategy</li><li>Drive continuous improvement across customer journeys</li><li>Localise and adapt the Global and regional activities for the Dutch Market  </li><li>Facilitate input from other functions Patient Affairs, Medical, Commercial, Marketing to enrich the multichannel strategy</li><li>Implement innovative Digital projects in the Dutch Market (AI, Virtual reality ect)</li><li>Analyze customer journey data and feedback to optimize touchpoints and improve overall experience.</li></ul><p></p><p><span class="emphasis"><b>Why you?</b></span></p><p><span class="emphasis"><b>Basic Qualifications:</b></span></p><ul><li>Level of education: Master in Business, Medical, Pharmacy, Biology</li><li>Minimum of 4 to 5 Y of marketing experience in pharmaceutical marketing experience (specialty TA preferred, ideally HIV or Injectable Therapeutic area), Product launch experience, additional sales experience preferable</li><li>Dutch pharmaceutical market specifics understanding</li><li>Experienced in multichannel and shaping customer journey</li><li>Can do attitude, think out of the box mindset</li><li>Strong team player</li><li>Fluent in English, Dutch speaking</li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications</b>:</span></p><p>If you have the following characteristics, it would be a plus:</p><ul><li>Strong communication and influencing skills with the ability to work collaboratively with key opinion leaders</li><li>Strong project management skills with an ability to lead multiple projects with various stakeholders</li><li>Strong customer focus with an ability to develop, leverage customer insights and translate them into tactics</li><li>Strong commercial and digital acumen</li></ul><p></p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;Dutch Salary Range: EUR 67,050 to EUR 111,750 &amp;#xa;&amp;#xa;The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.&amp;#xa;&amp;#xa;In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process.&amp;#xa;&amp;#xa;This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.&amp;#xa;<p></p><p><b>Why Us?</b></p><p>At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. </p><p></p><p>We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>GSK</u></span></a> and <a target="_blank" href="http://www.Pfizer.com"><span style="color:#0000ff"><u>Pfizer</u></span></a> in 2009, with <a target="_blank" href="http://www.Shionogi.com"><span style="color:#0000ff"><u>Shionogi</u></span></a> joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.</p><p></p><p>Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. </p><p></p><p>Having a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.</p><p></p><p>ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law                                                                                                                                                                                                                                                                                                                                                       </p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:HR.AmericasSC-CS&#64;gsk.com"><span style="color:#0000ff"><u>HR.AmericasSC-CS&#64;gsk.com</u></span></a> where you can also request a call.                                                                                                                                                                               </p><p></p><p>Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the link <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/brand-manager-gsk/6a0897522f1861929d253343</link><guid isPermaLink="true">http://biotechroles.com/brand-manager-gsk/6a0897522f1861929d253343</guid><pubDate>Sat, 16 May 2026 16:12:02 GMT</pubDate><company>GSK</company><location>Netherlands - Amersfoort</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Demand Analyst]]></title><description><![CDATA[<p><span><span><b>Role Summary</b></span></span></p><p><span><span>You will support the Demand Forecasting team by providing accurate and reliable data to enable better decision-making. You will work closely with Demand Forecasting Managers, Commercial teams, and Data Owners to develop, maintain, and enhance dashboards, reports, and tools related to forecasting insights. We value curiosity, attention to detail, and a collaborative mindset. This role gives you strong growth opportunities, visible impact on planning outcomes, and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.</span></span></p><p></p><p><span><span><b>Key Responsibilities</b></span></span></p><ul><li><p><span><span>Assist in the preparation and production of Pre-DRM tools and reports to support the commercial cycle, working alongside with the guidance of Senior Analysts.</span></span></p></li><li><p><span><span>Support the collection, validation, and upload of forecast volumes in relevant systems, ensuring data is accurately published.</span></span></p></li><li><p><span><span>Monitor and ensure data accuracy by managing reports (e.g. history, sales, KPI validations, DQIT) in systems, and escalate issues when necessary.</span></span></p></li><li><p><span><span>Assist in managing databases and repositories for the IBP cycle, ensuring that all data is consistently updated, organized, and easily retrievable.</span></span></p></li><li><p><span><span>Coordinate with data owners to ensure data consistency is maintained across systems and reports.</span></span></p></li><li><p><span><span>Support the preparation of standard dashboards and slide decks for functional users, ensuring timely delivery for monthly Pre-DRM/DRM meetings; assist in their creation and ensure they are up to date for presentations.</span></span></p></li><li><p><span><span>Identify and escalate system and technical issues to ensure timely execution of IBP activities.</span></span></p></li></ul><p><span> </span></p><p><span><span><b>Education, Experience &amp; Skills</b></span></span></p><ul><li><p><span><span>Bachelor’s degree in supply chain, business, engineering, statistics, analytics or a related field.</span></span></p></li><li><p><span><span>1 to 3 years of hands-on experience in demand forecasting, planning, or analytical roles.</span></span></p></li><li><p><span><span>Experience working in pharmaceutical, healthcare, or FMCG planning environments.</span></span></p></li><li><p><span><span>Practical experience with forecasting systems, preferably SAP APO or OMP.</span></span></p></li><li><p><span><span>Strong Microsoft Excel skills and familiarity with data visualization tools such as Power BI.</span></span></p></li><li><p><span><span>Good numerical and analytical skills with high attention to detail.</span></span></p></li><li><p><span><span>Clear communication skills and ability to collaborate across functions.</span></span></p></li><li><p><span><span>Ability to present insights to stakeholders and drive follow-up actions.</span></span></p></li><li><p><span><span>A proactive mindset focused on continuous improvement and process documentation.</span></span></p></li></ul><p></p><p><span><span><b>Working Arrangement</b></span></span></p><p><span><span>This role is on-site in Pakistan. You will work alongside local cross-functional teams and interact with regional stakeholders as required.</span></span></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?<br />Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Contact information:</b><br />You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/demand-analyst-gsk/6a0897522f1861929d253342</link><guid isPermaLink="true">http://biotechroles.com/demand-analyst-gsk/6a0897522f1861929d253342</guid><pubDate>Sat, 16 May 2026 16:12:02 GMT</pubDate><company>GSK</company><location>Pakistan - Sindh - Karachi</location><salary>$12000-22000</salary><type>Full time</type></item><item><title><![CDATA[Manager - Access Across Speciality]]></title><description><![CDATA[<p><b>Purpose of the Role:</b></p><p>As the Access Manager – Oncology, you will be responsible for shaping and driving the access strategy for GSK’s oncology portfolio within India’s public healthcare system. The role focuses on ensuring timely, sustainable access to GSK’s oncology innovations through strong advocacy, policy influence, stakeholder engagement, and health system shaping.</p><p>You will serve as the access manager for oncology, working closely with internal cross-functional teams and external stakeholders including government bodies, payers, public hospitals, policy influencers, and patient advocacy groups.</p><p></p><p><b>Key Responsibilities:</b></p><p><b>1. Public Access &amp; Policy Advocacy</b></p><ul><li><p>Drive formulary inclusion of GSK oncology brands across central and state public institutions (CGHS, ESI, RSBY, state-specific schemes).</p></li><li><p>Advocate for inclusion of GSK oncology therapies in rate contracts and health benefit packages through collaboration with health authorities.</p></li><li><p>Partner with policymakers, public health experts, and institutional administrators to shape reimbursement and funding frameworks.</p></li><li><p>Lead initiatives to increase fund allocation by therapy area in the public segment by XX% from baseline.</p></li></ul><p></p><p><b>2. Stakeholder Engagement &amp; Ecosystem Shaping</b></p><ul><li><p>Build and maintain high-quality relationships with public health stakeholders (NHM, MoHFW, state DoHs, AIIMS, PM-JAY, etc.).</p></li><li><p>Engage Tier 1 &amp; 2 oncologists, hospital decision-makers, and payers to align on standard-of-care (SOC) protocols including GSK therapies.</p></li><li><p>Support development and implementation of health system initiatives targeting barriers along the oncology patient journey (diagnosis to treatment).</p></li><li><p>Engage and manage Patient Advocacy Groups (Oncology PAG’s)</p></li></ul><ul><li><p>Ensure reduced turnaround time (TAT) from prescription to patient access by XX% from baseline.( In reimbursement ecosystem)</p></li></ul><ul><li><p>Monitor and evaluate access outcomes including patient reach, speed to access, and affordability support effectiveness.</p></li></ul><p><b>4. Internal &amp; Cross-Functional Collaboration</b></p><ul><li><p>Collaborate with medical, regulatory, commercial, policy, and compliance teams to enable holistic access strategies.</p></li><li><p>Work with legal and compliance to ensure all engagements are fully aligned with GSK and local governance standards.</p></li><li><p>Drive internal education around healthcare access trends, public procurement policies, and advocacy best practices.</p></li></ul><p></p><p><b>Qualifications &amp; Experience:</b></p><p><b>Education:</b></p><ul><li><p>Graduate in Life Sciences, Pharmacy, or related field; MBA or master&#39;s in public health (MPH) preferred.</p></li></ul><p><b>Experience:</b></p><ul><li><p>6 to 8years of experience in Market Access, Government Affairs, or Public Policy in the pharmaceutical or healthcare sector.</p></li><li><p>Strong exposure to oncology therapy area (1-2 years) and public healthcare systems in India.</p></li><li><p>Demonstrated success in health policy engagement and driving public access outcomes.</p></li></ul><p><b>Key Competencies:</b></p><ul><li><p>Strategic thinking with ability to navigate complex healthcare environments.</p></li><li><p>Strong stakeholder management, negotiation, and influence skills.</p></li><li><p>High business and policy acumen; understanding of Indian public healthcare landscape.</p></li><li><p>Ability to work cross-functionally and operate in a matrixed organization.</p></li><li><p>Agile, self-driven, and purpose-led mindset.</p></li></ul><p><b>Culture &amp; Ways of Working:</b></p><ul><li><p>Embrace GSK’s values of patient focus, integrity, respect, and transparency.</p></li><li><p>Demonstrate agility, accountability, and a networked team approach.</p></li><li><p>Ensure full compliance with internal policies and external regulatory frameworks.</p></li></ul><div><div><div><p> </p></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/manager-access-across-speciality-gsk/6a0897512f1861929d253341</link><guid isPermaLink="true">http://biotechroles.com/manager-access-across-speciality-gsk/6a0897512f1861929d253341</guid><pubDate>Sat, 16 May 2026 16:12:01 GMT</pubDate><company>GSK</company><location>India - Karnataka - Bengaluru</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Praktikant/Werkstudent (m/w/d) Marketing ViiV]]></title><description><![CDATA[<h1><b>Für unseren Standort München suchen wir einen Praktikant / Werkstudent (m/w/d) Marketing ViiV.</b></h1><div><div><div><div><div><div><div><div><div><p></p><p>Während Deiner Tätigkeit erhältst Du einen umfangreichen Einblick in Marketing von ViiV Healthcare. ViiV Healthcare ist ein unabhängiges, globales Unternehmen, welches sich zu 100% auf HIV fokussiert hat.</p><p></p><p>Komm in unser Team als Praktikant/Werkstudent (m/w/d)! Es warten vielfältige Tätigkeiten auf Dich!</p><p></p><p><b>Deine Aufgaben</b>:</p><ul><li><p>Unterstützung des Marketing-Teams bei den innovativen Therapieoptionen für HIV Patient*innen </p></li><li><p>Unterstützung bei der Umsetzung von Multichannel-Marketing Maßnahmen (Print und Digital) </p></li><li><p>Unterstützung bei der Planung und Durchführung von Meetings und Kongressen</p></li></ul><p></p><p><b>Dein Profil</b>:</p><ul><li><p>Du bist immatrikulierter Student (m/w/d) der Wirtschaftswissenschaften oder BWL, idealerweise mit dem Schwerpunkt Marketing oder vergleichbar</p></li><li><p>Du verfügst über routinierten Umgang mit den gängigen MS-Office Programmen und bist digital affin</p></li><li><p>Du bringst einen hohen Grad an Selbstverantwortung und Eigeninitiative mit und bist selbstständig arbeitend</p></li><li><p>Du bist ambitioniert, kreativ und dynamisch</p></li><li><p>Du hast Spaß an Teamarbeit und bist bereit neue Herausforderung zu suchen</p></li><li><p>Du bist ein offener Mensch, der sich wohlfühlt im Umgang mit Personen aus betroffenen Communities, einschließlich der LGBTQIA&#43; Community</p></li><li><p>Du hast fließende Deutsch- und gute Englischkenntnisse</p></li></ul><p></p><p><b>Was wir bieten</b>: </p><ul><li><p>Attraktives Gehalt</p></li><li><p>Die Möglichkeit für deine persönliche und fachliche Entwicklung</p></li><li><p>Einblick hinter die Kulissen eines innovativen und internationalen Biopharma Großkonzerns</p></li><li><p>Ein familienfreundliches, modernes und inklusives Arbeitsumfeld </p></li><li><p>Flexibilität am Arbeitsplatz – ob vor Ort in unserem neuen, renovierten Büro direkt am Prinzregentenplatz oder von deinem Zuhause aus</p></li><li><p>Weitere attraktive Zusatzleistungen, z.B. um deine Mobilität zu fördern </p></li><li><p>Vielfältige Veranstaltungen für Inclusion, Health &amp; Wellbeing etc.</p></li><li><p>Teilnahme an Corporate Social Responsibility Events</p></li></ul><p></p><p><b>Eckdaten</b>:</p><ul><li><p>Startdatum: 01. April 2026</p></li><li><p>Dauer: mind. 6 Monate</p></li><li><p>Vollzeitpraktikum: 37.5 St./Woche</p></li><li><p>Werkstudententätigkeit: 20 St./Woche</p></li><li><p>Arbeiten im Hybridmodus</p></li></ul></div></div></div></div></div></div></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:DE.Contact-Recruitment&#64;gsk.com"><span style="color:#0000ff"><u>DE.Contact-Recruitment&#64;gsk.com</u></span></a> where you can also request a call.</p><p></p><p>Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to <span style="font-size:14px">ethnicity</span>, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/ </u></span></a></p>]]></description><link>http://biotechroles.com/praktikantwerkstudent-mwd-marketing-viiv-gsk/6a0897512f1861929d253340</link><guid isPermaLink="true">http://biotechroles.com/praktikantwerkstudent-mwd-marketing-viiv-gsk/6a0897512f1861929d253340</guid><pubDate>Sat, 16 May 2026 16:12:01 GMT</pubDate><company>GSK</company><location>Munich - Office</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Alternance en compliance pharmaceutique / réglementaire site H/F]]></title><description><![CDATA[<p>Le Laboratoire GSK recherche un(e) <b>Alternant </b>– <b>Compliance Pharmaceutique / Réglementaire H/F</b> pour son site de production basé à<b> </b><b>Mayenne (53</b>)<b>. </b></p><p></p><p><b>MISSION :</b></p><p>Au sein de l&#39;équipe Qualité Réglementaire, vous aurez pour principales missions:</p><ul><li><p>Evaluer les impacts règlementaires selon les guidelines réglementaires des principaux marchés.</p></li><li><p>Assurer le maintien des Dossiers d&#39;AMM :</p></li><li><p>Évaluer les changements afin de définir l&#39;impact réglementaire et proposer une stratégie réglementaire</p></li><li><p>Communiquer le changement aux Affaires réglementaires centrales (GRA)</p></li><li><p>Communiquer et coordonner l&#39;obtention des documents et données nécessaires pour constituer le dossier réglementaire.</p></li><li><p>Préparer et archiver les documents nécessaires à la constitution des dossiers réglementaires (MSR).</p></li><li><p>Assurer la veille réglementaire et la conformité réglementaire par rapport aux réglementations applicables selon les marchés.</p></li><li><p>Vérification dossier et analyse écarts pratiques/exigences réglementaires</p></li><li><p>Proposer et participer à des actions d’amélioration continue de son secteur</p></li></ul><p></p><p></p><p><b>VOTRE PROFIL :</b></p><ul><li><p>Diplôme préparé : Ingénieur / Pharmacien avec un master spécialisé réglementaire</p></li></ul><ul><li><p>Langue : Anglais lu et écrit (Toeic min 750)</p></li></ul><ul><li><p>Savoir-être : Rigueur, méthodologie et curiosité </p></li></ul><p></p><p></p><p><b>Ce poste vous correspond ? Alors, rejoignez-nous !</b></p><p></p><p><b>A propos du site de Mayenne : </b> </p><p>Le site de Mayenne est spécialisé dans la production d’antibiotiques formes orales sèches (comprimés, gélules, sachets, poudre pour suspensions buvables). Il emploie environ 400 collaborateurs. </p><p></p><p><b>A propos de GSK</b> : </p><p>  </p><p>GSK est une entreprise biopharmaceutique de premier plan en France, en termes de présence et d’emploi, avec plus de 3.400 collaborateurs répartis sur 3 sites de production (Evreux, Mayenne et Saint-Amand-les-Eaux) et au siège social (Rueil-Malmaison). </p><p></p><p>Notre mission est d’unir la Science, la Technologie et les Talents pour devancer ensemble la maladie. Nous prévenons et traitons les maladies grâce aux vaccins et médicaments de médecine générale et de spécialité. Nous concentrons nos efforts sur la science du système immunitaire, la génétique humaine et les technologies de pointe. Nous investissons dans quatre domaines thérapeutiques essentiels (maladies infectieuses, VIH, oncologie et immunologie/respiratoire) et saisissons toutes les opportunités futures qui peuvent avoir un impact sur la santé à grande échelle. Notre objectif est d’avoir un impact sur la vie de plus de 2.5 milliards de personnes.  </p><p>Nous recrutons des personnes qui croient en notre mission, incarnent notre culture et veulent nous aider à atteindre nos ambitions. Dans notre environnement de travail, chacun est valorisé, intégré, apprécié pour sa personnalité et ses différences. Nous favorisons également l’épanouissement de nos collaborateurs, avec des projets stimulants qui répondent aussi bien à leurs aspirations qu’aux besoins futurs de nos activités.  </p><p><b>GSK France est certifié Top Employer France 2025. </b><a href="https://www.top-employers.com/fr/certified-top-employers-search/?country&#61;FR&amp;page&#61;1" target="_blank"><u>Découvrez les Top Employers (top-employers.com)</u></a> </p><p></p><p></p><p>Pour en savoir plus vous pouvez consulter les ressources suivantes :  </p><p><a href="http://www.gsk.fr/" target="_blank"><u>www.GSK.fr</u></a> </p><p><a href="http://www.gsk.com/" target="_blank"><u>www.GSK.com</u></a> </p><p><a href="https://www.linkedin.com/company/glaxosmithkline/life/6aa6b03b-77c5-423a-bf74-cded1e8d9ffa/" target="_blank"><u>GSK: Life | LinkedIn</u></a>  </p><p><b>*LI-GSK</b> </p>&amp;#xa;&amp;#xa;This is a temporary internship/apprenticeship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process.&amp;#xa;&amp;#xa;Il s’agit d’une opportunité de stage/alternance temporaire axée sur le développement professionnel. Tout remboursement, bourse, indemnité ou soutien financier sera accordé conformément aux lois et réglementations locales applicables, ainsi qu’aux politiques du site GSK. Des informations plus détaillées seront fournies au cours du processus de recrutement.<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on <a target="_blank" href="mailto:Fr-diversity.recruitment&#64;gsk.com​"><span style="color:#0000ff"><u>Fr-diversity.recruitment&#64;gsk.com​</u></span></a></p><p></p><p>Please note should your enquiry not relate to adjustments; we will not be able to support you through these channels.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/alternance-en-compliance-pharmaceutique-reglementaire-site-hf-gsk/6a0897502f1861929d25333f</link><guid isPermaLink="true">http://biotechroles.com/alternance-en-compliance-pharmaceutique-reglementaire-site-hf-gsk/6a0897502f1861929d25333f</guid><pubDate>Sat, 16 May 2026 16:12:00 GMT</pubDate><company>GSK</company><location>France - Mayenne</location><salary>$25000-32000</salary><type>Full time</type></item><item><title><![CDATA[Key Account Manager - Oncology]]></title><description><![CDATA[<p>GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.<br />Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.<br />Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.</p><p></p><p></p><p>This role is an exciting opportunity to make a meaningful impact in oncology care in Israel. You will lead strategic engagement with healthcare professionals and institutions, ensuring patients have access to innovative treatments.</p><p>Please note that this is a field based role.<br /><br />Responsibilities:</p><p><br />- Build and maintain strong relationships with healthcare professionals, hospitals, and oncology centers.<br />- Develop and execute strategic account plans aligned with local healthcare dynamics.<br />- Provide scientific education and support to healthcare professionals, ensuring optimal treatment decisions.<br />- Collaborate with internal teams, including medical, marketing, and market access, to deliver seamless customer experiences.<br />- Analyze market trends, competitor activities, and customer feedback to inform strategies.<br />- Ensure all activities comply with ethical standards and local regulations.<br /><br />Basic Qualifications &amp; Skills:<br /><br />- Bachelor’s degree in Life Sciences, Pharmacy, or a related field.<br />- Minimum 2 years of experience in oncology or hematology sales.<br />- Strong communication and relationship-building skills.<br />- Proficiency in Hebrew and English.<br />- Ability to travel within the country as required.<br /><br />Preferred Qualifications &amp; Skills:</p><p><br />- Master’s degree in Life Sciences or Business.<br />- Experience in key account management or product launches.<br />- Familiarity with Israel’s healthcare system and oncology landscape.<br />- Proven ability to work collaboratively in cross-functional teams.<br />- Comfortable using digital tools and CRM systems.<br /><br /><b>#LI-Remote</b></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any specific adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on <a target="_blank" href="mailto:isr-inclusion.recruitment&#64;gsk.com"><span style="color:#0000ff"><u>isr-inclusion.recruitment&#64;gsk.com</u></span></a>.</p><p></p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/ </u></span></a></p>]]></description><link>http://biotechroles.com/key-account-manager-oncology-gsk/6a08974f2f1861929d25333e</link><guid isPermaLink="true">http://biotechroles.com/key-account-manager-oncology-gsk/6a08974f2f1861929d25333e</guid><pubDate>Sat, 16 May 2026 16:11:59 GMT</pubDate><company>GSK</company><location>Field Worker - ISR</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[OC Experience & Content Strategy Lead]]></title><description><![CDATA[<p>GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.</p><p></p><p><b>OC Experience and Content Strategy Lead</b><br /> </p><p>You will lead content and experience strategy for omnichannel customer journeys in Türkiye. You will shape and deliver clear, useful content that meets local healthcare professional needs and supports our commercial objectives. You will work with marketing, medical, compliance, analytics and agency partners. We value practical thinking, collaboration and measurable impact. This role offers growth, visible impact and a chance to help GSK unite science, technology and talent to get ahead of disease together.</p><p></p><p><b>Responsibilities:</b></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><p></p><p>- Define content strategy for omnichannel customer journeys, aligning content to local customer needs and brand goals.</p><p>- Create and manage content calendars, ensuring timely delivery and channel fit.</p><p>- Set and uphold content governance for tone, voice, format and compliance with legal and internal standards.</p><p>- Work across marketing, medical, analytics, sales and external agencies to brief, review and deliver content.</p><p>- Use content performance data to improve relevance, personalization and impact.</p><p>- Lead content audits and design reusable content architectures for multi-channel use</p><p>- Develop customer-first content suited to face-to-face, digital and hybrid channels.</p><p>- Translate brand plans into clear content briefs and build-ready assets.</p><p>- Prioritise and manage multiple content streams to meet launch and business needs.</p><p>- Ensure all content passes required quality checks, references and local approvals.</p><p>- Coordinate agencies and vendors to keep delivery on time and on budget.</p><p>- Provide clear reporting and insights on content performance and optimisation.</p><p></p><p><b>Why You?</b></p><p><b>Basic Qualification</b></p><p></p><p>We are seeking professionals with the following required skills and qualifications to help us achieve our goals</p><p>- Bachelor’s degree in Marketing, Communications, Advertising, Journalism, or related field.</p><p>- Minimum 3 years of experience in brand mnagement, content strategy, content management, digital marketing or related roles.</p><p>- Experience working with cross-functional teams and external agencies.</p><p>- Strong written and spoken Turkish and professional English.</p><p>- Familiarity with content management systems and standard office tools.</p><p></p><p><b>Preferred Qualification</b></p><p></p><p>If you have the following characteristics, it would be a plus</p><p>- Experience in healthcare, pharma or life sciences communications, Oncology – Hematology experience preferred.</p><p>- Hands-on experience with CRM or content platforms (for example Promomats).</p><p>- Experience with marketing automation or email platforms (for example SFMC).</p><p>- Training or certification in digital or content marketing.</p><p>- Design awareness or basic skills with tools such as Canva, Photoshop or Illustrator.</p><p></p><p>Working Model</p><p>This position is hybrid. You will be based in Türkiye with a mix of on-site and remote work as agreed with the hiring manager.</p><p></p><p>What we value in you</p><p>- Clear, concise writing with strong attention to detail.</p><p>- A collaborative approach that brings people together.</p><p>- Practical decision-making and a focus on outcomes.</p><p>- Curiosity and a willingness to test and learn.</p><p>- Respect for compliance and ethical standards.</p><p>- A commitment to inclusion and creating spaces where colleagues can do their best work.</p><p></p><p>We want to hear from you.</p><p>If this role matches your skills and ambitions, please apply. Tell us how you would shape content to improve customer experience in Türkiye and the impact you would aim to deliver. #LI-Remote</p><p></p><p><b>Why GSK?</b></p><p></p><p>You will join a team focused on patient outcomes and scientific excellence. You will have development opportunities and access to global expertise. You will work in a supportive environment that values inclusion, respect and open feedback. If you are ready to use your clinical knowledge and relationship skills to make a difference, please apply today. We welcome applicants from all backgrounds.</p><p></p><p>What we offer</p><p>You will join an organisation that aims to make a real difference to patients. We invest in learning and development to help you grow. You will work with people who value inclusion and diverse perspectives. If you want to build a meaningful career in oncology and help shape better outcomes for patients, we encourage you to apply.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. #LI-Remote</p><p><br /> </p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at <a target="_blank" href="mailto:tr.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>tr.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p>Please note should your enquiry not relate to adjustments; we will not be able to support you through these channels</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/ </u></span></a></p>]]></description><link>http://biotechroles.com/oc-experience-and-content-strategy-lead-gsk/6a08974f2f1861929d25333d</link><guid isPermaLink="true">http://biotechroles.com/oc-experience-and-content-strategy-lead-gsk/6a08974f2f1861929d25333d</guid><pubDate>Sat, 16 May 2026 16:11:59 GMT</pubDate><company>GSK</company><location>Istanbul River Plaza</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Molecule Steward]]></title><description><![CDATA[<p><br /> </p><h1><span class="emphasis"><b>Molecule Steward</b></span><br /><br /> </h1><p><span class="emphasis"><b>Business Introduction</b></span><br /><br />We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.<br /><br /><br /><br /><span class="emphasis"><b>Position Summary</b></span><br /><br />This is a truly exciting opportunity for an experienced scientific professional to take end-to-end technical accountability for a given product, from bulk API manufacturing, formulation, packing and related support activities, providing strategic technical leadership to ensure successful new product introduction, quality robustness and productivity improvements across the lifecycle. </p><p>The Molecule Steward is aligned to a new asset at Commit to Commercial Development with responsibility for representing MSAT in the development of the Product Control Strategy.  When the product transfers to GSC accountability, the Molecule Steward co-ordinates Drug Substance, Drug Product, Analytical Strategy and if appropriate Device Leads to maintain the Product Control Strategy and ensure the product is maintained in the desired state of control throughout product lifecycle.</p><p>You will be responsible for developing and delivering the technical elements of the Global Supply Chain strategy with the GSC Strategy Lead and will be a recognised GSC expert in the given product or dose form.  In addition to strategic technical leadership, the role will be expected to provide deep technical expertise where required to ensure highest levels of quality and robustness.</p><p></p><p></p><h2><span class="emphasis"><b>Responsibilities</b></span></h2><p></p><ul><li><p>Representing MSAT as technical single-point accountable decision maker to CMC Matrix and Medicine Supply Chain teams, ensuring that a product control strategy is defined and maintained to drive a robust product that meets target manufacturability criteria.</p></li><li><p>Responsible for defining the End-to-End Product Performance Qualification and Ongoing Continuous Verification Strategy for the product, including trending and sampling plans and ensuring alignment and consistency across supply nodes.  </p></li><li><p>Maintaining accountability for the product, from transfer from R&amp;D throughout its lifecycle, ensuring improvement plans (including 2nd generation processes) are developed and delivered impacting the manufacturing process, analytical process, pack, device, and associated specifications to deliver value.  </p></li><li><p>Maintaining solid knowledge and understanding of complex scientific subject matter as well as evolving regulatory policies and guidelines and industry best practices.  This knowledge is used in developing improvement plans for the products.</p></li><li><p>Accountable from an MSAT perspective for defining technology strategy &amp; specific solutions as required to support the overall product or dose form lifecycle. </p></li><li><p>Responsible for leading Product Technical Lifecycle Teams, ensuring risks are identified and mitigated and technical issues are resolved in a timely manner.   </p></li><li><p>Responsible for co-ordinating the review of regulatory submissions and responses to technical questions within MSAT, ensuring review by appropriate SMEs and sites.  </p></li><li><p>Providing leadership and subject matter expertise where required for investigations and/or critical deviations, troubleshooting, and major change programmes. </p></li><li><p>Ensuring that product history and knowledge from development through lifecycle is maintained and aligns with knowledge management standards for the product or dose form within the GSC network. </p></li><li><p>Managing strong collaborations with technical staff across the Supply Chain sites, MSAT &amp; R&amp;D, with effective and clear communication on highly technical topics.  Must be able to lead and operate in an environment with high degree of change and uncertainty.</p></li></ul><p></p><p></p><h2><span class="emphasis"><b>Qualifications/Skills</b></span></h2><h2><span class="emphasis"><b>Basic Qualifications:</b></span></h2><p></p><ul><li><p>University Degree (minimum) in Chemistry, Chemical engineering, Pharmaceutical Sciences or similar area</p></li><li><p>Extensive years’ experience in pharmaceutical development and/or manufacturing, ideally in small molecule modality</p></li><li><p>Comprehensive knowledge of external regulatory requirements (MHRA, FDA), and internal/external quality and safety requirements</p></li><li><p>Experienced in technology transfer, with an understanding of the product development process</p></li><li><p>Knowledge of current and emerging Regulatory Strategies (Quality by Design, GMP for 21st century, ICH Q7, Q8, Q9, Q10) and Product Lifecycle Management</p></li><li><p>Demonstrated experience in the pharmaceutical industry in leading the technical aspects of Product Lifecycle Management, including supporting process investigations.</p></li></ul><p></p><p></p><h2><span class="emphasis"><b>Preferred Qualifications:</b></span></h2><p></p><ul><li><p>Project management and prioritization skills gained within a complex matrix</p></li><li><p>Excellent problem solver and ability to think and work creatively</p></li><li><p>Strong technical acumen and communication skills with the ability to articulate complex, technical details to stakeholders and enable cross functional collaboration across sites, supply chain, R&amp;D and suppliers</p></li><li><p>Experience managing external partners/CDMO’s in NPI and/or commercial supply</p></li><li><p>Ability to effectively influence stakeholders at all levels</p></li></ul><p></p><p></p><p><span class="emphasis"><b>Work Location:</b></span><br /><br />This role can be based in Ware, Worthing, Barnard Castle, UK or Upper Merion or Durham, USA  and offers a hybrid working model, combining on-site and remote work.</p><p></p><p></p><p><span class="emphasis"><b>Closing Date for Applications:</b></span> 29th May 2026</p><p></p><p></p><p>Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.</p><p></p><p></p><p>#Li-Hybrid</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/molecule-steward-gsk/6a08974d2f1861929d25333c</link><guid isPermaLink="true">http://biotechroles.com/molecule-steward-gsk/6a08974d2f1861929d25333c</guid><pubDate>Sat, 16 May 2026 16:11:57 GMT</pubDate><company>GSK</company><location>Ware</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[xCEL Trainee]]></title><description><![CDATA[Business Introduction
GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.<br>Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.<br>Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.


Position Summary
You will support and lead daily operational activities that keep our team focused and effective. You will work closely with senior managers and colleagues across functions and locations in India. We value people who are curious, dependable, and open to learning. This role offers clear growth paths, skill development, and a chance to make a measurable impact while helping GSK unite science, technology and talent to get ahead of disease together.

Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Translate objectives set with senior managers into clear daily plans and priorities.
- Create and maintain monitoring dashboards to track team workload, performance and service commitments.
- Communicate proactively with senior managers and follow up on meeting actions and decisions.
- Lead, coach and mentor team members to build capability, engagement and consistent service delivery.
- Manage routine operational tasks such as schedules, resources, equipment issues and material needs.
- Track and report compliance, completeness and timeliness of projects and customer requests.

Why You?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals
- Bachelor’s degree in administration, business, or a related field, or equivalent experience.
- Minimum 3 years of relevant experience in administration, operations, or team coordination.
- Strong written and verbal communication skills in English.
- Comfortable using common office software and creating dashboards (for example spreadsheets and presentation tools).
- Demonstrated ability to organise work, manage time and meet deadlines.
- This role is on-site in India and requires regular collaboration with local and regional teams.

Preferred Qualification
If you have the following characteristics, it would be a plus
- Postgraduate qualification in administration, business management or a related subject.
- Experience leading or developing a small team.
- Experience in customer service, stakeholder management or client-facing roles.
- Familiarity with process improvement or change initiatives.
- Basic understanding of resource planning and workforce scheduling.
- A proactive, solution-focused mindset and commitment to continuous learning.

Work Arrangement
This role is on-site in India. You will work from a GSK location and collaborate daily with colleagues and leaders.

What we value
We welcome people from different backgrounds and life experiences. We believe inclusion makes our teams stronger. We look for candidates who are respectful, curious, and committed to delivering high quality work. If you want to grow your skills, help others succeed, and contribute to meaningful work, we encourage you to apply.

How to apply
Ready to grow with us? Please submit your application and a short note about why this role matters to you. We look forward to learning how you can contribute.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/xcel-trainee-gsk/6a08974c2f1861929d25333b</link><guid isPermaLink="true">http://biotechroles.com/xcel-trainee-gsk/6a08974c2f1861929d25333b</guid><pubDate>Sat, 16 May 2026 16:11:56 GMT</pubDate><company>GSK</company><location>India - Maharashtra - Worli Mumbai</location><salary>$12000-18000</salary><type>Full time</type></item><item><title><![CDATA[Channel Deployment Specialist / Key Account Specialist (Rx)]]></title><description><![CDATA[<div><div><p></p><p></p><p></p><p>At GSK, millions of people rely on our prescription medicines every day. As a <b>Channel Deployment Specialist / Key Account Specialist (Rx)</b>, you will be responsible for <b>operational deployment and execution of commercial and distribution strategies for prescription medicines</b>, working closely with pharmacy chains and pharmaceutical wholesalers.</p><p></p><p>This role focuses on <b>ensuring appropriate product availability, continuity of supply and effective execution of agreed commercial terms</b>, in line with internal policies, compliance standards and applicable regulations.</p><p></p><p>The position is fully dedicated to <b>Rx products</b> and plays an important role in supporting patient access across Poland.</p><p></p><p></p><p><b>Key Responsibilities</b></p><p><b>Rx Channel &amp; Distribution Execution</b></p><ul><li><p>Support the <b>implementation of commercial and distribution activities for prescription medicines</b> in cooperation with pharmacy chains and pharmaceutical wholesalers.</p></li><li><p>Monitor <b>product availability, numeric distribution and continuity of Rx supply</b> to support reliable patient access.</p></li><li><p>Identify execution gaps, risks or deviations and escalate them in line with internal processes.</p></li></ul><p></p><p><b>Key Customer Cooperation (Operational Level)</b></p><ul><li><p>Maintain day-to-day cooperation with assigned pharmacy chains and wholesalers.</p></li><li><p>Support the execution of <b>commercial agreements, offers and contractual conditions</b>.</p></li><li><p>Prepare analyses, data and materials supporting commercial discussions led by senior stakeholders / Channel Deployment Managers (KAMs)</p></li></ul><p></p><p><b>Analysis &amp; Reporting</b></p><ul><li><p>Work with <b>GSK systems and analytical tools</b> to monitor:</p><ul><li><p>availability and distribution,</p></li><li><p>execution of commercial conditions,</p></li><li><p>sales and performance indicators.</p></li></ul></li><li><p>Prepare reports, dashboards and insights supporting business decision-making.</p></li></ul><p></p><p><b>Cross-Functional Collaboration</b></p><ul><li><p>Cooperate closely with <b>Marketing, Finance, Legal &amp; Compliance, Supply Chain and Customer Service</b> teams.</p></li><li><p>Support preparation and implementation of <b>commercial offers and contractual documentation</b> in line with internal standards.</p></li><li><p>Participate in selected <b>trade, channel execution and customer-focused initiatives</b>.</p></li></ul><p></p><p><b>Why You?</b></p><p><b>Basic Qualifications</b></p><ul><li><p><b>1/2 years of experience</b> in a commercial or customer facing role (Rx, OTC or food supplements).</p></li><li><p>Experience working with <b>pharmacies,</b> <b>pharmacy chains, buying groups and/or pharmaceutical wholesalers</b>.</p></li><li><p>Bachelor degree</p></li><li><p>Understanding of <b>pharmacy channel dynamics and distribution mechanisms</b>.</p></li><li><p>Strong analytical skills and ability to work with data.</p></li><li><p>Good organization, independence and ownership of tasks.</p></li><li><p>Strong interpersonal and communication skills.</p></li><li><p>Proficiency in <b>MS Office tools</b> (especially Excel and PowerPoint).</p></li><li><p>Driving license (category B) and readiness for business travel across Poland.</p></li><li><p>Fluent Polish speaker.</p></li></ul><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>Communicative level of English (spoken and written).</p></li><li><p>Experience in using <b>analytical, CRM, BI or advanced digital tools</b> (including AI-based solutions).</p></li><li><p>Bachelor’s degree in Sales, Marketing, Economics or a related field.</p></li></ul><p></p><p></p><p><b>Why GSK?</b></p></div><ul><li><p>Career at one of the leading global healthcare companies</p></li><li><p>Field based role.</p></li><li><p>Contract of employment</p></li><li><p>Attractive reward package (annual bonus &amp; awards for outstanding performance, recognition awards for additional achievements and engagement, holiday benefit)</p></li><li><p>Life insurance and pension plan</p></li><li><p>Private medical package with additional preventive healthcare services for employees and their eligible</p></li><li><p>Sports cards (Multisport)</p></li><li><p>Possibilities of development within the role and company’s structure</p></li><li><p>Personalized learning approach (internal trainings, mentoring, access to online training’ platforms: Keep Growing Campus, LinkedIn Learning, Business Skills, Harvard Manage Mentor, Skillsoft and external training)</p></li><li><p>Extensive support of work life balance (flexible working solutions, health &amp; well-being activities). </p></li><li><p>Supportive community and integration events</p></li></ul><p></p><p></p><p></p><p>#LI-GSK</p><p>#LI-REMOTE</p><p></p></div><p></p>&amp;#xa;The annual base salary in Poland for new hires in this position ranges from PLN 126,000 to PLN 210,000 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.   Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion).   All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave &amp; care of family member leave.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at <a target="_blank" href="mailto:pl.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>pl.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.    <b>                                                                                                                                                                                </b></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/channel-deployment-specialist-key-account-specialist-rx-gsk/6a08974c2f1861929d25333a</link><guid isPermaLink="true">http://biotechroles.com/channel-deployment-specialist-key-account-specialist-rx-gsk/6a08974c2f1861929d25333a</guid><pubDate>Sat, 16 May 2026 16:11:56 GMT</pubDate><company>GSK</company><location>Field Worker - POL</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Project Manager (EM-DS - External Manufacturing-Drug Substance)]]></title><description><![CDATA[<p></p><p><b>Job Purpose:</b></p><p>The External Manufacturing-Drug Substance (EM-DS) Project Manager is accountable for providing project leadership for Product Technical Transfers to external Contract Manufacturing Organization (CMO) Partners. These Technical Transfer (TT) projects can be from both internal and external donor sites and are delivered by a cross-functional PQTS&#43; Team (Procurement, Quality, Technical, Supply &#43; team) managed by the Project Manager (in partnership with the CMO).</p><p></p><p>The Project Manager acts as the main point of contact between GSK and the supplier to drive technology transfer activities (including mitigating risks and resolving issues).  The Project Manager leverages relationships with the supplier(s) to accomplish accelerated project timelines and delivery within budget.  This includes effective communication with GSK Senior Management and managing escalations for project(s).</p><p></p><p>The Project Manager will manage a cross-functional PQTS&#43; team and will be the interface between internal and external product schedules to drive a single schedule and manage critical path(s) to ensure technical transfer deliverables are met. Projects are sponsored by the Supply Director or NPI director (either of which the PM reports into to)</p><p></p><p><b>Key Responsibilities (include..,):</b></p><ul><li><p>Ownership (developing and delivering) of overarching project schedule that maintains critical path on the governed delivery dates and within budget.</p></li><li><p>Responsible for project management for two Tech Transfers, suppliers and/or assets/molecules.</p></li><li><p>Proactive risk identification and mitigation of issues that may delay critical path delivery.</p></li><li><p>Clearly articulate any issues or misalignments with the supplier / delivery plan and work with the relationship manager and/or Supply Director to mitigate with the supplier.</p></li><li><p>Build a strong relationship with project team members across the PQTS&#43; and external suppliers based on trust and collaboration.</p></li><li><p>Establish project organizational structure and maintain governance throughout the technology transfer.</p></li><li><p>Key point of contact for program milestones and escalation communication through established governance, across various management levels, as well as reporting of KPIs.</p></li><li><p>Key interface between the Quality and MSAT (Manufacturing Science and Technology) organizations within GSK and the suppliers to ensure the timely execution of all technology transfer deliverables.</p></li><li><p>Efficient and effective project management, including appropriate and timely escalation of project priorities, risks and issues to ensure project delivery.</p></li><li><p>Identifies and drives continuous improvement on project delivery with the assigned CMO(s) or asset(s) with internal and external stakeholders.</p></li><li><p>Ensure manufacturing know-how, relationship history and other technical knowledge is retained for future supply.</p></li></ul><p></p><p><b>Location:</b>  You can be based at any GSK manufacturing site in the UK (Ware, Barnard Castle, Worthing, Irvine or Montrose), or at GSK HQ (London, UK), or at the Upper Merion or Zebulon sites (USA).<br /> </p><p><b>Travel: </b> The successful applicant may need to travel as part of the delivery of their role to any of the sites in the network.  We anticipate that travel will be a maximum of 10% of their time.</p><p></p><p></p><p><b>CLOSING DATE for applications:  Friday 29th of May 2026 (COB).</b></p><p></p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Degree (or international equivalent) in Business, Supply Chain, Technical, Procurement, Biotechnology or Biologics related field, Engineering, Logistics, Finance or Quality.</p></li><li><p>Experience in Pharmaceutical Industry with a GMP background.</p></li><li><p>Experience in project management at an internal or external facility.</p></li><li><p>Experience in management of project governance and escalation processes including senior stakeholder communication and reporting</p></li><li><p>Experience in delivery of strategic business projects with associated responsibility for risk/issue, timeline and budget management – ideally of a Product Technical Transfer</p></li><li><p>Experience in product operational technologies as required by the supplier and product.</p></li><li><p>Experience in managing globally dispersed virtual matrix teams.</p></li><li><p>Experience in risk management and mitigation</p></li><li><p>Experienced in end-to-end Supply Chain Management and financial acumen</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>BS Degree or higher with PRINCE2 or PMP certification.</p></li><li><p>Proficiency in Microsoft Project online and Microsoft Power BI</p></li><li><p>Operational experience in: Drug substance supply chains and implementation of transfers and new product introduction &amp; launch.</p></li><li><p>Experience preparing and delivering presentations and negotiating agreements.</p></li><li><p>Ability to effectively facilitate both large and small groups in virtual environment.</p></li></ul><p></p><p>If you would like to learn more about our company wide benefits and life at GSK we would suggest looking at our webpage <a href="https://www.gsk.com/en-gb/careers/life-at-gsk/" target="_blank">Life at GSK | GSK</a>.</p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/project-manager-em-ds-external-manufacturing-drug-substance-gsk/6a08974b2f1861929d253339</link><guid isPermaLink="true">http://biotechroles.com/project-manager-em-ds-external-manufacturing-drug-substance-gsk/6a08974b2f1861929d253339</guid><pubDate>Sat, 16 May 2026 16:11:55 GMT</pubDate><company>GSK</company><location>UK - Hertfordshire - Ware</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Contracts Management Specialist  with German, Italian, French, Portuguese or Spanish language]]></title><description><![CDATA[<p></p><p></p><p></p><p>The Global Delivery Centre provides the critical Source to Contract and Contracts Management capability for GSK. Leading the delivery of a high volume of sourcing and contracting projects globally, the centre acts as the operational engine of the Procurement Organisation. As such, the GDC will play a critical role in delivering both the in-year savings and the functions long term operating model.</p><p>Are you passionate about contracts and enjoy working in a collaborative environment?</p><p>As a Contracts Specialist, you’ll play a key role in supporting our contracting processes. You’ll work closely with internal teams and external partners to ensure contracts are negotiated, executed, and managed effectively. We value candidates who are detail-oriented, proactive, and eager to contribute to a dynamic team. This role offers the opportunity to grow your skills and make a meaningful impact in a global organization.</p><p><br /><b> Key Responsibilities:</b></p><ul><li><p>Draft, negotiate, and execute contracts in line with defined procurement strategies and business requirements.</p></li><li><p>Apply basic legal principles and make system updates to support contract reporting.</p></li><li><p>Support metric reporting and system updates as required.</p></li><li><p>Build relationships and ensure effective communication with GSK stakeholders to understand business requirements, support non- standard workflow requests.</p></li><li><p>Provide metrics and reporting to track contract performance and identify areas for improvement.</p></li></ul><p></p><p><b>Why you?</b></p><p><b>Qualifications:</b></p><ul><li><p>University Degree (Law, Business, Finance, Sciences a related field).</p></li><li><p>Minimum 2- 3 years of Procurement and Contracts Management experience.</p></li><li><p>Full proficiency in English and German, Italian, French, Portuguese or Spanish language.</p></li><li><p>Strong attention to detail and organizational skills.</p></li><li><p>Problem solving skills and ability in navigating through organizational complexity, collaborating simultaneously with multiple teams.</p></li><li><p>Experience in using Procurment tools like Ariba or other equivalent CLM technology.</p></li></ul><p></p><p><b>Working model</b><br />This role is hybrid. You will be expected to work from our Poland office regularly and be available for in-person collaboration.</p><p></p><p><b>Why GSK?</b></p><ul><li><p>Career at one of the leading global healthcare companies.</p></li><li><p>Attractive reward package (annual bonus &amp; awards for outstanding performance, recognition awards for additional achievements and engagement, holiday benefit).</p></li><li><p>Life insurance and pension plan.</p></li><li><p>Private medical package with additional preventive healthcare services for employees and their eligible counterparts.</p></li><li><p>Sports cards (Multisport).</p></li><li><p>Possibilities of development within the role and company’s structure.</p></li><li><p>Personalized learning approach (mentoring, online training’ platforms: Pluralsight, Business Skills, Harvard Manage Mentor, Skillsoft and external training).</p></li><li><p>Extensive support of work life balance (flexible working solutions, short Fridays option, health &amp; well-being activities).</p></li><li><p>Supportive community and integration events.</p></li><li><p>Modern office with creative rooms, fresh fruits everyday.</p></li><li><p>Free car and bike parking, locker rooms and showers.</p></li></ul><p></p><p>#LI-GSK #LI-Hybrid</p><p></p>&amp;#xa;The annual base salary in Poland for new hires in this position ranges from PLN 110,250 to PLN 183,750 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.   Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion).   All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave &amp; care of family member leave.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at <a target="_blank" href="mailto:pl.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>pl.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.    <b>                                                                                                                                                                                </b></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/contracts-management-specialist-with-german-italian-french-portuguese-or-spanish-language-gsk/6a08974b2f1861929d253338</link><guid isPermaLink="true">http://biotechroles.com/contracts-management-specialist-with-german-italian-french-portuguese-or-spanish-language-gsk/6a08974b2f1861929d253338</guid><pubDate>Sat, 16 May 2026 16:11:55 GMT</pubDate><company>GSK</company><location>Warsaw</location><salary>$35000-50000</salary><type>Full time</type></item><item><title><![CDATA[Engineering Technician]]></title><description><![CDATA[<p></p><p>At GSK’s Barnard Castle site, we are looking to recruit an Engineering Technician to join our team.</p><p></p><p>GSK Barnard Castle is a key secondary manufacturing site and has invested heavily in industry 4.0 state of the art, bespoke equipment to support sustained new product introductions and volume increases, and as a key supplier of some of GSK’s blockbuster products, the site contributes revenues of ~$2Bn annually.</p><p></p><p>The engineering team provide technical expertise to support the manufacturing systems for all production operations across the Barnard Castle site.</p><p></p><p><b>Job Purpose:</b></p><p>Engineering Technicians provide comprehensive and professional engineering support service for the Steriles Business Unit (SBU) to meet business and regulatory needs.  You be responsible for engineering activities associated with the production process (operating across Inspect, Assembly, and Packaging operations) for syringes and vials.<br /> </p><p><b>Key responsibilities (include.,):</b></p><p>Equipment Maintenance &amp; Reliability</p><ul><li><p>Support day-to-day breakdown repairs of production and plant equipment.</p></li><li><p>Complete Planned Preventative Maintenance (PPM) schedules and breakdown maintenance activities.</p></li><li><p>Perform calibration of equipment instrumentation.</p></li><li><p>Lead equipment upgrades and manage equipment obsolescence through continuous improvement initiatives.</p></li></ul><p></p><p>GMP, Quality &amp; Safety</p><ul><li><p>Prepare, complete, and take ownership of GMP safety and quality documentation.</p></li><li><p>Maintain compliance with role, departmental, and site procedures, processes, and systems.</p></li><li><p>Supervise internal and external contractors, ensuring GMP standards are upheld and contract company details are reviewed for accuracy.</p></li><li><p>Positively engage with stakeholders to ensure relevant contract details remain accurate.</p></li></ul><p></p><p>Engineering Change &amp; Project Support</p><ul><li><p>Complete tasks within Engineering Change Controls.</p></li><li><p>Support localised area projects, including new product introduction activities.</p></li></ul><p></p><p>SAP / MERPS &amp; Data Management</p><ul><li><p>Accountable for the delivery of SAP/MERPS activities including Work Orders, Notifications, Data Maintenance, and ordering of plant spares.</p></li><li><p>Deliver data cleansing activities to ensure optimum data maintenance standards.</p></li><li><p>Manage data creations and changes to SAP vendor data.</p></li></ul><p></p><p>Continuous Improvement &amp; Performance</p><ul><li><p>Drive Continuous Improvement to increase performance in line with EHS and Quality improvement objectives and KPIs, utilising GPS tools.</p></li><li><p>Self-manage training compliance metrics to ensure ongoing personal and regulatory compliance.</p></li></ul><p></p><p><b>Shift:</b>  Please note that this role operates on a 24/5 shift rota:  Earlies (6:00 to 14:00), Lates (14:00 to 22:00), &amp; Nights (22:00 to 6:00).</p><p></p><p></p><p><b>About You: </b></p><p>Relevant engineering qualifications and / or experience is required (eg; HND / HNC, Engineering Apprenticeship).  A good standard of numeracy and literacy is essential.</p><p></p><p></p><p><b><span>CLOSING DATE for applications:   Friday 29th of May 2026 (COB).</span></b></p><p></p><p></p><p><b>Basic Qualifications / Skills:</b></p><ul><li><p>Relevant qualifications/certificates and engineering experience (e.g. <b>Engineering Apprenticeship</b>.  An <b>HNC / HND </b>Level qualification).</p></li><li><p>Applicants without an HNC level qualification need to have <b>EngTech status</b> (certificate) and have completed a recognised engineering apprenticeship.</p></li><li><p>A good standard of numeracy and literacy.</p></li><li><p>Hands-on experience of manufacturing processes and procedures (ideally obtained from working in a highly-regulated industry).</p></li><li><p>Knowledge of current Good Manufacturing Practice (cGMP).</p></li></ul><p></p><p>If you would like to learn more about our company wide benefits and life at GSK we would suggest looking at our webpage <a href="https://www.gsk.com/en-gb/careers/life-at-gsk/" target="_blank">Life at GSK | GSK</a>.</p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/engineering-technician-gsk/6a08974a2f1861929d253337</link><guid isPermaLink="true">http://biotechroles.com/engineering-technician-gsk/6a08974a2f1861929d253337</guid><pubDate>Sat, 16 May 2026 16:11:54 GMT</pubDate><company>GSK</company><location>UK - County Durham - Barnard Castle</location><salary>$35000-48000</salary><type>Full time</type></item><item><title><![CDATA[Alternant(e) Gestion de projet et Intelligence d'affaires]]></title><description><![CDATA[<h1></h1><h1></h1><h1><span class="emphasis"><b>Alternant(e) Gestion de projet et Intelligence d&#39;affaires  </b></span></h1><h1></h1><p>Nous recherchons un(e)<b> Alternant(e) </b>pour la rentrée de septembre 2026 pour notre site de Rueil.</p><p></p><p>Au sein de l&#39;équipe de <b><span>Excellence opérationnelle et performance</span></b><b>, </b>vous aurez pour <span class="emphasis">principales missions</span> :</p><ul><li><p>Soutenir notre équipe de chefs de projet (capabilities et planification d&#39;événements) et nos partenaires en intelligence d&#39;affaires afin de mener et de livrer des projets ayant un impact important sur notre entreprise et notre personnel</p></li><li><p>Ces projets peuvent inclure :</p><ul><li><p>la planification de notre séminaire national pour tous les employés de notre hub (FR et BE)</p></li><li><p>le soutien à la bonne réalisation de nos événements internes/externes</p></li><li><p>le lancement de nouveaux outils pour soutenir nos équipes terrain en vente et en médeival</p></li><li><p>l&#39;élaboration de rapports d&#39;intelligence concurrentielle</p></li><li><p>la création de tableaux de bord et le suivi de nos performances.</p></li></ul></li></ul><p></p><p></p><p><span class="emphasis"><b>Votre profil :</b></span></p><ul><li><p>Étudiant(e) en Bac&#43;4/5 (école de commerce, d’ingénieurs ou master universitaire) — spécialisation en gestion de projet, data / business intelligence, management ou équivalent.</p></li><li><p>Anglais (niveau minimum B2).</p></li><li><p>Esprit rigoureux et méthodologique, sens de l’analyse scientifique.</p></li><li><p>Prise d’initiative, autonomie et bonne organisation.</p></li><li><p>Intérêt pour l’innovation thérapeutique et/ou digitale.</p></li><li><p>Excellentes aptitudes relationnelles et facilité de communication.</p></li></ul><p></p><p>Le poste est rattaché au siège social basé à <b>Rueil-Malmaison (92)</b>. </p><p></p><p><span class="emphasis">A PROPOS DE VIIV HEALTHCARE</span><br /><br />Joint-venture, créée par GlaxoSmithKline et Pfizer en 2009, ViiV Healthcare est un laboratoire international et indépendant entièrement dédié à la recherche, au développement et à la commercialisation de médicaments dans le domaine du VIH. ViiV Healthcare accueille en 2012 un troisième associé et investisseur : Shionogi.<br /><br />ViiV Healthcare réunit deux expertises complémentaires dans le domaine du VIH, celle du laboratoire Pfizer et celle de GSK et repose sur un modèle de Recherche et Développement innovant entre GSK, pionnier des antirétroviraux avec Pfizer. Plus de 1500 collaborateurs sont répartis dans 16 filiales à travers le monde. Avec un portefeuille de 12 médicaments, ViiV Healthcare est un acteur majeur dans le domaine du VIH/SIDA.<br /><br />ViiV Healthcare France est la deuxième filiale dans le monde en termes :</p><ul><li><p>de poids dans la recherche clinique</p></li><li><p>d&#39;effectifs, avec plus de 70 salariés</p></li><li><p>de chiffre d&#39;affaires</p></li></ul><p></p><p>ViiV Healthcare a trois priorités :</p><ul><li><p>Apporter des solutions innovantes aux malades grâce à son programme de recherche et de développement spécifique</p></li><li><p>Consolider son engagement dans la durée grâce à son important portefeuille thérapeutique et à sa structure unique</p></li><li><p>Rechercher de nouveaux moyens pour faciliter l&#39;accès aux soins en collaborant avec le monde associatif</p></li></ul><p>Pour en savoir plus vous pouvez consulter la ressource suivante :</p><p><a href="https://viivhealthcare.com/fr-fr/" target="_blank">Page d&#39;accueil | ViiV Healthcare</a></p><p></p><p><i>ViiV Healthcare s’engage en faveur du pluralisme dans le cadre de ses recrutements.</i></p><p></p><p>*LI-GSK</p>&amp;#xa;&amp;#xa;This is a temporary internship/apprenticeship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process.&amp;#xa;&amp;#xa;Il s’agit d’une opportunité de stage/alternance temporaire axée sur le développement professionnel. Tout remboursement, bourse, indemnité ou soutien financier sera accordé conformément aux lois et réglementations locales applicables, ainsi qu’aux politiques du site GSK. Des informations plus détaillées seront fournies au cours du processus de recrutement.<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on <a target="_blank" href="mailto:Fr-diversity.recruitment&#64;gsk.com​"><span style="color:#0000ff"><u>Fr-diversity.recruitment&#64;gsk.com​</u></span></a></p><p></p><p>Please note should your enquiry not relate to adjustments; we will not be able to support you through these channels.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/alternante-gestion-de-projet-et-intelligence-daffaires-gsk/6a08974a2f1861929d253336</link><guid isPermaLink="true">http://biotechroles.com/alternante-gestion-de-projet-et-intelligence-daffaires-gsk/6a08974a2f1861929d253336</guid><pubDate>Sat, 16 May 2026 16:11:54 GMT</pubDate><company>GSK</company><location>France - Rueil Malmaison</location><salary>$18000-24000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Medical Strategy and Operations, Anti-Infectives and Respiratory]]></title><description><![CDATA[<p><b><span>Associate Director, Medical Strategy and Operations, Anti-Infectives and Respiratory</span></b></p><p></p><p><b><span>Location: Philadelphia, PA; Durham, NC</span></b></p><p></p><p>At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&amp;D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.</p><p>The Associate Director, Medical Strategy and Operations, Anti-Infectives and Respiratory is responsible for enabling high-quality execution of Medical Affairs plans and operational excellence within the Therapeutic Area (TA). The role partners closely with Asset Medical Leads and cross-functional stakeholders to ensure medical plans are operationally sound, resourced appropriately, executed with rigor, and tracked for impact.</p><p>This role serves as operational lead for medicines or high priority initiatives and cross-Therapeutic Area operations partner as needed. This includes facilitating medical planning, budgeting and resourcing, monitoring performance, and driving continuous improvement in ways of working across asset teams / the Therapeutic Area.  The Associate Director advances the operating model within the Therapeutic Area in alignment with enterprise operating model and ways of working, helping teams navigate change with agility.</p><p></p><p><span class="emphasis"><b>Key Responsibilities:</b></span></p><ul><li>Facilitate annual planning for assets, budget consolidation, forecasting, prioritization, and cross-team planning alignment, depending on organizational needs</li><li>Serve as the primary medical operations partner for 1 or multiple Anti-Infectives and/or Respiratory medicines, supporting Asset Medical Leads in the development and execution of Medical Affairs plans</li><li>Drive development of operational plans, including timelines, resourcing, budget assumptions, and execution milestones; support execution of tactics, ensuring alignment to strategic priorities and enterprise requirements</li><li>Track execution against plan, budget, and milestones; proactively identify risks, trade-offs, and mitigation strategies while ensuring adherence to established policies, SOPs, and governance expectations</li><li>Coordinate Medical Matrix Team meetings and broader cross-TA forums, preparing clear, concise status updates and performance insights, and effective communication to leadership and stakeholders  </li><li>Embed the therapeutic area operating model and ways of working, including shared tools, templates, governance practices, and cross-team routines</li><li>Identify opportunities to simplify workflows, improve transparency, and enhance speed and quality of execution within assigned assets; share best practices and lessons learned across assets and the broader community</li><li>Support change initiatives by helping teams adopt new processes, tools, and behaviors with a high degree of agility, practical problem solving, and trust building in all directions</li><li>Facilitate use of data, dashboards, and emerging digital and AI-enabled tools to improve planning quality, operational insights, and measurement of executional impact</li><li>Coordinate as needed across operational support, including vendors, agencies, or outsourced support aligned to asset or therapeutic area needs</li></ul><p></p><p><span class="emphasis"><b>Basic Qualifications:</b></span></p><ul><li>Bachelor’s degree in Business, Life Sciences, Public Health, or related field</li><li>Five or more years of experience in Medical Affairs operations, medical planning, business operations, or project/program management within pharma/biotech</li><li>Two or more years of experience supporting medical planning and execution for a brand, asset, or therapeutic area</li><li>Two or more years of experience tracking budgets, timelines, and execution metrics against plan</li><li>Experience supporting cross-functional teams in a matrix environment and contributing to changes in ways of working</li><li>Experience using data, dashboards, digital and AI-enabled tools to improve operational efficiency, insight generation, or impact measurement</li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications:</b></span></p><ul><li>Advanced degree (MBA, PharmD, PhD, or equivalent), PMP certification, or other formal project management training</li></ul><ul><li>Experience supporting Anti-Infectives and/or Respiratory Medical Affairs and/or launch or post-launch assets</li><li>Demonstrated ability to drive process improvement and improve ways of working across HQ and field teams</li><li>Proven ability to operate effectively in a matrix environment and manage multiple priorities simultaneously</li><li>Strong analytical, problem-solving, and stakeholder-management skills</li><li>Reputation as a reliable, execution-focused partner to medical and cross-functional leaders</li></ul><p></p><p><span class="emphasis"><b>Travel Expectations:</b></span></p><p>Ability to travel approximately <b><span>10–15%</span></b>, as needed</p><p></p><p>#Li-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/associate-director-medical-strategy-and-operations-anti-infectives-and-respiratory-gsk/6a08974a2f1861929d253335</link><guid isPermaLink="true">http://biotechroles.com/associate-director-medical-strategy-and-operations-anti-infectives-and-respiratory-gsk/6a08974a2f1861929d253335</guid><pubDate>Sat, 16 May 2026 16:11:54 GMT</pubDate><company>GSK</company><location>Durham Blackwell Street</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Regulatory Conformance Officer (12-month Fixed Term Contract (FTC) / Secondment)]]></title><description><![CDATA[<p></p><p>Are you passionate about ensuring the highest standards of regulatory compliance within the pharmaceutical industry? Do you have the expertise to maintain and enhance product licensing and regulatory conformance?</p><p>If so, we have an exciting fully site based Fixed term contract/secondment opportunity for you at our Barnard Castle site. </p><p></p><p>We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.</p><p></p><p>As a <b>Regulatory Conformance Specialist</b>, you will play a crucial role in ensuring our products meet all licensing requirements and company standards. Your responsibilities will include maintaining the approval status of product licenses for both new and established products, as well as upholding the manufacturer&#39;s licenses for our Barnard Castle facility.</p><p></p><p>You will be a key contributor to our business objectives by offering regulatory information and support for site transfers and variations to existing products within agreed customer deadlines. Join us and be part of a team dedicated to delivering excellence in regulatory conformance and compliance.</p><p></p><p>This role supports the delivery of critical regulatory projects across the product lifecycle. Key responsibilities include maintaining compliance with global market authorisations, supporting regulatory submissions, and ensuring site operations remain aligned with changing regulatory requirements.</p><p>Working closely with manufacturing and aseptic operations, the role contributes to the delivery of regulatory strategies, inspection readiness, and change implementation, ensuring that processes, specifications, and controls remain compliant and robust.</p><p></p><p><b><i>In this role you will… </i></b></p><ul><li><p>Collaborate with multiple functions across the site and the global network, establishing partnerships with Operational Quality, New Product Introduction, Analytical Laboratories, Validation, Logistics, R&amp;D, Global Regulatory Affairs, and Local Operating Companies.</p></li><li><p>Support the commercialization of new products from R&amp;D through development, clinical trials, and commercial submissions, coordinating submission authoring, reviewing, and approval for the site, and providing accurate and compliant information to support regulatory filings.</p></li><li><p>Represent Regulatory Conformance in project teams for new business, change projects, transfers, and network strategy, ensuring alignment with regulatory requirements.</p></li><li><p>Coordinate and prepare responses to questions from external regulatory authorities during technical reviews of submissions, variations, and renewals, managing the delivery of data/information to fulfil post-approval commitments.</p></li><li><p>Review site requests for change, assess regulatory impact, provide accurate advice to change owners/initiators, and support the Regulatory Implementation Strategy, communicating approval status to the site.</p></li><li><p>Assess regulatory changes for site impact, escalate issues to ensure compliance, review Quality and Regulatory Intelligence, communicate impacts to the site, report regulatory intelligence to Central Regulatory, and review Pharmacopoeia changes for specification impact.</p></li></ul><p></p><p></p><p><b>Please Note:</b>  This Fixed Term Contract (FTC) / secondment is expected to last circa 12 months in duration.  Please ensure you have spoken with your line-manager to ensure they are supportive of your application (this includes a timely-release from your current responsibilities should you be offered the Secondment).</p><p></p><p></p><p><b>CLOSING DATE for applications:  Friday 29th of May 2026 (COB).</b></p><p></p><p></p><p><b>Basic Qualifications &amp; Skills:</b></p><ul><li><p>HND or ‘A’ levels in Scientific disciplines or equivalent experience.</p></li><li><p>Background in analytical, laboratory, pharmaceutical industry, or regulatory roles.</p></li><li><p>Strong analytical approach with excellent attention to detail.</p></li><li><p>Understanding of the regulated industry and its requirements, including Quality and GxP.</p></li><li><p>Broad-based technical knowledge of manufacturing, quality, and regulatory activities/requirements, with knowledge of change control processes, registration, and regulatory procedures being desirable. Ability to interpret and apply registered details to ensure compliance in manufacturing and release processes.</p></li></ul><p></p><p><b>Preferred Qualifications &amp; Skills</b>:</p><p>If you have the following characteristics, it would be a plus:</p><ul><li><p>Broad-based technical knowledge of manufacturing, quality, and regulatory activities/requirements, with knowledge of change control processes, registration, and regulatory procedures being desirable. Ability to interpret and apply registered details to ensure compliance in manufacturing and release processes.</p></li><li><p>Degree in a scientific or related discipline (e.g., Microbiology, Pharmacy, Chemistry, or another related science).</p></li></ul><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/regulatory-conformance-officer-12-month-fixed-term-contract-ftc-secondment-gsk/6a0897492f1861929d253334</link><guid isPermaLink="true">http://biotechroles.com/regulatory-conformance-officer-12-month-fixed-term-contract-ftc-secondment-gsk/6a0897492f1861929d253334</guid><pubDate>Sat, 16 May 2026 16:11:53 GMT</pubDate><company>GSK</company><location>UK - County Durham - Barnard Castle</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Key Account Manager]]></title><description><![CDATA[<p><a href="https://www.gsk.com?utm_source&#61;chatgpt.com" target="_blank">GSK</a> mantiene su compromiso de alcanzar ambiciosos objetivos comerciales para el futuro. Para 2031, buscamos generar £40 mil millones en ventas anuales, aprovechando el sólido impulso de nuestro desempeño actual para incrementar significativamente nuestro impacto positivo en la salud de miles de millones de pacientes a nivel global. Nuestra estrategia <i>Ahead Together</i> se centra en la intervención temprana para prevenir y modificar el curso de las enfermedades, protegiendo así a las personas y apoyando a los sistemas de salud.</p><p>Nuestro portafolio diverso está compuesto por vacunas, medicamentos especializados y medicamentos generales.</p><p>A través de la innovación continua y un enfoque dedicado a la excelencia científica y técnica, buscamos desarrollar y lanzar nuevos tratamientos innovadores que respondan a desafíos críticos de salud.</p><p></p><h2>Resumen de la Posición</h2><p>Liderarás estrategias comerciales y de acceso para cuentas clave institucionales - Oncologia. Trabajarás de manera cercana con equipos multifuncionales para impulsar el acceso y los resultados del negocio. Valoramos la comunicación clara, la toma de decisiones basada en datos, la colaboración y el enfoque en resultados medibles.</p><p>Esta posición ofrece oportunidades de crecimiento, un impacto real en el acceso de los pacientes y la posibilidad de contribuir a la misión de GSK de unir ciencia, tecnología y talento para adelantarnos a las enfermedades juntos.</p><p></p><h2>Responsabilidades</h2><p>Este rol te brindará la oportunidad de liderar actividades clave para impulsar tu desarrollo profesional. Entre las responsabilidades se incluyen:</p><ul><li>Construir y ejecutar planes de cuenta para clientes institucionales - Oncologia, incluyendo aseguradoras de salud, distribuidores, IPS y otros socios estratégicos.</li><li>Gestionar el presupuesto de ventas y los pronósticos de tu territorio, monitorear el desempeño e implementar acciones correctivas.</li><li>Liderar negociaciones comerciales, licitaciones y propuestas para asegurar y ampliar el acceso.</li><li>Utilizar datos para gestionar inventarios, rotación y devoluciones, tomando decisiones oportunas para proteger la disponibilidad y la rentabilidad.</li><li>Colaborar con equipos de supply chain, finanzas, médico, marketing y comercial para resolver barreras de acceso y mejorar la experiencia del cliente.</li><li>Monitorear tendencias del mercado y necesidades de los stakeholders para identificar oportunidades de crecimiento y apoyar la estrategia.</li></ul><p></p><h2>¿Por qué tú?</h2><p>Requisitos Básicos</p><p>Buscamos profesionales con las siguientes habilidades y calificaciones:</p><ul><li>Título universitario en Administración de Empresas, Ingeniería Industrial, Farmacia, Economía o carreras afines.</li><li>Mínimo de 3 años de experiencia gestionando cuentas institucionales - Oncologia .</li><li>Experiencia manejando presupuestos de ventas, pronósticos y negociaciones comerciales en el portafolio de oncologia.</li><li>Experiencia comprobada participando en licitaciones y preparando propuestas comerciales.</li><li>Fuertes habilidades de comunicación y gestión de stakeholders.</li><li>Manejo de Microsoft Office, especialmente Excel, y capacidad para utilizar datos en la toma de decisiones.</li></ul><h2>Requisitos Deseables</h2><p>Será un plus si cuentas con:</p><ul><li>Experiencia comercial en Oncologia canales de cuidado especializado o vacunas.</li><li>Conocimiento de conceptos <i>gross-to-net</i> y estrategias comerciales para canales institucionales.</li><li>Experiencia trabajando en organizaciones grandes y multifuncionales.</li><li>Capacidad para analizar datos de mercado y clientes para apoyar decisiones estratégicas.</li><li>Nivel intermedio de inglés.</li><li>Experiencia gestionando relaciones con EPS, distribuidores o grandes clientes institucionales.</li></ul><h2>Cómo Aplicar</h2><p>Si esta posición se alinea con tu experiencia y aspiraciones profesionales, nos encantaría conocerte. Postúlate y cuéntanos cómo tus habilidades y valores pueden contribuir a mejorar el acceso de los pacientes y los resultados comerciales del equipo.</p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>If you require any adjustments or accommodation during the selection process to better showcase your abilities, please let our team know as soon as we contact you. We&#39;re here to support you.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Our inclusive workplace makes our employees feel engaged by the contribution they make, by affording them equal treatment regardless of actual or perceived characteristics. As so, when you apply for a job at GSK, it is not necessary to include on your resume information such as: race, color, ethnicity, age, gender, sexual orientation, marital status, religion, origin, photographs or any other personal characteristics.</p><p> </p><p>Find out what life at GSK is really like <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>www.gsk.com</u></span></a></p>]]></description><link>http://biotechroles.com/key-account-manager-gsk/6a0897492f1861929d253333</link><guid isPermaLink="true">http://biotechroles.com/key-account-manager-gsk/6a0897492f1861929d253333</guid><pubDate>Sat, 16 May 2026 16:11:53 GMT</pubDate><company>GSK</company><location>Colombia - Capital District - Bogota</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Territory Manager/Associate, Vaccines - ON North]]></title><description><![CDATA[<p></p><p>Are you a driven commercial professional who thrives in a field-based environment, builds strong relationships with healthcare providers, and is passionate about improving patient protection against vaccine-preventable diseases?<br /><br /><span>GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.</span>​</p><p><br /><span>Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.</span>​</p><p><br /><span>Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.</span></p><p></p><p><b>Job Purpose</b><br />GSK is looking to hire a Territory Manager/Associate, to join our Vaccines team. This role is field-based and reports directly to the District Sales Manager. <span><b>This position covers the Ontario North territory, including North Sudbury and surrounding areas extending as far as Sault Ste. Marie and North Bay</b>. The ideal candidate will reside in or near the covered territory.</span><br /> </p><p>As a Territory Manager/Associate, you will be responsible for executing strategic business plans that drive customer engagement and maximize the value of GSK’s innovative portfolio. You will lead business development initiatives, foster meaningful customer relationships, and collaborate cross-functionally to ensure the successful implementation of marketing strategies. Your ability to demonstrate business acumen, communicate effectively, and work autonomously will be critical to success. You will collaborate closely with cross-functional teams, including Medical Science Liaisons (MSLs), marketing, and other internal partners, to support GSK’s mission to help Canadians do more, feel better, and live longer.</p><p></p><p><b>Details (Your Responsibilities) </b> </p><p><i><span>This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following</span></i><i>:  </i></p><ul><li><p>Developing and executing strategic business plans to achieve sales targets within your assigned territory</p></li><li><p>Building and maintaining strong relationships with healthcare professionals to support their needs and improve patient outcomes</p></li><li><p>Communicating product information effectively and delivering tailored solutions to meet customer needs</p></li><li><p>Using data and insights to inform decision-making and optimize territory performance</p></li><li><p>Collaborating with cross-functional teams to identify opportunities and achieve business goals</p></li><li><p>Managing resources effectively to create value for customers and drive business success</p></li><li><p>Ensuring all activities align with internal compliance and regulatory standards</p></li></ul><p></p><p><b><i>Why you?</i></b><br /><b>Basic Qualifications:</b>  <br /><i><span>We are looking for professionals with these required skills to achieve our goals:</span></i> </p><ul><li><p>Bachelor’s degree in life sciences, marketing, or related field </p></li><li><p>Minimum 3 years of sales experience, preferably in healthcare or pharmaceuticals</p></li><li><p>Valid driver’s license and ability to travel within the assigned territory</p></li><li><p>Strong communication and interpersonal skills to build and maintain professional relationships</p></li><li><p>Proficiency in Microsoft Word, Excel, and PowerPoint</p></li><li><p>Ability to analyze data and use insights to inform strategy and decision-making<br /> </p></li></ul><p><b>Preferred Qualifications:</b>  <br /><i><span>If you have the following characteristics, it would be a plus:</span></i></p><ul><li><p>Experience in pharmaceutical sales or a related healthcare industry</p></li><li><p>Experience selling to specialists or running key account activitie</p></li><li><p>Proven ability to create and execute territory business plans</p></li><li><p>Skills interpreting scientific data and translating it for customers</p></li><li><p>Comfort with omnichannel engagement methods and digital customer interactions</p></li><li><p>Strong analytical skills to use data for decision-making</p></li><li><p>A local presence in Ontario and familiarity with the region’s healthcare system<br /> </p></li></ul><p><b>***This position requires the employee to drive routinely on company business and allows for the provision of a company-leased vehicle. However, to be eligible for this position and a company vehicle, GSK will need to obtain acceptable results from a license verification inquiry and drivers abstract review against its safe driver program requirements*** </b><br /><br /><b>#LI-GSK</b><br /><b>#LI-Field</b></p>&amp;#xa;In compliance with Ontario's provincial pay transparency legislation, this job posting includes a salary range to support equitable and informed hiring practices. The annual compensation for this role is CAD86,000 to CAD136,000 , determined based on experience, qualifications, and internal equity. GSK is dedicated to promoting transparency and fairness throughout our recruitment process.Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?<br />Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. GSK is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at <a target="_blank" href="mailto:canada-recruitment&#64;gsk.com">canada-recruitment&#64;gsk.com</a>.  Please do not send resumes to this e-mail and instead apply through the online application process of this posting.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/territory-managerassociate-vaccines-on-north-gsk/6a0897482f1861929d253332</link><guid isPermaLink="true">http://biotechroles.com/territory-managerassociate-vaccines-on-north-gsk/6a0897482f1861929d253332</guid><pubDate>Sat, 16 May 2026 16:11:52 GMT</pubDate><company>GSK</company><location>Canada – Ontario – Barrie/Vaughan</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Competitive Intelligence Director]]></title><description><![CDATA[<div><p></p><p><span><span>Are you a Competitive Intelligence</span><span><span> </span></span><span>or Vaccines</span><span><span> </span>professional seeking the next challenge in your career?</span><span><span> </span>This may be the perfect role for you.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>We are<span> </span></span><span>seeking</span><span><span> </span></span><span>a</span><span><span> </span>deeply curious, strategic thinker</span><span><span> </span>t</span><span>o join</span><span><span> </span>our<span> </span></span><span>Globa</span><span>l<span> </span></span><span>Vaccines<span> </span></span><span>Competitive Intelligence team</span><span>.<span> </span></span><span>In<span> </span></span><span>this role</span><span>,</span><span><span> </span>you will<span> </span></span><span>be</span><span><span> </span>a key partner to<span> </span></span><span>Global Product Strategy (GPS),<span> </span></span><span>R&amp;D and Medical</span><span><span> </span>teams<span> </span></span><span>within GSK’s Global Vaccines<span> </span></span><span>organization</span><span>. You will act as an objective,<span> </span></span><span>critical</span><span><span> </span>and strategic advisor based on your deep<span> </span></span><span>expertise</span><span><span> </span>in current and future competitive drivers in the vaccines market. This is an exciting opportunity to<span> </span></span><span>influence strategy development</span><span><span> </span>and investment<span> decisions and</span></span><span><span> </span>deliver insightful and forward-looking analysis and recommendations to help shape</span><span><span> </span>competitive</span><span><span> </span>GSK brand strategies.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The role </span><span>can be located in</span><span><span> </span>the UK (London) or the US (Upper Providence or Philadelphia).</span></span><span> </span></p><p></p><div><div><p><b><span>Key Responsibilities:</span></b></p><p><span><span>Describe the key deliverables to be achieved by the post holder and the ongoing responsibilities of the role</span></span><span> </span></p></div></div><div><div><ul><li><p><b><span>Partner</span></b><span><span><span> </span>–<span> </span></span><span>Act as<span> </span></span><span>a trusted strategic<span> </span></span><span>advisor<span> </span></span><span>to<span> </span></span><span>GPS, R&amp;D and Medical</span><span><span> </span>teams, providing dedicated competitive intelligence support for assigned brand(s) and program(s)<span> </span></span><span>on all relevant market and competition areas</span><span>, bringing<span> </span></span><span>objective, independent thinking</span><span>. Partner with other Vaccines functions and markets as needed to<span> </span></span><span>provide</span><span><span> </span>broader insight and analysis</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Analysis</span></b><span><span><span> </span>–<span> </span></span><span>Collect and<span> synthesize</span></span><span><span> </span>internal and external data with expert use of a wide range of information sources to derive<span> </span></span><span>proactive,<span> </span></span><span>timely</span><span><span> </span>and actionable competitive insight</span><span>.</span><span><span> </span></span><span>Develop holistic and predictive competitor landscape assessments based on a thorough understanding and analysis of internal and external business issues</span><span>,</span><span><span> </span>using robust CI sources and innovative methodologies<span> </span></span><span>as needed</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Recommendations</span></b><span><span><span> </span>– Use<span> </span></span><span>expertise</span><span><span> </span>on current and future competitive drivers in the marketplace to make critical recommendations</span><span><span> </span>from your analysis</span><span>, relating<span> </span></span><span>impact</span><span><span> </span>on our ability to be competitive</span><span><span> </span>and influencing without authority</span><span>.<span> </span></span><span>Proactively propose further areas of analysis relevant to the asset’s life cycle/place in market and</span><span><span> </span></span><span>that are relevant to our<span> </span></span><span>business<span> </span></span><span>strategies</span><span>.<span> </span></span><span>Ensure relevant<span> </span></span><span>CI<span> </span></span><span>analysis and deliverables are integrated into</span><span><span> </span>key</span><span><span> </span>stage</span><span><span> </span></span><span>gates of<span> </span></span><span>the<span> </span></span><span>commercialization</span><span><span> </span>process</span><span>, such as<span> </span></span><span>brand planning, forecasting, evidence generation and strategic decision making</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Rapid Key Event Coverage</span></b><span><span><span> </span>–<span> </span></span><span>Shape and direct</span><span><span> </span>coverage of key events relevant<span> </span></span><span>for</span><span><span> </span>your area</span><span>,<span> </span></span><span>ensuring</span></span><span><span><span> </span></span></span><span><span>effective integration, consolidation and<span> </span></span><span>rapid<span> </span></span><span>communication of analyses and insights</span><span>. H</span><span>elp develop systems</span><span>/</span><span>process</span><span>es</span><span><span> </span>that<span> </span></span><span>can<span> </span></span><span>enable fast response to unplanned/ad hoc analysis</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Congresses</span></b><span><span><span> </span>-<span> </span></span><span>Lead competitive intelligence planning</span><span><span> </span>and coverage</span><span><span> </span>for key congresses<span> </span></span><span>relevant to assigned brand(s) and disease area(s)<span> </span></span><span>with input from GSK teams and/or<span> </span></span><span>third-party</span><span><span> </span></span><span>agency</span><span>. Drive GSK team preparedness, ensure key intelligence questions<span> </span></span><span>are<span> </span></span><span>developed, align on-site activities<span> </span></span><span>as needed<span> </span></span><span>and<span> </span></span><span>consolidate</span><span><span> </span>key insights and<span> </span></span><span>disseminate</span><span><span> </span>post-congres</span><span>s</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>CI Capabilities</span></b><span><span><span> </span>– Working with the Head of Competitive Intelligence,<span> </span></span><span>contribute to and<span> </span></span><span>help shape evolution of the team to<span> </span></span><span>develop</span><span><span> </span>best-in-class CI capabilities, and increase the value of CI to GSK</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Indirect Team</span></b><span><span><span> </span>–</span><span>M</span><span>anage<span> </span></span><span>workflow</span><span><span> </span>and capabilities of the broader resource structure supporting<span> </span></span><span>the CI team</span><span>. Lead and coach these resources on high, focused performance</span><span>,<span> optimizing</span></span><span><span> </span>the team to deliver maximum value</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>External Research</span></b><span><span><span> </span>- E</span><span>ngage third party agencies as<span> </span></span><span>appropriate</span><span><span> </span>and e</span><span>nsure all CI research activities are conducted within<span> </span></span><span>appropriate GSK</span><span><span> </span>code of conduct,<span> </span></span><span>compliance</span><span><span> </span>and ethical business practices</span></span><span> </span></p></li></ul></div></div><div><div><p></p><p><b><span>Why you?</span></b><span> </span></p></div></div><div><div><p></p><p><b><span>Basic Qualifications:</span></b><span> </span></p></div><div><ul><li><p><span><span>Bachelor’s degree</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Minimum<span> </span></span><span>7</span><span><span> </span>years’ experience in healthcare,<span> </span></span><span>pharmaceutical</span><span>,<span> </span></span><span>strategy<span> </span></span><span>consultancy or financial institution</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Functional e</span><span>xperience in competitive intelligence</span><span>,</span><span><span> </span>gained either directly within a pharmaceutical company or from within a relevant healthcare CI,<span> </span></span><span>investment</span><span><span> </span>or consulting environment</span><span> </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong</span><span><span> </span></span><span>understanding</span><span><span> </span></span><span>of</span><span><span> </span>the</span><span><span> </span></span><span>medicine</span><span>/</span><span>vaccine</span><span><span> </span>development<span> </span></span><span>and<span> </span></span><span>commercialization</span><span><span> </span></span><span>process, including activities from preclinical through marketing of a product, and business knowledge of pharma</span><span>ceutical</span><span>/vaccine</span><span><span> </span>companies and their business practices</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Excellent ability to condense significant amounts of complex information</span><span><span> </span></span><span>into sharp,<span> </span></span><span>succinct</span><span><span> </span>and impactful deliverables</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experienced in matrix environment with ability to build strong relationships and drive impact across a range of functions, seniority, and geographical locations</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><b><span>Preferred Qualifications:</span></b><span> </span></p></div><div><ul><li><p><span><span>Ph.D.<span> </span></span><span>- Science</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Deep understanding of</span><span><span> </span>and experience in</span><span><span> </span>multiple vaccines indications that can be applied to competitive intelligence</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Previous</span><span><span> </span>experience</span><span><span> </span>working</span><span><span> </span>in commercial functions<span> </span></span><span>in a pharmaceutical company<span> </span></span><span>(global/regional, marketing,<span> </span></span><span>sales,<span> </span></span><span>etc</span><span>)</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proven ability to challenge, influence and support senior stakeholders</span></span><span> </span></p></li></ul><p></p><p><span>#LI-GSK</span></p></div></div><p></p></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/competitive-intelligence-director-gsk/6a0897472f1861929d253331</link><guid isPermaLink="true">http://biotechroles.com/competitive-intelligence-director-gsk/6a0897472f1861929d253331</guid><pubDate>Sat, 16 May 2026 16:11:51 GMT</pubDate><company>GSK</company><location>USA - Pennsylvania - Philadelphia</location><salary>$140000-200000</salary><type>Full time</type></item><item><title><![CDATA[Oncology Pipeline Director]]></title><description><![CDATA[<div><p><b><span>Uniting science, technology and talent to get ahead of disease together</span></b></p><p></p><p><span><span>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. </span></span><span>​</span></p></div><div><p><span><span>We prevent and treat disease with specialty medicines, vaccines and general medicines. We focus on the science of the immune system </span></span><span><span>and advanced technologies, investing in four core therapeutic areas – respiratory, immunology and inflammation; oncology; HIV; and </span></span><span><span>infectious diseases – to impact health at scale. </span></span><span>​</span></p></div><div><p><span>​</span></p></div><div><p><span><span>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment </span></span><span><span>where our people can perform and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and </span></span><span><span>doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</span></span></p></div><p></p><p><span><span>GSK </span></span><span><span>remains</span></span><span><span> committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, </span></span><span><span>leveraging</span></span><span><span> our existing </span></span><span><span>strong performance</span></span><span><span> momentum to significantly increase our positive impact on people’s health. </span></span><span>​</span></p><div><p><span><span>Our strategy is to prevent and treat disease with specialty medicines, </span></span><span><span>vaccines</span></span><span><span> and general medicines. ​</span></span><span>​</span></p></div><div><p><span><span>We combine the science of the immune system with advanced technologies, enhanced by targeted business development and world-class </span></span><span><span>partnerships, to develop new medicines and vaccines that can help transform people’s lives.</span></span></p></div><p><br /><b>Position Summary</b></p><p>The Oncology Pipeline Director is responsible for representing the Canadian commercial perspective across the lifecycle of key novel oncology assets or indications including ensuring development, commercialization strategy, and launch planning are optimized for the Canadian market. This role serves as the primary Canadian commercial leader interfacing with the global asset team and regional asset teams for all Oncology assets or indications, providing strategic guidance and input on Canadian needs for commercial readiness to maximize asset / indication value.</p><p></p><p>The Director will work cross-functionally with Medical Affairs, Market Access, Regulatory and Business Intelligence in Canada to shape the development path and commercialization strategy for the assets / indications including prioritization, resource and investment allocation / timing and business case / P&amp;L development. The role requires deep expertise in Canadian oncology market dynamics, competitive intelligence, payer landscape, and launch excellence, ensuring the Canadian perspective is considered and localized from global or regional strategy.</p><p><br /><b>Responsibilities</b><br />This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><p></p><p><b>Canada Oncology Asset / Indication Strategy Leadership:</b></p><ul><li><p>Serve as the Canadian commercial lead for all oncology assets / indications on global and regional teams, ensuring the Canadian perspective is considered in development and commercialization decisions.</p></li><li><p>Shape Canadian positioning strategy, value proposition, and differentiation relative to current and emerging competitors.</p></li><li><p>Member of the Oncology Leadership Team</p></li><li><p>Translate Canadian market insights into actionable strategy for local and global/regional teams as needed.</p></li><li><p>Partner with local Medical and Clinical teams to ensure understanding of local drivers and barriers of success of clinical trial sites in Canada and implications for potential commercial success or needs.</p></li><li><p>Identify opportunities to optimize label potential and market access positioning.</p></li></ul><p></p><p><b>Canada Market Intelligence &amp; Competitive Strategy:</b></p><ul><li><p>Lead the cross-functional team for Canada for market landscape assessments, including:</p><ul><li><p>Disease epidemiology</p></li><li><p>Treatment paradigms</p></li><li><p>Competitive intelligence</p></li></ul></li><li><p>Monitor evolving competitive pipelines across tumor types, translating insights into strategic implications.</p></li></ul><p></p><p><b>Forecasting &amp; Business Case Development:</b></p><ul><li><p>Collaborate with Business Intelligence to develop robust Canadian forecasts and scenario planning.</p></li><li><p>Lead assessment of commercial opportunity, pricing potential, and market uptake dynamics.</p></li><li><p>Provide strategic input into investment decisions and lifecycle planning.</p></li></ul><p></p><p><b>Cross-Functional Leadership:</b></p><ul><li><p>Serve as a key integrator across:</p><ul><li><p>Oncology Commercial Leadership</p></li><li><p>Medical Affairs</p></li><li><p>Market Access</p></li><li><p>Regulatory</p></li><li><p>Business Intelligence</p></li></ul></li><li><p>Drive alignment and integrated strategic plan development across stakeholders to ensure timely and strategic decision making.</p></li></ul><p></p><p><b>Leadership Competencies:</b></p><ul><li><p>Strategic thinking and ability to translate insights into actionable strategy</p></li><li><p>Enterprise leadership across complex global matrix organizations</p></li><li><p>Strong commercial acumen in oncology markets</p></li><li><p>Influencing without authority</p></li><li><p>Data-driven decision making</p></li></ul><p></p><p><b>Why You?</b><br /><b>Basic Qualifications</b><br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li><p>Bachelor’s degree in business, life sciences, healthcare, or related field.</p></li><li><p>10&#43; years of experience in the biopharmaceutical industry with 3-5&#43; years&#39; experience in oncology</p></li><li><p>Strong planning &amp; organizational skills, and the ability to work efficiently and effectively in a dynamic environment</p></li><li><p>Strong independent researching skills using a variety of modes from scientific publication, reputable internet and/or AI-supporting researching experience</p></li><li><p>Ability to influence without authority and drive towards a goal across multiple stakeholders</p></li><li><p>Effective time management skills. Ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity</p></li><li><p>Reliability, independence and punctuality (high level of professionalism)</p></li><li><p>Excellent verbal and written communication skills</p></li><li><p>Self-motivated, accountable, passionate, committed, invested in the business</p></li><li><p>Strong interpersonal skills</p></li><li><p>Ability to identify problems early and seek innovative solutions</p></li><li><p>Proficiency in Microsoft Office (Excel, PowerPoint &amp; Word)</p></li></ul><p><br /><b>Preferred Qualifications</b><br />If you have the following characteristics, it would be a plus:</p><ul><li><p>Advanced scientific degree (MD, MSc or PhD) and/or MBA</p></li><li><p>Specific training in marketing, forecasting/analytics, management consulting and leading teams</p></li><li><p>Bilingualism (English / French)</p></li><li><p>Experience supporting late-stage development, launch planning, or commercialization of oncology therapies</p></li></ul><p><br /><b>Working Pattern</b><br />This role is hybrid. You will be expected to be on-site in our Mississauga office 2-3 days per week for key meetings and team activities and work remotely as agreed with your manager.<br /><br /><b>What we offer</b><br />You will have the chance to shape programs that could change patient outcomes. You will work across diverse teams and grow your leadership and scientific expertise. We welcome applicants who bring curiosity, humility, and a commitment to inclusion. If you are motivated to make a real difference and to grow with us, please apply.</p><p></p><p>#LI-Hybrid</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?<br />Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. GSK is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at <a target="_blank" href="mailto:canada-recruitment&#64;gsk.com">canada-recruitment&#64;gsk.com</a>.  Please do not send resumes to this e-mail and instead apply through the online application process of this posting.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/oncology-pipeline-director-gsk/6a0897462f1861929d253330</link><guid isPermaLink="true">http://biotechroles.com/oncology-pipeline-director-gsk/6a0897462f1861929d253330</guid><pubDate>Sat, 16 May 2026 16:11:50 GMT</pubDate><company>GSK</company><location>Mississauga Milverton Drive</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Oncology Account Manager (Solid Tumor) Jacksonville, FL]]></title><description><![CDATA[<p><b>Territory includes </b><b><span>Jacksonville, FL, Ocala extending to some areas in Tallahassee. </span></b><b><b>The ideal candidat</b>e will live in Jacksonville, FL.</b></p><p>(Relocation assistance not provided).</p><p></p><p><span class="emphasis">Business Introduction:</span></p><p>Oncology is a core area of intensive focus at GSK, and while much progress has been made in the past few years, more can be done to REDEFINE EXPECTATIONS in cancer care. As we look to redefine expectations in Oncology, we need experienced, entrepreneurial-minded leaders to help us on this journey</p><p>.</p><p>Are you an experienced Oncology Sales Professional looking to be part of an innovative, dynamic and growing organization? GSK’s US Oncology team is looking for an Oncology Account Manager to manage the sales and business activities within a defined geographical business area. Key to this position is the ability to drive sales, leverage customer relationships and impact a variety of customer segments. This includes the design and implementation of business plans intended to increase revenue from targeted customers based upon strategic business analysis. You will understand and leverage roles and responsibilities of the cross functional team to drive sales results. These partners include Marketing, Medical Affairs, Market Access and Commercial Operations. Ideal candidates will have a deep knowledge of customers and accounts within Oncology, as well as the local dynamics that influence business in their area.</p><p>Being part of Oncology at GSK is being part of something special. The focus of the organization couldn’t be clearer – we are fueled by a personal passion to give our customers and our patients MORE. More of ourselves, more to fight for and more moments that matter!</p><p></p><p><span class="emphasis">Key Responsibilies:</span></p><p>This role will provide/give YOU the opportunity to lead key activities to progress YOUR career.</p><ul><li><p>Accountable for driving area sales results and ensuring open patient access to GSK therapies,</p></li><li><p>Develop and execute area business plans.</p></li><li><p>Identify and apply resources to the development of key prescribers/key account drivers within area.</p></li><li><p>Engage proactively with key customers and account groups to ensure the promotion of both GSK therapies and company image.</p></li><li><p>Work cross functionally to maximize brand availability and exposure within key accounts.</p></li><li><p>Work collaboratively with team and Regional Sales Director to ensure successful launch and/or ongoing promotion of branded products.</p></li><li><p>Engage with Regional Sales Director and cross functional partners on the development of programs and activities that will result in increased access to customers</p></li></ul><p></p><p><b>Why you?</b></p><p><span class="emphasis"><b>Basic Qualifications:</b></span></p><ul><li><p>4-year BA/BS degree from an accredited institution.</p></li><li><p>3&#43; years of pharmaceutical sales experience, Biologic/Specialty sales experience and/or 3&#43; years Clinical Oncology experience, Oncology education, patient care skills, and direct physician interface.</p></li><li><p>Valid Driver’s License - Must be able to drive or operate a vehicle – driving is an essential function of this role.</p></li><li><p>Must live in geography, no relocation assistance.</p></li><li><p>Ability to travel domestically as necessary, which may include overnight and/or weekend travel. The amount will depend on the specific territory size and may be up to 30%.</p></li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications:</b></span></p><p><b>If you have the following characteristics, it would be a plus:</b></p><ul><li><p>2&#43; years of Oncology sales and/or Specialty sales experience, Health System/Institutional experience is a strong preference.</p></li><li><p>Product marketing, specialty pharmacy, payer and state society experience a plus.</p></li><li><p>Strong organizational skills in order to maintain a high level of productivity, innovation and priority-setting in order to complete assignments on-time and on-budget.</p></li><li><p>Proven ability to think strategically and work with a high level of integrity, accuracy, and attention to detail.</p></li><li><p>Excellent oral and written communication skills for effectively interfacing with all levels of management and departments within the company.</p></li></ul><p></p><p>This role is field-based and requires regular travel within the assigned territory of up to 30%.<br /><br />We encourage you to apply if you are passionate about advancing oncology care and making a difference for patients and healthcare providers. Join us in shaping the future of cancer treatment.</p><p></p><p>#LI-GSK</p><p>#LI-REMOTE</p><p>#GSKOncology</p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/oncology-account-manager-solid-tumor-jacksonville-fl-gsk/6a0897452f1861929d25332f</link><guid isPermaLink="true">http://biotechroles.com/oncology-account-manager-solid-tumor-jacksonville-fl-gsk/6a0897452f1861929d25332f</guid><pubDate>Sat, 16 May 2026 16:11:49 GMT</pubDate><company>GSK</company><location>USA - Florida - Jacksonville</location><salary>$105000-145000</salary><type>Full time</type></item><item><title><![CDATA[Specialty Account Specialist (Respiratory) Phoenix, Arizona]]></title><description><![CDATA[<p><span class="emphasis">Business Introduction:</span><br />GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centered on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.<br />Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.<br />Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.<br /><br /><br /><span class="emphasis">Position Summary:</span><br />You will join our specialty respiratory team to support specialist healthcare providers across your territory. You will provide clear clinical education, help navigate access and reimbursement, and build strong professional relationships. We value curiosity, practical problem solving and teamwork. This role offers visible impact, career growth and a chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.</p><p></p><p><b>Territory Includes-</b><b> <span>Phoenix, Arizona, </span>Glendale, Peoria, Avondale, Litchfield Park, Prescott, Scottsdale, Sun City West.</b></p><p><b>The ideal candidate will reside in Phoenix, Arizona. </b></p><p><b>(Relocation assistance not provided).</b></p><p></p><p></p><p><span class="emphasis">Responsibilities:</span></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><ul><li><p>Build and maintain strong relationships with specialist customers, including pulmonologists, allergists, nurse specialists and practice managers.</p></li><li><p>Deliver clear, evidence-based clinical education and support to specialist teams.</p></li><li><p>Identify reimbursement and distribution needs and connect customers with appropriate support resources.</p></li><li><p>Develop tailored account plans and tactics to drive patient access and service.</p></li><li><p>Work closely with cross-functional partners, including market access, medical affairs, and marketing.</p></li><li><p>Adhere to compliance and ethical guidelines in all customer interactions.</p></li></ul><p><br /><b>Why You?</b><br /><br /><span class="emphasis">Basic Qualifications:</span><br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li><p>Bachelor’s degree from an accredited institution.</p></li><li><p>Experience engaging specialty healthcare providers in respiratory or related therapeutic areas.</p></li><li><p>Ability to travel domestically, including occasional overnight travel up to 30%.</p></li><li><p>Valid driver’s license and willingness to drive as required for the role.</p></li><li><p>The selected candidate will be hired at the appropriate level based on experience:</p><ul><li><p><b>Specialty Account Specialist (grade 8)</b>: 5&#43; years of pharmaceutical or medical device sales experience.</p></li><li><p><b>Senior Specialty Account Specialist (grade 7)</b>: 12&#43; years of pharmaceutical or medical device sales experience.</p></li></ul></li></ul><p></p><p><span class="emphasis">Preferred Qualifications:</span><br />If you have the following characteristics, it would be a plus:<br />Experience with specialty products using Buy &amp; Bill or specialty pharmacy distribution channels.</p><ul><li><p>Familiarity working with payer reimbursement or market access teams.</p></li><li><p>Background in biologic, rare disease, immunology or respiratory/pulmonology specialty sales.</p></li><li><p>Experience selling into integrated delivery networks (IDNs) or hospital systems.</p></li><li><p>Infusion experience.</p></li><li><p>Specialty pharmacy experience.</p></li><li><p>Proven ability to develop account plans and track measurable outcomes.</p></li><li><p>Comfortable working in a primarily remote role with occasional in-person and hybrid team activities.</p></li><li><p>Strong communication skills and a customer-focused mindset.</p></li></ul><p><br /><span class="emphasis">Work Arrangement/Location:</span></p><p>This position is primarily field-based and requires regular travel within an assigned territory. The role is hybrid in nature, combining remote work with in-person customer engagement and office collaboration as needed.</p><p></p><p>#LI-GSK</p><p>#SpecialtyCareers</p><p>#LI-Remote</p><p>#GSKCommercial</p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/specialty-account-specialist-respiratory-phoenix-arizona-gsk/6a0897452f1861929d25332e</link><guid isPermaLink="true">http://biotechroles.com/specialty-account-specialist-respiratory-phoenix-arizona-gsk/6a0897452f1861929d25332e</guid><pubDate>Sat, 16 May 2026 16:11:49 GMT</pubDate><company>GSK</company><location>USA - Arizona - Phoenix</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Specialty Account Specialist (Respiratory) Tucson, Arizona]]></title><description><![CDATA[<p><span class="emphasis">Business Introduction:</span><br />GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centered on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.<br />Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.<br />Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.<br /><br /><br /><span class="emphasis">Position Summary:</span><br />You will join our specialty respiratory team to support specialist healthcare providers across your territory. You will provide clear clinical education, help navigate access and reimbursement, and build strong professional relationships. We value curiosity, practical problem solving and teamwork. This role offers visible impact, career growth and a chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.</p><p></p><p><b>Territory Includes-</b><b> Tucson, Arizona, Mesa, Chandler, <span>Phoenix, Gilbert, and Flagstaff.</span> The ideal candidate will reside in Tucson, Arizona. </b></p><p><b>(Relocation assistance not provided).</b></p><p></p><p><span class="emphasis">Responsibilities:</span></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><ul><li><p>Build and maintain strong relationships with specialist customers, including pulmonologists, allergists, nurse specialists and practice managers.</p></li><li><p>Deliver clear, evidence-based clinical education and support to specialist teams.</p></li><li><p>Identify reimbursement and distribution needs and connect customers with appropriate support resources.</p></li><li><p>Develop tailored account plans and tactics to drive patient access and service.</p></li><li><p>Work closely with cross-functional partners, including market access, medical affairs, and marketing.</p></li><li><p>Adhere to compliance and ethical guidelines in all customer interactions.</p></li></ul><p><br /><b>Why You?</b><br /><br /><span class="emphasis">Basic Qualifications:</span><br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li><p>Bachelor’s degree from an accredited institution.</p></li><li><p>Experience engaging specialty healthcare providers in respiratory or related therapeutic areas.</p></li><li><p>Ability to travel domestically, including occasional overnight travel up to 30%.</p></li><li><p>Valid driver’s license and willingness to drive as required for the role.</p></li><li><p>The selected candidate will be hired at the appropriate level based on experience:</p><ul><li><p><b>Specialty Account Specialist (grade 8)</b>: 5&#43; years of pharmaceutical or medical device sales experience.</p></li><li><p><b>Senior Specialty Account Specialist (grade 7)</b>: 12&#43; years of pharmaceutical or medical device sales experience.</p></li></ul></li></ul><p></p><p><span class="emphasis">Preferred Qualifications:</span><br />If you have the following characteristics, it would be a plus:<br />Experience with specialty products using Buy &amp; Bill or specialty pharmacy distribution channels.</p><ul><li><p>Familiarity working with payer reimbursement or market access teams.</p></li><li><p>Background in biologic, rare disease, immunology or respiratory/pulmonology specialty sales.</p></li><li><p>Experience selling into integrated delivery networks (IDNs) or hospital systems.</p></li><li><p>Infusion experience.</p></li><li><p>Specialty pharmacy experience.</p></li><li><p>Proven ability to develop account plans and track measurable outcomes.</p></li><li><p>Comfortable working in a primarily remote role with occasional in-person and hybrid team activities.</p></li><li><p>Strong communication skills and a customer-focused mindset.</p></li></ul><p><br /><span class="emphasis">Work Arrangement/Location:</span></p><p>This position is primarily field-based and requires regular travel within an assigned territory. The role is hybrid in nature, combining remote work with in-person customer engagement and office collaboration as needed.</p><p></p><p>#LI-GSK</p><p>#SpecialtyCareers</p><p>#LI-Remote</p><p>#GSKCommercial</p><p></p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/specialty-account-specialist-respiratory-tucson-arizona-gsk/6a0897442f1861929d25332d</link><guid isPermaLink="true">http://biotechroles.com/specialty-account-specialist-respiratory-tucson-arizona-gsk/6a0897442f1861929d25332d</guid><pubDate>Sat, 16 May 2026 16:11:48 GMT</pubDate><company>GSK</company><location>USA - Arizona - Tucson</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Becario Area Finanzas Roche]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Sobre Roche</b></p><p></p><p>En Roche, nos impulsa el propósito de innovar en ciencia y apoyar transformaciones al sistema de salud para asegurar que las generaciones presentes y futuras disfruten de más y mejor tiempo con sus seres queridos. Creemos que la innovación no solo está en nuestros medicamentos, sino también en la excelencia de nuestros procesos internos.</p><p></p><p><b>La Oportunidad</b></p><p></p><p>Buscamos un becario proactivo con interés en tener una experiencia profesional de alto impacto en el área financiera, específicamente en Procurement y Supply Chain. En este rol, participarás en proyectos estratégicos para impulsar la eficiencia y agilidad operativa, experimentando la vida laboral en una farmacéutica de alta especialidad líder en el mundo.</p><p></p><p><b>Tus Responsabilidades</b></p><ul><li><p><b>Due Diligence:</b> Mantener el tracker al día y asegurar que la documentación esté completa en gDrive.</p></li><li><p><b>Procesos de Licitación:</b> Gestionar procesos de invitación a cotizar, asegurando el cumplimiento de los timelines y el resguardo de documentación.</p></li><li><p><b>Data &amp; Analytics:</b> Mantener actualizadas las gráficas del Dashboard de Procurement y realizar la extracción de reportes.</p></li><li><p><b>Gestión de Contenidos:</b> Actualizar el GSite de Procurement y el material de capacitación según los requerimientos.</p></li><li><p><b>Soporte Operativo:</b> Apoyo en el seguimiento al proceso de alta de proveedores.</p></li><li><p><b>Gestión de Órdenes:</b> Registro y seguimiento de órdenes de compra (OC), garantizando precisión en datos y disponibilidad de stock.</p></li><li><p><b>Cumplimiento Normativo:</b> Control y elaboración de cartas de canje y corta caducidad.</p></li><li><p><b>Reporting:</b> Extracción de datos para la actualización de indicadores clave (KPIs) del área.</p></li></ul><p></p><p><b>¿Quién eres?</b></p><p></p><p>Para destacar en este rol, buscamos el siguiente perfil:</p><ul><li><p><b>Formación:</b> Estudiante activo de <b>Ingeniería Industrial, Negocios Internacionales, Finanzas</b> o carreras afines.</p></li><li><p><b>Mindset:</b> Gran motivación por aprender, proactividad y una marcada orientación a resultados.</p></li><li><p><b>Pasión:</b> Interés por el manejo de información, el análisis de datos y la mejora continua de procesos.</p></li><li><p><b>Habilidades:</b> Capacidad para desarrollar visión estratégica y gestión de proyectos dentro del sector salud.</p></li></ul><p></p><p></p><p><b>Beneficios de reubicación no están disponibles para esta posición.</b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/becario-area-finanzas-roche-roche/6a0896772f1861929d25332c</link><guid isPermaLink="true">http://biotechroles.com/becario-area-finanzas-roche-roche/6a0896772f1861929d25332c</guid><pubDate>Sat, 16 May 2026 16:08:23 GMT</pubDate><company>Roche</company><location>Mexico City</location><salary>$8000-12000</salary><type>Full time</type></item><item><title><![CDATA[Process Owner - Administrative Engagement Services]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Como </span><b><b>Process Owner - Administrative Engagement Services</b><span>, </span></b><span>serás responsable de gestionar y optimizar los procesos administrativos de la célula de Engagement, la cual centraliza el soporte para las interacciones de Roche con actores clave del sector salud (profesionales, organizaciones, programas de pacientes y donaciones). En este rol, actuarás como guardián del cumplimiento normativo y líder de mejora continua, asegurando que cada contrato, pago o colaboración se ejecute con excelencia operativa y bajo los más altos estándares éticos. </span></p><p></p><p><b><b>The Opportunity</b></b></p><ul><li><p><span>Liderar proyectos de optimización, simplificación y automatización de procesos para mejorar los tiempos de respuesta y la eficiencia operativa.</span></p></li><li><p><span>Actuar como experto (SME) orientando a los stakeholders internos y externos en la ejecución correcta de interacciones con actores del sector salud.</span></p></li><li><p><span>Negociar y monitorear los Acuerdos de Nivel de Servicio (SLAs) con los clientes internos para alinear expectativas y capacidad de respuesta.</span></p></li><li><p><span>Gestionar el equipo de soporte transaccional y personal externo en el procesamiento de contratos, órdenes de compra y documentos de estudios clínicos o donaciones.</span></p></li><li><p><span>Definir y mantener actualizadas las políticas y procedimientos del área buscando la estandarización de los servicios bajo estándares de cumplimiento.</span></p></li><li><p><span>Implementar métricas y KPIs para evaluar la capacidad del equipo y realizar análisis de datos que apoyen la toma de decisiones estratégicas.</span></p></li><li><p><span>Aplicar principios de metodologías ágiles (Scrum y Lean Management) para gestionar el backlog de solicitudes y facilitar reuniones de seguimiento.</span></p></li></ul><p></p><p><b><b>Who you are</b></b></p><ul><li><p><span>Profesional en Ingeniería Industrial (preferiblemente), Ingeniería Química, Química Farmacéutica o Administración de Empresas.</span></p></li><li><p><span>Experiencia mínima de 2 a 4 años en gestión de procesos administrativos, centros de servicios compartidos (SSC), optimización de procesos o gestión de proyectos.</span></p></li><li><p><span>Experiencia previa en la industria farmacéutica o sector salud (preferible).</span></p></li><li><p><span>Dominio del idioma inglés a nivel avanzado (B2-C1) para interactuar en un entorno multinacional.</span></p></li><li><p><span>Conocimiento y aplicación demostrable de metodologías ágiles como Scrum, Six Sigma o Lean Management.</span></p></li><li><p><span>Mentalidad analítica y metódica con capacidad demostrada para influir en diversos stakeholders.</span></p></li></ul><p></p><p><span>Esta posición no ofrece beneficios de relocalización. </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/process-owner-administrative-engagement-services-roche/6a0896762f1861929d25332b</link><guid isPermaLink="true">http://biotechroles.com/process-owner-administrative-engagement-services-roche/6a0896762f1861929d25332b</guid><pubDate>Sat, 16 May 2026 16:08:22 GMT</pubDate><company>Roche</company><location>Bogota</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Patient Journey Partner Oncología - Fixed term 6 meses]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>En Roche Bolivia nos encontramos en búsqueda de un/a </span><b>Patient Journey Partner (PJP)</b> <span>para el área terapéutica de </span><b>Oncología</b> <span>idealmente basado en </span><b>Santa Cruz, Bolivia</b><span>, quien  es un líder empoderado y referente de contacto local con Roche, que se vincula con todos los actores del ecosistema de salud involucrados directamente a la jornada del paciente (en determinadas áreas de enfermedades o terapéuticas), de manera de co-crear soluciones significativas para su mejora, conectando con las capacidades que todo Roche puede disponer para ello.  </span></p><p></p><p><b>La oportunidad: </b></p><ul><li><p><span>Siendo un aliado confiable y punto de contacto primario (pero no exclusivo), se conecta </span><br /><span>con todos los actores involucrados en la jornada del paciente, buscando identificar las </span><br /><span>oportunidades para mejorarla lo más efectiva y rápidamente posible.  Para lograrlo, </span><br /><span>además conecta y pone a disposición del ecosistema toda la capacidad, la ciencia y el </span><br /><span>conocimiento del que Roche dispone.  </span></p></li><li><p><span>Al velar por la jornada del paciente en su totalidad, el/la PJP actúa como un pensador </span><br /><span>sistémico, con la capacidad de identificar un propósito compartido entre las partes </span><br /><span>interesadas y para co-crear soluciones en el ecosistema. </span></p></li><li><p><span>En alianza con todos los actores que participan en la jornada del paciente (incluidos </span><br /><span>los pacientes), busca remover barreras y desbloquear oportunidades para ofrecer </span><br /><span>soluciones valiosas a los pacientes y a la comunidad. </span></p></li><li><p><span>Comparte internamente las necesidades de los pacientes y los actores </span><br /><span>directamente vinculados, prioriza, asegura recursos y desarrolla soluciones que </span><br /><span>busquen mejorar los resultados lo más pronto posible.</span></p></li><li><p><span>Vela por el uso apropiado de los productos de Roche a lo largo de todo su ciclo de </span><br /><span>vida, lo que incluye entre otros, compartir información al respecto con profesionales </span><br /><span>de la salud en una forma veraz y balanceada.   </span></p></li><li><p><span>Está facultado para disponer de recursos a nivel local y de la red según sea </span><br /><span>necesario, incluida la colaboración con otros PJP y HSP.  </span></p></li><li><p><span>Busca garantizar una excelente experiencia, cada vez que las partes interesadas se </span><br /><span>relacionen con los empleados, los productos y los servicios de Roche. </span></p></li><li><p><span>Como empleado de Roche, comprende y respeta todas las políticas, programas, </span><br /><span>procedimientos e instrucciones relacionados a SHE, farmacovigilancia y compliance (esto incluye reportar incidentes e informar a quien sea apropiado en cada </span><br /><span>situación).  </span></p></li></ul><p></p><p><b>Quién eres</b><br /> </p><ul><li><p><span>Grado universitario (ciencias, economía o negocios) es altamente deseable. Un grado </span><br /><span>avanzado en ciencias de la vida y / o MBA es valorado. </span></p></li><li><p><span>Experiencia y conocimiento en el mercado de enfermedades raras, hematología y/o neurología del país.</span></p></li><li><p><span>Experiencia comercial, representación y/o visita médica, líder de cuentas claves entre otras. </span></p></li><li><p><span>Profundo conocimiento de la jornada del paciente y procedimientos médicos relacionados en determinada área de enfermedad, que permita el relacionamiento con especialistas en el tema.</span></p></li><li><p><span>Robusto conocimiento de estrategias y tácticas de asuntos médicos, incluyendo </span><br /><span>investigación clínica.    </span></p></li><li><p><span>Se requiere excelentes habilidades de relacionamiento con las partes interesadas, </span><br /><span>incluidos expertos del área terapéutica de oftalmología y organizaciones relacionadas.  </span><br /><span>Es altamente deseable experiencia en trabajo conjunto con agrupaciones de pacientes.  </span><br /><span>Sólida base y visión de negocio, con conocimientos en asuntos médicos, asuntos </span><br /><span>comerciales y experiencia del cliente.  </span></p></li><li><p><span>Se requiere experiencia en el liderazgo de equipos multifuncionales. Es muy deseable </span><br /><span>tener experiencia tanto en la formulación de estrategias multifuncionales como en la </span><br /><span>orquestación de equipos multifuncionales. </span></p></li><li><p><span>Capaz de comprender y aprovechar los medios y herramientas digitales.  </span><br /><span>Es deseable experiencia en formas de trabajo ágil.  </span></p></li><li><p><span>Manejo del idioma inglés es deseable. </span></p></li></ul><p></p><p><span>Note: This role does not have relocation benefits. </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/patient-journey-partner-oncologia-fixed-term-6-meses-roche/6a0896762f1861929d25332a</link><guid isPermaLink="true">http://biotechroles.com/patient-journey-partner-oncologia-fixed-term-6-meses-roche/6a0896762f1861929d25332a</guid><pubDate>Sat, 16 May 2026 16:08:22 GMT</pubDate><company>Roche</company><location>Santa Cruz</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Especialista de Compliance, Riscos e Auditoria]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><h2><span>Como Especialista de Compliance, Riscos e Auditoria, você irá atuar como um parceiro estratégico que assegura a conformidade com frameworks globais e legislação local. Você será responsável por monitorar o ciclo de riscos, conduzir auditorias e promover uma cultura de integridade, transformando análises complexas em planos de mitigação práticos e melhorias contínuas que protejam o negócio e suportem a tomada de decisão da liderança</span>.</h2><p></p><p><b><span>Sobre a oportunidade: </span></b></p><p></p><ul><li><p><span>Coordenação do ciclo anual de Riscos e Oportunidades, garantindo que a metodologia esteja alinhada às estratégias globais e locais.</span></p></li><li><p><span>Suporte às áreas de negócio na identificação de riscos e no desenvolvimento de planos de ação para ameaças estratégicas, operacionais e de compliance.</span></p></li><li><p><span>Acompanhamento constante da implementação das melhorias e reporte estruturado da evolução dos riscos para a alta liderança.</span></p></li><li><p><span>Revisão de políticas internas para garantir conformidade regulatória e condução de auditorias temáticas com foco em recomendações práticas.</span></p></li><li><p><span>Atuação como principal ponto de contato com o time global (Assuntos Governamentais e Assuntos Regulatórios), assegurando o alinhamento de diretrizes e a atualização de ferramentas corporativas.</span></p></li><li><p><span>Execução do programa local, com foco em </span><i>due diligence</i><span>, análise de riscos de parceiros e implementação de métricas de efetividade.</span></p></li><li><p><span>Revisão contínua de políticas e procedimentos internos para garantir total alinhamento entre as normas globais e as legislações locais.</span></p></li><li><p><span>Promoção da cultura de integridade por meio de treinamentos, campanhas de engajamento e planos de </span><i>lessons learned</i><span> baseados em desvios identificados.</span></p></li></ul><p></p><p><b><span>Habilidades e Experiências desejadas: </span></b></p><ul><li><p><span>Graduação completa em Contabilidade, Engenharia, Administração, Economia, Finanças ou áreas correlatas;</span></p></li><li><p><span>Inglês avançado e Espanhol desejável.</span></p></li><li><p><span>Experiência em Auditoria, Riscos e Compliance</span></p></li><li><p><span>Proficiência em normas e regulamentos de compliance, bem como em metodologias de gestão de risco</span></p></li><li><p><span>Conhecimento em frameworks (COSO, ISO), SAP,  ferramentas de análise de dados e governança corporativa</span></p></li><li><p><span>Experiência em gestão de projetos;</span></p></li><li><p><span>Disponibilidade para atuar em modelo híbrido (3x na semana no escritório - Zona Sul de São Paulo)</span></p></li></ul><p></p><h3>Os benefícios de realocação não estão disponíveis para essa posição.</h3><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/especialista-de-compliance-riscos-e-auditoria-roche/6a0896762f1861929d253329</link><guid isPermaLink="true">http://biotechroles.com/especialista-de-compliance-riscos-e-auditoria-roche/6a0896762f1861929d253329</guid><pubDate>Sat, 16 May 2026 16:08:22 GMT</pubDate><company>Roche</company><location>Sao Paulo</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Estagiario Tecnologia Informacao]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Sobre Roche:</b></p><p>Um futuro mais saudável. É isso que nos impulsiona a inovar. Avançar continuamente na ciência e garantir que todos tenham acesso à saúde - hoje e nas gerações futuras. Criando um mundo onde todos nós teremos mais tempo com as pessoas que amamos. É isso que nos faz Roche.</p><p><span>A Roche Diagnóstica, líder mundial em diagnósticos in vitro, dedica-se a soluções de diagnóstico laboratorial. Atuamos para oferecer produtos e serviços exclusivos, além de testes inovadores para pesquisadores, médicos, paciente</span>s, hospitais e laboratórios.</p><div></div><p><b>A Oportunidade:</b></p><ul><li><p><b>Suporte local (supervisionado):</b> Atuação em Soluções de Informação na resolução de problemas em clientes, realizando o escalonamento de casos para níveis superiores (Especialistas, Latam/GCS), quando necessário.</p></li><li><p><b>Colaboração técnica:</b> Interação direta com o Especialista e o Coordenador de Soluções de Informação para identificar e resolver problemas nos sistemas da Roche.</p></li><li><p><b>Análise e Investigação:</b> Investigação de problemas através da coleta e análise de dados, além da documentação e compreensão de demandas.</p></li><li><p><b>Comunicação:</b> Elaboração de relatórios, apresentações (PPT) e comunicações orais para o compartilhamento de informações técnicas.</p></li><li><p><b>Compliance:</b> Apoio às iniciativas da afiliada para reforçar nossa cultura de conformidade, atuando de forma ética e respeitando o Código de Conduta.</p></li></ul><p></p><p><b>Requerimentos:</b></p><ul><li><p><b>Formação:</b> Cursando graduação em áreas relacionadas à TI (Ciências da Computação, Sistemas de Informação, Engenharia de Software e correlatos).</p></li><li><p><b>Idiomas:</b> Inglês ou Espanhol em nível intermediário a avançado.</p></li><li><p><b>Autonomia:</b> Capacidade de desenvolver o trabalho sem supervisão constante.</p></li></ul><p></p><p><b>Sobre você:</b></p><p>Buscamos um perfil analítico, ágil e resolutivo. Você deve ser capaz de trabalhar de forma colaborativa com equipes multidisciplinares e possuir uma comunicação aberta para interagir com diferentes níveis da organização e clientes.</p><p></p><p></p><p><b>Benefícios de realocação não estão disponíveis para esta posição.</b></p><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/estagiario-tecnologia-informacao-roche/6a0896762f1861929d253328</link><guid isPermaLink="true">http://biotechroles.com/estagiario-tecnologia-informacao-roche/6a0896762f1861929d253328</guid><pubDate>Sat, 16 May 2026 16:08:22 GMT</pubDate><company>Roche</company><location>Sao Paulo</location><salary>$1000-1000</salary><type>Full time</type></item><item><title><![CDATA[Strategic Quality Partner]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><p style="text-align:inherit"></p><h3></h3><p></p><h3>The Position</h3><p><span>At Roche, we are passionate about transforming patients’ lives, and we are bold in both decision and action - we believe that good business means a better world. That is why we come to work every single day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. Roche is strongly committed to an inclusive workplace. We strive to build teams that represent a range of backgrounds, perspectives, and skills. Embracing inclusion and belonging enables us to create a great place to work and to innovate for patients.</span></p><p></p><p><span>The Strategic Quality Partner acts as a single point of contact within project teams (New product development / Product Change) for a portfolio of products assigned to them. The SQP leads and drives for decisions for strategic topics from a compliance and product quality perspective. The SQP partners with internal and external stakeholders across the value chain to accelerate the development process and incorporate learnings. Stakeholders include, but are not limited to Development Leads, Project Leaders, Regulatory Affairs, Operations, Global Customer Support, and Post-Market Quality.</span></p><p></p><p><b><b>The Opportunity</b></b></p><ul><li><p><span>Ensure consistent interpretation &amp; implementation of global requirements across Customer Areas (CAs)</span></p></li><li><p><span>Incorporate lessons learned from all areas of quality across Customer Areas (CA) into project support and ensure PostMarket Quality feedback is built into the requirements</span></p></li><li><p><span>Ensure development project plans contain the right deliverables according to the Design &amp; Development module to deliver safe and compliant solutions</span></p></li><li><p><span>Support internal and external audits</span></p></li><li><p><span>Lead and facilitate constructive discussions e.g. at project team meetings</span></p></li><li><p><span>Drive awareness and adoption of the Risk Enabler inside and outside of Global Quality &amp; Regulatory decision making; prepare and enable risk-based decisions</span></p></li><li><p><span>Partner to ensure effective resolution of issues (e.g. CAPA, NC)</span></p></li><li><p><span>Ensure effective feedback loops and information flow for milestone review.</span></p></li></ul><p></p><p><b><b>Who You Are</b></b></p><ul><li><p><span>Bachelor&#39;s degree in science, engineering, business administration or a related field. MBA or advanced degree is considered an advantage.</span></p></li><li><p><span>8&#43; years of experience in the diagnostics industry or a related field in business related</span> f<span>unctions</span></p></li><li><p><span>Strong scientific and technical background with sound product knowledge, ideally with assay/reagents/system/hardware/software development experience for IVD Products.</span></p></li><li><p><span>Strong business and financial acumen with an enterprise mindset</span></p></li><li><p><span>Knowledge of Regulations pertaining to the environment (i.e. ISO 13485, ISO 14971, GDP, GMP, others)</span></p></li><li><p><span>Excellent communication, presentation, and negotiation skills.</span></p></li><li><p><span>Strong agile knowledge and capabilities demonstrating new ways of working</span></p></li><li><p><span>Pragmatic decision making and ability to move forward without a perfect solution</span></p></li><li><p><span>Demonstrated thorough E2E understanding for lifecycle management</span></p></li><li><p><span>Strong leadership capabilities, with experience in leading cross-functional teams (Squad Lead, Matrix Lead) and driving change.</span></p></li></ul><p></p><p><b><b>Locations</b></b></p><p><span>You are located in Carlsbad, CA.  This is a primarily onsite role.</span></p><p></p><p><span>Relocation benefits are not available for this position.</span></p><p></p><p><span>The expected salary range for this position based on the primary location of Carlsbad is $103,800 and $221,780.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</span></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left"><span>GenMark is now a proud member of the Roche Group, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare.  As a global leader in healthcare, Roche Diagnostics offers a broad portfolio of products, tools and services that help in the prevention, diagnosis and management of diseases like HPV, HIV, hepatitis and diabetes as well as other medical conditions, such as fertility and blood coagulation. With the addition of GenMark to the Roche Group, syndromic infectious disease diagnostics is now added to the long list of disease states and conditions that the Roche Group addresses.  GenMark’s ePlex true sample-to-answer system offers unique solutions to address the most significant challenges facing clinical laboratories, while supporting hospital systems to deliver patient-centered, value-based care. ePlex streamlines the diagnostic workflow from physician order entry to the final test report and is the true sample-to-answer solution designed to improve patient care, reduce costs, and increase lab efficiency. GenMark is headquartered in Carlsbad, California.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>GenMark is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a target="_blank" href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/strategic-quality-partner-roche/6a0896762f1861929d253327</link><guid isPermaLink="true">http://biotechroles.com/strategic-quality-partner-roche/6a0896762f1861929d253327</guid><pubDate>Sat, 16 May 2026 16:08:22 GMT</pubDate><company>Roche</company><location>Carlsbad</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Security Engineer - Monitoring & Incident Response]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b><b>Let’s build a healthier future, together.  </b></b><br /><span>By combining our unique strengths, we’re redefining healthcare through sustainable action and innovation. Discover what it’s like to work at Roche.</span></p><p></p><p><span><b>The Opportunity</b></span></p><p>The Global Security Monitoring and Incident Response (MIR) team at Roche strives to keep our networks and users safe from constantly evolving threats. As a Security Engineer on the Vulnerability and Exposure Management Team, you will help protect sensitive data and defend computer systems and web applications from existing and emerging threats. You will not just be managing scanner output. You will help manage and reduce existing risks, assess and evaluate the weaponization of emerging risks, and act as a core builder of our future capabilities.</p><p></p><p><b>Responsibilities</b></p><ul><li><p>Triage, investigate, and respond to critical vulnerabilities affecting Roche</p></li><li><p>Evaluate and prioritize vulnerabilities found through our tools, including our bug-bounty program</p></li><li><p>Research emerging vulnerabilities and develop methods to confirm exploitability against our attack surface</p></li><li><p>Communicate risk and work with system owners and other stakeholders to mitigate security vulnerabilities</p></li><li><p>Assess company systems and web applications using both automated and manual tools</p></li><li><p>Maintain, improve, and engineer our scanning, detection, and automation solutions</p></li><li><p>Participating in security monitoring for a global environment</p></li></ul><p></p><p><b>Who you are</b></p><ul><li><p>Associate degree in relevant field or 5&#43; years in information security and fluent English.</p></li><li><p>Programming experience (Python, Node.js, JavaScript) and ability to write custom detection logic, scripts, and templates</p></li><li><p>Demonstrated ability to triage, analyze, and escalate vulnerabilities; experience validating vulnerabilities and basic exploit development in large global environments</p></li><li><p>Focus on web application, network, and computer security; cloud security experience; familiarity with attack surface management and AI-assisted development tools</p></li><li><p>Strong communication skills explaining complex risks to non-technical audiences; comfort balancing operational tasks with research; passion for security</p></li><li><p>Industry certifications in offensive security (OSCP, GWAPT, OSWE); open-source security project contributions</p></li></ul><p></p><p><b>Relocation benefits are not available for this job posting.</b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/security-engineer-monitoring-and-incident-response-roche/6a0896752f1861929d253326</link><guid isPermaLink="true">http://biotechroles.com/security-engineer-monitoring-and-incident-response-roche/6a0896752f1861929d253326</guid><pubDate>Sat, 16 May 2026 16:08:21 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Mexico Pharma Human Resources Director]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>This position has the mindset of a business leader and entrepreneur.  You will act as a strategic architect for the Mexico affiliate. You are responsible for translating long-term business strategy into &#34;fit-for-purpose&#34; P&amp;C initiatives that drive organizational agility and accelerated growth. You will partner flexibly across leadership areas to foster VACC leadership, advance organizational design, and secure future talent capabilities. In this role, you also serve as the Country Connector for Mexico, managing external system shaping and internal cultural stewardship for the site. Legal entity representation for the organization. The Mexico Pharma affiliate is home to &#43;280 collaborators and</span> generated CHF 423 million in revenue in 2025. <span>.</span></p><p></p><p><b>The Opportunity: </b></p><p></p><p><u>Business Acumen</u></p><ul><li><p><span>Aligns P&amp;C strategy, goals, and objectives to overall business strategies and objectives; translates P&amp;C strategies to drive key business results; provides guidance on talent management, workforce strategies, organization design and reward and recognition in partnership with Business Partners (Enterprise), other Chapters and subject-matter experts to develop high quality solution</span></p></li><li><p><span>Maintains broad-based knowledge of multiple leadership areas across the organization and its operations; uses knowledge of business and P&amp;C insights, metrics, expertise, and decision principles to effectively diagnose topics with a wide range of complexity</span></p></li><li><p><span>Recommends business practice/work process improvements to identify opportunities for leveraging human capital; ensures all P&amp;C initiatives have ROI that adds to organizational value</span></p></li><li><p><span>Maintains knowledge of external environment and other related information on peer and comparison groups to effectively diagnose and implement strategies to help drive business decisions</span></p></li></ul><p></p><p><u>Leadership</u></p><ul><li><p><span>Strategic Coaching: Act as a trusted partner and coach for senior leaders to foster a leadership culture aligned with the Roche Leadership Framework</span></p></li><li><p><span>HPO Leadership: Drive High-Performing Organization (HPO) transformations to evolve organizational behaviors, mindsets, and ways of working</span></p></li><li><p><span>Translates the business vision, mission, and strategy along with the 10 year ambition and P&amp;C Aspirational Goals into projects and initiatives with milestones and delivery schedules; leads or participates i n WPTs/squads to effectively meet planned objectives; develops clear action plans with results-oriented goals for measuring success; drives alignment and buy-in within multiple leadership areas as part of a network</span></p></li><li><p><span>Diagnoses P&amp;C needs and identifies interventions that address issues of retention, change leadership, employee engagement, and leadership development, partnering with Enterprise Business Partners, WPTs/squads and other P&amp;C Chapters as appropriate; uses appropriate tools for leadership competency and skills assessment.</span></p></li><li><p><span>Engagement &amp; Culture: Continuously improve the employee experience, driving measurable increases in satisfaction (eSAT) and fostering a diverse, inclusive culture.</span></p></li><li><p><span>Drives and implements change with proven ability to influence business leaders and P&amp;C professionals to required outcomes</span></p></li></ul><p></p><p><u>Strategic P&amp;C Insights &amp; Innovation</u></p><ul><li><p><span>Gathers and analyzes internal and external data, evidence-based research, benchmarks,</span></p></li><li><p><span>P&amp;C and business metrics to make critical decisions; shares insights with leaders and recommends innovative solutions based on the P&amp;C decision principles that support the culture, strategic direction and resources</span></p></li><li><p><span>Diagnoses root causes of work environment issues, disruptive team dynamics and ineffective organizational setups; initiates interventions and shapes solutions in collaboration and co-creation with key stakeholders across multiple leadership areas</span></p></li></ul><p><br /> </p><p><b>Who you are</b>:</p><ul><li><p><span>8&#43; years of broad and progressive strategic P&amp;C Business Partnering experience required, preferably within the biotechnology or pharmaceutical industries</span></p></li><li><p><span>Bachelor&#39;s degree in Human Resources (or related field) preferred, and/or equivalent work experience, advanced degree preferred</span></p></li><li><p><span>Exemplifies strong leadership skills, with or without direct reports and demonstrates the potential to take on broader and more impactful P&amp;C enterprise roles</span></p></li><li><p><span>Systems thinker, proven ability to work effectively across multiple business areas, teams and key leadership areas in a fast paced environment </span></p></li><li><p><span>Passion for and focus on building a diverse and inclusive work culture</span></p></li><li><p><span>Proven ability to lead with a creative mindset, acting as a coach and mentor for leaders </span></p></li><li><p><span>Ability to influence with courageous authenticity and build trust with individuals at all levels within the organization, challenging the status quo when appropriate</span></p></li><li><p><span>Effectively diagnosing long term P&amp;C needs, and shaping and leading initiatives to address them</span></p></li><li><p><span>Strong communication skills (written and verbal) to effectively address all organizational levels </span></p></li><li><p><span>Biotechnology or pharmaceutical industries, or sales organizations experience are preferred</span></p></li><li><p><span>Fluent in English and Spanish is a must</span></p></li></ul><p></p><p><span>The position may be elegible for relocation benefits.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/mexico-pharma-human-resources-director-roche/6a0896742f1861929d253325</link><guid isPermaLink="true">http://biotechroles.com/mexico-pharma-human-resources-director-roche/6a0896742f1861929d253325</guid><pubDate>Sat, 16 May 2026 16:08:20 GMT</pubDate><company>Roche</company><location>Mexico City</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Executive Assistant]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>As the Executive Assistant to the Country President, you will serve as a strategic partner and trusted advisor, ensuring operational excellence and enabling the Country President to focus on high-impact priorities. This role demands exceptional organizational skills, discretion, and agility to manage complex workflows in a fast-paced, multinational environment. You will coordinate the leadership team’s operating rhythm, manage sensitive information, and translate strategic priorities into actionable plans and measurable outcomes.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities</b></p><p></p><p><b>Executive Support &amp; Leadership Coordination</b></p><ul><li><p>Manage and optimize the Country President’s calendar, prioritizing strategic engagements and anticipating contingencies.</p></li><li><p>Prepare high-quality executive materials, including briefings, presentations, decision papers, and reports.</p></li><li><p>Maintain an action and decision tracker to ensure accountability and timely execution across leadership initiatives.</p></li></ul><p><b>Governance, Compliance &amp; Risk Management</b></p><ul><li><p>Oversee governance processes, including leadership meetings, quarterly reviews, compliance forums, and audit preparation.</p></li><li><p>Ensure strict adherence to company policies and local regulations, safeguarding confidentiality and compliance.</p></li><li><p>Coordinate mandatory reporting and maintain audit-ready documentation.</p></li></ul><p><b>Stakeholder Engagement &amp; Communication</b></p><ul><li><p>Act as a liaison between the Country President and internal/external stakeholders, including regional/global teams and industry bodies.</p></li><li><p>Support external engagements with strategic partners, ensuring protocol compliance.</p></li><li><p>Draft and review executive communications for internal and external audiences, maintaining tone and brand consistency.</p></li></ul><p><b>Project &amp; Event Management</b></p><ul><li><p>Track strategic initiatives, monitor progress, and manage interdependencies.</p></li><li><p>Organize leadership offsites, cycle meetings, and high-impact events, ensuring seamless execution from planning to follow-up.</p></li><li><p>Coordinate selected marketing activities within the region, including branding support for events, promotional materials, and alignment with corporate communication guidelines.</p></li><li><p>Collaborate with cross-functional teams to ensure events and marketing initiatives reinforce strategic priorities.</p></li></ul><p><b>Operational Excellence</b></p><ul><li><p>Oversee travel arrangements, expense management, and vendor coordination.</p></li><li><p>Maintain secure archiving of sensitive documents and enforce information governance standards.</p></li></ul><p></p><p><b>Qualifications &amp; Experience</b></p><ul><li><p>Bachelor’s degree in Business Administration, Communications, or related field; Master’s degree preferred.</p></li><li><p>7–10 years of experience supporting senior executives in a multinational environment; pharma/healthcare experience is a plus.</p></li><li><p>Fluency in French, Arabic and English required.</p></li><li><p>Advanced proficiency in Microsoft 365 and familiarity with enterprise tools ; Power BI knowledge is an advantage.</p></li><li><p>Proven ability to manage confidential information and exercise sound judgment.</p></li><li><p>Strong project management skills; certification is a plus.</p></li><li><p>Experience in event management and marketing coordination is highly desirable.</p></li></ul><p></p><p><b>Core Competencies &amp; Requirements</b></p><p></p><p><b>Core Competencies</b></p><ul><li><p>Handles sensitive matters with integrity and professionalism.</p></li><li><p>Builds trust and influences effectively across diverse teams.</p></li><li><p>Implements structured processes and ensures compliance.</p></li><li><p>Communicates clearly and delivers impactful messaging.</p></li><li><p>Adapts quickly to changing priorities and thrives under pressure.</p></li><li><p>Drives initiatives to completion with accountability.</p></li><li><p>Embodies company values and champions diversity and inclusion.</p></li><li><p>Managing crises and complex situations.</p></li><li><p>Working across cultures and collaborating beyond boundaries.</p></li></ul><p><b>Skills</b></p><ul><li><p>Quality decision-making and resource management.</p></li><li><p>Strategic thinking, creativity, and visioning.</p></li><li><p>Assertiveness and conflict resolution.</p></li><li><p>Challenging the status quo and driving innovation.</p></li><li><p>Influencing and persuading stakeholders.</p></li><li><p>Transaction structuring and franchise strategy prioritization.</p></li><li><p>Analyzing stakeholder requirements to inform decisions.</p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/executive-assistant-novartis/6a0895d12f1861929d253324</link><guid isPermaLink="true">http://biotechroles.com/executive-assistant-novartis/6a0895d12f1861929d253324</guid><pubDate>Sat, 16 May 2026 16:05:37 GMT</pubDate><company>Novartis</company><location>Casablanca</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Director Health Economics and Outcomes Research (HEOR)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI - Remote<br><br>Novartis has an exciting opportunity for a Director, HEOR Product Lead CRM for a Cardiovascular Product. You are directly responsible for leading relationships with the appropriate Medical Executive Directors/Directors and appropriate commercial leads (e.g., Value and Access) to ensure alignment on strategic priorities to ensure efficient and impactful tactical execution for the Cardiovascular Product. The Director along with the Evidence Generation Executive Director aligns with Medical SPOC (Single Point of Contact) for IPST (Integrated Product Strategy Team). The Director will also perform role as an individual contributor to execute tactical evidence initiatives to support medical product strategies. <br><br>This position can be based remotely anywhere in the U.S. (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 25% travel.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major Responsibilities:</b></p><ul><li>Represent the HEOR team in Medical Strategy Teams in the development of medical and HEOR strategies to demonstrate the value of products to payers, clinical decision-makers and patients.</li><li>Proactively generate and communicate evidence necessary to optimize patient access and value of Novartis products in the US market.</li><li>Exhibit medical leadership in strategic alignment with other areas and proactively propose new impactful ideas in cross-functional teams.</li><li>Manage multiple HEOR projects, associated budgets and external &amp; internal partners, while ensuring a high level of scientific rigor and alignment with stakeholders.</li><li>Build robust external institutional and individual level partnerships as needed.</li><li>Effectively communicate impactful research to diverse audiences.</li><li>Publish and present impactful research at scientific conferences and forums.</li><li>Business Partnering – Effectively partner with internal stakeholders at strategic and tactical levels to shape research partnerships; generate and disseminate robust HEOR findings in support of external stakeholders including SOCs and payers.</li><li>AI Fluency &amp; Digital Enablement - Leverages AI tools to streamline tasks, generate content, and support decision-making, demonstrating practical fluency in prompting, interpreting, and refining AI outputs to improve work quality and efficiency.</li></ul><p></p><p><b>Education and Work Experience: </b></p><p><b>Essential Requirements</b></p><ul><li>An advanced degree (Master’s or doctorate) in health economics, statistics, epidemiology, health policy or related field is required.</li><li>A minimum of 8 years’ experience in the pharma or healthcare sector, preferably in health economics, market access or related functions/fields is required.</li><li>Substantial experience in shaping HEOR and RWE strategy and hands-on execution supporting inline and pipeline products is required.</li><li>Candidates have consistently demonstrated ability to lead and execute and drive excellence in cross-functional teams both within their direct area of responsibility and across their organization.</li><li>Expert knowledge of Health Economics, Outcomes Research, and Real-World Evidence including study design, methodologies, modeling, data sources and analyses is required.</li><li>Deep knowledge of US healthcare financing and delivery system, US payer environment, evolving trends and competitive landscape is required.</li></ul><p><b>Preferred Requirements</b></p><ul><li>PhD or PharmD with strong focus in Health Economics, Public Health, Epidemiology or related field preferred.</li><li>Experience engaging or partnering with external organizations (e.g., SOCs, payers, universities, value assessors, regulatory agencies, etc.) is strongly preferred.</li></ul><p></p><p>Novartis Compensation Summary:</p><p>The salary for this position is expected to range between $185,500 and $344,500 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$185,500.00 - $344,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Agility, Cross-Functional Collaboration, Customer-Centric Mindset, Data Analysis, Employee Development, External Orientation, Finance, Go-To-Market Strategy, Healthcare Sector Understanding, Health Economics, Health Policy, Health Technology Assessment (HTA), Influencing Skills, Innovation, Inspirational Leadership, Market Access Strategy, People Management, Pharmacoeconomics, Pricing Strategy, Process Management, Product Launches, Project Management, Real World Evidence (RWE), Regulatory Affairs {+ 9 more}]]></description><link>http://biotechroles.com/director-health-economics-and-outcomes-research-heor-novartis/6a0895a92f1861929d253323</link><guid isPermaLink="true">http://biotechroles.com/director-health-economics-and-outcomes-research-heor-novartis/6a0895a92f1861929d253323</guid><pubDate>Sat, 16 May 2026 16:04:57 GMT</pubDate><company>Novartis</company><location>Remote Position (USA)</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Regulatory Affairs Senior Manager, CMC]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Location: East Hanover, NJ<br><br>This role is required to be in our East Hanover, NJ office 3x/week. <br><br>Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<br><br>We are looking for an experienced Senior Manager, Regulatory Affairs CMC to lead global regulatory strategy and execution across the product lifecycle. In this role, you will drive the development, submission, and approval of CMC dossiers, ensuring compliance with regulatory requirements while supporting timely access to innovative medicines for patients worldwide.<br><br>Working within a global, cross‑functional environment, you will provide strategic direction, manage regulatory risks, and act as a key interface with health authorities.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><u><b>Major Accountabilities</b></u></p><div><ul><li><p>Lead and implement global CMC regulatory strategies for assigned products and projects.</p></li><li><p>Plan, author, review, and coordinate high‑quality regulatory submissions.</p></li><li><p>Ensure regulatory compliance, technical accuracy, and alignment with global guidelines.</p></li><li><p>Identify risks, develop mitigation plans, and communicate key issues to stakeholders.</p></li><li><p>Collaborate across cross‑functional teams to support product development and lifecycle management.</p></li><li><p>Lead interactions with health authorities, including preparation and coordination of submissions and responses.</p></li><li><p>Support due diligence activities for business development opportunities.</p></li></ul></div><p>​</p><p><b><u>Essential Requirements</u></b></p><div><ul><li><p>5&#43; years of experience in regulatory affairs and/or the pharmaceutical industry.</p></li><li><p>Understanding of regulatory submission and approval processes.</p></li><li><p>Knowledge of chemistry, biotechnology, analytics, or pharmaceutical technology, with the ability to evaluate scientific data from a range of disciplines.</p></li><li><p>Experience working collaboratively in cross‑functional or global teams, with the ability to manage and prioritise multiple activities.</p></li><li><p>Ability to work independently as well as contribute effectively within team environments.</p></li><li><p>Strong planning, organisational, and communication skills.</p></li><li><p>Confidence using digital tools and systems relevant to the role.</p></li></ul><p></p><p>​<u><b>Benefits &amp; Rewards</b></u></p><p>The salary for this position is expected to range between $119,700 and $223,300 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p>To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p></div><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$119,700.00 - $222,300.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Change Control, Cross-Functional Teams, Documentation Management, Negotiation Skills, Regulatory Compliance, Risk Assessment, Risk Management, Waterfall Model]]></description><link>http://biotechroles.com/regulatory-affairs-senior-manager-cmc-novartis/6a0895a82f1861929d253322</link><guid isPermaLink="true">http://biotechroles.com/regulatory-affairs-senior-manager-cmc-novartis/6a0895a82f1861929d253322</guid><pubDate>Sat, 16 May 2026 16:04:56 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Peer to Peer Marketing (2 Positions)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI- Hybrid<br><br>This position will be located at East Hanover, NJ and will not have the ability to be located remotely. This position will require 20% travel as defined by the business (domestic and/ or international). Please note that this role would not provide relocation and only local candidates will be considered. <br><br>The Senior Manager, Peer to Peer Marketing (known as Senior Manager, HCP Education Delivery within Novartis), is a strategic marketing role within Integrated Marketing Organization of US Pharma. This position is dedicated to the consistent delivery of top-tier HCP education for Therapeutic Areas (TA)/Brands. Leveraging Novartis HCP Education capabilities and deep customer and TA/Brand in-sights, the role is designed to elevate peer to peer promotional activities and create a broad ecosystem of education. This role will also be the lead to create and execute educational experiences that not only inform and engage HCPs on DSE and unbranded education, but also foster confidence in appropriately selecting and prescribing Novartis products in line with marketing strategies.<br><br>There are 2 Positions available.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities:</b></p><ul><li>Design and deliver impactful peer-to-peer HCP education aligned with brand and therapeutic area strategies</li><li>Collaborate cross-functionally to ensure consistent, high-quality educational experiences across channels</li><li>Translate scientific data into engaging content tailored for diverse healthcare professional audiences</li><li>Lead multiple high-priority projects from concept to execution, ensuring timely and on-budget delivery</li><li>Drive initiatives that enhance the HCP experience and demonstrate measurable improvements</li><li>Apply strategic and analytical thinking to optimize educational program effectiveness</li><li>Maintain full compliance with regulatory standards while executing promotional education activities</li></ul><p></p><p>Education: Bachelor&#39;s degree in a related field is required; Master of Science, and/or MBA preferred</p><p><b>Essential Requirements:</b></p><ul><li>A minimum of 2 years of commercial marketing experience, with a proven track record of building scalable HCP education programs. Alternatively, candidates with 2 years of marketing experience and completion of a postdoctoral fellowship at a major pharmaceutical company will also be considered.</li><li>Demonstrated ability to communicate scientific data effectively to a variety of audiences.</li><li>Experience in driving enterprise-wide initiatives that enhance the HCP experience and demonstrate measurable improvements.</li><li>Proven project management skills, with the ability to lead and deliver multiple top-priority projects on time, within scope, and on budget. A strategic and analytical mindset is essential, as demonstrated by key projects or initiatives.</li><li>Accomplished cross-functional leadership skills, with the ability to collaborate effectively with various teams and stakeholders.</li></ul><p><b>Desirable Requirements:</b></p><ul><li>Multi-functional experience in Pharmaceutical or Healthcare</li><li>Prior work within a center of excellence model, where consistent standards, best practices, and knowledge sharing were effectively implemented</li></ul><p></p><p>The salary for this position is expected to range between $126,000 and $234,000 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and</p><p>experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published</p><p>salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the</p><p>role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and</p><p>disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In</p><p>addition, employees are eligible for a generous time off package including vacation, personal days,</p><p>holidays and other leaves.</p><p> To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p><p></p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$126,000.00 - $234,000.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Asset Management, Commercial Excellence, Cross-Functional Work, Customer-Oriented, Digital Marketing, Healthcare Sector Understanding, Influencing Skills, Marketing Strategies, Negotiation, Operational Excellence, Priority Disease Areas Expertise, Product Lifecycle Management (PLM), Product Marketing, Product Strategies, Speed and Agility Training (Inactive), Stakeholder Engagement, Stakeholder Management, Strategic Alliances]]></description><link>http://biotechroles.com/senior-manager-peer-to-peer-marketing-2-positions-novartis/6a0895a82f1861929d253321</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-peer-to-peer-marketing-2-positions-novartis/6a0895a82f1861929d253321</guid><pubDate>Sat, 16 May 2026 16:04:56 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison - Rheumatology - Boston MA & New England Coastal]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Medical Science Liaison (MSL) is a field based, customer-facing, non-promotional medical and scientific role. Their key objective is to create impact through advancing clinical practice within the territory that leads to improved <br>patient outcomes. The MSL must demonstrate deep therapeutic expertise, understand territory and market influences, engage scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop <br>their territory and execute all relevant activities in alignment with the medical strategic and tactical plan – while functioning within the Novartis Code of Conduct, Ethics/Compliance policies and Working Practice documents. <br>The MSL will Inform and shape medical strategy through application of a curious mindset to collect impactful and actionable insights, understanding the strategic impact of critical insights.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span>Key Responsibilities:</span></b></p><p></p><p>The MSL will leverage scientific expertise and market knowledge to establish and build professional relationships and engage with HCPs (including community physicians, pharmacists, medical experts, nurses, and other healthcare professionals) and other thought leaders in geographical area as aligned with medical strategy</p><p>• The primary responsibility of the MSL is to engage with customers - customer engagements may include but not be limited to emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle.</p><p>• Must demonstrate strategic territory vision and ensure appropriate territory identification, mapping, and planning of Medical Engagements (MEs) and Key Accounts as aligned to medical strategy and in collaboration with internal Novartis colleagues.</p><p>This includes:</p><p>a. identification of key stakeholders with influence in disease space throughout the product development journey to establish strategies for education, engagement, and partnership</p><p>b. identification of opportunities for partnership with academic centers, centers of excellence, and/or systems of care to drive impact within the assigned territory</p><p>c. identification of opportunities to involve HCPs or MEs when a specific medical need is identified (e.g., publications, clinical trial participation, etc.)</p><p>d. identification of opportunities for internal collaboration with other Novartis stakeholders to drive forward therapeutic area, clinical, or product goals as appropriate</p><p>• Provide clinical trial support for company sponsored trials and facilitating relevant medical activities, including but not limited to identification of appropriate sites, supporting clinical trials (subject recruitment, protocol questions, SIVs, etc.) at sites, and cross-functional collaboration with Medical Affairs and Clinical Operations colleagues</p><p>• Regularly collaborate with internal colleagues (e.g., HEOR, access, marketing, commercial) within the assigned therapeutic area and territory to advance clinical practice while maintaining customer centricity and a One Novartis approach in accordance with Novartis compliance standards</p><p>• Maintain in-depth knowledge of assigned therapeutic area and Novartis compounds to serve as a medical resource to customers and internal colleagues</p><p>• Maintain in-depth knowledge of internal policies and external regulations (e.g., field medical Working Practice Document (WPD), travel policy, expense policy, state and local laws, institutional policies) and how they affect the day-to-day</p><p>• Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner, including profiling of core customers and ensuring up-to-date information in the CRM</p><p>• Champion emerging responsibilities as strategic priorities and territory needs evolve</p><p>• Proactively drive personal and professional development</p><p>• Conduct yourself with the highest ethical standards and adhere to Novartis Code of Conduct. Comply with all relevant laws and regulations and Novartis Ethics, Risk &amp; Compliance policies, and procedures.</p><p></p><p><b><span>Essential Requirements: </span></b></p><ul><li><b><span>Education:</span></b> Graduate degree in science or healthcare required; doctoral degree preferred (MD, PhD, DNP, PharmD, etc.) </li><li>Minimum of 3 years’ experience in a Field Medical-based position within the pharmaceutical industry or as an MSL is preferred OR 5-7 years of relevant medical affairs, clinical research, or related experience in a scientific or clinical setting required.<ul><li>Strong clinical knowledge including pharmacotherapy, treatment guidelines, clinical research processes, medical expert engagement strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is required. </li><li>Candidates will perform their duties in accordance with applicable law, regulations, and Novartis policies. </li><li>Works within Ethics, Compliance and Promotional policies (Novartis &amp; Federal) and ensures those around them do the same. </li><li>Works to ensure a diverse and inclusive environment free from all forms of discrimination and harassment. </li><li>Adherence with Company policies, state and federal laws and regulations </li><li>Candidate must reside within territory, or within a reasonable daily commuting distance of 50 miles from the territory border. Field based, customer-facing position majority of the time with approximately 60-70% travel required to achieve performance and business objectives (face to face, virtual, email, telephone, etc.). Must have a valid driver’s license.</li></ul></li></ul><p></p><p><b><span>Desirable Requirements:</span></b></p><ul><li>Previous experience in assigned or related therapeutic area is preferred. </li></ul><p></p><p>The salary for this position is expected to range between $160,300.00 and $297,700.00 per year.</p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p>To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$160,300.00 - $297,700.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Building Construction, Business Analysis, Business Networking, Clinical Practices, Clinical Research, Clinical Study Reports, Collaboration, Curious Mindset, Disease Management, Diversity &amp; Inclusion, Drug Development, Epidemiology, Medical Information, Medical Research, Medical Writing, Microsoft Word, Phase Iv Clinical Trial, Product Placement, Scientific Support]]></description><link>http://biotechroles.com/medical-science-liaison-rheumatology-boston-ma-and-new-england-coastal-novartis/6a0895a82f1861929d253320</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-rheumatology-boston-ma-and-new-england-coastal-novartis/6a0895a82f1861929d253320</guid><pubDate>Sat, 16 May 2026 16:04:56 GMT</pubDate><company>Novartis</company><location>Field Non-Sales (USA)</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director HEOR Product Lead (2 Positions)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Remote<br><br>The HEOR Associate Director is responsible for the development and execution of robust health economics and outcomes research strategies and studies for products in a therapeutic area. This position will support developing product value propositions and HEOR evidence plans that addresses product differentiation, optimize commercialization and market access for products in different stages of their product lifecycle.<br><br>There are 2 Positions available.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p></p><p><span>The Associate Director will be a strategic partner for medical, commercial, and access colleagues. This role will require proactive participation in cross-functional team discussions, demonstration of strong leadership and strategic thinking in the areas of observational research, real-world evidence, economic modeling, patient reported outcomes, patient preference studies, registries, for both regulatory and payer decision-making. The Associate Director will collaborate with other senior members of the team supporting product related activities. </span></p><p></p><p><b>Major Accountabilities:</b></p><ul><li><p>Represent HEOR function in Medical Strategy Teams for developing medical and HEOR strategies – integrated evidence plans (IEPs), to demonstrate the value of therapeutic area products to payers, population health decision-makers and patients.</p></li><li><p>Proactively generate and communicate evidence necessary to optimize patient access and value of Novartis products in the US market.</p></li><li><p>Ensure all research is conducted with a high level of scientific rigor.</p></li><li><p>Publish and present research accomplishments at scientific conferences and forums and effectively communicate impactful research to diverse audiences.</p></li><li><p>Business Partnering – Effectively partner with internal stakeholders, such as RWE, VELs, Medical Affairs, Commercial, Market Access, Scientific Communications, Medical Information, at strategic and tactical levels to shape research partnerships; generate and disseminate robust HEOR findings in support of external stakeholders including SOCs and payers.</p></li><li><p>Manage multiple HEOR projects, associated budgets and external &amp; internal partners, while ensuring a high level of scientific rigor and alignment with stakeholders.</p></li><li><p>Build robust external institutional and individual level partnerships as needed.</p></li></ul><p></p><p><b>Position Requirements:</b></p><ul><li><p>An advanced degree (master’s or doctorate) in health economics, statistics, epidemiology, health policy or related field is required.</p></li><li><p>PhD or PharmD with strong focus in Health Economics, Public Health, Epidemiology or related fields is preferred.</p></li><li><p>Minimum 3 years of experience in the pharma or healthcare sector, in health economics, market access or related functions/fields is required.</p></li><li><p>Expert knowledge of Health Economics, Outcomes Research, and Real-World Evidence including study design, methodologies, economic modeling, data sources and analyses is required.</p></li></ul><p></p><p><b>Novartis Compensation and Benefit Summary:</b></p><p>The salary for this position is expected to range between $168,000.000 and $312,000.00 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In</p><p>addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p>To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$168,000.00 - $312,000.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Cross-Functional Work, Cross-Functional Work, Customer-Centric Mindset, Data Analysis, Employee Development, External Orientation, Finance, Go-to-Market Strategies, Government Affairs, Healthcare Policies, Healthcare Sector Understanding, Health Economics, Health Technology Assessment (HTA), Influencing Skills, Innovation, Inspirational Leadership, Market Access Strategies, People Management, Pharmacoeconomics, Pricing Strategies, Process Management, Product Launches, Real World Evidence (RWE), Regulatory Compliance, Reimbursement Strategies {+ 7 more}]]></description><link>http://biotechroles.com/associate-director-heor-product-lead-2-positions-novartis/6a0895a72f1861929d25331f</link><guid isPermaLink="true">http://biotechroles.com/associate-director-heor-product-lead-2-positions-novartis/6a0895a72f1861929d25331f</guid><pubDate>Sat, 16 May 2026 16:04:55 GMT</pubDate><company>Novartis</company><location>Remote Position (USA)</location><salary>$180000-240000</salary><type>Full time</type></item><item><title><![CDATA[Rheumatology Institutional Specialist – Miami]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Remote<br><br>This is a field-based and remote opportunity supporting the key accounts in an assigned geography.<br>Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible to you.<br><br>Company will not sponsor visas for this position.<br><br>The Rheumatology Institutional Specialist (IS) will be responsible for ensuring proper access pull-through in key hospitals with the rheumatology brand portfolio. Duties will include generating demand by creating, coordinating, and executing a strategic business plan for top priority hospitals within designated rheumatology academic and government institutions. The Institutional Specialist will work together with rheumatology sales, marketing, US market access, patient services, and other home office staff, as necessary, to implement programs centered on the institution that align with business unit strategic goals and legal and compliance policies.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span>Key Responsibilities:  </span></b></p><ul><li><span>Accountable for building institutional advocacy around formulary adoption of rheumatology brands to help drive appropriate utilization of approved products.</span></li><li><span>Increase demand by creating, organizing, and executing a strategic business plan specifically for the key strategic hospitals within the designated rheumatology academic and government institutions.</span></li><li><span>Collaborate with local partners to develop and sustain strategically focused business plans tailored to specific institutions, reflecting a comprehensive understanding of local market dynamics that impact product sales.</span></li><li><span>Exhibits a thorough understanding of the disease area, market dynamics, competitors, industry trends, and cross-functional strategies to proactively address and successfully navigate business opportunities and challenges.</span></li><li><span>Execute sales activities by delivering presentations on products and disease states, sharing approved clinical data with physicians and their teams. Establishes key business relationships within the hospital, engaging with essential clinicians, administrative staff, and influential decision-makers to network across the organization and collaborate on initiatives where opportunities emerge.</span></li><li><span>Facilitate cross-functional Area Team Meetings (ATMs) for designated hospital accounts, developing, executing, and revising business strategies to meet product access and sales targets. </span></li><li><span>Regularly evaluate key customer needs to provide tailored insights and hospital activities to both field and headquarters teams and collaborate on implementing new strategies to seize business opportunities.</span></li><li><span>Assist Area Business Leaders in pinpointing significant business opportunities and diagnosing essential business and implementation challenges within designated hospitals and their adjacent markets/landscape.</span></li></ul><p></p><p><b>Essential Requirements: </b></p><ul><li>Bachelor’s degree required from 4-year college or university.</li><li>5&#43; years’ experience in pharmaceutical, biotech, healthcare, or similarly structured industries with large, geographically dispersed sales teams; inclusive of 2&#43; years in hospital sales or similar sales role managing sophisticated accounts (including large academic centers) within the past 5 years. We also welcome candidates from other complex sales environments such as medical devices, diagnostics, life sciences services, insurance, consumer health, or B2B sectors, especially where strong field leadership and customer engagement are central to success.</li><li>Must have a high degree of understanding of the community and embody strong record of accomplishment of therapeutic area/product knowledge expertise.</li><li>Robust business background, with strong ability to collaborate and work cross-functionally within sophisticated matrix environments.</li><li>Candidate must reside within territory, or within a reasonable daily commuting distance of 100 miles from the territory border. Ability to travel 60-80% over a broad geography is required, with the ability to drive and/or fly within the territory. Must have a valid driver’s license.</li></ul><p></p><p><b>Desirable Requirements: </b></p><ul><li>Experience across therapeutic groups, disease states, account management strategy, and new product launches.</li><li>Broad understanding in patient services, market access, buy and bill, specialty pharmacy, reimbursement and/or medical calling on HCPs with respect to a sophisticated product or reimbursement pathway.</li></ul><p></p><p><b>Driving is an Essential Function of this Role: </b>Meaning it is fundamental to the purpose of this job and cannot be eliminated. Because driving is an essential function of the role, you must have a fully valid and unrestricted driver’s license to be qualified for this role. The company provides reasonable accommodations for otherwise qualified individuals with medical restrictions if an accommodation can be provided without eliminating the essential function of driving.</p><p></p><p><b>COVID-19 Vaccine Policy </b>(customer-facing roles only): While Novartis does not require vaccination for COVID-19 or proof of a recent negative test result for COVID-19 at this time, employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to <a href="mailto:Eh.occupationalhealth&#64;novartis.com" target="_blank">Eh.occupationalhealth&#64;novartis.com</a>.</p><p></p><p><b>For Field Roles with a Dedicated Training Period</b>: The individual hired for this role will be required to successfully complete certain initial training, including home study, eight (8) or fewer hours per day and forty (40) or fewer hours per week.</p><p></p><p><b>Novartis Compensation Summary</b><b>:</b></p><p>The salary for this position is expected to range between $145,600 and $270,400 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$145,600.00 - $270,400.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Analytical Skill, Change Management, Coaching, Collaboration, Commercial Excellence, Complexity Management, Compliance, health care industry, Leadership, Management, Mentorship, problem solving techniques, Professional Communication, Professional Ethics, Team Work]]></description><link>http://biotechroles.com/rheumatology-institutional-specialist-miami-novartis/6a0895a72f1861929d25331e</link><guid isPermaLink="true">http://biotechroles.com/rheumatology-institutional-specialist-miami-novartis/6a0895a72f1861929d25331e</guid><pubDate>Sat, 16 May 2026 16:04:55 GMT</pubDate><company>Novartis</company><location>Field Sales (USA)</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Senior / Medical Director, CVD]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>-Develops and implements strategic and operational TAs Global Medical Affairs programs, with a focus on innovative evidence and/or launch readiness and/or post-market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy addressing and delivering strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems <br>-Provides expertise in the development and execution of the overarching strategies, providing inputs during design and along the end-to-end execution of programs <br>-Develops and executes the Integrated Evidence Plan (IEP)/functional specific programs to maximize the value proposition for the prioritized launch portfolio and impact of our medicines.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities:</b></p><ul><li><p>Demonstrate solid competencies as a Medical Leader within the US Medical Affairs organization; preferably with launch experience in the CV space</p></li><li><p>Build positive, effective partnerships with Medical and Commercial as well as US and Global colleagues.</p></li><li><p>Key member of the cross-functional Medical Strategy Team (MST), which drives Medical tactical development and excellence in execution.</p></li><li><p>Drive a robust data generation program to support current indication, as well as pelacarsen’s lifecycle.</p><ul><li><p>Co-develop strategically aligned study programs with Health Economics &amp; Outcomes Research (HE&amp;OR) colleagues</p></li><li><p>Lead Investigator-Initiated Trial (IIT) program</p></li><li><p>Lead US based Phase 3b/4 studies</p></li><li><p>Collaborate with global team on lifecycle management studies on strategy for USA</p></li></ul></li><li><p>Foster strong relationships with not only National, but also key Regional and Local Medical Experts, including Investigators. Support Medical Expert Engagement Strategy.</p></li><li><p>Drive advisory boards and work closely with Field Medical on insight-gathering initiatives.</p></li></ul><p></p><p><b>Essential Requirements: </b></p><p><b>Education (minimal/desirable):</b></p><p>·       Bachelors or equivalent 4-Year University Degree required.</p><p>·       Doctorate level degree (MD, PharmD, DO, or PhD in Health Sciences or related field) or Nurse Practitioner (NP)/ Physician’s Assistant (PA) degree with significant relevant clinical experience required.</p><p><br /><b>Work Experience: </b></p><ul><li><p>Strong Medical Affairs background.</p></li><li><p>Launch experience in CV.</p></li><li><p>Strategy Development.</p></li><li><p>Cross-functional collaboration.</p></li></ul><p></p><p><span>The pay range for this position at commencement of employment is between </span><span>$204,000.00 - $379,600.00 a year</span><span>. </span><span>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</span></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p>To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$204,400.00 - $379,600.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Agility, Clinical Practices, Cross-Functional Collaboration, Data Analysis, Drug Development, Employee Development, Healthcare Sector Understanding, Health Sciences, Influencing Skills, Innovation, Inspirational Leadership, Integrated Evidence Generation, Medical Affairs, Medical Communication, Medical Education, Patient Care, People Management, Pharmaceutics, Priority Disease Areas Expertise, Product Launches, Product Strategy, Real World Evidence (RWE), Regulatory Compliance, Research Methodologies {+ 4 more}]]></description><link>http://biotechroles.com/senior-medical-director-cvd-novartis/6a0895a72f1861929d25331d</link><guid isPermaLink="true">http://biotechroles.com/senior-medical-director-cvd-novartis/6a0895a72f1861929d25331d</guid><pubDate>Sat, 16 May 2026 16:04:55 GMT</pubDate><company>Novartis</company><location>Remote Position (USA)</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[HR Business Partner Director (Mexico-based, Supporting US Organization).]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The HR Business Partner Director is dedicated to supporting the US Organization, reporting directly to the Head People &amp; Organization (HR) Customer Engagement USA. The HR Business Partner Director will spend approximately 70% of their time supporting the US Customer Engagement organization and 30% supporting US Global Functions.<br><br>#LI-Hybrid <br>Location: CDMX, Mexico<br><br>Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities: </b></p><ul><li>Strategic People &amp; Organization (HR) Partnering: Translate strategy and functional plans to design and implement P&amp;O interventions that enable the business agenda while applying data driven and external insights with People &amp; Organization (HR) metrics.</li><li>Talent Management: Develop talent and leadership development strategy and plan; drive the talent agenda in partnership with the business, establishing quality succession planning for critical positions, development plans of key talent and talent strategy to build the leadership pipeline.</li><li>Organizational Development: Develop an organizational design / plan for client groups by utilizing organizational diagnostics; hold the knowledge and outlook for the 3–5-year business plans; establish strategic workforce plans with leaders and develop organization design efficiencies to enable the long-term business strategy</li><li>Data Analytics: Have knowledge of People &amp; Organization (HR) systems. Ability and interest to leverage data &amp; analytics for business insights to inform decisions</li><li>Diversity &amp; Inclusion: Activate business ownership and advise on and handle diversity, equity, and inclusion at all levels</li><li>Rewards &amp; Recognition: Contribute to the development of recognition strategies that facilitate and support the attraction and retention of top performers.</li><li>Leadership: Provide coaching, feedback, learning opportunities and mentoring to support and enable People &amp; Organization (HR) team members in their development.</li><li>Project &amp; Initiatives: Contribute actively to the People &amp; Organization (HR)  community and network; actively participate in complex, enterprise People &amp; Organization (HR)  projects or initiatives; ensure business representation and alignment.</li></ul><p></p><p><b>Minimum Requirements: </b></p><ul><li>Bachelor’s degree required; Master’s degree in Human Resources, Psychology, or related field preferred.</li><li>Minimum 10 years of HR experience in Multinational/ global environments, with proven talent management expertise.</li><li>Broad HR expertise (Rewards, Organizational Development, People Analytics, Business Partnering).</li><li>Strong change management, project management, and people leadership skills.</li><li>Experience leading cross-disciplinary, matrixed HR and client teams.</li><li>Strong people leadership skills and experience, including coaching and mentoring skills</li><li>Strong people analytics skills, effectiveness with data/metrics/reporting to inform decision making</li></ul><p></p><p>Commitment to Diversity &amp; Inclusion:</p><p>We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/hr-business-partner-director-mexico-based-supporting-us-organization-novartis/6a0895a72f1861929d25331c</link><guid isPermaLink="true">http://biotechroles.com/hr-business-partner-director-mexico-based-supporting-us-organization-novartis/6a0895a72f1861929d25331c</guid><pubDate>Sat, 16 May 2026 16:04:55 GMT</pubDate><company>Novartis</company><location>INSURGENTES</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Senior Clinical Data Scientist]]></title><description><![CDATA[<p><span><b>ROLE SUMMARY </b></span></p><p></p><p><span>As part of the Clinical Data and Information Sciences (CDIS) group, an integral delivery unit within the Clinical Development &amp; Operations (CD&amp;O) organization, the Manager, Senior Clinical Data Scientist (Sr CDS) is responsible for timely and high-quality data management deliverables supporting the Pfizer portfolio. The Sr CDS delivers asset level information strategies and services for optimal use and reuse of internal and external information that will advance research, development, and commercialization of the Pfizer portfolio and further precision medicine. The Sr CDS designs, develops, and maintains key data management deliverables used to collect, review, monitor, and ensure the integrity of clinical data, applies standards, data review and query management, and is accountable for quality study data set release and consistency in asset/submission data. The Sr CDS may have one or more direct reports.</span></p><p></p><p><span><b>ROLE RESPONSIBILITIES</b></span></p><ul><li><p><span>Serves as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDIS activities including selection and application of data acquisition standards, Data Management Plan, selection of quality risk indicators, third party study data due diligence.</span></p></li><li><p><span>May functionally manage a team of Associate Data Managers, Senior Data Managers, be responsible for resource allocation, training and development.</span></p></li><li><p><span>Works with Asset Leads to establish strategy, timelines, and adequate resourcing of DMs at Asset/Study level.</span></p></li><li><p><span>Ensures appropriate documentation across the lifespan of the study/asset for all DM deliverables and ensures the required study specific CDIS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously.</span></p></li><li><p><span>May likely be involved in development of TA specific standards.</span></p></li><li><p><span>Provides project management leadership to DM teams – Responsible for managing issues at the study level as they arise and proactively communicating to Asset Lead and Management while serving to provide solutions.</span></p></li><li><p><span>Acts as the key scientific and technical data management expert; contribute to department level initiatives and ensure effective reporting of study status and metrics to Management.</span></p></li><li><p><span>Ensures work carried out on behalf of CDIS is in accordance with applicable SOPs and working practices.</span></p></li><li><p><span>Serves as Subject Matter Expert (SME) for and oversees the design, documentation, testing and implementation of clinical data collection tools, both CRF and non-CRFs using and electronic data capture (EDC) system and/or other data collection systems.</span></p></li><li><p><span>May act as data management contact for regulatory inspections/audits in liaison with the appropriate Quality and Safety groups with Pfizer.</span></p></li></ul><p></p><p><span><b>QUALIFICATIONS</b></span></p><ul><li><p><span>Bachelor’s degree required. Degree in scientific field preferred. Master’s degree preferred.</span></p></li><li><p><span>Minimum 7 years Data Management experience required, including experience in team leadership.</span></p></li><li><p><span>Demonstrated successful experience in all relevant clinical data management activities in a Biopharmaceutical or CRO setting.</span></p></li><li><p><span>Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review.</span></p></li><li><p><span>Strong Project and Risk Management.</span></p></li><li><p><span>CRO and vendor oversight experience preferred.</span></p></li><li><p><span>Strong verbal and written communication skills.</span></p></li><li><p><span>Consistent, detail oriented, communicative, dedicated to do a job well done.</span></p></li><li><p><span>Knowledge of clinical research, FDA &amp; ICH, GCP, GCDMP, and related regulatory requirements.</span></p></li><li><p><span>Proficient experience using commercial clinical data management systems and/or EDC products (Medidata RAVE, Oracle RDC, Inform preferred).</span></p></li><li><p><span>Experience using relational databases (e.g. MS SQL Server, MS Access, or Oracle) and data visualization tools (e.g. Spotfire, jReview).</span></p></li><li><p><span>Strong knowledge of MedDRA/WHO-Drug.</span></p></li><li><p><span>Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.).</span></p></li></ul><p></p><p><span>Please apply by sending your CV and a motivational letter in English</span></p><p> <br />Work Location Assignment: Hybrid</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Medical<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/manager-senior-clinical-data-scientist-pfizer/6a08949a2f1861929d25331b</link><guid isPermaLink="true">http://biotechroles.com/manager-senior-clinical-data-scientist-pfizer/6a08949a2f1861929d25331b</guid><pubDate>Sat, 16 May 2026 16:00:26 GMT</pubDate><company>Pfizer</company><location>Greece - Thessaloniki Pylaia</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Scientific AI Engineer]]></title><description><![CDATA[<p><span style="font-size:14px">Pfizer Oncology is building an AI-first R&amp;D engine where artificial intelligence is a foundational capability shaping how medicines are discovered, developed, and delivered to patients. We are seeking</span><span style="font-size:14px"> a Scientific AI Engineer to design and build end-to-end AI solutions that directly impact Oncology R&amp;D decision-making. This role sits at the intersection of deep scientific understanding and hands on AI engineering, translating complex biological, translational, and clinical questions into applied AI solutions.</span></p><p></p><p>In this role, you will partner closely with Oncology scientists, clinicians, and product leaders to prototype, iterate, and deliver AI enabled insights, with a strong emphasis on speed, scientific rigor, and real-world usability.</p><p></p><p><b>Key Responsibilities</b></p><ul><li><p>Design, develop, and prototype AI/ML solutions addressing Oncology discovery, translational, and clinical development challenges.</p></li><li><p>Apply advanced analytical and machine learning methods to multimodal datasets (e.g., molecular, clinical, real-world, literature).</p></li><li><p>Own solutions end-to-end, from problem framing and data exploration through model development and user facing outputs.</p></li><li><p>Collaborate closely with domain experts to ensure solutions are scientifically grounded and decision relevant.</p></li><li><p>Rapidly iterate on prototypes based on user feedback and evolving scientific needs.</p></li><li><p>Contribute technical expertise to solution design discussions led by the Oncology AI Product &amp; Engineering Lead.</p></li><li><p>Document methods, assumptions, and limitations to support transparency and responsible AI practices.</p></li></ul><p></p><p><b>Basic Qualifications</b></p><ul><li><p>Bachelor&#39;s degree and 6&#43; years of relevant work experience <b>OR </b>Master’s degree and 5&#43; years of experience <b>OR </b>PhD and 1&#43; years of experience. Advanced degree in computational biology, data science, machine learning, engineering, or related field strongly preferred.</p></li><li><p>Demonstrated experience building applied AI/ML solutions in life sciences, healthcare, or advanced analytics environments.</p></li><li><p>Strong hands-on programming skills (e.g., Python) and experience working with data pipelines and ML frameworks.</p></li><li><p>Solid understanding of Oncology biology, translational science, or clinical development workflows.</p></li><li><p>Ability to operate independently in ambiguous problem spaces and deliver working prototypes.</p></li></ul><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>Experience in pharma, biotech, or AI driven health technology startups.</p></li><li><p>Familiarity with prototyping approaches for AI products rather than long cycle production systems.</p></li><li><p>Experience working with large, heterogeneous datasets common to Oncology R&amp;D.</p></li></ul>&amp;#xa;The annual base salary for this position ranges from $139,100.00 to $231,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Information &amp; Business Tech&amp;#xa;]]></description><link>http://biotechroles.com/senior-manager-scientific-ai-engineer-pfizer/6a0894972f1861929d25331a</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-scientific-ai-engineer-pfizer/6a0894972f1861929d25331a</guid><pubDate>Sat, 16 May 2026 16:00:23 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$180000-280000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, AI, and Data Engineering]]></title><description><![CDATA[<p>Pfizer Oncology is building an AI-first R&amp;D engine where artificial intelligence is a foundational capability shaping how medicines are discovered, developed, and delivered to patients. We are seeking AI &amp; Data Engineers to focus on generalist, use case driven AI solutions where process, workflow, and data engineering are as critical as advanced science. This role is ideal for engineers who thrive in rapid prototyping environments and enjoy translating real-world problems into practical, AI enabled tools.<br /> </p><p>In this role, you will partner with scientific, clinical, and operational teams to develop data pipelines, analytics, and machine learning solutions that enhance the effectiveness of Oncology R&amp;D workflows.</p><p><b>Key Responsibilities</b></p><ul><li><p>Build and prototype AI enabled solutions supporting Oncology R&amp;D workflows and decision making.</p></li><li><p>Develop and maintain data pipelines, feature engineering workflows, and analytical models.</p></li><li><p>Apply machine learning techniques to structured and unstructured healthcare data.</p></li><li><p>Collaborate with scientific and product partners to understand needs and deliver usable tools.</p></li><li><p>Focus on speed, iteration, and usability, with production scaling supported by enterprise Digital teams as appropriate.</p></li><li><p>Contribute to shared engineering standards, documentation, and best practices.</p></li></ul><p></p><p><b>Basic Qualifications</b></p><ul><li><p>Bachelor&#39;s degree and 6&#43; years of relevant work experience OR Master’s degree and 5&#43; years of experience OR PhD and 1&#43; years of experience. Advanced degree in computer science, machine learning, artificial intelligence, computational biology, bioinformatics, statistics, engineering, or a related quantitative or scientific field strongly preferred.</p></li><li><p>Demonstrated hands‑on experience building data, analytics, or ML solutions in healthcare, life sciences, or health tech.</p></li><li><p>Strong programming skills and experience with modern data and ML tooling.</p></li><li><p>Ability to rapidly prototype and adapt solutions based on feedback.</p></li><li><p>Strong collaboration and communication skills.</p></li></ul><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>Experience working on research or clinical workflows.</p></li><li><p>Background in healthcare technology companies or AI startups.</p></li><li><p>Exposure to cloud‑based data and ML environments.</p></li></ul><p></p>&amp;#xa;The annual base salary for this position ranges from $139,100.00 to $231,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Research and Development&amp;#xa;]]></description><link>http://biotechroles.com/senior-manager-ai-and-data-engineering-pfizer/6a0894962f1861929d253319</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-ai-and-data-engineering-pfizer/6a0894962f1861929d253319</guid><pubDate>Sat, 16 May 2026 16:00:22 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Director, Oncology AI Product & Engineering Lead]]></title><description><![CDATA[<p>Pfizer Oncology is building an AI-first R&amp;D engine where artificial intelligence is a foundational capability shaping how medicines are discovered, developed, and delivered to patients. We are seeking a Director, Oncology AI Product &amp; Engineering Lead to own the translation of Oncology R&amp;D needs into high impact AI products and solutions.<br /> </p><p>In this role, you will lead a multidisciplinary team of AI engineers and science focused technologists, define the Oncology AI product roadmap, and partner closely with scientific, clinical, digital, and enterprise stakeholders to identify opportunities for process automation / simplification and ensure solutions are adopted, scalable, and decision relevant. This role does not require hands on coding, but does require strong technical fluency, scientific credibility, and product leadership.</p><p></p><p><b>Key Responsibilities</b></p><ul><li>Own the Oncology AI product strategy and roadmap across discovery, translational science, clinical development, and real-world evidence.</li><li>Lead and manage a cross functional team of AI engineers, providing technical direction, prioritization, and coaching.</li><li>Translate complex scientific and operational problems into clear AI product requirements, success metrics, and delivery plans.</li><li>Partner with Oncology scientific leaders, clinical teams, Digital, Enterprise AI, and IT to ensure solutions are aligned with enterprise platforms and governance.</li><li>Evaluate AI concepts, prototypes, and technical approaches, providing informed guidance and trade‑off decisions.</li><li>Assess Oncology workflows to identify and propose opportunities for automation and process improvements.</li><li>Drive stakeholder engagement, change management, and adoption, ensuring AI solutions move beyond pilots to sustained impact.</li><li>Establish lightweight governance, delivery standards, and value tracking for Oncology AI initiatives.</li><li>Represent Oncology AI initiatives in leadership forums and cross-enterprise discussions.</li></ul><p></p><p><b>Basic Qualifications</b></p><ul><li>PhD in Computer Science, Machine Learning, Data Science, Software Engineering, AI, or a related discipline and a minimum of 5 years of applied analytical experience with demonstrated impact in operations, automation, business analytics, or decision support <b>OR</b></li><li>Master’s in Computer Science, Machine Learning, Data Science, Software Engineering, AI, or a related discipline and a minimum of 7 years of applied analytical experience with demonstrated impact in operations, automation, business analytics, or decision support.</li><li>Demonstrated impact leading AI enabled products, platforms, or analytics solutions in pharma, biotech, healthcare technology, or AI startups.</li><li>Strong understanding of Oncology R&amp;D workflows and the role of data and AI in scientific and clinical decision making.</li><li>Proven ability to lead multidisciplinary technical teams in a matrixed environment.</li><li>High technical fluency enabling effective evaluation of AI/ML approaches without hands on development.</li><li>Excellent communication and stakeholder management skills.<br /> </li></ul><p><b>Preferred Qualifications</b></p><ul><li>Experience operating at the intersection of science, product management, and engineering.</li><li>Familiarity with AI/ML concepts including data pipelines, model development, and prototyping workflows.</li><li>Experience scaling AI solutions in large, regulated organizations.</li></ul>&amp;#xa;The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Information &amp; Business Tech&amp;#xa;]]></description><link>http://biotechroles.com/director-oncology-ai-product-and-engineering-lead-pfizer/6a0894932f1861929d253318</link><guid isPermaLink="true">http://biotechroles.com/director-oncology-ai-product-and-engineering-lead-pfizer/6a0894932f1861929d253318</guid><pubDate>Sat, 16 May 2026 16:00:19 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$220000-320000</salary><type>Full time</type></item><item><title><![CDATA[Senior Oncology Account Specialist Hematology Maine New Hampshire]]></title><description><![CDATA[<p></p><p>Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is innovative and customer oriented. Whether you are involved in manufacturing, testing, or compliance, your contribution will directly impact patients.</p><p></p><p>The Senior Oncology Account Specialist (SOAS) will have a variety of responsibilities, ranging from promoting Pfizer’s product portfolio to health care providers and specialists, to educating members of the healthcare community regarding the appropriate use of Pfizer products, to calling on accounts and organized customers to help improve patients’ experience with Pfizer products, as well as the overall quality of patient care delivered. <br /> <br />The SOAS plays a critical role in increasing Pfizer’s brand with high-value target customers by linking an insightful assessment of the account and/or business landscape with a strong understanding of Pfizer’s products and resources. </p><p></p><p><b>BASIC QUALIFICATIONS</b></p><ul><li><p>BA/BS Degree from an accredited institution BA/BS Degree from an accredited institution OR an associate’s degree with 8&#43; years of experience; OR a high school diploma (or equivalent) with 10&#43; years of relevant experience.</p></li><li><p>Ability to travel domestically and stay overnight as necessary </p></li><li><p>Valid US driver’s license and driving record in compliance with company standards.  Any DUI/DWI or other impaired driving citation within the past 7 years will disqualify you from being hired</p></li><li><p>Minimum of 4 years of previous Pharmaceutical Sales experience or minimum of 4 years of previous Oncology Healthcare Professional (HCP) experience working with key Oncology thought leaders or high influence customers in hospitals, large group practices or managed care organizations. </p></li><li><p>A demonstrated track record of success and accomplishment with previous Pharmaceutical Sales experience or Healthcare Professional (HCP) experience </p></li><li><p>Exceptional aptitude for learning and ability to communicate technical and scientific product and disease management information to a wide range of customers </p></li><li><p>Demonstrated high degree of business acumen </p></li><li><p>Proficiency using complex digital applications and able to adapt to Pfizer’s long-range technology model in bringing relevant Pfizer information to market. </p></li></ul><p></p><p><b>PREFERRED QUALIFICATIONS</b></p><ul><li><p>3-5 years of Oncology sales experience </p></li><li><p>Experience in Hematology</p></li><li><p>Master’s Degree </p></li><li><p>Advanced Healthcare Professional (HCP) Degree </p></li><li><p>Experience calling on institutions, NCI centers and Key Opinion Leaders </p></li></ul><p></p><p><b>Functional / Technical Skills can include:</b> </p><ul><li><p>Promote broad portfolio of products; Strong knowledge of disease states, therapeutic areas, and products </p></li><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li><li><p>Generate demand for Pfizer products in assigned accounts </p></li><li><p>Strategic account selling and management skills.  Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li><li><p>Maintain relationships throughout institutions </p></li><li><p>Overcome obstacles to gain access to difficult to see health care providers and customers. </p></li><li><p>Cultivate relationships with KOLs; build lasting relationships with top priority customers </p></li><li><p>Assess needs of target physicians/accounts; Address needs with responsive approach, targeted skills, and appropriate resources </p></li><li><p>Superior selling, technical and relationship building skills </p></li><li><p>Demonstrated ability to engage, influence and support customers throughout the selling process; excellent communication and interpersonal and leadership skills.  </p></li><li><p>Demonstrated ability to quickly learn and embrace new ways of working in a rapidly changing environment. </p></li><li><p>Possess the ability to work in a matrix environment and to leverage multiple resources to meet customer needs and deliver results. </p></li></ul><p></p><p><b>Other Job Details</b></p><p>Last Day to Apply May 29 2026</p><p>the BOSTON Territory includes but is not limited to: Maine, New Hampshire and parts of Upstate NY</p><p>Relocation might be offered</p><p></p><p>The annual base salary for this position ranges from $108,600 - $250,700. During initial new hire sales training, you will be classified as a salary non-exempt employee which entitles you to overtime pay. Upon your training certification, you will become an overtime exempt employee. In addition, this position offers an additional Sales Incentive bonus. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits| (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to any location outside of the United States.  </p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Sales&amp;#xa;]]></description><link>http://biotechroles.com/senior-oncology-account-specialist-hematology-maine-new-hampshire-pfizer/6a08948d2f1861929d253317</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-account-specialist-hematology-maine-new-hampshire-pfizer/6a08948d2f1861929d253317</guid><pubDate>Sat, 16 May 2026 16:00:13 GMT</pubDate><company>Pfizer</company><location>United States - New Hampshire - Remote</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Prevnar 20 Pediatric Senior Manager - HCP]]></title><description><![CDATA[<p><span><b>ROLE SUMMARY</b></span></p><p><span><span>Pfizer’s pediatric pneumococcal vaccine, Prevnar 20, was approved by the FDA in April 2023 and received its ACIP recommendation in June 2023.  This vaccine expands serotype coverage to 20 and aims to further protect children from serious pneumococcal disease. This next generation vaccine is a “blockbuster” for the U.S. and is a critical brand within the Vaccines portfolio.</span></span><br /> </p><p><span>The U.S. Prevnar 20 Pediatric Senior Manager </span><span><span>is a mission critical role responsible for HCP materials development and execution for Prevnar 20 Pediatric.  The person in this r</span></span><span>ole works extensively on a daily basis with the Prevnar 20 three Pediatric HCP Directors and the Senior Director, Prevnar 20 Pediatric Lead. </span></p><p><span> </span></p><p><span><span>This individual will lead the development and execution of HCP tactics for the brand.   This work will span HCP efforts and competitive strategy for the brand, working collaboratively with relevant U.S. and Global stakeholders to drive preference vs. competition and build effective campaigns. The candidate will also help set execute the brand’s vision for AI/digital transformation to effectively reach customers, drive planning and cross-functional collaboration to achieve desired outcomes. </span></span></p><p><span> </span></p><p><span>The candidate needs to demonstrate the ability to engage people, lead within a highly matrixed structure, have excellent communication skills, have high learning agility, and be able to work seamlessly with the global marketing team in preparation for launch.</span></p><p><span> </span></p><p><span><span>This role requires strong strategic, communication and analytical thinking as well as creativity, prioritization skills, and an ability to inspire and partner with external and internal stakeholders.</span></span></p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><p><span> <b><u>HCP Strategy &amp; Tactics:</u></b></span><span><span> </span></span></p><ul><li><p><span>In collaboration with the HCP Directors, own the development and execution of the Prevnar 20 HCP strategy and tactical plan.</span></p></li><li><p><span><span>Drive the pull through of HCP tactics for Prevnar 20 Pediatric such as communication of scientific information and emphasizing the value of Prevnar 20 vs. competition.</span></span></p></li><li><p><span><span>Develop, deliver, and measure marketing solutions that differentiate Prevnar 20 Pediatric with HCPs through innovative CFC delivered digital engagement. As part of execution the Sr. Mgr. will assess digital metrics, insights and make recommendations for content and channel optimization.</span></span></p></li><li><p><span><span>Develop effective resources to help transition customers from competition to Prevnar 20.</span></span></p></li><li><p><span><span>Expand vaccine confidence efforts with HCPs to help foster vaccine initiation and adherence.</span></span></p></li><li><p><span><span>Engage with sales and account management leads to solicit insights, provide solutions, and drive utilization of materials, and ensure programs and resources are of value to and empower customer facing colleagues.</span></span></p></li><li><p><span><span>Develop training resources for use with CFCs and ensure they are appropriately prepared to drive business and are empowered to defend against competition.</span></span></p></li><li><p><span><span>Collaborate with the creative agency and manage the respective promotional budget for tactics owned; manage trade-offs across the brand team’s advertising and promotion.</span></span></p></li><li><p><span><span>Lead/assist with other critical responsibilities/business planning deliverables as needed– e.g. leadership reports, presentations, brand metrics.</span></span><br /><br /><span> </span></p></li></ul><p><span><b>BASIC QUALIFICATIONS</b></span></p><p>Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><ul><li><p><span><span>Bachelor’s degree in related area – e.g., Marketing, Life Sciences, etc.</span></span></p></li><li><p><span><span>Minimum 1 year of experience with PhD/DrPH/ScD/PharmD; minimum of 5 years of experience with MS/MPH; minimum of 6 years of experience with a Bachelor’s degree.</span></span></p></li><li><p><span><span>Ability to work independently across stakeholders and demonstrates judgement of what needs to be escalated</span></span></p></li><li><p><span><span>Excellent communication and presentation skills (oral and written)</span></span></p></li><li><p><span><span>Robust analytical/planning skills and ability to multi-task under pressure</span></span></p></li><li><p><span><span>Self-starter, comfortable with ambiguity</span></span></p></li><li><p><span><span>Solid understanding of today’s U.S. pharmaceutical environment, incl. Regulatory, Legal and Compliance</span></span></p></li></ul><p></p><p><span><b>PREFERRED QUALIFICATIONS</b></span></p><ul><li><p><span><span>3&#43; years experience in the U.S. pharmaceutical industry preferred</span></span></p></li><li><p><span><span>Previous marketing experience preferred</span></span></p></li><li><p><span><span>MBA, MPH or similar</span></span></p></li></ul><p><span> </span></p><p><b>Other Job Details:</b></p><ul><li><p>Last Date to Apply for Job: May<b> 29, 2026.</b></p></li><li><p>Locations: United States - New York - HQ; United States - Pennsylvania - Collegeville Site</p></li><li><p>Ability to travel domestically and internationally based on business needs</p></li><li><p>Ability to work in all US time zones</p></li><li><p>NOT eligible for Relocation Package</p></li><li><p>This position is hybrid and requires working onsite 2 to 3 days per week</p></li></ul>&amp;#xa;The annual base salary for this position ranges from $124,400.00 to $207,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/prevnar-20-pediatric-senior-manager-hcp-pfizer/6a08948c2f1861929d253316</link><guid isPermaLink="true">http://biotechroles.com/prevnar-20-pediatric-senior-manager-hcp-pfizer/6a08948c2f1861929d253316</guid><pubDate>Sat, 16 May 2026 16:00:12 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Key Account Director - Puerto Rico]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><p>The Key Account Director is responsible for Biosimilars – Oncology and I&amp;I sales; Is a critical component to the growth of the overall business with increasing consolidation and complexity in how these accounts conduct their business and manage patients, this individual will be required to effectively work in a dynamic business environment.</p><p>The primary function is to develop, maintain and grow strategic long-term HCPs, SPPs, Alternate Site, PBMs/Plans and Key Stakeholders customer relationships, develop and execute customer business plans and ultimately maximize sales and margin growth within assigned Accounts</p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><p><b>Essential Functions:</b></p><p><b><u>Customer Relationship Management:</u> </b>Developing, maintaining and enhancing strategic customer relationships across the entire HCPs, SPPs and accounts’ organization including but not limited to Pharmacy/Procurement, clinical, PBMs/Plans and other critical stakeholders. Other Customer Relationship Management responsibilities include</p><ul><li><p>Ensure that HCPs, SPPs, PBMs/Plans and accounts have a positive experience when dealing with Pfizer.</p></li><li><p>Effectively navigate through complex organizations to grow HCPs contacts within the territory to gain influence among key decision makers; establish and leverage relationships to expand access to product offering.</p></li><li><p>Effectively articulate value proposition statements conveying economic, clinical and other key differentiators and quickly assess the success of messaging, revising strategy &amp; tactics if/when required.</p></li></ul><p></p><p><b><u>Business Planning &amp; Strategic Execution:</u> </b>Develop and execute strategies that achieve growth targets that are aligned to business unit objectives and strategic initiatives. Other responsibilities include:</p><ul><li><p>Understand assigned HCPs, SPPs and accounts business model; find mutually beneficial economic solutions to increase Pfizer value proposition.</p></li><li><p>Develop and adapt focused and customized strategies for each assigned HCPs, SPPs and customers (and their members for GPO’s); ensure alignment of PBMs/plans with Pfizer business objectives and strategic initiatives and adapt strategies based on market conditions.</p></li><li><p>Conduct monthly (or as needed) business reviews with assigned accounts.</p></li><li><p>Effectively utilize and deploy resources (people, systems, information and products) to accomplish sales goals and support key customer objectives and business strategy.</p></li></ul><p></p><p><b><u>Leadership:</u></b> Provide strong leadership to internal stakeholders to effectively accomplish the following:</p><ul><li><p>Provide a collaborative environment for all members within a matrix to effectively serve our HCPs/IDN/PMBs/Plans/SPPs/Alternate Site/Key Stakeholders customers and resolve concerns/issues our customers may have.</p></li><li><p>Provide a positive environment where accountability, collaboration, ingenuity and problem solving are expected and encouraged.</p></li></ul><p></p><p><b><u>Contracting:</u> </b>Manage HCPs, SPPs, PMBs, Plans and customer contracts by liaising with customers and internal contracting team</p><ul><li><p>Analyze current contracts and identify opportunities to drive contract compliance, product portfolio expansion and gain support for inclusion of products in the next contracting cycle.</p></li></ul><p></p><p><b><u>Internal Relationship:</u> </b>Collaborate closely with BU Lead, Customers facing, Contracting and Trade to develop strategies and value add programs that help maintain and grow the business as well as improve contract compliance.</p><p></p><p><b>Secondary Functions:</b></p><ul><li><p>Perform special project and assignments as directed by the Supervisor</p></li></ul><p></p><p><b>QUALIFICATIONS</b></p><p><b>Education: </b></p><p>• BA/BS Degree from an accredited institution</p><p>• MBA or advanced degree is a plus</p><p>• Ability to travel domestically and stay overnight as necessary.</p><p>• Valid US driver’s license and driving record in compliance with company standards.  Any DUI/DWI or other impaired driving citation within the past 7 years will disqualify you from being hired.</p><p>• Candidate must reside in San Juan, Puerto Rico preferred – Local Candidates Only.</p><p></p><p><b>Experience:</b></p><ul><li><p>The Key Account Director must have a minimum of 8 years of successful healthcare sales experience with proven results and must possess strong leadership skills</p></li><li><p>They also must have demonstrated ability to serve customers’ needs (immediate follow-up, addressing issues promptly) and collaborate with multiple and diverse product lines, customer segments, and levels of internal/external stakeholders.</p></li></ul><p></p><p><b>Other Requirements:</b></p><ul><li><p>This person must have strong business management skills, demonstrate an excellent understanding of marketing practices, be able to develop and execute strategic plans, and understand and apply the fundamentals of financial management to perform profit and loss analyses to plan strategies</p></li><li><p>This person must have strong analytical and problem-solving skills, a demonstrated ability to gather, understand, evaluate information from various sources (establishes links between sources of data, draws logical conclusions and provides appropriate options, makes recommendations and wise decisions in a timely manner, and has the ability to utilize various analytical tools to gather, understand and evaluate information (Excel, etc.).</p></li><li><p>This person must have well-developed project management/organizational skills to manage multiple projects and priorities. The candidate will have a proactive, results-oriented willingness to drive changes across the organization while working effectively with cross-functional teams in a matrix environment, focusing energy in the right places to work efficiently.</p></li><li><p>This person must have a high degree of self-direction with the ability to constantly seek innovative ways to perform tasks in an efficient and timely manner.</p></li><li><p>This person must be fully bilingual (English &amp; Spanish)</p></li><li><p>Proficient in Microsoft Excel, Word, and PowerPoint</p></li><li><p>Occasional travel; mainly to USA (i.e. Sales/Business meetings), POAs, trainings, etc.</p></li><li><p>Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p></li></ul><p></p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p>Ability to walk all day and ability to perform mathematical calculations and ability to perform complex data analysis.</p><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p></p><p>Participation in business reviews / Operating Plans / territory analysis and / or in its preparation. Ability to work After hours<br />Participation in conventions or activities on weekdays and / or weekends.<br />Occasional trips; mainly to USA (i.e. sales meetings), POAs, trainings, etc.</p><p><br /><b>Other Job Details</b></p><p>Last Day to apply: May 22, 2026</p>&amp;#xa;The annual base salary for this position ranges from $139,100.00 to $231,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Sales&amp;#xa;]]></description><link>http://biotechroles.com/key-account-director-puerto-rico-pfizer/6a08948b2f1861929d253315</link><guid isPermaLink="true">http://biotechroles.com/key-account-director-puerto-rico-pfizer/6a08948b2f1861929d253315</guid><pubDate>Sat, 16 May 2026 16:00:11 GMT</pubDate><company>Pfizer</company><location>Puerto Rico - Remote</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[(1 Year Temporary Contract) Medical Operations Support]]></title><description><![CDATA[<ol><li>To support contract process /finalization related to Medical Affairs initiated consultancy, according to Local/Global Policies and Local Regulation.</li><li>Ensure regular updates on project status and progress</li><li>Review and manage contracts with external providers</li><li>Interface effectively with service providers</li></ol><p>Responsibilities include but are not limited to the following:</p><ol><li>Support TALs (Therapeutic Area Leaders) in planning, supervising, and developing Advisory Board meetings</li><li>Carry out financial/administrative activities related to prioritized Medical Affairs Projects (ie Advisory Board Meetings):<ol><li>HCP Engagement for prioritized activity : Collect documentation and verify service performed&#xa0;</li><li>Logistics Contract Management: Development, finalization, and closure of logistics contracts&#xa0;</li></ol></li><li>Ensure project activities comply with regulations, internal policies, and the Farma Industria code</li><li>Collaborate with various company functions (e.g., OEC, Regulatory Affairs, Legal, Procurement, CEX) for proper project implementation</li><li>Support preparation for audits/inspections.</li></ol>]]></description><link>http://biotechroles.com/(1-year-temporary-contract)-medical-operations-support-abbvie/6a0840922f1861929d253310</link><guid isPermaLink="true">http://biotechroles.com/(1-year-temporary-contract)-medical-operations-support-abbvie/6a0840922f1861929d253310</guid><pubDate>Sat, 16 May 2026 10:01:54 GMT</pubDate><company>AbbVie</company><location>Rome, Roma</location><salary>$35000-48000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist II]]></title><description><![CDATA[<p>12-month Fixed Term Contract | AbbVie Westport</p><p>Join AbbVie in Westport and contribute to the development and delivery of innovative medicines that make a meaningful difference to patients. This 12-month fixed term contract offers an exciting opportunity to work within the Product Development, Science &amp; Technology (PDS&amp;T) team, supporting new product introductions and analytical method lifecycle activities in a collaborative, science-driven environment.</p><p>&#xa0;</p><p><strong>Role Purpose</strong></p><p>The Scientist II, PDS&amp;T Analytical will lead and support the development, qualification, validation, and transfer of analytical methods, primarily ELISA, HPLC, and related assays, to support New Product Introductions (NPIs) at AbbVie Westport. This role ensures methods are scientifically robust, compliant with applicable regulatory and quality requirements, and effectively integrated into production and QC workflows to support clinical and commercial supply.</p><p>The successful candidate will also support NPI product leads and lifecycle management activities, including stability and specification documentation, data trending, third-party method transfers, sample coordination, reagent requalification, and procurement support. In addition, this role will support QC activities through coordination of release and stability samples, investigation support, and cross-functional collaboration.</p><p>Key Responsibilities</p><ul><li>Lead and/or support the development, qualification, validation, and transfer of analytical methods, with a focus on HPLC and ELISA, for new product introductions.</li><li>Apply Quality by Design principles to ensure methods are scientifically sound, GMP compliant, and suitable for QC implementation.</li><li>Support technology transfer activities from R&amp;D to manufacturing and QC, ensuring smooth handover and minimal disruption to operations.</li><li>Plan, execute, and track analytical projects related to method development, validation, and transfer to ensure timely delivery of project milestones.</li><li>Prepare, review, and maintain technical documentation, including protocols, reports, specifications, stability documentation, and SOPs.</li><li>Support NPI product leads with analytical data compilation, trending, stability and specification updates, sample shipment coordination, reagent requalification, and procurement-related activities.</li><li>Coordinate release and stability sample activities in partnership with QC and other cross-functional stakeholders.</li><li>Support and participate in investigations, troubleshooting, and root cause analysis related to analytical methods and testing.</li><li>Collaborate closely with R&amp;D, QC, Manufacturing, Regulatory Affairs, and Quality to resolve technical challenges and support project execution.</li><li>Train and support QC and cross-functional team members in the transfer and execution of new analytical methods, as appropriate.</li></ul>]]></description><link>http://biotechroles.com/scientist-ii-abbvie/6a0840912f1861929d25330f</link><guid isPermaLink="true">http://biotechroles.com/scientist-ii-abbvie/6a0840912f1861929d25330f</guid><pubDate>Sat, 16 May 2026 10:01:53 GMT</pubDate><company>AbbVie</company><location>Westport, Westport</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist I]]></title><description><![CDATA[<p>Fixed-Term Contract | 1 Year</p><p>About the Role</p><p>We are currently seeking a Scientist I to join our talented and ambitious analytical team on a 1-year fixed term contract. This is an exciting opportunity to contribute to a collaborative, science-led environment where you will support routine analytical testing and play a key role in the development, validation, and continuous improvement of analytical methods.</p><p>In this role, you will perform routine testing using ELISA, HPLC, Karl Fischer, and other compendial methods while contributing to the delivery of high-quality data in support of project and operational needs.</p><p>Key Responsibilities</p><ul><li>Perform routine testing using ELISA, HPLC, Karl Fischer, and other compendial analytical methods.</li><li>Participate in the development, optimization, and validation of analytical methods in line with project requirements, regulatory standards, and company procedures.</li><li>Accurately document, review, and interpret experimental results and observations.</li><li>Troubleshoot and resolve technical issues related to analytical instrumentation and methodologies.</li><li>Maintain laboratory equipment, manage reagents and consumables, and help ensure a safe and well-organized laboratory environment.</li><li>Collaborate effectively with team members to support efficient workflow and timely project completion.</li><li>Communicate clearly and professionally with colleagues and management regarding project status, results, and any technical issues.</li><li>Understand and adhere to corporate standards, including Good Manufacturing Practice (GMP), code of conduct, safety requirements, and appropriate handling of materials such as controlled drug compounds, as applicable.</li></ul>]]></description><link>http://biotechroles.com/scientist-i-abbvie/6a08408f2f1861929d25330e</link><guid isPermaLink="true">http://biotechroles.com/scientist-i-abbvie/6a08408f2f1861929d25330e</guid><pubDate>Sat, 16 May 2026 10:01:51 GMT</pubDate><company>AbbVie</company><location>Westport, Westport</location><salary>$75000-95000</salary><type>Full-time</type></item><item><title><![CDATA[Technician, Manufacturing II (Monday-Friday, 6:00am - 2:30pm)]]></title><description><![CDATA[<p>Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.</p><p>Responsibilities</p><ul><li>Shipping finished materials</li><li>Maintaining inventory levels</li><li>Sampling of in process and raw materials</li><li>Running glass washer / autoclave</li><li>Buffer / media preparation</li><li>Equipment preparation (CIP/SIP)</li><li>Cell culture (from vial thaw to production scale)</li><li>Column chromatography</li><li>Tangential flow filtration</li></ul>]]></description><link>http://biotechroles.com/technician-manufacturing-ii-(monday-friday-6:00am-2:30pm)-abbvie/6a08408e2f1861929d25330d</link><guid isPermaLink="true">http://biotechroles.com/technician-manufacturing-ii-(monday-friday-6:00am-2:30pm)-abbvie/6a08408e2f1861929d25330d</guid><pubDate>Sat, 16 May 2026 10:01:50 GMT</pubDate><company>AbbVie</company><location>Worcester, Worcester</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Product Specialist / Medical Representative]]></title><description><![CDATA[<p><strong>This position title on contract - PRODUCT SPECIALIST.</strong></p><p><strong>Territorial scope (districts): mazowieckie, warmińsko-mazurskie, podlaskie.</strong></p><p><strong>Job purpose:</strong></p><p>The Product Specialist’s primary responsibility is to coordinate Allergan’s relationships with the customers - physicians and pharmacies in its designated area (i.e. HCPs/injectors, pharmacies). The Product Specialist works strategically to increase the awareness and appropriate use of designated &#xa0;AA products. Works in combination with affiliate sales management to define and implement the most effective approach and is responsible for the sales performance of the designated portfolio. Develops, manages and implements business plans and programs in the assigned geographic region to ensure that not only growth targets are achieved but also to establish long term loyalty and commitment with the customers based on ethical principles.</p><p><strong>Key responsibilities:</strong></p><p>1.&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;<u>Commercial Management &#xa0;&#xa0;</u>&#xa0;&#xa0; &#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0; &#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;</p><ul><li>Responsible for the sales performance of the designated portfolio by engaging with customers in placing orders, presenting commercial policy and seasonal offers benefits.</li><li>Achieve the quantitative objectives defined for designated geographic territory.</li><li>Development of sales strategies aligned with AA overall strategic plan.</li><li>Leverage portfolio and increase market share of AA products within the territory.</li><li>Develop &amp; manage relationships with relevant internal stakeholders.</li></ul><p>2.&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;<u>Customer Relationship Management&#xa0;&#xa0;&#xa0;&#xa0;</u>&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;</p><ul><li>Develops long-term customer relationship based on ethical principles.</li><li>Makes presentations and organizes group events for HCPs, as well as works with contacts on a one-to-one basis.</li><li>Provide training and support about the proper use of AA products.</li><li>Identify new opportunities in the territory for further strategic synergies and target group development.</li></ul><p>3.&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;<u>&#xa0;Planning&#xa0;&#xa0;&#xa0;</u>&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0; &#xa0; &#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0; &#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;&#xa0;</p><ul><li>Plans daily activities based on actual targeting in order to achieve assigned sales targets.&#xa0;</li><li>Maximise time spent with the customer by correct monthly and daily call planning by using CRM system and reporting KPIs.</li><li>Effectively use of the budget.</li><li>Constantly keep the business plan up to date and implement improvements.</li><li>Adhere to Company ethical code and promotional strategy.</li></ul>]]></description><link>http://biotechroles.com/product-specialist-medical-representative-abbvie/6a08408c2f1861929d253308</link><guid isPermaLink="true">http://biotechroles.com/product-specialist-medical-representative-abbvie/6a08408c2f1861929d253308</guid><pubDate>Sat, 16 May 2026 10:01:48 GMT</pubDate><company>AbbVie</company><location>Warsaw, Warszawa</location><salary>$35000-55000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Parkinson's - El Paso, TX]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.&#xa0; <strong>This territory includes Austin, El Paso and Lubbock</strong><br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-parkinson&apos;s-el-paso-tx-abbvie/6a08408b2f1861929d253307</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-parkinson&apos;s-el-paso-tx-abbvie/6a08408b2f1861929d253307</guid><pubDate>Sat, 16 May 2026 10:01:47 GMT</pubDate><company>AbbVie</company><location>El Paso, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Gross to Net Finance Analyst]]></title><description><![CDATA[<p>Responsible for credit and accrual rebate process, in line with commercial agreements for pharma markets in Cluster North LATAM countries.</p>]]></description><link>http://biotechroles.com/gross-to-net-finance-analyst-abbvie/6a08408a2f1861929d253306</link><guid isPermaLink="true">http://biotechroles.com/gross-to-net-finance-analyst-abbvie/6a08408a2f1861929d253306</guid><pubDate>Sat, 16 May 2026 10:01:46 GMT</pubDate><company>AbbVie</company><location>Bogotá, Bogota Cundinamarca</location><salary>$28000-45000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Parkinson's - Lubbock, TX]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.&#xa0;&#xa0;<strong>This territory includes Austin, El Paso and Lubbock</strong><br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-parkinson&apos;s-lubbock-tx-abbvie/6a0840882f1861929d253305</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-parkinson&apos;s-lubbock-tx-abbvie/6a0840882f1861929d253305</guid><pubDate>Sat, 16 May 2026 10:01:44 GMT</pubDate><company>AbbVie</company><location>Lubbock, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Manufacturing Software / Control Engineer]]></title><description><![CDATA[<p>•As&#xa0;<strong>Software / Control Engineer,&#xa0;</strong>you are responsible for basic configuration and programming per AbbVie’s change management procedures for the manufacturing process, utilities and facilities control systems. This position performs system troubleshooting during and outside business hours as necessary. Responsible for the maintenance of assigned site operations technologies (OT) systems per applicable departmental procedures.</p><p><strong>Responsibilities</strong></p><ul><li>Develop basic control configuration or programming in accordance with the design documents to meet the functional requirements.</li><li>Provide first line technical support to Project Engineers, Maintenance, Production and Technical Operation personnel in automation related problems as need arises. Provides training for OT Systems users in automation technologies and process control applications.</li><li>Diagnose and troubleshooting Control System hardware, software, and networking issues, replace defective components as needed.</li><li>Perform site OT systems (PLC’s, SCADA, and Data Historian) upgrades and data migrations activities.</li><li>Develop and execute qualification protocols plus associated technical documentation like System’s Functional and\or Design Specifications following OT Systems lifecycle validation activities.</li><li>Perform scheduled OT Systems administration and maintenance tasks such as operating systems (OS) and anti-virus updates, users accounts managements, critical data back-up and others.</li><li>Evaluate and provide input and recommendations regarding control system improvements. Establish monitoring and reporting project techniques to support equipment performance reliability.</li><li>Provide production support during off-peak hours. This might require working overtime, overnight or on weekends.</li><li>Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.</li></ul>]]></description><link>http://biotechroles.com/manufacturing-software-control-engineer-abbvie/6a0840872f1861929d253303</link><guid isPermaLink="true">http://biotechroles.com/manufacturing-software-control-engineer-abbvie/6a0840872f1861929d253303</guid><pubDate>Sat, 16 May 2026 10:01:43 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$85000-115000</salary><type>Full-time</type></item><item><title><![CDATA[Metrology Engineer]]></title><description><![CDATA[<p>We are looking for an experienced and versatile Senior Scientist I/Development Engineer to join our Injection Device Development team to help us accelerate AbbVie’s combination products from proof-of-concept through submission, industrialization and launch.</p><p>Our team has end-to-end accountability for commercial development, submission, industrialization and marketed product support for injection devices that enable the delivery of AbbVie’s innovative medicines. In the course of our work, we collaborate with early-stage CMC, Quality Assurance, Regulatory Affairs, Internal and External Manufacturing, and other cross-functional colleagues to ensure timeliness, robustness and market success.</p><p>As a Senior Scientist I/Development Engineer at AbbVie you will be part of a multi-disciplinary team of professionals working at the intersection of engineering and biopharmaceuticals. The problems you would help to solve relate not only to the function of innovative injection systems, but also the way in which they interact with drug products and the human body. You would be responsible for advancing programs that combine proven delivery systems with viable commercial drug assets. If you are a self-motivated person who thrives on solving complex problems and are excited by the idea of putting life-changing therapies in the hands of patients, this might be the opportunity for you.</p><p>Key Responsibilities:&#xa0;</p><ul><li>Design and execute laboratory studies supporting product development and on-market investigations</li><li>Develop new and maintain existing test methods</li><li>Create and execute test method validation/transfer protocols, and author validation reports</li><li>Maintain product design documentation</li><li>Support design transfer and industrialization activities</li><li>Support design changes and continuous improvement effort</li><li>Perform 3D and 2D CAD development in PDM environment</li><li>Collaborating with third party developers and suppliers</li><li>Position required up to 25% of travel time</li></ul>]]></description><link>http://biotechroles.com/metrology-engineer-abbvie/6a0840852f1861929d253302</link><guid isPermaLink="true">http://biotechroles.com/metrology-engineer-abbvie/6a0840852f1861929d253302</guid><pubDate>Sat, 16 May 2026 10:01:41 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[HR Systems Analyst - Time and Attendance]]></title><description><![CDATA[<p>An HR Systems Analyst specializing in UKG or Workday&#xa0;acts as a technical bridge between Human Resources and Information Technology, responsible for the configuration, maintenance, reporting, and optimization of HR Information Systems (HRIS). This role ensures that workforce data—covering payroll, time tracking, benefits, and talent management—is accurate, secure, and fully utilized.</p><p><strong>Responsibilities&#xa0;</strong></p><ul><li><strong>System Administration &amp; Configuration:</strong>&#xa0;Serve as the primary administrator for UKG Pro/Dimensions and/or Workday, configuring business processes, security roles, and workflows.</li><li><strong>Integration Support:</strong>&#xa0;Monitor and manage data feeds/integrations&#xa0;pertain to Time and Absence&#xa0;ensuring seamless data flow between payroll, timekeeping, and HR system.</li><li><strong>Continuous&#xa0;</strong><strong>Improvement &amp; Optimization: </strong>Understand current business processes to identify improvements, implementing new features to enhance user experience and efficiency.</li><li><strong>User Support:</strong>&#xa0;Provide&#xa0;timely&#xa0;technical support to end-users,&#xa0;ensure adherence to AbbVie System Life Cycle (SLC) process, and resolve system-related inquires or issues efficiently.&#xa0;</li></ul>]]></description><link>http://biotechroles.com/hr-systems-analyst-time-and-attendance-abbvie/6a0840842f1861929d253301</link><guid isPermaLink="true">http://biotechroles.com/hr-systems-analyst-time-and-attendance-abbvie/6a0840842f1861929d253301</guid><pubDate>Sat, 16 May 2026 10:01:40 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$85000-115000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist I, In Vitro Electrophysiologist]]></title><description><![CDATA[<p>We are seeking a highly motivated in vitro electrophysiologist to join our collaborative Migraine and Pain drug discovery team.&#xa0; The ideal candidate will bring deep expertise in ion channel biology and patch-clamp electrophysiology to support functional, pharmacological, and mechanistic studies that advance novel therapeutics.</p><p><strong>Key Responsibilities Include:</strong></p><ul><li>Design and execute manual patch-clamp electrophysiology experiments to characterize ion channel pharmacology, biophysical properties, and cellular excitability in relevant cell and disease models including primary, hiPSC-derived, and recombinant cell lines.</li><li>Lead design, execution, and analysis of studies on automated patch-clamp platforms (e.g. SyncroPatch).&#xa0; This will include both operation and training/guidance of more junior scientists on the instrument.</li><li>Contribute to studies utilizing multi-electrode (MEA) recordings and complimentary fluorescence-based assays (e.g. calcium imaging, membrane potential assays) as needed.</li><li>Support target identification, validation, and compound profiling to advance our Neuroscience pipeline, with a focus on pain-relevant ion channel families including both voltage-and ligand-gated channels.</li><li>Apply broad cell and molecular biology skills to support mechanistic studies and complement electrophysiology-based work (e.g., cell culture, Western blot, Microscopy, transient transfection, RNAi approaches, etc).</li><li>Read and adapt scientific literature to stay current in the field and advance techniques and innovative approaches</li><li>Independently generate precise, reliable, and reproducible data in a timely manner; interpret and effectively communicate results to cross-functional project teams and diverse audiences.</li><li>Contribute to scientific publications and present findings at internal and external scientific meetings and conferences.</li></ul>]]></description><link>http://biotechroles.com/senior-scientist-i-in-vitro-electrophysiologist-abbvie/6a0840832f1861929d253300</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-i-in-vitro-electrophysiologist-abbvie/6a0840832f1861929d253300</guid><pubDate>Sat, 16 May 2026 10:01:39 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Publications - Oncology]]></title><description><![CDATA[<p>Lead Publications Teams in the execution of publication plans for assigned assets, and oversee the execution of scientific publications (ie, clinical manuscripts, abstracts, posters, and oral presentations) that fulfill strategic publication plan and scientific communications objectives for the asset. Ensure Publication Plan is in alignment with the strategic publication plan as developed by the Scientific Communication Platform lead or Medical Affairs plans as applicable. In partnership with the Publications Director ensure resources and personnel are aligned and optimized to meet with needs of their therapeutic area. Provide managerial oversight to staff members, including performance assessment, training and feedback, resolution of personnel issues, and management of talent retention.</p><p>Responsibilities</p><p>Serve as the leader of cross-functional Publications Team(s) for assigned assets, including leading team meetings/discussions and driving the execution of publication plans, incorporating input from key global stakeholders</p><ul><li>Lead tactical execution of publication plans (ie, clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets</li><li>Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications</li><li>Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics</li><li>Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets</li><li>Provide managerial oversight to internal and external medical writers regarding assigned projects, ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures</li><li>Provide direction to external vendors to effectively complete the execution of publication projects, within specified timelines, and ensure quality publication deliverables</li><li>Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff</li><li>Address and resolve publications-related issues for assigned therapeutic areas and assets.Ensure project information in publication records and resourcing tools is accurate and up-to-date</li></ul>]]></description><link>http://biotechroles.com/senior-manager-publications-oncology-abbvie/6a0840822f1861929d2532fe</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-publications-oncology-abbvie/6a0840822f1861929d2532fe</guid><pubDate>Sat, 16 May 2026 10:01:38 GMT</pubDate><company>AbbVie</company><location>Irvine, Mettawa</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist II, Precision Medicine Translational Research Immunology]]></title><description><![CDATA[<p>The Precision Medicine Immunology department is&#xa0;seeking&#xa0;a highly motivated and talented Scientist with a background in immunology or immuno-oncology and experience in single-cell or spatial genomics, molecular biology, and cell biology to join the Translational Research team. This individual will provide leadership in clinical biomarker discovery by profiling clinical samples using single-cell and spatial omics approaches to better understand drug mechanism of action and pharmacodynamics, while driving data-informed patient selection strategies. The role will support drug development programs across inflammatory and autoimmune disease areas, including Dermatology, Gastroenterology, Rheumatology, and Fibrosis, from late-stage discovery through clinical trials. The successful candidate will join a growing translational research group and collaborate with cross-functional teams both internally and externally.&#xa0;</p><p>Key Responsibilities&#xa0;</p><ul><li><p>Independently lead the design, execution, and analysis of complex genomic profiling experiments, including single-cell RNA-Seq, CITE-Seq, and spatial transcriptomics/proteomics.&#xa0;</p></li></ul><ul><li><p>Perform image analysis tasks for spatial transcriptomics and proteomics datasets, including de-array and alignment for multi-omics integration, cell&#xa0;segmentation&#xa0;and phenotyping.&#xa0;</p></li></ul><ul><li><p>Design, develop and implement computational pipelines for processing and analyzing spatial omics datasets, including spatial transcriptomics and proteomics.&#xa0;</p></li></ul><ul><li><p>Proactively&#xa0;identify&#xa0;technical artifacts, interpret quality control results,&#xa0;optimize&#xa0;assay performance, and ensure high quality and reproducible data delivery on&#xa0;timely&#xa0;deadlines.&#xa0;</p></li></ul><ul><li><p>Stay at the forefront of the single-cell and spatial genomics field by surveying, evaluating,&#xa0;testing&#xa0;and&#xa0;validating&#xa0;novel scientific methodologies.&#xa0;</p></li></ul><ul><li><p>Present work plans and&#xa0;acquired&#xa0;data clearly and precisely to cross-functional stakeholders through formal written reports and verbal updates</p></li></ul>]]></description><link>http://biotechroles.com/senior-scientist-ii-precision-medicine-translational-research-immunology-abbvie/6a0840802f1861929d2532fd</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-ii-precision-medicine-translational-research-immunology-abbvie/6a0840802f1861929d2532fd</guid><pubDate>Sat, 16 May 2026 10:01:36 GMT</pubDate><company>AbbVie</company><location>Waltham, Waltham</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Territory Manager, Downtown Toronto - West, Facial Aesthetics]]></title><description><![CDATA[<p>Joining Allergan Aesthetics (AA), an AbbVie company means you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients’ lives. AA exists to empower confidence for consumers and customers, creating products and technologies that drive the advancement of aesthetic medicine. We believe in the power of shaping your own life, your own business, your own look – and we continue to evolve our business around the needs of those we serve. United by our shared belief in what we do and a commitment to doing what is right, we bring our best every day to empower confidence.</p><p>Are you looking for an exciting full-time career, where development and high-performance are valued? AbbVie Canada is looking to connect with a Territory Manager to join our commercial sales team. This role is based in Downtown Toronto- West.</p><p>Our Territory Manager develops robust business plans to execute brand strategies and tactics in the field. They deliver sales performance, build strong customer relationships and support customer needs to maximize short- and long-term sales targets, all while placing the patient at the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p><strong>Key responsibilities:</strong></p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives in order to meet or exceed business objectives</li><li>Create pre-call plans and execute post-call evaluation to continuously improve sales performance</li><li>Proactively and continuously engage and collaborate with key stakeholders in support of their needs, expectations, and challenges, to build trusted relationships</li><li>Execute a call plan that achieves set metrics and optimizes coverage of key customers, to maximize sales opportunities</li><li>Continuously build understanding of customer needs and expectations, territory landscape, competitors, market segments/dynamics, accounts, products, and clinical expertise. Share this market intelligence information with district manager and respective team members, in order to achieve alignment, to anticipate environmental change and to optimize brand strategy and its execution.</li><li>Differentiate Allergan Aesthetics value proposition with healthcare providers and identify, develop and maintain knowledge, market insights and speakers/advocates to maximize brand performance</li></ul><p>&#xa0;</p>]]></description><link>http://biotechroles.com/territory-manager-downtown-toronto-west-facial-aesthetics-abbvie/6a08407f2f1861929d2532fc</link><guid isPermaLink="true">http://biotechroles.com/territory-manager-downtown-toronto-west-facial-aesthetics-abbvie/6a08407f2f1861929d2532fc</guid><pubDate>Sat, 16 May 2026 10:01:35 GMT</pubDate><company>AbbVie</company><location>Toronto, Toronto</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist II / Principal Scientist I, Biologics Drug Product Development]]></title><description><![CDATA[<p><strong>Description:&#xa0;</strong></p><p>Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie’s R&amp;D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy).</p><p>AbbVie is seeking a highly motivated candidate for the position of Senior Scientist II / Principal Scientist I, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product formulation and process development, scale-up and tech transfer. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Represent Bio DPD in the cross-functional Product Presentation and Device Strategy Team (PPDST) and the CMC Team.</li><li>Effectively and timely communicate development plans, risks, and mitigation plans to stakeholders and line management.</li><li>Support scale-up and technology transfer activities to internal and external manufacturing sites.</li><li>Lead the design and execution of biologics drug product formulation and process development, characterization and robustness studies.</li><li>Initiate and/or support scientific initiatives to drive innovation, continuously enhance capabilities and platforms, and improve business processes.</li></ul>]]></description><link>http://biotechroles.com/senior-scientist-ii-principal-scientist-i-biologics-drug-product-development-abbvie/6a08407e2f1861929d2532fb</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-ii-principal-scientist-i-biologics-drug-product-development-abbvie/6a08407e2f1861929d2532fb</guid><pubDate>Sat, 16 May 2026 10:01:34 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Strategic Account Executive - Oncology - Southwest]]></title><description><![CDATA[<p><strong>*Must be located within a reasonable driving distance from Los Angeles-CA or Phoenix-AZ*</strong></p><p>The Strategic Account Executive will play a pivotal role in the successful launch and promotion of a new oncology drug designed to treat an ultra-rare blood cancer. This position requires a dynamic and strategic professional with a strong background in pharmaceutical sales. The Strategic Account Executive will be responsible for developing and maintaining productive relationships with key stakeholders, including healthcare professionals, to drive the adoption of the new therapy.</p><p>It is an exciting time to join AbbVie’s established hematology team as we pursue our mission to have a remarkable impact on the lives of people affected by cancer and build organizational capabilities around ultra rare diseases. Come join an inclusive AbbVie Oncology culture that fosters trust in each other, curiosity, growth in ourselves and our organization, and joy in what we do! AbbVie Oncology offers you immense opportunities to explore your interests and help you achieve your goals. Hear directly from our AbbVie Oncology colleagues to learn more about our culture, growth opportunities, and what makes AbbVie Oncology a great place to work!&#xa0;<a href="https://www.abbvie.com/join-us/oncology-opportunities.html" rel="noopener noreferrer">https://www.abbvie.com/join-us/oncology-opportunities.html</a></p><p><strong>Key Responsibilities Include:</strong></p><ul><li>Establish and maintain relationships with key opinion leaders where appropriate.</li><li>Monitor and analyze territory level sales data</li><li>Proactively communicate with the marketing team through ongoing feedback on the development and implementation of effective selling materials.</li><li>Participate on cross-functional teams to support key accounts within the geography</li><li>Teamwork with other account managers across the country</li><li>Key account management that engages the entire care team</li><li>Educate on the preparation and administration requirements of approved products; and adverse event mitigation, monitoring, and management.</li><li>Educate patient care teams about initiation and managing patients per protocols associated with the product.</li><li>Represent AbbVie as a partner of choice in the ultra-rare Hematology space with HCP and Patient Organizations.&#xa0;</li><li>Attend and actively participate in local oncology society meetings, conferences, patient programs, support groups, advocacy events, etc., some of which occur in the evenings or weekends.</li><li>An essential requirement of your position is to meet health care industry representative (HCIR) credentialing requirements for entry into facilities and organizations that are in your assigned territory. These HCIR credentialing requirements may include, but not limited to, background checks, drug screens, and proof of immunization/vaccination for various diseases.</li></ul><p>&#xa0;</p><ul></ul>]]></description><link>http://biotechroles.com/strategic-account-executive-oncology-southwest-abbvie/6a08407c2f1861929d2532f9</link><guid isPermaLink="true">http://biotechroles.com/strategic-account-executive-oncology-southwest-abbvie/6a08407c2f1861929d2532f9</guid><pubDate>Sat, 16 May 2026 10:01:32 GMT</pubDate><company>AbbVie</company><location>Phoenix, US-Virtual Office</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - Florence, AL]]></title><description><![CDATA[<p>Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-florence-al-abbvie/6a08407b2f1861929d2532f8</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-florence-al-abbvie/6a08407b2f1861929d2532f8</guid><pubDate>Sat, 16 May 2026 10:01:31 GMT</pubDate><company>AbbVie</company><location>Florence, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Quality Engineer, Combo Product External Quality]]></title><description><![CDATA[<p>The Senior Quality Engineer – Combination Products External Quality is responsible for the quality of assigned suppliers/contract manufacturers to ensure business objective are me with regards to on time delivery of product while assuring compliance to AbbVie requirements, applicable external regulations, and standards.&#xa0;&#xa0; Products include injection molded components, and critical device components used to manufacture AbbVie On Body Injection Delivery Systems.&#xa0;&#xa0;</p><p>Responsibilities<em><strong>:</strong></em></p><ul><li>Support supplier quality development projects and continuous improvement activities.</li><li>Investigate/coordinate supplier quality issues resolution with the appropriate department, including the dispositioning of non-conforming product, event, deviation, and market complaints.&#xa0;</li><li>Initiate and follow up on Supplier Corrective Action Requests (SCARs).</li><li>Validate supplier corrective actions involving design and/or process changes to ensure they are robust, sustainable, and implemented for similar potential concerns across manufacturing lines and/or suppliers</li><li>Coordinate supplier change notifications and ensure supplier changes are appropriately assessed for impact and change plans opened to mitigate any impact to AbbVie product / processes.</li><li>Work with Product Development and Manufacturing/Process Engineers to develop appropriate receiving inspection test methods, sampling plans and acceptance criteria for new and existing components and materials, including first article inspection.</li><li>Review and monitor strategic supplier performance, including providing trend analysis, investigation, and CAPA for monthly quality review.</li><li>Liaise with internal customers to ensure effective problem resolution, develop metrics, develop reports, and identify supplier non-conformance trends.</li><li>Develop and implement product quality plans, documents, and systems by creating product and quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members.</li><li>Assist management in implementing and maintaining a quality system that adheres to European, US, Canadian and other regulatory and Quality System requirements (ISO 13485, CFR 820 QSMR, EU MDR, and ISO 14971).</li><li>Assist with internal Regulatory or Notified Body audits.</li><li>Perform continuous improvement activities/projects to improve Product Quality, Compliance, and the Quality System.</li><li>Establish and maintain relationships, including quality agreements with assigned suppliers/contract manufacturers.</li><li>Plan, execute, and deliver projects effectively within defined time/cost parameters.</li><li>Support supplier qualification activities for suppliers as needed.</li></ul>]]></description><link>http://biotechroles.com/senior-quality-engineer-combo-product-external-quality-abbvie/6a0840792f1861929d2532f7</link><guid isPermaLink="true">http://biotechroles.com/senior-quality-engineer-combo-product-external-quality-abbvie/6a0840792f1861929d2532f7</guid><pubDate>Sat, 16 May 2026 10:01:29 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist II - Biocompatibility]]></title><description><![CDATA[<p>The Scientist II - Biocompatibility is a SME which will provide highly skilled support for biocompatibility and non-clinical safety evaluations of medical devices, tissue products, and combination products as a part of AbbVie Research &amp; Development. The position will be responsible for supporting cross-functional and cross-site collaborations involving recommendations for biocompatibility activities with limited supervision. This individual must possess a working knowledge of ISO-10993 and other applicable standards. The position will be responsible for supporting cross-functional and cross-site teams and recommendations of biocompatibility activities. This includes establishing requirements, planning, execution, and approval of biocompatibility requirements in support of regulatory submissions, project teams, operations, with a large focus on marketed product support.</p><p><strong>This is an onsite role based out of our Branchburg, NJ.&#xa0;</strong></p><p><u><strong>Main Responsibilities</strong></u></p><ul><li>Function as a representative for ISO-10993 (biocompatibility) assessments, with minimal supervision from Biocompatibility senior team members and therapeutic area SMEs. This will include the design, execution, and interpretation of biocompatibility evaluation strategies and programs per the applicable regulatory requirements, including biological risk assessments, technical documentation, and other documents for internal and external distribution and regulatory submissions.</li><li>Responsible for supporting Project Plans for biocompatibility with realistic deliverables with timelines. Actively involved in the planning, execution and management of experimental studies for the safety and efficacy characterization of new and existing products.</li><li>Serve as dedicated biocompatibility resource for product development teams, working closely with other colleagues in Development Science. Provide skilled technical knowledge to support cross-functional project initiatives.</li><li>Maintain knowledge of medical device regulations to assure compliance and conformance of programs for evaluation of medical devices and other products, including performing gap analysis relevant to changes in biocompatibility standards or guidance, inclusive of updating of internal product files for component/process changes.</li><li>Prepare and deliver technical presentations to internal and external stakeholders with minimal supervision. Assist the team in functional training initiatives.</li><li>Support global change control activities as they relate to Biocompatibility.</li><li>Build and maintain strong connections and relationships with Contract Research Organizations, Toxicologists and Consultants for Biological Risk Assessments as needed.</li></ul><p>&#xa0;</p>]]></description><link>http://biotechroles.com/scientist-ii-biocompatibility-abbvie/6a0840782f1861929d2532f6</link><guid isPermaLink="true">http://biotechroles.com/scientist-ii-biocompatibility-abbvie/6a0840782f1861929d2532f6</guid><pubDate>Sat, 16 May 2026 10:01:28 GMT</pubDate><company>AbbVie</company><location>Branchburg, Branchburg</location><salary>$110000-145000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist I Medical Device Mechanical Engineer]]></title><description><![CDATA[<p>Purpose</p><p>We are looking for an experienced Scientist I Medical Device Mechanical Engineer to join our Injectables Device Development team to help us accelerate AbbVie’s combination products from proof-of-concept through submission, industrialization and launch.</p><p>Our team has end-to-end accountability for commercial development, submission, industrialization and marketed product support for injection devices that enable the delivery of AbbVie’s innovative medicines. In the course of our work, we collaborate with early-stage CMC, Quality Assurance, Regulatory Affairs, Internal and External Manufacturing, and other cross-functional colleagues to ensure timeliness, robustness and market success.</p><p>As a Scientist I Medical Device Mechanical Engineer at AbbVie you will be part of a multi-disciplinary team of professionals working at the intersection of engineering and biopharmaceuticals. The problems you would help to solve relate not only to the function of innovative injection systems, but also the way in which they interact with drug products and the human body. You would be responsible for advancing programs that combine proven delivery systems with viable commercial drug assets. If you are a self-motivated person who thrives on solving complex problems and are excited by the idea of putting life-changing therapies in the hands of patients, this might be the opportunity for you.</p><p>Responsibilities</p><ul><li>Design and execute laboratory studies supporting product development and on-market investigations</li><li>Support design transfer and industrialization activities</li><li>Support manufacturing process development activities</li><li>Maintain product design documentation</li><li>Support product design changes and continuous improvement effort</li><li>Perform statistical data analysis</li><li>Perform 3D and 2D CAD development in PDM environment</li><li>Develop protocols, and document test results</li><li>Position required up to 25% of travel time</li></ul><p>Preferred Qualifications</p><ul><li>BS in Mechanical or Biomedical Engineering (MS preferred)</li><li>3-5 years of experience (MS up to 2 years) ideally in the medical device, drug delivery or other regulated industry</li><li>Strong communication skills (both written and verbal)</li><li>Strong design and analytical skills</li><li>Experience with:<ul><li>Laboratory environment, experiment planning, material control and recordkeeping</li><li>Physical prototyping (including 3D printing, manual machining, etc.) and reverse engineering</li><li>3D CAD modeling, detailed engineering drawings, product database management environment and GD&amp;T</li><li>Statistical analysis tools</li><li>Manufacturing processes</li><li>Design controls (in accordance with ISO 13485 / CFR 820.30)</li><li>Toolroom environment</li></ul></li><li>Knowledge of material properties, material selection and testing methodologies</li><li>The ability to follow assigned schedules and work in team environment</li></ul>]]></description><link>http://biotechroles.com/scientist-i-medical-device-mechanical-engineer-abbvie/6a0840762f1861929d2532f5</link><guid isPermaLink="true">http://biotechroles.com/scientist-i-medical-device-mechanical-engineer-abbvie/6a0840762f1861929d2532f5</guid><pubDate>Sat, 16 May 2026 10:01:26 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$95000-125000</salary><type>Full-time</type></item><item><title><![CDATA[Specialist, Quality Systems]]></title><description><![CDATA[<p><strong>Purpose</strong></p><p>The Specialist Quality Systems is responsible for providing quality assurance support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ensure that all product, process or system related quality activities from raw material inspection through shipment of final product are in compliance with Corporate and governmental regulations.</p><p>Responsibilities</p><ul><li>Assist with proper integration and support of quality regulations: drug, biologics, device and/or combination products.</li><li>Assist project teams in planning, preparation, review and approval of quality documentation.</li><li>Complete and route change requests for process document creation, maintenance, and implementation.</li><li>Create quality system documentation and specifications with guidance from technical teams following approved templates and guidelines.</li><li>Assist with or co-lead audits of documentation, facilities and equipment.</li><li>Assist in the design of effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality system.</li><li>Perform assessments to determine compliance to processes and regulations to identify potential gaps and mitigate and implement improvements within our quality system.</li><li>Participate in training and education programs for various aspects of quality assurance.</li></ul>]]></description><link>http://biotechroles.com/specialist-quality-systems-abbvie/6a0840752f1861929d2532f4</link><guid isPermaLink="true">http://biotechroles.com/specialist-quality-systems-abbvie/6a0840752f1861929d2532f4</guid><pubDate>Sat, 16 May 2026 10:01:25 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Consumer Marketing - OTC (Eye Care)]]></title><description><![CDATA[<p><strong>Job Description</strong></p><p>The Associate Director, Consumer Marketing serves as the patient, brand, and product subject matter expert for Over-The-Counter (OTC) consumer business, driving overall brand performance through strategic, data-driven marketing across varied channels. Lead cross-functional collaboration and external agency management, implementing eCommerce strategies to bolster online reach, and consumer engagement.</p><p><strong>Key Responsibilities</strong></p><ul><li>Lead brand strategy evolution, including value proposition, positioning, segmentation, and omni-channel strategy, with integration of eCommerce.</li><li>Direct development and execution of creative consumer marketing tactics and omnichannel campaigns—including TV, digital, social, website, CRM, and eCommerce platforms.</li><li>Collaborate extensively with external agencies and a broad range of internal stakeholders to ensure consistency, compliance, and excellence in brand messaging and marketing execution.</li><li>Drive brand annual planning, representing direct-to-consumer (DTC) needs foremost, while ensuring digital commerce initiatives are incorporated as supportive growth channels.</li><li>Oversee measurement, analytics, and optimization of marketing performance. Utilize KPIs for continuous campaign improvement and innovation.</li><li>Support business development opportunities, leverage digital and eCommerce data insights, and provide ad hoc competitive analyses as needed.</li><li>Advise senior leadership on market challenges and opportunities, offering creative thought leadership for consumer marketing and eCommerce initiatives.</li></ul>]]></description><link>http://biotechroles.com/associate-director-consumer-marketing-otc-(eye-care)-abbvie/6a0840732f1861929d2532f3</link><guid isPermaLink="true">http://biotechroles.com/associate-director-consumer-marketing-otc-(eye-care)-abbvie/6a0840732f1861929d2532f3</guid><pubDate>Sat, 16 May 2026 10:01:23 GMT</pubDate><company>AbbVie</company><location>Irvine, Irvine</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Cost Analyst]]></title><description><![CDATA[<p>The Newly formed Packaging Region in Internal Manufacturing includes 4 critical manufacturing sites. These sites package nearly all of AbbVie’s key products, including Skyrizi, Ubrelvy, Rinvoq, Venetoclax, and Vyalev.&#xa0; This role will function as a shared resource across the Packaging region with a focus on AP16 &amp; Cincinnati sites. The role will lead process improvement initiatives including the implementation and maintenance of regional reporting in Wdesk, drive standardization &amp; consistent accounting treatment across sites. This role will also get the opportunity to gain direct cost accounting &amp; business support experience through working with the Site and Assistant Controllers for AP16 &amp; Cincinnati.</p><p>The Analyst, Finance is responsible for driving process improvements, consolidation, cost allocation, and collection of data and preparation of reports that maintain AbbVie’s cost accounting systems for businesses supported.</p><p>Responsibilities</p><ul><li>Serves as a shared resource across the Packaging Region, providing financial support to multiple sites and ensuring alignment of processes and reporting.</li><li>Leads standardization efforts across the packaging Region, identifying opportunities to harmonize financial processes, reporting templates, and cost allocation methodologies across all regional sites.</li><li>Implements and maintains regional reporting in Wdesk, including developing standardized templates, ensuring data accuracy, and training site teams on reporting requirements.</li><li>Drives continuous process improvements across the region, identifying inefficiencies and implementing solutions to enhance financial close processes, reporting accuracy, and operational effectiveness.</li><li>Financial support for Actuals, LBE Plan and Update. Review and understand variances from Plan/Update/LBE. Provide mid-month analysis of actuals and trend against LBE to Region Management.</li><li>Prepare and analyze journal entries and account reconciliations as needed during month-end close process to maintain appropriate internal controls.</li><li>Provide ad hoc analysis to support complex decision making.</li></ul>]]></description><link>http://biotechroles.com/cost-analyst-abbvie/6a0840722f1861929d2532f2</link><guid isPermaLink="true">http://biotechroles.com/cost-analyst-abbvie/6a0840722f1861929d2532f2</guid><pubDate>Sat, 16 May 2026 10:01:22 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$75000-95000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Migraine - Kokomo, IN]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.<br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers.</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance.</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-migraine-kokomo-in-abbvie/6a0840712f1861929d2532f1</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-migraine-kokomo-in-abbvie/6a0840712f1861929d2532f1</guid><pubDate>Sat, 16 May 2026 10:01:21 GMT</pubDate><company>AbbVie</company><location>Indianapolis, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Analyst, Business Systems]]></title><description><![CDATA[<p>Advance your career with an organization that strategically invests in its long-term success, technology, and people. The AbbVie Business Technology Solutions (BTS) team drives our digital transformation, vital to ensuring our treatments positively impact patients’ lives. As a Senior Analyst, Business Systems, you will tackle complex challenges, broaden your professional experience, and help others grow their skills.&#xa0;</p><p>The Senior Analyst, Business Systems works closely with business partners in Clinical Development Operations to understand and document requirements for technology solutions. This involves conducting interviews, workshops, and surveys to gather critical information. You will analyze these requirements to identify gaps, define project objectives, and collaborate with solution architects to propose solutions aligned with business goals. As a bridge between business stakeholders and technical teams, you will ensure requirements are clear, complete, and feasible. You will also contribute to the design, development, testing, maintenance, and enhancement of business applications, applying specialized technical or business knowledge to system projects. This position is essential for developing, identifying, and implementing system modifications that drive productivity improvements.&#xa0;</p><p>Responsibilities:&#xa0;</p><ul><li><p>Gain a deep understanding of business processes related to Clinical Development Operations technology solutions.&#xa0;</p></li></ul><ul><li><p>Respond to questions and provide consultation to business users regarding current and prospective system inputs, processes, and outputs.&#xa0;</p></li></ul><ul><li><p>Research and analyze system issues and determine appropriate resolutions.&#xa0;</p></li></ul><ul><li><p>Develop comprehensive business user requirements, functional requirements, user stories, system documentation, workflow procedures, and data models.&#xa0;</p></li></ul><ul><li><p>Drive alignment between business and technology teams regarding plans, requirements, sprint schedules, trade-offs, and showcases, ensuring all parties understand project scope and goals.&#xa0;</p></li></ul><ul><li><p>Consult with functional areas to develop an understanding of the varied, complex business needs supported by the system.&#xa0;</p></li></ul><ul><li><p>Assess how evolving business needs will affect existing systems.&#xa0;</p></li></ul><ul><li><p>Analyze the broader impact of systems and provide recommendations for their evolution.&#xa0;</p></li></ul><ul><li><p>Advancing efficiency and automation leveraging emerging technologies.&#xa0;</p></li></ul><ul><li><p>Create and manage system change requests and documentation supporting implementations.&#xa0;</p></li></ul><ul><li><p>Assist in the communication of system changes and issues to all levels of management.&#xa0;</p></li></ul><ul><li><p>Ensure up-to-date system documentation and coordinate or lead testing of system modifications for both validated and non-validated systems.&#xa0;</p></li></ul><ul><li><p>Provide system expertise and support for training, educational tools, and materials.&#xa0;</p></li></ul><ul><li><p>Apply analytical thinking to diagnose issues and make system recommendations.&#xa0;</p></li></ul><ul><li><p>Collaborate effectively with both technical and business team members.&#xa0;</p></li></ul>]]></description><link>http://biotechroles.com/senior-analyst-business-systems-abbvie/6a0840702f1861929d2532f0</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-business-systems-abbvie/6a0840702f1861929d2532f0</guid><pubDate>Sat, 16 May 2026 10:01:20 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$110000-145000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, I - Drug Substance Analytical R&D]]></title><description><![CDATA[<p>AbbVie Analytical Research &amp; Development (Analytical R&amp;D) is a global analytical scientific organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products.  Our scope includes AbbVie's diverse pipeline of innovative small molecule medicines and spans from the selection of Discovery candidate molecules to Late Stage Clinical.  We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines.  Careers in AbbVie Analytical R&amp;D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies.  We are looking for diverse candidates with strong scientific experience to join the AbbVie Analytical R&amp;D team and can offer exciting and rewarding career opportunities for these candidates.<strong>&#xa0;</strong></p><p>&#xa0;</p><p><strong>Position Description:&#xa0;</strong></p><p>For the Senior Scientist I position, we are seeking a highly motivated candidate who can conceive, implement and execute novel scientific research and development. The candidate can independently develop and optimize new methods and techniques to generate reliable and reproducible data in a timely manner, demonstrate broad versatile technical expertise. He/she should possess understanding of core disciplines and support early phase development of New Chemical Entities (NCEs) drug substance in both preclinical and clinical space. He/she will collaborate within the global Analytical R&amp;D organization and with R&amp;D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), and Quality Assurance (QA) and CMC-Regulatory. &#xa0;</p><p>This position will focus primarily on drug substance (active pharmaceutical ingredient) programs in a dynamic environment from pre-clinical through first-in-human clinical stages. The individual will independently create phase-appropriate analytical methods to facilitate process development, assess stability, control manufacturing impurities, and enable release testing of pre-clinical and clinical drug substances. They will work closely with synthetic organic chemists in Process Chemistry to establish appropriate proposed regulatory starting materials, design efficient control strategies, support reaction troubleshooting, and identify manufacturing impurities or degradants. Candidates should be comfortable discussing organic chemistry topics relevant to analytical chemistry, such as stereoisomers, common functional groups, and pKa values. Experience with chromatographic analysis (such as HPLC or GC) is preferred but not required. Experience with analysis of peptides and solid-phase peptide synthesis (SPPS) is preferred but not required.</p><p><strong>Responsibilities:</strong></p><ul><li>Apply analytical separation and detection modes for complex impurity profiling of pharmaceutical drug substances to further the understanding of emerging non-GMP and cGMP manufacturing processes.</li><li>Responsible for leading the analytical aspects of a project while working with other functional areas to advance projects through the development pipeline.</li><li>Utilize understanding of a range of analytical techniques to conduct research and development studies related to small-molecule drug substances, intermediates, starting materials, impurities, and impurity profiling.</li><li>Support new product development with advanced method development and validation, technical transfer packages, and generation of technical data in support regulatory requirements.</li><li>Highly autonomous and productive in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor.</li><li>Formulate conclusions and design follow-on experiments based on multidisciplinary data.</li><li>May initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a research or development program.</li><li>Process, interpret, and visualize data to facilitate project team decisions.</li><li>Communicate and collaborate with cross-functional groups and departments, especially process chemistry, process engineering, and technical operations.</li><li>Routinely demonstrate scientific initiative and creativity in research or development activities and maintain a high level of productivity in the lab.</li><li>Responsible for method development, testing procedures, and implementation of analytical control strategies to help the advancement of drug discovery candidates.</li><li>Raises the bar and is never satisfied with the status quo.</li><li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, and GxP compliance, where applicable.</li></ul><p>&#xa0;</p><p>&#xa0;</p><p>&#xa0;</p>]]></description><link>http://biotechroles.com/senior-scientist-i-drug-substance-analytical-randd-abbvie/6a08406e2f1861929d2532ef</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-i-drug-substance-analytical-randd-abbvie/6a08406e2f1861929d2532ef</guid><pubDate>Sat, 16 May 2026 10:01:18 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$130000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Project Manager, Clinical Supply]]></title><description><![CDATA[<p>Forecasts, plans, schedules, coordinates and executes, ensuring timely availability of investigational drug supplies and related services to clinical sites and depots for clinical supply chain activities. This position is the entry-level position for the GDSM Project Management function. Works on the less complex clinical studies and will require significant guidance through the learning curve process.&#xa0;</p><p><strong>Responsibilities</strong></p><ul><li>Maintains and adheres to applicable Corporate and Divisional Policies and procedures. Represents CDSM activities as a member of the Clinical Study Team.</li><li>With guidance, provides input to Clinical Study Teams to influence clinical protocol design to ensure most efficient utilization of supply chain resources. Translates clinical study design into packaging design.</li><li>Develops protocol specific labeling compliant with applicable global regulations. Identifies, develops, communicates and tracks project timelines, activities, logistics, and milestones.</li><li>Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with QA, GPAS, and clinical team partners, ensuring timely availability of clinical supplies. Forecasts and coordinates the execution of required packaging jobs including retest expiry label updates.</li><li>Participates in CDSM Knowledge Management Meetings and presents relevant topics on an ad hoc basis. Proactively provides input on process improvement opportunities.</li><li>Successfully participates in Process Improvement initiatives. Partners with Clinical Statistics and CDSM Coordination staff to prepare appropriate protocol specific randomization code files and blind breaker envelopes, as required.</li><li>Coordinates with CDSM Materials Management to establish study specific distribution plans for shipment of packaged supplies. Manages inventory of finished goods and ancillary supply through study completion. Tracks retest dates and subsequent dating extensions of study medication.</li><li>With mentoring, participates in troubleshooting and resolving clinical supply related issues ensuring that project needs and priorities are understood by key team members. Effectively utilizes MS Project to manage key project activities.</li><li>With guidance, may be responsible for project management of IVRS/IWRS activities. Provides input and recommendation to CSPMs / DSMs on project timing, resource requirements, and budget projections.</li></ul>]]></description><link>http://biotechroles.com/project-manager-clinical-supply-abbvie/6a08406d2f1861929d2532ee</link><guid isPermaLink="true">http://biotechroles.com/project-manager-clinical-supply-abbvie/6a08406d2f1861929d2532ee</guid><pubDate>Sat, 16 May 2026 10:01:17 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$75000-95000</salary><type>Full-time</type></item><item><title><![CDATA[National Partnership Manager – Oncology / Hematology]]></title><description><![CDATA[<p>Joining AbbVie means you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada.</p><p>When choosing your career path, choose to be remarkable.</p><p>AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio.</p><p>We are presently recruiting for a National Partnership Manager position in our Oncology business, reporting to the Business Unit Head - Hematology.&#xa0; The candidate will build strategic plans with key AbbVie Hematology stakeholders and accounts across Canada, aligns cross-functional teams, and manages account planning, local and national congress engagement, and regional initiatives to advance business objectives.</p><p>The National Partnership Manager<strong> </strong>(NPM) is intended to be the face of AbbVie to identified Strategic Accounts across Canada to continue to build on and develop the long-term customer relationships. The NPM will also support the coordination of effective IFT Reginal Meetings and develop regional tactics aligned with the brands priorities.</p><p>Location ONTARIO OR QUEBEC</p><p><strong>Key Responsibilities</strong>:</p><ul><li>Acts as manager of the AbbVie Hematology Strategic partnerships with Key accounts and HCP Associations. &#xa0;</li><li>Develops and maintains a macro view of customer relationships and works cross-functionally within AbbVie to maximize engagement with Strategic Accounts.</li><li>Works closely with multiple stakeholders, both internal and external, to ensure internal team members understand and effectively execute against the customer strategy and commercial expectations.</li><li>Acts in the best interests of AbbVie looking for areas of mutual interest to AbbVie and the key accounts. The NPM identifies predictive and responsive opportunities to co-develop solutions and growth projects within the key accounts.</li><li>Mapping of key stakeholders and decision makers to help develop account specific strategies in accordance with AbbVie’s guidelines and values.</li><li>Builds deep and broad engagements within the C-suite of key account to understand key priorities, structure, and business environment to align with AbbVie Hematology priorities.&#xa0;</li><li>The NPM will also support key accounts by identifying growth opportunities within the market.&#xa0; The NPM will be able to recommend and support growth strategy for all key accounts.</li><li>The NPM will act as a liaison between IFT cross-functional stakeholders to align on implementation of Strategic Account plans and support internal cross-functional team members and leadership in identifying the right stakeholders for the right needs.</li><li>Proficiently manage overall budget &amp; resource allocation for all accounts.</li><li>Tracking and monitoring of the execution and success.<ul><li>Perform quarterly business reviews for internal and external stakeholders.</li></ul></li><li>Develop, build, and execute growth strategies for Hematology portfolio:<ul><li>Manage monthly reporting for Strategic Accounts leveraging Symphony.</li><li>Conduct quarterly business reviews with BUH.</li><li>Collaborate with IFT Managers in implementing value added projects where appropriate.</li><li>Collaborate with Oncology Therapeutic Specialists.</li><li>Anticipate and recommend solutions to business problems.</li></ul></li></ul>]]></description><link>http://biotechroles.com/national-partnership-manager-oncology-hematology-abbvie/6a08406b2f1861929d2532ed</link><guid isPermaLink="true">http://biotechroles.com/national-partnership-manager-oncology-hematology-abbvie/6a08406b2f1861929d2532ed</guid><pubDate>Sat, 16 May 2026 10:01:15 GMT</pubDate><company>AbbVie</company><location>Montreal, Quebec City</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Portfolio Program Management]]></title><description><![CDATA[<p>The Director, Portfolio Program Management (PPM) will partner with the Asset Strategy Leader, asset strategy planner, and deliverable team project managers and co-chairs to develop asset strategy, align execution plans, and drive implementation across the product portfolio. This includes the development and launch of novel medical device products, new clinical indications, and global expansion of existing products within Aesthetics Medicine. As the operational leader of the asset and asset team, the Director will lead complex, high-impact programs requiring strong leadership, advanced project management expertise, and a strategic enterprise mindset.</p><p>This role requires the ability to bring clarity to complex situations, communicate effectively with diverse stakeholders at all levels, influence decisions across the organization, and foster accountability for commitments and outcomes. The Director will also contribute to and lead departmental initiatives, mentor team members, and work independently with minimal oversight. In addition, the role may include oversight of Aesthetics Therapeutic Area Council meetings, either as a primary responsibility or in support of the meeting manager.</p><p>The ideal candidate will have deep experience in new product development and the pharmaceutical industry, strong cross-functional collaboration skills, proficiency with enterprise-level project management tools, and the ability to guide teams in aligning operational plans with approved asset strategy, and leading proactive risk management and mitigation strategies. &#xa0;</p><p><strong>Key Duties / Responsibilities</strong></p><p><strong>1. Project Strategy and Planning:</strong></p><ul><li>Strategic partner with the Deliverable Team Chair and Portfolio Program Manager (PPM) and Portfolio Program Planner (Planner</li><li>In partnership with Deliverable Team Chair develops the deliverables team global strategy and drives the execution of the strategy across products and indications for the asset.</li><li>Project manages the development of the deliverable team strategy across indications and ensures aligned execution plan</li><li>Develop, monitor, and control the project cross functional plans, timeline, budget, milestones, ensuring both cross-functional alignment and alignment with the asset project management team (PMT).</li><li>Member of the Asset Program Management Team (PMT)</li><li>At each stage gate, supports the Asset Leadership team to gain approval from the governance</li><li>Evaluate, monitor, and control project risks.</li></ul><p><strong>2. Project Execution</strong></p><ul><li>Support the cross functional teams to execute the project on time per agreed to milestones/timelines and within budget.</li><li>Accountable for the deliverable team timeline and project timeline in partnership with the Project Planner.Act proactively and assertively to ensure team members meet their commitments as planned, and work to the appropriate standards.</li><li>Drives cross functional project team and deliverable team effectiveness.</li></ul><p><strong>3. Meeting Facilitation:</strong></p><ul><li>Manage the cross functional project team operational activities to ensure milestones and goals are met.</li><li>Schedule cross functional project team and other relevant meetings.</li><li>Manage effective and efficient project team meetings, scheduling, clear agendas and meeting minutes capturing action items and decisions. Proactively follow-up action items.</li></ul><p><strong>4. Communication:</strong></p><ul><li>Ensure management decisions are provided to Deliverables Team and cross functional project team in a timely manner</li><li>Monitor and record progress of project activities, milestones and forecasts and periodically report status to management</li><li>Ensure and maintain open communication with and between Asset Strategy Team/ Deliverables Team and sub-team members</li></ul><p><strong>5. Issue resolution:</strong></p><ul><li>Actively respond to project risks, mitigate, prevent and/or resolve potential risks or issues.</li><li>Identify issues with Asset Strategy Team/ Deliverables Team needing resolution with management or governance.</li></ul><p><strong>6. Decision Analysis:</strong></p><ul><li>Define with the teams the appropriate key decision points and go/no go criteria.</li><li>Provide decision analysis expertise and tools to the project teams in strategic planning and operational execution, ensure timely and well-informed decision making.</li><li>Support the Asset Strategy Team and Deliverables Team for management meetings to ratify decisions.</li></ul><p><strong>7. Training:</strong></p><ul><li>Train and coach team members on project team processes including project governance, roles /responsibilities of Asset Strategy Team/ Deliverables Team members, planning processes, project goals and milestones, use and application of project management tools including Global Development Strategy, Gantt charts, decision trees, project costing, and forecasting.</li></ul>]]></description><link>http://biotechroles.com/director-portfolio-program-management-abbvie/6a08406a2f1861929d2532ec</link><guid isPermaLink="true">http://biotechroles.com/director-portfolio-program-management-abbvie/6a08406a2f1861929d2532ec</guid><pubDate>Sat, 16 May 2026 10:01:14 GMT</pubDate><company>AbbVie</company><location>Irvine, Irvine</location><salary>$160000-240000</salary><type>Full-time</type></item><item><title><![CDATA[Chef, Partenariats nationaux – Oncologie / Hématologie]]></title><description><![CDATA[<p>Vous joindre à AbbVie signifie que vous ferez partie d’une équipe de professionnels exceptionnels qui se sont engagés à avoir un impact remarquable sur la vie des patients. Chez AbbVie, nous effectuons des recherches scientifiques révolutionnaires à l’échelle mondiale au quotidien. AbbVie&#xa0;Canada est l’un des meilleurs lieux de travail au Canada.</p><p>En choisissant votre cheminement de carrière, choisissez d’être remarquable.</p><p>AbbVie a pour mission de découvrir et d’offrir des médicaments novateurs pour répondre à des besoins importants en matière de santé aujourd’hui et relever les défis médicaux de demain. AbbVie met tout en œuvre afin d’avoir un impact remarquable sur la vie des gens dans divers secteurs thérapeutiques clés, dont l’immunologie, l’oncologie, les neurosciences, les soins oculaires, la virologie, la gynécologie et la gastroentérologie, de même que dans le domaine de l’esthétique par le truchement des produits et services d’Allergan&#xa0;Aesthetics.</p><p>Nous sommes actuellement à la recherche d’un Chef, Partenariats nationaux, au sein de notre section commerciale Oncologie, sous la responsabilité du Gestionnaire en chef, section commerciale Hématologie. Le candidat élaborera des plans stratégiques en collaboration avec les comptes et les parties prenantes clés d’AbbVie en hématologie au Canada, harmonisera les équipes interfonctionnelles et gérera la planification des comptes, la participation à des congrès locaux et nationaux, ainsi que les initiatives régionales pour faire progresser les objectifs de l’entreprise.</p><p><strong>Résumé du poste&#xa0;:</strong></p><p>Le Chef, Partenariats nationaux, vise à représenter AbbVie auprès des comptes stratégiques identifiés au Canada, afin de renforcer et d’établir des relations à long terme avec la clientèle. Le Chef, Partenariats nationaux, facilitera la coordination de réunions régionales efficaces des équipes sur le terrain et élaborera des stratégies régionales qui s’aligneront sur les priorités des marques.</p><p><strong>Principales responsabilités</strong>&#xa0;:</p><ul><li>Agir comme chef des partenariats stratégiques d’AbbVie en hématologie avec les associations de professionnels de la santé et les comptes clés.&#xa0;</li><li>Développer et maintenir une vision globale des relations avec la clientèle et collaborer de façon interfonctionnelle chez AbbVie pour maximiser l’engagement auprès des comptes stratégiques.</li><li>Collaborer étroitement avec plusieurs parties prenantes, tant à l’interne qu’à l’externe, afin que les membres de l’équipe interne comprennent et mettent en œuvre de façon efficace la stratégie auprès des clients et les attentes commerciales.</li><li>Agir dans l’intérêt d’AbbVie en recherchant les domaines d’intérêt commun entre AbbVie et les comptes clés; identifier les occasions prévisionnelles et adaptées aux besoins, afin d’élaborer conjointement des solutions et des projets de croissance au sein des comptes clés.</li><li>Se charger de la cartographie des décideurs et des parties prenantes clés pour contribuer à l’élaboration de stratégies propres aux comptes, conformément aux lignes directrices et aux valeurs d’AbbVie.</li><li>Établir des relations étroites et approfondies avec les cadres supérieurs des comptes clés, afin de connaître leurs principales priorités, leur structure et leur environnement commercial, tout en s’alignant sur les priorités d’AbbVie en hématologie.&#xa0;</li><li>Aider les comptes clés en identifiant les occasions de croissance sur le marché; recommander et soutenir une stratégie de croissance pour tous les comptes clés.</li><li>Assurer la liaison entre les parties prenantes interfonctionnelles des équipes sur le terrain, non seulement pour établir un consensus sur la mise en œuvre des plans de comptes stratégiques, mais aussi pour aider les équipes interfonctionnelles internes et la direction à trouver les parties prenantes appropriées qui répondront à des besoins spécifiques.</li><li>Gérer efficacement le budget global et la répartition des ressources pour l’ensemble des comptes.</li><li>Suivre et surveiller l’exécution et la réussite.<ul><li>Réaliser des revues commerciales trimestrielles pour les parties prenantes internes et externes.</li></ul></li><li>Élaborer, bâtir et mettre en œuvre des stratégies de croissance pour la gamme de produits d’hématologie&#xa0;:<ul><li>Gérer les rapports mensuels pour les comptes stratégiques qui utilisent Symphony.</li><li>Mener des revues commerciales trimestrielles avec le Chef, section commerciale.</li><li>Collaborer avec les chefs des équipes sur le terrain pour mettre en œuvre des projets à valeur ajoutée, le cas échéant.</li><li>Collaborer avec des spécialistes thérapeutiques, Oncologie.</li><li>Prévoir les problèmes d’affaires et proposer des solutions.</li></ul></li></ul>]]></description><link>http://biotechroles.com/chef-partenariats-nationaux-oncologie-hematologie-abbvie/6a0840692f1861929d2532eb</link><guid isPermaLink="true">http://biotechroles.com/chef-partenariats-nationaux-oncologie-hematologie-abbvie/6a0840692f1861929d2532eb</guid><pubDate>Sat, 16 May 2026 10:01:13 GMT</pubDate><company>AbbVie</company><location>Montreal, Quebec City</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Operator, Production API - Rotating shift schedule]]></title><description><![CDATA[<p>Sets up equipment for routine processes. Under general supervision operates complex equipment and monitors manufacturing process. Becomes conversant with overall functionality of departmental processes. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout the operations and assists in the implementation of changes both in physical operations and written documents. Operates assigned jobs and maintains operating conditions within the desired range under supervision. May work with certified or qualified Trainer to learn equipment and manufacturing process, based on previous experience. Sets up equipment to accommodate minor processing changes. Becomes more knowledgeable on work processes to assist with identifying and implementing work improvements.</p><p>Responsibilities</p><ul><li>Knowledgeable of basic jobs in assigned area of responsibility and Good Manufacturing Practice (GMP) policies. Demonstrates compliance to local and industry quality and safety standards.</li><li>Proficient in either manual or controlled process equipment</li><li>Learns and expands knowledge with the help of the certified and qualified trainer. Comprehends and applies all required technical, regulatory, and safety training.</li><li>Ability to troubleshoot problem situations with occasional assistance.&#xa0;</li><li>Under occasional supervision makes timely decision to accomplish department goals. Recommends improved manufacturing and departmental processes, and takes some ownership of tasks, small projects; 5S implementation&#xa0;and SOP reviews.</li><li>Listens actively to acquire information and understand work procedures. Participates in the sharing of information to promote overall efficiency of production. Attends and actively participates in meetings.</li><li>Works to resolve conflict in professional and constructive manner with individuals inside and outside operating environment.</li><li>Rotating shift schedule:</li><li>1st weeks (Sunday - Thursday) 11:00pm to 7:00am</li><li>2nd week (Monday - Friday) 3:00pm to 11:00pm.</li><li>3rd - 4th weeks (Monday - Friday) 7:00am to 3:00pm.</li><li>Overtime requirements every other weekend Saturday and Sunday.</li></ul>]]></description><link>http://biotechroles.com/associate-operator-production-api-rotating-shift-schedule-abbvie/6a0840672f1861929d2532ea</link><guid isPermaLink="true">http://biotechroles.com/associate-operator-production-api-rotating-shift-schedule-abbvie/6a0840672f1861929d2532ea</guid><pubDate>Sat, 16 May 2026 10:01:11 GMT</pubDate><company>AbbVie</company><location>Wyandotte, Wyandotte</location><salary>$45000-60000</salary><type>Full-time</type></item><item><title><![CDATA[Clinical Educator, AMI Clinical Engagement- Atlanta, GA]]></title><description><![CDATA[<p>The Clinical Educator will play an integral role in deploying AMI (Allergan Medical Institute) training by leading on-site educational programs at Allergan Training Centers. This role includes working with leadership to uphold training center policies and procedures. The Clinical Educator also participates in ongoing learning, including anatomy labs and hands-on training.</p><p><strong>Essential Duties and Responsibilities:</strong></p><ul><li>Execute AMI training strategies for facial training sessions.</li><li>Delivering presentations and clinical training during training programs.</li><li>Assess and optimize clinical workflows to identify areas for improvement and implement strategies to enhance efficiency.</li><li>Travel to support clinical HCP educational engagement training programs.</li><li>Collaborate with leadership and supervisors to monitor and report clinical activities with AMI Training Centers.</li><li>Collaborate with the AMI Curricula team by providing feedback on clinical training programs aimed to expand reach, increase effectiveness, and further strengthen AMI brand sentiment.</li><li>Participate in ongoing job-related clinical training such as anatomy labs.</li><li>Partner closely with Clinical Operations, Environmental Health, and Safety, Medical, Legal, Regulatory, and Compliance to ensure that all guidelines, regulations, and standards are met.</li><li>Promote a safety-conscious work environment and maintain good housekeeping practices.</li><li>Assist with the development of clinical content for the ongoing optimization of training curricula.</li><li>Perform other duties as assigned.</li></ul>]]></description><link>http://biotechroles.com/clinical-educator-ami-clinical-engagement-atlanta-ga-abbvie/6a0840662f1861929d2532e9</link><guid isPermaLink="true">http://biotechroles.com/clinical-educator-ami-clinical-engagement-atlanta-ga-abbvie/6a0840662f1861929d2532e9</guid><pubDate>Sat, 16 May 2026 10:01:10 GMT</pubDate><company>AbbVie</company><location>Atlanta, Atlanta</location><salary>$85000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Finance Analyst, External Manufacturing]]></title><description><![CDATA[<p>External Manufacturing Finance provides financial planning and reporting support for the Company Operations External Manufacturing organization. This includes financial oversight for third party manufacturing of key regulatory starting materials and various production stages of oral solid dose pharmaceuticals, biologics, aesthetics, and devices. The team also provides financial and strategic support for third party negotiations and contracting.</p><p>The Finance Analyst for Third Party Manufacturing (TPM) is responsible for supporting financial reporting and analysis for Pharmaceutical products sourced from Third Party Manufacturers. More specifically, the Finance Analyst will partner closely with the broader Third-Party Manufacturing, and Supply Chain teams to ensure that brands are available for our patients, all internal controls are applied appropriately, and insightful financial analyses are provided to achieve strategic and day-to-day business objectives. This is a Cost Accounting role and will provide exposure to cost accounting principles, variance analytics, and inventory valuation.</p><p>Responsibilities</p><ul><li>Assist in the preparation of monthly TPM Product and Project accruals, reclasses and various cost allocation journal entries, in partnership with Finance Shared Services.</li><li>Assist in analysis of key financial drivers on Pharma portfolio impacting US &amp; OUS actuals.</li><li>Ensure that all financial transactions are accounted for appropriately.&#xa0;</li><li>Assist in the coordination, consolidation and reporting of Actuals, Plan, Update, Latest Best Estimate (LBE) and Long-Range Plan (LRP) including product variances, project expense, and headcount.</li><li>Assist in the standards development for Pharmaceutical brands.</li><li>Assists with financial support to functional business partners.</li><li>Assist in the annual Physical Inventory counts at Third Party Manufacturers in scope.</li><li>Perform monthly inventory reconciliations for AbbVie consigned inventory at TPMs.</li></ul>]]></description><link>http://biotechroles.com/finance-analyst-external-manufacturing-abbvie/6a0840652f1861929d2532e8</link><guid isPermaLink="true">http://biotechroles.com/finance-analyst-external-manufacturing-abbvie/6a0840652f1861929d2532e8</guid><pubDate>Sat, 16 May 2026 10:01:09 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$75000-105000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, Regulatory Affairs-Chemistry Manufacturing & Controls (CMC)]]></title><description><![CDATA[<p>The <strong>Manager, Regulatory Affairs for Chemistry Manufacturing &amp; Controls (CMC) - Biologics Product Lead</strong>, works with internal and external partners in order to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals under limited management supervision. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new market applications and supplements/variations with limited management supervision. Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research &amp; Development (R&amp;D) organizations. Represents RA CMC on product development and life-cycle management teams to negotiate, influence, and provide strategic advice to peers in RA, R&amp;D, and Operations.</p><p><u><strong>Responsibilities:</strong></u></p><ul><li>Prepares CMC regulatory product strategies with limited supervision. Prepares regulatory submissions, including new IND/CTA applications and amendments, renewals, annual reports, supplements and variations under limited supervision.</li><li>Analyzes and interprets information that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions</li><li>Reviews and revises regulatory submission documentation to effectively present data and strategy to regulatory agencies under limited supervision</li><li>Responds to global regulatory information requests under limited supervision.</li><li>Develops strategies for CMC-related agency interactions and manages preparation of agency meeting requests and information packages, under limited supervision</li><li>Manages products and change control with an understanding of regulations, agency guidance and company policies and procedures with limited supervision. Analyzes and approves manufacturing change records with limited supervision.</li><li>Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations Product Teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions and stays abreast of regulatory procedures and changes in the external regulatory environment.</li><li>Analyzes legislation, regulation and guidance and provides analysis to the organization under limited supervision</li><li>Contributes to creation of white papers and policies to illustrate current regulatory thinking under supervision of manager. Participates in initiatives internal to RA CMC</li><li>May act as a formal or informal mentor to others.</li><li>This position will work a hybrid work schedule (3 days in office) from the AbbVie Lake County, IL; Irvine, CA or Waltham, MA headquarters.&#xa0;</li></ul><p>Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required</p>]]></description><link>http://biotechroles.com/manager-regulatory-affairs-chemistry-manufacturing-and-controls-(cmc)-abbvie/6a0840632f1861929d2532e5</link><guid isPermaLink="true">http://biotechroles.com/manager-regulatory-affairs-chemistry-manufacturing-and-controls-(cmc)-abbvie/6a0840632f1861929d2532e5</guid><pubDate>Sat, 16 May 2026 10:01:07 GMT</pubDate><company>AbbVie</company><location>Waltham, North Chicago</location><salary>$130000-170000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, Regulatory Affairs for Chemistry Manufacturing & Controls (CMC)]]></title><description><![CDATA[<p>The <strong>Manager, Regulatory Affairs for Chemistry Manufacturing &amp; Controls (CMC) - Biologics Product Lead</strong>, works with internal and external partners in order to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals under limited management supervision. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new market applications and supplements/variations with limited management supervision. Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research &amp; Development (R&amp;D) organizations. Represents RA CMC on product development and life-cycle management teams to negotiate, influence, and provide strategic advice to peers in RA, R&amp;D, and Operations.</p><p><strong><u>Responsibilities:</u></strong></p><ul><li>Prepares CMC regulatory product strategies with limited supervision. Prepares regulatory submissions, including new IND/CTA applications and amendments, renewals, annual reports, supplements and variations under limited supervision.</li><li>Analyzes and interprets information that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions</li><li>Reviews and revises regulatory submission documentation to effectively present data and strategy to regulatory agencies under limited supervision</li><li>Responds to global regulatory information requests under limited supervision.</li><li>Develops strategies for CMC-related agency interactions and manages preparation of agency meeting requests and information packages, under limited supervision</li><li>Manages products and change control with an understanding of regulations, agency guidance and company policies and procedures with limited supervision. Analyzes and approves manufacturing change records with limited supervision.</li><li>Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations Product Teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions and stays abreast of regulatory procedures and changes in the external regulatory environment.</li><li>Analyzes legislation, regulation and guidance and provides analysis to the organization under limited supervision</li><li>Contributes to creation of white papers and policies to illustrate current regulatory thinking under supervision of manager. Participates in initiatives internal to RA CMC</li><li>May act as a formal or informal mentor to others.</li><li>This position will work a hybrid work schedule (3 days in office) from the AbbVie Lake County, IL; Irvine, CA or Waltham, MA headquarters.&#xa0;</li></ul><p>Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required</p>]]></description><link>http://biotechroles.com/manager-regulatory-affairs-for-chemistry-manufacturing-and-controls-(cmc)-abbvie/6a0840622f1861929d2532e4</link><guid isPermaLink="true">http://biotechroles.com/manager-regulatory-affairs-for-chemistry-manufacturing-and-controls-(cmc)-abbvie/6a0840622f1861929d2532e4</guid><pubDate>Sat, 16 May 2026 10:01:06 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Dermatology - Nashville, TN]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. <em>Talent will be hired at a level commensurate with experience.</em>&#xa0;</p><p><strong>This geography covers the areas surrounding:</strong><strong> Nashville, Clarksville, Bowling Green, KY.</strong></p><p>Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p><strong>Responsibilities:</strong></p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. in order to meet or exceed on those objectives.</li><li>Create pre-call plan using SMART objectives and execute post-call evaluation in order to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action in order to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges in order to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers.</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers in order to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop and maintain disease state experts and speakers/advocates in order to maximize brand performance.</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-dermatology-nashville-tn-abbvie/6a0840602f1861929d2532e1</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-dermatology-nashville-tn-abbvie/6a0840602f1861929d2532e1</guid><pubDate>Sat, 16 May 2026 10:01:04 GMT</pubDate><company>AbbVie</company><location>Clarksville, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Customer Experience Representative II]]></title><description><![CDATA[<p><strong>Customer Experience Representatives (CXR) that support the Facial Aesthetics (FA) department receive emails from Health Care Providers, internal sales personnel, and administrative personnel to place orders and process credits for product returns for Allergan Aesthetics products. &#xa0;</strong></p><p>CXRs serve as first-line representatives responsible for handling email inquiries, processing transactions, and act as subject matter experts as needed. Representatives are responsible for fax and/or email order processing and resolution of issues that may prevent orders from shipping, processing credit for product returns and product complaints.&#xa0;Under general supervision, CXRs process internal and external customer requests in a timely, accurate and professional manner. CXRs foster the growth of a strong customer base through creating positive interactions and building strong relationships.</p><p><strong><em>Responsibilities:</em></strong></p><ul><li>Receive and answer 60-80 customer inquiries regarding product orders, order status, lot number research, physician certification, product returns, requests for credits, product search, and pricing and services offered.&#xa0; &#xa0;</li><li>Ability to use critical thinking skills to resolve inquiries to meet service levels.</li><li>Support additional projects and requests as needed.</li><li>Partner with sales and other operational departments to provide exceptional customer service within designated service levels to complete order transactions and other informational call follow up.</li><li>Deliver an excellent customer experience, while acting in a professional and courteous manner.</li></ul><p>&#xa0;</p><ul></ul>]]></description><link>http://biotechroles.com/customer-experience-representative-ii-abbvie/6a08405f2f1861929d2532e0</link><guid isPermaLink="true">http://biotechroles.com/customer-experience-representative-ii-abbvie/6a08405f2f1861929d2532e0</guid><pubDate>Sat, 16 May 2026 10:01:03 GMT</pubDate><company>AbbVie</company><location>Austin, Austin</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Rheumatology - Saint Louis North]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. <em>Talent will be hired at a level commensurate with experience.</em>&#xa0;</p><p><strong>This geography covers the areas surrounding:</strong>&#xa0;Northern Saint Louis, Columbia, Southern Illinois</p><p>Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p><strong>Responsibilities:</strong></p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. in order to meet or exceed on those objectives.</li><li>Create pre-call plan using SMART objectives and execute post-call evaluation in order to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action in order to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges in order to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers.</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers in order to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop and maintain disease state experts and speakers/advocates in order to maximize brand performance.</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-rheumatology-saint-louis-north-abbvie/6a08405e2f1861929d2532df</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-rheumatology-saint-louis-north-abbvie/6a08405e2f1861929d2532df</guid><pubDate>Sat, 16 May 2026 10:01:02 GMT</pubDate><company>AbbVie</company><location>St. Louis, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Innovation & Portfolio Marketing – US Specialty]]></title><description><![CDATA[<p><strong>Role Overview:</strong> The Associate Director for Innovation &amp; Portfolio Marketing – US Specialty is responsible for leading innovation and portfolio marketing strategy across the US Specialty business. The role is foundational to modernizing commercial models, accelerating digital enablement, and cultivating future-ready marketing expertise that fuels growth for all Specialty brands.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Drive the strategic development and execution of Innovation &amp; Portfolio Marketing initiatives for the entire US Specialty portfolio, ensuring alignment with business-wide objectives and executive direction.</li><li>Champion partnership excellence by orchestrating seamless, value-driven collaborations across marketing, sales, analytics, IT, and enterprise resources like Digital Lab, APEX, and BTS to solve challenges and unlock opportunities for Specialty brands.</li><li>Enable and scale portfolio innovation by guiding omnichannel strategy evolution, leading enterprise-level digital initiatives and sharing cutting-edge best practices for broader adoption.</li><li>Advance "Marketer of the Future" education by identifying upskilling needs across the portfolio, designing learning initiatives with Brand and Marketing Excellence teams, and catalyzing personalized and omnichannel marketing capability across all brands.</li><li>Serve as influencer and connector within matrixed teams—driving alignment, building consensus, and delivering results through strong stakeholder management rather than formal authority.</li><li>Manage, coach, and develop the direct report, instilling a culture of continuous improvement, collaboration, and innovative thinking.</li></ul>]]></description><link>http://biotechroles.com/associate-director-innovation-and-portfolio-marketing-us-specialty-abbvie/6a08405c2f1861929d2532de</link><guid isPermaLink="true">http://biotechroles.com/associate-director-innovation-and-portfolio-marketing-us-specialty-abbvie/6a08405c2f1861929d2532de</guid><pubDate>Sat, 16 May 2026 10:01:00 GMT</pubDate><company>AbbVie</company><location>Florham Park, Florham Park</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Gastroenterology - Kansas]]></title><description><![CDATA[<p><strong><em>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.&#xa0;</em></strong></p><p><em>This geography covers the state of Kansas.</em></p><p>Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities:</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. in order to meet or exceed on those objectives.</li><li>Create pre-call plan using SMART objectives and execute post-call evaluation in order to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action in order to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges in order to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers.</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers in order to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop and maintain disease state experts and speakers/advocates in order to maximize brand performance.</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-gastroenterology-kansas-abbvie/6a08405b2f1861929d2532dd</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-gastroenterology-kansas-abbvie/6a08405b2f1861929d2532dd</guid><pubDate>Sat, 16 May 2026 10:00:59 GMT</pubDate><company>AbbVie</company><location>Kansas City, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[District Manager, Rheumatology - Boston, MA]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. <em>Talent will be hired at a level commensurate with experience.</em>&#xa0;</p><p>Coordinate commercial activity within in-field teams to ensure targets are reached for increasing sales within an assigned geography. Create, implement, and communicate District Sales Plan and monitor progress.</p><p><strong>Responsibilities:</strong></p><ul><li>Coordinate in-field activity to achieve results and agreed-upon targets. Maximize market, segment, and team dynamics to drive both top- and bottom-line results.</li><li>Ensure smooth, collaborative efforts in both day to day and long term business execution. Set tone and pace for business process and organization.</li><li>Understand and present a market and franchise/business point of view when leading teams and championing in-field meeting by developing a mastery of product and disease state information, as well as pertinent Market dynamics, including Managed Care landscape.</li><li>Coach, mentor, educate and develop direct and indirect team members to enhance individual skills and elevate overall team performance. Hold direct reports accountable to behaviors and expectations.</li><li>Provide direction and insights to key internal partners in business planning process. Consistently exemplify the AbbVie Ways of Working.</li></ul>]]></description><link>http://biotechroles.com/district-manager-rheumatology-boston-ma-abbvie/6a08405a2f1861929d2532db</link><guid isPermaLink="true">http://biotechroles.com/district-manager-rheumatology-boston-ma-abbvie/6a08405a2f1861929d2532db</guid><pubDate>Sat, 16 May 2026 10:00:58 GMT</pubDate><company>AbbVie</company><location>Boston, US-Virtual Office</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Account Specialist, Anti Infectives - Torrance, CA]]></title><description><![CDATA[<p><strong><em>This role is field-based and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.</em></strong></p><p>The Account Specialist is responsible for maximizing opportunities for the product portfolio in single layer geography. This individual will develop and maintain strategic business relationships with a wide spectrum of customers to include Hospitals, IDN’s, Academic Institutions, Outpatient Accounts, Long Term Care Facilities, Government Accounts, and Specialty Private Practice. Business relationships will focus on increasing patient access to portfolio products, consistent with approved labels, developing new business, expanding current business, maximizing resource utilization, and increasing sales to achieve geography sales goals through a solution oriented and collaborative approach. The role will involve networking, client services, and a thorough understanding of institutional and medical practices.</p><p>Responsibilities</p><ul><li>Advances hospital and specialty customers along the sales continuum and gains prescriber commitments through effective questioning, active listening, and utilization of approved data and resources. Delivers on-label presentations/sales calls to appropriately highlight the benefits and risks of the product portfolio to create awareness of product solutions and address gaps in therapeutic areas, resulting in sales goal achievement.</li><li>Develops professional relationships and differentiates the Anti-Infective portfolio’s value proposition at all levels (C-Suite, Physicians, Hospital Staff, Support Personnel) within accounts and departments to further the use of the product portfolio.</li><li>Strong understanding and ability to problem solve product and patient flow through Specialty Pharmacy, Specialty Distribution, and Buy and Bill channels. Ability to coordinate and mobilize key stakeholders across multiple departments with competing goals to align individuals on patient focused solutions.</li><li>Uses opportunities to understand and address customer needs. Builds strong relationships that provide market intelligence and support development of compliant and innovative programs and initiatives. Builds and maintains relationships across accounts that result in opportunities to benefit patients, physicians, and other HCPs within the geography.</li><li>Ability to achieve success in a complex, matrixed, account-based selling environment in which the need for collaboration and cross functional discipline is critical. Consistently partners with AbbVie in-field (MSLs, National Director of Accounts and Key Account Directors) to and in-house teams to identify, design, and/or adapt appropriate approaches and tactics.</li><li>Creates, develops, executes, and monitors strategic geography business plans. Determines appropriate department, channel, HCP focus and frequency by account to deliver on sales objectives. Aligns appropriate resources to support tactic execution and adjusts as needed.</li><li>Sources, interprets and utilizes key data by account to develop and maintain working account profiles and relationship maps for all territory accounts to maximize call continuum and communication. Consistently targets key stakeholders and decision makers within each hospital/institution/outpatient setting to expand physician usage and customer base.</li><li>Attend and actively participate in local boards, societies, conventions, and other HCP meetings when appropriate. Represent AbbVie and assigned products at such venues, build/improve new/existing relationships. Channel key information, developments, or findings to internal partners/stakeholders. All communications in these forums are on-label.</li><li>Complete all AbbVie required training and maintain adherence to all company policies and OEC/Legal procedures.<br>
Meet health care industry representative credentialing requirements to gain entry into facilities and organizations that are in assigned territory. These HCIR credentialing requirements may include, but are not limited to, background checks, drug screens, and proof of immunization/vaccination for various diseases.</li><li>Proactively collaborates across multiple departments within healthcare institutions and across organizations. Seamlessly works with cross-functional partners including National Director of Accounts and Key Account Directors to develop processes within the account base while working with Medical Science Liaisons to develop compliant communication strategies.</li></ul>]]></description><link>http://biotechroles.com/account-specialist-anti-infectives-torrance-ca-abbvie/6a0840582f1861929d2532da</link><guid isPermaLink="true">http://biotechroles.com/account-specialist-anti-infectives-torrance-ca-abbvie/6a0840582f1861929d2532da</guid><pubDate>Sat, 16 May 2026 10:00:56 GMT</pubDate><company>AbbVie</company><location>Torrance, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Account Specialist, Anti Infectives - East Bay, CA]]></title><description><![CDATA[<p><strong><em>This role is field-based and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.</em></strong></p><p>The Account Specialist is responsible for maximizing opportunities for the product portfolio in single layer geography. This individual will develop and maintain strategic business relationships with a wide spectrum of customers to include Hospitals, IDN’s, Academic Institutions, Outpatient Accounts, Long Term Care Facilities, Government Accounts, and Specialty Private Practice. Business relationships will focus on increasing patient access to portfolio products, consistent with approved labels, developing new business, expanding current business, maximizing resource utilization, and increasing sales to achieve geography sales goals through a solution oriented and collaborative approach. The role will involve networking, client services, and a thorough understanding of institutional and medical practices.</p><p>Responsibilities</p><ul><li>Advances hospital and specialty customers along the sales continuum and gains prescriber commitments through effective questioning, active listening, and utilization of approved data and resources. Delivers on-label presentations/sales calls to appropriately highlight the benefits and risks of the product portfolio to create awareness of product solutions and address gaps in therapeutic areas, resulting in sales goal achievement.</li><li>Develops professional relationships and differentiates the Anti-Infective portfolio’s value proposition at all levels (C-Suite, Physicians, Hospital Staff, Support Personnel) within accounts and departments to further the use of the product portfolio.</li><li>Strong understanding and ability to problem solve product and patient flow through Specialty Pharmacy, Specialty Distribution, and Buy and Bill channels. Ability to coordinate and mobilize key stakeholders across multiple departments with competing goals to align individuals on patient focused solutions.</li><li>Uses opportunities to understand and address customer needs. Builds strong relationships that provide market intelligence and support development of compliant and innovative programs and initiatives. Builds and maintains relationships across accounts that result in opportunities to benefit patients, physicians, and other HCPs within the geography.</li><li>Ability to achieve success in a complex, matrixed, account-based selling environment in which the need for collaboration and cross functional discipline is critical. Consistently partners with AbbVie in-field (MSLs, National Director of Accounts and Key Account Directors) to and in-house teams to identify, design, and/or adapt appropriate approaches and tactics.</li><li>Creates, develops, executes, and monitors strategic geography business plans. Determines appropriate department, channel, HCP focus and frequency by account to deliver on sales objectives. Aligns appropriate resources to support tactic execution and adjusts as needed.</li><li>Sources, interprets and utilizes key data by account to develop and maintain working account profiles and relationship maps for all territory accounts to maximize call continuum and communication. Consistently targets key stakeholders and decision makers within each hospital/institution/outpatient setting to expand physician usage and customer base.</li><li>Attend and actively participate in local boards, societies, conventions, and other HCP meetings when appropriate. Represent AbbVie and assigned products at such venues, build/improve new/existing relationships. Channel key information, developments, or findings to internal partners/stakeholders. All communications in these forums are on-label.</li><li>Complete all AbbVie required training and maintain adherence to all company policies and OEC/Legal procedures.<br>
Meet health care industry representative credentialing requirements to gain entry into facilities and organizations that are in assigned territory. These HCIR credentialing requirements may include, but are not limited to, background checks, drug screens, and proof of immunization/vaccination for various diseases.</li><li>Proactively collaborates across multiple departments within healthcare institutions and across organizations. Seamlessly works with cross-functional partners including National Director of Accounts and Key Account Directors to develop processes within the account base while working with Medical Science Liaisons to develop compliant communication strategies.</li></ul>]]></description><link>http://biotechroles.com/account-specialist-anti-infectives-east-bay-ca-abbvie/6a0840572f1861929d2532d9</link><guid isPermaLink="true">http://biotechroles.com/account-specialist-anti-infectives-east-bay-ca-abbvie/6a0840572f1861929d2532d9</guid><pubDate>Sat, 16 May 2026 10:00:55 GMT</pubDate><company>AbbVie</company><location>South San Francisco, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Stock Administration and Payroll]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-size: 12pt; font-family: arial, helvetica, sans-serif;&quot;&gt;Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Eikon Therapeutics is seeking a Senior Manager, Stock Administration and Payroll to lead and scale the company’s equity administration and payroll functions during a period of significant growth and increased regulatory complexity. This role will oversee all aspects of stock administration and payroll operations, ensuring accuracy, compliance, operational excellence, and a strong employee experience as the company continues operating as a public company.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;The Senior Manager will partner closely with senior leadership across Finance, Legal, Total Rewards, HR Operations, People Team, and external vendors to drive compliant, scalable, and efficient processes across equity and payroll administration. This role requires a strategic, detail-oriented leader who can operate in ambiguity, balance hands-on execution with operational leadership, and build strong controls and infrastructure to support a growing organization.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;About You&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;You are a strategic, battle-tested stock administration and payroll leader who thrives in complex, fast-moving environments. You bring deep expertise in equity programs and payroll operations and understand the importance of precision, controls, compliance, and employee experience — particularly as companies scale toward or operate as public entities. You are comfortable partnering with senior leaders, reconciling differing stakeholder perspectives, and guiding decisions that have lasting impact on employees and the organization. You balance hands-on execution with strategic oversight and enjoy building scalable processes, strengthening operational controls, and continuously improving how equity and payroll programs are administered and communicated.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;What You’ll Do&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Lead end-to-end payroll processing and operations, ensuring timely, accurate, and compliant payroll administration, including bonuses, commissions, equity transactions, leave of absence, terminations, relocations, and other complex employee events&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Oversee the company&#39;s stock administration function, including administration of stock options, RSUs, ESPPs, and all equity lifecycle activities such as grants, vesting, exercises, releases, cancellations, and terminations&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Partner closely with Finance, HR Operations, Legal, and external vendors to ensure accurate data inputs, reconciliations, reporting, accounting treatment, and compliance with internal controls, SOX requirements, SEC regulations, tax laws, and company policies&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Perform and support stock-based compensation accounting and analyses under ASC 718, including forecasts, modifications, repricing activities, and equity pool tracking, utilization, and forecasting&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Prepare and maintain audit-ready documentation, governance materials, reporting, and controls supporting payroll and equity administration processes&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Partner with senior leadership to support compensation and equity strategy execution, including refresh grants, employee programs, and operational scaling initiatives&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Oversee relationships with payroll providers, stock administration vendors, transfer agents, and external advisors to ensure strong service delivery, compliance, and data integrity&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Continuously improve payroll and equity processes, systems, controls, integrations, and workflows to support scalability, operational efficiency, and risk mitigation&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Stay current on payroll, tax, FASB, and SEC regulatory developments and partner with internal and external stakeholders to assess impact and support complex transactions and compliance requirements&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Provide responsive support and guidance to employees and leaders regarding payroll, taxation, and equity-related matters with a strong focus on accuracy, professionalism, and employee experience&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Bachelor&#39;s degree with 12+ years of experience, or a post-graduate degree in Finance, HR, or a related discipline with 10+ years of experience in stock administration, payroll, finance, HR operations, compensation, or related functions&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Strong payroll processing experience with comprehensive knowledge of payroll operations, payroll tax compliance, controls, and audit requirements&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Extensive experience administering equity compensation programs in a high-growth public company environment, with strong knowledge of equity vehicles, stock-based compensation accounting, tax implications, and regulatory requirements including SEC and SOX compliance&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Proven ability to navigate complex, ambiguous issues and translate business strategy into scalable operational processes and solutions&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Experience partnering with senior leadership and managing competing priorities across cross-functional stakeholders to drive business outcomes&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Strong communication, analytical, and influencing skills, with the ability to engage effectively with executives, employees, auditors, vendors, and cross-functional partners&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Experience in biotech, life sciences, or another highly regulated industry preferred&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Experience with equity and HR/payroll platforms such as E*TRADE (Equity Edge Online) and SAP SuccessFactors preferred&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;The expected salary range for this role is $145,000 to $158,650 depending on skills, competency, and the market demand for your expertise.&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-size: 12pt; font-family: arial, helvetica, sans-serif;&quot;&gt;Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; font-family: arial, helvetica, sans-serif;&quot;&gt;We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-stock-administration-and-payroll-eikon-therapeutics/6a07ebe52f1861929d2532d5</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-stock-administration-and-payroll-eikon-therapeutics/6a07ebe52f1861929d2532d5</guid><pubDate>Sat, 16 May 2026 04:00:37 GMT</pubDate><company>Eikon Therapeutics</company><location>Millbrae, CA</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Engagement Manager - Commercial]]></title><description><![CDATA[<div>
<div><span style="font-size: 16px;">Veeva is building the industry cloud for Life Sciences through software, data, AI, and Business Consulting working together. Learn more about our products, vision and values, and status as a public benefit corporation on our </span><a rel="noopener noreferrer" href="http://veeva.com/" style="font-size: 16px;" class="postings-link">website</a><span style="font-size: 16px;">.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">Consulting is changing, and we’re not like other firms. </span><a rel="noopener noreferrer" href="https://www.veeva.com/services/business-consulting-services/" style="font-size: 16px;" class="postings-link">Veeva Business Consulting</a><span style="font-size: 16px;"> was launched in 2019 and has grown quickly and organically to a global organization of over 400 people. Our team is focused on making the life sciences industry more efficient and effective through software, data, and consulting working together.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">We expect significant growth in Business Consulting as we look towards 2030, and are looking for great people to make it happen.</span></div>
</div><div><br></div><div>
<h3><span style="font-size: 18px;">The Role</span></h3>
<div>As an <strong>Engagement Manager</strong> in our <strong>Commercial Business Consulting</strong> practice, you won’t just advise on the future of Life Sciences - you’ll be building it. We help our customers bring treatments to patients faster by fundamentally transforming their operating models, powered by the industry’s most advanced technology, AI and data. Unlike traditional firms, we move beyond "slides and theory" to deliver tangible, scalable execution that others simply cannot replicate.</div>
</div></br><b>What You'll Do</b></br><div>

<li><strong>Strategic Delivery: </strong>Act as the end-to-end lead on Veeva’s most complex, large-scale, and global engagements</li>
<li><strong>Account Leadership:</strong> Build and navigate senior customer relationships, leading proposals for significant project wins and driving long-term account strategy</li>
<li><strong>People Leadership:</strong> Lead and inspire teams of 4+ consultants across multiple projects simultaneously, fostering a culture of excellence</li>
<li><strong>Financial Oversight:</strong> Manage project budgets of $1M+, acting as the primary point of contact for project health and commercial success</li>
<li><strong>Practice Building:</strong> Support brand-building activities and the development of internal IP to keep Veeva Business Consulting at the forefront of the industry</li>

</div></br><b>Requirements</b></br><div>

<li><strong>Experience:</strong> 8+ years in Life Sciences Consulting (Business or Management Consulting preferred)</li>
<li><strong>Leadership:</strong> Proven track record of managing large project teams and $1M+ engagements</li>
<li><strong>Domain Knowledge:</strong> Proven and recognised expertise in Go-to-Market strategy, Brand Planning, Product Launch, Omnichannel strategy, Segmentation and targeting, as well as the broader Life Sciences industry</li>
<li><strong>Mindset:</strong> A highly analytical approach to problem-solving with the ability to influence C-suite stakeholders</li>
<li><strong>Education:</strong> Bachelor’s degree or higher</li>

</div></br><div>
<h6><span style="font-size: 10px;">#RemoteSpain</span></h6>
<h6><span style="font-size: 10px;">#LI-MidSenior</span></h6>
</div><div><br></div><div>
<div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.</div>
<div>&nbsp;</div>
<div>If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>
</div>]]></description><link>http://biotechroles.com/engagement-manager-commercial-veeva/6a07ebe62f1861929d2532d8</link><guid isPermaLink="true">http://biotechroles.com/engagement-manager-commercial-veeva/6a07ebe62f1861929d2532d8</guid><pubDate>Sat, 16 May 2026 04:00:37 GMT</pubDate><company>Veeva</company><location>Spain - Barcelona</location><salary>$65000-95000</salary><type>Full-Time</type></item><item><title><![CDATA[Director - Veeva Regulatory]]></title><description><![CDATA[<div>Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.</div>
<div>&nbsp;</div>
<div>At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a&nbsp;<a href="https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6">public benefit corporation</a>&nbsp;(PBC), legally bound to balancing the interests of customers, employees, society, and investors.</div>
<div>&nbsp;</div>
<div>As a&nbsp;<a href="https://careers.veeva.com/work-anywhere/">Work Anywhere</a>&nbsp;company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.</div>
<div>&nbsp;</div>
<div>Join us in&nbsp;<a href="https://www.youtube.com/watch?v=TaPSP8cCSKY&amp;ab_channel=Forbes">transforming the life sciences industry</a>, committed to making a positive impact on its customers, employees, and communities.</div><div><br></div><h3>The Role</h3>
<p>You are the definitive authority on Regulatory Information Management (RIM) for Veeva. This is not a people-management role; it is a Mastery-level position. You will bridge the gap between complex regulatory requirements and modern software solutions. In this role you will be responsible for growing Veeva’s Regulatory product market share.</p>
<p><strong>Why This Role is Unique</strong></p>
<ul>
<li>Influence, Not Admin: You aren't managing a team's PTO or budgets. You are managing the strategy of how fast growing biotech upstarts handle their pivotal health authority submissions.</li>
<li>The "Credibility" Factor: You use your dual background (Operator + Consultant) to provide advice that sticks. When a customer says, "That won't work in a global submission," you have the lived experience to show them exactly how it will.</li>
<li>Commercial Impact: You aren't just "supporting" sales; you are the secret weapon. You identify market gaps and work directly with Product teams to ensure Veeva remains the industry standard.</li>
</ul>
<div>
<p><strong>What This Job Is NOT</strong></p>
<ul>
<li>NOT People Management: You are an elite individual contributor. Your success is measured by market impact, not headcount.</li>
<li>NOT Regulatory Affairs or Science: We aren't developing regulatory strategy for sponsors. We are architecting the systems that manage their deliverables and speed their products to market.</li>
<li>We deliver working, transformative technology solutions.</li>
</ul>
</div></br><b>What You'll Do</b></br><div>

<li>Act as the “CEO of your deal” during the sales cycle for complex deals. You bring together the best of Veeva to propose business capability improvements with tangible business value to senior executives.</li>
<li>Serve as the "Face of Veeva Regulatory." You will speak at key conferences such as Veeva Summit and DIA to shape the industry's conversation around RIM AI, IDMP, eCTD, and data governance.</li>
<li>Be the voice of the customer for our Product and Engineering teams. You tell them what the industry needs before the industry even knows it needs it.</li>
<li>While you have no direct reports, you will lead "by influence," aligning Sales, Marketing, and Services teams to ensure a unified market strategy.</li>

</div></br><b>Requirements</b></br>
<li>5+ years of experience with regulatory submission document authoring, submission publishing / validation / viewing, registration and commitment tracking, and regulatory document archiving</li>
<li>4+ years of experience consulting for the regulatory operations area of a life sciences company</li>
<li>3+ years of experience selling software and/or services to life sciences organizations</li>
<li>Proven ability to innovate across business processes and technology solutions</li>
<li>Ability to hold strategic conversations with heads of regulatory and IT regarding the regulatory applications and their use within Regulatory execution</li>
<li>Understanding of global drug development &amp; regulatory process</li>
<li>Ability to travel for customer meetings and presentations</li>
</br><h6><span style="font-size: 10px;">#LI-RemoteUS</span></h6>
<h6><span style="font-size: 10px;">#LI-Director</span></h6><div><br></div><div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>]]></description><link>http://biotechroles.com/director-veeva-regulatory-veeva/6a07ebe62f1861929d2532d7</link><guid isPermaLink="true">http://biotechroles.com/director-veeva-regulatory-veeva/6a07ebe62f1861929d2532d7</guid><pubDate>Sat, 16 May 2026 04:00:37 GMT</pubDate><company>Veeva</company><location>Massachusetts - Boston</location><salary>$180000-260000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Research Associate (Contractor)]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;About this opportunity:&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;At Freenome, we are seeking a Senior Research Associate to help grow our Genomics Assay Development team. At Freenome, you will help develop the assay technologies used to analyze patient samples and contribute to our mission of early cancer detection. The ideal candidate will work to develop assay technologies for our multiomic platform manually and on robotic platforms. You will develop, characterize, verify, and validate clinical-grade assays to measure complex, blood-based analytes (e.g., whole-genome sequencing of cfDNA). You will work cross-functionally with Research &amp;amp; Development teams, automation and process engineering, computational science, and clinical operations to develop and transfer NGS-based assays in a regulated, high-throughput environment. You are passionate about developing life saving diagnostics using NGS technologies, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;The role reports to the Manager of Genomics Late Stage Development. This role will be an onsite role based in our Brisbane, California headquarters.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What you’ll do:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Apply knowledge of molecular biology, nucleic-acid biochemistry, and next-generation sequencing to develop assays for DNA, including genome-wide and targeted approaches&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Participate in experimental design and independently plan and execute mission-critical experiments to optimize and characterize assay performance&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Create and manipulate high impact assay inputs, including use of biological samples and formulation of contrived samples and reagents as required&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Gather high-quality data, take detailed notes, and openly communicate on lessons learned while performing experiments&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Perform data analysis, create summary presentations, and present results cross-functionally&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Perform technical troubleshooting, identify and implement process improvements across the lab by thinking critically about the execution of all experiments&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Build productive working relationships and collaborate with engineers and clinical laboratory members to transition development protocols into clinical production, including automation, validation experiments, and SOP development&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Contribute to writing study protocols and reports. Diligently apply current Good Laboratory and Documentation Practices (cGLP, cGDP)&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Must haves:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Bachelor’s or Master’s degree in molecular biology, biochemistry, genetics, or a related field with at least 4 years of professional experience in the life sciences. Prior experience in clinical diagnostics and/or working in a start-up environment is preferred&amp;nbsp;&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Experience executing verification and validation studies for IVD assays in a regulated laboratory environment (GLP)&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Hands-on experience in Next-gen sequencing (NGS) based assay development including extraction, library preparation, target capture, and sequencing&amp;nbsp;&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Familiarity with molecular biology, genomics, NGS, assay development, sample preparation, reagent handling, or related laboratory workflows (e.g. plasma separation processes, DNA/RNA extraction, purification, and quantification, NGS library preparation)&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Experience designing, planning, and executing successful experiments, interpreting results, preparing data for review, and giving effective scientific presentations&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;High attention to detail and ability to record accurate and detailed observations, assess impact, and perform troubleshooting as required&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Ability to manually pipette with high confidence, accuracy, and precision&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Clear and proactive communication skills and ability to collaborate effectively with team members in the same and adjacent disciplines&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Strong organizational skills and the ability to contribute the design and implementation of new processes&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-weight: 300;&quot;&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Flexible and highly motivated to learn new skills and comfortable adapting to changing priorities&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Nice to haves:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Experience in working with with methylated ctDNA/cfDNA as an analyte in liquid biopsy workflows &lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Experience with automated liquid handlers, laboratory information systems, sample tracking systems, and equipment scheduling/status tools&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Familiarity with programing in a scientific programming language (e.g., Python or R)&lt;br&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Contractors may be hired through a third-party provider and will be considered contingent workers. &lt;/span&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;We invite you to check out our career page @ &lt;em&gt;&lt;a href=&quot;http://freenome.com/job-openings/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://freenome.com/job-openings/&amp;amp;source=gmail&amp;amp;ust=1708620295766000&amp;amp;usg=AOvVaw0K-a4lTJ0RquYagpqS-yp4&quot;&gt;freenome.com/job-openings/&lt;/a&gt;&lt;/em&gt; &lt;/span&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;for additional company information.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Freenome is proud to be an equal opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local &lt;/span&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;law.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Applicants have rights under Federal Employment Laws.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;&lt;em&gt;&lt;a href=&quot;https://www.dol.gov/agencies/whd/posters/fmla&quot; target=&quot;_blank&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Family &amp;amp; Medical Leave Act (FMLA)&lt;/span&gt;&lt;/em&gt;&lt;/a&gt;&lt;/em&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;&lt;em&gt;&lt;a href=&quot;https://www.dol.gov/agencies/ofccp/posters&quot; target=&quot;_blank&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Equal Employment Opportunity (EEO)&lt;/span&gt;&lt;/em&gt;&lt;/a&gt;&lt;/em&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;&lt;em&gt;&lt;a href=&quot;https://www.dol.gov/agencies/whd/posters/employee-polygraph-protection-act&quot; target=&quot;_blank&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;Employee Polygraph Protection Act (EPPA)&lt;/span&gt;&lt;/em&gt;&lt;/a&gt;&lt;/em&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #ecf0f1;&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-weight: 300;&quot;&gt;#LI-ONSITE&lt;/span&gt;&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-research-associate-(contractor)-freenome/6a07ebe22f1861929d2532d4</link><guid isPermaLink="true">http://biotechroles.com/senior-research-associate-(contractor)-freenome/6a07ebe22f1861929d2532d4</guid><pubDate>Sat, 16 May 2026 04:00:34 GMT</pubDate><company>Freenome</company><location>Brisbane, California</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager / Associate Director, Healthcare Compliance]]></title><description><![CDATA[<div>More than one million people in the United States today are fighting blood cancer. While a traditional <a href="https://www.mayoclinic.org/tests-procedures/allogeneic-stem-cell-transplant/pyc-20384863" class="postings-link">allogeneic stem cell transplant</a> has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.<strong>&nbsp;</strong><span style="font-size: inherit;">With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.</span></div><div><br></div><div><strong>Position Summary: </strong>Orca Bio is building its first in-house healthcare compliance function and is seeking a motivated and adaptable compliance professional to support the development and execution of that program. Reporting to the SVP/Head of Legal, the Senior Manager or Associate Director, Healthcare Compliance will work cross-functionally to lead key elements of a pre-commercial compliance program—including policy and SOP development, transparency and aggregate spend reporting, training, and commercial and promotional compliance review. The role will also support future field engagements following potential product approval.</div>
<div>&nbsp;</div>
<div>Travel: ~25%. Remote applicants accepted, with preference for those near Orca Bio HQ.</div></br><b>Key Responsibilities</b></br>
<li>Assist in the ongoing development, implementation, and maintenance of the Company’s compliance program that aligns with industry standards and regulatory requirements, including federal, state, and international regulations, as appropriate.</li>
<li>Develop policies and procedures that provide appropriate guidance and instruction to Company employees.</li>
<li>Lead the development and delivery of compliance training programs for employees at all levels.</li>
<li>Conduct regular compliance audits, monitoring and risk assessments to identify potential areas of compliance vulnerability and risk.</li>
<li>Assist in the completion of activities related to federal and relevant state transparency-driven compliance requirements. &nbsp;</li>
<li>Manage the Company’s whistleblower hotline.</li>
<li>Collaborate with legal, regulatory, and operational teams to provide compliance guidance and support for new initiatives and projects.</li>
<li>Investigate compliance-related issues and coordinate with relevant stakeholders to ensure appropriate corrective actions are taken.</li>
<li>Stay current with industry trends, regulatory changes, and best practices in compliance.</li>
<li>Engage in such other activities as directed by the Senior Vice President, Legal.&nbsp;</li>
</br><b>Required Experience:</b></br>
<li>Bachelor’s degree in life sciences, law, business, or a related field; advanced degree (e.g., JD, MBA) preferred.</li>
<li>Minimum of 6 years of experience in compliance, regulatory affairs, or a related field within the pharmaceutical or biotech industry.</li>
<li>Strong knowledge of FDA regulations, GxP standards, and other relevant compliance frameworks.</li>
<li>Proven ability to interpret and apply complex regulations and guidelines to business practices.</li>
<li>Excellent analytical, problem-solving skills.</li>
<li>Well-rounded, experienced compliance expert who has played a key role on matters relating to the marketing and promotion of pharmaceutical products and possesses excellent business judgment concerning overall healthcare compliance and risk management.</li>
<li>Ability to work effectively in cross-functional teams with a collaborative and hands-on approach.</li>
<li>Ability to manage multiple tasks independently and simultaneously.</li>
</br><div>The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Who we are</strong></div>
<div>&nbsp;</div>
<div>We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.</div>
<div>&nbsp;</div>
<div>We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.</div>
<div>&nbsp;</div>
<div>We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.</div>
<div>&nbsp;</div>
<div>We maintain a start-up culture of camaraderie and leadership by example, regardless of title.</div>
<div>&nbsp;</div>
<div>We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Notice to staffing firms</strong></div>
<div>&nbsp;</div>
<div>Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.</div>]]></description><link>http://biotechroles.com/senior-manager-associate-director-healthcare-compliance-orca-bio/6a07ebe12f1861929d2532d3</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-associate-director-healthcare-compliance-orca-bio/6a07ebe12f1861929d2532d3</guid><pubDate>Sat, 16 May 2026 04:00:33 GMT</pubDate><company>Orca Bio</company><location>Menlo Park, CA</location><salary>$160000-220000</salary><type>Regular, Full-Time Employee</type></item><item><title><![CDATA[Research Associate, Compound Management]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;Your work will change lives. Including your own.&amp;nbsp;&lt;/h2&gt;
&lt;p&gt;&lt;iframe style=&quot;width: 655px; height: 367px;&quot; src=&quot;https://www.youtube.com/embed/NzerLX6koWI?si=KaDRt0AYxcwmtZus&quot; width=&quot;655&quot; height=&quot;367&quot;&gt;&lt;/iframe&gt;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Impact You’ll Make&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Recursion Pharmaceuticals is pioneering a new approach to drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking a Research Associate for our Compound Management group to help accelerate our discovery programs and clinical portfolio. In this role, you will supply drug candidates and disease perturbants, handling the ordering, weighing, and solubilization of reagents while running automated systems to generate the assay plates that power our platform.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;You will manage multiple projects simultaneously, using pipetting skills and &lt;strong&gt;software-driven&lt;/strong&gt; instrumentation to prepare reagents for high-throughput screening. This position offers a collaborative environment and substantial scope for continuous learning, encouraging you to evaluate and deploy the latest technological developments to create efficient, scalable workflows. We are seeking an individual with strong analytical skills who can thrive as both a team player and an independent contributor.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;In this role, you will:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build the foundational data source for the discovery platform by managing inventory projection with careful attention to detail, consistency, and documentation while delivering high-quality reagent samples for high-throughput screening.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Create and innovate new processes where needed by collaborating with our biological, engineering, and computational science teams to develop the most efficient path to success for compound delivery and assay execution.&lt;/li&gt;
&lt;li&gt;Expand your skillsets in Chemistry, Molecular Biology, and Data Science to adopt cutting-edge techniques and solve complex laboratory challenges.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Optimize and maintain the organization of a growing Compound Management lab to ensure scalable, high-precision reagent delivery.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The Team You’ll Join&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;You will join our Compound Management team, a lean, high-impact and collaborative group of scientists who own the end-to-end lifecycle of Recursion’s small-molecule, guide, and biological inventory. Serving as the critical physical link between inventory sourcing and biological data generation, our team ensures all reagents are assay-ready for internal programs and external partners.&lt;/p&gt;
&lt;p&gt;As a member of this group, you will maintain the backbone of our discovery engine by leveraging industrial-scale automation to provide the high-volume throughput necessary for large-scale model builds. You will thrive in a fast-paced environment where your work directly supports iterative drug discovery cycles and the generation of high-quality multi-omics data.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Experience You’ll Need&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in Chemistry or a similar life science field OR some college with 3+ years of experience in sample management within a laboratory.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Proficiency in fundamental lab operations, including solubilization and precision weighing; we are looking for someone who is ready to hit the ground running with these core skills.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;A track record of process improvement, showing you are proactive in identifying and optimizing laboratory workflows rather than simply following established protocols.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Hands-on experience with manual pipetting and operating automated laboratory instrumentation (e.g., liquid handlers); experience with software-driven systems is preferred.&lt;/li&gt;
&lt;li&gt;Comfort with computational tools and a data-first mindset, embracing the efficiency of integrated automation and digital workflows.&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills, with the judgment to know when to ask for insights from teammates and when to independently troubleshoot solutions.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;A passion for a fast-paced startup culture where you’ll leverage creativity and independent thinking to drive results.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Working Location &amp;amp; Compensation:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This is a full-time, onsite position at our US headquarters located in &lt;strong&gt;Salt Lake City, Utah&lt;/strong&gt;.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;At Recursion, we believe that every employee should be compensated fairly. Based on the skill and level of experience required for this role, the estimated current annual base range for this role is &lt;strong&gt;$77,500 to $97,800 (USD)&lt;/strong&gt;. You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;#LI-BO1&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;The Values We Hope You Share:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;We act boldly with integrity. &lt;/strong&gt;We are unconstrained in our thinking, take calculated risks, and push boundaries, but never at the expense of ethics, science, or trust.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;We care deeply and engage directly. &lt;/strong&gt;Caring means holding a deep sense of responsibility and respect - showing up, speaking honestly, and taking action.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;We learn actively and adapt rapidly. &lt;/strong&gt;Progress comes from doing. We experiment, test, and refine, embracing iteration over perfection.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;We move with urgency because patients are waiting. &lt;/strong&gt;Speed isn’t about rushing but about moving the needle every day.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;We take ownership and accountability.&lt;/strong&gt; Through ownership and accountability, we enable trust and autonomy—leaders take accountability for decisive action, and teams own outcomes together.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;We are One Recursion. &lt;/strong&gt;True cross-functional collaboration is about trust, clarity, humility, and impact. Through sharing, we can be greater than the sum of our individual capabilities.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Our values underpin the employee experience at Recursion. They are the character and personality of the company demonstrated through how we communicate, support one another, spend our time, make decisions, and celebrate collectively.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;More About Recursion &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Recursion (NASDAQ: RXRX) is a clinical-stage TechBio company decoding biology to radically improve lives. Recursion is advancing a portfolio of differentiated investigational medicines across its wholly owned and partnered pipeline in oncology, rare disease, neuroscience, immunology, and other therapeutic areas with significant unmet need. Enabling its mission is the Recursion OS, an AI-native, end-to-end drug discovery and development platform integrating biology, chemistry, and clinical development into a unified intelligence system. Powered by proprietary multimodal data, purpose-built AI models, and bilingual teams fluent in both science and AI, the Recursion OS is designed to translate complex science into medicines that matter — faster, better, and at scale — for patients who are waiting.&lt;br&gt;&lt;br&gt;Recursion’s platform infrastructure is anchored in Salt Lake City, Utah and Milton Park, Oxfordshire, where its automated biology and chemistry laboratories generate proprietary data at industrial scale. Recursion also maintains offices in New York, Montréal, and London, three global hubs for talent and leadership at the intersection of AI and scientific innovation. Learn more at &lt;u&gt;&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=RX8_3OmD5YHn9KPS0dIZWI5SJTXw7o78IX71mdHWAptB3UnjQ7VNutoXIyTbG5D_sBzYYsRPGsSI2UDwEODguVwc0tsA_7kbn2hIXe7Xb8g=&quot; target=&quot;_blank&quot;&gt;www.recursion.com&lt;/a&gt;&lt;/u&gt;, or connect on &lt;u&gt;&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=PEN8v5P4NfB9Je1Ehd4M665lSNOQWhGtMQkvFASBLBI-jFZV3X4qcj21uQ1akOvCKbQGxe8fC1gw7KzH_yFxhw==&quot; target=&quot;_blank&quot;&gt;X&lt;/a&gt;&lt;/u&gt; and &lt;u&gt;&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=NZ3-__S7n3thuUCJDwe4LbKB3mL3beP5InfKrkM-PaMYe7yHWExchDgzH5kpuanTnSQt567E9X4FJ-sc4RRSbXAPzNGE7JsoG7bLhL2f84LlAk2rLmDecui7soYSVpUY&quot; target=&quot;_blank&quot;&gt;LinkedIn&lt;/a&gt;&lt;/u&gt;.&lt;/p&gt;
&lt;p&gt;Recursion is an Equal Opportunity Employer.&amp;nbsp; All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable federal, state, local, or provincial human rights legislation.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-weight: 400;&quot;&gt;Accommodations are available on request for candidates taking part in all aspects of the selection process.&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;h5&gt;&lt;span style=&quot;font-weight: 400;&quot;&gt;Recruitment &amp;amp; Staffing Agencies: Recursion Pharmaceuticals and its affiliate companies do not accept resumes from any source other than candidates. The submission of resumes by recruitment or staffing agencies to Recursion or its employees is strictly prohibited unless contacted directly by Recursion’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Recursion, and Recursion will not owe any referral or other fees. Our team will communicate directly with candidates who are not represented by an agent or intermediary unless otherwise agreed to prior to interviewing for the job.&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;/span&gt;&lt;/h5&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/research-associate-compound-management-recur/6a07ebdf2f1861929d2532d2</link><guid isPermaLink="true">http://biotechroles.com/research-associate-compound-management-recur/6a07ebdf2f1861929d2532d2</guid><pubDate>Sat, 16 May 2026 04:00:31 GMT</pubDate><company>Recur</company><location>Salt Lake City, Utah</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[VP, Commercial Operations]]></title><description><![CDATA[<div>
<p>Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values — Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome — we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.</p>
<p><strong>Title</strong>: Vice President, Commercial Operations<br><strong>Reports to</strong>: Chief Commercial Officer<br><strong>Location</strong>: Remote (West Coast preferred) or Emeryville, CA Hybrid</p>
<p><strong>Position Summary</strong></p>
<p>Kyverna is seeking a strategic and execution-oriented Vice President, Commercial Operations to build and lead a world-class commercial operations organization supporting the launch and commercialization of innovative cell therapies for autoimmune diseases.</p>
<p>As part of the Commercial Leadership Team, the VP will be responsible for developing scalable commercial infrastructure, analytics, forecasting, field operations, CRM, incentives, data strategy, market insights, and operational excellence across the commercial organization. The ideal candidate brings extensive experience leading commercial operations in biotechnology, including launch preparation, specialty therapeutics, cell therapy products, buy-and-bill reimbursement models, and complex patient journeys.&nbsp; Experience supporting autoimmune, neurology, CAR-T, rare disease, or specialty biologics launches is strongly preferred.</p>
</div></br><b>Responsibilities</b></br><div>
<p><strong>Commercial Strategy &amp; Launch Readiness</strong></p>

<li>Build and scale the Commercial Operations function to support pre-commercial through commercial-stage growth.</li>
<li>Partner with Commercial Leadership to develop launch strategies, go-to-market models, field deployment plans, and operational infrastructure.</li>
<li>Lead launch readiness activities including territory alignment, targeting, incentive compensation, CRM implementation, analytics, and reporting.</li>
<li>Develop operational frameworks to support specialty product commercialization, including infused and buy-and-bill reimbursement environments.</li>
<li>Support long-range planning, annual operating planning, and commercial forecasting activities.</li>

<p>&nbsp;</p>
<p><strong>Sales &amp; Field Operations</strong></p>

<li>Lead all field operations activities including sales force sizing, structure, alignment, targeting, call planning, and performance analytics.</li>
<li>Oversee incentive compensation design, administration, and optimization aligned with business objectives.</li>
<li>Establish KPIs, dashboards, and reporting frameworks to measure commercial effectiveness and drive data-informed decision-making.</li>
<li>Partner with field leadership to optimize execution, productivity, and customer engagement strategies.</li>
<li>Ensure operational excellence across CRM systems, field tools, data governance, and commercial technologies.</li>

<p>&nbsp;</p>
<p><strong>Commercial Analytics &amp; Insights</strong></p>

<li>Lead forecasting, market analytics, competitive intelligence, and business insights capabilities.</li>
<li>Translate complex market, customer, and performance data into actionable commercial strategic recommendations.</li>
<li>Partner with Market Access and Finance to support pricing, reimbursement, and access planning activities.</li>
<li>Build scalable data infrastructure and reporting capabilities to support executive decision-making.</li>
<li>Drive adoption and optimization of analytics platforms and commercial technologies.</li>

<p>&nbsp;</p>
<p><strong>Cross-Functional Leadership</strong></p>

<li>Collaborate closely with Marketing, Sales, Market Access, Medical Affairs, Patient Services, Regulatory, Compliance, and IT to ensure coordinated commercial execution.</li>
<li>Serve as a key strategic advisor to executive leadership on commercialization strategy and operational planning.</li>
<li>Partner with Compliance and Legal to develop Field Compliance SOPs and ensure all commercial activities adhere to regulatory and corporate standards.</li>
<li>Support alliance management and cross-functional governance processes as needed.</li>
<li>Team Leadership</li>
<li>Recruit, develop, and lead a high-performing Commercial Operations organization.</li>
<li>Foster a culture of accountability, collaboration, innovation, and continuous improvement.</li>
<li>Mentor and develop team members while building scalable organizational capabilities aligned with company growth.</li>

</div></br><b>Qualifications</b></br><div>

<li>Bachelor’s degree required; MBA or advanced degree preferred.</li>
<li>15+ years of biotechnology or pharmaceutical commercial experience with significant leadership experience in Commercial Operations.</li>
<li>Demonstrated success supporting multiple product launches in specialty therapeutics, oncology, cell therapy, CAR-T, neurology, rare disease, or other complex treatment settings strongly preferred.</li>
<li>Deep expertise in commercial operations including forecasting, analytics, field operations, CRM, incentive compensation, targeting, and reporting.</li>
<li>Strong understanding of specialty pharmacy, infused products, buy-and-bill reimbursement, and complex patient access models preferred.</li>
<li>Experience building commercial infrastructure in emerging or growth-stage biotechnology companies highly preferred.</li>
<li>Proven leadership in cross-functional commercial launch planning and execution.</li>
<li>Strong analytical and strategic thinking capabilities with ability to synthesize multiple data points, assess trends and translate into actionable business insights.</li>
<li>Experience with commercial systems and platforms including CRM, data visualization, incentive compensation, and analytics tools.</li>
<li>Excellent executive presence, communication, and stakeholder management skills.</li>
<li>Demonstrated ability to operate effectively in highly matrixed, fast-paced environments.</li>
<li>Strong people leadership, organizational development, and talent management capabilities.</li>
<li>Ability to travel as needed for commercial meetings, field engagement, conferences, and company activities.</li>

</div></br><div>
<p>The national salary range for this position is $300K to $340K USD annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on factors including experience, education, geographic location, internal equity, and market data. This position is also eligible for annual bonus, equity, benefits, and participation in the Company’s stock plan.</p>
</div>]]></description><link>http://biotechroles.com/vp-commercial-operations-kyverna/6a07ebdd2f1861929d2532d1</link><guid isPermaLink="true">http://biotechroles.com/vp-commercial-operations-kyverna/6a07ebdd2f1861929d2532d1</guid><pubDate>Sat, 16 May 2026 04:00:29 GMT</pubDate><company>Kyverna</company><location>Remote</location><salary>$220000-350000</salary><type>Full Time</type></item><item><title><![CDATA[Director, Field Medical]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p style=&quot;margin: 0in; font-family: Calibri; font-size: 11.0pt;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif; font-size: 10pt;&quot;&gt;Using living cells to treat – and sometimes even cure – cancer is one of the most dramatic advances in modern medicine. Patients with hematologic malignancies have been successfully treated with cell therapies. However, these profound results have not yet been achieved in patients with solid tumors, representing approximately 90% of all cancers. And for patients with hematologic malignancies, there is a need for next-generation cell therapies that can deliver increased response rates and longer duration of response.&amp;nbsp; We are a clinical-stage company advancing a pipeline of next-generation CAR T-cell therapies for patients with solid tumors or hematologic malignancies. Lyell’s product candidates are enhanced with novel technology designed to generate T cells that resist exhaustion and have qualities of durable stemness in order to drive durable tumor cytotoxicity and achieve consistent and long-lasting clinical response. We were founded by cell therapy pioneers whose decades of research elevated the broader understanding of T-cell biology and its interaction with cancer. In our quest to advance next-generation CAR T-cell therapies, we have built a fully integrated company capable of discovering new technologies, translating science into therapies, manufacturing cell therapy products, and clinically evaluating them in patients. Our culture is based on Science, Respect, Collaboration, and Courage and reflects who we are, the environment we create, and our mission&#39;s urgency.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;As a critical member of Lyell&#39;s inaugural U.S. Field Medical Team, the Director, Field Medical will serve as a field-based subject matter expert on cellular therapy for the external health care professional (HCP) community and internal partners. Reporting directly to the Senior Director, Field Medical, this high-performing field medical professional will be responsible for driving strategic regional external engagement, deep therapeutic expertise, pivotal clinical trial support, and advanced insight generation across hematologic and solid tumors—particularly within cellular therapy to establish Lyell as the partner of choice in the rapidly evolving cellular therapy landscape. This role is expected to model AI-fluency for field medical — leveraging emerging tools for scientific synthesis, insight generation, and engagement planning to operate with the speed and impact of a team.&lt;/p&gt;
&lt;p&gt;This role will initially operate as an individual contributor with a defined pathway to people management. As Lyell&#39;s field team expands, the Director, Field Medical will assume responsibility for recruiting, coaching, and leading a team of MSLs within their region.&lt;/p&gt;
&lt;h3&gt;KEY ROLE AND RESPONSIBILITIES&lt;/h3&gt;
&lt;p&gt;&lt;strong&gt;Strategic Territory Ownership &amp;amp; Team Foundation&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design and execute comprehensive, insight-driven regional territory plan aligned with Medical Affairs strategy through sophisticated mapping and engagement of HCPs, cellular therapy treatment centers, CAR-T referring networks, disease-area influencers, and institutional decision makers.&lt;/li&gt;
&lt;li&gt;Leverage advanced knowledge of the CAR-T ecosystem — augmented by AI-powered landscape tools, literature synthesis platforms, and digital signal monitoring — to anticipate scientific, clinical, and operational needs across the territory.&lt;/li&gt;
&lt;li&gt;Apply strategic acumen and innovation to shape regional medical priorities and tactics.&lt;/li&gt;
&lt;li&gt;Serve as foundational member of inaugural field medical team, contributing to creation of standardized field medical processes, external and internal resources, and mentorship and supervision of future MSL hires.&lt;/li&gt;
&lt;li&gt;Prepare for future team leadership by contributing to MSL hiring, onboarding frameworks, and performance management processes in partnership with the Senior Director, Field Medical.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Scientific Exchange &amp;amp; Stakeholder Engagement&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Function as the regional scientific expert in cellular immunotherapy, delivering high-impact, fair-balanced scientific exchange tailored to the needs of:
&lt;ul&gt;
&lt;li&gt;Key Opinion Leaders (KOLs)&lt;/li&gt;
&lt;li&gt;Academic investigators&lt;/li&gt;
&lt;li&gt;Transplant and cell therapy centers&lt;/li&gt;
&lt;li&gt;Community oncology and hematology treaters&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Drive deep, peer-to-peer scientific discussions across complex topics such as CAR-T mechanism, safety management, durability, immune cell fitness, and trial protocols.&lt;/li&gt;
&lt;li&gt;Represent the organization with field presence at local regional conferences and major scientific meetings (e.g., ASH, ASCO, ESMO, SITC).&lt;/li&gt;
&lt;li&gt;Utilize AI-assisted tools for pre-call planning, scientific literature synthesis, and post-interaction insight capture to maximize the quality and consistency of HCP engagements.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Strategic Impact &amp;amp; Quality Adherence&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Generate high-quality, actionable medical insights by synthesizing signals across scientific conversations, clinical practice patterns, competitive intelligence, and emerging translational science — using AI-enabled tools to accelerate pattern recognition, summarization, and insight delivery to internal stakeholders.&lt;/li&gt;
&lt;li&gt;Serve as strategic, scientific thought partner of choice through proactively synthesizing data and insights that meaningfully inform:
&lt;ul&gt;
&lt;li&gt;Evidence generation plans, clinical trial design, and protocol amendments&lt;/li&gt;
&lt;li&gt;Launch readiness and positioning&lt;/li&gt;
&lt;li&gt;Cross-functional strategies (Clinical Operations, HEOR, R&amp;amp;D)&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Partner closely with Clinical Operations to accelerate site identification, study start-up and enrollment, and scientific training to investigators, sub investigators, research staff, and referral sites for pivotal clinical trials.&lt;/li&gt;
&lt;li&gt;Maintain strict adherence to compliance standards and accurate and timely documentation of field activity, insights, and expenses.&lt;/li&gt;
&lt;li&gt;Champion the responsible adoption of AI tools within the field medical function, while maintaining compliance and data integrity standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;PREFERRED EDUCATION&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;PharmD, PhD, MD, or DO with residency/fellowship and board certification for clinical degrees preferred. Advanced degree in health sciences (NP, PA, RN) considered if extensive clinical/medical experience in therapeutic areas.&lt;/li&gt;
&lt;li&gt;Oncology/hematology specialty required; lymphoma and/or CAR-T cell therapy experience strongly preferred. Solid tumor experience (particularly GI oncology) valued.&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;PREFERRED EXPERIENCE&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;5+ years pharmaceutical/biotech industry experience in a field medical or MSL role. Prior experience in a Senior MSL, Principal/Executive MSL, or field medical leadership capacity preferred.&lt;/li&gt;
&lt;li&gt;Demonstrated success engaging multi-disciplinary high-level academic and community providers.&lt;/li&gt;
&lt;li&gt;Demonstrated track record of solving complex problems and proactive field medical innovation.&lt;/li&gt;
&lt;li&gt;Demonstrated experience incorporating technology such as AI tools into field medical workflows, with a track record of rapid technology adoption.&lt;/li&gt;
&lt;li&gt;Experience contributing to or leading MSL team development, hiring, or onboarding a plus.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;KNOWLEDGE, SKILLS, AND ABILITIES&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Strong knowledge of clinical trial processes, CAR-T operational pathways, and latest immuno-oncology science.&lt;/li&gt;
&lt;li&gt;Expertise tailoring complex scientific and clinical data into relevant scientific exchange.&lt;/li&gt;
&lt;li&gt;Exceptional communication, presence, and scientific storytelling abilities.&lt;/li&gt;
&lt;li&gt;Comfort operating at the intersection of immuno-oncology science and emerging technology, including AI-enabled field operations.&lt;/li&gt;
&lt;li&gt;Ability to work autonomously in a rapidly evolving, high-growth biotech environment.&lt;/li&gt;
&lt;li&gt;Strategic and systems-level thinker and doer with deep scientific curiosity and expertise.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to mentor, coach, or informally lead peers in a field medical setting.&lt;/li&gt;
&lt;li&gt;Exceptional collaboration and influence.&lt;/li&gt;
&lt;li&gt;High adaptability and comfort with ambiguity.&lt;/li&gt;
&lt;li&gt;Strong ethical judgment and integrity.&lt;/li&gt;
&lt;li&gt;Passion for transforming patient outcomes through cutting-edge science.&lt;/li&gt;
&lt;li&gt;Frequent travel (up to 50-70%), including visits to cellular treatment centers, community practices, and local regional conferences.&lt;/li&gt;
&lt;/ul&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;Lyell offers its employees a range of compensation and benefits. To assist you with your decision to apply for this role, the following decision to apply for this role, the following information and links to our site highlight our &lt;span id=&quot;page3R_mcid13&quot; class=&quot;markedContent&quot;&gt;competitive market position and support to our employees and their dependents. &lt;/span&gt;&lt;/div&gt;
&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;&lt;span id=&quot;page3R_mcid15&quot; class=&quot;markedContent&quot;&gt;The salary range for this position is $240,000 - $280,000, annually, with the opportunity to earn an annual bonus. The salary range is an estimate, and the actual salary may vary based on Lyell’s compensation practices and an applicant’s qualifications and experience. Employees are also eligible to participate in Lyell’s Equity Incentive Plan.&amp;nbsp;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;At Lyell, we believe that highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse and inclusive culture for all employees. Lyell is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws.&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;We’ve learned from experience that some of the best people don’t always match our requirements perfectly - if you’re interested and think you could fit, please don’t hesitate to apply.&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p style=&quot;margin: 0in; font-family: helvetica; font-size: 10.0pt;&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p style=&quot;margin: 0in; font-family: Calibri; font-size: 11.0pt;&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-field-medical-lyell-immunopharma/6a07ebdc2f1861929d2532d0</link><guid isPermaLink="true">http://biotechroles.com/director-field-medical-lyell-immunopharma/6a07ebdc2f1861929d2532d0</guid><pubDate>Sat, 16 May 2026 04:00:28 GMT</pubDate><company>Lyell Immunopharma</company><location>USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Strategic Account Manager, Miami]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;ABOUT US&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;There are more than 9 million immunocompromised people in the United States. Almost half a million of those represent a population that are moderately to severely immunocompromised and at highest risk for severe COVID-19, including stem cell and solid organ transplant patients as well as those with hematologic cancers.&lt;/p&gt;
&lt;p&gt;At Invivyd, Inc., we take those numbers very seriously and we come to work each day on a mission to deliver protection from serious viral infectious diseases, beginning with SARS-CoV-2. Invivyd deploys a proprietary integrated technology platform unique in the industry designed to assess, monitor, develop, and adapt to create best in class antibodies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;In March 2024&lt;/strong&gt;, Invivyd received emergency use authorization (EUA) from the U.S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;In October 2025&lt;/strong&gt;, the FDA cleared the company&#39;s Investigational New Drug (IND) application and provided feedback to advance the company&#39;s REVOLUTION clinical program, Invivyd&#39;s development program for VYD2311, a vaccine alternative monoclonal antibody being investigated for the prevention of COVID-19.&lt;/p&gt;
&lt;p&gt;Be part of making a difference. Be part of Invivyd.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Location: &lt;/strong&gt;Remote (Miami)&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;At &lt;span class=&quot;hover:entity-accent entity-underline inline cursor-pointer align-baseline&quot;&gt;&lt;span class=&quot;whitespace-normal&quot;&gt;Invivyd&lt;/span&gt;&lt;/span&gt;, we’re building a new category of infectious disease prevention. With an authorized product already on the market, a next-generation program in Phase 3 and a strong pipeline behind it, we are at a defining moment of growth.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We have an exciting opportunity for a Strategic Account Manager who will play a pivotal role at Invivyd. This is an incredible opportunity for someone who is passionate about making a difference for patients, executing successful sales strategies and supporting a culture of adaptability and compliance. In this role, you will lead strategic territory planning, cultivate high-value partnerships across key accounts, and deliver clear, compliant education on approved messaging to diverse healthcare stakeholders.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;The Strategic Account Manager is responsible for providing solutions to our customers by acting as a key business owner of Invivyd resources and solutions for a variety of customers, including Health Care Providers, Health Care Organizations, Centers of Excellence, Integrated Delivery Network (IDN) Stakeholders, Veterans Affairs (VA) Centers, Reimbursement Personnel, and Practice Administrators and is accountable for working collaboratively to help ensure customer inquiries are resolved&lt;/li&gt;
&lt;li&gt;Facilitate clinical dialogue that compels the customer to act on behalf of their patients and engage the entire account to understand any obstacles that exist to provide appropriate solutions&lt;/li&gt;
&lt;li&gt;Identify shared priorities and leverage knowledge and tactics within full account to develop a strategic territory business plan that drives product demand by meeting the needs of key partners and ultimately their patients to drive superior results&lt;/li&gt;
&lt;li&gt;Collaborate with cross-functional partners on overall account and territory strategy to maximize internal/external knowledge on how to access products and services&lt;/li&gt;
&lt;li&gt;Aggregate customer, market data, and insights to effectively apply multiple channels to drive total selling engagements&lt;/li&gt;
&lt;li&gt;Utilize data driven approach to prioritize customers/accounts to maximize impact aligned to strategic plan&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree strongly preferred; candidates without a degree with significant relevant, related industry experience will be considered&lt;/li&gt;
&lt;li&gt;Proven track record of consistent high performance, and well versed in navigating and successfully selling to large accounts and key customer segments&lt;/li&gt;
&lt;li&gt;Ability to travel up to 100% over a broad geography is required, with the ability to drive and/or fly within the territory&lt;/li&gt;
&lt;li&gt;Candidate is required to be in the field five days a week, conducting visits, while also completing all administrative tasks related to the role&lt;/li&gt;
&lt;li&gt;Candidates must live within the stated territory&lt;/li&gt;
&lt;li&gt;Strong ability to communicate clinical product information&lt;/li&gt;
&lt;li&gt;Diverse experience in a matrixed environment and exposure to Reimbursement, Buy-and-Bill, Specialty Pharmacies, IDNs, and Federal channels is required&lt;/li&gt;
&lt;li&gt;Strong understanding and experience with following the laws, regulations, and industry codes (e.g., the PhRMA Code on Interactions with Healthcare Professionals) that govern appropriate interactions with Healthcare Professionals and Healthcare Organizations&lt;/li&gt;
&lt;li&gt;Demonstrates knowledge of the Veterans Affairs (VA) system within territory and the rules and regulations to conduct business within the VA system&lt;/li&gt;
&lt;li&gt;Must be results oriented and can demonstrate time management skills&lt;/li&gt;
&lt;li&gt;Possess a broad understanding of case management, market access, reimbursement and selling a medical benefit product&lt;/li&gt;
&lt;li&gt;Has experience working with Hem/Onc, Rheumatology, Transplant, Hospital/IDN, Veterans Affairs, immunology, account management strategy, and new product launches&lt;/li&gt;
&lt;li&gt;Demonstrated effective time management, organizational and interpersonal skills to prioritize opportunities&lt;/li&gt;
&lt;li&gt;Proven winning attitude and experience demonstrated by sales numbers that consistently beat quotas, Presidents Club wins and other awards won&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Pay Range&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;$152,000 - $202,000&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The pay range represents the expected full-time base salary for this role at the time of posting. Actual base pay will be determined based on a variety of factors, including relevant experience, skills, and education. In addition to base pay, this role is eligible for both an annual short-term incentive (e.g., bonus or sales incentive) and an annual long-term incentive (e.g., equity), reflecting our commitment to rewarding strong performance and long-term impact. Learn more about our total rewards by visiting &lt;a href=&quot;https://www.invivyd.com/careers/&quot;&gt;https://www.invivyd.com/careers/&lt;/a&gt;.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;em&gt;At Invivyd we strive to create a welcoming and inclusive environment. Here all applicants will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Invivyd is proud to be an equal opportunity employer.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We do not accept unsolicited resumes from agencies.&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/strategic-account-manager-miami-invivyd/6a07ebda2f1861929d2532cf</link><guid isPermaLink="true">http://biotechroles.com/strategic-account-manager-miami-invivyd/6a07ebda2f1861929d2532cf</guid><pubDate>Sat, 16 May 2026 04:00:26 GMT</pubDate><company>Invivyd</company><location>Remote (Miami)</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Virology Care Specialist/Strategic Account Manager, New Orleans]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;ABOUT US&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;There are more than 9 million immunocompromised people in the United States. Almost half a million of those represent a population that are moderately to severely immunocompromised and at highest risk for severe COVID-19, including stem cell and solid organ transplant patients as well as those with hematologic cancers.&lt;/p&gt;
&lt;p&gt;At Invivyd, Inc., we take those numbers very seriously and we come to work each day on a mission to deliver protection from serious viral infectious diseases, beginning with SARS-CoV-2. Invivyd deploys a proprietary integrated technology platform unique in the industry designed to assess, monitor, develop, and adapt to create best in class antibodies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;In March 2024&lt;/strong&gt;, Invivyd received emergency use authorization (EUA) from the U.S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;In October 2025&lt;/strong&gt;, the FDA cleared the company&#39;s Investigational New Drug (IND) application and provided feedback to advance the company&#39;s REVOLUTION clinical program, Invivyd&#39;s development program for VYD2311, a vaccine alternative monoclonal antibody being investigated for the prevention of COVID-19.&lt;/p&gt;
&lt;p&gt;Be part of making a difference. Be part of Invivyd.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Location: &lt;/strong&gt;Remote - local to assigned territory&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;At &lt;span class=&quot;hover:entity-accent entity-underline inline cursor-pointer align-baseline&quot;&gt;&lt;span class=&quot;whitespace-normal&quot;&gt;Invivyd&lt;/span&gt;&lt;/span&gt;, we’re building a new category of infectious disease prevention. With an authorized product already on the market, a next-generation program in Phase 3 and a strong pipeline behind it, we are at a defining moment of growth.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We have an exciting opportunity for a Senior Virology Care Specialist/Strategic Account Manager who will play a pivotal role at Invivyd. This is an incredible opportunity for someone who is passionate about making a difference for patients, executing successful sales strategies and supporting a culture of adaptability and compliance. In this role, you will lead strategic territory planning, cultivate high-value partnerships across key accounts, and deliver clear, compliant education on approved messaging to diverse healthcare stakeholders.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;The Senior Virology Care Specialist/Strategic Account Manager is responsible for providing solutions to our customers by acting as a key business owner of Invivyd resources and solutions for a variety of customers, including Health Care Providers, Health Care Organizations, Centers of Excellence, Integrated Delivery Network (IDN) Stakeholders, Veterans Affairs (VA) Centers, Reimbursement Personnel, and Practice Administrators and is accountable for working collaboratively to help ensure customer inquiries are resolved&lt;/li&gt;
&lt;li&gt;Facilitate clinical dialogue that compels the customer to act on behalf of their patients and engage the entire account to understand any obstacles that exist to provide appropriate solutions&lt;/li&gt;
&lt;li&gt;Identify shared priorities and leverage knowledge and tactics within full account to develop a strategic territory business plan that drives product demand by meeting the needs of key partners and ultimately their patients to drive superior results&lt;/li&gt;
&lt;li&gt;Collaborate with cross-functional partners on overall account and territory strategy to maximize internal/external knowledge on how to access products and services&lt;/li&gt;
&lt;li&gt;Aggregate customer, market data, and insights to effectively apply multiple channels to drive total selling engagements&lt;/li&gt;
&lt;li&gt;Utilize data driven approach to prioritize customers/accounts to maximize impact aligned to strategic plan&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree strongly preferred; candidates without a degree with significant relevant, related industry experience will be considered&lt;/li&gt;
&lt;li&gt;Proven track record of consistent high performance, and well versed in navigating and successfully selling to large accounts and key customer segments&lt;/li&gt;
&lt;li&gt;Ability to travel up to 100% over a broad geography is required, with the ability to drive and/or fly within the territory&lt;/li&gt;
&lt;li&gt;Candidate is required to be in the field five days a week, conducting visits, while also completing all administrative tasks related to the role&lt;/li&gt;
&lt;li&gt;Candidates must live within the stated territory&lt;/li&gt;
&lt;li&gt;Strong ability to communicate clinical product information&lt;/li&gt;
&lt;li&gt;Diverse experience in a matrixed environment and exposure to Reimbursement, Buy-and-Bill, Specialty Pharmacies, IDNs, and Federal channels is required&lt;/li&gt;
&lt;li&gt;Strong understanding and experience with following the laws, regulations, and industry codes (e.g., the PhRMA Code on Interactions with Healthcare Professionals) that govern appropriate interactions with Healthcare Professionals and Healthcare Organizations&lt;/li&gt;
&lt;li&gt;Demonstrates knowledge of the Veterans Affairs (VA) system within territory and the rules and regulations to conduct business within the VA system&lt;/li&gt;
&lt;li&gt;Must be results oriented and can demonstrate time management skills&lt;/li&gt;
&lt;li&gt;Possess a broad understanding of case management, market access, reimbursement and selling a medical benefit product&lt;/li&gt;
&lt;li&gt;Has experience working with Hem/Onc, Rheumatology, Transplant, Hospital/IDN, Veterans Affairs, immunology, account management strategy, and new product launches&lt;/li&gt;
&lt;li&gt;Demonstrated effective time management, organizational and interpersonal skills to prioritize opportunities&lt;/li&gt;
&lt;li&gt;Proven winning attitude and experience demonstrated by sales numbers that consistently beat quotas, Presidents Club wins and other awards won&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Pay Range&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Senior Virology Care Specialist: $120,000 - $160,000&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Strategic Account Manager: &lt;/strong&gt;&lt;strong&gt;$152,000 - $202,000&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The pay range represents the expected full-time base salary for this role at the time of posting. Actual base pay will be determined based on a variety of factors, including relevant experience, skills, and education. In addition to base pay, this role is eligible for both an annual short-term incentive (e.g., bonus or sales incentive) and an annual long-term incentive (e.g., equity), reflecting our commitment to rewarding strong performance and long-term impact. Learn more about our total rewards by visiting &lt;a href=&quot;https://www.invivyd.com/careers/&quot;&gt;https://www.invivyd.com/careers/&lt;/a&gt;.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;em&gt;At Invivyd we strive to create a welcoming and inclusive environment. Here all applicants will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Invivyd is proud to be an equal opportunity employer.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We do not accept unsolicited resumes from agencies.&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-virology-care-specialiststrategic-account-manager-new-orleans-invivyd/6a07ebd82f1861929d2532ce</link><guid isPermaLink="true">http://biotechroles.com/senior-virology-care-specialiststrategic-account-manager-new-orleans-invivyd/6a07ebd82f1861929d2532ce</guid><pubDate>Sat, 16 May 2026 04:00:24 GMT</pubDate><company>Invivyd</company><location>Remote (New Orleans)</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Head of Sales, Cosmetic Active Ingredients – Korea]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;About Debut&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Debut is the unconventional innovation lab spearheading the next generation of big business. Only Debut has a scalable, integrated, climate-positive creation model powered by biotechnology that puts human wellbeing at the center of everything we do—setting the new standard for profitable business and a new pace for an ever-changing world. &amp;nbsp;Our hybrid biotechnology approaches unlock latent markets, providing access to sustainably produced, natural ingredients with health benefits that cannot be obtained through other methods. We are committed to traversing the entire process, from ingredient discovery to the scaling of these products, for consumer markets. If you are passionate, enjoy fast-paced innovation and collaborative teams, then Debut is for you. &amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Summary &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Debut is seeking a dynamic and results-driven Head of Sales, Cosmetic Active Ingredients in Korea to drive market penetration of our high-performing, novel biotechnology-derived ingredients across contract manufacturers. Based in Korea, this role is directly responsible for growing Debut’s Korea business by establishing and expanding relationships with major contract manufacturers (CMs) throughout the region. The successful candidate will report to the Chief Executive Officer and will serve as the primary commercial driver ensuring Debut’s ingredients are adopted and integrated across all key CMs in Korea.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential Functions &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Own and execute the commercial strategy for ingredient sales across Korea, with a primary focus on achieving deep integration of Debut&#39;s active ingredient portfolio into CM formulation libraries and with responsibility for building the commercial infrastructure that supports future formulation expansion.&lt;/li&gt;
&lt;li&gt;Identify, engage, and develop deep partnerships with contract manufacturers South Korea with the objective of achieving broad ingredient adoption across all major CMs in the region.&lt;/li&gt;
&lt;li&gt;Serve as the primary relationship holder and commercial point of contact for CMs, driving ingredient specification, formulation integration, securing long-term ingredient supply agreements, and establishing Debut&#39;s actives as the preferred performance ingredient across key CM formulation libraries.&lt;/li&gt;
&lt;li&gt;Travel to meet with clients, attend industry events, conduct product presentations, and close business, with travel to the United States 1-2 times per year as needed.&lt;/li&gt;
&lt;li&gt;Plan and organize regional trade shows and industry events in coordination with the marketing team and other sales hires in Asia, including identifying the right shows, managing logistics, coordinating booth presence, and arranging for senior leadership and technical team members to attend and present as appropriate.&lt;/li&gt;
&lt;li&gt;Translate local market intelligence, including regional trends, CM needs, competitive dynamics, regulatory shifts, and customer feedback—into actionable insights that inform Debut’s broader global commercial strategy, product roadmap, and go-to-market planning.&lt;/li&gt;
&lt;li&gt;Develop and maintain a robust sales pipeline with clear forecasting, reporting directly to the Chief Executive Officer on progress, pipeline health, market intelligence and strategic partnership development.&lt;/li&gt;
&lt;li&gt;Work autonomously and at pace to capitalize on market opportunities, requiring minimal day-to-day oversight while maintaining strong alignment with global commercial objectives.&lt;/li&gt;
&lt;li&gt;Collaborate with Debut’s R&amp;amp;D, formulations, marketing, and operations teams to ensure customer needs are met and that Debut’s ingredient value proposition is effectively communicated.&lt;/li&gt;
&lt;li&gt;Represent Debut at trade shows, industry conferences, and customer events across the region and build a team as needed for broader penetration across the Asia region.&lt;/li&gt;
&lt;li&gt;This position is based in Korea.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Education and Experience &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Important: Candidates who do not meet the minimum experience requirement below will not be considered for this role. &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in Chemistry or Cosmetic Science, or a related field; advanced degree preferred.&lt;/li&gt;
&lt;li&gt;Minimum of 10 years of direct experience in cosmetic ingredient sales to beauty contract manufacturers in Korea. This is a strict requirement. Candidates must clearly demonstrate this specific experience in their application; those who do not will not advance in the selection process.&lt;/li&gt;
&lt;li&gt;Exceptional, established network of contacts and relationships with major cosmetic contract manufacturers across Korea. Candidates must be able to demonstrate existing, active relationships with key CMs in the region.&lt;/li&gt;
&lt;li&gt;Deep knowledge of the CM landscape in Korea, including key players, decision-making processes, formulation workflows, and procurement practices.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to work independently, move quickly, and deliver results with minimal oversight in a fast-paced, entrepreneurial environment.&lt;/li&gt;
&lt;li&gt;Strong commercial acumen with experience managing complex B2B sales cycles, from prospecting through to contract execution.&lt;/li&gt;
&lt;li&gt;Excellent communication, presentation, and negotiation skills with the ability to translate technical ingredient value propositions into compelling commercial narratives.&lt;/li&gt;
&lt;li&gt;Fluency in English and Korean required.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential Physical Characteristics &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The physical characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Frequent sitting, standing, and walking during customer meetings, trade shows, and extended travel.&lt;/li&gt;
&lt;li&gt;Repetitive use of hands to operate computers, mobile devices, and presentation equipment.&lt;/li&gt;
&lt;li&gt;Ability to carry and transport sales materials and samples weighing up to 30 pounds.&lt;/li&gt;
&lt;li&gt;Frequent air travel, including long-haul international flights across time zones.&lt;/li&gt;
&lt;li&gt;Ability to navigate diverse physical environments including manufacturing facilities, trade show floors, and customer offices.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Condition of Employment &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;As part of Debut’s pre-employment process, prospective candidates will undergo a background check prior to beginning employment. Additional types of background investigations may be conducted based on the job-related activities of the position.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Debut is an equal opportunity employer. All applicants will be considered for employment without attention to age, nationality, sex, marital status, pregnancy status, caregiving responsibilities, race, religion, language, disability, or mental health conditions. Employment decisions at Debut are based on merit, qualifications, and business needs.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;This role is based in Korea. Employment is subject to the candidate&#39;s eligibility to work in the Republic of Korea in accordance with applicable immigration and work authorization requirements. Debut complies with all obligations under the Labor Standards Act, the Equal Employment Opportunity and Work-Family Balance Assistance Act, the Act on Prohibition of Age Discrimination in Employment and Elderly Employment Promotion, and all other applicable Korean labor laws and regulations.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Additional Information&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Location: Korea&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Reports To: CEO&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Type: Full-Time&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Salary Range: &lt;strong&gt;₩150M – ₩220M&lt;/strong&gt; (~$110K–$160K USD) + performance-based incentives, commensurate with experience&lt;/p&gt;]]></description><link>http://biotechroles.com/head-of-sales-cosmetic-active-ingredients-korea-debut-biotech/6a07ebd72f1861929d2532cd</link><guid isPermaLink="true">http://biotechroles.com/head-of-sales-cosmetic-active-ingredients-korea-debut-biotech/6a07ebd72f1861929d2532cd</guid><pubDate>Sat, 16 May 2026 04:00:23 GMT</pubDate><company>Debut Biotech</company><location>Korea</location><salary>$120000-200000</salary><type>Full-time</type></item><item><title><![CDATA[Warehouse Associate - Romeoville, IL]]></title><description><![CDATA[<div>Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients in nearly every single county in the United States, including 99% of primary care deserts.</div>
<div>&nbsp;</div>
<div>Ro is consistently recognized as a top workplace in Health Care, in New York, and for Women and Parents—earning more than 20 honors from Fortune, Great Place to Work, and PEOPLE since 2021. In 2025 alone, we ranked top 5 among medium workplaces in Health Care and New York, and top 50 nationwide.</div><div><br></div><div><span style="font-size: 16px;">As a </span><strong style="font-size: 16px;">Warehouse Associate</strong><span style="font-size: 16px;">, you will play a key role in the day-to-day operations of our Romeoville warehouse facility. You will be responsible for picking and packing items for shipment, operating forklifts and pallet jacks, maintaining organized inventory, and supporting inbound and outbound logistics. You will help ensure accuracy in inventory counts and work to maintain a clean, safe, and efficient warehouse environment. You’re a versatile team player who thrives in a fast-paced setting and takes pride in organization and operational precision.</span></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">We are looking for a Warehouse Associate with </span><strong style="font-size: 16px;">full-time</strong><span style="font-size: 16px;"> availability. This position is located </span><strong style="font-size: 16px;">on-site in Romeoville, Illinois</strong><span style="font-size: 16px;">.</span></div>
<div>&nbsp;</div></br><b>What You'll Do:</b></br>
<li>Support daily warehouse activities including receiving, stocking, picking, packing, and shipping inventory</li>
<li>Package and ship patient orders accurately and efficiently in accordance with company SOPs</li>
<li>Operate warehouse equipment including forklifts and pallet jacks</li>
<li>Receive and inspect inbound inventory and ensure accurate stocking of materials</li>
<li>Perform regular inventory cycle counts and assist in reconciliation processes</li>
<li>Monitor supply levels during daily operations and report low stock to team leads or management</li>
<li>Maintain cleanliness and organization across all warehouse areas</li>
<li>Collaborate with warehouse team members to complete daily tasks and meet shipping deadlines</li>
<li>Follow established workflows and operational protocols to ensure safety, quality, and productivity standards</li>
<li>Communicate clearly and respectfully with team members to ensure a smooth and coordinated workflow</li>
<li>Perform other warehouse-related tasks as assigned by supervisors or team leads</li>
</br><b>What You’ll Bring to the Team:</b></br>
<li>Strong attention to detail with a commitment to accuracy and quality control</li>
<li>Ability to follow safety protocols and maintain a clean, organized work area</li>
<li>Comfortable working in a fast-paced environment and adapting to changing priorities</li>
<li>Effective communication skills and the ability to work collaboratively with cross-functional teams</li>
<li>Willingness to learn and take direction, with a positive attitude and proactive approach to problem-solving</li>
<li>Dependable and punctual, with a strong work ethic and team-oriented mindset</li>
<li>Long periods of standing, must be able to bend at the waist and knee, occasionally lift up to 50 lbs</li>
<li>Forklift certification preferred or willingness to obtain</li>
</br><div>The hourly rate for new hires in this position ranges from $19 to $21/hour, in addition to a competitive equity and benefits package (as applicable). When determining compensation, we analyze and carefully consider several factors, including location, job-related knowledge, skills, and experience. These considerations may cause your compensation to vary.</div><div><br></div><div>Ro recognizes the power of in-person collaboration, while supporting the flexibility to work anywhere in the United States. For our Ro’ers in the tri-state (NY) area, you will join us at HQ on Tuesdays and Thursdays. For those outside of the tri-state area, you will be able to join in-person collaborations throughout the year (i.e., during team on-sites).</div>
<div>&nbsp;</div>
<div>At Ro, we believe that our diverse perspectives are our biggest strengths — and that embracing them will create real change in healthcare. As an equal opportunity employer, we provide equal opportunity in all aspects of employment, including recruiting, hiring, compensation, training and promotion, termination, and any other terms and conditions of employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, familial status, age, disability and/or any other legally protected classification protected by federal, state, or local law.</div>
<div>&nbsp;</div>
<div>Ro is committed to providing reasonable accommodations for qualified individuals with disabilities in our application and interview process. If you require a reasonable accommodation in the application or interview process, please contact us at talent@ro.co.</div>
<div>&nbsp;</div>
<div>See our California Privacy Policy <span class="postings-link"><a href="https://ro.co/job-applicant-privacy-policy/">here</a></span>.</div>]]></description><link>http://biotechroles.com/warehouse-associate-romeoville-il-ro/6a07ebd22f1861929d2532cc</link><guid isPermaLink="true">http://biotechroles.com/warehouse-associate-romeoville-il-ro/6a07ebd22f1861929d2532cc</guid><pubDate>Sat, 16 May 2026 04:00:18 GMT</pubDate><company>Ro</company><location>Romeoville, IL</location><salary>$35000-45000</salary><type>Full-time</type></item><item><title><![CDATA[GTM Lead]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Our mission: to eliminate every barrier to mental health.&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;At Spring Health, we’re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. Our clinically validated technology,&lt;strong&gt; &lt;/strong&gt;&lt;a href=&quot;https://www.springhealth.com/our-approach&quot;&gt;&lt;strong&gt;Precision Mental Healthcare&lt;/strong&gt;&lt;/a&gt;, empowers us to deliver the right care at the right time—whether it’s therapy, coaching, medication, or beyond—tailored to each individual’s needs.&lt;/p&gt;
&lt;p&gt;We proudly partner with over 450 companies, from startups to multinational Fortune 500 corporations, as a leading provider of mental health service, providing care for 10 million people. Our clients include brands you use and know like Microsoft, Target, and Delta Airlines, all of whom trust us to deliver best-in-class outcomes for their employees globally. With our innovative platform, we’ve been able to generate a &lt;a href=&quot;https://www.springhealth.com/news/first-net-roi-performance-guarantee-in-mental-health?utm_medium=DSMN8&amp;amp;utm_source=LinkedIn&quot;&gt;&lt;strong&gt;net positive ROI&lt;/strong&gt;&lt;/a&gt; for employers and we are the only company in our category to earn &lt;a href=&quot;https://www.springhealth.com/news/validation-institute-certifies-spring-health-delivers-net-savings-for-customers&quot;&gt;&lt;strong&gt;external validation&lt;/strong&gt;&lt;/a&gt; of net savings for customers.&lt;/p&gt;
&lt;p&gt;We have raised capital from prominent investors including Generation Investment, Kinnevik, Tiger Global, Northzone, RRE Ventures, and many more. Thanks to their partnership and our latest Series E Funding, our current valuation has reached $3.3 billion. We’re just getting started—join us on our journey to make mental healthcare accessible to everyone, everywhere.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;We’re looking for a Senior B2B Marketing Manager to help take a brand-new product from early traction to a repeatable go-to-market motion. This is a true 0→1 role: new product, new brand, and early customers, with the opportunity to define how we show up in the market from the ground up.&lt;/p&gt;
&lt;p&gt;You’ll own positioning, launches, and early demand, working closely with the founders, product, and design to turn a complex AI product into something customers clearly understand and want to buy.&amp;nbsp; This IC role will report directly to the General Manager of the New Venture. This role defines our first real footprint in the market. You’ll help shape how customers understand the product, influence early revenue, and build the foundation for a scalable marketing function as the company grows. Occasional travel may be required for team or company events. There is a strong preference for this position to be based in NYC and operate under a hybrid model, with &lt;strong&gt;three days per week in our HQ at 60 Madison Ave office.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What you’ll do:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Define our initial go-to-market strategy for a new AI product&lt;/li&gt;
&lt;li&gt;Establish positioning, messaging, and category narrative from scratch&lt;/li&gt;
&lt;li&gt;Lead early product launches and customer-facing storytelling&lt;/li&gt;
&lt;li&gt;Design and run early demand experiments to find what works&lt;/li&gt;
&lt;li&gt;Partner closely with sales on enablement, feedback loops, and early deals&lt;/li&gt;
&lt;li&gt;Work with product and design to shape onboarding and first impressions&lt;/li&gt;
&lt;li&gt;Turn early customer learnings into sharper messaging and GTM focus&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What success looks like in this role:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Generate and influence high-quality demo, pilot, and sales conversations with our ICP, focusing on signal and conversion quality over raw volume.&lt;/li&gt;
&lt;li&gt;Develop and validate messaging that clearly explains the New Venture&#39;s value, differentiation, and role within an existing benefits stack, and measurably improves conversion across website, outbound, and sales materials.&lt;/li&gt;
&lt;li&gt;Design and run experiments, turn buyer and customer insight into action, and partner cross-functionally to create repeatable GTM foundations for growth.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What you’ll bring:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;5-7+ years of B2B marketing experience, with 0→1 or early-stage products&lt;/li&gt;
&lt;li&gt;Experience bringing new products or brands to market&lt;/li&gt;
&lt;li&gt;Strong ability to simplify complex or technical products (AI experience a plus, not required)&lt;/li&gt;
&lt;li&gt;Comfortable operating with limited data, evolving strategy, and high ownership&lt;/li&gt;
&lt;li&gt;Hands-on operator who can execute while setting direction&lt;/li&gt;
&lt;li&gt;Strong cross-functional collaborator with product, design, and sales&lt;/li&gt;
&lt;li&gt;Experience marketing AI, data, or technical B2B products preferred&lt;/li&gt;
&lt;li&gt;Background in early-stage startups or venture-backed companies preferred&lt;/li&gt;
&lt;li&gt;Experience shaping early ICP definition and GTM motion preferred&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The target base salary range for this position is&lt;strong&gt;&lt;em&gt; $121,500 -&amp;nbsp; $153,830&lt;/em&gt;&lt;/strong&gt; and is part of a competitive total rewards package including equity and benefits. Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations. We review all employee pay and compensation programs annually using &lt;a href=&quot;https://springhealth.link/jd-2022-09-radfordcomp&quot;&gt;&lt;strong&gt;Radford Global Compensation Database&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; &lt;/strong&gt;at minimum to ensure competitive and fair pay.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Benefits provided by Spring Health:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Note&lt;/strong&gt;: We have even more benefits than listed &lt;a href=&quot;https://www.springhealth.com/careers#:~:text=Our%20perks%20%26%20benefits&quot;&gt;here&lt;/a&gt; and below, your recruiter will provide more in-depth information as you continue in the interview process. Benefits are subject to individual plan requirements and eligibility criteria. &lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Health, Dental, Vision benefits start on your first day at Spring. You and your dependents also receive access to &lt;a href=&quot;https://www.onemedical.com/membership/&quot;&gt;&lt;strong&gt;One Medical&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; &lt;/strong&gt;accounts HSA and FSA plans are also available, with Spring contributing up to $1K for HSAs, depending on your plan type.&lt;/li&gt;
&lt;li&gt;Employer sponsored 401(k) match of up to 2% for retirement planning&lt;/li&gt;
&lt;li&gt;A yearly allotment of no cost visits to the Spring Health network of therapists, coaches, and medication management providers for you and your dependents.&lt;/li&gt;
&lt;li&gt;We offer competitive paid time off policies including vacation, sick leave and company holidays.&lt;/li&gt;
&lt;li&gt;At 6 months tenure with Spring, we offer parental leave of 18 weeks for birthing parents and 16 weeks for non-birthing parents.&lt;/li&gt;
&lt;li&gt;Access to &lt;a href=&quot;https://www.noom.com/&quot;&gt;&lt;strong&gt;Noom&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt;, &lt;/strong&gt;a weight management program—based in psychology, that’s tailored to your unique needs and goals.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Access to fertility care support through &lt;a href=&quot;https://springhealth.link/jd-2023-07-carrotbenefit&quot;&gt;&lt;strong&gt;Carrot&lt;/strong&gt;&lt;/a&gt;, in addition to $4,000 reimbursement for related fertility expenses.&lt;/li&gt;
&lt;li&gt;Access to&lt;strong&gt; &lt;/strong&gt;&lt;a href=&quot;https://springhealth.link/jd-2023-07-gympassbenefit&quot;&gt;&lt;strong&gt;Wellhub&lt;/strong&gt;&lt;/a&gt;,&amp;nbsp; which connects employees to the best options for fitness, mindfulness, nutrition, and sleep in one subscription&lt;/li&gt;
&lt;li&gt;Access to &lt;a href=&quot;https://www.brighthorizons.com/&quot;&gt;&lt;strong&gt;BrightHorizons&lt;/strong&gt;&lt;/a&gt;, which provides sponsored child care, back-up care, and elder care&lt;/li&gt;
&lt;li&gt;Up to $1,000 Professional Development Reimbursement a year.&lt;/li&gt;
&lt;li&gt;$200 per year donation matching to support your favorite causes.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;Not sure if you meet every requirement?&lt;/strong&gt; &lt;a href=&quot;https://pubsonline.informs.org/doi/10.1287/mnsc.2023.4907&quot;&gt;Research shows&lt;/a&gt; that women and people from historically underrepresented communities often hesitate to apply for roles unless they meet every qualification compared to other similarly-qualified candidates. At Spring Health, we are committed to fostering a workplace where everyone feels valued, empowered, and supported to &lt;a href=&quot;https://www.springhealth.com/careers&quot;&gt;Thrive&lt;/a&gt;. If this role excites you, we encourage you to apply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Ready to do the most impactful work of your life? Learn more about our values, what it’s like to work here, and how hypergrowth meets impact at Spring Health:&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://drive.google.com/file/d/1TjOJ7_OtSkacBqhs5-jMsrMV6lySQXdw/view?usp=sharing&quot;&gt;&lt;strong&gt;Our Values&lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Our privacy policy:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;a href=&quot;https://springhealth.com/privacy-policy/&quot;&gt;&lt;strong&gt;&lt;em&gt;https://springhealth.com/privacy-policy/&lt;/em&gt;&lt;/strong&gt;&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Spring Health is proud to be an equal opportunity employer. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex, marital status, ancestry, disability, genetic information, veteran status, gender identity or expression, sexual orientation, pregnancy, or other applicable legally protected characteristic. We also consider qualified applicants regardless of criminal histories, consistent with applicable legal requirements. Spring Health is also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans. If you have a disability or special need that requires accommodation, please let us know.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/gtm-lead-spring-health/6a07ebd12f1861929d2532cb</link><guid isPermaLink="true">http://biotechroles.com/gtm-lead-spring-health/6a07ebd12f1861929d2532cb</guid><pubDate>Sat, 16 May 2026 04:00:17 GMT</pubDate><company>Spring Health</company><location>New York (Hybrid)</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Strategy & Program Management, Member Growth]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Our mission: to eliminate every barrier to mental health.&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;At Spring Health, we’re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. Our clinically validated technology,&lt;strong&gt; &lt;/strong&gt;&lt;a href=&quot;https://www.springhealth.com/our-approach&quot;&gt;&lt;strong&gt;Precision Mental Healthcare&lt;/strong&gt;&lt;/a&gt;, empowers us to deliver the right care at the right time—whether it’s therapy, coaching, medication, or beyond—tailored to each individual’s needs.&lt;/p&gt;
&lt;p&gt;We proudly partner with over 450 companies, from startups to multinational Fortune 500 corporations, as a leading provider of mental health service, providing care for 10 million people. Our clients include brands you use and know like Microsoft, Target, and Delta Airlines, all of whom trust us to deliver best-in-class outcomes for their employees globally. With our innovative platform, we’ve been able to generate a &lt;a href=&quot;https://www.springhealth.com/news/first-net-roi-performance-guarantee-in-mental-health?utm_medium=DSMN8&amp;amp;utm_source=LinkedIn&quot;&gt;&lt;strong&gt;net positive ROI&lt;/strong&gt;&lt;/a&gt; for employers and we are the only company in our category to earn &lt;a href=&quot;https://www.springhealth.com/news/validation-institute-certifies-spring-health-delivers-net-savings-for-customers&quot;&gt;&lt;strong&gt;external validation&lt;/strong&gt;&lt;/a&gt; of net savings for customers.&lt;/p&gt;
&lt;p&gt;We have raised capital from prominent investors including Generation Investment, Kinnevik, Tiger Global, Northzone, RRE Ventures, and many more. Thanks to their partnership and our latest Series E Funding, our current valuation has reached $3.3 billion. We’re just getting started—join us on our journey to make mental healthcare accessible to everyone, everywhere.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;This role sits at the intersection of strategy and execution — translating company priorities into structured, accountable programs that deliver breakthrough outcomes for members and the business. You&#39;ll partner across Product, Engineering, Data, Revenue, and Finance to diagnose what&#39;s working, challenge what isn&#39;t, and move decisively on opportunities that drive meaningful, measurable growth.&lt;/p&gt;
&lt;p&gt;This role requires a rigorous, data-driven operator who thrives in ambiguity, excels at bringing clarity and accountability to complex cross-functional work, and combines analytical depth with stakeholder influence to deliver results on high-stakes programs. Your initial focus will be a portfolio of member growth initiatives — identifying the right bets, pressure-testing assumptions, and executing with precision to move the needle on engagement and business outcomes.&lt;/p&gt;
&lt;p&gt;This role will report into Vice President, Member Experience for Product and Growth Marketing. Please note that this is a hybrid role based in New York City, with an expectation to be in the office 2–3 days per week at our 60 Madison Avenue location. Candidates must be based in the NYC metro area or able to relocate independently within 90 days of their start date. Occasional travel will be required for team on-sites.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What you will do:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Leverage data-driven insights to diagnose underperforming growth levers, drive those initiatives with product, customer/member marketing and customer success teams, identify high-impact opportunities, and align cross-functional teams around the most critical priorities.&lt;/li&gt;
&lt;li&gt;Lead end-to-end program planning, execution, and delivery across product, marketing, engineering, and cross-functional teams — translating strategy into structured plans with clear milestones, owners, and outcomes.&lt;/li&gt;
&lt;li&gt;Define and rigorously track success metrics tied to member growth and program impact, using insights to continuously sharpen priorities and drive better outcomes.&lt;/li&gt;
&lt;li&gt;Translate complex program data into clear, executive-ready narratives — surfacing progress, risks, and tradeoffs to enable fast, high-confidence decision-making.&lt;/li&gt;
&lt;li&gt;Act as connective tissue across departments — aligning stakeholders, resolving dependencies, and mobilizing teams quickly on the highest-priority opportunities.&lt;/li&gt;
&lt;li&gt;Identify and integrate AI-leveraged workflows and scalable tools to increase program efficiency, reduce manual overhead, and accelerate speed-to-impact.&lt;/li&gt;
&lt;li&gt;Identify, pilot, and scale AI-leveraged workflows and automation tools across programs — reducing manual overhead, improving reporting fidelity, and accelerating speed-to-impact across the team.&lt;/li&gt;
&lt;li&gt;Foster a culture of continuous improvement through retrospectives, process iteration, and feedback loops that make every program more effective than the last.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What success looks like:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;You don&#39;t just deliver programs on time — you drive outcomes that outperform original projections and redefine what growth looks like for the business. You&#39;ve moved high-stakes initiatives from ambiguity to sustainable operations ahead of schedule, with clear data showing impact on member engagement and business results. Senior stakeholders rely on you as the source of clarity and accountability in the room — confident that risks are surfaced early, decisions are grounded in evidence, and execution follows through without friction. Continuous improvement practices you&#39;ve introduced have materially raised the bar on how programs run, and your work is directly traceable to company growth goals.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What we expect from you:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;10+ years of program management, product operations, or project management experience within a high-performing tech org, preferably embedded in product, engineering, or marketing.&lt;/li&gt;
&lt;li&gt;Critical Thinking and Analytical Rigor: Ability to deconstruct complex, ambiguous growth problems into actionable priorities and drive evidence-based decisions across competing stakeholders.&lt;/li&gt;
&lt;li&gt;AI Competency: Familiarity with AI and automation tools and a demonstrated ability to leverage them to increase your own output and unlock program efficiency at scale.&lt;/li&gt;
&lt;li&gt;Communication and Mobilizing Teams: Exceptional ability to create clarity, earn trust, and align diverse stakeholders — including at the executive level — to move fast on shared goals.&lt;/li&gt;
&lt;li&gt;Grit and Accountability: A track record of owning outcomes, not just outputs — maintaining focus and momentum even as priorities shift and blockers emerge.&lt;/li&gt;
&lt;li&gt;Organizational Rigor: Proven ability to manage a high volume of complex, interdependent work with tight timelines and a consistent bias toward on-time, high-quality delivery.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;The target base salary range for this position is &lt;strong&gt;$180,00 - $227,000,&lt;/strong&gt;&amp;nbsp;and is part of a competitive total rewards package including equity and benefits. Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations. We review all employee pay and compensation programs annually using &lt;a href=&quot;https://springhealth.link/jd-2022-09-radfordcomp&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Radford Global Compensation Database&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; &lt;/strong&gt;at minimum to ensure competitive and fair pay.&lt;/em&gt;&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;Benefits provided by Spring Health:&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;p&gt;&lt;strong&gt;Note&lt;/strong&gt;: We have even more benefits than listed &lt;a href=&quot;https://www.springhealth.com/careers#:~:text=Our%20perks%20%26%20benefits&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt; and below, your recruiter will provide more in-depth information as you continue in the interview process. Benefits are subject to individual plan requirements and eligibility criteria. &lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Health, Dental, Vision benefits start on your first day at Spring. You and your dependents also receive access to &lt;a href=&quot;https://www.onemedical.com/membership/&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;One Medical&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; &lt;/strong&gt;accounts HSA and FSA plans are also available, with Spring contributing up to $1K for HSAs, depending on your plan type.&lt;/li&gt;
&lt;li&gt;Employer sponsored 401(k) match of up to 2% for retirement planning&lt;/li&gt;
&lt;li&gt;A yearly allotment of no cost visits to the Spring Health network of therapists, coaches, and medication management providers for you and your dependents.&lt;/li&gt;
&lt;li&gt;We offer competitive paid time off policies including vacation, sick leave and company holidays.&lt;/li&gt;
&lt;li&gt;At 6 months tenure with Spring, we offer parental leave of 18 weeks for birthing parents and 16 weeks for non-birthing parents.&lt;/li&gt;
&lt;li&gt;Access to &lt;a href=&quot;https://www.noom.com/&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Noom&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt;, &lt;/strong&gt;a weight management program—based in psychology, that’s tailored to your unique needs and goals.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Access to fertility care support through &lt;a href=&quot;https://springhealth.link/jd-2023-07-carrotbenefit&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Carrot&lt;/strong&gt;&lt;/a&gt;, in addition to $4,000 reimbursement for related fertility expenses.&lt;/li&gt;
&lt;li&gt;Access to&lt;strong&gt; &lt;/strong&gt;&lt;a href=&quot;https://springhealth.link/jd-2023-07-gympassbenefit&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Wellhub&lt;/strong&gt;&lt;/a&gt;,&amp;nbsp; which connects employees to the best options for fitness, mindfulness, nutrition, and sleep in one subscription&lt;/li&gt;
&lt;li&gt;Access to &lt;a href=&quot;https://www.brighthorizons.com/&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;BrightHorizons&lt;/strong&gt;&lt;/a&gt;, which provides sponsored child care, back-up care, and elder care&lt;/li&gt;
&lt;li&gt;Up to $1,000 Professional Development Reimbursement a year.&lt;/li&gt;
&lt;li&gt;$200 per year donation matching to support your favorite causes.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;Not sure if you meet every requirement?&lt;/strong&gt; &lt;a href=&quot;https://pubsonline.informs.org/doi/10.1287/mnsc.2023.4907&quot;&gt;Research shows&lt;/a&gt; that women and people from historically underrepresented communities often hesitate to apply for roles unless they meet every qualification compared to other similarly-qualified candidates. At Spring Health, we are committed to fostering a workplace where everyone feels valued, empowered, and supported to &lt;a href=&quot;https://www.springhealth.com/careers&quot;&gt;Thrive&lt;/a&gt;. If this role excites you, we encourage you to apply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Ready to do the most impactful work of your life? Learn more about our values, what it’s like to work here, and how hypergrowth meets impact at Spring Health:&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://drive.google.com/file/d/1TjOJ7_OtSkacBqhs5-jMsrMV6lySQXdw/view?usp=sharing&quot;&gt;&lt;strong&gt;Our Values&lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Our privacy policy:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;a href=&quot;https://springhealth.com/privacy-policy/&quot;&gt;&lt;strong&gt;&lt;em&gt;https://springhealth.com/privacy-policy/&lt;/em&gt;&lt;/strong&gt;&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Spring Health is proud to be an equal opportunity employer. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex, marital status, ancestry, disability, genetic information, veteran status, gender identity or expression, sexual orientation, pregnancy, or other applicable legally protected characteristic. We also consider qualified applicants regardless of criminal histories, consistent with applicable legal requirements. Spring Health is also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans. If you have a disability or special need that requires accommodation, please let us know.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-strategy-and-program-management-member-growth-spring-health/6a07ebd02f1861929d2532ca</link><guid isPermaLink="true">http://biotechroles.com/director-strategy-and-program-management-member-growth-spring-health/6a07ebd02f1861929d2532ca</guid><pubDate>Sat, 16 May 2026 04:00:16 GMT</pubDate><company>Spring Health</company><location>New York (Hybrid)</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Fulfillment Pharmacist - Torrance, CA]]></title><description><![CDATA[<div>Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients in nearly every single county in the United States, including 99% of primary care deserts.</div>
<div>&nbsp;</div>
<div>Ro is consistently recognized as a top workplace in Health Care, in New York, and for Women and Parents—earning more than 20 honors from Fortune, Great Place to Work, and PEOPLE since 2021. In 2025 alone, we ranked top 5 among medium workplaces in Health Care and New York, and top 50 nationwide.</div><div><br></div><div><span style="font-size: 16px;">As a Pharmacist, you will be front and center ensuring members get accurate orders on time. You will report directly to the Lead Pharmacist and have the opportunity to work with multiple teams to deliver an uncommonly seamless pharmacy experience for members. You are passionate about improving the patient experience and want to help shape the future of the industry.&nbsp;</span></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">This posting is for our location in </span><strong style="font-size: 16px;">Torrance, California</strong><span style="font-size: 16px;">. This hire is for a Full-Time role.&nbsp;</span></div></br><b>What You'll Do</b></br>
<li>Process and review medication orders for members</li>
<li>Work with the doctor or care team when clinical intervention is needed</li>
<li>Respond to clinical questions from members</li>
<li>Work with a multidisciplinary team of doctors, engineers, product managers, and more</li>
<li>Work with team members to improve current procedures and workflow</li>
<li>Find creative, fun, and professional ways to deliver the best possible experience for our patients</li>
<li>Offer clinical expertise in evaluating drug regimens to provide the best patient care</li>
<li>Collaborate with healthcare professionals to ensure optimal patient care&nbsp;</li>
</br><b>What You'll Bring to the Team</b></br>
<li>Bachelor of Science in Pharmacy or Doctor of Pharmacy from an accredited college of pharmacy</li>
<li>Valid California Pharmacy License</li>
<li>Ability to work 40 hours per week in fast paced, high volume location</li>
<li>Unrivaled empathy and patience when helping patients</li>
<li>Ability to think quickly and work autonomously</li>
<li>Strong organization skills and attention to detail</li>
<li>You connect with the mission of Ro</li>
<li>Innovative individuals looking to share ideas and implement change</li>
<li>Aptitude in problem-solving and decision-making</li>
<li>Team player with outstanding communication skills</li>
</br><div><span style="font-size: 16px;">We welcome qualified candidates of all races, creeds, genders, and sexuality to apply.</span></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">The target hourly rate for this position ranges from $64.42 to $68.27, in addition to a competitive equity and benefits package (as applicable). When determining compensation, we analyze and carefully consider several factors, including location, job-related knowledge, skills and experience. These considerations may cause your compensation to vary.</span></div><div><br></div><div>At Ro, we believe that our diverse perspectives are our biggest strengths — and that embracing them will create real change in healthcare. As an equal opportunity employer, we provide equal opportunity in all aspects of employment, including recruiting, hiring, compensation, training and promotion, termination, and any other terms and conditions of employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, familial status, age, disability and/or any other legally protected classification protected by federal, state, or local law.</div>
<div>&nbsp;</div>
<div>Ro is committed to providing reasonable accommodations for qualified individuals with disabilities in our application and interview process. If you require a reasonable accommodation in the application or interview process, please contact us at talent@ro.co.</div>
<div>&nbsp;</div>
<div>See our California Privacy Policy <a href="https://ro.co/job-applicant-privacy-policy/" class="postings-link">here</a>.</div>]]></description><link>http://biotechroles.com/fulfillment-pharmacist-torrance-ca-ro/6a07ebd02f1861929d2532c9</link><guid isPermaLink="true">http://biotechroles.com/fulfillment-pharmacist-torrance-ca-ro/6a07ebd02f1861929d2532c9</guid><pubDate>Sat, 16 May 2026 04:00:16 GMT</pubDate><company>Ro</company><location>Los Angeles, CA</location><salary>$130000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist, Peptide Chemistry]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Who We Are:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico’s highly innovative technology labs, its commitment to curiosity-driven discovery science, and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Description&lt;/strong&gt;:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We are seeking a scientist to join our Peptide Chemistry team. In this role, you will drive peptide drug discovery projects that sit at the nexus of empirical medicinal chemistry and Calico’s proprietary Machine Learning (ML) peptide design platform. You will collaborate cross-functionally with ML scientists, medicinal chemists, automation specialists, and biologists to explore structure-activity relationships (SAR). By leveraging a rapid design-make-test cycle, you will accelerate the optimization of therapeutic peptides and contribute to the evolution of a world-class synthetic engine.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Drive Discovery: Lead peptide drug discovery campaigns from initial hit identification through to IND-enabling studies&lt;/li&gt;
&lt;li&gt;Innovate Synthetic Workflows: Onboard and optimize novel chemistries for high-throughput, automated peptide synthesis; troubleshoot complex synthetic challenges to generate high-quality leads, and curate a custom library of building blocks&lt;/li&gt;
&lt;li&gt;Cross-Functional Partnership: Collaborate with biology, software, automation, assay, and pharmacology teams to ensure seamless execution of ML platform objectives and drug discovery milestones&lt;/li&gt;
&lt;li&gt;Mentorship and Management: Actively mentor junior scientists, fostering a culture of technical excellence, continuous learning, and collaborative innovation&lt;/li&gt;
&lt;li&gt;Manage external collaborations and CROs efficiently, including teams of chemists, DMPK scientists and formulation experts&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Position Requirements&lt;/strong&gt;:&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in Organic Chemistry, Peptide Chemistry, or a related discipline with 0-2 years of industry experience in drug discovery&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience in peptide hit discovery, SAR campaigns, ADMET optimization, and peptide formulation&lt;/li&gt;
&lt;li&gt;Proven experience building and interpreting complex assay cascades, including biophysical characterization, functional protein/cell-based assays, and ADMET screening&amp;nbsp;&lt;/li&gt;
&lt;li&gt;High proficiency in automated synthesis, purification (HPLC, Flash, SPE), and characterization (LCMS, NMR, CD, etc.)&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Demonstrated ability to implement diverse chemistries, including backbone-modifications, macrocyclization, stapling, and bioconjugation via solid- or solution-phase strategies&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Excellent problem-solving and analytical skills&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Exceptional interpersonal and communication skills for effective collaboration across diverse functional groups&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Must be willing to work onsite 5 days per week&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Nice to Have:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with organic synthesis, including transition metal catalysis and synthesis of non-canonical amino acids, is highly desired&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience with automation, software, and data-science integration into chemistry workflows&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ability to utilize AI-tools to improve efficiency of research and build programs for data analysis or synthesis&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Knowledgeable on the key principles of ML-design for peptide therapeutics&lt;/li&gt;
&lt;li&gt;Prior experience with peptide-specific computational tools for hit discovery, SAR prioritization, molecular modeling, and physicochemical characterization&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The estimated base salary range for this role is $135,000 - $145,000. Actual pay will be based on a number of factors including experience and qualifications. This position is also eligible for two annual cash bonuses.&lt;/p&gt;
&lt;h2 id=&quot;ojxVC&quot; class=&quot;wLzlc&quot;&gt;&lt;/h2&gt;]]></description><link>http://biotechroles.com/scientist-peptide-chemistry-calico-labs/6a07ebcd2f1861929d2532c8</link><guid isPermaLink="true">http://biotechroles.com/scientist-peptide-chemistry-calico-labs/6a07ebcd2f1861929d2532c8</guid><pubDate>Sat, 16 May 2026 04:00:13 GMT</pubDate><company>Calico Labs</company><location>South San Francisco, CA</location><salary>$120000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Security Operations Lead (SecOps)]]></title><description><![CDATA[<div>At Sword, we’re building AI to heal billions and unlock humanity’s full potential. In doing so, we’re pioneering AI Care, a fundamentally new approach to healthcare built for medical reasoning, safety, and real-time treatment, not generic technology applied after the fact. As both a clinical-centric frontier AI lab and an applied AI platform, Sword is reimagining how care is delivered at scale, removing traditional barriers like appointments, waiting rooms, and stigma so more people can access the care they need—and ultimately get back to lives lived in full.<br><br>Since 2020, Sword has expanded across physical therapy, women’s health, cardiometabolic, and mental health, and is now moving beyond the session to a fully AI-native, 24/7 care program that brings physical activity, therapeutic exercise, psychotherapy, nutrition, and behavior change into one connected experience. More than 700,000 members across three continents have completed over 10 million AI sessions, helping 1,000+ enterprise clients avoid more than $1 billion in unnecessary healthcare costs. Backed by 42 clinical studies, 44+ patents, and more than $500 million raised from leading investors including Khosla Ventures, General Catalyst, and Founders Fund, Sword is defining a new standard for healthcare.</div><div><br></div><div>
<p>As Security Operations Lead, you'll lead our SecOps squad and own how Sword detects, investigates, and responds to threats. You'll help structure how this function operates — setting the direction on SIEM architecture, detection engineering, and incident response — and use automation and AI to scale a focused team across a fast-growing, multi-continent footprint. You'll be a core voice in our security strategy, and the systems, processes, and culture you build will set the bar for how Sword protects 700,000+ members.</p>
<p><strong>If&nbsp; Tech role</strong>: To get to know more about our Tech Stack, check <a href="https://stackshare.io/sword-health/sword-health">here</a>.</p>
</div></br><b></b></br><div><strong>AI</strong>&nbsp;<strong>Proficiency at Sword Health</strong>
<p>AI fluency is a core expectation at Sword Health. Every candidate is assessed against our three-level framework — be ready to share real examples of how AI is already part of how you work.</p>

<li>
<p>Explorer (Level 1) — Uses AI daily to boost personal productivity</p>
</li>
<li>
<p>Builder (Level 2) — Creates workflows and tools that elevate the whole team</p>
</li>
<li>
<p>Integrator (Level 3) — Embeds AI into products and processes at scale</p>
</li>

<p>Every hire must demonstrate at least Level 1. The expected level will vary depending on the seniority of the role.</p>
</div></br><b>What you’ll be doing</b></br><div>

<li>
<p>Set the strategy and technical direction for Sword’s Security Operations Center — defining the operating model, SIEM and detection architecture, incident response capability, and the roadmap to scale them as the company grows.</p>
</li>
<li>
<p>Drive an AI- and automation-first transformation of security operations: design SOAR playbooks, agentic and LLM-assisted triage workflows, and ML-driven detection to reduce MTTD/MTTR, expand coverage, and let a lean team operate at enterprise scale.</p>
</li>
<li>
<p>Lead the SOC/CSIRT team technically — mentoring detection and response engineers, raising the bar on investigations, running on-call and escalation models, and acting as commander for major incidents.</p>
</li>
<li>
<p>Own the SIEM end-to-end (architecture, data sources, normalization, retention, cost, and tuning) and evolve detection-as-code content aligned to MITRE ATT&amp;CK and Sword’s threat model.</p>
</li>
<li>
<p>Lead high-severity incident response from detection through containment, eradication, recovery, and post-incident review, partnering with engineering, IT, legal, and executive stakeholders during critical events.</p>
</li>
<li>
<p>Run the threat intelligence and threat hunting programs, converting emerging TTPs into new detections, proactive hardening, and informed risk decisions.</p>
</li>
<li>
<p>Define and report on SOC performance — MTTD, MTTR, coverage, automation rate, false-positive rate, on-call health — and use those metrics to drive measurable, continuous improvement.</p>
</li>
<li>
<p>Influence security architecture and engineering decisions across the company, ensuring detection, response, and recovery are built into new products, platforms, and infrastructure from day one.</p>
</li>
<li>
<p>Establish and continuously improve incident response playbooks, runbooks, and tabletop exercises to ensure organizational readiness.</p>
</li>

</div></br><div><span data-sheets-root="1">*This range includes base, variable and equity<br><br>These compensation bands are just the starting point. Once someone joins and proves they’re outlier talent, we adjust quickly to ensure their compensation aligns with their impact.<br><br>Our job titles may span more than one career level. Actual pay is determined by skills, qualifications, experience, location, market demand, and other factors. Compensation details listed in this posting reflect the base salary and any potential variable, bonus or sales incentives, and the Company’s estimation of the value of private company stock options, if applicable. The pay range is subject to change, future value of company stock options is not guaranteed, and compensation may be modified in the future. In addition to our total compensation, Sword offers a number of benefits as listed below.</span></div>
<div>&nbsp;</div>
<div><strong>Portugal - Sword Benefits &amp; Perks:</strong></div>
<div>&nbsp;</div>
<div>• Health, dental and vision insurance</div>
<div>• Meal allowance</div>
<div>• Equity shares</div>
<div>• Remote work allowance</div>
<div>• Flexible working hours</div>
<div>• Work from home</div>
<div>• Discretionary vacation</div>
<div>• Snacks and beverages</div>
<div>&nbsp;</div>
<div><strong>Note:</strong>&nbsp;Please note that this position does not offer relocation assistance. Candidates must possess a valid EU visa and be based in Portugal.</div>
<div>&nbsp;</div>
<div>Sword Health complies with applicable Federal and State civil rights laws and does not discriminate on the basis of Age, Ancestry, Color, Citizenship, Gender, Gender expression, Gender identity, Gender information, Marital status, Medical condition, National origin, Physical or mental disability, Pregnancy, Race, Religion, Caste, Sexual orientation, and Veteran status.</div>]]></description><link>http://biotechroles.com/security-operations-lead-(secops)-sword-health/6a07ebcd2f1861929d2532c6</link><guid isPermaLink="true">http://biotechroles.com/security-operations-lead-(secops)-sword-health/6a07ebcd2f1861929d2532c6</guid><pubDate>Sat, 16 May 2026 04:00:13 GMT</pubDate><company>Sword Health</company><location></location><salary>$120000-160000</salary><type></type></item><item><title><![CDATA[Design Manager]]></title><description><![CDATA[<div>At Sword, we’re building AI to heal billions and unlock humanity’s full potential. In doing so, we’re pioneering AI Care, a fundamentally new approach to healthcare built for medical reasoning, safety, and real-time treatment, not generic technology applied after the fact. As both a clinical-centric frontier AI lab and an applied AI platform, Sword is reimagining how care is delivered at scale, removing traditional barriers like appointments, waiting rooms, and stigma so more people can access the care they need—and ultimately get back to lives lived in full.<br><br>Since 2020, Sword has expanded across physical therapy, women’s health, cardiometabolic, and mental health, and is now moving beyond the session to a fully AI-native, 24/7 care program that brings physical activity, therapeutic exercise, psychotherapy, nutrition, and behavior change into one connected experience. More than 700,000 members across three continents have completed over 10 million AI sessions, helping 1,000+ enterprise clients avoid more than $1 billion in unnecessary healthcare costs. Backed by 42 clinical studies, 44+ patents, and more than $500 million raised from leading investors including Khosla Ventures, General Catalyst, and Founders Fund, Sword is defining a new standard for healthcare.</div><div><br></div><div>We are looking for a Design Manager who is both a hands-on designer and a strategic leader. This role focuses on creating high-performing experiences that drive client and member acquisition across multiple channels, including email, website, landing pages, and enrollment/onboarding flows.<br><br>You will be responsible for executing and optimizing best-in-class experiences while managing and mentoring a team. This position requires expertise in brand visuals and product design, ensuring every touchpoint is both visually compelling and conversion-driven.<br><br><strong>Critically, this role operates in a highly matrixed environment, spanning multiple product and engineering teams, as well as marketing and business leadership. Success here requires strong communication, the ability to build alignment without direct authority, and the confidence to navigate competing priorities across organizations.</strong></div></br><b></b></br><div><strong>AI</strong>&nbsp;<strong>Proficiency at Sword Health</strong>
<p>AI fluency is a core expectation at Sword Health. Every candidate is assessed against our three-level framework — be ready to share real examples of how AI is already part of how you work.</p>

<li>
<p>Explorer (Level 1) — Uses AI daily to boost personal productivity</p>
</li>
<li>
<p>Builder (Level 2) — Creates workflows and tools that elevate the whole team</p>
</li>
<li>
<p>Integrator (Level 3) — Embeds AI into products and processes at scale</p>
</li>

<p>Every hire must demonstrate at least Level 1. The expected level will vary depending on the seniority of the role.</p>
</div></br><b>What you’ll be doing:</b></br>
<li>
<p>Own and drive design initiatives that optimize acquisition and conversion across key touchpoints;</p>
</li>
<li>
<p>Design and iterate on high-impact growth experiences, including campaigns, client emails, landing pages, and onboarding flows;</p>
</li>
<li>
<p>Balance strong brand storytelling with conversion-driven design principles to maximize performance;</p>
</li>
<li>
<p>Drive alignment across marketing, product, engineering, and data teams, navigating competing priorities, advocating for design quality, and ensuring work lands with clarity at every level of the organization;</p>
</li>
<li>
<p>Communicate design strategy and rationale clearly to senior leadership and executive stakeholders, translating design decisions into business impact;</p>
</li>
<li>
<p>Navigate ambiguity and conflicting priorities across teams, building trust and consensus without direct authority;</p>
</li>
<li>
<p>Leverage data, A/B testing, and insights to continuously refine and improve user journeys;</p>
</li>
<li>
<p>Manage, mentor, and inspire a team of designers, ensuring high-quality execution and professional growth;</p>
</li>
<li>
<p>Ensure insights, assets, and learnings are shared and leveraged across your direct team;</p>
</li>
<li>
<p>Advocate for user-centered design while balancing growth and performance goals;</p>
</li>
<li>
<p>Follow experimentation methodologies and frameworks to test and validate design decisions;</p>
</li>
<li>
<p>Analyze user behavior, conversion rates, and engagement metrics to inform iterative improvements;</p>
</li>
<li>
<p>Stay up-to-date with industry trends, tools, and best practices in growth and performance design.</p>
</li>
</br><div><span data-sheets-root="1">*This range includes base, variable and equity<br><br>These compensation bands are just the starting point. Once someone joins and proves they’re outlier talent, we adjust quickly to ensure their compensation aligns with their impact.<br><br>Our job titles may span more than one career level. Actual pay is determined by skills, qualifications, experience, location, market demand, and other factors. Compensation details listed in this posting reflect the base salary and any potential variable, bonus or sales incentives, and the Company’s estimation of the value of private company stock options, if applicable. The pay range is subject to change, future value of company stock options is not guaranteed, and compensation may be modified in the future. In addition to our total compensation, Sword offers a number of benefits as listed below.</span></div>
<div>&nbsp;</div>
<div><strong>Portugal - Sword Benefits &amp; Perks:</strong></div>
<div>&nbsp;</div>
<div>• Health, dental and vision insurance</div>
<div>• Meal allowance</div>
<div>• Equity shares</div>
<div>• Remote work allowance</div>
<div>• Flexible working hours</div>
<div>• Work from home</div>
<div>• Discretionary vacation</div>
<div>• Snacks and beverages</div>
<div>&nbsp;</div>
<div><strong>Note:</strong>&nbsp;Please note that this position does not offer relocation assistance. Candidates must possess a valid EU visa and be based in Portugal.</div>
<div>&nbsp;</div>
<div>Sword Health complies with applicable Federal and State civil rights laws and does not discriminate on the basis of Age, Ancestry, Color, Citizenship, Gender, Gender expression, Gender identity, Gender information, Marital status, Medical condition, National origin, Physical or mental disability, Pregnancy, Race, Religion, Caste, Sexual orientation, and Veteran status.</div>]]></description><link>http://biotechroles.com/design-manager-sword-health/6a07ebcd2f1861929d2532c7</link><guid isPermaLink="true">http://biotechroles.com/design-manager-sword-health/6a07ebcd2f1861929d2532c7</guid><pubDate>Sat, 16 May 2026 04:00:13 GMT</pubDate><company>Sword Health</company><location></location><salary>$120000-160000</salary><type></type></item><item><title><![CDATA[Head of Peptide Drug Discovery]]></title><description><![CDATA[&lt;h4&gt;&lt;strong&gt;Who We Are:&lt;/strong&gt;&lt;/h4&gt;
&lt;p&gt;Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico’s highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Description:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Calico is seeking an accomplished and motivated individual to lead peptide drug discovery efforts as Head of Peptide Drug Discovery within the Calico Drug Discovery organization. This leader will collaborate with innovative and diverse scientists and play a pivotal role in advancing Calico’s Preclinical pipeline to deliver oral peptide drug candidates to our development portfolio. The ideal candidate will leverage deep and proven expertise in the lead optimization of oral peptide drug candidates, provide leadership for discovery and development stage projects, and be an effective people leader capable of attracting key talent and developing our internal team of peptide drug discovery scientists.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Act as a peptide drug discovery Subject Matter Expert (SME) to deliver peptide Drug Candidates for the Calico pipeline&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Be a strong and collaborative partner with leaders of the Calico Small Molecule Drug Discovery, Machine Learning Platform, Discovery Technologies, Research, CMC, DMPK, Toxicology and Clinical Development functions&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Bridge Computation &amp;amp; Chemistry: Serve as the primary technical liaison and advisor to the ML team, ensuring chemical intuition effectively informs algorithmic design and vice versa&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Provide leadership, mentorship, and development of the existing peptide chemistry team to achieve a cutting-edge peptide drug discovery group&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Maintain oversight of external CROs to support chemistry, formulation, and DMPK for peptide drug discovery&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Contribute to global regulatory submissions (e.g., IBs, Briefing Books, INDs, NDAs)&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Represent Calico in external scientific collaborations, committees, and consortia in the field of peptide drug discovery&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Position Requirements:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in organic/peptide/medicinal chemistry with 12+ years of drug discovery experience in biotech or pharma&lt;/li&gt;
&lt;li&gt;Proven track record of successfully delivering peptide drug candidates that have achieved preclinical candidate nomination and progressed into clinical development&lt;/li&gt;
&lt;li&gt;Effective communication with ML-peptide design team to deliver prioritized design concepts through strong collaboration&lt;/li&gt;
&lt;li&gt;Strong working knowledge of the synthesis of peptide libraries and the scale-up of peptide lead molecules&lt;/li&gt;
&lt;li&gt;Strong organic chemistry skills to direct the synthesis of non-canonical amino acids&lt;/li&gt;
&lt;li&gt;Deep knowledge in the use of formulation excipients to enhance oral bioavailability of peptide drug candidates&lt;/li&gt;
&lt;li&gt;Self-motivated, enthusiastic, and highly adaptable with the ability to quickly identify project challenges and pivot strategies in a fast-paced environment&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Exceptional oral communication and writing skills, with record-keeping and data organization skills&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Must be willing to work onsite 5 days a week&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Nice to Have:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with evaluation of AI/ML generated peptides in Hit Generation-Lead Optimization&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The estimated base salary range for this role is $320,000 - $350,000. Actual pay will be based on a number of factors including experience and qualifications. This position is also eligible for two annual cash bonuses.&lt;/p&gt;
&lt;h2 id=&quot;ojxVC&quot; class=&quot;wLzlc&quot;&gt;&lt;/h2&gt;]]></description><link>http://biotechroles.com/head-of-peptide-drug-discovery-calico-labs/6a07ebcb2f1861929d2532c5</link><guid isPermaLink="true">http://biotechroles.com/head-of-peptide-drug-discovery-calico-labs/6a07ebcb2f1861929d2532c5</guid><pubDate>Sat, 16 May 2026 04:00:11 GMT</pubDate><company>Calico Labs</company><location>South San Francisco, CA</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Member Engagement & Optimization]]></title><description><![CDATA[<div>
<div>Everlywell is a digital health company pioneering the next generation of biomarker intelligence—combining AI-powered technology with human insight to deliver personalized, actionable health answers. We transform complex biomarker data into life-changing insights—seamlessly integrating advanced diagnostics, virtual care, and patient engagement to reshape how and where health happens.</div>
<div>&nbsp;</div>
<div>Over the past decade, Everlywell has delivered close to 1 billion personalized health insights, transforming care for 60 million people and powering hundreds of enterprise partners. In 2025, an estimated 1 in 94 U.S. adults received an Everlywell test, solidifying our spot as the #1 at-home testing company in the country. Fueled by AI and built for scale, we’re breaking down barriers, closing care gaps, and unlocking a more connected healthcare experience that is smarter, faster, and more personalized.</div>
<p>We are hiring a strategic, marketing-forward leader to own and evolve member engagement strategy across Everlywell’s health plan and enterprise programs. This role will lead engagement strategy across channels including&nbsp;<strong>telemarketing and live agent outreach, IVR, SMS, email, and direct mail</strong>, with a focus on improving activation, conversion, kit return, visit completion, and follow-through across complex healthcare populations.</p>
<p>This person should bring strong healthcare marketing judgment and meaningful experience designing engagement and activation programs in payer, Medicare Advantage, Medicaid, or broader health plan environments. They will partner closely with Analytics, ML / AI, Operations, Clinical, Product, Compliance, and client-facing teams to improve targeting, optimize cadence and channel mix, and increase member action rates through both stronger engagement design and smarter use of predictive models.</p>
</div></br><b>What You'll Do:</b></br>
<li>
<p>Own member engagement strategy across key channels, with <strong>telemarketing / live agent outreach</strong> as a critical lever alongside IVR, SMS, email, direct mail, and related touchpoints.</p>
</li>
<li>
<p>Design end-to-end engagement journeys that improve member activation and action across use cases such as opt-in, kit activation, kit return, visit scheduling, and downstream follow-through.</p>
</li>
<li>
<p>Build segmentation, messaging, and channel strategies tailored to health plan populations including Medicare Advantage, Medicaid, Commercial ACA, and other relevant lines of business.</p>
</li>
<li>
<p>Partner with Analytics, ML / AI, and operations teams to build targeting approaches, decision frameworks and reporting that help us understand what is and is not working across programs, with particular focus on telemarketing and live agent outreach performance.</p>
</li>
<li>
<p>Help shape how predictive models and ML-driven recommendations can be used to prioritize outreach, improve telemarketing targeting, optimize outreach cadence and channel selection, and increase member action rates.</p>
</li>
<li>
<p>Lead A/B testing and optimization across messaging, scripts, creative, timing, sequencing, and channel mix, with particular attention to what improves connection and conversion in telemarketing and phone-based outreach.</p>
</li>
<li>
<p>Partner with teams responsible for scripts, templates, print, digital comms, and implementation to ensure engagement strategy is translated into effective, compliant execution.</p>
</li>
<li>
<p>Partner with client-facing and commercial teams to bring engagement strategy into health plan conversations early, helping shape program design, channel approach, and performance expectations upfront.</p>
</li>
</br><b>Who You Are:</b></br><div>

<li>
<p>6-10+ years of experience in healthcare marketing, member engagement, lifecycle marketing, growth, or related strategy roles</p>
</li>
<li>
<p>Strong experience designing engagement or activation programs in payer, health plan, managed care, provider, population health, or healthcare services environments</p>
</li>
<li>
<p>Deep understanding of member behavior and how to drive action across regulated, high-friction healthcare journeys</p>
</li>
<li>
<p>Meaningful experience with <strong>telemarketing, live agent, or call-based engagement strategy</strong>, especially in contexts where phone outreach is a major conversion driver.</p>
</li>
<li>
<p>Strong marketer with sound judgment on messaging, positioning, testing, and performance optimization</p>
</li>
<li>
<p>Experience partnering with analytics, data science, or ML / AI teams to improve targeting, prioritization, and engagement outcomes</p>
</li>
<li>
<p>Comfortable operating in regulated environments and partnering closely with Compliance and Legal</p>
</li>
<li>
<p>Experience with Medicare Advantage and government-aligned populations is strongly preferred, but the role should not be limited to Medicare-only telemarketing expertise.</p>
</li>

</div></br>]]></description><link>http://biotechroles.com/senior-manager-member-engagement-and-optimization-everly-health/6a07ebca2f1861929d2532c3</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-member-engagement-and-optimization-everly-health/6a07ebca2f1861929d2532c3</guid><pubDate>Sat, 16 May 2026 04:00:10 GMT</pubDate><company>Everly Health</company><location>United States</location><salary>$130000-180000</salary><type></type></item><item><title><![CDATA[IACUC Coordinator, Contract]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Our Mission&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Our mission is to restore cell health and resilience through cell rejuvenation to reverse disease, injury, and the disabilities that can occur throughout life.&lt;/p&gt;
&lt;p&gt;For more information, see our website at &lt;a href=&quot;https://altoslabs.com/&quot; target=&quot;_blank&quot;&gt;altoslabs.com.&lt;/a&gt;&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;Our Value&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Our Single Altos Value: &lt;strong&gt;Everyone Owns Achieving Our Inspiring Mission&lt;/strong&gt;.&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;Diversity at Altos&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Altos Labs has been named one of the Top 3 Biotech Companies and ranked for the second year on the Forbes 2026 Best Startups in America list. &amp;nbsp;At Altos, exceptional scientists and industry leaders from around the world work together to advance a shared mission. Our intentional focus is on Belonging, so that all employees know that they are valued for their unique perspectives. We are all accountable for sustaining a diverse and inclusive environment.&lt;/p&gt;&lt;/div&gt;&lt;h2&gt;What You Will Contribute To Altos&lt;/h2&gt;
&lt;p&gt;The contract IACUC Administrator will be responsible for the day‑to‑day administration and coordination of the Institutional Animal Care and Use Committee (IACUC) at Altos Labs™. This role supports a small, high‑standards animal research program with a limited number of protocols and no USDA‑covered species, potentially distributed across multiple Altos sites.&lt;/p&gt;
&lt;p&gt;You will help ensure that animal research at Altos is conducted ethically and in compliance with applicable standards (including PHS Policy and the Guide for the Care and Use of Laboratory Animals), with the goal of operating at AAALAC‑level quality even without formal accreditation. You will coordinate protocol review processes, committee activities, semiannual program reviews, facility inspections and training; ensure harmonized practices across sites; and serve as the functional lead for Altos’ electronic IACUC management system (e.g., @tune). You will collaborate closely with scientists, attending veterinarian, animal facility staff, and compliance colleagues to support a culture of integrity, animal welfare, and scientific excellence.&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;IACUC Program Administration &amp;amp; Compliance&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Coordinate receipt, pre‑review, and routing of animal use protocols, amendments, and continuing/annual reviews; track approval and expiration dates and follow up with research staff as needed.&lt;/li&gt;
&lt;li&gt;Organize IACUC meetings including agendas, materials, and minutes; maintain accurate, audit‑ready IACUC records.&lt;/li&gt;
&lt;li&gt;Support consistent IACUC processes across Altos sites to ensure standardized procedures and documentation.&lt;/li&gt;
&lt;li&gt;Help ensure that IACUC activities align with applicable regulations and guidance (e.g., PHS Policy, the Guide for the Care and Use of Laboratory Animals) and relevant Altos policies; flag key regulatory updates and suggest policy/procedure adjustments.&lt;/li&gt;
&lt;li&gt;Coordinate and support semiannual program reviews and facility inspections, prepare draft reports, track findings, and monitor completion of corrective actions to help ensure facilities meet high animal care and use standards.&lt;/li&gt;
&lt;li&gt;Collaborate with the IACUC Chair and attending veterinarian to respond to animal welfare concerns, support related investigations, and document follow‑up actions and resolutions.&lt;/li&gt;
&lt;li&gt;Support communication, documentation, and tracking of Post‑Approval Monitoring activities.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;strong&gt;Research Staff Support, Training &amp;amp; Quality Improvement&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Serve as a primary point of contact for research staff regarding IACUC policies, protocol preparation, and review processes.&lt;/li&gt;
&lt;li&gt;Develop and deliver concise orientation and refresher compliance/process training for research staff and IACUC members (e.g., how to submit protocols/amendments, what the IACUC looks for, and reporting expectations).&lt;/li&gt;
&lt;li&gt;Create and maintain clear written guidance (e.g., checklists, SOPs, FAQs, quick‑start guides) to support consistent, high‑quality submissions and reviews.&lt;/li&gt;
&lt;li&gt;Lead IACUC‑related communications, including coordinating content for a quarterly animal research/IACUC newsletter and other periodic updates to research staff and stakeholders.&lt;/li&gt;
&lt;li&gt;Partner with the IACUC and animal facility leadership to clearly communicate which hands‑on animal care, handling, and procedure training are required for protocol personnel.&lt;/li&gt;
&lt;li&gt;Coordinate basic post‑approval monitoring activities (e.g., brief site visits or protocol checks) and work with research and veterinarian to support ongoing adherence to IACUC‑approved practices and continuous improvement where needed.&lt;/li&gt;
&lt;li&gt;Maintain and update training modules in the electronic training system (Velocity AT&amp;amp;L) and ensure accurate tracking of training completion records.&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;strong&gt;Electronic IACUC System&amp;nbsp;&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the functional lead for implementation and ongoing use of Altos’ electronic IACUC/protocol management system (e.g., @tune).&lt;/li&gt;
&lt;li&gt;Work with the vendor, IT, IACUC, research staff, and other stakeholders to configure practical workflows, forms, roles, and review processes that reflect Altos policies and regulatory requirements.&lt;/li&gt;
&lt;li&gt;Oversee initial entry or migration of existing protocols and help ensure records remain accurate and current.&lt;/li&gt;
&lt;li&gt;Develop and maintain streamlined templates, reviewer checklists, and standard communications within the system to promote consistency and efficiency.&lt;/li&gt;
&lt;li&gt;Provide focused training and front‑line support to research staff, IACUC members, and other users on system use and compliance‑related processes, partnering with veterinary and facility staff for any animal‑procedure content.&lt;/li&gt;
&lt;li&gt;Monitor system queues and basic reports to support timely review, follow‑up, and required institutional reporting, and collaborate with leadership and the vendor on periodic updates and improvements&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;strong&gt;Other Duties As Assigned&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Support related research compliance or program improvement initiatives as needed.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Who You Are&lt;/h2&gt;
&lt;p&gt;&lt;strong&gt;Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in a scientific or related field (e.g., biology, animal science, biomedical science, or similar).&lt;/li&gt;
&lt;li&gt;Experience in animal research administration, research compliance, or laboratory animal science in an industry research environment (e.g., biotech, pharma, or related life sciences company)&lt;/li&gt;
&lt;li&gt;Familiarity with the Guide for the Care and Use of Laboratory Animals and PHS Policy; willingness to deepen expertise as needed.&lt;/li&gt;
&lt;li&gt;Strong organizational skills with attention to detail and the ability to manage multiple tasks within a part‑time schedule.&lt;/li&gt;
&lt;li&gt;Clear and professional written and verbal communication skills, including the ability to explain regulatory and process concepts to researchers and staff.&lt;/li&gt;
&lt;li&gt;Ability to work collaboratively with investigators, veterinary staff, IACUC members, and institutional leadership, and to maintain confidentiality and professionalism.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to work effectively across sites or functions and to support consistent practices in a multi‑site environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Prior direct experience supporting an IACUC or animal care and use program.&lt;/li&gt;
&lt;li&gt;Experience with an electronic protocol management system.&lt;/li&gt;
&lt;li&gt;CPIA certification (Certified Professional IACUC Administrator) a plus.&lt;/li&gt;
&lt;li&gt;Experience in a small research program or startup environment where one position covers multiple responsibilities.&lt;/li&gt;
&lt;li&gt;Experience in an AAALAC‑accredited or AAALAC‑aligned program.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The salary range for &lt;strong&gt;San Diego, CA&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;IACUC Coordinator&lt;/strong&gt;: $43 - $55 / hr.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Exact compensation may vary based on skills, experience, and location.&lt;/p&gt;
&lt;p&gt;#LI-NN1&lt;/p&gt;
&lt;p&gt;For UK applicants, before submitting your application:&lt;/p&gt;
&lt;p&gt;- Please click here to read the Altos Labs EU and UK Applicant Privacy Notice (&lt;a href=&quot;https://bit.ly/eu_uk_privacy_notice&quot; target=&quot;_blank&quot;&gt;bit.ly/eu_uk_privacy_notice&lt;/a&gt;)&lt;br&gt;- This Privacy Notice is not a contract, express or implied and it does not set terms or conditions of employment.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h2&gt;&lt;strong&gt;Equal Opportunity Employment&lt;/strong&gt;&lt;/h2&gt;
&lt;p class=&quot;s6&quot;&gt;&lt;span class=&quot;s5&quot;&gt;We value collaboration and scientific excellence.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;s6&quot;&gt;&lt;span class=&quot;s5&quot;&gt;We believe that a culture of belonging are foundational to scientific innovation and inquiry. At Altos Labs, exceptional scientists and industry leaders from around the world work together to advance a shared mission. Our intentional focus is on Belonging, so that all employees know that they are valued for their unique perspectives. We are all accountable for sustaining an inclusive environment.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;s6&quot;&gt;&lt;span class=&quot;s5&quot;&gt;Altos Labs provides equal employment opportunities to all employees and applicants for employment, without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Altos&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;prohibits&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;unlawful discrimination and harassment.&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Thank you for your interest in Altos Labs where we strive for a culture of scientific excellence, learning, and belonging.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Note: Altos Labs will not ask you to download a messaging app for an interview or outlay your own money to get started as an employee. If this sounds like your interaction with people claiming to be with Altos, it is not legitimate and has nothing to do with Altos. Learn more about a common job scam at &lt;a href=&quot;https://www.linkedin.com/pulse/how-spot-avoid-online-job-scams-biron-clark/&quot; target=&quot;_blank&quot;&gt;https://www.linkedin.com/pulse/how-spot-avoid-online-job-scams-biron-clark/&lt;/a&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/iacuc-coordinator-contract-alto-labs/6a07ebc82f1861929d2532c2</link><guid isPermaLink="true">http://biotechroles.com/iacuc-coordinator-contract-alto-labs/6a07ebc82f1861929d2532c2</guid><pubDate>Sat, 16 May 2026 04:00:08 GMT</pubDate><company>Alto Labs</company><location>San Diego, CA</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Clinical Veterinarian, Part-time Contract]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Our Mission&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Our mission is to restore cell health and resilience through cell rejuvenation to reverse disease, injury, and the disabilities that can occur throughout life.&lt;/p&gt;
&lt;p&gt;For more information, see our website at &lt;a href=&quot;https://altoslabs.com/&quot; target=&quot;_blank&quot;&gt;altoslabs.com.&lt;/a&gt;&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;Our Value&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Our Single Altos Value: &lt;strong&gt;Everyone Owns Achieving Our Inspiring Mission&lt;/strong&gt;.&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;Diversity at Altos&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Altos Labs has been named one of the Top 3 Biotech Companies and ranked for the second year on the Forbes 2026 Best Startups in America list. &amp;nbsp;At Altos, exceptional scientists and industry leaders from around the world work together to advance a shared mission. Our intentional focus is on Belonging, so that all employees know that they are valued for their unique perspectives. We are all accountable for sustaining a diverse and inclusive environment.&lt;/p&gt;&lt;/div&gt;&lt;h2&gt;What You Will Contribute To Altos&lt;/h2&gt;
&lt;p&gt;This part-time, contract Clinical Veterinarian will serve as a key veterinary and regulatory leader supporting in vivo research across multiple Altos sites. In this role, you will act as the Attending Veterinarian (AV) for Altos Labs and provide veterinary oversight, clinical care, and technical training.&lt;/p&gt;
&lt;p&gt;You will help ensure that animal research is conducted ethically, with scientific rigor and in full compliance with applicable standards, including Public Health Service (PHS) Policy and the Guide for the Care and Use of Laboratory Animals. You will play a central role in shaping a program that emphasizes animal welfare, regulatory excellence, and continuous refinement of in vivo models.&lt;/p&gt;
&lt;p&gt;You will also help establish core guidelines, best practices, and the Post-Approval Monitoring (PAM) program needed to support consistent execution, protocol adherence, animal welfare, and continuous improvement across sites.&lt;/p&gt;
&lt;p&gt;You will partner closely with scientists, operations, IACUC coordinator, and external collaborators to enable high-quality discovery and preclinical development programs. This includes providing expert veterinary input, strengthening biosecurity and clinical care programs, and driving a culture of care that integrates animal welfare, scientific excellence, and operational discipline&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;h4&gt;&lt;strong&gt;Regulatory Oversight &amp;amp; IACUC Leadership&lt;/strong&gt;&lt;/h4&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the Attending Veterinarian (AV) for the Altos Labs (Redwood City &amp;amp; San Diego). Some travel to Redwood City may be required.&lt;/li&gt;
&lt;li&gt;Ensure protocol quality, appropriate humane endpoints, and continuous improvement aligned with the 3Rs: Replacement, Reduction, and Refinement.&lt;/li&gt;
&lt;li&gt;Lead regulatory programs to ensure compliance with Animal Welfare Act, The Guide, and other applicable standards.&lt;/li&gt;
&lt;li&gt;Establish and maintain veterinary and IACUC-related guidelines, best practices, and program standards to ensure consistent, humane, and scientifically rigorous animal use across sites.&lt;/li&gt;
&lt;li&gt;Develop and support the Post-Approval Monitoring (PAM) program, including protocol adherence checks, procedure observations, documentation review, and feedback loops for training, refinement, and continuous improvement.&lt;/li&gt;
&lt;li&gt;Maintain inspection readiness; lead site inspections, and applicable audits.&lt;/li&gt;
&lt;/ul&gt;
&lt;h4&gt;&lt;strong&gt;Veterinary Care &amp;amp; Program Oversight&lt;/strong&gt;&lt;/h4&gt;
&lt;ul&gt;
&lt;li&gt;Provide direct clinical veterinary care for rodent species.&lt;/li&gt;
&lt;li&gt;Lead and enhance biosecurity, disease prevention, and health surveillance programs.&lt;/li&gt;
&lt;li&gt;Drive continuous improvement in enrichment and behavioral management programs.&lt;/li&gt;
&lt;li&gt;Support and participate in the veterinary on-call program.&lt;/li&gt;
&lt;/ul&gt;
&lt;h4&gt;&lt;strong&gt;Training, Technical Excellence &amp;amp; Model Refinement&lt;/strong&gt;&lt;/h4&gt;
&lt;ul&gt;
&lt;li&gt;Lead technical training and development programs for in vivo research teams.&lt;/li&gt;
&lt;li&gt;Mentor scientists and staff in technical excellence and best practices, fostering a strong culture of care.&lt;/li&gt;
&lt;li&gt;Guide refinement of animal models, ensuring scientific rigor and humane practices.&lt;/li&gt;
&lt;li&gt;Proactively prepare the organization for novel models and emerging technologies, ensuring technical and operational readiness.&lt;/li&gt;
&lt;/ul&gt;
&lt;h4&gt;&lt;strong&gt;Leadership &amp;amp; Cross-Functional Partnership&lt;/strong&gt;&lt;/h4&gt;
&lt;ul&gt;
&lt;li&gt;Foster cross-functional partnerships to drive continuous improvements in animal welfare, compliance, and execution excellence.&lt;/li&gt;
&lt;li&gt;Deliver program performance through both direct leadership and indirect influence across teams.&lt;/li&gt;
&lt;li&gt;Support development of team members in technical capability, continuous improvement, and career growth.&lt;/li&gt;
&lt;li&gt;Help shape a scalable, standardized veterinary and animal care model across sites.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;&lt;strong&gt;Who You Are&lt;/strong&gt;&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;DVM or equivalent veterinary degree; licensed or eligible for licensure in California.&lt;/li&gt;
&lt;li&gt;Board certification, such as ACLAM, strongly preferred.&lt;/li&gt;
&lt;li&gt;Significant experience in laboratory animal medicine, including rodent and non-rodent species.&lt;/li&gt;
&lt;li&gt;Deep understanding of regulatory frameworks, including USDA/Animal Welfare Act, AAALAC, and IACUC processes.&lt;/li&gt;
&lt;li&gt;Demonstrated experience with inspections, audits, accreditation activities, and animal welfare investigations&lt;/li&gt;
&lt;li&gt;Experience developing guidelines, best practices, training programs, or PAM activities preferred.&lt;/li&gt;
&lt;li&gt;Strong leadership, communication, and cross-functional collaboration skills.&lt;/li&gt;
&lt;li&gt;Experience supporting discovery and preclinical development programs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The salary range for &lt;strong&gt;San Diego, CA&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Clinical Veterinarian: $92 - $117 / hr.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Exact compensation may vary based on skills, experience, and location.&lt;/p&gt;
&lt;p&gt;#LI-NN1&lt;/p&gt;
&lt;p&gt;For UK applicants, before submitting your application:&lt;/p&gt;
&lt;p&gt;- Please click here to read the Altos Labs EU and UK Applicant Privacy Notice (&lt;a href=&quot;https://bit.ly/eu_uk_privacy_notice&quot; target=&quot;_blank&quot;&gt;bit.ly/eu_uk_privacy_notice&lt;/a&gt;)&lt;br&gt;- This Privacy Notice is not a contract, express or implied and it does not set terms or conditions of employment.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h2&gt;&lt;strong&gt;Equal Opportunity Employment&lt;/strong&gt;&lt;/h2&gt;
&lt;p class=&quot;s6&quot;&gt;&lt;span class=&quot;s5&quot;&gt;We value collaboration and scientific excellence.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;s6&quot;&gt;&lt;span class=&quot;s5&quot;&gt;We believe that a culture of belonging are foundational to scientific innovation and inquiry. At Altos Labs, exceptional scientists and industry leaders from around the world work together to advance a shared mission. Our intentional focus is on Belonging, so that all employees know that they are valued for their unique perspectives. We are all accountable for sustaining an inclusive environment.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;s6&quot;&gt;&lt;span class=&quot;s5&quot;&gt;Altos Labs provides equal employment opportunities to all employees and applicants for employment, without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Altos&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;prohibits&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;unlawful discrimination and harassment.&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;s5&quot;&gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Thank you for your interest in Altos Labs where we strive for a culture of scientific excellence, learning, and belonging.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Note: Altos Labs will not ask you to download a messaging app for an interview or outlay your own money to get started as an employee. If this sounds like your interaction with people claiming to be with Altos, it is not legitimate and has nothing to do with Altos. Learn more about a common job scam at &lt;a href=&quot;https://www.linkedin.com/pulse/how-spot-avoid-online-job-scams-biron-clark/&quot; target=&quot;_blank&quot;&gt;https://www.linkedin.com/pulse/how-spot-avoid-online-job-scams-biron-clark/&lt;/a&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/clinical-veterinarian-part-time-contract-alto-labs/6a07ebc62f1861929d2532c1</link><guid isPermaLink="true">http://biotechroles.com/clinical-veterinarian-part-time-contract-alto-labs/6a07ebc62f1861929d2532c1</guid><pubDate>Sat, 16 May 2026 04:00:06 GMT</pubDate><company>Alto Labs</company><location>San Diego, CA</location><salary>$120000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Facilities Technician II]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><p style="text-align:inherit"></p><h3></h3><p></p><h3>The Position</h3><p><b>The Opportunity</b></p><p></p><p><u>Work shift: M-F 2:00pm - 10:30pm</u></p><h3></h3><p>The Facilities Technician II at GenMark Diagnostics, A Member of the Roche Group, is responsible for the overall maintenance, upkeep, and cleanliness of the designated facility, preventative or otherwise. In this position, you are</p><ul><li><p><b>Preventative Maintenance &amp; Operations</b> – Perform routine maintenance on HVAC and central plant equipment, conduct daily facility tours, monitor all rooftop and building systems, and make necessary operational adjustments</p><p>• <b>Work Request Management &amp; Response</b> – Handle internal customer facility work requests, respond to alarm system alerts 24/7, investigate and document process alarms, and provide on-call coverage</p><p>• <b>Equipment &amp; Inventory Support</b> – Maintain spare parts inventory, manage repair parts for work requests, conduct maintenance on specialized systems (water purification, heating/cooling, humidity control, building controls), and support validation protocols</p><p>• <b>Quality &amp; Compliance</b> – Ensure all duties comply with ISO, FDA, and regulatory requirements; demonstrate awareness of quality consequences and potential device defects; support Quality Management System implementation</p><p>•<b> Coordination &amp; Professional Development</b> – Coordinate contractor/vendor site escorts and training, support cross-functional staff training, collaborate with technicians on daily tasks, and maintain professionalism with internal and external stakeholders</p></li></ul><p></p><p><b>Who you are</b></p><ul><li><p>You possess a High School Diploma, or Technical Education with 2 to 4 years of maintenance experience preferably in Biotech, cGMP, medical or health related environment or equivalent.</p></li><li><p>You must be available to work any shift and be “on call” via pager and/or cell phone.</p></li><li><p>You possess a clean &amp; valid CA driver’s license</p></li></ul><p></p><p><b>Behaviors, Competencies, and Qualities of the ideal applicant.</b></p><ul><li><p>Proficiency with power tools and machine shop equipment, knowledge of HVAC systems, refrigeration systems, and plumbing; ability to read schematics and drawings.</p></li><li><p>Experience in high-paced manufacturing environments, routine building and grounds maintenance, and familiarity with welding and precision tools (drill press, hand tools).</p></li><li><p>Excellent understanding and application of safety procedures; knowledge of federal regulations including QSR, ISO, and ISO 13485 standards; CMDR familiarity preferred.</p></li><li><p>Ability to prioritize multiple tasks and work independently; basic computer skills (MS Word, Excel, Access, Google); excellent documentation and record-keeping abilities.</p></li><li><p>Strong interpersonal, communication, and cooperation skills; ability to work effectively with diverse teams in regulated environments.</p></li></ul><p></p><p><b>Work Environment </b></p><p>The essential functions of the job are usually performed in an environmentally controlled facility where the noise level in the work environment is usually moderate.  This position may involve a combination of office and biotechnology laboratory environments. You <i>may</i> be exposed to hazardous chemicals, blood-borne, pathogens and automated equipment.</p><p></p><p>While performing the job duties, you are regularly required to sit; reach with hands and arms and talk or hear. You are frequently required to stand and walk.  You may sometimes be required to lift and/or move up to 35 pounds.  Specific vision abilities required by this job include close vision, distance vision, color vision, and ability to adjust focus.</p><p></p><p>Relocation benefits are not offered for this job posting</p><p></p><p> The expected salary range for this position based on California is 53,800.00 - 99,800 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><b><u>Benefits</u></b></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left"><span>GenMark is now a proud member of the Roche Group, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare.  As a global leader in healthcare, Roche Diagnostics offers a broad portfolio of products, tools and services that help in the prevention, diagnosis and management of diseases like HPV, HIV, hepatitis and diabetes as well as other medical conditions, such as fertility and blood coagulation. With the addition of GenMark to the Roche Group, syndromic infectious disease diagnostics is now added to the long list of disease states and conditions that the Roche Group addresses.  GenMark’s ePlex true sample-to-answer system offers unique solutions to address the most significant challenges facing clinical laboratories, while supporting hospital systems to deliver patient-centered, value-based care. ePlex streamlines the diagnostic workflow from physician order entry to the final test report and is the true sample-to-answer solution designed to improve patient care, reduce costs, and increase lab efficiency. GenMark is headquartered in Carlsbad, California.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>GenMark is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a target="_blank" href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/facilities-technician-ii-roche/6a0746492f1861929d2532c0</link><guid isPermaLink="true">http://biotechroles.com/facilities-technician-ii-roche/6a0746492f1861929d2532c0</guid><pubDate>Fri, 15 May 2026 16:14:01 GMT</pubDate><company>Roche</company><location>Carlsbad</location><salary>$65000-85000</salary><type>Full time</type></item><item><title><![CDATA[Record to Report Period End Close Senior Analyst]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><b>The Opportunity:</b></p><p></p><h2>As a <b>R2R Period-End Close Senior Analyst</b> based in San José, Costa Rica, you will be an integral part of our Global Shared Services organization. This role serves as a subject matter expert, delivering advanced accounting support and complex financial analysis while driving process improvements and automation initiatives. You will act as a key point of contact for accounting and reporting matters, serving as a trusted advisor for our supported affiliates.</h2><p></p><p><b>Your key responsibilities will include:</b></p><ul><li><p><b>Accounting Expertise &amp; Audit Leadership:</b> Lead complex accounting analyses and audit activities for assigned areas. You will serve as a subject matter expert for affiliates and internal stakeholders, ensuring technical accounting excellence.</p></li><li><p><b>Financial Reporting &amp; Close Activities:</b> Prepare and review complex financial statements and reports. You will manage month-end close activities, including journal entries, cost allocations, and reconciliations, while maintaining a proper audit trail and compliance with standards.</p></li><li><p><b>Analysis, Commentary &amp; Advisory:</b> Analyze financial results to investigate variances and provide clear, actionable insights to management. You will interpret and communicate financial data effectively to both internal and external stakeholders.</p></li><li><p><b>Compliance &amp; Governance:</b> Ensure strict compliance with company policies, accounting standards, and regulatory requirements.</p></li><li><p><b>Team Development:</b> Support the growth of the team through coaching, reviewing work, and contributing to cross-functional initiatives and global projects.</p></li><li><p><b>Continuous Improvement:</b> Drive process improvements and support automation initiatives to increase the efficiency of the Record-to-Report flow.</p></li></ul><p></p><p><b>Who you are:</b></p><p></p><p>You are a highly analytical finance professional with a strong attention to detail, capable of working independently in a fast-paced environment to meet tight deadlines.</p><p><b>Requirements and Qualifications:</b></p><ul><li><p><b>Education:</b> Bachelor’s degree in <b>Accounting, Finance</b>, or a related field. A professional certification (<b>CPA, ACCA</b>, or equivalent) is preferred.</p></li><li><p><b>Experience:</b> Minimum of <b>4&#43; years</b> of experience in accounting or finance. Prior experience in a Finance Shared Services environment is preferred. Experience in the pharmaceutical or healthcare industry is a plus.</p></li><li><p><b>Technical Skills:</b> * Strong knowledge of <b>US GAAP and/or IFRS</b>.</p><ul><li><p>Experience with ERP systems, specifically <b>SAP</b> (FI, CO/PA, MM, FA, FCC) and <b>BlackLine</b> is highly desirable.</p></li><li><p>Advanced proficiency in Microsoft Excel and Google Workspace.</p></li></ul></li><li><p><b>Languages:</b> Excellent written and verbal communication skills; fluent in <b>English and Spanish</b>. Portuguese and or French is preferred.</p></li><li><p><b>Core Competencies:</b> * Strong stakeholder management and collaboration abilities.</p></li><li><p>Problem-solving mindset with a focus on process automation and continuous improvement.</p></li><li><p>Ability to manage multiple priorities with minimal supervision.</p></li></ul><p></p><p><i><b>Relocation benefits are not available for this posting.</b></i></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/record-to-report-period-end-close-senior-analyst-roche/6a0746492f1861929d2532bf</link><guid isPermaLink="true">http://biotechroles.com/record-to-report-period-end-close-senior-analyst-roche/6a0746492f1861929d2532bf</guid><pubDate>Fri, 15 May 2026 16:14:01 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Controls Engineer]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p>At <b>Roche Near Patient Care</b>, we create the tools that help people with diabetes think less about their daily routine and more about their lives. Our Indianapolis site is a global hub for blood glucose strip manufacturing and the future home of our next-generation continuous glucose monitoring (CGM) sensors.</p><p></p><p><b>The Opportunity</b></p><p>As a <b>Controls Engineer</b>, you are the technical backbone of our automated production lines. You won’t just be sitting at a desk; you’ll be hands-on with high-speed equipment, ensuring our manufacturing processes are stable, validated, and constantly improving.</p><p></p><p><b><b>What You’ll Do</b></b></p><ul><li><p><b><b>Optimize &amp; Innovate:</b></b><span> Lead the evolution of our automation and electromechanical processes. You’ll use data and operator feedback to make our lines faster, smarter, and more reliable.</span></p></li><li><p><b><b>Launch New Tech:</b></b><span> Partner with R&amp;D and Process Development to bridge the gap between design and high-volume manufacturing for new product launches.</span></p></li><li><p><b><b>Own the Controls:</b><span> </span></b><span>Program, modify, and troubleshoot the &#34;brains&#34; of our machines, ensuring every sensor, motor, and PLC is performing at peak efficiency.</span></p></li><li><p><b><b>Manage Quality &amp; Validation:</b><span> </span></b><span>Lead equipment qualifications (IQ/OQ/PQ) and ensure all process changes meet strict regulatory standards without sacrificing production speed.</span></p></li><li><p><b><b>Strategic Leadership:</b><span> </span></b><span>Manage multiple project lifecycles, mentor junior staff, and provide expert on-call support to keep our 24/7 operations running smoothly.</span></p></li><li><p><b><b>On-Site: </b><span> </span></b><span>Engineers are dedicated to the Indianapolis site. Travel typically &lt; 10%.</span></p></li></ul><p></p><p><b><b>What You’ll Bring</b></b></p><ul><li><p><b><b>PLC &amp; HMI Proficiency:</b><span> </span></b><span>Deep experience with Allen Bradley (RSLogix/Studio 5000) and FactoryTalk View. You are comfortable modifying code to drive continuous improvement.</span></p></li><li><p><b><b>The &#34;Troubleshooter&#34; Mindset:</b><span> </span></b><span>Strong knowledge of electromechanical systems, motion controls (Servos/VFDs), Distributed I/O, sensors, and Cognex/Keyence Vision Systems.</span></p></li><li><p><b><b>Validation Expertise:</b><span> </span></b><span>Proven ability to develop and execute equipment qualification protocols and write clear, technical documentation.</span></p></li><li><p><b><b>Vendor Management:</b><span> </span></b><span>Experience collaborating with external partners to source specialized solutions or navigate component obsolescence.</span></p></li><li><p><b><b>Analytical Drive:</b><span> </span></b><span>A highly logical approach to problem-solving, with the ability to run simulations and use test data to make informed decisions.</span></p></li></ul><p></p><p><b><b>Who You Are</b></b></p><ul><li><p><span>Bachelor’s degree in Engineering or closely related discipline with a minimum of 2 years of related experience; advanced degree may substitute for previous experience or equivalent experience</span></p></li><li><p><span>Related experience must include troubleshooting, modifying, and/or developing industrial equipment controls systems (PLCs, HMIs, Motion Control, etc.)</span></p></li></ul><p></p><p><b><b>Preferred:</b></b></p><ul><li><p><span>Familiar with GMP in a regulated environment (Medical Device or Pharmaceutical).</span></p></li><li><p><span>Strong electro-mechanical skills that can look at the machine from all engineering aspects: mechanical, electrical, and controls.</span></p></li><li><p><span>Previous experience troubleshooting controls systems of high volume/speed manufacturing equipment.</span></p></li><li><p><span>Previous training or experience in Process Improvement Methodologies (e.g. LSS, PDCA, etc.).</span></p></li><li><p><span>Demonstrates excellent interpersonal, communication, and teamwork skills.</span></p></li><li><p><span>Strong ability to teach and educate key stakeholders and other colleagues.</span></p></li><li><p><span>Deep commitment to cross-functional collaboration and breaking down silos to achieve the best results for the organization.</span></p></li></ul><p></p><p><b><b>This is an onsite role in Indianapolis. Relocation benefits are not available.</b></b></p><p></p><p><span>The expected salary range for the Manufacturing Engineer position based on the primary location of Indiana is $68,800 - $127,800 Annual.  Actual pay will be determined based on experience, qualifications and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance, as well as participation in a long-term incentive program.  This position also qualifies for the benefits detailed at the link provided below.</span> <a href="http://hrportal.ehr.com/roche" target="_blank">Benefits</a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/controls-engineer-roche/6a0746482f1861929d2532be</link><guid isPermaLink="true">http://biotechroles.com/controls-engineer-roche/6a0746482f1861929d2532be</guid><pubDate>Fri, 15 May 2026 16:14:00 GMT</pubDate><company>Roche</company><location>Indianapolis</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Principal Software Development Engineer]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><span>At Roche, we are working to make next-generation sequencing simple and accessible enough for routine use. By accelerating clinical research, streamlining workflows, and expanding assay menus, we are broadening access to genomic data and lowering barriers to adoption. From robust sample isolation and preparation tools to novel sequencing technology and advanced bioinformatics, we are developing differentiated, highly integrated end-to-end solutions for next-generation sequencing, resulting in a sample in, result out workflow.</span></p><p><br /><span>Our Verification and Validation team, a part of Roche Sequencing Solutions, is responsible for ensuring a software product meets its specified requirements and performs as intended by rigorously testing and analyzing the software throughout its development lifecycle. </span></p><p></p><p><span>As a Principal Software Developer in Test, you will be responsible for test design, development, automation, deployment, execution, and reporting. Specifically, you will develop an integrated hardware-software framework for end-to-end test automation that leverages a third-party Hardware-in-the-Loop solution. In this role, you will represent quality engineering and verification on behalf of your team in all events and activities related to this effort, working closely with software and hardware engineers across multiple global locations.</span></p><p></p><p><b><b>The Opportunity</b></b></p><ul><li><p><span>You develop solutions for Hardware-in-the-Loop testing for end-to-end testing of embedded instrument software</span></p></li><li><p><span>You author and confirm correctness of requirements-driven tests, covering aspects including:</span></p><ul><li><p><span>Testing approaches (exploratory, white box, black box, etc.)</span></p></li><li><p><span>Testing level (end-to-end, system, integration, unit, etc.)</span></p></li><li><p><span>Testing types (functional, performance, scalability, etc.)</span></p></li></ul></li><li><p><span>You automate and execute front-end and back-end tests, covering for:</span></p><ul><li><p><span>Instrument software</span></p></li><li><p><span>Web applications</span></p></li></ul></li><li><p><span>You automate deployment and testing pipelines across branches and stages</span></p></li><li><p><span>You report quality metrics and enhancing quality dashboards</span></p></li><li><p><span>You perform root cause analysis of defects and discoveries</span></p></li><li><p><span>You develop automation frameworks and validate automation toolchains</span></p></li><li><p><span>You ensure regulatory compliance of quality engineering deliverables</span></p></li><li><p><span>You partner with Test Architects, Test Leads, and Verification &amp; Validation Leads on practices</span></p></li><li><p><span>You collaborate with designers, architects, developers, system engineers and testers on product development</span></p></li><li><p><span>You participate in all development events, and activities and guide junior testing team members as needed</span></p></li><li><p><span>Technologies which may be utilized</span>: <span>C&#43;&#43;, Java, Cucumber (Behavior-Driven Development), Gherkin, Playwright, Windows, Cypress/JDI/Selenium/WebDriver/TestNG, Typescript/Javascript, Angular, Docker, Jenkins, Groovy, Bash, Jira, Github, Confluence, Google Suite, macOS/Linux, MS SQL, Vector HIL Solutions</span></p></li></ul><p></p><p></p><p><b><b>Who You Are</b></b></p><ul><li><p><span>You have a Bachelors Degree in Computer Science, Mathematics, Physics, Electrical Engineering, or related. Advanced degree preferred. An equivalent combination of education and experience may be considered, with three years of experience for each year of missing education</span></p></li><li><p><span>You have 10&#43; years related experience or equivalent combination of education and experience with Java, Javascript, C&#43;&#43;/Object-oriented programming, software architecture, networking, and distributed systems, and/or UNIX/NT development</span></p></li><li><p><span>You have a minimum of 5 years of software development experience with exposure to instrument control programming</span></p></li><li><p><span>You have 4&#43; years of experience in quality engineering or similar field</span></p></li><li><p><span>You have excellent analytical and problem-solving skills, with a proven ability to debug complex issues at the software/hardware interface</span></p></li><li><p><span>You have expert knowledge of core software engineering concepts, object-oriented programming, and the software development life cycle</span></p></li><li><p><span>You have experience in regulated industries, specifically Medical Devices/Digital Health/Lifesciences (preferred)</span></p></li><li><p><span>You have strong experience or exposure to technical capabilities such as: </span></p><ul><li><p><span>Programming proficiency in C&#43;&#43;, Java, and Python</span></p></li><li><p><span>Multi-threaded programming, real-time control algorithms, and concurrent systems</span></p></li><li><p><span>Message passing design patterns</span></p></li><li><p><span>Automating front-end and back-end applications, automation frameworks and corresponding languages</span></p></li><li><p><span>Development and deployment on Unix derivatives</span></p></li><li><p><span>Behavior-Driven Development and Gherkin specifications</span></p></li><li><p><span>Agile methodologies including Scrum and Scaled Agile Framework</span></p></li><li><p><span>Experience with databases including writing queries</span></p></li></ul></li><li><p><span>You have excellent communication skills, both written and oral</span></p></li></ul><p></p><p><i>Work Environment and Role Expectations</i><br /><span>This role combines software testing responsibilities with hands-on interaction in a lab environment where our medical device systems are built, integrated, and verified. While many tasks—such as test planning, automation development, and documentation—are completed in an office setting, a significant portion of the work involves executing and troubleshooting software tests directly on physical hardware in a lab.</span></p><p></p><p><span>Candidates should be comfortable working around electromechanical systems, automated instruments. Lab work may include initiating test runs, collecting data from real devices, analyzing system behavior, and collaborating closely with software, hardware, systems, and manufacturing teams.</span></p><p></p><p><b><b>Locations</b></b></p><p><span>This position is based in Santa Clara, CA.</span></p><p></p><p><span>Relocation benefits are not available.</span></p><p></p><p><span>The expected salary range for this position based on the primary location of Santa Clara is $165,800 to $307,900.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</span></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/principal-software-development-engineer-roche/6a0746482f1861929d2532bd</link><guid isPermaLink="true">http://biotechroles.com/principal-software-development-engineer-roche/6a0746482f1861929d2532bd</guid><pubDate>Fri, 15 May 2026 16:14:00 GMT</pubDate><company>Roche</company><location>Santa Clara</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Enterprise Identity Management Engineer]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>We are seeking a <b>Enterprise Identity Management Engineer</b> to serve as a senior primary architect of our Enterprise Identity Management (IGA) future. This is a high-impact, hands-on role where you will design, build, and deliver next-generation identity solutions operating at global scale. Positioned at the intersection of security engineering and business enablement, you&#39;ll create resilient frameworks that protect critical systems while enabling seamless, automated access. As a technical visionary, you&#39;ll tackle the most complex identity challenges within our large-scale enterprise ecosystem.</p><p></p><p><b><span>The </span><span>Opportunity </span></b></p><p></p><p><span>In </span><span>this </span><span>pivotal </span><span>role, </span><span>you </span><span>will </span><span>act </span><span>as </span><span>a </span><span>primary </span><span>architect </span><span>driving </span><span>the </span><span>evolution </span><span>of </span><span>our </span><span>Enterprise </span><span>Identity </span><span>Management </span><span>strategy. </span><span>You&#39;ll </span><span>own </span><span>the </span><span>complete </span><span>technical </span><span>lifecycle, from </span><span>designing </span><span>scalable </span><span>solutions </span><span>to </span><span>delivering </span><span>resilient </span><span>implementations </span><span>across </span><span>our </span><span>global </span><span>infrastructure.</span></p><p></p><p><b><span>Main Responsibilities</span></b></p><ul><li><p><span>Lead end-to-end technical design of EIM solutions aligned with enterprise standards and security policies</span></p></li><li><p><span>Define and standardize architecture patterns, best practices, and reusable frameworks</span></p></li><li><p><span>Conduct design reviews and provide technical governance for scalable, high-quality implementations</span></p></li><li><p><span>Translate security and business requirements into actionable technical solutions</span></p></li><li><p><span>Architect, build, test, and deploy SailPoint-based IAM solutions from the ground up</span></p></li><li><p><span>Deliver resilient identity solutions across complex, distributed environments</span></p></li><li><p><span>Collaborate with cross-functional teams to ensure smooth implementation and production rollout</span></p></li><li><p><span>Own delivery lifecycle end-to-end, including planning, estimation, timelines, and risk management</span></p></li><li><p><span>Act as Tier 3 escalation point, leading root cause analysis and long-term fixes</span></p></li><li><p><span>Drive innovation through PoCs and adoption of modern EIM Integrations (APIs, cloud integrations)</span></p></li></ul><p></p><p></p><p><b>Who You Are</b></p><p><b>Core Expertise &amp; Experience</b></p><p></p><ul><li><p><span>Minimum of 8 years of hands-on experience in Identity Management within large-scale, global environments.</span></p></li><li><p><span>3&#43; years experience working in a multinational work environment (Healthcare Industry experience a plus) as an Engineer/Technical team member</span></p></li><li><p><span>Strong customer engagement and presentation skills with the ability to communicate across all levels (senior and/or small audiences)</span></p></li><li><p><span>Deep technical expertise in SailPoint, specifically in design, custom development, troubleshooting, and architecture.</span></p></li><li><p><span>Ability to work effectively with team members and virtual teams from different locations and different cultural background </span></p></li><li><p><span>Ability to function independently with little supervision</span></p></li><li><p><span>Advanced programming proficiency in Java for developing custom connectors, rules, and complex workflows.</span></p></li><li><p><span>Proven experience implementing Integration solutions with Active Directory and  cloud environments such as AWS, Azure, or GCP.</span></p></li><li><p><span>Familiarity with CI/CD, DevOps, and modern architecture (APIs, microservices, cloud)</span></p></li><li><p><span>Strong understanding of RBAC, Segregation of Duties (SoD), and access governance frameworks.</span></p></li></ul><p></p><p><b>Education</b></p><ul><li><p><span>Bachelor’s or Advanced degree in Computer Science, Cyber Security, Information Technology, or a related Engineering field.</span></p></li><li><p><span>Professional Information Security certifications (e.g., CISSP) is a plus.</span></p></li></ul><p></p><p>If you&#39;re an experienced identity architect with deep SailPoint expertise, a passion for solving complex security challenges, and the drive to own end-to-end technical delivery in a multinational environment, we want to hear from you.</p><p></p><p>Relocation benefits are not available for this job posting.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/enterprise-identity-management-engineer-roche/6a0746472f1861929d2532bc</link><guid isPermaLink="true">http://biotechroles.com/enterprise-identity-management-engineer-roche/6a0746472f1861929d2532bc</guid><pubDate>Fri, 15 May 2026 16:13:59 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$55000-85000</salary><type>Full time</type></item><item><title><![CDATA[Identity & Access Management Engineer]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>We are seeking a skilled <b>Identity &amp; Access Management Engineer</b> to join our growing IAM team. This role offers a unique opportunity for a Java Developer to expand their expertise into the Identity and Access Management space, with a focus on SailPoint technologies and application integration. You will work on solving complex business problems through practical application of your development skills, contributing to the design, implementation, and evolution of enterprise-scale identity solutions. In this position, you will take on meaningful responsibility for technical design decisions, build resilient IAM infrastructure, and play an active role in shaping how our organization manages identity and access across the enterprise.</p><p></p><div></div><p><b>The Opportunity</b></p><p>This role positions you at the intersection of software development and information security, where you&#39;ll apply your Java expertise to solve complex identity and access management challenges within a large global enterprise.</p><p></p><div></div><p><b>Your Responsibilities</b></p><ul><li>Contribute to the end-to-end design of IAM infrastructure solutions and create and maintain related component standards</li><li>Produce and maintain comprehensive documentation for designs, design patterns, and component standards</li><li>Interact with senior internal and external partners on significant technical matters related to organizational priorities</li><li>Strengthen the Information Security community by building bridges and collaborating with peers and stakeholders</li><li>Contribute to determining success criteria and evaluating promising solutions and technologies via Proofs of Concept (PoCs) and feasibility studies</li><li>Design, build, test, and implement integrated, resilient, and reliable IAM solutions</li><li>Advise, influence, and collaborate with various IT partners and line-of-business stakeholders, integrating their feedback</li><li>Ensure designs and solutions align with organizational policies, standards, and strategic directions</li><li>Contribute to estimating engineering resources and timelines for successful project delivery</li><li>Write and contribute to position papers, white papers, technical recommendations, and best practices documentation for the IAM solution space</li><li>Remain proactive in identifying operational challenges and opportunities, working with support teams to ensure solutions meet quality and regulatory standards</li><li>Collaborate closely with Identity Management Support and Operations teams on incident management, problem management, and continuous service improvement</li><li>Embrace our Infrastructure as Code tool chain and adhere to coding best practices</li></ul><p></p><div></div><p><b>Who You Are</b></p><p></p><p><b>Technology Skills &amp; Experience</b></p><ul><li>Deep expertise in Java development with proven ability to apply it within enterprise security contexts</li><li>Hands-on experience with Identity Management technologies; SailPoint experience is highly desired</li><li>Demonstrated experience following CI/CD and DevOps practices</li><li>Knowledge of microservices architectures, API design, and REST APIs</li><li>Understanding of distributed architectures and the challenges they present</li><li>Experience working in an Agile environment</li><li>Proficiency in Python and scripting languages (Perl, JavaScript, PowerShell, etc.) is desired</li><li>Background in Identity and Access Management, Directory Services, or Cyber Security is a plus</li></ul><p></p><div></div><p><b>Core Competencies &amp; Qualifications</b></p><ul><li>Bachelor&#39;s degree or equivalent professional experience</li><li>5&#43; years of overall experience in relevant technology areas</li><li>2&#43; years working in a multinational environment as an Engineer or Technical team member (Healthcare Industry experience a plus)</li><li>Effective interpersonal and communication skills with the ability to engage across all organizational levels</li><li>Demonstrated delivery focus and strong problem-solving capabilities</li><li>Ability to work effectively with team members and virtual teams across different locations and cultural backgrounds</li><li>Ability to function independently with minimal supervision</li><li>Fluent oral and written communication skills in English</li><li>Proven project and time management skills is a plus</li><li>Industry certifications are valuable</li><li>Willingness to travel moderately and work across multiple time zones</li></ul><p></p><div></div><h2></h2><p>We&#39;re looking for a talented Java Developer ready to grow into the Identity and Access Management space. If you&#39;re passionate about solving complex security challenges, have a strong foundation in Java development, and are eager to deepen your expertise in SailPoint and IAM technologies, we&#39;d like to speak with you.</p><p></p><div></div><p>This is an excellent opportunity to advance your career within a global enterprise while making a meaningful impact on how we secure and manage identity and access across our organization.</p><p></p><div></div><p>Relocation benefits are not available for this job posting.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/identity-and-access-management-engineer-roche/6a0746472f1861929d2532bb</link><guid isPermaLink="true">http://biotechroles.com/identity-and-access-management-engineer-roche/6a0746472f1861929d2532bb</guid><pubDate>Fri, 15 May 2026 16:13:59 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Statistician]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>This role is within Biostatistics,  a core function within Product Development Data Science and Analytics (PDD) that provides strategic leadership and scientific rigor across Development at Roche. Biostatistics identifies opportunities to apply the full breadth of data, digital, and design capabilities to deploy innovative methods across PDD, PD and the broader Roche Pharma  organization.</p><p></p><p>As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to drive scientifically rigorous programmatic decisions across Roche’s Development portfolio; Biostatistics designs robust trials and analysis plans that increase the probability of technical success, accelerating timelines to advance Roche’s clinical pipeline and promote regulatory success — ultimately bringing medicines to our patients faster.</p><p></p><p><b><u>The Opportunity: </u></b><br />The Statistician is a key member of the cross-functional study or molecule team, responsible for applying statistical expertise to the design, conduct, analysis, and interpretation of individual clinical trials. This role ensures the scientific rigor and regulatory compliance of the study by contributing to protocol development, authoring statistical analysis plans, performing or overseeing data analyses, and supporting the interpretation and communication of results. The Statistician plays a critical role in ensuring that each study generates robust, meaningful data to support decision-making and regulatory submissions.</p><p></p><ul><li><p>You contribute to trial design under guidance, applying standard statistical methods</p></li><li><p>You draft and review protocols, statistical analysis plans (SAPs), and case report forms (CRFs) using templates and precedents</p></li><li><p>You perform or support statistical analyses as per statistical analysis plans, escalating issues when needed</p></li><li><p>You represent Biostatistics and PDD at the Study Team level, ensuring statistical and scientific rigor of study deliverables under guidance</p></li><li><p>You collaborate with study team members to meet deliverables, following existing processes</p></li><li><p>You summarize findings clearly with support from senior colleagues</p></li><li><p>You contribute to CSR development and regulatory responses using established templates</p></li><li><p>You apply judgment to address moderately complex statistical or data issues, balancing scientific rigor with appropriate flexibility, and seek guidance when facing novel or ambiguous situations</p></li><li><p>You adhere to functional standards by participating in peer review and mentoring relationships to uphold quality and build methodological and regulatory expertise</p></li></ul><p></p><p><b><u>Who You Are:</u></b></p><ul><li><p>You hold an MSc or PhD in Statistics, Biostatistics, or a closely related quantitative field</p></li><li><p>You have 1-3 years of relevant experience in clinical trial statistics within a pharmaceutical, biotech, or CRO setting</p></li><li><p>You are familiar with ICH guidelines, GCP, and regulatory requirements (e.g., FDA, EMA)</p></li><li><p>You have a strong understanding of statistical principles and methodology relevant to clinical trial design and analysis</p></li><li><p>You are proficient in SAS and/or R and familiar with CDISC standards</p></li><li><p>You demonstrate capacity for independent thinking and ability to make decisions based upon sound principles</p></li><li><p>You bring excellent strategic agility including problem-solving and critical thinking skills, and agility that extends beyond the technical domain</p></li><li><p>You demonstrate respect for cultural differences when interacting with colleagues in the global workplace</p></li><li><p>You have excellent verbal and written communication skills, specifically in the areas of presentation and writing, with the ability to explain complex technical concepts in clear language</p></li></ul><p></p><p><b><u>Preferred:</u></b></p><ul><li><p>Experience working in cross-functional teams</p></li><li><p>Effective communication skills with the ability to translate complex statistical concepts for non-statistical audiences</p></li><li><p>Experience with multiple phases of drug development (early and/or late stage)</p></li><li><p>Excellent communication skills, including the ability to influence and translate complex data for non-technical stakeholders</p></li><li><p>Strategic mindset with the ability to contribute to portfolio-level decisions</p></li></ul><p></p><p>Relocation benefits are not available for this posting  </p><p></p><p>#PPDT</p><p>#PDDMiss</p><p><span><span>.</span></span></p>The expected salary range for this position based on the primary location of Mississauga is 89,256.00 and 117,148.50 of hiring range.  Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.<p></p><p>We use artificial intelligence to screen, assess or select applicants for this role.</p><p></p><p>This posting is for an existing vacancy at Hoffmann-La Roche Ltd.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/statistician-roche/6a0746462f1861929d2532ba</link><guid isPermaLink="true">http://biotechroles.com/statistician-roche/6a0746462f1861929d2532ba</guid><pubDate>Fri, 15 May 2026 16:13:58 GMT</pubDate><company>Roche</company><location>Mississauga</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[Project Manager (contract)]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><b>1 year contract</b></p><p><b>Mississsauga, ON</b></p><p></p><p><span>The Project Manager is accountable for the end-to-end strategy, planning, execution, monitoring, and change management of Patient Support Programs (PSPs) between our partners, ensuring business continuity and an uninterrupted, high-quality patient experience.</span></p><p></p><p><span>In this role, the Project Manager will be a key partner to cross-functional teams, responsible for translating Therapeutic Area/Brand strategies into a comprehensive change management strategy that prioritizes patient continuity and operational excellence. This accountability spans the full transition lifecycle, from transition design and vendor onboarding to execution, stabilization, and optimization. The Program Manager will proactively manage risks, timelines, and dependencies while ensuring seamless coordination between outgoing and incoming vendors.</span></p><p></p><p></p><p><b><u>The Opportunity:</u></b></p><p></p><p></p><p><span>Program &amp; Transition Management</span></p><ul><li><p><span>Lead end-to-end planning and execution of the Patient Support Program transition between vendor</span></p></li><li><p><span>Develop and manage detailed transition roadmaps, timelines, milestones, and deliverables</span></p></li><li><p><span>Identify risks, dependencies, and mitigation strategies to ensure uninterrupted patient services</span></p></li><li><p><span>Coordinate with internal teams (commercial, medical, compliance, finance, legal) and external vendors</span></p></li><li><p><span>Monitor program performance, track KPIs, and ensure adherence to scope, budget, and timelines</span></p></li></ul><p></p><p></p><p><span>Change Management &amp; Stakeholder Engagement</span>:</p><p></p><ul><li><p><span>Design and implement a structured change management approach to support the transition</span></p></li><li><p><span>Engage and align key stakeholders, including leadership, vendors, and cross-functional teams</span></p></li><li><p><span>Develop communication strategies to ensure transparency and clarity throughout the transition</span></p></li></ul><p></p><p></p><p><span>Patient Centric Design &amp; Continuous Improvement:</span></p><ul><li><p><span>Apply design thinking principles to optimize patient experience during and after the transition</span></p></li><li><p><span>Ensure continuity of care by minimizing disruption to patient services and support programs</span></p></li></ul><p></p><p></p><p><b>Who you are:</b></p><p></p><ul><li><p>Bachelor’s degree in Business Administration, Healthcare, Life Sciences, or related field; Master’s degree is an asset</p></li><li><p>You possess 5&#43; years of relevant program management, large-scale transition, or related experience and you have 7&#43; years of experience in Healthcare, Pharmaceutical, or Patient Services environments</p></li><li><p>Strong program management and change management capabilities, with experience leading complex transitions</p></li><li><p>Experience managing vendor transitions, outsourcing, or operational transformations preferred</p></li><li><p>PSP or patient services is an asset</p></li><li><p>Strong stakeholder management skills, including influencing, negotiation, and navigating complex environments</p></li><li><p>Ability to translate strategy into execution with strong business and operational acumen</p></li><li><p>Ability to work cross-functionally and align internal teams and external partners (including vendors)</p></li><li><p>Experience with digital tools, automation, or AI-enabled solutions is an asset</p></li><li><p>Bilingual (English/French) is an asset</p></li></ul><p></p><p></p><p>Relocation assistance is not available for this job posting.</p>The expected salary range for this position based on the primary location of Mississauga is 136,936.00 and 179,728.50 of hiring range.  Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.<p></p><p>We use artificial intelligence to screen, assess or select applicants for this role.</p><p></p><p>This posting is for an existing vacancy at Hoffmann-La Roche Ltd.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/project-manager-contract-roche/6a0746462f1861929d2532b9</link><guid isPermaLink="true">http://biotechroles.com/project-manager-contract-roche/6a0746462f1861929d2532b9</guid><pubDate>Fri, 15 May 2026 16:13:58 GMT</pubDate><company>Roche</company><location>Mississauga</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[Internship - Automation Developer]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>As an Automation Intern, you will be part of our Data Science &amp; Automation (D&amp;A) team within the Business Analytics function. This internship is designed as a hands-on learning experience, where you will explore automation technologies, support ongoing initiatives, and contribute fresh ideas to improve how we work.</p><p></p><p>You will gain exposure to real-world business challenges, automation tools, and emerging AI capabilities, while working alongside experienced Business Analysts, Automation Developers, and Business Partners.</p><p>This role is ideal for someone who is curious about technology, enjoys simplifying complex ideas, and is eager to learn how automation and data-driven solutions can create business impact.</p><p></p><p>You will be part of RSS Business Analytics - a global team with regional presence in Switzerland, India, Costa Rica, Hungary, Latvia and Malaysia. We operate in an agile organizational set-up without extensive hierarchical structure, where all our employees lead from every seat. Inspirational leadership, service oriented behavior and entrepreneurial customer centric mindset are our core values.</p><p></p><p><span>As part of your 6-month journey, you will have the chance to dive into one or more of these core areas:</span></p><ul><li><p><span>Hands-on Development: Work on internal automation projects using UiPath, Python, or scripting to streamline our own team&#39;s workflows.</span></p></li><li><p><span>MS migration analysis: Research our upcoming move to Microsoft 365, evaluating the effects on existing automations and proposing best practices for a smooth bot migration.</span></p></li><li><p><span>Solution Strategy &amp; Showcase: Develop an &#34;Automation Toolkit&#34; (decision trees and tool matrices) to match business problems with the right tech (AI vs. RPA). You’ll then bring this to life by curating a digital &#34;Solution Catalogue&#34; to showcase our team’s capabilities and toolkit.</span></p></li><li><p>Ad-hoc Exploration: Stay agile! You’ll support various team initiatives as they arise, giving you a 360-degree view of Business Analytics.</p></li></ul><p></p><p>Require:</p><ul><li><p>Basic understanding of programming or scripting concepts</p></li><li><p>Familiarity with any language such as Python, JavaScript, or similar (academic or personal projects is sufficient)</p></li><li><p>Strong curiosity and willingness to learn new technologies</p></li><li><p>Ability to break down complex ideas into simple, structured formats</p></li><li><p>Good communication and presentation skills (written and verbal in English)</p></li></ul><p></p><p>Nice to have (not mandatory)</p><ul><li><p>Exposure to automation tools (e.g. UiPath, Power Automate, Google Apps Script)</p></li><li><p>Experience creating presentations, documentation, or visual content</p></li></ul><p></p><p>What we offer:</p><ul><li><p>Mentorship: Regular 1:1s with experienced Data Scientists and Automation Developers.</p></li><li><p>Real Impact: Your projects (like the Tool Matrix or Solution Catalogue) will be used by the team long after your internship ends.</p></li><li><p>Global Exposure: Experience how a leading healthcare company uses technology to impact patients&#39; lives.</p></li><li><p>Flexible Environment: A culture that values &#34;leading from every seat&#34; and prioritizes your development over a rigid job title.</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/internship-automation-developer-roche/6a0746452f1861929d2532b8</link><guid isPermaLink="true">http://biotechroles.com/internship-automation-developer-roche/6a0746452f1861929d2532b8</guid><pubDate>Fri, 15 May 2026 16:13:57 GMT</pubDate><company>Roche</company><location>Petaling Jaya</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Global Product Planner - Molecular]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><span>Are you ready to take your career to the next level with a dynamic and global role? As a Global Product Planner, you will be at the forefront of supply chain management, driving operational excellence and ensuring product availability across our hubs and nodes.. You will develop and manage supply plans utilizing both affiliate and statistical forecasts to create accurate and efficient supply chains. By proactively addressing supply and demand planning issues, you will maintain seamless operations and ensure the accuracy and continuous optimization of MRP master data. Leading bottleneck management, allocation, reserve management, and scrap mitigation across the network will be vital components of your role.</span></p><p></p><p><span>In this position, you will be the primary point of contact for product supply-related communications with suppliers, regions, business areas, and affiliates. You will guarantee the timely supply of finished goods to regional and local warehouses, aligning with service level agreements (SLAs), and strive to meet customer service objectives at the lowest possible total costs, including distribution, inventory, and write-offs.</span></p><p></p><p><span>We are looking for someone with specialized and comprehensive knowledge in supply chain management or a related business area. Your analytical and problem-solving skills will be engaged in varied and complex duties involving research, analysis, and solution development. You will provide expert guidance to department leadership in setting strategic direction and utilize originality and ingenuity in your daily responsibilities and decision-making processes. Applying a wide range of principles, practices, and procedures to navigate more complex and challenging assignments will be crucial. Additionally, your commitment to maintaining and continuously improving the planning objectives and goals through daily actions will be key.</span></p><p></p><p><span>This is your opportunity to make a significant impact in a highly professional and strategic role. Join us and contribute to our mission of delivering exceptional service and operational efficiency. Apply now to be part of a global team committed to excellence!</span></p><p></p><p><b>The Opportunity</b></p><ul><li><p><b>End-to-End Inventory Management:</b><span> Accountable to ensure global product availability across all regional and central warehouse locations for a defined portfolio, including the strategic setting and continuous monitoring of global safety levels.</span></p></li><li><p><b>Supply Planning &amp; Optimization:</b><span> Responsible for the creation and accuracy of global supply plans by aligning demand inputs with manufacturing and supplier capabilities; provides robust recommendations regarding Master Production Schedules (MPS) and Rough Cut Capacity Planning (RCCP).</span></p></li><li><p><b>Lifecycle &amp; Launch Coordination:</b><span> Accountable to liaise with functional leads and lifecycle teams to manage complex product transitions, ensuring seamless availability during critical launch and phase-out periods.</span></p></li><li><p><b>Operational Execution &amp; Data Integrity:</b><span> Responsible for the ongoing optimization and accuracy of MRP master data and executes logistics interventions, including batch reservations, to guarantee uninterrupted product flow during emergencies.</span></p></li><li><p><b>Crisis Management &amp; S&amp;OP Leadership</b><span><b>:</b> Serves as the primary lead for initiating escalation processes regarding global availability and orchestrates S&amp;OP meetings to resolve critical supply-demand imbalances across the network.</span></p></li><li><p><b>Global Allocation &amp; Process Excellence</b><span><b>:</b> Manages global product allocations in collaboration with cross-functional partners and assumes the subject matter expert role to ensure supply chain processes reflect real-life business scenarios.</span></p></li></ul><p></p><p><b><b>Who you are</b></b></p><ul><li><p><span>Bachelor’s Degree in Business or related field</span></p></li><li><p><span>5 years of experience in logistics, marketing, production, inventory control or purchasing functions with an international focus</span></p></li><li><p><span>Highly proficient in materials management and supply chain data analysis.  Supporting tools include SAP &amp; OMP</span></p></li><li><p><span>Excellent problem solving &amp; negotiation skills to impact the status quo and influence decisions to achieve business decisions</span></p></li><li><p><span>Strong expertise in stakeholder management and excellent communication skills</span></p></li><li><p><span>Project Management skills</span></p></li></ul><p></p><p></p><p><i>Relocation benefits are not available for this posting</i></p><p>The expected salary range for this position based on the primary location of Indianapolis, IN is $78,600 - $146,000.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below. <a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/global-product-planner-molecular-roche/6a0746432f1861929d2532b7</link><guid isPermaLink="true">http://biotechroles.com/global-product-planner-molecular-roche/6a0746432f1861929d2532b7</guid><pubDate>Fri, 15 May 2026 16:13:55 GMT</pubDate><company>Roche</company><location>Indianapolis</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Head of Service & Support]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p>A healthier future. It is what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That is what makes us Roche.</p><p></p><p><span>The Head of Service and Support manages the day-to-day operations of the service team to effectively execute after-sales support strategies and objectives to deliver customer experience beyond expectations. </span></p><p></p><p><span><b><u>Key Responsibilities</u></b><u><b> include</b></u></span></p><p></p><p><span>a) Leads and manages the service team’s overall activities by implementing effective strategies and detailed plans aligned with company objectives. </span></p><p><span>b) Ensures all initiatives are properly executed in accordance with the strategies set by the GCS. </span></p><p><span>c) Align the strategy to operational process, and people resulting in a great customer experience </span></p><p><span>d) Provides technical information to Sales and Marketing for Roche projects across all stages of the buying cycle. </span></p><p><span>e) Implement Regional and Global initiatives as relevant</span></p><p><span>f) Serves as a core member of the DLT in an advisor capacity to the team and helps to set the direction of the Customer Services team with a special emphasis on how and what to implement to achieve current and future direction. </span></p><p><span>g) Responsible for planning the budget of the service team. </span></p><p><span>h) Oversees management and maintains inventory of relevant spare parts at an acceptable level </span></p><p><span>i) Ensure all service activities of the service team are promptly encoded into customer relationship management (CRM) </span></p><p></p><p><span><b>Organizational Relationship </b></span></p><p><span>a) Liaises with other affiliates in APAC/Global for technical initiatives and support requirements of the team. </span></p><p><span>b) Drive the culture of collaboration across the stakeholders </span></p><p><span>c) Maintain key partners, companies, distribution partners, etc. </span></p><p><span>d) Develop and implement strategies to build a customer-centric culture in the team. </span></p><p></p><p><span><b>Team Management </b></span></p><p><span>a) Coaches and motivates the team to perform all duties and responsibilities to resolve key internal and external challenges. </span></p><p><span>b) Ensure skills enhancement of the service team (direct and distributor teams) regarding required technical capabilities. </span></p><p><span>c) Long-term strategic planning of excellent customer experience, cost reduction, and team efficiency. </span></p><p></p><p><span><b>SHE Responsibilities: </b></span></p><p><span>● Promote awareness and participation to Security, Safety, Health and Environmental Protection policies and programs at site to create a safe work environment to all employees. </span></p><p></p><p><span><b>Quality / Regulatory Responsibilities: </b></span></p><p><span>● Ensure full compliance with applicable regulatory requirements and perform activities following global Roche quality standards and local SOPs. </span></p><p></p><p><span><b><u>Liaises with</u> </b></span></p><p><span>● External customer, distributors, and suppliers </span></p><p><span>● Relevant internal team members, including Sales, Marketing, Finance, Supply Chain, and other Departments /areas as required </span></p><p><span>● External Relevant Company, Distribution Partner, etc. </span></p><p><span>● APAC and Global team for service support, updates, and inquiries relevant to the team </span></p><p></p><p><b><u>Who you are</u></b></p><p></p><p><span>● Bachelor&#39;s Degree in Science or Engineering with substantial multinational companies&#39; experience in Diagnostics industry preferred</span></p><p><span>● A manager&#39;s manager with minimum 5 years of experience in leading and managing a large service team in a similar industry </span></p><p><span>● Computer Skills (Microsoft Office Application and or Google Productivity Tools) </span></p><p><span>● Excellent interpersonal and communication skills in English (spoken and written)</span></p><p><span>● Strong leadership skills and a team player </span></p><p><span>● Analytical, precise, pragmatic, enthusiastic, result-oriented, and strong commercial awareness </span></p><p><span>● Selling and negotiation skills </span></p><p><span>● Creative problem-solving and issue-resolution skills </span></p><p><span>● Customer handling skill </span></p><p><span>● Planning, organization and time management skill </span></p><p><span>● Self-Initiative and Proactive </span></p><p></p><p>Ability to travel interstate and internationally as required by the position</p><p></p><p>We do not accept any unsolicited resumes or enquiries from recruitment agencies- Roche has a dedicated in-house Talent Acquisition team.</p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/head-of-service-and-support-roche/6a0746422f1861929d2532b6</link><guid isPermaLink="true">http://biotechroles.com/head-of-service-and-support-roche/6a0746422f1861929d2532b6</guid><pubDate>Fri, 15 May 2026 16:13:54 GMT</pubDate><company>Roche</company><location>Taguig City</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Praktikum bei MSAT Analytics (m/w/d)]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><h2><b>Deine Abteilung</b></h2><div><div><div><div><div><div><div><div><div><p></p><p>Unser 18-köpfiges Team, bestehend aus Analytikern, Projektleitern und Gruppenleiter im Bereich der chemischen und biochemischen Analytik, freut sich auf tatkräftige Unterstützung von einem hilfsbereiten und flexiblen neuen Teammitglied. Du solltest Spaß an neuen Herausforderungen haben und Dich in unsere positive Arbeitsatmosphäre einfügen.</p><p></p><p>Wir möchten Dir als Praktikant (m/w/d) einen Einblick in das „<i>daily business</i>“  in der Abteilung Manufacturing Science &amp; Technology (MSAT) geben. Dabei wirst Du auch die Möglichkeit haben, Dich selbstständig mit Projektarbeiten zu befassen, um bestehende Prozesse zu optimieren.</p><p></p><p><b>Deine Aufgaben</b></p><p></p><ul><li><p>Unterstützung unserer Projektarbeiten im Bereich <i>Design Transfer &amp; Product Care</i></p></li><li><p>Analytik von chemischen, biochemischen und biologischen Einsatzstoffen im diagnostischen Umfeld</p></li></ul><p></p><p><b>Dein Profil</b></p><p></p><ul><li><p>Du bist aktuell in einem naturwissenschaftlichen Studium (Bachelor oder Master in Chemie / Biochemie / Molekularbiologie / Lebensmittelchemie / Life Science oder vergleichbar) immatrikuliert oder Du befindest Dich in Deinem Gap-Year</p></li><li><p>Du bringst Kenntnisse in der chemischen und/oder biochemischen Analytik mit</p></li><li><p>Du bist motiviert, neugierig und möchtest Deine Ideen einbringen</p></li><li><p>solide Deutschkenntnisse sind erforderlich</p></li></ul><p></p><p><b>Deine Vorteile</b></p><p></p><ul><li><p>Flexible Zeiteinteilung</p></li><li><p>2268 € Vergütung im Monat für ein Vollzeitpraktikum &gt; 3 Monate</p></li><li><p>Vernetzung mit anderen Studierenden (online/offline)</p></li><li><p>Ermäßigte Preise (-50 %) in unserer Kantine</p></li><li><p>Fitnessstudio auf dem Roche Campus</p></li><li><p>Weiterbildungsmöglichkeiten und spannende Gastvorträge</p></li><li><p>Möglichkeit der Unterbringung im Roche Boardinghaus</p></li><li><p>Gut organisierte Verkehrsanbindung nach München mit unserem Roche-Shuttle</p></li></ul><p></p><p></p><p><b>Deine Bewerbung</b></p><p></p><p>Denke daran, daß sich dieses Praktikum an Studierende (m/w/d) bei laufender Immatrikulation während des gesamten Zeitraums des Praktikums richtet oder alternativ an Personen in einem maximal einjährigen Gap-Year (zwischen Bachelor und Master Studium), wo es schriftlich nachgewiesen werden kann, auf welcher Universität/Hochschule und genau wann (Monat/Jahr) innerhalb eines Jahres die Studien fortgesetzt werden.</p><p></p><p>Beachte bitte, dass Empfehlungen für alle studentischen Tätigkeiten (z.B. Praktika, Abschlussarbeiten, etc.) ausgeschlossen sind.</p><p></p><p><b>Zeitraum</b>:  ab sofort oder nach Vereinbarung für die Dauer von 6 Monaten</p><p></p><p><b>Wir freuen uns auf Deine Bewerbung!</b></p></div></div></div></div></div></div></div></div></div><p><b> </b></p><p><b> </b></p><h3></h3><h1>Your contact to us! With people. For people.</h1><p style="text-align:left">Do you need further support?</p><p style="text-align:left">Please have a look at our FAQs, you will find them via <a href="https://careers.roche.com/global/en/faq" target="_blank"><span><span><span><span class="WCO0">https://careers.roche.com/global/en/faq</span></span></span></span></a>.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b><span>Roche is an Equal Opportunity Employer.</span></b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/praktikum-bei-msat-analytics-mwd-roche/6a0746422f1861929d2532b5</link><guid isPermaLink="true">http://biotechroles.com/praktikum-bei-msat-analytics-mwd-roche/6a0746422f1861929d2532b5</guid><pubDate>Fri, 15 May 2026 16:13:54 GMT</pubDate><company>Roche</company><location>Penzberg</location><salary>$2000-3000</salary><type>Full time</type></item><item><title><![CDATA[Digital & Innovation Hub Intern]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span style="color:#000000"><b>Job Description:</b> </span></p><p><span style="color:#000000">Join our <b>Innovation Hub</b> to pioneer the next generation of AI-driven pharmaceutical solutions. Unlike a traditional data role, this internship focuses on bridging the gap between cutting-edge LLM (Large Language Model) research and practical healthcare applications.</span></p><p></p><p><span style="color:#000000"><b>Key Responsibilities:</b></span></p><ul><li style="color:#000000 !important"><p><span style="color:#000000"><b>Full-Stack AI Development:</b> Architect and build AI-driven applications from the ground up.</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Cloud Architecture &amp; Publishing:</b> Take ownership of the deployment process. You will containerize applications and <b>publish them to Cloud environments (AWS, Azure, or GCP)</b>, ensuring they are accessible and scalable.</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Database Management:</b> Design and implement basic data storage architectures to handle application state, session memory, and knowledge retrieval.</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>End-to-End Ownership:</b> Monitor the live application, troubleshoot cloud environment issues, and iterate on model performance independently.</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Technical Translation:</b> Work with stakeholders to refine project requirements and ensure the final product meets pharmaceutical industry standards.</span></p></li></ul><p></p><p><span style="color:#000000"><b>Required Skills and Qualifications:</b></span></p><ul><li style="color:#000000 !important"><p><span style="color:#000000">You are a self-starter, independent &amp; highly motivated. </span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Internship Duration: </b>Capability to commit to a 6-month full-time internship (highly preferred).</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>AI Solution Engineering: </b>Proven ability to build an AI application from scratch (Portfolio/GitHub evidence of independent projects is highly preferred).</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Technical Proficiencies:</b> Strong hands-on experience with <b>Python</b></span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Database Basics:</b> Understanding of how to store and retrieve data from a database (e.g., NoSQL, Vector DBs, or simple Cloud Storage)</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>AI Fundamentals:</b> Familiarity with LLM architectures, API integrations, and the basics of Natural Language Processing (NLP).</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Software Engineering Basics:</b> Familiarity with Git for version control and the SDLC.</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Education:</b> Currently pursuing a Bachelor’s or Master’s degree in Computer Science, AI, Data Science, or Software Engineering, or a related field. </span></p></li></ul><p></p><p><span style="color:#000000"><b>What We Offer:</b></span></p><ul><li style="color:#000000 !important"><p><span style="color:#000000"><b>End-to-End Project Ownership:</b>  You won’t just be assisting; you will be the lead developer of your assigned project, responsible for its architecture and success.</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Production Experience:</b> A rare opportunity to see your &#34;from-scratch&#34; builds published and running in an enterprise-grade cloud environment.</span></p></li><li style="color:#000000 !important"><p><span style="color:#000000"><b>Corporate Working Environment &#64; a leading MNC</b>: You will be part of a qualified and engaged professional team and organization where you will experience corporate culture at the intersection of healthcare industry and digital innovation in a globally leading pharma company</span></p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/digital-and-innovation-hub-intern-roche/6a07463a2f1861929d2532b4</link><guid isPermaLink="true">http://biotechroles.com/digital-and-innovation-hub-intern-roche/6a07463a2f1861929d2532b4</guid><pubDate>Fri, 15 May 2026 16:13:46 GMT</pubDate><company>Roche</company><location>Subang Jaya</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Team Lead Engineering Commercial Data]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h2></h2><p style="text-align:inherit"></p><h3>The Position</h3><p></p><p><b>Team Lead Engineering Commercial Data</b></p><p></p><p><span>At Roche, we believe every individual can make a difference. We are looking for a <b>Team Lead Engineering Commercial Data</b> to join our team in a role that sits at the intersection of engineering excellence and business impact. </span><span><span>In this position, you will lead and grow high-performing data and analytics engineering teams to deliver scalable, reliable, and business-critical solutions that support commercial decision-making across sales, marketing, pricing, and customer engagement</span></span><span>.</span></p><p></p><p>The Commercial Data, Analytics and AI area supports Service, Marketing, Sales, and Commercial Operations across Roche Diagnostics’ global organization, enabling data-driven decision-making and operational excellence at scale. The area spans global, regional, and country-level teams and covers a wide range of commercial activities, including customer engagement, sales effectiveness, service performance, pricing, installed base management, and operational optimization.</p><p></p><p>Operating in a highly regulated, global environment, the Commercial Data &amp; Analytics function partners closely with business, IT, Digital, and central Data &amp; AI platform teams to deliver trusted data foundations, analytics, and AI-enabled insights. Solutions are designed to be scalable, compliant, and reusable across markets, while remaining flexible enough to address local needs.</p><p></p><p>By providing reliable data products, analytics capabilities, and advanced insights, the area plays a critical role in improving commercial effectiveness, service quality, and customer experience, ultimately supporting Roche Diagnostics’ mission to deliver innovative diagnostics solutions to patients worldwide.</p><p></p><p><b>The Opportunity:</b></p><ul><li><p><span><span>Lead and develop high-performing data and analytics engineering teams, fostering a culture of technical excellence, accountability, and continuous professional growth</span></span><span>.</span></p></li><li><p><span><span>Scale engineering capabilities to support diverse Commercial use cases across Service, Marketing, Sales, and Operations through modern data modeling and transformation</span></span><span>.</span></p></li><li><p><span><span>Drive technical standards by establishing and enforcing best practices for dbt-based development, CI/CD, automated testing, and comprehensive documentation</span></span><span>.</span></p></li><li><p><span><span>Evolve data onboarding as a service to enable efficient, standardized, and scalable ingestion of new data sources while maintaining strict security and governance</span></span><span>.</span></p></li><li><p><span><span>Design robust pipelines that power advanced analytics and AI/ML solutions, ensuring all datasets are production-grade and &#34;AI-ready&#34; for downstream science teams</span></span><span>.</span></p></li><li><p><span><span>Collaborate with platform teams to align commercial data solutions with enterprise architecture, ensuring the reuse of platform capabilities and avoiding tool duplication</span></span><span>.</span></p></li><li><p><span><span>Manage team delivery on a day-to-day basis, translating complex commercial requirements into reliable analytics layers and high-impact insight products</span></span><span>.</span></p></li><li><p><span><span>Champion engineering craftsmanship by reviewing technical designs and guiding your team toward maintainable, cost-efficient, and scalable architectural decisions</span></span><span>.</span></p><p></p></li></ul><p><b>Who you are:</b></p><ul><li><p><span><span>Experienced Leader: You possess 5&#43; years of experience in data engineering leadership or architecture, with a proven track record of building high-performing teams</span>.</span></p></li><li><p><span><span>Industry Expert: You bring 2&#43; years of experience within the pharmaceutical, biotechnology, or regulated healthcare technology industry to navigate complex compliance needs</span>.</span></p></li><li><p><span><span>Formally Educated: You hold a Bachelor’s or advanced degree in Computer Science or a similar field, with a strong foundation in Business or IT specifications</span>.</span></p></li><li><p><span><span>Technical Specialist: You have hands-on expertise with Snowflake, including data modeling, performance optimization, and secure access patterns in a cloud environment</span>.</span></p></li><li><p><span><span>Modern Stack Proficient: You are highly skilled in analytics engineering using dbt, orchestration tools like Airflow, and modern CI/CD integration practices</span>.</span></p></li><li><p><span><span>Visionary Architect: You understand data quality and observability practices, including automated testing and lineage, to ensure reliability in an enterprise setting</span>.</span></p></li><li><p><span><span>Collaborative Leader: You exhibit &#34;VACC&#34; (servant and creative) leadership behaviors, with the ability to navigate ambiguity and empower teams to act autonomously</span></span><span>.</span></p><p></p></li></ul><p><b>What you get*:</b></p><ul><li><p><span>Monthly salary range: 19,075 - 35,425 PLN gross<i><span> </span></i>based on the employment contract.</span></p></li><li><p><span>Annual bonus payment based on your performance (target 20%).</span></p></li><li><p><span>Company car or car allowance.</span></p></li><li><p><span>Dedicated training budget (training, certifications, conferences, diversified career paths etc.).</span></p></li><li><p><span>Recharge Fridays (2 Fridays off per quarter available).</span></p></li><li><p><span>Hybrid work model (min. 2 days in the office weekly)</span></p></li><li><p><span>Take time Program (up to 3 months of leave to use for any purpose).</span></p></li><li><p><span>Vacation subsidy available.</span></p></li><li><p><span>Flex Location (possibility to perform our work from different places in the world for a certain period of time).</span></p></li><li><p><span>Take Time for Charity (additional paid leave of maximum 2 weeks to engage in the charity action of your choice).</span></p></li><li><p><span>Private healthcare (LuxMed packages), group life insurance (UNUM) and Multisport.</span></p></li><li><p><span>Stock share purchase additions.</span></p></li><li><p><span>Yearly sales of company laptops and cars and many more!</span></p></li></ul><p></p><p><i><span>*Please note that the compensation details provided pertain specifically to our offices in Poland (Warsaw &amp; Poznan). For other locations, compensation packages will be discussed with the local Talent Acquisition Partner during the interview process.</span></i></p><p></p><p>Ready to bring your unique qualities to Roche and make an impact? Apply now and join us in our mission to shape the future of healthcare.</p><p></p><p><b>#RDT2026</b></p><p></p><h3><b>Compensation &amp; Benefits</b></h3>The expected salary range for this position, based on the primary location of Warsaw Grafit is 228’900.00 PLN-425’100.00 PLN. Final compensation will be determined by a number of factors, including your skills, experience, qualifications, and location. In addition to base pay, this role may be eligible for a discretionary annual bonus with a target of 20% subject to both individual and company performance.<p></p><p>This position also offers an attractive <a target="_blank" href="https://cdn.phenompeople.com/CareerConnectResources/prod/ROCHGLOBAL/documents/PolandBenefitsBrochureMyrewards-1763649233034.pdf"><span style="color:#0000ff"><u>benefits package</u></span></a>.</p><p></p><p><a target="_blank" href="https://roche.phenompro.com/global/en/compensation-philosophy"><span style="color:#0000ff"><u>Learn more</u></span></a> about how we reward our employees at Roche.</p>This job is posted in multiple locations. If you're applying for the role in an alternative location where pay transparency regulations apply, the Talent Acquisition Partner will share the local pay information with you ahead of any business interview.<p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/team-lead-engineering-commercial-data-roche/6a0746392f1861929d2532b3</link><guid isPermaLink="true">http://biotechroles.com/team-lead-engineering-commercial-data-roche/6a0746392f1861929d2532b3</guid><pubDate>Fri, 15 May 2026 16:13:45 GMT</pubDate><company>Roche</company><location>Warsaw</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[(Sr) Automation Engineer]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><u>Engineering Project Support and Operation Readiness:</u></p><ul><li>Act as the Automation representative on the project team, contributing to design, construction, and qualification activities. This includes reviewing URS (User Requirement Specification) and executing FAT and SAT to contribute to project delivery.</li><li>Lead or act as the automation maintenance team coordinate with Engineering department, production department, quality department, vendors, etc. for cooperation to achieve the positive goal.</li><li>Establish and develop the automation system in alignment with the Roche standards including maintenance management system, people training and qualification, CCS strategy and implementation to support robust operation readiness.</li><li>Support manager to develop a competent team through coaching, mentoring and training by having in place a skill competencies development and appraisal program to strengthen the technical expertise and capabilities.</li><li>Participate in tech transfer, collaboration with other functions to ensure the success of new product manufacturing.</li><li>Represents the automation during regulatory inspections and audits and participates in the response of regulator audit and global quality audit.</li></ul><p><u>Routine Operation &amp; Maintenance:</u></p><ul><li>Implementations Support</li></ul><ul><li>Improve management of, and access to, business-critical scientific data for all scientific disciplines across Roche.</li><li>Provide consultation with regards to automation systems, computerized systems and software, implementation and validation.</li></ul><ul><li>Business Partnering and Solution Provision</li></ul><ul><li>Strive to provide the best workable solution using the software/systems and systems available in alignment with the sites digital strategy.</li><li>Develop an in-depth understanding of Automation/IT and business initiatives, strategies and needs for the future and ensure alignment of Automation/OT strategy.</li><li>Be aware of current and emerging technologies which could benefit/add value to the site and promote these opportunities internally.</li><li>Provide strategic directions to the automation group specifically around the areas of software and hardware. Responsible for implementing site digital roadmap according to Roche global strategy.</li></ul><ul><li>Automation Operations</li></ul><ul><li>Provide SME support to manufacturing and other departments for the design and operation of process automation equipment.</li><li>Conduct troubleshooting and technical analyses on manufacturing equipment and process automation system including PI data analyses, code review/troubleshooting, etc.</li><li>Act as controls engineer for tech transfer or new process into the facilities.</li><li>Support production and project teams in all questions of Automation and controls</li><li>Develop technical knowledge on manufacturing equipment and process automation system.</li><li>Secures professional and economic execution of all activities and high availability of manufacturing unit and equipment.</li><li>Also provide training to site users to ensure the operational use, and shop floor service during production.</li><li>Create/Revise/Review Automation and manufacturing related SOP&#39;s Functional Specs, work instructions, equipment and process changes.</li><li>Perform high level system administration of Automation systems: managing the user roles, including their configurations, security rights and access rights.</li><li>On call for system emergent complex trouble shooting escalated from technicians.</li><li>Ensure that all relevant information relating to activities within your scope are tracked, captured and forwarded in due time to your manager or the head of department</li><li>Compliance:</li><li>Ensure audit readiness by adhering to GMP, regulatory, and statutory requirements to protect product quality and prevent compliance observations.</li><li>Troubleshooting &amp; Improvement:</li></ul><ul><li>Respond to critical alarms and provide timely technical support for complex issues.</li><li>Drive continuous improvement initiatives to enhance sustainability, safety, and asset reliability.</li><li>Ensure in time response to critical alarms in compliance with the SOP and related procedures.</li><li>Evaluate the alarm trends and establish corrective actions to avoid repeat events.</li></ul><ul><li>Assets Lifecycle Management &amp; Reliability</li></ul><ul><li>Evaluate the system capacity and provide related Operational &amp; Maintenance data for project initiation.</li><li>As the automation system owner and SME, actively participate in the design, review, comment, commissioning and handover of site new projects according to Site CAPEX process.</li><li>Responsible for the implementation of the site Reliability Engineering process within owned areas.</li><li>Establish and maintain a strategic and technical roadmap for the responsible area to support the site&#39;s strategic development and product lifecycle.</li></ul><p></p><p><span style="font-size:14px">Qualification and Experience </span></p><div><p>Education/Qualifications </p><ul><li><p><span>Bachelor’s degree or above in Automation or a related field.</span></p></li></ul> <p>Job Required Competencies</p><ul><li><p>Experience: <span>Minimum of 8 years of electrical management or engineering experience in injection pharmaceutical industry, MNC Bio-pharma preferred.</span></p></li><li><p>Expertise:</p></li></ul><ul><li><p><span>Experience with MES/PI/LIMS/EMS/BAS/SCADA/PLC and related software.</span></p></li><li><p><span>Familiar with Visualization Platform.</span></p></li><li><p><span>Expertise on data integrity.</span></p></li><li><p><span>General knowledge of network, cyber security, firewalls, operation system, </span></p></li></ul><ul><li><p>Startup Experience:<span> Experienced in new facility startup readiness and operation ramp-up.</span></p></li><li><p>Communication:<span> Fluent in written and spoken English, with strong collaboration skills to effectively work with diverse teams and stakeholders.</span></p></li><li><p>Strategy Thinking<span>: Able to think strategically and translate strategies into actionable plans, understand and apply agile ways of working</span></p></li></ul> <p>Preferred Qualifications (Nice to Have)</p><ul><li><p><span>Experience with Lean Manufacturing or Six Sigma methodologies.</span></p></li><li><p><span>PMP or other project management certifications.</span></p></li></ul></div><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/sr-automation-engineer-roche/6a0746392f1861929d2532b2</link><guid isPermaLink="true">http://biotechroles.com/sr-automation-engineer-roche/6a0746392f1861929d2532b2</guid><pubDate>Fri, 15 May 2026 16:13:45 GMT</pubDate><company>Roche</company><location>Shanghai</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Product Lead - Pathology Lab]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b><u>Job Summary:</u></b></p><ul><li><p>This role is heavily focused on strategic products marketing and identifying qualified opportunities for Roche Pathology Lab product lines.</p></li><li><p>The primary resource for technical information regarding products and applications in the areas of expertise.</p></li><li><p>Work closely with sales, technical product specialists and marketing staff throughout the region to identify market opportunities, drive sales, and maintain relationships in key accounts</p></li></ul><p></p><p><b><u>The Opportunity:</u></b></p><ul><li><p>Understand internal and external market situation and deliver short term and long term product strategy and annual bonus policy etc.</p></li><li><p>Frequently work closely with global marketing and product management to develop relevant materials used in China market like promotion material, training material, FAQs for internal and external use.</p></li><li><p>Timely deliver product sales forecast and work closely with sales team to drive successful implementation of opportunity</p></li><li><p>Develop and maintain relationships with key accounts as well as market influencers.</p></li><li><p>Develop new product launch plan and lead the product registration, market access, product position, price and strategy through cooperation with relative departments.</p></li><li><p>Create market promotion plan and work closely with sales, regional market team etc. to hold market promotion events to deliver medical value efficiently and drive market potential</p></li><li><p>Timely provide product training to sales team, distributor partner etc.</p></li></ul><p><b><u>Who you are:</u></b></p><ul><li><p><span>A Bachelor degree or above in the medical area. </span>Completion of an advanced degree in business (MBA) or related science is strongly desired.</p></li><li><p>Proficiency in both spoken and written English</p></li><li><p>Good command of MS office software application</p></li><li><p>Product &amp; marketing expertise</p></li><li><p>Good track record for working in a MNC company for eight or more years, with related supervisory work experience in sales, application support, customer service or training</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/product-lead-pathology-lab-roche/6a0746372f1861929d2532b1</link><guid isPermaLink="true">http://biotechroles.com/product-lead-pathology-lab-roche/6a0746372f1861929d2532b1</guid><pubDate>Fri, 15 May 2026 16:13:43 GMT</pubDate><company>Roche</company><location>Shanghai</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Product Expert - Pathology Lab]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><u><b>Job Summary:</b></u><br />1. This role is heavily focused on creating medical messaging and clinical value on strategic products and<br />identifying qualified opportunities for Pathology Lab product lines.<br />2. Work closely with sales, technical product specialists and marketing staff to train and align on medical<br />messaging<br />3. Act as the primary resource for medical information regarding products and applications in the areas of<br />expertise.<br />4. Develop and maintain relationships with distributors and key opinion leaders</p><p><br /><u><b>The Opportunity:</b></u><br /><u>Medical messaging and product support</u></p><ul><li><p>Provide product input/ messages to strategic plans including product lifecycle, launch and tactical plans.</p></li><li><p>Provide comprehensive marketing input across product line to Marketing, Sales, Regulatory Affairs, and Corporate Affairs</p></li><li><p>Support development of promotional and PR materials, market access submissions, training of sales representatives and other personnel in product messaging</p></li><li><p>Present MSA approved medical information and data related to Roche products to external audiences. Ensure accuracy, credibility, strategic alignment and product positioning and support high medical-value product-related publications.</p></li></ul><p></p><p><u>Key opinion leader development management</u></p><ul><li><p>Identify and develop key product opinion leaders in alignment with product objectives</p></li><li><p>Utilize peer relationships to influence the development and/or update of therapeutic guidelines to ensure optimal product positioning and commercial message consistency.</p></li><li><p>Persuade key opinion leaders on complex issues and product support</p></li></ul><p></p><p><u><b>Who you are:</b></u></p><ul><li><p>MD with Clinical Research experience.</p></li><li><p>5 years of diverse diagnostics industry experience in either Sales, Clinical Research or Marketing</p></li><li><p>Able to work as a member of a cross functional team</p></li><li><p>Able to focus on developing and delivering key messages</p></li><li><p>Proficiency in both spoken and written English</p></li><li><p>Good track record for working in a MNC company for five or more years, with related supervisory work experience in sales, application support, customer service or training</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/product-expert-pathology-lab-roche/6a0746372f1861929d2532b0</link><guid isPermaLink="true">http://biotechroles.com/product-expert-pathology-lab-roche/6a0746372f1861929d2532b0</guid><pubDate>Fri, 15 May 2026 16:13:43 GMT</pubDate><company>Roche</company><location>Shanghai</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Procurement Specialist - Research & Development (Clinical Laboratories)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Procurement Specialist - Research &amp; Development (Clinical Laboratories)</b></p><p><b>Roche India – Roche Services &amp; Solutions</b></p><p><b>Hyderabad</b></p><p></p><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</p><p></p><p>Healthcare is evolving, and Global Procurement is responding by continuously striving for the highest possible performance, taking innovative and strategic approaches to business and supplier partnerships.  Global Procurement proactively manages the entire supplier ecosystem, making a vital contribution to improving health outcomes, reducing costs for patients and global healthcare systems, and ensuring that Roche continues doing now what patients need next.</p><p></p><p><b>The Opportunity</b></p><p></p><p>This role sits within the Indirect Procurement Delivery group, which covers the core procurement activities from category management, strategic and operational sourcing, supplier management, contracting, content strategy definition, and execution. The Indirect Procurement Delivery group comprises many communities grouping categories of the same value chain or having commonality, including Research &amp; Development, Commercial and Corporate Services, Digital &amp; Technology, and Facilities. The communities are key enablers of strong category expertise while allowing flexibility in the procurement delivery response to the evolving needs of our customers.</p><p></p><p>As a <b>Procurement Specialist in Clinical Laboratories,</b> you will bring analytical thinking, planning, execution, and focus to the procurement sourcing and delivery capability area. Applying both general procurement and specialized knowledge or expertise in a specific commodity or spend area, you will ensure effective and efficient delivery of core procurement services and continuous improvement of automation and content availability. </p><p></p><p>You will collaborate closely with internal procurement (i.e. Chapters and capability areas such as customer relationship management, contracting, solutions, analytics, etc.) and business stakeholders to translate business needs into sourcing and spend management activities and content enhancement.</p><p></p><p>You will work closely with other team members to support customer demand, improve the customer buying experience, deliver on day-to day operational activities, and provide capacity and expertise to deliver productivity and other customer oriented projects/solutions.</p><p></p><p>As a <b>Procurement Specialist</b> <b>in</b> <b>Clinical Laboratories,</b> you will play a variety of roles according to your experience, knowledge, and general business requirements, including but not limited to:</p><ul><li><p>You are a Category and sourcing subject matter specialist in Clinical Laboratories conducting market and internal analysis to develop strategies and tactical plans for how Roche should source and negotiate for third party goods and services in order to satisfy stakeholder requirements.</p></li><li><p>You are a Procurement delivery practitioner delivering and executing sourcing strategies by leveraging spend, category know-how, robust sourcing, negotiation, contracting, supplier management methodologies and frameworks and project management skills.  </p></li><li><p>You develop content and automation, translating sourcing outcomes and opportunities into content and automated buying channels that improve business adoption, satisfaction, and overall efficiency. </p></li></ul><p><i> </i></p><p><b>Who you are: </b></p><ul><li><p>You hold a university degree, preferably in a scientific related discipline like Biological/Life Sciences, Chemistry, Biochemistry or related field.</p></li><li><p>You have 5&#43; years procurement experience in strategic sourcing, category strategy building and strategic project execution with general contracting understanding and proficiency or relevant related commodity experience, preferably in the Pharmaceutical industry.</p></li><li><p>You have experience in procurement systems and processes.</p></li><li><p>You possess knowledge and experience in the Clinical Laboratories commodity area (Genomics and Genetics, Bioanalytics, Soluble Biomarkers, Flow Cytometry, Histopathology, Central laboratories) and awareness of adjacent commodities. </p></li><li><p>You have deep knowledge and experience in supplier management, contract negotiations, cost optimization, market research &amp; analysis in R&amp;D categories, and understand the related R&amp;D regulations (e.g. GCP, GDPR).</p></li><li><p>You demonstrate curiosity, active listening and a willingness to experiment and test new ideas when appropriate, with the focus very much on continuous learning and improvement.</p></li><li><p>You are open-minded and inclusive, generously sharing ideas and knowledge, while being receptive to ideas and feedback from others.</p></li><li><p>You have skills in project management.</p></li><li><p>Business level fluency in English.</p></li></ul><p></p><p>Join our team and enable the strong capability expertise needed to meet the evolving needs of our customers.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/procurement-specialist-research-and-development-clinical-laboratories-roche/6a0746292f1861929d2532af</link><guid isPermaLink="true">http://biotechroles.com/procurement-specialist-research-and-development-clinical-laboratories-roche/6a0746292f1861929d2532af</guid><pubDate>Fri, 15 May 2026 16:13:29 GMT</pubDate><company>Roche</company><location>Hyderabad</location><salary>$18000-35000</salary><type>Full time</type></item><item><title><![CDATA[Senior Software Engineer (Java)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Roche Information Solutions provides integrated digital solutions to deliver on the promise of affordable, high-quality, and accessible healthcare. RIS is accountable for the development and delivery of digital solutions, common Diagnostics architecture, and data management. Digitalization in healthcare is of increasing importance to deliver customer and patient value, and shape healthcare.</p><p>The Platform team is building the foundation on which a myriad of healthcare and research software applications can be delivered to patients, from the cloud to the lab. The Platform Engineering team is responsible for platform services including the development, testing, deployment, and operation of software. In addition, the function manages platform onboarding and developer experience.</p><p>Roche’s single vision is to improve the lives of patients, and the RIS Platform team is dedicated to using the latest cloud software technologies as a means to deliver this vision. If you would rather improve health outcomes for millions instead of helping sell ads on the Internet, this is the job for you.</p><p></p><h1><b>The Position</b></h1><p>This position is a key technical leadership role within a team operating across <b>one to two Scrum teams</b>, and is responsible for driving the design, technical direction, and successful implementation of complex, enterprise-scale software systems.</p><p>This role is suited for a highly experienced engineer who operates above the Senior Engineer level and combines strong technical depth with leadership in architecture, design execution, and cross-team collaboration. This role is expected to <b>own and drive designs from concept to implementation</b>, ensuring alignment across architects, peers, and engineering teams.</p><p>The role includes <b>creating solution designs, leading technical discussions, resolving design and implementation blockers, and guiding teams through execution</b>. This role will work closely with architects, partner teams, and peers to resolve conflicts, gain alignment and approvals, and ensure smooth delivery.</p><p>In addition, this role is expected to <b>identify opportunities for introducing new tools, capabilities, and engineering improvements</b>, and to proactively raise concerns and propose changes where processes, practices, or technical approaches can be improved. This role also plays an important part in mentoring engineers, influencing engineering excellence, and ensuring scalable, reliable, and maintainable solutions.</p><p></p><h1><b>Your Responsibilities</b></h1><h2><b>Technical Leadership &amp; Design Ownership</b></h2><ul><li><p>Lead the technical design of complex features, services, and platform capabilities from ideation through implementation.</p></li><li><p>Create, drive, and evolve solution designs, ensuring they are scalable, maintainable, and aligned with architectural standards.</p></li><li><p>Lead design discussions and provide technical direction to engineering teams during implementation.</p></li><li><p>Work closely with architects, peers, and other stakeholders to resolve design conflicts, close gaps, and secure necessary approvals.</p></li><li><p>Ensure designs are translated effectively into implementation, supporting teams until successful delivery.</p></li></ul><p></p><h2><b>Implementation Guidance &amp; Blocker Resolution</b></h2><ul><li><p>Act as the primary technical point of contact for the team during implementation.</p></li><li><p>Identify and resolve technical blockers faced by implementation teams, providing hands-on guidance where needed.</p></li><li><p>Bridge design and execution by ensuring engineering teams understand requirements, trade-offs, and technical decisions.</p></li><li><p>Proactively identify risks, dependencies, and design gaps, and drive timely resolution.</p></li></ul><h2><b>Software Development &amp; Engineering Excellence</b></h2><ul><li><p>Contribute hands-on to the development of high-quality, scalable, and maintainable software using Java, Spring Boot, REST APIs, and microservices architecture.</p></li><li><p>Guide engineering best practices across coding, testing, code reviews, observability, and reliability.</p></li><li><p>Support robust system design and implementation for enterprise-scale cloud applications.</p></li></ul><p></p><h2><b>Cloud &amp; Platform Engineering</b></h2><ul><li><p>Bring strong exposure and experience with AWS cloud services to build robust, scalable, and high-performing cloud-native solutions.</p></li><li><p>Ensure platform services and applications are resilient, scalable, secure, and cost-effective.</p></li><li><p>Contribute to platform engineering capabilities, shared services, and developer experience improvements.</p></li></ul><h2><b>Innovation, Tools &amp; Continuous Improvement</b></h2><ul><li><p>Identify, evaluate, and introduce new tools, frameworks, and technical capabilities that can improve team productivity and platform quality.</p></li><li><p>Drive Proof of Concepts (POCs) and exploratory initiatives to assess new technologies or approaches.</p></li><li><p>Proactively raise concerns where engineering processes, tools, or delivery practices can be improved, and help drive those improvements within the team.</p></li><li><p>Champion continuous improvement in design practices, development workflows, and team effectiveness.</p></li></ul><p></p><h2><b>Collaboration &amp; Mentorship</b></h2><ul><li><p>Mentor and guide engineers on technical design, implementation quality, and problem-solving approaches.</p></li><li><p>Collaborate across teams to align on architecture, dependencies, and delivery plans.</p></li><li><p>Foster strong engineering practices and help build technical capability within the team.</p></li><li><p>Act as a technical leader who influences without formal authority and drives alignment across multiple stakeholders.</p></li></ul><p></p><h1><b>Your Qualifications</b></h1><ul><li><p>BE/BTech/Master’s degree in Computer Science or a related discipline</p></li><li><p><b>6&#43; years of hands-on experience</b> in software engineering, with strong technical leadership experience</p></li><li><p>Strong hands-on expertise in Java, Spring Boot, REST APIs, and microservices architecture</p></li><li><p>Strong experience in system design, design patterns, engineering principles, and scalable architecture</p></li><li><p>Proven experience driving technical design and guiding implementation teams through delivery</p></li><li><p>Demonstrated ability to resolve technical conflicts and align multiple stakeholders across teams</p></li><li><p>Strong exposure and experience with AWS cloud services to build robust, scalable, and high-performing solutions</p></li><li><p>Experience building, deploying, and supporting enterprise-scale cloud applications</p></li><li><p>Strong understanding of Agile development environments and engineering delivery practices</p></li><li><p>Proven ability to identify design and implementation gaps proactively and drive them to resolution</p></li><li><p>Strong problem-solving skills and ability to work effectively in complex technical ecosystems</p></li><li><p>Experience mentoring engineers and influencing engineering best practices</p></li><li><p>Healthcare domain experience or familiarity is preferred (understanding of healthcare workflows, data, or regulatory considerations is a plus)</p></li></ul><p></p><h1><b>Nice to Have</b></h1><ul><li><p>Frontend experience with modern frameworks (React, Angular, etc.)</p></li><li><p>Experience contributing to platform engineering or shared services teams</p></li><li><p>Exposure to developer experience, internal developer platforms, or engineering productivity initiatives</p></li><li><p>Experience working closely with enterprise or solution architects in large-scale organizations</p></li><li><p>Experience driving process improvements, tooling adoption, or cross-team engineering standardization</p></li></ul><h1><b>What Success Looks Like in This Role</b></h1><ul><li><p>Designs are clearly defined, aligned, and successfully implemented across teams</p></li><li><p>Implementation teams receive timely technical guidance and blocker resolution</p></li><li><p>Design conflicts and technical dependencies are proactively managed and resolved</p></li><li><p>Engineering practices, tools, and processes continuously improve over time</p></li><li><p>The team delivers scalable, high-quality solutions with strong technical leadership and alignment</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/senior-software-engineer-java-roche/6a0746292f1861929d2532ae</link><guid isPermaLink="true">http://biotechroles.com/senior-software-engineer-java-roche/6a0746292f1861929d2532ae</guid><pubDate>Fri, 15 May 2026 16:13:29 GMT</pubDate><company>Roche</company><location>Pune</location><salary>$80000-120000</salary><type>Full time</type></item><item><title><![CDATA[Integration Governance Expert - Data Platforms]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><h2><span>The Integration Governance Expert is responsible for defining, implementing, and continuously improving governance frameworks for enterprise integrations, including APIs, event-driven architectures, and AI-driven and A2A integrations. This role ensures that integrations are discoverable, reusable, compliant, high-quality, and AI-ready through effective management of metadata, schemas, and standards. </span><span><span>You will drive governance practices across integration platforms, enabling consistent design, implementation, and lifecycle management of integration assets. </span></span></h2><h2></h2><h2></h2><h2>The Opportunity:</h2><ul><li><h2><span><b><span>Lead the evolution</span></b><span> of integration governance frameworks across APIs, events, and AI-driven systems to ensure enterprise-wide scalability. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Drive schema governance</span></b><span> by designing, versioning, and validating standards such as OpenAPI, AsyncAPI, and JSON Schema to maintain high-quality assets. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Shape the integration strategy</span></b><span> aligned with global digital, data, and AI goals, promoting metadata-driven approaches for maximum reuse. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Ensure AI-readiness</span></b><span> by implementing semantically structured metadata and schemas that support advanced analytics and automation. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Collaborate with architects and engineers</span></b><span> to align on governance standards, providing the enablement needed for consistent global practices. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Resolve complex integration challenges</span></b><span> by performing root cause analysis and debugging issues to improve overall landscape compliance. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Maximize discoverability</span></b><span> of integration assets, ensuring they are well-documented and easily accessible across multiple platforms and domains. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Operate as a Subject Matter Expert</span></b><span> in metadata management, balancing strategic design with practical implementation across MCP interactions. </span></span></h2><h2></h2><h2></h2></li></ul><h2>Who you are:</h2><ul><li><h2><span><b><span>Experienced professional</span></b><span> with a proven track record in integration engineering, architecture, or governance roles within complex enterprise environments. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Educated specialist</span></b><span> holding a degree in Computer Science, Information Technology, or a related technical field. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Technical expert</span></b><span> with advanced knowledge of API design (REST, SOAP, microservices) and management practices. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Systems architect</span></b><span> with strong experience in event-driven architectures, messaging systems, and metadata management (APIs, events, MCP). </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Standardization advocate</span></b><span> with expertise in schema governance, lifecycle management, and quality assessment through validation and observability. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Tech-savvy collaborator</span></b><span> familiar with DevOps, CI/CD, and hands-on experience in Mulesoft, Solace, IBM Sterling, or SAP IS. </span></span></h2><h2></h2><h2></h2></li><li><h2><span><b><span>Strategic influencer</span></b><span> possessing excellent communication skills to engage stakeholders and drive improvement without direct authority. </span></span></h2><h2></h2><h2></h2></li></ul><h2></h2><h2>Ready to bring your unique qualities to Roche and make an impact? Apply now and join us in our mission to shape the future of healthcare.</h2><h2>#RDT2026</h2><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/integration-governance-expert-data-platforms-roche/6a0746292f1861929d2532ad</link><guid isPermaLink="true">http://biotechroles.com/integration-governance-expert-data-platforms-roche/6a0746292f1861929d2532ad</guid><pubDate>Fri, 15 May 2026 16:13:29 GMT</pubDate><company>Roche</company><location>Pune</location><salary>$65000-110000</salary><type>Full time</type></item><item><title><![CDATA[Data Steward - Lead]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Data Steward Lead</b></p><p><b>Roche India - Roche Services &amp; Solutions</b></p><p><b>Hyderabad</b></p><p></p><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</p><p></p><p>Healthcare is evolving, and Global Procurement (GP) is responding by continuously striving for the highest possible performance, taking innovative and strategic approaches to business and supplier partnerships. Global Procurement proactively manages the supplier ecosystem, making a vital contribution to improving health outcomes, reducing costs for patients and global healthcare systems, and ensuring that Roche continues doing now what patients need next.</p><p></p><p><b>The Opportunity</b></p><p></p><p>This role sits within the <b>Enablement Chapter, in Global Procurement Analytics &amp; Insights, </b>where we drive operational and financial effectiveness by delivering trusted data, actionable insights, stronger performance management, and robust decision support for GP leadership and chapters.</p><p></p><p>As <b>Data Steward Lead</b>, you will play a senior role in shaping how Global Procurement defines, governs, documents, validates, and uses its critical data products.</p><p></p><p>You will act as the data stewardship lead for priority procurement data products, ensuring that business definitions, metadata, lineage, data quality expectations, ownership, access requirements, and usage guidance are clear, trusted, and consistently applied. You will work closely with procurement, finance, governance, informatics, data engineering, analytics, and business stakeholders to improve trust in critical metrics such as spend, savings, supplier, category, contract, and sustainability data.</p><p></p><p>This is a senior stewardship and data product governance role. You will connect business meaning with technical implementation, helping ensure that data products are not only built, but also understandable, reusable, well-governed, and fit for decision-making.</p><p></p><p><b>Responsibilities include</b></p><ul><li><p>Leading data stewardship for priority Global Procurement data products, including business definitions, metric logic, ownership, metadata, lineage, data quality expectations, and approved usage.</p></li><li><p>Defining and maintaining data product standards and data product contracts, including product purpose, data grain, source dependencies, business rules, ownership, service expectations, and release-readiness criteria.</p></li><li><p>Partnering with business owners and domain experts to resolve conflicting metric definitions and align on certified business logic for critical procurement data products.</p></li><li><p>Working with data engineering teams to translate business rules into governed data products using modern data platforms and tools such as Snowflake, dbt, GitLab, and related data engineering practices.</p></li><li><p>Ensuring that production-grade data products are properly documented and registered in enterprise cataloging tools such as Collibra, including technical metadata, business glossary terms, ownership, stewardship, and lineage.</p></li><li><p>Supporting data access and policy alignment in partnership with governance, informatics, and security teams, including Role-Based Access Control (RBAC), Immuta-enabled policy controls, masking requirements, and Personally Identifiable Information (PII) handling where applicable.</p></li><li><p>Leading data quality issue triage for critical data products by identifying root causes, coordinating resolution, tracking open risks, and escalating issues that may impact leadership reporting or business-critical decisions.</p></li><li><p>Helping embed stewardship into the data product lifecycle, including intake, requirements clarification, Definition of Done, change control, release readiness, cataloging, and ongoing product support.</p></li><li><p>Supporting the transition from legacy reporting logic, manual workflows, and dashboard-level calculations into governed, reusable data products.</p></li><li><p>Coaching colleagues and stakeholders on data stewardship practices, business glossary quality, metadata standards, documentation discipline, and responsible data usage.</p></li></ul><p></p><p><b>Who you are</b></p><ul><li><p>You hold a university degree in Information Management, Data Science, Business Analytics, Computer Science, Information Systems, Engineering, Business Administration, Supply Chain, Procurement, Finance, or a related field.</p></li><li><p>You have significant 7&#43; years of experience in data stewardship, data governance, data management, analytics, metadata management, data quality, business analysis, or data product delivery.</p></li><li><p>You have strong understanding of how data moves from source systems into analytical products, dashboards, and business decision-making.</p></li><li><p>You can translate between business definitions, data models, quality rules, access requirements, and downstream reporting needs.</p></li><li><p>You have strong Structured Query Language (SQL) literacy and can investigate data issues, joins, grain, duplicates, mappings, reconciliation gaps, and metric logic.</p></li><li><p>You have experience defining or supporting data dictionaries, business glossaries, metadata, lineage, data quality rules, data ownership, and usage documentation.</p></li><li><p>You are familiar with modern data platforms and tools such as Snowflake, dbt, GitLab, Collibra, Immuta, Tableau, Power BI, Alteryx, or similar technologies.</p></li><li><p>You can operate independently in ambiguous situations, structure complex problems, and drive alignment across business, governance, and technical teams.</p></li><li><p>You have strong stakeholder management skills and can influence teams without direct authority in a global, cross-functional environment.</p></li><li><p>You communicate clearly in English, both verbally and in writing, and can explain complex data topics in simple business language.</p></li></ul><p></p><p><b>Preferred</b></p><ul><li><p>Certification or training in data management, data governance, Snowflake, Collibra, DAMA / Certified Data Management Professional (CDMP), procurement, supply chain, or analytics is a plus.</p></li><li><p>Knowledge of Data Mesh, data product management, data contracts, semantic layers, Findable, Accessible, Interoperable, and Reusable (FAIR) data principles, or enterprise data governance frameworks.</p></li><li><p>Experience with data privacy, security, classification, or access-control requirements in a large global organization.</p></li><li><p>Experience supporting data migration or modernization from legacy reporting environments into governed cloud data platforms.</p></li><li><p>Experience in procurement, supply chain, finance, spend analytics, savings, sourcing, contracts, supplier data, category management, or sustainability data.</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/data-steward-lead-roche/6a0746282f1861929d2532ac</link><guid isPermaLink="true">http://biotechroles.com/data-steward-lead-roche/6a0746282f1861929d2532ac</guid><pubDate>Fri, 15 May 2026 16:13:28 GMT</pubDate><company>Roche</company><location>Hyderabad</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Senior Subject Matter Expert (SME) - E2E Accounts Receivable & R2R]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p>This role is based in Roche Services Americas, one of our worldwide Shared Services Centers providing Finance and Procurement services to various countries in the Americas region. As the <b>Record to Report (R2R) CRM SME</b>, you will be based in San José, Costa Rica, reporting to the Cluster Section Lead CRM NALA.</p><p></p><p><b>The Opportunity:</b></p><p></p><p>In this specialized role, you will be responsible for executing high-level AR operational activities and serving as a Subject Matter Expert (SME) for our systems and processes. Your focus will be on maintaining technical excellence and driving regional process harmonization.</p><p></p><p>Your responsibilities include:</p><ul><li><p><b>SME Leadership:</b> Maintain deep knowledge of accounts receivable processes, flows, and systems. Serve as the technical expert for &#34;AS IS&#34; processes during global project implementations.</p></li><li><p><b>Operational Execution:</b> Coordinate and perform complete, stringent, and timely financial tasks including bank reconciliation, cash application, and clearing of AR/bank suspense accounts.</p></li><li><p><b>Process Improvement:</b> Propose and coordinate system enhancements, sharing best practices from global organizations and following through on implementations.</p></li><li><p><b>Credit &amp; Data Management:</b> Execute Customer Credit Analysis, manage dispute resolutions, and maintain customer credit master data.</p></li><li><p><b>Project Coordination:</b> Support the resolution of gaps found during project rollouts, coordinating testing and documentation to ensure seamless transitions.</p></li><li><p><b>Training &amp; Mentorship:</b> Maintain a training network to ensure knowledge flows across the organization, providing functional guidance to team members.</p></li><li><p><b>Stakeholder Communication:</b> Handle incoming inquiries via calls and emails with a focus on customer service, and facilitate cross-functional communication to resolve complex issues.</p></li></ul><h3></h3><p><b>Who you are:</b></p><ul><li><p>You hold a <b>Bachelor’s degree</b> in Accounting, Finance, Project Management or Engineering.</p></li><li><p>You bring <b>5&#43; years</b> of finance and accounting experience, with a deep understanding of R2R and AR process flows.</p></li><li><p>You are characterized by a high level of social competence and are fluent in both <b>English and Spanish</b>; Portuguese is a plus.</p></li><li><p>You possess strong technical expertise in Finance Shared Services systems such as <b>SAP, BlackLine, and SNOW</b>. SAP FS-CM and Power BI a plus.</p></li><li><p>You are an expert at organizing tasks with limited direction and managing multiple competing priorities in a fast-paced environment.</p></li><li><p>You are well known for your independent, yet collaborative working style and your ability to act as a <b>technical bridge </b>between local teams and global projects.</p></li></ul><p></p><p><b>Preferred:</b></p><ul><li><p>Advanced knowledge of computerized environments (Excel, G-Suite, PowerPoint, Power BI) for data analysis.</p></li><li><p>Demonstrated experience in project testing and documentation (UAT) within a Shared Service Center environment.</p></li></ul><p></p><p><b><i>Relocation benefits are not available for this posting.</i></b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/senior-subject-matter-expert-sme-e2e-accounts-receivable-and-r2r-roche/6a0746262f1861929d2532ab</link><guid isPermaLink="true">http://biotechroles.com/senior-subject-matter-expert-sme-e2e-accounts-receivable-and-r2r-roche/6a0746262f1861929d2532ab</guid><pubDate>Fri, 15 May 2026 16:13:26 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Field Service/Support Engineer]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Contratacion requerida de Person con Discapacidad PCD </p><p>Principales responsabilidades:</p><ul><li><p>Recepción y registro: Atender requerimientos a nivel nacional que se generen frente a las soluciones digitales ofertadas por Roche, registrando de forma clara y detallada cada caso.</p></li><li><p>Diagnóstico inicial: Categorizar el requerimiento y determinar el nivel de urgencia según impacto al cliente.</p></li><li><p>Resolución en primer nivel: Brindar solución de primer nivel a los reportes técnicos generados por el cliente por medio de herramientas de acceso remoto o de manera telefónica.</p></li><li><p>Interoperabilidad soluciones de terceros ofertadas por Roche: brindar soporte básico a los LIS de terceros ofrecidos por Roche, asegurando que los resultados lleguen de forma correcta.</p></li><li><p>Guía sobre soluciones digitales: brindar al cliente guía paso a paso en el uso básico de las soluciones digitales ofrecidas por Roche.</p></li><li><p>Soporte de conectividad: validar estados de red y configuración básica de puertos que permitan la transmisión de datos entre los dispositivos y las soluciones digitales.</p></li><li><p>Escalamiento proactivo: transferir casos complejos a segundo nivel cuando la solución no esté al alcance del soporte de primer nivel, asegurando que el cliente siempre se mantenga actualizado del estado de su requerimiento.</p></li><li><p>Seguimiento de SLAs: garantizar que los tiempos de respuesta se cumplan de acuerdo a lo acordado con los clientes.</p></li><li><p>Actualización de base de conocimiento: documentar soluciones nuevas para para alimentar repositorio de errores conocidos para mejorar tiempos de respuesta a futuros.</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/field-servicesupport-engineer-roche/6a0746252f1861929d2532aa</link><guid isPermaLink="true">http://biotechroles.com/field-servicesupport-engineer-roche/6a0746252f1861929d2532aa</guid><pubDate>Fri, 15 May 2026 16:13:25 GMT</pubDate><company>Roche</company><location>Bogota</location><salary>$25000-40000</salary><type>Full time</type></item><item><title><![CDATA[Team Leader RCSC]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><p>Technical Manager - Regional Customer Support Centre </p><p><br /></p><p>Are you looking for an exciting challenge?</p><p></p><p>Are you ready to lead a specialist team in delivering world-class diagnostic support across the UK, Ireland and Northern Europe?  </p><p></p><p>Roche Diagnostics is looking for a Technical Manager to lead our SWA/Core Lab Hardware remote support team. Based within our Regional Customer Support Centre (RCSC) in Burgess Hill, you will be the strategic lead for a team of 16 specialists providing critical technical and systems support for the Roche Core Laboratory portfolio.</p><p></p><p>The Role</p><p>As Technical Manager, you will lead a team of 16 specialists who provide remote technical and systems support for the Roche Core Laboratory portfolio, alongside customer and staff training. You will be the driving force behind the team’s operational and strategic success, ensuring we deliver a &#34;best-in-class&#34; customer experience.</p><p></p><p>You will be accountable for the successful delivery of service requirements across the UK, Ireland, Nordics and the wider EMEA-LATAM region.</p><p></p><p>Key Responsibilities:</p><ul><li><p>Leadership &amp; Coaching: Use your skills to empower your team, remove obstacles and foster high performance.</p></li><li><p>Line Management: Drive recruitment of ideal skill sets, manage performance and take ownership of the team&#39;s professional development.</p></li><li><p>Strategic Collaboration: Partner with Sales, Marketing, and Regional Service Managers to ensure the technical service offering aligns with broader business goals.</p></li><li><p>Operational Excellence: Oversee the delivery of high-value remote support and the implementation of Roche Global standards.</p></li></ul><p></p><p>Location &amp; Flexibility</p><p>This is an office based role with an expectation of a minimum of 2 days a week in our office in Burgess Hill, Sussex.</p><h3></h3><p>Who you are</p><p>You are a resilient  leader who thrives in a fast-paced environment. You don’t just manage tasks; you inspire innovation and possess a &#34;questioning&#34; approach that challenges the status quo to exceed customer expectations.</p><p></p><p>Essential Requirements:</p><ul><li><p>Education: A degree in a relevant field OR a proven track record of technical mastery and leadership in an engineering environment.</p></li><li><p>Experience: A minimum of 3 years experience of leading technical teams</p></li><li><p>Technical Background: A proven track record of supporting complex healthcare instrumentation and/or deep experience within a Blood Sciences laboratory.</p></li><li><p>Leadership: Proven experience in line management or a clear ability to demonstrate the leadership competencies required to coach and develop a high-performing team.</p></li><li><p>Technical Proficiency: Strong IT skills, including Microsoft Office, Google Suite, and CRM systems (e.g., Salesforce).</p></li><li><p>Communication: Excellent verbal and written communication skills, with the ability to influence stakeholders in a matrix environment.</p></li><li><p>IT Literacy: Strong digital skills, including Microsoft/Google Suite and CRM systems (e.g., Salesforce).</p></li></ul><p></p><p>Investing in you</p><p>Roche is a company that invests as much in its people as it does in R&amp;D (over £6.5 billion worldwide). In addition to a competitive salary and benefits package, you will receive recognised product training and continuous support to build your knowledge and potential.</p><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.</span></p>]]></description><link>http://biotechroles.com/team-leader-rcsc-roche/6a0746242f1861929d2532a9</link><guid isPermaLink="true">http://biotechroles.com/team-leader-rcsc-roche/6a0746242f1861929d2532a9</guid><pubDate>Fri, 15 May 2026 16:13:24 GMT</pubDate><company>Roche</company><location>Burgess Hill</location><salary>$85000-110000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison - Solid Tumor - OH, WV, PA Territory]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Medical Science Liaison (MSL) is a field based, customer-facing, non-promotional medical and scientific role. Their key objective is to create impact through advancing clinical practice within the territory that leads to improved <br>patient outcomes. The MSL must demonstrate deep therapeutic expertise, understand territory and market influences, engage scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop <br>their territory and execute all relevant activities in alignment with the medical strategic and tactical plan – while functioning within the Novartis Code of Conduct, Ethics/Compliance policies and Working Practice documents. <br>The MSL will Inform and shape medical strategy through application of a curious mindset to collect impactful and actionable insights, understanding the strategic impact of critical insights.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities:</b></p><p></p><p>The MSL will leverage scientific expertise and market knowledge to establish and build professional relationships and engage with HCPs (including community physicians, pharmacists, medical experts, nurses, and other healthcare professionals) and other thought leaders in geographical area as aligned with medical strategy</p><p>• The primary responsibility of the MSL is to engage with customers - customer engagements may include but not be limited to emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle.</p><p>• Must demonstrate strategic territory vision and ensure appropriate territory identification, mapping, and planning of Medical Engagements (MEs) and Key Accounts as aligned to medical strategy and in collaboration with internal Novartis colleagues.</p><p>This includes:</p><p>a. identification of key stakeholders with influence in disease space throughout the product development journey to establish strategies for education, engagement, and partnership</p><p>b. identification of opportunities for partnership with academic centers, centers of excellence, and/or systems of care to drive impact within the assigned territory</p><p>c. identification of opportunities to involve HCPs or MEs when a specific medical need is identified (e.g., publications, clinical trial participation, etc.)</p><p>d. identification of opportunities for internal collaboration with other Novartis stakeholders to drive forward therapeutic area, clinical, or product goals as appropriate</p><p>• Provide clinical trial support for company sponsored trials and facilitating relevant medical activities, including but not limited to identification of appropriate sites, supporting clinical trials (subject recruitment, protocol questions, SIVs, etc.) at sites, and cross-functional collaboration with Medical Affairs and Clinical Operations colleagues</p><p>• Regularly collaborate with internal colleagues (e.g., HEOR, access, marketing, commercial) within the assigned therapeutic area and territory to advance clinical practice while maintaining customer centricity and a One Novartis approach in accordance with Novartis compliance standards</p><p>• Maintain in-depth knowledge of assigned therapeutic area and Novartis compounds to serve as a medical resource to customers and internal colleagues</p><p>• Maintain in-depth knowledge of internal policies and external regulations (e.g., field medical Working Practice Document (WPD), travel policy, expense policy, state and local laws, institutional policies) and how they affect the day-to-day</p><p>• Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner, including profiling of core customers and ensuring up-to-date information in the CRM</p><p>• Champion emerging responsibilities as strategic priorities and territory needs evolve</p><p>• Proactively drive personal and professional development</p><p>• Conduct yourself with the highest ethical standards and adhere to Novartis Code of Conduct. Comply with all relevant laws and regulations and Novartis Ethics, Risk &amp; Compliance policies, and procedures.</p><p></p><p><b>Essential Requirements: </b></p><ul><li><b>Education:</b><span> </span>Graduate degree in science or healthcare required; doctoral degree preferred (MD, PhD, DNP, PharmD, etc.) </li></ul><ul><li><span>Minimum of 3 years’ experience in a Field Medical-based position within the pharmaceutical industry or as an MSL is preferred OR 5-7 years of relevant medical affairs, clinical research, or related experience in a scientific or clinical setting required.</span><ul><li><span>Strong clinical knowledge including pharmacotherapy, treatment guidelines, clinical research processes, medical expert engagement strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is required. </span></li><li><span>Candidates will perform their duties in accordance with applicable law, regulations, and Novartis policies. </span></li><li><span>Works within Ethics, Compliance and Promotional policies (Novartis &amp; Federal) and ensures those around them do the same. </span></li><li><span>Works to ensure a diverse and inclusive environment free from all forms of discrimination and harassment. </span></li><li><span>Adherence with Company policies, state and federal laws and regulations </span></li><li><span>Candidate must reside within territory, or within a reasonable daily commuting distance of 50 miles from the territory border. Field based, customer-facing position majority of the time with approximately 60-70% travel required to achieve performance and business objectives (face to face, virtual, email, telephone, etc.). Must have a valid driver’s license.</span></li></ul></li></ul><p></p><p><b><span>Desirable Requirements:</span></b></p><ul><li><span>Previous experience in assigned or related therapeutic area is preferred. </span></li></ul><p></p><p><span>NOTE: Above level experience criteria are not an exhaustive list.</span></p><p><span>Driving is an Essential Function of this Role: </span><span>Meaning it is fundamental to the purpose of this job and cannot be eliminated. Because driving is an essential function of the role, you must have a fully valid and unrestricted driver’s license to be qualified for this role. The company provides reasonable accommodations for otherwise qualified individuals with medical restrictions if an accommodation can be provided without eliminating the essential function of driving.</span></p><p></p><p>The salary for this position is expected to range between $160,300.00 and $297,700.00 per year.</p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p>To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$160,300.00 - $297,700.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Building Constructions, Business Analysis, Business Networking, Clinical Protocols, Clinical Research, Clinical Study Reports, Communication, Curious Mindset, Disease Management, Diversity and Inclusion (D&amp;I), Drug Development, Epidemiology, Medical Information, Medical Research, Medical Writing, Microsoft Word, Phase Iv Clinical Trial, Product Placement, Scientific Support]]></description><link>http://biotechroles.com/medical-science-liaison-solid-tumor-oh-wv-pa-territory-novartis/6a0745912f1861929d2532a8</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-solid-tumor-oh-wv-pa-territory-novartis/6a0745912f1861929d2532a8</guid><pubDate>Fri, 15 May 2026 16:10:57 GMT</pubDate><company>Novartis</company><location>Field Non-Sales (USA)</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Executive Assistant & PSP Coordinator]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br><br>The Executive Assistant and PSP coordinator is responsible for providing multifunctional, operational, and digital administrative support to the Country President &amp; CCFO.  As the executive assistant, this role shall support in planning, coordination and execution of internal and external events and meetings as needed. As the PSP coordinator interacts with all the relevant Local, Regional and Global functions to ensure adequate monitoring, tracking and review of Patient Support Program (PSP) controls framework.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major accountabilities: </b></p><p><b>Provide administrative support to the Country President and CCFO</b></p><ul><li><p>Manage superiors&#39; calendars, ensuring that all important meetings and events are scheduled ahead of time.</p></li><li><p>Manage superiors&#39; travel requirements, ensuring adherence to policies and guidelines</p></li><li><p>Monitor and ensure that reports required by Global, Region, Cluster and local IMI organization are submitted on time.</p></li><li><p><span>Coordinate and manage logistical support for LT meetings, quarterly business review meetings, business reviews with above-country stakeholders, and country governance meetings.</span></p></li><li><p>Ensure accurate minutes of key meetings, for example LT meetings and timely and consistent follow-through of action points. Update the minutes and provide copies to the attendees.</p></li><li><p>Maintain systematic filing of office documents including digital archiving for safekeeping and easy retrieval.</p></li><li><p>Coordinate and arrange logistics of all official Global/ Region/ Cluster visits to the country as may be required.</p></li><li><p>Organize meetings in coordination with Superiors’</p><p>o   Prepare venue of meeting including materials for presentation.</p><p>o   Attend to logistics needed in organizing meetings.</p></li></ul><p></p><p><b>Communication/ Support as Change Agent</b></p><ul><li><p>Responsible for the preparation and communication for the Country President and CCFO.</p></li><li><p>Maintain confidentiality of information contained in correspondence and communication.</p></li></ul><p></p><p><b>PSP Coordinator</b></p><ul><li><p>Responsible for coordinating with all PSP stakeholders to obtain evidence and complete the PSP self-assessment</p></li><li><p>Responsible for tracking, monitoring, reporting and follow-up on all PSP CAPAs/ remediation actions by relevant control owners</p></li><li><p>Performing a periodic review on PSP programs in line with Local/ Regional/ Global reporting requirements</p></li><li><p>Ensure timely updates and escalations to Country President on the various programs.</p></li></ul><p></p><p></p><p><b>Minimum Requirements: </b></p><ul><li><p>Graduate of any four-year course, preferably business degree.</p></li><li><p>Fluent spoken and written English</p></li><li><p>Minimum of 5 years’ experience in providing administrative support to senior leaders.</p></li><li><p>Above average computer knowledge, is adept and can navigate digital technology and tools with ease.</p></li><li><p>Strong communication and interpersonal skills.</p></li><li><p>Proficient in Microsoft office, Teams, and other IT tools essential for documentation and collaboration</p></li><li><p>Prior project management experience is a bonus.</p></li><li><p>Enterprise and strategic mindset with strong analytical skills to interpret data and KPIs</p></li></ul><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/executive-assistant-and-psp-coordinator-novartis/6a0745912f1861929d2532a7</link><guid isPermaLink="true">http://biotechroles.com/executive-assistant-and-psp-coordinator-novartis/6a0745912f1861929d2532a7</guid><pubDate>Fri, 15 May 2026 16:10:57 GMT</pubDate><company>Novartis</company><location>Makati City</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Director, Decision Science Product Lead – Neuroscience (1 of 2 roles)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: <br>#LI-Hybrid<br><br>The Insights and Analytics team is dedicated to enabling improved decision making at Novartis by leveraging data and advanced analytics capabilities to generate actionable insights that drive business growth. We collaborate closely with the US business, bringing insights and challenging ideas to empower smarter, data-driven decision-making. Reporting into the ED, Decision Science Product Lead Neuroscience, this role is crucial in enabling proactive and integrated insight-driven decision making for the brand, addressing business problems, shaping strategy and implementing decision science through Insights &amp; Analytics capabilities.<br><br>The Decision Science Product Lead is a strategic leader responsible for transforming complex data into actionable insights that drive brand success. This role is pivotal in integrating and synthesizing information from diverse sources to provide comprehensive, actionable answers that align with brand strategic imperatives. By supporting the generation and analysis of insights throughout the product lifecycle as the connector between the Insights &amp; Analytics and product team, the individual ensures continuous insight-generation and strategic alignment, fostering in-novation and informed decision-making. Leading a team of high-performing Insights &amp; Analytics POD at product level, this role is instrumental in shaping the brand's strategic direction, ensuring that insights are effectively leveraged to achieve business goals.<br><br>	<br>This position will be located at the East Hanover, NJ or Cambridge, MA sites and will not have the ability to be located remotely. This position will require 10% travel as defined by the business (domestic and/ or international).<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities:</b></p><ul><li>Shape the strategic direction of a neuromuscular brand by leveraging insights to identify opportunities, address challenges, and optimize performance</li><li>Integrate and synthesize insights from across I&amp;A functions to deliver comprehensive, actionable recommendations that address key brand objectives and take into account rare disease approaches and models</li><li>Actively participate in IPST discussions and decision-making, contributing data-driven insights and challenging established thinking to refine strategies</li><li>Understand and help craft the brand narrative for IPST meetings and conversations with senior leadership</li><li>Serve as the primary point of contact and proactive strategic thought partner for the Integrated Product Strategy Team (IPST) and General Management (GM), driving brand performance narrative, and ensuring consistent communication and alignment</li><li>Collaborate with the IPST Lead to further refine analyses &amp; sharpen insights / recommendations</li><li>Lead POD at product level by working across I&amp;A pillars to direct and synthesize information to help drive brand performance</li><li>Closely coordinate with other neuromuscular product illuminators for areas of synergistic value across neuromuscular brands given the common footprints and rare disease characteristics.</li><li>Share key insights with the IPST, while actively pressure-testing and challenging current thinking to drive innovation and informed decision-making</li><li>Support the generation and analysis of insights throughout the entire product lifecycle, ensuring continuous improvement and alignment with brand goals</li><li>Synthesize large volumes of analytics provided by GM, ensuring that insights are translated into actionable strategies for the brand</li><li>Pressure-test insights and analyses to ensure robust, high-quality recommendations that drive brand success</li><li>Integrate performance analytics (e.g., diagnose current results with aligned KPIs and drivers, provide clarity on root cause) and predictive analytics (e.g., data-driven scenarios and simulations) to explore/address business issues in the context of the brand</li><li>Support neuromuscular above-brand initiatives in building rare disease capabilities.</li></ul><p></p><p>Novartis seeks an individual with extensive experience in the pharmaceutical or healthcare industry, with a deep understanding of product lifecycle management, market dynamics, and regulatory environments. A proven track record in brand performance management, strategic planning, or a similar role, the person should demonstrate the ability to develop strategic insights that drive brand success and align with organizational goals. Highly desirable is experience with rare diseases given the unique insights and analytics due to rare disease go-to-market models, data analytics, patient services, market access and diagnostic testing needs associated with rare disease brands.  The candidate should be able to manage high performing teams, fostering a collaborative and innovative work environment.</p><p></p><p><b>Essential Requirements</b><b>:</b></p><ul><li>Minimum 8&#43; years of experience in the pharmaceutical or healthcare industry, with a deep understanding of brand management, product lifecycle management and market dynamics</li><li>A bachelor’s degree in business administration, Life Sciences, Data Science or a related field; an MBA or advanced degree is strongly preferred</li><li>Strong background in therapeutic area strategy, product lifecycle management, and early-stage asset planning, ideally with experience in both established and launch products.</li><li>Minimum 5&#43; years of domain expertise in these areas are highly desired: secondary data analytics, data science, primary market research, field analytics and insights, market access and patient service analytics, or other related strategic analytics and management consulting, preferably with rare diseases.</li><li>Expertise in synthesizing complex data from diverse sources to drive actionable, business-aligned insights and inform strategic decisions across the product lifecycle</li><li>Ability to work effectively with cross-functional teams and drive strategic brand initiatives, including ability to influence without authority</li><li>Excellent communication skills, capable of effectively collaborating with senior leadership and aligning diverse teams around strategic goals for IPST.</li><li>Proficiency in insight and hypothesis generation, behavioral science, data science, and primary and secondary research methodologies.</li><li>Ability to thrive in a fast-paced, dynamic environment and adapt to changing business needs and priorities</li></ul><p></p><p><b>Novartis Compensation Summary:</b></p><p>The salary for this position is expected to range between $185,500.00 and $344,500.00 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p></p><p></p><p></p><p></p><p></p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$185,500.00 - $344,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Agility, Brand Analysis, Brand Awareness, Commercial Excellence, Cross-Functional Collaboration, Customer Engagement, Customer Experience, Customer Insights, Data Strategy, Digital Marketing, Go-To-Market Strategy, Healthcare Needs, healthcare outcomes, Influencing Skills, Inspirational Leadership, launch products, Marketing Strategy, Media Campaigns, People Management, Product Marketing, Product Roadmap, Return on Investment (ROI), Stakeholder Engagement, Stakeholder Management {+ 2 more}]]></description><link>http://biotechroles.com/director-decision-science-product-lead-neuroscience-1-of-2-roles-novartis/6a0745902f1861929d2532a6</link><guid isPermaLink="true">http://biotechroles.com/director-decision-science-product-lead-neuroscience-1-of-2-roles-novartis/6a0745902f1861929d2532a6</guid><pubDate>Fri, 15 May 2026 16:10:56 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Director - Strategy & Operations Neuroscience]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI -Hybrid <br><br>This position will be located at the East Hanover, New Jersey site and will not have the ability to be located remotely. This position will require travel as defined by the business (domestic and/ or international).<br><br>Please note that this role would not provide relocation, and only local candidates will be considered.<br><br><br>The role of the Director, NPS Program Strategy &amp; Management is to serve as a leader for product and program strategy in support of patient access to achieve gene therapy product and/or portfolio objectives. This role owns ongoing planning, evaluation/measurement, and optimization of short-term and long-term program performance to enable impact for Novartis and patients. This is inclusive of end-to-end patient and provider journeys, as well as all NPS programs and services (onboarding, co-pay, adherence, e-services, hub operations, product ordering &amp; fulfillment experience, external landscape/monitoring, and shifting market dynamic).  <br>This role requires a highly collaborative and agile leader to liaise with multiple NPS Centers of Excellence and cross-functional teams, including, but not limited to, Product Strategy, Marketing, Market Access, Customer Engagement (Sales), Field Reimbursement, Ethics and Compliance, Legal, Data Analytics, and Training.  Finally, this role is accountable for driving strong business performance.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Your responsibilities will include, but are not limited to:</b></p><ul><li>Lead a core team of cross-functional NPS stakeholders focused on ongoing patient support program refinement and measurement specific to the post-prescription experience in partnership with Program Data Insights and Analytics Center of Excellence (starting and staying on appropriate therapy) </li><li>Serve as NPS subject matter expert on gene therapy &amp; indicated disease states and provide key inputs to Portfolio Strategy &amp; Lifecycle Management Center of Excellence for program designs related to onboarding, co-pay, adherence, e-services, hub operations, and product ordering &amp; fulfillment experience to ensure reconciliation with product P&amp;L and objectives</li><li>Drive integration of NPS priorities and program performance with identified product priorities, strategies and KPIs</li><li>Liaising with NPS Enterprise Intelligence and Insights team to gather insights on external and competitive benchmarking, scanning global best practices and liaising across network internal resources (marketing, sales reps, patient coordinators, reimbursement managers) </li><li>Supports successful implementation of any new services launched/administered for NPS including planning, managing, budgeting and launching along with ensuring adequate staffing for operational support</li><li>Maintain close alignment with NPS Advanced Technology Platform team to ensure that all program design decisions are in alignment with the platform strategy, tactics, and capabilities</li></ul><p></p><p><b>What you’ll bring to the role: </b></p><p>Education: Bachelor’s degree required; Advanced degree MPH, PharmD, MBA, or equivalent preferred</p><p>Experience:</p><ul><li>7&#43; Pharma commercial experience or Healthcare or Consulting, with 2 of those years of experience operating in patient services space and/or market access is preferred</li><li>Ability to connect commercial, financial, and clinical perspectives to develop enhanced value messages and strategies</li><li>Strong written and verbal communication skills, including comfort level with senior management presentations</li><li>Proven track record leading across cross-functional teams</li></ul><p></p><p>Preferred Experience:</p><ul><li>In-depth knowledge and understanding of patient services challenges and opportunities </li><li>Previous consultant or vendor experience</li></ul><p></p><p><br />Novartis Compensation Summary:</p><p></p><p>The salary for this position is expected to range between $185,000 and $344,500 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$185,500.00 - $344,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Asset Management, Business Strategy, Commercial Excellence, Cross-Functional Collaboration, Customer Orientation, Digital Marketing, Healthcare Sector Understanding, Influencing Skills, Inspirational Leadership, Marketing Strategy, Negotiation Skills, Operational Excellence, People Management, Priority Disease Areas Expertise, Product Lifecycle Management (PLM), Product Marketing, Product Strategy, Stakeholder Engagement, Stakeholder Management, Strategic Partnerships]]></description><link>http://biotechroles.com/director-strategy-and-operations-neuroscience-novartis/6a07458f2f1861929d2532a5</link><guid isPermaLink="true">http://biotechroles.com/director-strategy-and-operations-neuroscience-novartis/6a07458f2f1861929d2532a5</guid><pubDate>Fri, 15 May 2026 16:10:55 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Director, Forecasting - Neuroscience]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: <br>#LI-Hybrid<br><br>The Insights and Analytics team is dedicated to enabling improved decision making at Novartis by leveraging superior data to identify actionable insights that drive enhanced performance. We collaborate closely with the US business, bringing insights and challenging ideas to empower smarter, data-driven decision-making. Reporting into the ED Forecasting, the Director, Forecasting – Neuroscience is crucial in developing forecasts that align with brand strategies, ensuring that the organization is well-prepared to navigate market dynamics and capitalize on opportunities.<br><br>The Director, Forecasting – Neuroscience plays a pivotal role in delivering high-quality, timely insights that drive informed decision-making and strategic planning. This position plays a crucial role in supporting launch preparations, guiding teams in performance tracking, and ensuring that forecasts are both realistic and adaptable to changing conditions. <br><br>This role will enable the business organization to drive optimal decisions on investments based on an accurate understanding of brand potential. This individual will work closely with the Business Performance, Decision Science, Data Science and Functional Excellence Reporting teams, ensuring accurate forecast information is disseminated to all relevant stakeholders.<br><br>This position will be located at East Hanover, NJ site and will not have the ability to be located remotely. This position will require 10% travel as defined by the business (domestic and/ or international).<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities:</b></p><ul><li>Develop realistic, transparent, and assumption-driven demand forecasts, challenging assumptions and apply forecasting methodologies to support the brand strategy</li><li>Prepare robust forecast assumptions by leveraging expertise and analogs from in-line Forecasting team and research from Insights and Analytics team</li><li>Support launch preparations and guide the teams to set up clear post-launch performance tracking by creating and monitoring the short-term revenue forecasts, comparable to actuals in future, and recommending adjustments when applicable</li><li>Maintain accountability for high quality, timely service delivery of forecasting analytic service requests, including requests for solutions requiring sophisticated statistical and machine learning approaches</li><li>Ensure consistent delivery of analytics that drive informed decision-making, including the definition and development of models to be used in answering business and operational questions</li><li>Develop new and innovative analytics models / methods for untapped opportunities, enabling the automation of routine measurements</li><li>Create a checklist for best practices on decomposing forecasts into the granular elements at a subnational, segment level and ensure consistency with other forecast leads</li><li>Coordinate with the IC team in CE Ops to provide territory-level growth goals that aggregate up to the national level</li><li>Drive patient count requests for internal comms, external comms, and IR for all US</li><li>Ensure that value assessments address the impact of key market dynamics and that internal events are logically designed and well-documented</li></ul><p></p><p>Novartis seeks an individual with extensive experience in the pharmaceutical or healthcare industry, with a strong understanding of market dynamics and regulatory environments. A proven track record of implementing forecasting strategies and driving business outcomes through data driven insights is crucial for this role. The candidate should excel in driving quality forecasts that align closely with actual outcomes.</p><p></p><p><b>Essential Requirements</b><b>:</b></p><ul><li>A Bachelor&#39;s degree in Business Administration, Statistics, Data Science, Economics, or a related field; an MBA or advanced degree is preferred</li><li>Minimum 8&#43;years of experience in forecasting, analytics, and strategic planning, or a similar role within the pharmaceutical or healthcare industry</li><li>Commitment to driving and enabling data-driven decision making throughout all levels of the organization</li><li>Experience in developing and applying various forecasting methodologies to support brand strategies and business objectives in the context of the pharmaceutical industry</li><li>Demonstrated experience in fostering a culture of innovation and continuous improvement, developing new models and methods to enhance forecasting accuracy and efficiency</li><li>Experience in managing multiple projects simultaneously, ensuring timely delivery and alignment with business goals</li><li>Experience in managing relationships with key stakeholders, including senior leadership and external partners</li><li>Ability to work effectively with cross-functional teams and drive strategic initiatives</li><li>Excellent verbal and written communication skills to articulate and present forecast results to key stakeholders persuasively</li><li>Strong analytical and problem-solving skills with the ability to interpret complex data and generate actionable insights</li><li>Proficiency in data analysis, statistical modeling, and machine learning techniques</li><li>Ability to thrive in a fast-paced, dynamic environment and adapt to changing business needs and priorities</li></ul><p></p><p><b>Novartis Compensation Summary:</b></p><p>The salary for this position is expected to range between $185,500.00 and $344,500.00 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p></p><p></p><p></p><p></p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$185,500.00 - $344,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Agility, Brand Analysis, Brand Awareness, Commercial Excellence, Cross-Functional Collaboration, Customer Engagement, Customer Experience, Customer Insights, Data Strategy, Digital Marketing, Go-To-Market Strategy, Healthcare Needs, healthcare outcomes, Influencing Skills, Inspirational Leadership, launch products, Marketing Strategy, Media Campaigns, People Management, Product Marketing, Product Roadmap, Return on Investment (ROI), Stakeholder Engagement, Stakeholder Management {+ 2 more}]]></description><link>http://biotechroles.com/director-forecasting-neuroscience-novartis/6a07458f2f1861929d2532a4</link><guid isPermaLink="true">http://biotechroles.com/director-forecasting-neuroscience-novartis/6a07458f2f1861929d2532a4</guid><pubDate>Fri, 15 May 2026 16:10:55 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Omnichannel Engagement Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Omnichannel Engagement Manager<br><br>Location: Cairo, Egypt<br> <br>#Hybrid<br><br>About the Role:<br>Join us in shaping the future of customer engagement within different specialties across Egypt. The OCE manager key accountability is to manage Novartis relation with mass number of HCPs from targeted specialty to deliver valuable knowledge and promote our brands through digital engagement model (digital tools only). They must have a deep understanding in the respective disease strategy. Maintain and enhance knowledge of disease areas, products, product strategy, positioning, key messages, programs, company developments, customers, and competitors.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major accountabilities: </b></p><ul><li><p>Identify market insights and opportunities through customer interactions, while scouting centers, key opinion leaders (KOLs), and opinion leaders (OLs) by disease within the assigned territory.</p></li><li><p>Execute marketing activities at both central and regional levels, collaborating with Marketing and Medical teams to maximize impact and address specific needs for each patient segment.</p></li><li><p>Monitor product performance and external environment using appropriate tools, taking corrective actions when necessary to achieve business objectives and ensure alignment with market dynamics.</p></li><li><p>Monitor and control brand budgets, forecasts and expenses and assess the marketing mix of the product to evaluate cost effectiveness and results.</p></li><li><p>Strong ability to design and orchestrate a full omnichannel engagement experience.</p></li></ul><ul><li><p>Deliver exceptional customer experience through orchestrating the Omni-channels ‘customer engagements and delivering personalized content (Right message/content, Right channel, Right time) to address the customer needs within the specific customer journey.</p></li><li><p>Experimenter for different engagement models, sharing feedback and insights and suggestions for improvement.</p></li><li><p>Continuously assessing Customer Experience (CX) and promptly attending to Customer feedback and suggestions.</p></li><li><p>In depth understanding of patient journey pains and gains.</p></li></ul><p></p><p><b>Minimum Requirements: </b></p><ul><li><p>Bachelor&#39;s degree in any discipline.</p></li><li><p>Minimum 3 years of experience in digital marketing or Customer Digital Engagement in pharmaceutical industry</p></li><li><p>Digital Savvy and demonstrated ability to use digital tools</p></li><li><p>Strong communication skills with ability to collaborate cross functionally</p></li><li><p>Fluency in English and Arabic Languages</p></li></ul><p></p><p></p><p><b>Commitment to Diversity and Inclusion:</b></p><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.</p><p></p><p><i><span>Novartis is a proud member of the</span></i><a href="http://www.businessanddisability.org/members/" target="_blank"><i><span> ILO Global Business and Disability Network</span></i></a><i><span> and the </span></i><a href="https://www.thevaluable500.com/members" target="_blank"><i><span>Valuable 500</span></i></a><i><span>, promoting the inclusion of people with disabilities in workplaces around the world. We also collaborate with international partners, such as </span></i><a href="https://disabilityin.org/" target="_blank"><i><span>Disability:IN</span></i></a><i><span>, </span></i><a href="https://www.purplespace.org/" target="_blank"><i><span>Purple Space</span></i></a><i><span>, and </span></i><a href="https://businessdisabilityforum.org.uk/" target="_blank"><i><span>Business Disability Forum</span></i></a><i><span> to identify and develop best practice solutions to enable people with disabilities to participate as equal members of our organization.</span></i></p><p></p><p><u>tc.</u></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Analytical Thinking, Brand Awareness, Cross-Functional Collaboration, Digital Marketing, Marketing Strategy, Media Campaigns, Project Management, Project Planning, Sales, Stakeholder Engagement, Strategic Marketing]]></description><link>http://biotechroles.com/omnichannel-engagement-manager-novartis/6a07458f2f1861929d2532a3</link><guid isPermaLink="true">http://biotechroles.com/omnichannel-engagement-manager-novartis/6a07458f2f1861929d2532a3</guid><pubDate>Fri, 15 May 2026 16:10:55 GMT</pubDate><company>Novartis</company><location>New Cairo</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Director, Precision Medicine Data Science & AI]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: <br>#LI-Hybrid<br><br>This role sits at the intersection of AI/ML, real-world data, digital health, and commercial pharma strategy within the Strategy, Platforms &amp; Transformation Personalized &amp; Precision Medicine (PPM) team. The Director will architect, develop, deploy, and scale patient identification models, HCP prioritization algorithms, and site-of-care analytics across Novartis's US portfolio.<br><br>This is a multidisciplinary role requiring deep technical expertise in machine learning, hands-on implementation experience in healthcare/clinical settings, and the strategic acumen to manage external partnerships with health systems, AI/CDS vendors, real-world data aggregators, and digital health developers. The successful candidate thrives in ambiguity, operates with a high degree of independence, and brings a builder mindset to an evolving precision medicine function.<br><br>This position will be located at East Hanover, NJ site and will not have the ability to be located remotely. This position will require 10% travel as defined by the business (domestic and/ or international)<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities:</b></p><ul><li>Lead end-to-end development and deployment of patient identification, HCP targeting AI/ML, ensuring clinical validity and commercial impact across therapeutic areas.</li><li>Design clinical decision support (CDS) algorithms to improve patient outcomes via accelerating time to diagnosis, and treatment leveraging real-world data sources including claims, EHR, lab, genomic, patient generated health data, and registry data. Own and advance external partnership strategies with health systems, AI/CDS vendors to integrate these algorithms into clinical workflows leading to measurable impact on clinical outcomes.</li><li>Architect scalable model lifecycle frameworks — from ideation through development, validation, deployment, monitoring, optimization, and sunsetting — ensuring governance, fairness, and reproducibility.</li><li>Navigate regulatory and compliance requirements related to AI/ML in healthcare, including FDA CDS guidance frameworks, HIPAA, and anti-kickback safe harbor considerations.</li><li>Collaborate cross-functionally with Brand/Marketing, Medical Affairs, HEOR, Legal/Compliance, Field Teams, and Patient Support to translate clinical and commercial needs into actionable AI/ML solutions.</li><li>Drive integration of advanced AI technologies including large language models (LLMs), generative AI, deep learning, and foundation models into precision medicine workflows where applicable.</li><li>Develop go-to-market frameworks and field activation resources that enable model-adjacent materials for commercial teams to act on model outputs.</li><li>Champion a culture of experimentation, continuous improvement, and scientific rigor — contributing to peer-reviewed publications, conference presentations, and open-source model externalization where appropriate.</li><li>Operate with a high level of autonomy and self-direction, proactively identifying opportunities, managing ambiguity, and driving initiatives forward without close supervision.</li><li>Serve as a thought leader within Strategy, Platforms &amp; Transformation and across the Novartis US organization on the convergence of AI, real-world data, and precision medicine in commercial pharma.</li></ul><p></p><p><b>Essential Requirements</b><b>:</b></p><ul><li>Master&#39;s degree required; PhD or doctoral degree preferred. Relevant fields: Data Science, Computer Science, Bioinformatics, Health Informatics, Computational Biology, Statistics, Epidemiology, or related quantitative/health sciences discipline. Clinical or health-focused education or research background is a plus.</li><li>Minimum 10&#43; years of experience in data science, AI/ML, or digital health, with at least 5 years in pharmaceutical, medical device, health-tech, or digital health settings.</li><li>Demonstrated hands-on expertise building and deploying machine learning models (classification, NLP, deep learning, recommendation systems) using Python, Spark, TensorFlow, PyTorch, or equivalent.</li><li><i>Experience designing and executing model validation frameworks — ensuring accuracy, reliability, clinical validity, and reproducibility of AI/ML algorithms prior to clinical or commercial deployment</i></li><li>Proven experience with cloud-based ML infrastructure (AWS, Azure, GCP) for scalable model deployment.</li><li>Deep working knowledge of healthcare data: EHR (structured and unstructured), medical/pharmacy claims, lab results, genomic data, and patient registries.</li><li><i>Working knowledge of clinical terminologies and coding systems (e.g., ICD-10, SNOMED CT, LOINC, RxNorm, CPT) used in model feature engineering and clinical data interpretation</i></li><li><i>Proven ability to communicate complex AI/ML concepts and strategies to senior executive leadership and non-technical audiences, translating technical outputs into business value narratives.</i></li><li>Experience implementing or partnering on AI/ML solutions in clinical or healthcare delivery settings, including clinical decision support integration into EHR workflows.</li><li>Track record managing external partnerships with health systems, AI/CDS vendors, EHR platforms, data aggregators, or digital health companies.</li><li>Working knowledge of regulatory and compliance landscape for AI in healthcare: FDA CDS frameworks, HIPAA, anti-kickback statutes.</li><li>Experience working in complex, matrixed organizational environments with demonstrated ability to influence without authority across commercial, medical, legal, and technical stakeholders.</li><li>Knowledge of large language models (LLMs) such as GPT, BERT, Cohere, and their practical applications in healthcare and commercial pharma.</li></ul><p></p><p><b>Desirable Requirements:</b></p><ul><li>External thought leadership (publications, conference presentations, industry working groups) is a plus.</li></ul><p></p><p><b>Novartis Compensation Summary:</b></p><p>The salary for this position is expected to range between $194,600.00 and $361,400.00 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p></p><p></p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$194,600.00 - $361,400.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agile (Programming Methodology), Artificial Intelligence (AI), Business Value Creation, Change Management, Curious Mindset, Data Governance, Data Literacy, Data Quality, Data Science, Data Strategy, Data Visualization, Deep Learning, Learning Agility, Machine Learning (ML), Machine Learning Algorithms, Mentorship, Nlp (Neuro-Linguistic Programming) And Genai, Organization Awareness, Stakeholder Engagement, Statistical Analysis, Time Series Analysis, Vision, Visualization]]></description><link>http://biotechroles.com/director-precision-medicine-data-science-and-ai-novartis/6a07458e2f1861929d2532a2</link><guid isPermaLink="true">http://biotechroles.com/director-precision-medicine-data-science-and-ai-novartis/6a07458e2f1861929d2532a2</guid><pubDate>Fri, 15 May 2026 16:10:54 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Director, Marketing Strategy- CAR-T Immunology]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Lead the marketing vision behind a next‑generation CAR‑T therapy poised to redefine treatment for autoimmune disease. As Director, Marketing Strategy, you will set and drive the end‑to‑end marketing strategy for a CAR‑T cell therapy within Novartis’ Immunology portfolio, translating breakthrough science into human‑centric campaigns, behavioral strategies, and connected experiences. Partnering closely with cross‑functional leaders, you will orchestrate strategy and execution for a product developed using T‑Charge™—Novartis’ next‑generation CAR‑T platform—bringing meaningful innovation to patients living with autoimmune disorders.<br><br>This position is based in East Hanover, NJ and will not have the ability to be located remotely. Please note that Novartis is unable to offer relocation support for this role; please only apply if this location is accessible for you, as only local candidates will be considered. This position will require up to 20% travel as defined by the business (domestic and/or international).<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities: </b></p><ul><li>Lead the development and implementation of the strategic marketing for the brand</li><li>Monitor the product performance, competitive environment and customer base to quickly identify plan changes</li><li>Manage ROI assessments of tactical programs while collaborating with Sales leadership, ensure proper execution throughout the field force(s)</li><li>Lead interactions with extended brand team members including other functional areas (Sales, Managed Markets, Medical, Clinical, Regulatory, Training, and Finance), building consensus/buy-in among these team members</li><li>Present to senior management on strategy and action plans to address competitive threats and/or exogenous market events</li><li>Collaborate with Global on critical brand issues related to development, aligning as appropriate to the global brand strategy.</li><li>Provide leadership to the brand team and extended brand team members including coaching, advising, and developing team members</li><li>Lead the preparation and launch of new indication(s), defining market size, opportunity, forecast, while aligning with Global&#39;s pre-marketing &amp; marketing plans, participating in negotiations and execution of plan</li><li>Oversee market research initiatives as part of brand plans while anticipating market reactions and changes</li><li>Provides strategic leadership with cross-functional GPT members (i.e., DRA, Clinical, TRD, etc.) to ensure cohesion &amp; brand integrity, pricing, safety messaging, pharmacovigilance, regulatory interactions, manufacturing, packaging, distribution and supply forecasting across indications within a disease area</li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li><p>Bachelor&#39;s/undergraduate degree required; MBA in Marketing or a related field preferred</p></li><li><p>Minimum of 8 years of experience in commercial Marketing required; multi-functional experience in pharmaceutical, healthcare or consumer packaged goods preferred</p></li><li><p>Demonstrated experience in utilizing data, insights, analytics, and behaviors into optimizing marketing performance and outcomes.</p></li><li><p>Experience in supporting high performing brands in highly competitive categories within the US; recent launch experience for blockbuster specialty treatments preferred</p></li><li><p>Strong cross-functional leadership and ability to collaborate effectively with various stakeholders and teams including General Management, Communications, Legal, Regulatory, Compliance and Global</p></li><li><p>Excellent written and oral communication skills with the ability to effectively communicate complex ideas and information to a range of audiences and stakeholders</p></li><li><p>Strong track record of developing talent and building high performing teams</p></li><li><p>Understanding of complex brands within a specialty distribution.</p></li><li><p>Ability to navigate regulatory, compliance, and legal environments to launch new programs.</p></li></ul><p></p><p><b>Desirable Requirements:</b></p><ul><li><p>Experience in all aspects of marketing across the early product lifecycle (pre-launch and launch)</p></li><li><p>Familiarity with agile approaches to marketing strategy and execution</p></li></ul><p></p><p><b>Novartis Compensation Summary<span>:</span></b></p><p>The salary for this position is expected to range between $185,500 and $344,500 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><ul></ul><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$185,500.00 - $344,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Asset Management, Business Strategy, Commercial Excellence, Cross-Functional Collaboration, Customer Orientation, Digital Marketing, Healthcare Sector Understanding, Influencing Skills, Inspirational Leadership, Marketing Strategy, Negotiation Skills, Operational Excellence, People Management, Priority Disease Areas Expertise, Product Lifecycle Management (PLM), Product Marketing, Product Strategy, Stakeholder Engagement, Stakeholder Management, Strategic Partnerships]]></description><link>http://biotechroles.com/director-marketing-strategy-car-t-immunology-novartis/6a07458e2f1861929d2532a1</link><guid isPermaLink="true">http://biotechroles.com/director-marketing-strategy-car-t-immunology-novartis/6a07458e2f1861929d2532a1</guid><pubDate>Fri, 15 May 2026 16:10:54 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Senior Product Specialist]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>As a Product Specialist at Novartis, you’ll build strong relationships with healthcare professionals and deliver solutions that make a real difference for patients. By personalizing your approach, using data, and working closely with your team, you’ll help us achieve our mission—making every interaction and outcome matter.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Job Title-Senior Product Specialist</b></p><p><b>#LI-Remote </b></p><p><b>Job Location-Chandigarh</b></p><p><b>Key Responsibilities</b></p><ul><li><p>Drive sales of priority oncology molecules across premium pharma accounts and hospital networks</p></li><li><p>Build strong relationships with key decision-makers and KOLs to support product adoption</p></li><li><p>Manage state government business including tenders, empanelment, and institutional access</p></li><li><p>Ensure product availability in hospitals and support stock liquidation and repurchase cycles</p></li><li><p>Generate demand through targeted engagement with doctors and medical service teams</p></li><li><p>Handle both trade and government channels to maximize reach and impact</p></li><li><p>Collaborate with hospitals for medical service empanelment and account activation</p></li><li><p>Use data insights to plan territory actions and optimize sales performance</p></li></ul><p><b>Role Requirements:</b></p><ul><li><p>Minimum 5 years of over all pharma sales experience in Trade/ Institutional, Government Instituitions</p></li><li><p>Strong knowledge of the assigned territory and customer landscape in Chandigarh</p></li><li><p>Bachelor’s degree in science or pharmacy (B.Sc or B.Pharma)</p></li><li><p>Excellent communication and relationship-building skills</p></li><li><p>Proven ability to collaborate across teams and deliver customer value</p></li><li><p>Experience in Medical Oncology, breast cancer portfolio</p></li></ul><p><b>Desirable Requirements</b></p><p>Experience in oncology sales or working with oncology-focused healthcare professionals</p><p>Familiarity with Novartis’ therapeutic portfolio and patient-centric engagement strategies</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Breast Cancer, Breast Oncology, Cancer, Commercial Excellence, Communication Skills, Compliance, Conflict Management, Cross-Functional Coordination, Customer Insights, health care industry, Influencing Skills, Key Account Management, Negotiation Skills, Oncology Sales, Professional Ethics, Relationship Building, Selling Skills, Technical Skills]]></description><link>http://biotechroles.com/senior-product-specialist-novartis/6a07458e2f1861929d2532a0</link><guid isPermaLink="true">http://biotechroles.com/senior-product-specialist-novartis/6a07458e2f1861929d2532a0</guid><pubDate>Fri, 15 May 2026 16:10:54 GMT</pubDate><company>Novartis</company><location>Chandigarh (Territory)</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Manager - International CoE]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>About the role:<br><br>Lead all BPA activities within a country ,unit, or function, a region or globally (depending on the division size), providing insightful and value-added analysis and decision support to the business leadership.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Requirements:</b></p><ul><li>Manage the execution of regional / global strategies for own part of the organization and the correct and timely implementation of BPA processes and policies and ensure adherence thereof.</li><li>Deliver core management reporting and financial planning processes to ensure the effective and timely delivery of insightful, recurring or ad-hoc financial information.</li><li>Lead the development of detailed budget and financial forecasts for use in Global and Regional, country, Business Franchise (BF), and Business Unit (BU) planning.</li><li>Design and maintain early warning systems for financial tracking, ensuring accurate advance warning for all financial results.</li><li>Proactively drive performance and carry out value-added analyses on financial data: Sales trends, Functional Expenses, Other Income and Expenses, Impairment review, Management Cash Flow, Capital Investments, life time costs for projects, NPV etc</li><li>Support the organization’s leadership team with financial analysis (including Risks and Opportunities analysis), cost analysis and control and drive corrective actions.</li><li>Conduct value added analyses, e.g. Resource Allocation, Profitability analyses, Benchmarking to recommend short -and long-term targets and improvement areas.</li><li>Manage and ensure the development of a team of experienced BPA professionals.</li><li>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt</li><li>Distribution of marketing samples (where applicable)</li></ul><p><br /><b>Essential Requirements: </b></p><ul><li><span>CA / MBA Finance, 5-8 years.</span></li><li><span>Advanced Excel skills, Inhouse tools (if Internal), </span></li><li><span>Problem Solving Skills, Self-motivated, ability to drive things Independently</span></li></ul><p></p><p><b>Desirable Requirements: </b></p><ul><li><span>FP&amp;A Exposure</span></li><li><span>Multi-tasking, and MNC exposure</span></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Ability To Influence Key Stakeholders, advance excel, AI Driven, Building Effective Teams, Capital Allocation, Critical Thinking, Data Cleansing / Normalization, Data Visualization, excel, Financial And Management Reporting, Financial Data, Financial Databases, Giving And Receiving Feedback, Insight Generation, Interpersonal Savvy, Managing Ambiguity, Market Understanding, Planning &amp; Analysis, Pmi (Post-Merger Integration), Process Optimization, Rapid Problem Solving, Understanding Value Drivers]]></description><link>http://biotechroles.com/manager-international-coe-novartis/6a07458d2f1861929d25329f</link><guid isPermaLink="true">http://biotechroles.com/manager-international-coe-novartis/6a07458d2f1861929d25329f</guid><pubDate>Fri, 15 May 2026 16:10:53 GMT</pubDate><company>Novartis</company><location>Telangana</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Clinical Quality Assurance - Program Lead (Associate Director)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Employment Type: Full‑time | Regular, Hybrid, #LI-hybrid<br>Location: London (The Westworks) or Dublin (NOCC)<br><br>Novartis is unable to offer relocation support for this role: please only apply if the locations of Westworks, London or Dublin are accessible for you<br><br>The Associate Director, Clinical Quality Assurance (QA) will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to patients’ safety, rights and well-being.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major Accountabilities:</b></p><ul><li><p>Proactively provide QA leadership to the business strategy for assigned programs/trials by ensuring considerable organization awareness (e.g. Interrelationship of departments and business priorities),</p></li><li><p>Drive implementation of quality strategy within Global Clinical Team (GCT )/ Clinical Trial Team (CTT) under responsibility</p></li><li><p>Regularly monitor the implementation of the annual Quality Plan pertaining to the assigned programs/studies</p></li><li><p>Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that Clinical Trial Process (CTP) are in control</p></li><li><p>Provide robust and clear quality oversight in the following areas of clinical development: Support/collaborate with key stakeholders (e.g., Country Development Quality (CDQ), Development Units (DUs), GCT and/or CTT members) to ensure that risks are detected and remediated.Support core governance for quality incident management for critical and major deviations pertinent to the programs being assigned and ensure timely escalation when required.Provide Good Clinical Practice (GCP) guidance to day-to-day questions arising from Clinical trials deliverables.Collaborate with Country Development QA and External Service Providers (ESP) QA to drive initiatives relevant to internal monitoring and outsourced activities Quality oversight.Lead inspections preparation and facilitation in collaboration with other QA groups within Research &amp; Development Quality (RDQ).Support audits and inspections follow-up activities including Corrective &amp; preventative Actions (CAPA) preparation.</p></li><li><p>Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.</p></li><li><p>Active participation in continuous improvement initiatives (including Work streams) and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability</p></li><li><p>Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.</p></li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li><p>Bachelor’s degree in life science or healthcare field required.  Advanced degree or equivalent education/degree in life sciences/healthcare preferred (PhD/MD/ PharmD/ Masters).</p></li><li><p>Extensive experience of involvement in regulated activities (GCP/ Pharmacovigilance (PV)), clinical development and/or QA positions with strong understanding on clinical trials</p></li><li><p>Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product development.</p></li><li><p>Ability to work independently and in a global/matrix environment.</p></li><li><p>Experience in managing projects.</p></li><li><p>Strong skills in GCP, quality and/or clinical development</p></li></ul><p></p><p><b>Why Novartis:</b><span> </span>Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?<span> </span><a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a></p><p></p><p><b>Benefits and Rewards:</b><span> </span>Learn about all the ways we’ll help you thrive personally and professionally.<br /><a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">Read our handbook (PDF 30 MB)</a></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Business Partnering, Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Organizational Saviness, Problem Solving Skills, Regulatory Requirements knowledge, Risk Management, Stakeholder Management]]></description><link>http://biotechroles.com/clinical-quality-assurance-program-lead-associate-director-novartis/6a07458b2f1861929d25329e</link><guid isPermaLink="true">http://biotechroles.com/clinical-quality-assurance-program-lead-associate-director-novartis/6a07458b2f1861929d25329e</guid><pubDate>Fri, 15 May 2026 16:10:51 GMT</pubDate><company>Novartis</company><location>Dublin (NOCC)</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Program manager DDIT PO&CF AskNovartis]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The AskNovartis Enterprise Product Leader is a senior, cross functional role responsible for leading the strategy, delivery, adoption, and continuous improvement of AskNovartis, Novartis’ AI enabled front door for employee services and tasks.<br>AskNovartis is a cornerstone of Novartis’ digital employee experience agenda—shifting the company from fragmented service delivery toward a single, intelligent, self service first experience that enables employees to get work done quickly, consistently, and with minimal friction across DD&amp;IT and corporate functions.<br>The Product Leader is accountable for ensuring AskNovartis delivers measurable employee value across priority journeys and scales responsibly across domains without fragmentation. The role is deliberately dual shaped, reflecting the enterprise nature of AskNovartis:<br>•	Enterprise Product Leader for AskNovartis as a single platform and experience<br>•	Product Lead for the DD&amp;IT domain (Ask IT), accountable for DD&amp;IT service outcomes delivered through AskNovartis<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><div><p><b><span>Location:</span></b><span><span><span> Prague</span></span></span></p><p><b><span>#L</span><span>I</span><span>-Hybrid</span></b><span><span> </span> (</span><span>12 days/month in office)</span></p></div><div><p></p></div><p><b>Key Accountabilities:</b></p><ul><li><b>Platform Strategy &amp; Enterprise Readiness</b> -The Product Leader sets the strategic direction for how AskNovartis evolves—from PoC through MVP and enterprise scale ensuring the platform remains focused on value, trust, and usability as scope expands. This includes maintaining a clear product vision for AskNovartis, prioritizing high‑value, high‑volume employee use cases across domains and governing scope, release sequencing, and go‑live decisions to balance speed with readiness.</li></ul><p></p><ul><li><b>Service Transformation &amp; Ask IT Ownership</b> - As Product Lead for Ask IT, the role drives the transformation of DD&amp;IT services through AskNovartis Key responsibilities include prioritizing DD&amp;IT use cases across areas such as access &amp; identity, devices, network, applications and end‑to‑end automation and service redesign. The role needs to drive automation and ticket elimination through integrations with ServiceNow, Microsoft Intune and other system of records.<b> </b>The focus is on faster resolution and reduced effort for employees.</li></ul><p></p><ul><li><b>Service Design &amp; Knowledge Quality</b>- The Product Leader ensures that DD&amp;IT services are properly defined, structured and reflected in the platform’s service catalog and designed together with service owners. The Product Leader ensures that services and knowledge across participating domains are designed for self‑service and AI‑assisted interaction with clear ownership and maintenance models, so quality is sustained over time. In this role, strong service and knowledge design is foundational to drive the long‑term scalability of AskNovartis.</li></ul><p></p><ul><li><b> </b><b>Adoption, Experience &amp; Deployment</b> -The Product Leader is accountable for AskNovartis becoming the default employee entry point for prioritized services and tasks. The leader needs to ensure adoption is designed into product strategy and release planning, aligning priorities and sequencing across domains and channels. Central enablement and change teams lead execution, the Product Lead ensures the product experience and value proposition justify adoption at scale.</li></ul><p></p><ul><li><b>Testing and Quality Assurance</b> - The product leader is responsible for the testing with end users of all DD&amp;IT related services, queries and workflows on the platform – validating that AI generated answers, routing logic and ticket management flows perform correctly. Leading organisations show that a human expert in the loop approach ensures minimized back and forth between employees and IT support teams.</li></ul><p></p><ul><li><b>AI Trust &amp; Platform Integration</b> -The Product Leader ensures that AI‑enabled interactions within AskNovartis meet enterprise standards for transparency, usability, trust, and control. The role partners closely with platform, architecture, and engineering teams to ensure AskNovartis integrates cleanly with enterprise systems such as ServiceNow, Workday, and Intune, and remains production‑grade as capabilities expand.</li></ul><p></p><ul><li><b>Partner &amp; Investment Governance</b> -The Product Leader governs a multi‑partner ecosystem to scale delivery capacity while maintaining clear accountability and enterprise ownership. Responsibilities include shaping investment cases across phases (PoC, MVP, scale) and aligning co‑funding across DD&amp;IT and participating domains. The role also involves tracking value realization through adoption, automation and experience outcomes</li><li></li></ul><p><b>Commitment to Diversity and Inclusion:</b></p><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</p><p></p><p><b>What you will receive:</b></p><p>Monthly pension contribution matching your individual contribution up to 3% of your gross monthly base salary; Risk Life Insurance (full cost covered by Novartis); 5-week holiday per year; (1 week above the Labour Law requirement) ; 4 paid sick days within one calendar year in case of absence due to sickness without a medical sickness report; Cafeteria employee benefit program – choice of benefits from Benefit Plus Cafeteria in the amount of 17,500 CZK per year; Meal vouchers in amount of 90 CZK for each working day (full tax covered by company); transportation allowance; MultiSport Card. Find out more about Novartis Business Services: <a href="https://www.novartis.cz/" target="_blank">https://www.novartis.cz/</a></p><p></p><p><b>Accessibility and accommodation:</b><br />Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</p><p><b>Why Novartis:</b> Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a></p><p></p><p><b>Benefits and Rewards:</b> Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">https://www.novartis.com/careers/benefits-rewards</a></p><p></p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Budget Management, Business Acumen, Digital capabilities, Effective use of technology, Operational Excellence Projects, Performance Management, Project Management, Risk Management, Service Delivery Management, Stakeholder Management, Strategic Leadership, Strategic Planning, Talent Development]]></description><link>http://biotechroles.com/program-manager-ddit-poandcf-asknovartis-novartis/6a07458b2f1861929d25329d</link><guid isPermaLink="true">http://biotechroles.com/program-manager-ddit-poandcf-asknovartis-novartis/6a07458b2f1861929d25329d</guid><pubDate>Fri, 15 May 2026 16:10:51 GMT</pubDate><company>Novartis</company><location>Prague</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[QA Officer Operations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>-Manages Quality aspects and projects within area of responsibility. <br>-Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major Accountabilities:</b></p><ul><li>QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &amp; cleanliness zones, Functional Breadth, Collaborating across boundaries</li><li>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt</li><li>Distribution of marketing samples (where applicable)</li></ul><p><br /><b>Key Performance Indicators:</b></p><ul><li>On-time and GMP-compliant release of dosage forms</li><li>No complaints about inspections by authorities in your own area of responsibility without these being noticed &amp; communicated beforehand</li><li>Successfully support continuous improvement projects&lt;LI&gt;Executes batch release in compliance with registration</li></ul><p><br /><b>Work Experience:</b></p><ul><li>Quality Assurance</li><li>Quality Control</li><li>Quality Management Systems</li><li>Technological Expertise</li><li>Environmental Monitoring</li><li>Release Management</li><li>Good Manufacturing Practices (cGMP)</li><li>Audit &amp; Inspection Management</li><li>Quality Compliance</li><li>Technological Expertise</li></ul><p><br /><b>Skills:</b></p><ul><li>Collaboration</li><li>Dealing With Ambiguity</li><li>Operational Excellence</li><li>Regulatory requirements knowledge</li><li>Problem Solving Skills</li><li>Leadership</li><li>Communication skills</li><li>Data Integrity</li><li>Digital saviness</li></ul><p></p><p><b>Languages:</b></p><ul><li>English.</li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge]]></description><link>http://biotechroles.com/qa-officer-operations-novartis/6a07458b2f1861929d25329c</link><guid isPermaLink="true">http://biotechroles.com/qa-officer-operations-novartis/6a07458b2f1861929d25329c</guid><pubDate>Fri, 15 May 2026 16:10:51 GMT</pubDate><company>Novartis</company><location>Zaragoza</location><salary>$55000-80000</salary><type>Full time</type></item><item><title><![CDATA[Senior Analyst, CRM, Data Integrations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>We are seeking a Senior Analyst, CRM to support the integration and migration of CRM platforms, data, and field force operations as part of a large-scale acquisition and platform change programs. This role focuses on ensuring that CRM data, configurations, business logic, and field-facing functionality are assessed, mapped, and migrated into the target organization's / target platform’s CRM ecosystem with minimal disruption to field operations and customer engagement.<br><br>The individual will act as a bridge between CRM product teams, data engineering, field operations, and business stakeholders from both entities — coordinating data integration requirements, managing enhancement and release readiness during transition, and ensuring data quality and adoption continuity throughout the migration lifecycle.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><div><p><b>Key Responsibilities: </b></p><p><b>Location: Hyderabad # Hybrid</b></p><ul><li><b>CRM discovery &amp; documentation</b> of the current platform configuration (data model, automation, rules) and integration touchpoints</li><li><b>Cross-platform mapping &amp; gap analysis</b> between source and target CRM (field definitions, business logic), producing a field-level crosswalk</li><li><b>Integration coordination</b> across upstream data teams (for example master data and segmentation) and downstream consumers (analytics, reporting, dashboards)</li><li><b>Migration wave readiness &amp; coordination</b>, including timelines, testing dependencies, stakeholder communication, and roadmap support</li><li><b>Testing &amp; quality assurance</b> across unit/integration/UAT with defined data-quality checkpoints</li><li><b>Adoption &amp; change support</b> post-migration, tracking usage, addressing adoption gaps, and reinforcing governance</li><li><b>Continuous improvement</b> to strengthen data quality, streamline integrations, and improve field user experience</li></ul></div><p></p><p><b>Essential Requirements:</b></p><div><ul><li>Education: Bachelor’s degree in a relevant discipline</li><li>Experience: 3–5&#43; years with field CRM platforms (Veeva, Salesforce Health Cloud, IQVIA OCE, etc.)</li><li>Strong understanding of pharma field operations (call planning, territory alignment, sample management, closed-loop marketing)</li><li>Practical knowledge of CRM data models and configuration (objects, relationships, workflows, validation rules)</li><li>Proven experience in CRM migration / platform transition / system consolidation (not just BAU administration)</li><li>Hands-on exposure to data mapping and field-level crosswalk creation</li><li>Experience coordinating end-to-end data integration flows (MDM, segmentation, analytics, reporting)</li><li>Exposure to testing and quality assurance in migration contexts (UAT, defect tracking, test plans)</li><li>Strong analytical mindset and ability to support data-driven decisions. Strong communication &amp; stakeholder coordination skills . High attention to detail and documentation rigor.</li></ul><p></p></div><p><b>Desirable Requirement:</b></p><ul><li><p>CRM platform certifications (e.g., Salesforce Admin, Veeva CRM certification, or equivalent).</p></li><li><p>Prior experience in <b>US or global field operations teams</b> within the pharma/life sciences industry.</p></li><li><p>Experience with <b>CRM-adjacent systems</b> such as alignment/roster tools, incentive compensation, content management (CLM/Approved Email), or sample accountability platforms.</p></li></ul><p></p><p><span><span><b>Commitment to Diversity &amp; Inclusion</b></span></span></p><p><span><span>We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</span></span></p><p><span> </span></p><p><span><span><b>Accessibility and accommodation</b></span></span></p><p><span><span>Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Advertising Campaigns, Alteryx, Analytical Thinking, Brand Awareness, Business Networking, Curiosity, Digital Marketing, Marketing Communications, Marketing Plans, Marketing Strategy, Media Campaigns, Process Documentation, Statistical Analysis, Strategic Marketing]]></description><link>http://biotechroles.com/senior-analyst-crm-data-integrations-novartis/6a07458a2f1861929d25329b</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-crm-data-integrations-novartis/6a07458a2f1861929d25329b</guid><pubDate>Fri, 15 May 2026 16:10:50 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$30000-50000</salary><type>Full time</type></item><item><title><![CDATA[Senior Analyst, Master Data Management, Data Integrations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>We are seeking an experienced Senior Analyst, Master Data Management to play a critical role in the integration and migration of master data domains as part of a large-scale acquisition and platform migration programs. This role sits at the intersection of data governance, data quality, and business stakeholder engagement, ensuring that master data from one entity is profiled, reconciled, harmonized, and migrated into the target organization's / target platform’s MDM ecosystem with full golden record integrity.<br><br>The role will be responsible for managing the end-to-end lifecycle of master data during the integration — from discovery and overlap analysis through to matching, survivorship resolution, conflict adjudication, and post-cutover validation. This individual will work across multiple data domains (e.g., customer, product, account, healthcare provider/organization, territory, hierarchy) and will partner closely with domain owners, data engineers, governance leads, and business stakeholders.<br><br>This role demands not only deep MDM expertise but also the ability to operate in ambiguity — navigating differences in data standards, business rules, platform capabilities, and organizational culture that are inherent to any large scale organizational / platform integration. The ideal candidate brings a structured yet adaptable approach to data stewardship in high-complexity, time-sensitive migration programs.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location: Hyderabad #Hybrid</b></p><p><b>Key Responsibilities</b></p><div><ul><li><b>Discovery &amp; profiling:</b> Baseline data quality metrics (completeness, uniqueness, referential integrity), inventory assets, document dependencies, capture tribal knowledge/workarounds.</li><li><b>Overlap analysis &amp; reconciliation:</b> Duplicate/overlap analysis using match keys (IDs, tax IDs, MDM IDs), quantify conflicts, run reconciliation workshops, define survivorship/exception rules.</li><li><b>Migration execution &amp; stewardship:</b> Own DCR workflow end-to-end (intake → triage → validation/enrichment → approvals → execution), run match/merge/survivorship, steward queues/SLAs, update reference data.</li><li><b>Business rules translation:</b> Harmonize business rules and mastering logic across functions; document matching algorithms, survivorship hierarchies, validation logic; drive resolution of rule conflicts via governance.</li><li><b>Validation &amp; QA:</b> Reconciliation protocols by wave (counts, field-level checks, hierarchy integrity, downstream impact), operational reporting (KPIs, backlogs, exception trends).</li><li><b>Governance &amp; continuous improvement:</b> Metadata/data dictionary/glossary registration in enterprise catalog; propose AI/automation use cases (duplicate detection, DCR triage, anomaly detection, prioritization).</li></ul><p></p><p><b>Essential Requirements</b></p></div><div><ul><li><b>Experience:</b> 4&#43; years in MDM/data stewardship/data operations, including <b>at least 2 years</b> in migration/integration context.</li><li><b>Hands-on MDM:</b> Experience with one or more MDM platforms (examples provided: Informatica, Reltio, SAP MDG, Semarchy, Profisee).</li><li><b>MDM concepts depth:</b> Matching algorithms, survivorship, hierarchy management, reference data governance, trust scoring, golden record lifecycle.</li><li><b>Technical:</b> SQL &#43; data profiling tools; familiarity with APIs and ETL/ELT/integration patterns; understanding of downstream systems (CRM/ERP/BI/marketing).</li><li><b>Governance:</b> Working knowledge of data governance frameworks (classification, ownership/RACI, metadata management).</li><li><b>Scale &amp; complexity:</b> Demonstrated overlap analysis &#43; survivorship strategy &#43; reconciliation at scale (100K&#43; records), in ambiguity/time-bound environments.</li><li><b>Industry context:</b> Regulated industry exposure preferred; strong preference called out for <b>pharma/life sciences commercial data domains</b> (HCP/HCO, product, territory/alignment).</li><li><b>Ways of working:</b> Strong facilitation (workshops), stakeholder communication (incl. senior), strong documentation and analytical rigor.</li></ul></div><p></p><p><b>Desirable Reequipments:</b></p><div><ul><li>MDM tool-to-tool migration experience (e.g., Informatica → Reltio).</li><li>Cloud data platforms familiarity (Snowflake/Databricks/Azure Synapse) and cloud-native data architectures.</li></ul><p></p><p><span><span><b>Commitment to Diversity &amp; Inclusion</b></span></span></p><p><span><span>We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</span></span></p><p><span> </span></p><p><span><span><b>Accessibility and accommodation</b></span></span></p><p><span><span>Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></span></p></div><p></p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Advertising Campaigns, Alteryx, Analytical Thinking, Brand Awareness, Business Networking, Curiosity, Digital Marketing, Marketing Communications, Marketing Plans, Marketing Strategy, Media Campaigns, Process Documentation, Statistical Analysis, Strategic Marketing]]></description><link>http://biotechroles.com/senior-analyst-master-data-management-data-integrations-novartis/6a07458a2f1861929d25329a</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-master-data-management-data-integrations-novartis/6a07458a2f1861929d25329a</guid><pubDate>Fri, 15 May 2026 16:10:50 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Senior Analyst, BI Visualization, Data Integrations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>We are seeking a Senior Analyst, BI Visualization to support the migration, redesign, and continuity of business intelligence dashboards and reporting solutions as part of a large-scale acquisition and platform change programs. This role ensures that the reporting ecosystem — dashboards, KPI visualizations, field-facing reports, and self-service analytics — is cataloged, mapped, rebuilt, and validated within the target organization's / target platform’s BI infrastructure with zero disruption to business decision-making.<br><br>The individual will work closely with analytics leads, data engineering teams, and business stakeholders from both entities to migrate and re-connect dashboards to new data sources, validate visual and metric accuracy against legacy outputs, and ensure that field, commercial, medical, and leadership reporting is fully operational on the target platform through each migration wave.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location:</b> <b>Hyderabad # Hybrid</b></p><p><b>Key Responsibilities</b></p><ul><li><p><b>Dashboard Discovery &amp; Inventory:</b> Catalog all dashboards, reports, and visualization assets — documenting data sources, refresh schedules, business owners, user audience, access permissions, and criticality tier. Classify each asset as migration-critical (e.g., field-facing, leadership, patient services) vs. deferrable.</p></li><li><p><b>Dashboard Migration &amp; Rebuild:</b> Design, develop, and rebuild dashboard solutions on the target BI platform, re-connecting to migrated data sources (curated/consumption-layer datasets). Ensure that visual design, interactivity, filters, drill-throughs, and calculated measures faithfully replicate reporting experience — or improve upon it where consolidation creates opportunity.</p></li><li><p><b>Data Source Re-Mapping:</b> Work with data engineering teams to map legacy dashboard data connections (tables, views, semantic layers, direct queries) to their equivalents in the target data platform. Validate that underlying datasets are complete, accurate, and refreshing on schedule before connecting dashboards.</p></li><li><p><b>Metric Validation &amp; Quality Assurance:</b> Execute side-by-side validation of legacy vs. migrated dashboards — comparing KPI values, aggregations, trend lines, filters, and edge cases. Document discrepancies, perform root-cause analysis (data issue vs. calculation logic vs. visualization error), and drive resolution. Maintain quality checklists and SOPs for each migration wave.</p></li><li><p><b>Access &amp; Permissions Configuration:</b> Coordinate with security and governance teams to configure dashboard access, workspace permissions, row-level security, and distribution lists on the target BI platform. Ensure that user access models are translated appropriately to the target organization&#39;s / target platform’s security framework.</p></li><li><p><b>Stakeholder Communication &amp; UAT:</b> Serve as the interface between data/analytics teams and business consumers during dashboard migration. Coordinate UAT with field users, home office teams, and leadership — prepare test scenarios, collect feedback, triage defects, and drive to sign-off. Maintain regular communication on migration progress, timelines, and known issues.</p></li><li><p><b>Documentation &amp; Standardization:</b> Develop, document, and maintain SOPs, quality checklists, and dashboard specification documents for all migrated reporting assets. Identify opportunities to standardize reports across brands, domains, and functions enabled by platform consolidation — reducing redundancy and improving consistency.</p></li><li><p><b>Continuous Improvement:</b> Continuously build technical and analytical capability by adopting new tools, approaches, and methods aligned to the target platform&#39;s evolving capabilities — including AI-powered analytics features where appropriate. Identify reporting enhancements made possible by migration (e.g., richer data, new domains, improved refresh frequency).</p></li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li><p>Bachelor&#39;s degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related field.</p></li><li><p>3&#43; years of hands-on experience in data visualization and BI development, with strong expertise in Power BI (or equivalent enterprise BI platform such as Tableau or QlikSense).</p></li><li><p>Basic to intermediate working knowledge of SQL, Microsoft Excel, PowerPoint, and ETL/data preparation concepts.</p></li><li><p>Good interpersonal and communication skills with the ability to work across technical and business teams.</p></li><li><p>Demonstrated learning agility including the ability to leverage AI-powered tools to improve efficiency in day-to-day tasks.</p></li><li><p>Ability to manage <b>multiple dashboard migrations in parallel</b> across different business domains and stakeholder groups.</p></li></ul><p></p><p><b>Desirable Requirement:</b></p><ul><li><p>Hands-on experience with side-by-side metric validation between legacy and migrated dashboards — including KPI reconciliation, trend comparison, and root-cause analysis for discrepancies.</p></li><li><p>Experience coordinating dashboard UAT with business users — test scenario preparation, feedback collection, defect triage, and sign-off management across multiple stakeholder groups (field, commercial, leadership).</p></li><li><p>Strong focus on documentation, SOPs, and quality checklists — ability to maintain rigorous standards while operating under tight, wave-based migration timelines.</p></li></ul><p></p><p><span><span><b>Commitment to Diversity &amp; Inclusion</b></span></span></p><p><span><span>We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</span></span></p><p><span> </span></p><p><span><span><b>Accessibility and accommodation</b></span></span></p><p><span><span>Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message</span></span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Advertising Campaigns, Alteryx, Analytical Thinking, Brand Awareness, Business Networking, Curiosity, Digital Marketing, Marketing Communications, Marketing Plans, Marketing Strategy, Media Campaigns, Process Documentation, Statistical Analysis, Strategic Marketing]]></description><link>http://biotechroles.com/senior-analyst-bi-visualization-data-integrations-novartis/6a07458a2f1861929d253299</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-bi-visualization-data-integrations-novartis/6a07458a2f1861929d253299</guid><pubDate>Fri, 15 May 2026 16:10:50 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Senior Analyst, Brand Data Enablement, Data Integrations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>We are seeking a Senior Analyst, Brand Data Enablement to support the migration, integration, and continuity of brand-level data enablement deliverables as part of a large-scale acquisition and platform change programs. This role ensures that the brand data products, operational datasets, and performance reporting pipelines are assessed, translated, and re-established within the target organization's / target platform’s data and infrastructure ecosystem — without disruption to brand teams' decision-making capabilities.<br><br>The individual will work across brand operations, data engineering, and analytics functions from both entities, ensuring that commercial datasets, brand KPI frameworks, and enablement workflows are mapped, migrated, and validated through evolving infrastructure landscapes. This role requires a blend of data enablement expertise, pharma commercial domain knowledge, and the structured execution discipline essential to data &amp; platform integration programs.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location:</b> Hyderabad #Hybrid</p><p><b>Key Responsibilities</b></p><ul><li><p><b>Brand Data Discovery &amp; Inventory:</b> Catalog all brand-level data enablement deliverables — including datasets, KPI outputs, recurring reports, SOPs, and operational workflows. Document data sources, refresh cadence, business owners, downstream consumers, and quality standards for each deliverable.</p></li><li><p><b>Data Enablement Migration:</b> Design, develop, and maintain data enablement solutions that translate brand performance datasets into the target organization&#39;s infrastructure. Ensure that commercial data feeds (e.g., prescription data, promotional activity, patient-level data, specialty pharmacy, affiliations) are re-mapped and re-connected on the target platform with full fidelity.</p></li><li><p><b>Cross-Entity Dataset Reconciliation:</b> Map commercial data sources to the target organization&#39;s equivalent datasets (e.g., patient-level data, prescription audits, promotional feeds, third-party syndicated data). Identify gaps, overlaps, and definition conflicts. Produce field-level crosswalk documents and drive alignment with relevant stakeholders.</p></li><li><p><b>Quality &amp; SOP Management:</b> Maintain and adapt standard operating procedures (SOPs) and quality checklists for all brand enablement outputs during migration. Ensure that data quality checkpoints are preserved or enhanced as deliverables move from legacy to target infrastructure. Define acceptance criteria for each migrated deliverable.</p></li><li><p><b>Validation &amp; Delivery:</b> Deliver migrated brand enablement outputs as per agreed timelines, accuracy, and quality standards. Execute side-by-side validation of legacy vs. migrated outputs — including metric reconciliation, trend continuity, and edge case testing. Coordinate with brand stakeholders for UAT and sign-off.</p></li><li><p><b>Stakeholder Communication &amp; Coordination:</b> Maintain exemplary communication with all partners — brand teams, data engineering, analytics, and leadership — through regular updates focused on migration progress, quality metrics, risks, and key milestones. Support leads with appropriate documentation throughout the delivery lifecycle.</p></li><li><p><b>Knowledge Sharing &amp; Continuous Improvement:</b> Participate in and contribute to cross-team knowledge sharing sessions to propagate migration learnings, improve quality deliverables, and accelerate enablement for all brands/teams transitioning to the new platform. Identify opportunities to standardize and improve brand data products enabled by platform consolidation.</p></li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li><p>3–5 years of experience in a data enablement role, preferably in US pharma commercial operations.</p></li><li><p>Familiarity with data tools such as SQL, Dataiku, Power BI, Python, and project management tools (e.g., Jira).</p></li><li><p>Exposure to US pharma commercial datasets such as patient-level data (APLD), specialty pharmacy (SP), prescription audits (e.g., IQVIA Xponent), claims/diagnosis data, promotional activity, HCP affiliations, and CRM data.</p></li><li><p>Experience developing and coordinating project plans across design, development, and production stages with delivery against defined KPIs.</p></li><li><p>Strong collaboration skills with cross-functional teams including brand, technical, analytics, and data engineering functions.</p></li><li><p>Strong communication and presentation skills with good learning agility and an analytical mindset.</p></li></ul><p></p><p><b>Desirable Requirement:</b></p><ul><li><p>Demonstrated experience in migrating or re-building brand data enablement deliverables during a platform transition, data and platform integration, or large-scale infrastructure change — not just steady-state delivery.</p></li><li><p>Proven ability to map and reconcile commercial pharma datasets across two entities or platforms — including field-level crosswalks for prescription data, patient-level data, promotional feeds, and third-party syndicated sources.</p></li><li><p>Hands-on experience with data quality management during transitions — maintaining SOPs, quality checklists, and validation protocols while underlying infrastructure is changing.</p></li></ul><p></p><p><span><span><span><span><b>Commitment to Diversity &amp; Inclusion</b></span></span></span></span></p><p><span><span><span><span>We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</span></span></span></span></p><p><span><span><span> </span></span></span></p><p><span><span><span><span><b>Accessibility and accommodation</b></span></span></span></span></p><p><span><span><span><span>Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></span></span></span></p><p><span><span><span><span> </span></span></span></span></p><p><span><span><span> </span></span></span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Advertising Campaigns, Alteryx, Analytical Thinking, Brand Awareness, Business Networking, Curiosity, Digital Marketing, Marketing Communications, Marketing Plans, Marketing Strategy, Media Campaigns, Process Documentation, Statistical Analysis, Strategic Marketing]]></description><link>http://biotechroles.com/senior-analyst-brand-data-enablement-data-integrations-novartis/6a07458a2f1861929d253298</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-brand-data-enablement-data-integrations-novartis/6a07458a2f1861929d253298</guid><pubDate>Fri, 15 May 2026 16:10:50 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Director, Internal Audit, TechOps]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Location: Barcelona, Spain<br><br>You will play a pivotal role in safeguarding and strengthening Novartis’ Technical Operations by providing independent, strategic assurance across manufacturing and supply. As Director, Internal Audit, TechOps, you will lead complex, high‑impact audit and advisory engagements that shape how risks are identified, mitigated, and managed across end‑to‑end operations. Partnering closely with senior and executive stakeholders, you will bring deep operational insight, sound judgment, and a forward‑looking mindset to influence better outcomes, advance audit innovation, and help ensure we continue to deliver quality medicines to patients worldwide.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key responsibilities:</b></p><ul><li><p>Oversee and provide overall direction for complex, risk‑based audit and advisory engagements across manufacturing and supply operations</p></li><li><p>Ensure audit scopes address end‑to‑end Technical Operations risks, including quality, compliance, technology, and third‑party models</p></li><li><p>Support audit planning and audit program development by identifying key Manufacturing &amp; Supply risks and acting as a technical reference to ensure audit coverage remains risk‑based, relevant, and aligned to business priorities</p></li><li><p>Review audit findings and reports to ensure technical accuracy, clarity, and evidence‑based conclusions</p></li><li><p>Drive pragmatic, value‑adding recommendations that strengthen controls and enable measurable operational improvement</p></li><li><p>Act as a trusted advisor to senior leaders, maintaining independence while fostering constructive, credible partnerships</p></li><li><p>Provide direct line management to Senior Managers, setting clear strategic direction, overseeing performance and development, and ensuring consistent, high‑quality delivery of risk‑focused audit and advisory engagements across Technical Operations</p></li><li><p>Coach and develop auditors through hands‑on guidance, feedback, and knowledge‑sharing in Manufacturing and Supply</p></li><li><p>Advance digital, data‑driven, and artificial intelligence‑enabled audit practices in collaboration with enablement teams</p></li></ul><p></p><p><i>Please be advised that this role has a global travel requirement circa <span>25%.</span></i></p><p></p><p><b>Essential Requirements:</b></p><ul><li><p>Degree in technical or scientific discipline related to manufacturing, supply chain, logistics, or production planning</p></li><li><p>Substantial experience within internal audit functions in highly regulated industries, preferably pharmaceuticals, biotechnology, or medical devices</p></li><li><p>Strong practical knowledge of end-to-end processes in manufacturing operations, supply chain management, quality systems, and external manufacturing models</p></li><li><p>Proven experience leading audit and advisory engagements, managing senior stakeholders, and delivering high‑impact outcomes</p></li><li><p>Solid understanding of pharmaceutical regulations and standards, including Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and global health authority requirements such as FDA, EMA, and other international regulatory bodies</p></li><li><p>Demonstrated ability to operate in complex environments, influence senior leaders, and communicate audit conclusions with confidence and tact</p></li><li><p>Strong people management experience, with a track record of leading, developing, and motivating high‑performing teams.</p></li><li><p>Fluency in English (written and verbal) is required; additional languages are an advantage</p></li></ul><p></p><p><b>Desirable Requirements:</b></p><ul><li><p>Professional internal audit or supply chain certification, such as Certified Internal Auditor or Certified Supply Chain Professional</p></li><li><p>Experience applying data analytics or artificial intelligence‑enabled tools within internal audit or regulated operating environments</p></li></ul><p></p><p><b>Commitment to Diversity and Inclusion </b></p><p></p><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</p><p></p><p></p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Building Effective Teams, Compliance And Controls, Critical Thinking, E2E Process View, Effective Communications, Financial Accounting, Financial And Management Reporting, People Development, Process Optimization, Rapid Problem Solving]]></description><link>http://biotechroles.com/director-internal-audit-techops-novartis/6a0745892f1861929d253297</link><guid isPermaLink="true">http://biotechroles.com/director-internal-audit-techops-novartis/6a0745892f1861929d253297</guid><pubDate>Fri, 15 May 2026 16:10:49 GMT</pubDate><company>Novartis</company><location>Barcelona Gran Vía</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Senior Analysts, Data & Analytics Enablement, Data Integrations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>We are seeking an experienced Senior Analysts, Data &amp; Analytics Enablement to drive the integration and migration of data products across a layered/medallion architecture as part of a large-scale acquisition and platform change programs. This role ensures that data is ingested, curated, quality-checked, and provisioned into the data platform in a manner that preserves business logic, data quality standards, and downstream consumer continuity.<br><br>The individual will own the end-to-end data enablement lifecycle during integration — translating transformation logic between platforms, aligning layer definitions and naming conventions, implementing data quality controls, and ensuring that curated data products are available to analytics, reporting, and operational consumers on schedule and in compliance with governance and regulatory standards. This role bridges data engineering, data stewardship, and business stakeholder engagement across both entities.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location:</b> Hyderabad #Hybrid</p><p><b>Key Responsibilities</b></p><ul><li><p><b>Architecture Alignment &amp; Layer Mapping:</b> Assess and document data architecture layers (e.g., raw/staging, intermediate/curated, consumption/marts) and map them to the target organization’s / target platform’s medallion or layered architecture. Identify semantic differences and define a unified layer strategy for the integrated platform.</p></li><li><p><b>Transformation Logic Migration:</b> Inventory all transformation models, business rules, and data curation logic (across tools such as dbt, Python, ETL/ELT platforms). Translate and re-implement this logic within the target platform&#39;s tooling and standards, ensuring full preservation of business intent and data lineage.</p></li><li><p><b>Data Quality &amp; compliance controls:</b> Implement standard data quality checks (completeness, uniqueness, referential integrity, timeliness, validity) at each architecture layer for migrated data. Ensure appropriate compliance controls, including PII/PHI masking, row-level security, and classification-based access policies — are applied consistently across migrated datasets.</p></li><li><p><b>Data Product Provisioning:</b> Curate and provision cleaned, validated, integration-ready datasets for downstream consumers (analytics teams, BI/reporting, data science, operational systems). Manage provisioning layer schemas and ensure consumer-facing data products meet agreed SLAs for freshness, completeness, and accuracy.</p></li><li><p><b>Cross-Entity Stakeholder Engagement:</b> Partner with domain owners, business analysts, and data consumers from both entities to validate that migrated data products meet business requirements. Facilitate domain-by-domain walkthroughs to confirm business logic preservation, flag gaps, and prioritize remediation.</p></li><li><p><b>Governance, Metadata &amp; Documentation:</b> Register all migrated data assets (schemas, tables, columns, business rules) in the enterprise data catalog. Maintain data dictionaries, business glossary entries, and end-to-end lineage documentation. Ensure compliance with data governance policies, regulatory requirements, and FAIR data principles (Findable, Accessible, Interoperable, Reusable).</p></li><li><p><b>Continuous Improvement:</b> Identify opportunities to optimize pipeline performance, reduce data latency, and improve quality automation during and after migration. Evaluate and recommend AI/ML-driven approaches for quality monitoring, anomaly detection, and automated data profiling.</p></li></ul><p></p><p><b>Essential Requirement:</b></p><div><ul><li><p>3–6 years in data engineering / stewardship / analytics enablement; at least 2 years in migration/integration</p></li><li><p>Strong layered data architecture &#43; data warehouse fundamentals (dimensional modeling, slowly changing dimensions, star/snowflake)</p></li><li><p>Hands-on with extract-transform-load / extract-load-transform tooling &#43; cloud data platforms</p></li><li><p>Strong Structured Query Language and Python. Data modeling &#43; data quality frameworks</p></li><li><p>Governance: metadata, cataloging, lineage, classification.</p></li><li><p>Proven large-scale migration/integration experience (logic &#43; curated datasets).</p></li><li><p>Layer mapping/reconciliation across two architectures.</p></li><li><p>Translating transformation logic between tools/frameworks.</p></li></ul><p></p></div><p><b>Desirable Requirements:</b></p><ul><li><p>Experience with <b>orchestration tool migration</b> (e.g., transitioning from one scheduler/orchestrator to another — such as Dagster to Airflow, Control-M to Airflow, or similar).</p></li><li><p>Familiarity with <b>data catalog and lineage tools</b> (e.g., Collibra, Alation, Atlan, Purview) and experience registering assets during a migration.</p></li></ul><p></p><p><span><span><b>Commitment to Diversity &amp; Inclusion</b></span></span></p><p><span><span>We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</span></span></p><p><span> </span></p><p><span><span><b>Accessibility and accommodation</b></span></span></p><p><span><span>Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></span></p><p><span><span> </span></span></p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Advertising Campaigns, Alteryx, Analytical Thinking, Brand Awareness, Business Networking, Curiosity, Digital Marketing, Marketing Communications, Marketing Plans, Marketing Strategy, Media Campaigns, Process Documentation, Statistical Analysis, Strategic Marketing]]></description><link>http://biotechroles.com/senior-analysts-data-and-analytics-enablement-data-integrations-novartis/6a0745892f1861929d253296</link><guid isPermaLink="true">http://biotechroles.com/senior-analysts-data-and-analytics-enablement-data-integrations-novartis/6a0745892f1861929d253296</guid><pubDate>Fri, 15 May 2026 16:10:49 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Senior Hematology Medical Science Liaison - Riyadh]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>To serve as a liaison to the medical/ scientific community and responsible for establishing, devel-oping and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Ex-perts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemina-tion of clinical and scientific information regarding Novartis’ compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders’ scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.<br><br>#LI-Onsite<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><h3><b>Medical Expert Engagement</b></h3><ul><li><p>Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).</p></li><li><p>Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.</p></li></ul><h3><b>Scientific Information &amp; Requests</b></h3><ul><li><p>Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.</p></li><li><p>Involve HCPs in advisory boards, educational activities, and publications when relevant.</p></li></ul><h3><b>Clinical Research Support</b></h3><ul><li><p>Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.</p></li><li><p>Facilitate IIT submissions and material transfer agreements for independent research.</p></li></ul><h3><b>Scientific Exchange &amp; Insights</b></h3><ul><li><p>Promote scientific exchange on emerging principles and trends.</p></li><li><p>Collect and report HCP insights to inform medical strategy and IPS planning.</p></li></ul><h3><b>Internal Contributions</b></h3><ul><li><p>Act as a local medical resource for disease area and product training.</p></li><li><p>Contribute to IPS and Medical Affairs strategy design and execution.</p></li></ul><h3><b>Compliance &amp; Integrity</b></h3><ul><li><p>Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).</p></li><li><p>Foster a diverse, inclusive, and harassment-free environment.</p></li></ul><h3><b>Education &amp; Communication</b></h3><ul><li><p>Provide scientific and educational information to HCPs on patient-critical issues.</p></li><li><p>Support internal capability building through training and knowledge sharing.</p></li></ul><p></p><p><b>Minimum Requirements</b></p><ul><li><p>A degree in PharmD, PhD, MD (Medical Doctor) is essential.</p></li><li><p>At least 1-year experience as Medical Science Liaison, specific experience in Hematology is a plus.</p></li><li><p>Fluent in both Arabic and English languages.</p></li></ul><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Biostatistics, Clinical Practices, Clinical Research, Clinical Study Reports, Curious Mindset, Customer Relationship Management (CRM) Software, Disease Management, Drug Development, Education, Epidemiology, IT Tools, Medical Information, Medical Research, Medical Writing, Phase Iv Clinical Trial, Product Placement, Scientific Support]]></description><link>http://biotechroles.com/senior-hematology-medical-science-liaison-riyadh-novartis/6a0745892f1861929d253295</link><guid isPermaLink="true">http://biotechroles.com/senior-hematology-medical-science-liaison-riyadh-novartis/6a0745892f1861929d253295</guid><pubDate>Fri, 15 May 2026 16:10:49 GMT</pubDate><company>Novartis</company><location>Riyadh</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Head Talent Management US]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>We’re a team of dedicated and passionate people united by a drive to achieve together. <br>You will shape and deliver the talent and development strategy for US Commercial, partnering with P&amp;O (People &amp; Organization) Business Partners and business leaders to translate enterprise talent priorities into local action. Provide data and market-informed talent diagnostics, leverage technology and predictive analytics to strengthen workforce planning, and ensure high-quality talent data for decision-making. You will enable critical roles and succession outcomes through OTR facilitation, high-potential and priority-group development, early careers and capability mapping, and cross-functional mobility programs—coordinating end-to-end interventions across Recruitment Solutions, Operational Development, LDCE, and Rewards to build diverse pipelines and a future-ready, continuous-development culture.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p>The ideal location for this role is East Hanover site but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific East Hanover site for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager.</p><p></p><p><span>We’re a team of dedicated and passionate people united by a drive to achieve together. You will shape and deliver the talent and development strategy for US Commercial, partnering with P&amp;O (People &amp; Organization) Business Partners and business leaders to translate enterprise talent priorities into local action. Provide data and market-informed talent diagnostics, leverage technology and predictive analytics to strengthen workforce planning, and ensure high-quality talent data for decision-making. You will enable critical roles and succession outcomes through OTR facilitation, high-potential and priority-group development, early careers and capability mapping, and cross-functional mobility programs—coordinating end-to-end interventions across TA, OD, LDCE, and Rewards to build diverse pipelines and a future-ready, continuous-development culture.</span></p><p><span> </span></p><p><span>Key Responsibilities:  </span></p><ul><li><p><span>Strategic talent partnership: Advise leaders and P&amp;O Business Partners; translate enterprise talent strategy into country priorities informed by business needs and external market dynamics.</span></p></li><li><p><span>Succession and talent reviews: Support Critical Role identification; lead succession planning for roles in scope with diverse, high-quality internal and external pipelines; facilitate OTR sessions and ensure clear outcomes and action follow-through.</span></p></li><li><p><span>Future-ready talent (cohorts, capabilities, priority groups): Drive assessment and development planning for successors and HiPos; deliver local talent strategies for priority groups; support strategic cohort execution and critical capability mapping and interventions (hire, develop, retain), including Early Careers where applicable.</span></p></li><li><p><span>Mobility and talent brokering: Enable cross-unit and cross-functional development and movement by running local talent brokering forums and rotation opportunities; lead Future Me activities and local talent forums as needed.</span></p></li><li><p><span>Data and insights: Maintain high-quality Workday talent data; leverage analytics tools to provide talent diagnostics, improve decisions, and support workforce planning.</span></p></li><li><p><span>Integrated P&amp;O delivery: Coordinate with TA, OD, LD and CE, Rewards, and P&amp;O Business Partners to sequence and deliver holistic talent solutions and high-impact projects.</span></p></li><li><p><span>Culture and capability building: Act as a Talent Ambassador, coaching leaders on succession excellence and future-ready practices; reinforce a continuous development and enterprise mindset.</span></p></li></ul><p><span> </span></p><p><span>Essential Criteria: </span></p><ul><li><p><span>Bachelor’s degree in a business discipline </span></p></li><li><p><span>Extensive P&amp;O (HR) experience in Talent Management and Scouting or in an adjacent discipline with genuine commitment to broaden skillset within Talent &amp; Transformation work</span></p></li><li><p><span>Strategic collaborator with P&amp;O and business leaders at executive levels.</span></p></li><li><p><span>Comfort working in partnership with C-Suite leaders to drive business outcomes. Driven by achieving outcomes rather than by running processes</span></p></li><li><p><span>Deep experience establishing and delivering internal talent mobility interventions grounded in and guided by the business strategy</span></p></li><li><p><span>Builder and creator mindset.</span></p></li><li><p><span>Fluent in English </span></p></li></ul><p><span> </span></p><p><span>Desirable Criteria: </span></p><ul><li><p><span>Commercial AI or Technology background</span></p></li><li><p><span>Pharma or Tech industry experience </span></p></li></ul><p></p><p></p><p>Benefits &amp; Rewards</p><p>The salary for this position is expected to range between $194,600.00 and $361,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p>Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a></p><p></p><p>Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: <a href="https://talentnetwork.novartis.com/network" target="_blank">https://talentnetwork.novartis.com/network</a></p><p>Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">https://www.novartis.com/careers/benefits-rewards</a></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$194,600.00 - $361,400.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, AI Solutions, Business Partnering, Change Management, Coaching, Communication Skills, Consulting, Data Analytics and AI Integration, Digital Literacy, Facilitation, Governance frameworks, Influencing Without Authority, Organizational Development (OD), Organization Design, Relationship Building, Resilience, Stakeholders Management, Strategic Workforce Planning, Talent Management, Team Leadership]]></description><link>http://biotechroles.com/head-talent-management-us-novartis/6a0745882f1861929d253294</link><guid isPermaLink="true">http://biotechroles.com/head-talent-management-us-novartis/6a0745882f1861929d253294</guid><pubDate>Fri, 15 May 2026 16:10:48 GMT</pubDate><company>Novartis</company><location>East Hanover</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Assoc. Dir. DDIT IES - HPC Infrastructure Sr. Engineer]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>-Associate Director of Novartis Core Infrastructure Services/Engineering organization is responsible for execution, continuous improvement, service delivery and operations of a specific function/platform <br>-OR Develop and maintain a technology roadmap which supports the respective Service Strategies of a specific function/platform.<br>-Oversee the operational health deployment and lifecycle of the technology and/or platform solutions OR Design and deploy technology solutions and/or act as L4 support during major and critical incidents.<br>-Automation of service deployments and management to enable modern delivery flows including DevOps and SRE with a goal of providing efficiency flexibility and speed at the lowest aggregate cost. <br>-Recruit coach and mature a team that is consistently over performing and delivering on business and technology objectives.  Drive change management and culture change by adhering to and evangelizing Novartis values and behaviors.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p>Major accountabilities</p><p></p><p>High Performance Computing (HPC) Specialist for Novartis Core Infrastructure Services team performs the operational health deployment and lifecycle of HPC technology</p><p>Designs innovative solutions utilizing projects and qualification frameworks to run and optimize our complex infrastructures.</p><p>Act as technical and organizational escalation point during major and critical incidents.</p><p>Responsible to track suppliers and partner for effective and efficient delivery of projects</p><p>Contributes to service / platform strategy development</p><p>Commitment to Diversity &amp; Inclusion: We are committed to building an outstanding, inclusive work environment and diverse teams, representative of the patients and communities we serve.</p><p></p><p>What you’ll bring to the role</p><p></p><p>6&#43; years’ IT experience, of which at least 3 in an HPC/scientific computing environment</p><p>Experience designing and building infrastructure within a public cloud platform (e.g. AWS, GCP or Azure) as they relate to HPC workloads</p><p>Hands-on experience with system administrative task in Linux environment, and fluency in scripting (shell scripting in bash required, Python knowledge would be advantageous)</p><p>Can build software from sources including knowledge of build systems (e.g. Make, CMake...)</p><p>Extensive knowledge of one or more HPC scheduling mechanisms (e.g. Grid Engine, Slurm, LSF... etc.)</p><p>Extensive knowledge of one or more HPC cluster management software packages (e.g. Bright Cluster Manager / Base Command Manager, xCat, OpenHPC… etc.)</p><p>Hands-on knowledge of network- and distributed filesystems (e.g. NFS, GPFS, Gluster, BeeGFS, Lustre or other parallel file systems, etc.)</p><p>Worked in environments with high speed / low latency network (e.g. InfiniBand)</p><p>Strong knowledge of Unix systems performance tuning</p><p>Working knowledge of DevOps (e.g. Ansible, Chef, CICD etc.) tools and practices</p><p>Desired: experience setting up, maintaining, and tuning infrastructure for AI/ML workloads</p><p>Desired: experience with HPC infrastructure supporting a scientific / research / pharmaceutical / bioinformatics / cheminformatics environment</p><p></p><p><b>Why consider Novartis?</b></p><p>Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!<br />Learn more here:<br />https://www.novartis.com/about/strategy/people-and-culture<br /><br /><b>Commitment to Diversity and Inclusion: </b><br />Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.<br /> </p><p>Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:<br />https://talentnetwork.novartis.com/network</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Business Acumen, Communication Skills, Digital Capabilities, Effective use of Technology, IT Infrastructures, IT Operations, IT Service Management, Operational Excellence Projects, Problem Solving Skills, Stakeholder Engagement, System Integration, Vendor Management]]></description><link>http://biotechroles.com/assoc-dir-ddit-ies-hpc-infrastructure-sr-engineer-novartis/6a0745882f1861929d253293</link><guid isPermaLink="true">http://biotechroles.com/assoc-dir-ddit-ies-hpc-infrastructure-sr-engineer-novartis/6a0745882f1861929d253293</guid><pubDate>Fri, 15 May 2026 16:10:48 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director: Data Integrations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Associate Director, Data Integrations will be responsible for responsible for implementing the integration of data across various systems and platforms, ensuring seamless data flow and accuracy. This role requires a deep understanding of data integration techniques, strong leadership skills, and the ability to work collaboratively with cross-functional teams.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location</b>: Hyderabad #Hybrid</p><p><b>Key Responsibilities</b></p><ul><li><p>Lead and manage the data integration team, providing guidance and support to ensure successful project delivery.</p></li><li><p>Design, develop, and implement data integration solutions to meet business requirements.</p></li><li><p>Collaborate with stakeholders to understand data needs and develop integration plan and roadmap.</p></li><li><p>Explicitly reference MDM strategy and Snowflake‑based ecosystems in requirements</p></li><li><p>Emphasize architectural (Medallion architecture &amp; Snowflake experience) understanding and platform‑level integration experience</p></li><li><p>Retain leadership and influence expectations (this is not a purely technical role)</p></li><li><p>Ensure data quality and integrity by implementing best practices and data governance policies.</p></li><li><p>Troubleshoot and resolve data integration issues in a timely manner.</p></li><li><p>Stay up to date with the latest trends and technologies in data integration and recommend improvements.</p></li></ul><p></p><p></p><p><b>Essential Requirements: </b></p><ul><li><p>Strong understanding of Master Data Management (MDM) concepts: data mastering, golden records, survivorship rules, hierarchies, downstream integrations</p></li><li><p>Solid technical grounding in Snowflake: data modeling and platform‑level integration patterns</p></li><li><p>Experience integrating MDM platforms with Snowflake‑centric data ecosystems</p></li><li><p>Ability to translate MDM strategy into business‑level outcomes, not just tooling discussions</p></li><li><p>Minimum of 10 years of experience in data and analytics, with a focus on leadership and enablement.</p></li><li><p><span>Strong knowledge of data integration tools and technologies (e.g., ETL, API, middleware).</span></p></li><li><p>Proven track record of leading cross-functional teams and driving organizational change.</p></li><li><p>Strong leadership and team management skills. Proficiency in data management tools and software.</p></li></ul><p></p><p><b>Desirable Requirement:</b></p><ul><li><p>10-12 years of experience in the pharmaceutical or healthcare industry, with a strong focus on provider data management in a healthcare setting.</p></li></ul><ul><li><p>5&#43; years of people management experience. Proven track record of enabling data-driven decision-making at a senior leadership level, including addressing complex business challenges.</p></li></ul><ul><li><p>Strong analytical background, strategic thinking and problem-solving skills, with the ability to translate complex data into actionable insights and aligning them with business priorities to drive impactful results </p></li></ul><p></p><p><span><span><b>Commitment to Diversity &amp; Inclusion</b></span></span></p><p><span><span>We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</span></span></p><p><span> </span></p><p><span><span><b>Accessibility and accommodation</b></span></span></p><p><span><span>Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Cross-Functional Collaboration, Customer Engagement, Customer Experience, Customer Insights, Data Analytics, Data Strategy, Digital Marketing, Marketing Strategy, Market Research, Media Campaigns, Product Marketing, Stakeholder Engagement, Stakeholder Management, Team Leadership, Waterfall Model]]></description><link>http://biotechroles.com/associate-director-data-integrations-novartis/6a0745882f1861929d253292</link><guid isPermaLink="true">http://biotechroles.com/associate-director-data-integrations-novartis/6a0745882f1861929d253292</guid><pubDate>Fri, 15 May 2026 16:10:48 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Intern Supply operations (LCI)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Intern – Supply Operations:<br>• Support the Novartis Technical Operations (TechOps) – Lifecycle Implementation team in the<br>leading and managing implementation product lifecycle projects such launch, transfer, change,<br>divestment and pruning etc. in compliance with Good Manufacturing Practices (GMP) &amp;<br>Regulatory requirements while creating value for the stakeholders across Novartis divisions<br>across geographies.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b> Major accountabilities: </b> </p><ul><li><p>Support and collaborate implementation of assigned product lifecycle projects / brands as per the</p><p>relevant SOPs, business matrix and SLA timelines</p><p>• Assist in delivering and maintaining a detailed Change Over Plan (COP) for LC projects regarding</p><p>implementation dates, according to the overall strategic project/ program plan</p><p>• Assist and support with a broad variety of stakeholders: Actively seek alignment with the experts</p><p>from different functions (e.g. Supply Support Team (SST) members, CPO DRA, CPO demand</p><p>planning, site tactical/ operational schedulers, Master Data Governance, Demand Management</p><p>Centre, other Supply Chain functions) and is in close collaboration with Project Lead / Life Cycle</p><p>Manager.</p><p>• Assist for the up-to-date assortment at SKU level of the assigned brands.</p><p>• Assist in plans and execution of changeover activities with all involved functions and proactively</p><p>addresses/resolves or escalates potential issues through the Project Lead or project team</p><p>• Assist in reporting all deviations through timely escalations.</p><p>• Responsible for block management</p><p>• Assist in data collection and reporting of KPIs</p><p>• Assist in continuous improvement initiatives</p><p>• Completion of Project / Thesis with guidance from Lead – LCI</p><p>• Completion of on job trainings imparted by the SME</p><p>• Grasping of Knowledge Session for better knowledge and understanding of business</p></li></ul><p><b> Key performance indicators: </b></p><p>Quality / Accuracy / Right First Time</p><p>• Timeliness</p><p>• Productivity</p><p>• Cross functional training</p><p><b> Minimum Requirements: </b> <br /> <b> Work Experience: </b></p><ul><li><p>NA.</p></li></ul><p><b> Skills: </b></p><ul><li><p>NA.</p></li></ul><p><b> Languages :</b></p><ul><li><p>English.</p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/intern-supply-operations-lci-novartis/6a0745872f1861929d253291</link><guid isPermaLink="true">http://biotechroles.com/intern-supply-operations-lci-novartis/6a0745872f1861929d253291</guid><pubDate>Fri, 15 May 2026 16:10:47 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$1000-3000</salary><type>Full time</type></item><item><title><![CDATA[AwOps- Associate ACC]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>•	Responsible for executing various Artwork Operations activities supporting the manufacturing sites to ensure quality &amp; compliant artwork creation and implementation on time, every time, safely and efficiently with full satisfaction of our customers within the framework of regulatory compliance and operating within high standards of GMP, HSE and good working practices.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p></p><p>•        Manage the Artwork Supply Chain for packaging site, starting from when an Artwork Request is received up to the point where the print-ready artwork is handed over to the manufacturing site.</p><p>•        Ensure “On Time in Full” delivery of high-quality artworks fully compliant with Novartis standards and in-country regulatory, marketing, manufacturing &amp; legal compliance to internal Artwork customers &amp; stakeholders. Manage Artwork Change Requests and communication &amp; alignment with Country Organizations, different site stakeholders to ensure timely implementation of artworks</p><p>•        Support various types of projects – regular launches, regular text changes, technical changes, transfers, mock-ups, divestments etc. in the Novartis Artwork landscape.</p><p>•        Execute technical check of artworks according to manufacturing site technical parameters.</p><p>•        Collect &amp; align all the necessary data / inputs required for Finished Product Bill of Material management.</p><p>•        Manage Artwork implementation in the Finished Product Bills of Materials based on the relevant data collected</p><p>•        Manage various Finished Product Bill of Material Life-Cycle events – creation, maintenance, deactivation etc. (for Production BoMs) in accordance with GMP and manufacturing site standards &amp; requirements.</p><p>•        Proactively report all deviations through timely escalations &amp; ensure implementation of relevant CAPAs and performance improvements.</p><p>•        Ensure Training on relevant procedures before taking up any GxP activities.</p><p>•        Implement continuous process improvement projects to enhance quality &amp; productivity.</p><p>•        Ensure compliance with GMP, regulatory requirements, HSE (including record management).</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management]]></description><link>http://biotechroles.com/awops-associate-acc-novartis/6a0745862f1861929d253290</link><guid isPermaLink="true">http://biotechroles.com/awops-associate-acc-novartis/6a0745862f1861929d253290</guid><pubDate>Fri, 15 May 2026 16:10:46 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$12000-18000</salary><type>Full time</type></item><item><title><![CDATA[Višji ekspert upravljanja kakovosti – skladnost (m/ž/d) / Regulatory CMC Facilitator (m/f/d)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Lokacija: Mengeš, Slovenia<br>Interni naziv pozicije / Internal job title: Višji ekspert upravljanja kakovosti – skladnost  /  Senior QA Compliance Expert<br>Relocation Support: This role is based in Mengeš, Slovenia. Novartis is unable to offer relocation support: please only apply if accessible.<br> <br>Ste pripravljeni na karierno priložnost, kjer bo vaš prispevek ključen pri uvajanju inovativnih zdravil na trg? Na našem oddelku za kakovost – skladnost, male molekule, iščemo strokovnjaka za upravljanje kakovosti, ki bo s svojim znanjem in izkušnjami povezoval in usklajeval regulativne CMC aktivnosti, povezane z lansiranjem zdravil ter aktivnostmi po njihovi odobritvi. Če vas veseli delo, ki neposredno vpliva na pravočasno dostopnost naprednih terapij ter zagotavljanje najvišjih standardov kakovosti, vas vabimo, da se nam pridružite in pustite svoj pečat.<br><br>_______________<br><br>Are you ready for a career opportunity where your contribution plays a key role in bringing innovative medicines to market? Within our Quality – Compliance, Small Molecules department, we are looking for a Quality Management expert who will leverage their expertise to coordinate and align CMC regulatory activities related to product launches and post-approval processes. If you are motivated by work that enables timely patient access to advanced therapies while upholding the highest quality standards, we invite you to join us and make your mark.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><h3><span>Vaše ključne odgovornosti:</span></h3><ul><li><span>Delovati kot osrednja kontaktna oseba in strokovni svetovalec za globalno CMC regulativno obveščenost na lokaciji.</span></li><li><span>Tesno sodelovati z Global Regulatory CMC ter spremljati in uvajati nove regulativne zahteve, strategije in trende.</span></li><li><span>Izvajati neodvisne predhodne ocene zahtevkov za spremembe ter potrjevati ustrezno klasifikacijo kategorije I ali II.</span></li><li><span>Zagotavljati pravilnost, popolnost in pravočasnost regulativno relevantnih informacij v zahtevkih za spremembe.</span></li><li><span>Podpirati lokacijo pri razvoju učinkovitih strategij nadzora sprememb z večjim vplivom na produkte ali lokacije.</span></li><li><span>Omogočati pripravo visokokakovostne CMC dokumentacije in modulov v skladu z dogovorjenimi CMC strategijami.</span></li><li><span>Usposabljati in razvijati sodelavce glede regulativnih vidikov upravljanja sprememb ter krepiti kulturo skladnosti.</span></li></ul><p></p><h3><span>Vaš doprinos k delovnem mestu:</span></h3><ul><li><span>Univerzitetna izobrazba farmacevtske, biološke, kemijske, mikrobiološke ali druge ustrezne naravoslovne smeri.</span></li><li><span>Aktivno znanje angleškega jezika.</span></li><li><span>Najmanj dve leti delovnih izkušenj na področju proizvodnje, razvoja ali kakovosti v reguliranem okolju.</span></li><li><span>Dobro poznavanje lokalnih in globalnih regulativnih zahtev ter postopkov za nove kemične enote (NCE) in upravljanje življenjskega cikla izdelkov.</span></li><li><span>Odlične komunikacijske in pogajalske sposobnosti ter sposobnost strateškega razmišljanja v kompleksnem okolju.</span></li><li><span>Dobro poznavanje orodij Microsoft Office, projektnega dela ter sistemov za upravljanje dokumentacije, z visoko sposobnostjo učenja novih orodij.</span></li></ul><p><br /> </p><p>Z izbranim kandidatom bomo sklenili delovno razmerje za <b>nedoločen čas</b> s poskusno dobo <b>6 mesecev</b>. Prijavo oddajte z življenjepisom v angleškem jeziku. </p><p><b> </b> </p><p><b>Ugodnosti in nagrajevanje:</b> Konkurenčen plačni paket, letni bonus, fleksibilen način dela z možnostjo prilagajanja urnika in delom od doma, pokojninska shema, možnost vključitve v kolektivno zdravstveno zavarovanje,  shema nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju fizičnega in duševnega dobrega počutja ter delovne obremenitve (Polni življenja), številne priložnosti za učenje in razvoj.   </p><p></p><p>Preberite naš priročnik, da spoznate načine, s katerimi bomo spodbujali vaš osebni in profesionalni razvoj: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank"><u>https://www.novartis.com/careers/benefits-rewards</u></a>     </p><p></p><p><b>Predani smo raznolikosti in vključenosti: </b>Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.   </p><p></p><p><b>Zakaj Novartis:</b> Pomagati bolnikom in njihovim družinam zahteva več kot le inovativno znanost. Potrebna je skupnost zavzetih ljudi, kot ste vi. V Novartisu cenimo sodelovanje, podporo in navdihovanje drug drugega za razvoj prebojnih terapij, ki spreminjajo življenja pacientov. Ste pripravljeni ustvariti svetlejšo prihodnost skupaj z nami? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank"><u>https://www.novartis.com/about/strategy/people-and-culture</u></a>     </p><p>___________________________________</p><p></p><h3><span>Key Responsibilities:</span></h3><ul><li><span>Act as the primary contact and expert advisor for global CMC regulatory intelligence at the site.</span></li><li><span>Collaborate closely with Global Regulatory CMC to monitor and implement new regulatory requirements and strategies.</span></li><li><span>Perform independent pre-assessments of change requests and confirm appropriate Category I or II classification.</span></li><li><span>Ensure accuracy, completeness, and timeliness of regulatory-relevant information within change documentation.</span></li><li><span>Support the site in developing effective change control strategies with broader product or site impact.</span></li><li><span>Enable timely preparation of high-quality CMC documentation and modules aligned with agreed CMC strategies.</span></li><li><span>Train and develop site colleagues on regulatory change management to strengthen compliance capabilities.</span></li></ul><p></p><h3><span>Essential Requirements:</span></h3><ul><li><span>University degree in pharmacy, biology, chemistry, microbiology, or another relevant life science discipline.</span></li><li><span>Proficient command of the English language.</span></li><li><span>At least two years of professional experience in manufacturing, development, or quality within a regulated environment.</span></li><li><span>Solid knowledge of local and global regulatory requirements, including submission processes for new chemical entities (NCE) and product lifecycle management.</span></li><li><span>Strong communication and negotiation skills combined with strategic thinking in a cross-functional setting.</span></li><li><span>Proficiency in Microsoft Office tools, project-based work, and document management systems, with a strong ability to learn new tools quickly.</span></li></ul><p><br /> </p><p>We offer <b>permanent employment </b>with <b>6 months</b> of probation period. Submit your application with the CV in English language. </p><p>  </p><p>  </p><p><b>Benefits and Rewards: </b>Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, possibility of joining collective health insurance scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical and mental well-being and managing workload (Well-being), Unlimited learning and development opportunities.   </p><p>   </p><p><b>Commitment to Diversity and Inclusion:</b> Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Decision Making, Digital saviness, Leadership, Organizational Saviness, Regulatory Requirements knowledge, Risk Management]]></description><link>http://biotechroles.com/visji-ekspert-upravljanja-kakovosti-skladnost-mzd-regulatory-cmc-facilitator-mfd-novartis/6a0745862f1861929d25328f</link><guid isPermaLink="true">http://biotechroles.com/visji-ekspert-upravljanja-kakovosti-skladnost-mzd-regulatory-cmc-facilitator-mfd-novartis/6a0745862f1861929d25328f</guid><pubDate>Fri, 15 May 2026 16:10:46 GMT</pubDate><company>Novartis</company><location>Mengeš</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Head People Partner, India]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br><br>Location: Hyderabad, India<br><br>About The Role <br><br>Novartis India is a significant part of the global Novartis network, contributing to various business units and strategic priorities. Novartis Hyderabad is the largest global Operations capability center, supporting domains such as Data Digital and Information Technology (DDIT), People &amp; Organization (P&amp;O) Services, Procurement, Financial Reporting and Accounting (FRA), Development and Research. The site has over 9200 employees largely based in Hyderabad with the commercial business operating out of Mumbai (approx. 700 employees). The Hyderabad site focuses on driving productivity, innovation, and simplification by nurturing an ecosystem of agile inter-team collaboration and leveraging partnerships with external innovators. There are two offices in Hyderabad – Novartis Healthcare Private Limited at the Sattva Knowledge Park as well as our research center in Genome Valley. We also have an office for the commercial business in Mumbai with around 700 plus employees. <br>	<br>The People Partner head plays a critical role within the India operations for Novartis, closely works with the country P&amp;O Head in delivering the people plan across all our sites, in partnership with the COE’s and BP’s. This role also plays a critical role working closely with the Global People Partner Head based out of Switzerland as well as is a part of a broader community of People Partner Head operating out of the large Novartis offices in US, Switzerland, China, Japan and Germany. In this role you will be part of India P&amp;O Leadership team and drive One P&amp;O (People &amp; Organisation) mindset across all the P&amp;O functions in India (approx. 400 FTE) and has direct reporting accountability of 25 plus People Partners with a layer of management.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities </b></p><ul><li>Lead the India People Partnering organization (~25) as a leader of leaders (~3&#43;), building a high-performing cross-divisional team that delivers consistent, credible, and end-to-end P&amp;O support to 9,000&#43; employees.</li><li>Strengthen the One P&amp;O mindset by harmonizing People Partnering processes, standards, and ways of working across business units, while collaborating with Country P&amp;O, Business Partners, Global Business Partners, COEs, and site leaders to deliver integrated people solutions.</li><li>Shape and execute the India People Partnering agenda in alignment with business priorities and global P&amp;O strategy, driving key people initiatives, organizational change, culture and people experience efforts, compliance, and future-ready capability building.</li><li>Build and sustain a high performing India People Partnering team, fostering a collaborative and accountable culture that enables impact, agility, and an enterprise mindset in an evolving organizational landscape.</li><li>Lead leaders effectively by setting clear direction, building capability, driving accountability, and ensuring outcomes are delivered through empowered, high performing teams.</li><li>Role model and strengthen the “One P&amp;O” ethos across People Partnering and the broader P&amp;O ecosystem, enabling seamless collaboration across country, regional, and global stakeholders.</li><li>Engage proactively with site leaders and key stakeholders, building strong partnerships to clarify expectations, shape priorities, and ensure consistent execution of people initiatives.</li><li>Influence without authority in a matrixed environment by cultivating strong global and local partnerships with COEs, Business Partners, Global Business Partners, and other critical internal and external stakeholders.</li><li>Sponsor, lead, and inspire country level people initiatives, ensuring strong alignment with business priorities and disciplined execution across sites and functions.</li><li>Identify and manage interdependencies across cross functional teams and COEs, driving clarity, connecting the dots, and enabling integrated planning, timely execution, and organizational agility.</li><li>Provide leadership on India wide labour compliance, institutionalizing robust governance, audit discipline, and risk mitigation frameworks in close partnership with cross functional teams.</li><li>Own and lead P&amp;O policy at the country level, shaping line manager and employee experience; act as the single point of contact for standards, controls, and risk management, and serve as the escalation point for exceptions, deviations, and appeals.</li><li>Lead the local implementation of large scale organizational changes, including structural transformations, transitions, and integrations, ensuring effective change management, business continuity, and alignment with country policies.</li><li>Demonstrate a growth mindset and exploratory approach to challenge the status quo, leveraging AI tools, agents, and emerging capabilities to drive efficiency and elevate value creation. Continuously reassess practices to stay relevant, while adapting to new ways of working and role modelling curiosity and experimentation.</li><li>Leverage data, insights, and metrics to anticipate demand trends, assess team capacity, identify risks, and ensure the People Partnering team is equipped to meet evolving business needs.</li><li>Act as a critical liaison with the global people partner excellence teams driving the implementation of global initiatives at a local level, ensuring there is a good understanding of local implications on people and operating models for successful global roll outs (e.g EPIC, India labour code etc)</li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li>20&#43; years of experience in HR partnering role/s with strong experience in people management.</li><li>MBA or equivalent in Human Resources is preferred.</li><li>Ability to partner with senior business leaders and HR peers to deliver the talent agenda, with strong stakeholder management and influencing capabilities.</li><li>Role‑model self‑awareness and a growth mindset through continuous learning, acknowledging gaps, and personal accountability.</li><li>Enterprise mindset with a decisive bias for action.</li><li>Business acumen – connecting the dots to balance strategic and operational priorities.</li><li>Lead as a coach and servant leader, enabling others to succeed.</li><li>Exceptional stakeholder management with strong influencing capability.</li></ul><p></p><p><b>Desirable Requirements: </b></p><ul><li>Experience in leveraging AI to simplify people processes, reduce duplication, and shift team capacity toward higher impact, value adding work.</li><li>Experience in Global/ MNC and complex &amp; matrixed organizations.</li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Change Management, Client Counseling, Coaching, Commercial Acumen, Compliance &amp; Risk Management, Connecting The Dots, Data-Driven Decision Making, Influencing, Leadership Training and Development, Matrix Collaboration, Organizational Structures, Organization Health, Stakeholder Management, Strategic Workforce Planning, Talent Development, Talent Pipeline, Vision &amp; Purpose (Strategy To Story), Waterfall Model]]></description><link>http://biotechroles.com/head-people-partner-india-novartis/6a07443c2f1861929d25328e</link><guid isPermaLink="true">http://biotechroles.com/head-people-partner-india-novartis/6a07443c2f1861929d25328e</guid><pubDate>Fri, 15 May 2026 16:05:16 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Principal Scientist I/II - Oncology]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: Cambridge, MA - Onsite <br><br>The Oncology Translational Research (OTR) group at BR is seeking a highly motivated individual to serve as a lab head investigating the mechanisms of efficacy and resistance to radioligand therapy (RLT). This role involves collaborative work with various groups across the drug development spectrum, including drug discovery, data science, and early clinical development groups, located in Watertown (Mariana site) and Cambridge (Oncology BR site). The successful candidate will be responsible for leading a team and will be tasked with the design &amp; execution of preclinical translational studies and clinical biomarker plans.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key responsibilities:</b></p><ul><li>Supervise translational experimental plan and biomarker strategies for various RLT drug discovery programs</li><li>Design and conduct translational studies including in vitro assays with RLT, dissection of mechanism of action, and testing of drug combinations</li><li>Collaborate with groups across Mariana and BR Oncology</li></ul><p><b>Essential Requirements:</b></p><ul><li>This is a dual post. The final level and title of the role offered will be determined by the hiring team based on the skills, experience &amp; capabilities required to perform the role at the level offered (Principal Scientist I/II):<ul><li>Principal Scientist I: Post Doc experience or 3 years of relevant experience in academia or industry.</li><li>Principal Scientist II: Post Doc experience plus 2 years of relevant industry experience after the postdoctoral period.</li></ul></li><li>Ph.D. in molecular, cellular, cancer biology or related fields.</li><li>Strong foundational knowledge and experience working on cell death mechanisms, experience in the field of DNA damage response and repair, and/or and RLT.</li><li>Proficiency with data mining and computational skills.</li><li>Deep understanding of cancer cell biology, familiarity with innovative cell and molecular biology techniques.</li><li>Excellent creative thinking and problem-solving skills.</li><li>Enthusiasm for scientific collaboration and teamwork, positive attitude, scientific curiosity, dedication, agility.</li><li>Desire to work collaboratively, manage a research team and scientific projects, as well as clearly communicate scientific findings.</li></ul><p></p><p><span><b>Novartis Compensation and Benefit Summary: </b></span></p><p>The salary for this position is expected to range between $108,500 and $201,500 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and</p><p>experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published</p><p>salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the</p><p>role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and</p><p>disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In</p><p>addition, employees are eligible for a generous time off package including vacation, personal days,</p><p>holidays and other leaves.</p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$108,500.00 - $201,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills, Curious Mindset, Data, Data Analysis, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory, Lifesciences, Machine Learning (ML), Management, Medical Research, Molecular Biology {+ 10 more}]]></description><link>http://biotechroles.com/principal-scientist-iii-oncology-novartis/6a07443c2f1861929d25328d</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-iii-oncology-novartis/6a07443c2f1861929d25328d</guid><pubDate>Fri, 15 May 2026 16:05:16 GMT</pubDate><company>Novartis</company><location>Cambridge (USA)</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[LDC Deployment Manager - Manufacturing]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>This role will help drive the execution of Novartis’ ambition to turn data and digital into a strategic asset to drive actionable insights across the organization. This ambition is one of key pillars in the broader digital transformation happening at Novartis to be a focused medicines company powered by data and digital.<br><br>Accountability for the design in the respective work package, build and deployment of LDC in-scope processes and data based on the user-requirements defined in conjunction with the domain pillars and the E2E data team. Working with architecture to identify new technologies and the new possibilities arising out of it. <p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p></p><p><b>MAJOR ACCOUNTABILITIES</b></p><ul><li><p>Accountable for the LDC implementation/ adoption in the area responsible based on the business requirements based on the Novartis architectural standards, performance, quality and security principles</p></li><li><p>Accountable for deciding on implemetation for complex issues in strong collaboration with the respective functional GPOs and LDC Pillars based on a detailed rational and interpretation to fully understand implications of the proposal for the integrated solution</p></li><li><p>Accountable that the solution:</p><ul><li><p>meets business and user requirements</p></li><li><p>adheres to high level conceptual design and it is tracable</p></li><li><p>it is aligned with architectual roadmap</p></li><li><p>improves and sustains standardization efficient while respecting regulatory/control requirements (e.g., NFCM-control requirements, P3, TPRM, GxP)</p></li><li><p>supports the development, execution and operations of solutions</p></li></ul></li><li><p>Work (together with the IT Expert) in the assigned area and ensuring integrated solutions by strongly being connected to experts in connected workpackages, data &amp; analytics, by applying a continuous improvement mindset</p></li><li><p>Accountable that dedicated project work is delivered to agreed time, cost and quality constraints following the release calendars</p></li><li><p>Accountable for the solutions are peer reviewed, formally documented and signed off by domain pillars and business functions</p></li><li><p>Accountable that solution user acceptance testing is performed and meet quality standards</p></li><li><p>Champion the need to stay standard from a customisation perspective by establish standardized design and development processes to enable cost effective delivery</p></li><li><p>Ensure adherence with all relevant internal / external security and compliance policies and procedures (e.g. FDA, Novartis IGM framework)</p></li><li><p>Guide data cleansing, data migration and building the master data dictionary, in close collaboration with the local data owners</p></li><li><p>Simplify user profile definition and absorb local profiles into global profiles where feasible. Guide the sites with profile mapping to users</p></li><li><p>Guide business cutover planning, data double maintenance, ramp down and ramp up/ Hypercare support</p></li><li><p>Support country discovery activities for identifying additional needs going beyond the existing LDC core solution</p></li><li><p>Ensure close collaboration with pillar teams and country reference group members, regular meetings and workshops are conducted and feedback from operations is taken into consideration.</p></li></ul><p> </p><p><b>KEY PERFORMANCE INDICATORS / MEASURES OF SUCCESS</b></p><p>Delivery of key milestones of the program on time, in quality and within budget, </p><p>with full buy-in and support of country and global teams</p><p> </p><p><b>JOB DIMENSIONS</b></p><p>Complexity:</p><ul><li><p>Execution of a specfic functional area  in a very high complex program impacting all countries and regions</p></li></ul><p>Influence:</p><ul><li><p>Stakeholder management with LDC domain pillar teams, GPOs and country/hubs/sites reference groups</p></li><li><p>Large and geographically broad scope; high change impact</p></li></ul><p>Knowledge &amp; Skills:</p><ul><li><p>Business acumen: very good understanding of various worldwide data models, required capabilities and operational pain points in the area responsible</p></li><li><p>Curious and forward looking: looks for signals both inside and outside the company to identify new trends and future expectations to set the goals of the commercial workstream.</p></li><li><p>Digital savvy: very good grasp of the impacts and opportunities of data and technology will create to Novartis</p></li><li><p>Leadership skills: ability to inspire change, involve country-experts and effectively communicate to GPOs and relevant stakeholders</p></li></ul><p> </p><p> </p><p><b>EDUCATION &amp; EXPERIENCE</b></p><ul><li><p>University level degree</p></li><li><p>Additional Project Management training, a certification/designation desirable</p></li><li><p>Lean / Six Sigma Certified preferred</p></li><li><p>At least 3 years’ experience in country and global roles</p></li></ul><p> </p><p><b>LANGUAGES</b></p><p>English as a must and additional language(s) preferred.</p><p> </p><p><b>FINANCIAL RESPONSIBILITY</b></p><p>Support a<span style="color:#cd5937"> </span>very large program over 5&#43; years potentially in the magnitude of &gt;500mUSD.</p><p> </p><p><b>COMPETENCY PROFILE</b></p><ul><li><p>Contributes to the project efficiently, with an ‘value creation’ mentality by maintaining a key focus on value creation and process optimization</p></li><li><p>Leverage best in class examples, key expert input to design the appropriate project management and change approach for all phases of the program/project lifecycle.</p></li><li><p>Keeps deadlines and gets the team to produce high quality output</p></li><li><p>Leverages business understanding and its requirements in the design of the Transformation Program agreed end states/outcomes</p></li><li><p>Problem solving and root cause identification skills</p></li><li><p>Strong analytic and decision making abilities</p></li><li><p>Able to work effectively at all levels in an organization</p></li><li><p>Excellent communication and collaboration skills with proven speaking, presentation and facilitation experience in internal and external environments</p></li><li><p>Able to leverage networks of professionals across functions and business areas</p></li><li><p>Understands the competing organizational needs beyond own part of business</p></li><li><p>Able to interpret complex information and to influence internal and external peers</p></li><li><p>Role model for Novartis’ values and behaviours</p></li><li><p>Analytical mindset and ability to understand situations, interdependencies and challenges in a holistic way</p></li><li><p>Ability to effectively prioritize and execute tasks in a high-pressure environment</p></li><li><p>Demonstrate ability to work effectively in a multi-national and complex matrix organization</p></li><li><p>Can conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities</p></li><li><p>Flexible and reacts to changes promptly and efficiently</p></li><li><p>High cultural awareness</p></li><li><p>Proactive, result orientated and with a strong customer centric attitude</p></li><li><p>Interest to learn, explore and develope within the given role </p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Data Analytics, digital skills, General Hse Knowledge  , gmp knowledge, process excellence, Resilience]]></description><link>http://biotechroles.com/ldc-deployment-manager-manufacturing-novartis/6a07443c2f1861929d25328c</link><guid isPermaLink="true">http://biotechroles.com/ldc-deployment-manager-manufacturing-novartis/6a07443c2f1861929d25328c</guid><pubDate>Fri, 15 May 2026 16:05:16 GMT</pubDate><company>Novartis</company><location>İstanbul Kurtköy</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Senior Medical Information Manager 1]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>This role is responsible for delivering complex Medical Information (MI) activities and for providing functional and therapeutic area/brand expertise to support the development of Medical Information documents. It also involves developing high‑quality responses to escalated medical enquiries received from Novartis country affiliates worldwide across the Novartis product portfolio.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major accountabilities: </b></p><ul><li><p>Provide timely and quality responses to medical enquiries escalated from Novartis country affiliates for products</p></li><li><p>Write MI deliverables such as Global Guidance Documents (GGDs), MI Q&amp;As to ensure they meet quality requirements – scientifically balanced and evidence-based, adhere to topic, using appropriate language and correct grammar, and regulatory/safety/legal aspects are considered</p></li><li><p>Provide input into MI processes and standards to ensure optimal efficiency and productivity</p></li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li><p><span>Healthcare professional degree or degree in a healthcare-related field. Advanced</span><span> degree (PhD, PharmD, MD) in life science/healthcare</span></p></li><li><p><span>Minimum 2 years’ experience in a Medical Information/Communications role specifically in the Pharmaceutical Industry (or a related Medical Affairs role with significant MI responsibility in the Pharmaceutical Industry)</span></p></li><li><p><span>Experience with delivering MI services at Global and local level</span></p></li><li><p><span>Product and disease area knowledge in Novartis therapeutic areas</span></p></li><li><p><span>Strong knowledge of good practices in medical information writing, and experience with mentoring others</span></p></li><li><p><span>Strong clients focus and cross-functional skills and proven experience in collaboration with other departments/groups</span></p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Clinical Research, Clinical Trials, Detail-Oriented, Medical Writing, Safety]]></description><link>http://biotechroles.com/senior-medical-information-manager-1-novartis/6a07443b2f1861929d25328b</link><guid isPermaLink="true">http://biotechroles.com/senior-medical-information-manager-1-novartis/6a07443b2f1861929d25328b</guid><pubDate>Fri, 15 May 2026 16:05:15 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Communications & Patient Engagement Partner (PEP) Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>- To contribute from an executional and collaborative perspective on all strategic brand communications, media &amp; content strategies, engagement &amp; partnership with patient organizations and internal communications to support positive employee engagement.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b> Major accountabilities: </b> </p><ul><li><p>Coordinate and provide specialist knowledge across all specific area of communications.</p></li><li><p>Drive and lead internal employee communications plan through various approved channels.</p></li><li><p>Establish, develop, and execute local communication plans in-line with Country, Region and Global strategic goals, and desired market position for key brands.</p></li><li><p>Disseminate information to relevant public (marketable customers, regulators, shareholders) through appropriate use of the media and press releases.</p></li><li><p>Develop and execute social media strategies and campaigns for corporate and executive channels, including media planning/buying for paid campaigns.</p></li><li><p>Managing editorial social calendar and delivering rich content for multiple social media platforms.</p></li><li><p>Manage crises and issues communication in close collaboration with the Country Leadership team as well as global communications function.</p></li><li><p>Act as a strategic partner to the business and create and support implementation of communications strategies across different therapeutic areas.</p></li><li><p>Externally, the role focuses on building strong relationships with patients and patient organizations to improve outcomes, implementing, and localizing global integrated patient-inclusive product communications campaigns for launch and established products, and leveraging corporate initiatives and CSR activities. Simultaneously full preparation for potential crisis &amp; issues should be guaranteed.</p></li><li><p>Yearly integrated/aligned plans for brand communications, corporate communications, internal communications, social media, and patient relations.</p></li><li><p>Successful implementation of communications plans in close cooperation with key business partners.</p></li><li><p>Identification, anticipation, and management of issues by working with appropriate functions and counsel management.</p></li><li><p>Establish and drive patient advocacy strategies, manage relationships with local patient organizations or support in initiating establishment of patient organizations.</p></li><li><p>Develop and lead disease patient advocacy initiatives aligned and integrated with key business partners (franchises, market access, medical affairs, and development).</p></li><li><p>Facilitate/support patient organization events and align expectations with common areas of interest focused on improving patient outcomes through a patient centric approach.</p></li><li><p>Ensure consistency of Novartis brand and market position in external communications, by ensuring alignment across the Enterprise and by putting in place necessary communication-control processes</p></li><li><p>Measuring the impact of channels and campaigns towards achieving business objectives by using the measurement template.</p></li><li><p>Supervise the implementation of assigned project or communications activity.</p></li><li><p>Build relationships with and Brand managers/business leads, P&amp;O Partners and /or senior Communications colleagues.</p></li><li><p>Manage and liaise with agencies to create engaging multimedia content and community management for all platforms, setting targets, increasing engagement and track KPIs/best practices to secure maximum return on investment, operational excellence and business impact.</p></li><li><p>Use and coordinate available communications resources to achieve required results by ensuring effective deployment of project information /materials.</p></li><li><p>To ensure compliance in all interaction throughout the organization and maintain regular liaison with the Regional and Local compliance function to ensure that all processes and activities comply with internal and external policies.</p></li></ul><ul><li><p>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt.</p></li></ul><p><b>Ethics and Compliance:</b></p><ul><li><p>Work within any given legal framework, Novartis Ethics and Compliance policies and ensure those around him/her do the same.</p></li><li><p>Work to ensure a diverse and inclusive environment, free from all forms of discrimination and harassment</p></li></ul><p></p><p><b> Minimum Requirements: </b></p><ul><li><p>5 years combination working experience in agency and a MNC &#43; matrixed organization - preferably with exposure or experience in innovative medicines, pharmaceutical industry.</p></li><li><p>Cross Cultural Experience. Collaborating with internal / external stakeholders</p></li><li><p>Project Management. Operations Management and Execution.</p></li><li><p>Significant experience in pharmaceutical industry communications positions, and excellent understanding of healthcare innovative medicines communication concerns regarding public, media, and employee relations preferred</p></li><li><p>Demonstrated ability to influence high level media, patient organizations</p></li><li><p>Excellent written and oral communication skills</p></li></ul><ul><li><p>Good team skills: ability to manage and achieve results through influence; credible high performing manager with experience in managing people and projects.</p></li></ul><p></p><p><b> Skills: </b></p><ul><li><p>Communication Medium.</p></li><li><p>Corporate Communication.</p></li><li><p>Creativity.</p></li><li><p>Internal Communications (Ic).</p></li><li><p>Interviewing Skills.</p></li><li><p>Marketing.</p></li><li><p>Media Campaigns.</p></li><li><p>Media Relations.</p></li><li><p>Multimedia.</p></li><li><p>Social Media.</p></li></ul><p><b> Languages :</b></p><ul><li><p>English.</p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Communication Medium, Corporate Communication, Creativity, Internal Communications (Ic), Interviewing Skills, Marketing, Media Campaigns, Media Relations, Multimedia, Social Media]]></description><link>http://biotechroles.com/communications-and-patient-engagement-partner-pep-manager-novartis/6a07443b2f1861929d25328a</link><guid isPermaLink="true">http://biotechroles.com/communications-and-patient-engagement-partner-pep-manager-novartis/6a07443b2f1861929d25328a</guid><pubDate>Fri, 15 May 2026 16:05:15 GMT</pubDate><company>Novartis</company><location>Jakarta</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Ultra-Rare Disease Territory Account Specialist – Beverly Hills, CA]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Remote<br><br>This is a field-based and remote opportunity supporting key accounts in an assigned geography.<br>Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible to you.<br><br>Company will not sponsor visas for this position.<br><br>The Ultra‑Rare Disease Territory Account Specialist is a self‑driven business leader who shapes thoughtful, personalized customer experiences aligned to the unique needs of Health Care Providers and their patients. Serving as the primary point of contact, this role partners closely with customers to identify shared priorities, solve complex challenges, and connect seamlessly to Novartis resources in support of improved patient outcomes. Operating with autonomy in a highly dynamic environment, the Ultra‑Rare Disease Territory Account Specialist orchestrates patient‑focused solutions across clinical, operational, and access pathways, informed by a deep understanding of patient flow and ultra‑rare disease access dynamics. While retaining core demand‑generation responsibilities, this role brings expanded focus to access, operational excellence, and continuity of care to help enable timely treatment initiation and sustained patient support.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities: </b></p><ul><li>Proactively identify and navigate any account‑level challenges, partnering with customers to deliver thoughtful, compliant solutions that support patient care.</li><li>Develop and execute Health Care Provider (HCP) and account‑level business plans rooted in shared priorities, informed by clinical insight, access considerations, and operational understanding.</li><li>Educate Health Care Providers and practice teams on non‑clinical barriers to care, including access and reimbursement tools relevant to ultra‑rare disease management.</li><li>Maintain a strong understanding of patient flow, drug acquisition, and practice dynamics to help support timely treatment initiation and continuity of care.</li><li>Collaborate closely with field‑based and home‑office partners to address Health Care Provider needs and share relevant market access insights.</li><li>Leverage deep knowledge of the ultra‑rare disease landscape, competitors, and industry trends to anticipate opportunities and navigate evolving challenges.</li><li>Analyze territory‑level data and market trends to inform strategy, drive pull‑through, and lead meaningful virtual and in‑person engagements with Health Care Providers.</li><li>Lead cross‑functional planning discussions to solve complex Health Care Provider challenges with urgency, alignment, and a patient‑first mindset.</li><li>Serve as the primary orchestrator of Novartis resources for assigned Health Care Providers, compliantly coordinating across Medical, Access, and Patient Support teams while personalizing engagement through omni‑channel capabilities.</li></ul><p></p><p><b>Essential Requirements:  </b></p><ul><li>Bachelor’s degree required from 4-year college or university. </li><li>Experience (see leveling guidelines below) in pharmaceutical, biotech, healthcare, or similarly structured industries with large, geographically dispersed sales teams within the last 5 years. We also welcome candidates from other complex sales environments such as medical devices, diagnostics, life sciences services, insurance, consumer health, or B2B sectors, especially where strong field leadership and customer engagement are central to success<i>. </i><i>For Associate Level opportunities, applicants with limited prior sales experience are encouraged to apply.</i></li><li>Proven track-record of consistent high-performance, and well-versed in navigating and successfully selling to large accounts and key customers. </li><li>Self-starter with analytic abilities to seek out, prioritize, and apply relevant information to solve problems to meet the needs of key customers, while also demonstrating ethical leadership and ability to foster environment that promotes ethical behavior and compliance with company policies and laws. </li><li>Candidate must reside within territory, or within a reasonable daily commuting distance of 50 miles from the territory border. Ability to travel 60-80% over a broad geography is required, with the ability to drive and/or fly within the territory. Must have a valid driver’s license.</li></ul><p></p><p><b>Desirable Requirements: </b></p><ul><li>Experience supporting ultra‑rare or specialty disease states, including familiarity with sophisticated access and reimbursement pathways (e.g., buy‑and‑bill, injectable, or biologic products).</li><li>Broad experience across therapeutic areas, patient services, market access, reimbursement models, account strategy, and/or new product launches, with an understanding of engaging Health Care Providers around complex treatment and access pathways.</li></ul><p></p><p><b>Leveling Guidelines:</b> The position will be filled at level commensurate with experience.</p><ul><li><b>Associate Territory Account Specialist:</b> Recently separated from the US Military with 4&#43; years of military service in a leadership capacity (Platoon Leader, Executive Officer, Company Commander, etc.), or applicants with limited prior sales experience.<ul><li><i>Demonstrates strong ability to collaborate, work cross-functionally within a matrix environment, and communicate product information effectively.</i></li><li><i>Preferred experience in the 2-year Novartis Sales Internship Program; demonstrated proven leadership experience in student sports, fraternities, clubs, activities, and other extracurricular activities.</i></li></ul></li><li><b>Territory Account Specialist:</b> 2&#43; years’ experience in specialty pharmaceutical, biotech, healthcare, medical device, diagnostics, life sciences services, insurance, consumer health, B2B sectors or sales role of similar complexity within the last 5 years. Strong ability to collaborate, work cross-functionally within a matrix environment and can communicate clinical product information.</li><li><b>Senior Territory Account Specialist:</b> 5&#43; years’ experience in specialty pharmaceutical, biotech, healthcare, medical device, diagnostics, life sciences services, insurance, consumer health, B2B sectors or sales role of similar complexity within the last 5 years. Strong ability to collaborate, work cross-functionally within a matrix environment and can communicate clinical product information.</li><li><b>Executive Territory Account Specialist:</b> 10&#43; years’ experience in specialty pharmaceutical, biotech, healthcare, medical device, diagnostics, life sciences services, insurance, consumer health, B2B sectors or sales role of similar complexity within the last 5 years. Strong ability to collaborate, work cross-functionally within a matrix environment and can communicate clinical product information.</li></ul><p></p><p><b>Driving is an Essential Function of this Role:</b> Meaning it is fundamental to the purpose of this job and cannot be eliminated. Because driving is an essential function of the role, you must have a fully valid and unrestricted driver’s license to be qualified for this role. The company provides reasonable accommodations for otherwise qualified individuals with medical restrictions if an accommodation can be provided without eliminating the essential function of driving.</p><p></p><p><b>COVID-19 Vaccine Policy (customer-facing roles only):</b> While Novartis does not require vaccination for COVID-19 or proof of a recent negative test result for COVID-19 at this time, employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to Eh.occupationalhealth&#64;novartis.com.</p><p></p><p><b>For Field Roles with a Dedicated Training Period:</b> The individual hired for this role will be required to successfully complete certain initial training, including home study in eight (8) or fewer hours per day and forty (40) or fewer hours per week.</p><p></p><p><b>Novartis Compensation Summary:</b></p><p>The salary for this position is expected to range between:</p><ul><li>Associate Territory Account Specialist: $81,200 and $150,800 per year</li><li>Territory Account Specialist: $114,100 and $211,900 per year</li><li>Senior Territory Account Specialist: $132,300 and $245,700 per year</li><li>Executive Territory Account Specialist: $145,600 and $270,400 per year</li></ul><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$132,300.00 - $245,700.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Commercial Excellence, Communication Skills, Compliance, Conflict Management, Cross-Functional Coordination, Customer Insights, health care industry, Influencing Skills, Key Account Management, Negotiation Skills, Professional Ethics, Selling Skills, Technical Skills]]></description><link>http://biotechroles.com/ultra-rare-disease-territory-account-specialist-beverly-hills-ca-novartis/6a07443a2f1861929d253289</link><guid isPermaLink="true">http://biotechroles.com/ultra-rare-disease-territory-account-specialist-beverly-hills-ca-novartis/6a07443a2f1861929d253289</guid><pubDate>Fri, 15 May 2026 16:05:14 GMT</pubDate><company>Novartis</company><location>Field Sales (USA)</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Quality Manager (ecompliance)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Provide quality assurance expertise, guidance and support to operational activities in development and research organizations to ensure compliance with applicable regulatory requirements and Novartis procedures and quality standards.  Manage projects, including Quality Plan initiatives, and processes that support quality objectives to assure their compliance with GxP regulations. Responsible for operational eCompliance support for Biomedical Research, ensuring compliance, validation oversight, and inspection readiness for GxP and non-GxP systems and associated supplier activities.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities</b></p><ul><li><p>Support initiatives to maintain or improve quality performance and compliance of operational activities including risk management, health authority reporting, IT systems</p></li><li><p>Manage and Support quality aspects of projects and activities, including those related to third parties, analytical instruments, manufacturing equipment, quality plans, training, IT validations, etc.</p></li><li><p>Provide operational eCompliance support for ~20 active systems (GxP and non-GxP), including Periodic Review, review of validation and change control deliverables, HLCCD review and sign-off</p></li><li><p> Support operational aspects of new system implementations, ensuring adherence to compliance and validation requirements </p></li><li><p>Perform technical aspects of IT / Technology Vendor Qualification and assessments </p></li><li><p>Provide inspection support for systems supported by the eCompliance manager</p></li><li><p> Provide input on technical aspects of SOPs, guidance, standards, and health authority (HA) regulation gap assessments </p></li><li><p>Support operational aspects of CAPAs and remediation activities, including review of CAPA documentation </p></li></ul><p>Minimum Requirement</p><div><ul><li>Bachelor’s degree with ~5 years of experience or Master’s degree with ~2 years of experience in quality, compliance, or clinical development.</li><li>Strong experience in audit &amp; inspection management, quality management systems (QMS), quality assurance, and regulatory compliance across drug development.</li><li>Proven expertise in SOP management and working within GxP-regulated environments (GCP, GLP, GMP).</li><li>Solid understanding of computer system validation (CSV), change control processes, and IT supplier qualification and audits.</li><li>Demonstrated experience supporting inspection readiness with strong attention to detail and regulatory alignment.</li></ul></div><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Business Partnering, Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge]]></description><link>http://biotechroles.com/quality-manager-ecompliance-novartis/6a0744392f1861929d253288</link><guid isPermaLink="true">http://biotechroles.com/quality-manager-ecompliance-novartis/6a0744392f1861929d253288</guid><pubDate>Fri, 15 May 2026 16:05:13 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$18000-35000</salary><type>Full time</type></item><item><title><![CDATA[Specialist, Quality Control - Physical Chemistry]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Specialist, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring conformance to established quality processes and standards for manufacturing and production.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location: </b></p><ul><li>This position will be located in Durham, NC and will be an On-Site role.</li><li>Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.</li></ul><p></p><p><b>Key Responsibilities:</b></p><ul><li>Execute routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to chromatography (HPLC, UPLC), AUC, SEC, compendial assays (pH, Conductivity, Osmolality), electrophoresis (CE, Western Blot) and assist with data review.</li><li>Execute method verifications/transfers as required for various projects.</li><li>Assist with enrollment of vendors, ordering reagents and consumables for new assays.</li><li>Initiate all paperwork (LIMS, SOPs, assay forms) for testing and transfers of methods for projects.</li><li>Assists in the evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards.</li><li>Reviews data obtained for compliance with specifications and reports abnormalities. Performs trend analysis of methods /environmental data / assay controls &amp; standards and draws conclusions.</li><li>Capable of delivering to assigned work schedule with attention to detail and accuracy.</li><li>Support department risk assessments and participate in audit walkthroughs.</li><li>Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance with specifications and reports. Investigates and resolves non-conforming test results by completing thorough Deviation, OOS/OOT/OOE and Investigation.</li><li>Authors new/revise Standard Operating Procedures, Protocols / Summary Reports / Analytical Master Plans for QC.</li><li>Oversee special projects on analytical and instrument problem solving. May develop testing and analysis methods and procedures in accordance with established guidelines.</li><li>Supports training of departmental personnel in appropriate techniques and related topics.</li><li>Other related job duties as assigned.</li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li>Bachelor&#39;s degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field with 5 years’ experience in GMP environment or 4 years’ at GTx.</li><li>Excellent interpersonal, verbal and written communication skills with strong technical writing experience required. Previous investigation experience a plus.</li><li>Proven ability to work effectively in a team environment. Collaborates cross functionally with other departments to achieve site goals.</li><li>Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. </li><li>Exercises judgment within defined procedures and practices to determine appropriate action including critical thinking, troubleshooting and problem-solving skills.</li><li>Normally receives general instructions on routine work, detailed instructions on new projects or assignments.</li><li>Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of core duties.</li></ul><p></p><p><b>Novartis Compensation and Benefit Summary:</b></p><p>The salary for this position is expected to range between $41.06 and $76.25 per hour.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p>#LI-Onsite</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$85,400.00 - $158,600.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Business Partnering, Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge, Risk Management, Stakeholder Management]]></description><link>http://biotechroles.com/specialist-quality-control-physical-chemistry-novartis/6a0744372f1861929d253287</link><guid isPermaLink="true">http://biotechroles.com/specialist-quality-control-physical-chemistry-novartis/6a0744372f1861929d253287</guid><pubDate>Fri, 15 May 2026 16:05:11 GMT</pubDate><company>Novartis</company><location>Durham</location><salary>$75000-105000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Sales Representative]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>- Responsible for executing the in-field commercial strategy for assigned priority brands within a defined territory. The role focuses on high-quality customer engagement, effective execution of brand and tactical plans, generating demand, and delivery of agreed sales objectives, in line with Novartis policies, ethical standards, and compliance requirements.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major accountabilities:</b></p><ul><li><p>Execute the ICE field execution framework by:</p><ul><li><p>segmenting customers according to company standards (e.g., via ViP tool),</p></li><li><p>applying value-based tiering,</p></li><li><p>using tailored promotional content and key messages by segment audience,</p></li><li><p>adhering to data driven call plans suggestions (e.g., via IDS&#43;),</p></li><li><p>consistently deploying personalized omnichannel customer journeys enabled by global International digital tools (e.g., RepAI, IDS&#43;, OnCore,Veeva, etc.),</p></li><li><p>timely documenting customers visits.</p></li></ul></li><li><p>Deliver high-quality, compliant product promotion in-field activities and customer engagements, in alignment with brand and TA strategies and by:</p><ul><li><p>applying approved messages through the 6 Impact Behaviors (6IBs) selling model,</p></li><li><p>leveraging technology enablement to enhance customer engagement (e.g. RepAI, IDS&#43;, OnCore, Veeva, CRM, etc.),</p></li><li><p>continuously improving execution quality through building on coaching feedback inputs, field effectiveness assessment reports (STEM) and performance insights (e.g. BEST, C360, etc.) with respective area manager and/or sales head.</p></li></ul></li><li><p>Act as a trusted  therapeutic area commercial partner to HCPs, explaining clinical data, evidence, and appropriate product use.</p><p></p></li><li><p>Maximize technology enablement support systems, e.g. “next best action” proposals, to enhance customer engagement impact.</p><p></p></li><li><p>Collect, interpret, and share field insights on best practices, customer needs, market dynamics, competitor activity, and  territory needs and priorities, to develop actions to address them.</p><p></p></li><li><p>Participate in or contribute to local events, meetings, and promotional activities in compliance with governance standards.</p><p></p></li><li><p>Collaborate cross-functionally with TA Marketing, Medical TA, Value &amp; Access, and Execution Excellence partners.</p></li><li><p>Operate fully in line with Novartis policies, ethical standards, and local regulatory requirements.</p></li><li><p>Live by Novartis Code of Ethics and Values and Behaviors.</p></li><li><p>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt.</p></li></ul><p></p><p><b>Key performance indicators: </b></p><ul><li><p>To be populated at local level, based on the guidance that will follow from IMI Field Engagement Performance Management Council outcomes.</p></li><li><p>Achievement of sales targets and objectives.</p></li><li><p>Quality and effectiveness of customer interactions, including adherence to: 6IBs selling model, value-based tiering and personalized omnichannel customer engagement targets achievement.</p></li><li><p>Coverage and frequency against suggested call plans.</p></li><li><p>Adherence to compliance, reporting, and CRM standards.</p></li><li><p>Quality of insights provided to cross-functional teams.</p></li><li><p>Progress on field effectiveness assessment (incl Capability building requirements).</p></li><li><p>Adherence to International Commercialization Excellence – field sales guidelines and targets.</p></li><li><p>Completed product and disease knowledge tests (if applicable).</p></li></ul><p></p><p><b>Minimum Requirements:</b></p><ul><li><p>University degree in<b> life sciences, business, or a related field</b>.</p></li><li><p>Proven experience in pharmaceutical or healthcare sales.</p><p></p></li><li><p>Strong customer engagement and relationship management skills.</p><p></p></li><li><p>Ability to execute omnichannel customer journeys effectively.</p><p></p></li><li><p>Commercial mindset with strong execution focus.</p><p></p></li><li><p>Analytical skills to interpret data and KPIs.</p><p></p></li><li><p>Strong communication and interpersonal skills.</p><p></p></li><li><p>Ability to work independently while collaborating across teams.</p><p></p></li><li><p>Proven ability to use digital/AI tools as part of daily work.</p></li><li><p>High standards of integrity, ethics, and compliance awareness.</p></li></ul><p></p><p><b>Skills: </b></p><ul><li><p>Key Account Management</p></li><li><p>Commercial Excellence</p></li><li><p>Communication Skills</p></li><li><p>Compliance</p></li><li><p>Conflict Management</p></li><li><p>Cross-Functional Coordination</p></li><li><p>Customer Insights</p></li><li><p>Professional Ethics</p></li><li><p>Health care Industry</p></li><li><p>Influencing Skills</p></li><li><p>Negotiation Skills</p></li><li><p>Selling Skills</p></li><li><p>Technical Skills</p></li></ul><p></p><p><b>Languages:</b></p><ul><li><p>English is optional.</p></li><li><p>Local Language.</p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Commercial Excellence, Communication Skills, Compliance, Conflict Management, Cross-Functional Coordination, Customer Insights, health care industry, Influencing Skills, Key Account Management, Negotiation Skills, Professional Ethics, Selling Skills, Technical Skills]]></description><link>http://biotechroles.com/sr-sales-representative-novartis/6a0744362f1861929d253286</link><guid isPermaLink="true">http://biotechroles.com/sr-sales-representative-novartis/6a0744362f1861929d253286</guid><pubDate>Fri, 15 May 2026 16:05:10 GMT</pubDate><company>Novartis</company><location>Field Force (Indonesia)</location><salary>$35000-60000</salary><type>Full time</type></item><item><title><![CDATA[Mehanik v enoti pakiranje (m/ž/d)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Onsite <br>Lokacija: Ljubljana<br>Interni naziv pozicije: Mehanik III<br><br>V enoti pakiranje v pretisne omote v Ljubljani iščemo Mehanika (m/ž/d), ki bo odgovoren za samostojno, zahtevnejše vzdrževanje strojev in naprav ali objektov, zagotavljanje ustreznih pogojev na strojih in samostojno izvajanje nastavitve in menjave strojnih delov. <br>Zadolženi boste za sodelovanje pri uvajanju nove strojne tehnologije, prenašanje znanja na sodelavce ter za zagotavljanje realizacije proizvodnje, skladno z zakonodajo, internimi predpisi, dobrimi praksami in poslovnimi cilji.<br><br>Sodelavci so vključeni v izmenski delovnik. Delo poteka en teden v nočni izmeni, en teden popoldne in en teden dopoldne. <br><br>This role is based in Ljubljana, Slovenia. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span>Vaše ključne odgovornosti:</span></b></p><ul><li>Samostojno izvajanje nastavitve in menjave strojnih delov.</li><li>Sodelovanje pri izvajanju servisov s strani zunanjih izvajalcev.</li><li>Izvajanje rednih letnih remontov ter sodelovanje s proizvodnim inženiringom.</li><li>Podajanje predlogov tehničnih in drugih izboljšav.</li><li>Sodelovanje pri planiranih in neplaniranih posegih ter odpravi napak na opremi in sistemih.</li><li>Sodelovanje pri zagonih in kvalifikacijah nove in obstoječe opreme in sistemov.</li><li>Odpravljanje neplaniranih zastojev.</li><li>Izvajanje nalog s področja vzdrževanja strojev in naprav.</li><li>Sodelovanje v proizvodnem procesu (posluževanje stroja, IPC kontrole, kontrole senzorjev, čiščenja).</li></ul><p></p><p><b><span>Vaš doprinos k delovnem mestu: </span></b></p><ul><li>Srednješolska poklicna stopnja izobrazbe strojne, elektro ali druge ustrezne smeri.</li><li>Aktivno znanje slovenskega jezika.</li><li>Poznavanje orodja Microsoft Office.</li><li>Zaželene delovne izkušnje s področja proizvodnje in vzdrževanja.</li></ul><p></p><p>Z izbranim kandidatom bomo sklenili delovno razmerje za <b><span>določen čas enega leta</span></b> s poskusno dobo <b><span>6 mesecev</span></b>.  </p><p></p><p></p><p><b><span>Ugodnosti in nagrajevanje: </span></b>Konkurenčen plačni paket, letni bonus, pokojninska shema, možnost vključitve v kolektivno zdravstveno zavarovanje,  shema nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju fizičnega in duševnega dobrega počutja ter delovne obremenitve (Polni življenja), številne priložnosti za učenje in razvoj. </p><p></p><p>Preberite naš priročnik, da spoznate načine, s katerimi bomo spodbujali vaš osebni in profesionalni razvoj: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank"><span>https://www.novartis.com/careers/benefits-rewards</span></a>   </p><p></p><p><b><span>Predani smo raznolikosti in vključenosti: </span></b>Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo. </p><p></p><p></p><p><b><span>Zakaj Novartis:</span></b> Pomagati bolnikom in njihovim družinam zahteva več kot le inovativno znanost. Potrebna je skupnost zavzetih ljudi, kot ste vi. V Novartisu cenimo sodelovanje, podporo in navdihovanje drug drugega za razvoj prebojnih terapij, ki spreminjajo življenja pacientov. Ste pripravljeni ustvariti svetlejšo prihodnost skupaj z nami? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank"><span>https://www.novartis.com/about/strategy/people-and-culture</span></a>   </p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>General Hse Knowledge  , gmp knowledge]]></description><link>http://biotechroles.com/mehanik-v-enoti-pakiranje-mzd-novartis/6a0744362f1861929d253285</link><guid isPermaLink="true">http://biotechroles.com/mehanik-v-enoti-pakiranje-mzd-novartis/6a0744362f1861929d253285</guid><pubDate>Fri, 15 May 2026 16:05:10 GMT</pubDate><company>Novartis</company><location>Ljubljana</location><salary>$25000-35000</salary><type>Full time</type></item><item><title><![CDATA[Senior Engineer, MS&T]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Step into a high-impact role where your expertise will directly shape the delivery of life-saving therapies. As a key member of Manufacturing Science and Technology, you’ll lead process improvements and drive innovation in sterile drug product manufacturing, partnering cross-functionally to ensure quality, efficiency, and reliability. This is your opportunity to solve complex challenges, influence production outcomes, and play a critical role in bringing medicines to patients.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location: </b></p><ul><li>This position will be located in Durham, NC and will be an onsite role.</li><li>Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.</li></ul><p></p><p><b>Key Responsibilities:</b></p><ul><li>Lead process investigations to resolve manufacturing issues and drive continuous improvements</li><li>Analyze process verification data to identify trends and ensure consistent product quality</li><li>Partner with manufacturing to meet production schedules and maintain reliable drug supply</li><li>Monitor critical quality attributes and process parameters to control variability and drift</li><li>Implement process improvements in collaboration with operations and engineering teams</li><li>Support startup and qualification of new equipment, systems, and manufacturing processes</li><li>Document and manage updates to manufacturing processes in compliance with quality standards</li><li>Provide technical expertise for projects, including remediation and process enhancement initiatives</li><li>Support technology transfer to ensure seamless transition into compliant GMP manufacturing</li><li>Collaborate with Quality to maintain a compliant and inspection-ready production environment</li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li>Bachelor of Science degree with 6 years, Master of Science with 4 years, or PhD with 2 years of biopharmaceutical manufacturing experience</li><li>Strong experience supporting GMP drug product manufacturing environments, including aseptic processing and fill/finish operations</li><li>Proven ability to analyze data and apply scientific principles to solve complex process issues</li><li>Excellent written and verbal communication skills with strong technical writing capability</li><li>Demonstrated ability to collaborate effectively across cross-functional teams</li><li>Familiarity with global regulatory requirements for drug products, validation, and qualification</li><li>Ability to manage multiple priorities and contribute to continuous improvement initiatives</li></ul><p></p><p><b>Novartis Compensation and Benefit Summary:</b></p><p>The salary for this position is expected to range between <span>$114,100 to $211,900 </span><span>annually</span></p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p>#LI-Onsite</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$114,100.00 - $211,900.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Applied Statistics, Change Control, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Manufacturing Technologies, Operational Excellence, Process and Cleaning Validation, Process Control, Quality Compliance, Regulatory Compliance, Resilience and Risk Management, Technical Leadership, Technology Transfer]]></description><link>http://biotechroles.com/senior-engineer-msandt-novartis/6a0744362f1861929d253284</link><guid isPermaLink="true">http://biotechroles.com/senior-engineer-msandt-novartis/6a0744362f1861929d253284</guid><pubDate>Fri, 15 May 2026 16:05:10 GMT</pubDate><company>Novartis</company><location>Durham</location><salary>$130000-170000</salary><type>Full time</type></item><item><title><![CDATA[Operater v enoti pakiranja (m/ž/d)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Onsite<br>Lokacija: Ljubljana<br>Interni naziv: Operater III<br><br>V enoti pakiranje v pretisne omote v Ljubljani iščemo Operaterja (m/ž/d), ki bo odgovoren za samostojno izvajanje posameznih proizvodnih operacij na različnih linijah in v različnih enotah, za realizacijo proizvodnje, skladno z zakonodajo, internimi predpisi, dobrimi praksami in poslovnimi cilji.<br><br>Iščemo zanesljivo in natančno osebo za izvajanje ter vodenje proizvodnih procesov, ki bo skrbela za skladnost z GMP smernicami, dosledno dokumentiranje aktivnosti ter nemoteno delovanje in urejenost proizvodnega okolja.<br><br>Sodelavci so vključeni v izmenski delovnik. Delo poteka en teden v nočni izmeni, en teden popoldne in en teden dopoldne.<br><br>This role is based in Ljubljana, Slovenia. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p>Vaše ključne odgovornosti:</p><p><span><span>·<span>         </span></span></span>Izvajanje operacij v proizvodnih procesih in/ali vodenje proizvodnih procesov.</p><p><span><span>·<span>         </span></span></span>Izvajanje vseh dodeljenih dejavnosti v skladu s proizvodnim planom in veljavnimi GMP smernicami in navodili ter dosledno dokumentiranje vseh aktivnosti.</p><p><span><span>·<span>         </span></span></span>Odgovornost za pravočasno in točno pregledovanje in dokumentiranje evidenc o serijah.</p><p><span><span>·<span>         </span></span></span>Pravilno in pravočasno izvajanje čiščenj ter priprave in sterilizacije  proizvodne opreme in proizvodnih prostorov.</p><p><span><span>·<span>         </span></span></span>Odgovornost za vzdrževanje proizvodnih površin (čiščenje, urejanje in pospravljanje po 5S sistemu-vsak element na za to predpisanem mestu).</p><p><span><span>·<span>         </span></span></span>Odgovornost za spremljanje strojev (linij) v obratovanju in ustrezna esklalacija v primeru težav.</p><p><span><span>·<span>         </span></span></span>Po potrebi vzorčenje, razdeljevanje, distribuiranje in izvajanje medprocesnih kontrol.</p><p>Vaš doprinos k delovnem mestu:</p><p><span><span>·<span>         </span></span></span>Srednješolska poklicna stopnja izobrazbe (katerekoli smeri).</p><p><span><span>·<span>         </span></span></span>Aktivno znanje slovenskega jezika.</p><p><span><span>·<span>         </span></span></span>Poznavanje orodja Microsoft Office.</p><p>Zaželene izkušnje:</p><p><span><span>·<span>         </span></span></span>Delovne izkušnje s poznavanjem proizvodnega procesa v različnih organizacijskih enotah in linijah.</p><p></p><p></p><p>Z izbranim kandidatom bomo sklenili delovno razmerje za <b>določen čas</b> s poskusno dobo <b>6 mesecev</b>. Prijavo oddajte z življenjepisom v slovenskem jeziku.</p><p></p><p></p><p><b>Ugodnosti in nagrajevanje: </b>Konkurenčen plačni paket, letni bonus, fleksibilen način dela z možnostjo prilagajanja urnika, pokojninska shema, možnost vključitve v kolektivno zdravstveno zavarovanje, shema nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju fizičnega in duševnega dobrega počutja ter delovne obremenitve (Polni življenja), številne priložnosti za učenje in razvoj.</p><p>Preberite naš priročnik, da spoznate načine, s katerimi bomo spodbujali vaš osebni in profesionalni razvoj: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">https://www.novartis.com/careers/benefits-rewards</a> </p><p><b>Predani smo raznolikosti in vključenosti: </b>Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.</p><p><b>Zakaj Novartis: </b>Pomagati bolnikom in njihovim družinam zahteva več kot le inovativno znanost. Potrebna je skupnost zavzetih ljudi, kot ste vi. V Novartisu cenimo sodelovanje, podporo in navdihovanje drug drugega za razvoj prebojnih terapij, ki spreminjajo življenja pacientov. Ste pripravljeni ustvariti svetlejšo prihodnost skupaj z nami? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a> </p><p><b>Pridružite se Novartisu:</b> Ni pravo delovno mesto za vas? Prijavite se v našo bazo talentov, da ostanete v kontaktu z nami in se seznanite z ustreznimi kariernimi priložnostmi takoj, ko se pojavijo: <a href="https://talentnetwork.novartis.com/network" target="_blank">https://talentnetwork.novartis.com/network</a> </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>General Hse Knowledge  , gmp knowledge]]></description><link>http://biotechroles.com/operater-v-enoti-pakiranja-mzd-novartis/6a0744352f1861929d253283</link><guid isPermaLink="true">http://biotechroles.com/operater-v-enoti-pakiranja-mzd-novartis/6a0744352f1861929d253283</guid><pubDate>Fri, 15 May 2026 16:05:09 GMT</pubDate><company>Novartis</company><location>Ljubljana</location><salary>$22000-30000</salary><type>Full time</type></item><item><title><![CDATA[Executive Director, Clinical Data Technology Platforms]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Executive Director, Clinical Data Technology Platforms occupies a pivotal organizational position to collaborate with ASCEND Functional and Service Area Leads, orchestrating the development of a cohe-sive strategy and overseeing the delivery of highly complex Development technology transformation pro-grams. This role ensures organizational congruence and flawless cross-functional execution for the pro-grams under purview (e.g., IDR, CDP, RBQM, Digital Protocol, NextGen Development Data Platform, and SCAPE).<br><br>In the capacity of Executive Director, Clinical Data Technology Platforms of Strategic Programs, there may be occasions to act on behalf of the Head of ASCEND Strategy &amp; Transformation, serving as a leader and representative for ASCEND’s Portfolio/Program Management Office. This encompasses the realms of Program Management, Process, Product, and Change Management. The Executive Director is charged with the comprehensive scoping, delivery, and execution of strategic technology transformation programs within the ASCEND framework.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities</b></p><div><ul><li>Lead strategic oversight and execution of transformation programs (e.g., IDR, CDP, RBQM, NextGen Data Platform, Cloudscapes), ensuring alignment across Development functions.</li><li>Define and drive integrated, standardized approaches leveraging technology to deliver scalable, end-to-end solutions.</li><li>Partner with ASCEND chapter leads and cross-functional teams to translate strategy into executable integrated plans.</li><li>Champion adoption of AI/GenAI through PoCs and scalable solutions, aligned with enterprise AI initiatives.</li><li>Ensure quality, consistency, and excellence of all program deliverables, strategic artifacts, and documentation.</li><li>Drive transparent communication on delivery status, risks, and issues, enabling informed decision-making.</li><li>Identify resource gaps, propose mitigation strategies, and escalate as needed to ensure program continuity.</li><li>Lead complex cross-functional collaborations and external partnerships, fostering alignment and innovative problem-solving.</li><li>Set delivery priorities, monitor execution, and drive enterprise-level outcomes across multiple initiatives.</li><li>Provide leadership, coaching, and governance across teams, fostering a high-performance, innovation-driven culture.</li></ul><p></p><p><b>Minimum Responsibilities</b></p><div><ul><li>20&#43; years of cross-industry experience, including ~10 years in pharma, with extensive leadership across complex, global, and cross-functional teams.</li><li>Proven expertise in leading large-scale global technology transformation programs with strong portfolio and program management capabilities.</li><li>Strong executive presence with the ability to influence senior stakeholders, navigate complex environments, and drive strategic decision-making, scenario planning, and risk mitigation.</li><li>Deep expertise in stakeholder engagement, executive communication, and bridging scientific and business functions to deliver impactful outcomes.</li><li>Advanced planning, prioritization, and tracking capabilities with proficiency in program management tools, managing multiple high-priority initiatives simultaneously.</li></ul></div></div><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Accountability, Agility, Cross-Functional Teams, Decision Making Skills, Drug Development, Entrepreneurship, Health Authorities Interactions, Leadership, Program Management, Project Delivery, R&amp;D, Risk Management, Strategy]]></description><link>http://biotechroles.com/executive-director-clinical-data-technology-platforms-novartis/6a0744352f1861929d253282</link><guid isPermaLink="true">http://biotechroles.com/executive-director-clinical-data-technology-platforms-novartis/6a0744352f1861929d253282</guid><pubDate>Fri, 15 May 2026 16:05:09 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Regional Director of Medical Science Liaison - Great Lakes Region]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Remote<br><br>This is a field-based and remote opportunity supporting a team in an assigned geography. Ability to travel 60-70% over a broad geography is required, with the ability to drive and/or fly within the territory. Must have a valid driver’s license. Preferred candidate resides within region, or within a reasonable commuting distance from region border.<br><br>Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. <br><br>Company will not sponsor visas for this position.<br><br>As Regional Director, Medical Science Liaison (MSL), you will set the standard for Field Medical Excellence across the region or local CPO translating strategy into action by driving Field Medical plans, ensuring launch readiness for key products (including MSL deployment, tools, and resources), and strengthening the systems and processes that enable high-impact field execution. You will partner closely with Regional Medical Directors, the Global FME group, and Franchise/Global Medical Affairs teams to deliver results.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities</b></p><ul><li>Lead and guide the Field Medical Team (MSL Managers), ensuring the effective implementation of a Field Medical organization within the assigned region or medical unit</li><li>Drive the implementation of Field Medical Intelligence and insights, enabling cross-functional exchange, engagement strategy development, and execution</li><li>Support and ensure Field Medical launch excellence and all related launch activities</li><li>Build and strengthen regional/CPO Field Medical capabilities, including onboarding, soft skills development, and coaching excellence</li><li>Plan, coordinate, and deliver MSL and MSL Manager training in collaboration with Global FME and Global Medical Affairs Franchise teams, ensuring local implementation of training curricula and individual development plans</li><li>Adapt and leverage therapeutic medical resources for external use by MSLs</li><li>Develop and maintain regional deployment maps across all brands, align on standardized FME/CPO KPIs, ensure tracking, and provide regular reporting of deployment, KPIs, and insights to regional/country and global medical leadership</li><li>Provide coaching and talent development for direct reports; ensure compliant reporting of technical complaints, adverse events, and special cases within 24 hours, and oversee the distribution of marketing samples where applicable</li></ul><p><b>Essential Requirements</b></p><ul><li><b>Education:</b> Graduate degree in science or healthcare required; doctoral degree preferred (MD, PhD, DNP, PharmD, etc.) </li><li>Minimum of 7 years’ experience in a Field Medical-based position within the pharmaceutical industry or as an MSL is preferred OR 8&#43; years of relevant medical affairs, clinical research, or related experience in a scientific or clinical setting required.  </li><li>Strong clinical knowledge including pharmacotherapy, treatment guidelines, clinical research processes, medical expert engagement strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is required.   </li><li>History of organizational or enterprise impact through strategic thinking, working within a matrix organization and leading others through collaborative teams in a Field Medical-based position required. </li><li>Candidates will perform their duties in accordance with applicable law, regulations, and Novartis policies. </li><li>Works within Ethics, Compliance and Promotional policies (Novartis &amp; Federal) and ensures those around them do the same. </li><li>Works to ensure a diverse and inclusive environment free from all forms of discrimination and harassment. </li><li>Adherence with Company policies, state and federal laws and regulations </li></ul><p><b>Desirable Requirements:</b></p><ul><li>Previous experience in assigned therapeutic area (Cardiovascular) or related therapeutic area is preferred. </li></ul><p></p><p>NOTE: Above level experience criteria are not an exhaustive list. </p><p><b>Driving is an Essential Function of this Role: </b>Meaning it is fundamental to the purpose of this job and cannot be eliminated. Because driving is an essential function of the role, you must have a fully valid and unrestricted driver’s license to be qualified for this role. The company provides reasonable accommodations for otherwise qualified individuals with medical restrictions if an accommodation can be provided without eliminating the essential function of driving.</p><p><b>COVID-19 Vaccine Policy (customer-facing roles only):</b> While Novartis does not require vaccination for COVID-19 or proof of a recent negative test result for COVID-19 at this time, employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to Eh.occupationalhealth&#64;novartis.com.</p><p><b>For Field Roles with a Dedicated Training Period:</b> The individual hired for this role will be required to successfully complete certain initial training, including home study, eight (8) or fewer hours per day and forty (40) or fewer hours per week.</p><p><b>Novartis Compensation Summary: </b></p><p>The pay range for this position at commencement of employment is expected to be between $225,400 and $418,600 year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p>To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$225,400.00 - $418,600.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Clinical Research, Clinical Study Reports, Customer Engagement, Customer Insights, Disease Management, Health Economics, Internal Medicine, Medical Communication, Medical Information, Microsoft PowerPoint, Microsoft Word, Patient Care, Phase Iv Clinical Trial, Product Placement, Scientific Support, Strategic Direction, Team Player, Teamwork, Utilization Management (Um)]]></description><link>http://biotechroles.com/regional-director-of-medical-science-liaison-great-lakes-region-novartis/6a0744342f1861929d253281</link><guid isPermaLink="true">http://biotechroles.com/regional-director-of-medical-science-liaison-great-lakes-region-novartis/6a0744342f1861929d253281</guid><pubDate>Fri, 15 May 2026 16:05:08 GMT</pubDate><company>Novartis</company><location>Field Non-Sales (USA)</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Assoc. Director Visualization(Power BI)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: Hyderabad<br><br>Accountable as the Business System Owner for the Enterprise Visualization Platform, ensuring Business adoption, value realization, and effective utilization.<br>Partners with DDIT and platform teams to align demand with business priorities, support platform roadmap execution, and ensure adherence to architecture, governance, and experience standards.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major Accountabilities</b></p><ul><li><p>Own the business vision and value realization of the Enterprise visualization platform.</p></li><li><p>Align platform capabilities with business outcomes and KPIs. Drive demand intake, prioritization, and backlog alignment to business needs.</p></li><li><p>Contribute to platform roadmap execution and adoption strategy. Define and track value metrics (usage, impact, decision enablement). Support onboarding of new use cases aligned with governance and architecture.</p></li><li><p>Lead legacy BI decommissioning (e.g., Qlik) aligned with platform roadmap. Drive continuous improvement across platform capabilities and operations.</p></li><li><p>Enable governed self-service analytics through standardized environments and certified assets. Establish governance and quality reviews ensuring adherence to architecture, engineering, and security standards.</p></li><li><p>Build and scale enablement models (training, playbooks, community) to drive adoption.</p></li><li><p>Own business governance, funding, and cost optimization for platform usage while ensuring value realization.Ensure full compliance with Information Security &amp; Compliance (ISC), legal, ethical, and regulatory requirements, including GxP where applicable.</p></li><li><p>Embed security, privacy, compliance, and risk considerations into platform architectures, delivery standards, and operational processes. Define funding and charging model for platform usage and track cost vs value optimization.</p></li></ul><p></p><p><b>Min Requirements:</b></p><ul><li><p>10&#43; years in Data &amp; Analytics / BI.</p></li><li><p>5&#43; years leading enterprise analytics/visualization platforms in a global matrix environment.</p></li><li><p>Deep expertise in Power BI and Microsoft Fabric (semantic modelling, performance, governance, RLS, deployment pipelines).</p></li><li><p>Working knowledge of modern data platforms and integration patterns (incl. Databricks and Snowflake).</p></li><li><p>Proven experience operating a centralized delivery model (intake/prioritization/capacity/SLA reporting) and scaling adoption via COE practices.</p></li><li><p>AWS experience preferred; relevant cloud architecture certification is a plus.</p></li><li><p>Pharma / life-sciences domain exposure preferred; experience working in regulated contexts (GxP) is an advantage.</p></li><li><p>Strong vendor and stakeholder management;</p></li></ul><p><b>Why Novartis?</b></p><p>Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!<br />Learn more here:<br /><br />https://www.novartis.com/about/strategy/people-and-culture<br /><br />Commitment to Diversity and Inclusion:<br />Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.<br />Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:<br />https://talentnetwork.novartis.com/network</p><h1></h1><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>power bi]]></description><link>http://biotechroles.com/assoc-director-visualizationpower-bi-novartis/6a0744342f1861929d253280</link><guid isPermaLink="true">http://biotechroles.com/assoc-director-visualizationpower-bi-novartis/6a0744342f1861929d253280</guid><pubDate>Fri, 15 May 2026 16:05:08 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Senior Brand Manager, Oncology]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>As a Senior Brand Manager, Oncology, you will play a key role in driving the growth and performance of the oncology portfolio in Canada. Partnering closely with Medical, Field Force, and cross-functional teams, you will lead the execution of strategic and tactical initiatives to maximize brand value across the lifecycle. This role requires strong business acumen, execution excellence, and the ability to operate effectively in a highly collaborative, matrix environment.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><div><p><b>#LI-Hybrid</b><br /><b>Location:</b> Toronto, Ontario</p><p><br />This role is based in Toronto, Canada. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.</p><p></p><p><b>This job posting is not for an existing position.</b></p><div><p></p></div><p><b>Key responsibilities:</b></p><ul><li><p>Drive performance of key oncology assets through effective brand planning and execution</p></li><li><p>Develop and implement tactical marketing plans aligned with strategic brand objectives and lifecycle management</p></li><li><p>Generate high-quality, timely market insights to optimize brand positioning, targeting, and segmentation</p></li><li><p>Partner with Medical, Brand Director, and Field teams to ensure strong cross-functional alignment and execution excellence</p></li><li><p>Plan and execute promotional activities, including campaign development, media strategy, and events</p></li><li><p>Lead demand planning, forecasting, and financial discipline across brand-related investments</p></li><li><p>Support annual brand planning, budget development, and monthly forecasting processes</p></li><li><p>Track performance through defined KPIs and provide regular insights and recommendations to stakeholders</p></li><li><p>Ensure consistency of approach within the customer marketing team and alignment across stakeholders</p></li><li><p>Ensure compliance with Novartis policies, including reporting of adverse events within 24 hours</p></li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li><p>Proven experience in brand management within the pharmaceutical industry</p></li><li><p>Strong strategic thinking with demonstrated ability to translate strategy into execution</p></li><li><p>Experience working in cross-functional teams (e.g., Medical, Sales, Marketing)</p></li><li><p>Strong project management and operational execution skills</p></li><li><p>Ability to build trust-based relationships with key stakeholders</p></li><li><p>Business acumen with focus on driving sales growth and performance</p></li><li><p>Strong communication and collaboration skills in a matrix environment</p></li></ul><p></p><p><b>Desirable Requirements:</b></p><ul><li><p>Experience in Oncology or specialty care therapeutic areas</p></li><li><p>Experience in multinational or large pharmaceutical organizations</p></li></ul><p></p><p></p><p><b><span>At </span><span>Novartis Canada</span><span>,</span><span> </span></b><span>we are determined to be a valued partner and advocate, with a deep understanding of patient needs along the entire care journey – from drug development, to diagnosis, to access and beyond. Part of the way we are doing this is by leveraging data, technology, and partnerships.</span></p><p><span> </span></p><p><span>Research &amp; Development</span><span>:</span><span> we focus on four core therapeutic areas: Cardiovascular, Renal &amp; Metabolic, Immunology, Neuroscience and Oncology. We also develop and deliver treatments through other promoted and established brands, which today are helping millions of patients. Over the last three years, our average annual research and development investment in Canada was over $30 million, and we conduct clinical trial research in every region throughout Canada.</span></p><p><span> </span></p><p><span>Commitment to Diversity and Inclusion</span><span>:</span><span> Novartis is committed to building outstanding, inclusive work environment and diverse team’s representatives of the patients and communities we serve.</span></p></div><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Asset Management, Commercial Excellence, Cross-Functional Collaboration, Customer Orientation, Digital Marketing, Healthcare Sector Understanding, Influencing Skills, Marketing Strategy, Negotiation Skills, Operational Excellence, Priority Disease Areas Expertise, Product Lifecycle Management (PLM), Product Marketing, Product Strategy, Stakeholder Engagement, Stakeholder Management, Strategic Partnerships]]></description><link>http://biotechroles.com/senior-brand-manager-oncology-novartis/6a0744342f1861929d25327f</link><guid isPermaLink="true">http://biotechroles.com/senior-brand-manager-oncology-novartis/6a0744342f1861929d25327f</guid><pubDate>Fri, 15 May 2026 16:05:08 GMT</pubDate><company>Novartis</company><location>Toronto</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Patient Access  Lead]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>As a Global Market Access Lead, you will play a critical role in shaping and driving the integrated access strategy for innovative therapies within Neuroscience and Gene Therapy. You will lead global reimbursement efforts for a high-priority asset, partnering cross-functionally to ensure optimal patient access across key markets. This is a highly strategic role requiring deep expertise in market access, strong leadership, and the ability to influence and align diverse stakeholders globally.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><div><b>#LI-Hybrid</b><br /><b>Location:</b> Toronto, Ontario</div><div><br />This role is based in Toronto, Canada. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.</div><div><br /><b>This job posting is for an existing position</b></div><p></p><div></div><div><div><h3><b>Key responsibilities:</b></h3><ul><li>Lead the global integrated product access strategy across the full product lifecycle, ensuring clear differentiation and strong value proposition for payers, patients, and healthcare stakeholders</li><li>Drive the global reimbursement process for OAV101, including leading advocacy efforts to secure public reimbursement</li><li>Develop and execute market access strategies in partnership with Medical, Commercial, HEOR, and Public Affairs teams</li><li>Support country teams in payer negotiations and ensure timely delivery of high-quality access materials</li><li>Ensure access perspectives are embedded in TPPs, clinical development programs, BD&amp;L assessments, and lifecycle planning</li><li>Identify and drive evidence generation (beyond registration trials) to meet payer, HTA, and stakeholder requirements in key geographies</li><li>Collaborate closely with HEOR and PCO teams to integrate robust economic and outcomes evidence into cross-franchise strategies</li><li>Lead and develop a team (3 direct reports: 2 leads, 1 manager across Toronto and Montreal) while managing budgets and access community initiatives</li><li>Ensure compliance with pharmacovigilance requirements, including reporting adverse events within 24 hours</li></ul><p></p><h3><b>Essential Requirements:</b></h3><ul><li>Minimum 5&#43; years of experience in Market Access, Pricing, or HEOR roles within the pharmaceutical industry</li><li>Experience in early drug development and/or product launch strategy execution</li><li>Proven ability to lead cross-functional initiatives in a matrix environment and influence senior stakeholders</li><li>Strong experience driving commercial strategies through access, pricing, or HEOR insights</li><li>Demonstrated strategic thinking and data-driven decision-making capabilities</li><li>Excellent communication and stakeholder engagement skills</li><li>Ability to lead complex global projects and advocacy efforts</li></ul><p></p><h3><b>Desirable Requirements:</b></h3><ul><li>7&#43; years of experience in Market Access</li><li>Experience in Neuroscience, Gene Therapy, or other relevant therapeutic areas</li></ul><p></p><h2></h2><p><b>At Novartis Canada, </b>we are determined to be a valued partner and advocate, with a deep understanding of patient needs along the entire care journey – from drug development, to diagnosis, to access and beyond. Part of the way we are doing this is by leveraging data, technology, and partnerships.</p><p></p><p>Research &amp; Development: we focus on four core therapeutic areas: Cardiovascular, Renal &amp; Metabolic, Immunology, Neuroscience and Oncology. We also develop and deliver treatments through other promoted and established brands, which today are helping millions of patients. Over the last three years, our average annual research and development investment in Canada was over $30 million, and we conduct clinical trial research in every region throughout Canada.</p><p></p><p>Commitment to Diversity and Inclusion: Novartis is committed to building outstanding, inclusive work environment and diverse team’s representatives of the patients and communities we serve.</p></div></div><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Access And Reimbursement Strategy, Agility, Analytical Skill, Analytical Thinking, Cross-Functional Collaboration, Customer-Centric Mindset, Employee Development, Finance, Go-To-Market Strategy, Healthcare Sector Understanding, Health Economics, Health Policy, Health Technology Assessment (HTA), Innovation, Inspirational Leadership, Market Access Strategy, Negotiation Skills, People Management, Process Management, Project Management, Public Affairs, Real World Evidence (RWE), Regulatory Compliance, Risk Management, Value Propositions]]></description><link>http://biotechroles.com/patient-access-lead-novartis/6a0744332f1861929d25327e</link><guid isPermaLink="true">http://biotechroles.com/patient-access-lead-novartis/6a0744332f1861929d25327e</guid><pubDate>Fri, 15 May 2026 16:05:07 GMT</pubDate><company>Novartis</company><location>Toronto</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Customer Operations Manager – Radioligand Therapy (RLT)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>We are seeking an experienced and patient-focused professional to join our Radioligand Therapy (RLT) team as Manager, Customer Operations. In this role, you will lead the end-to-end ordering and delivery process, ensuring seamless, compliant, and high-quality service to healthcare providers. You will play a critical role in enabling operational excellence and supporting access to highly specialized therapies in a complex and regulated environment.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>#LI-Hybrid</b></p><p><b>Location:</b> Toronto, Ontario</p><p><br />This role is based in Toronto, Canada. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.</p><p><br /><b>This job posting is not for an existing position.</b></p><p></p><div><div><p><b>Key responsibilities:</b></p><ul><li><p>Oversee end-to-end customer operations, including order processing, case management, escalations, and communications with healthcare providers and treatment centers</p></li><li><p>Act as the primary point of contact for healthcare professionals and institutions, ensuring a high-quality customer experience</p></li><li><p>Monitor and drive key operational KPIs (e.g., on-time delivery, issue resolution, unused dose management), providing insights and continuous improvement recommendations</p></li><li><p>Collaborate cross-functionally (Supply Chain, Manufacturing, Quality, Medical, Regulatory, Commercial, Field) to support therapy adoption and operational excellence</p></li><li><p>Lead onboarding and operational readiness of RLT treatment centers, ensuring standardized processes and compliance</p></li><li><p>Drive continuous improvement initiatives by leveraging analytics to optimize performance and enhance the customer journey</p></li><li><p>Ensure adherence to regulatory, compliance, and pharmacovigilance standards, including timely reporting of adverse events</p></li><li><p>Support governance, SOP standardization, and operational discipline in a highly regulated radiopharmaceutical environment</p></li></ul><p></p><p><b>Essential Requirements:</b></p><p></p><p></p><ul><li><p>Bachelor’s degree in Business, Life Sciences, Healthcare Management, or a related field</p></li><li><p>3–5&#43; years of experience in supply chain, customer service, or operations within pharmaceuticals, medical devices, or healthcare</p></li><li><p>Experience working in regulated environments with strong understanding of compliance requirements, CRM and ERP systems</p></li><li><p>Proven ability to collaborate effectively in cross-functional teams within complex environments</p></li><li><p>Strong customer-centric mindset with demonstrated operational rigor and process excellence</p></li><li><p>Excellent communication, problem-solving, and project management skills</p></li><li><p>Ability to manage complexity and drive execution with a patient-first mindset</p></li></ul><p></p><p><b>Desirable Requirements:</b></p><ul><li><p>Experience supporting highly specialized therapies and/or hospital-based care models</p></li><li><p>Digital and technology proficiency (e.g., analytics tools, supply chain systems, emerging technologies)</p></li></ul><p></p><p></p><p>Rewards</p><p>At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.</p><p>Expected Remuneration Range for role:</p><p></p><p><i>Salary range in the xls file shared with RBP&#39;S </i></p><ul><li><p>CAD 125,120 - 173,696</p></li></ul><p></p><p>The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.</p><p>The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.</p><p>Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.</p><p></p><p>Read our <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">brochure</a> to learn more about our global total rewards offering: <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf</a></p><p><i>Note: Benefits and compensation may vary by country and are subject to local legal requirements. A full overview of your compensation package applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.</i></p><p></p><p><b><span>At </span>Novartis Canada<span>,</span> </b><span>we are determined to be a valued partner and advocate, with a deep understanding of patient needs along the entire care journey – from drug development, to diagnosis, to access and beyond. Part of the way we are doing this is by leveraging data, technology, and partnerships.</span></p><p></p><p><b>Research &amp; Development<span>:</span></b><span><b> </b>we focus on four core therapeutic areas: Cardiovascular, Renal &amp; Metabolic, Immunology, Neuroscience and Oncology. We also develop and deliver treatments through other promoted and established brands, which today are helping millions of patients. Over the last three years, our average annual research and development investment in Canada was over $30 million, and we conduct clinical trial research in every region throughout Canada.</span></p><p></p><p><b>Commitment to Diversity and Inclusion<span>:</span></b><span><b> </b>Novartis is committed to building outstanding, inclusive work environment and diverse team’s representatives of the patients and communities we serve.</span></p></div></div><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Analytical Thinking, Brand Awareness, Business Analytics, Cross-Functional Collaboration, Digital Marketing, Marketing Strategy, Media Campaigns, Project Management, Project Planning, Sales, Stakeholder Engagement, Stakeholder Management, Strategic Marketing, Waterfall Model]]></description><link>http://biotechroles.com/customer-operations-manager-radioligand-therapy-rlt-novartis/6a0744332f1861929d25327d</link><guid isPermaLink="true">http://biotechroles.com/customer-operations-manager-radioligand-therapy-rlt-novartis/6a0744332f1861929d25327d</guid><pubDate>Fri, 15 May 2026 16:05:07 GMT</pubDate><company>Novartis</company><location>Toronto</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Director, Data Science]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><p></p><p>Global Commercial Analytics (GCA) harnesses the power of data to drive robust analytical insights that inform some of Pfizer&#39;s most critical business questions. With colleagues across the globe, GCAs rigorous analytical expertise is depended on as the compass and decision support for the enterprise. Our dynamic, exciting team of subject-matter experts comes from diverse backgrounds and experiences, including market research, data science, digital analytics, finance, and consulting. As a team, we partner to turn data into meaningful insights that will have a direct impact on patient&#39;s lives and the future of Pfizer as a data-driven organization.</p><p></p><p>The Director (T/L), Data Science is accountable for delivering data science driven strategic and tactical support for multiple brands. As a strategic partner to the US Commercial team, this person will develop and implement models and data-science derived insights that drive brands’ strategic priorities. This will include driving the execution and interpretation AI/ML models, framing problems, and shaping solutions. Also, this person will help shape the brands’ strategies and tactics by interfacing closely with Data</p><p>Science Solutions team to develop bespoke AI/ML models to meet evolving needs and will also interface closely with sales-operations to drive execution.</p><p></p><p>This role is dynamic, fast-paced, highly collaborative, and covers a broad range of strategic topics that are critical to our business. The successful candidate will join GCA colleagues worldwide that are constantly supporting business transformation through their proactive thought leadership, innovative analytical capabilities, and their ability to communicate highly complex and dynamic information in new and creative ways.</p><p></p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><p></p><p>Role definition and key accountabilities include, but are not limited to:</p><p><b> </b></p><p><b>Commercial Data Science and Insights</b></p><ul><li><p>Provide data science and insights to US Commercial teams to drive brand tactic decisions</p></li><li><p>Act as strategic partner to frame, investigate, translate complex data related models, and answer key business questions related to the identification and evaluation of Commercial brand strategies and tactics</p></li><li><p>Lead a team of Data Scientists and manage their career development.</p></li><li><p>Connect machine learning models and insights together to identify Commercial brand opportunities and tactics to execute</p></li><li><p>Guide stakeholders via compelling and persuasive story</p></li><li><p>Strengthen the Brand and Sales teams understanding of marketplace performance and opportunities by analyzing impacts of brand strategies and tactics and partnering on data product solutions.</p></li></ul><p></p><p><b>Collaboration with other GCA and Analytics teams</b></p><ul><li><p>Partner with GCA IIS leads to incorporate data science capabilities and insights into analytics plans and recommendations</p></li><li><p>Ensure alignment across GCA Data Science teams and Data Science Solutions teams to ensure cohesive activities with our stakeholders</p></li><li><p>Partner with other analytic functions to advance the use of novel data sources, including RWD</p></li></ul><p></p><p><b>PROFESSIONAL CHARACTERISTICS</b></p><ul><li><p><span><b>Analytical Thinker</b>: Understands how to synthesize facts and information from varied data sources, both new and pre-existing, into discernable insights and perspectives; takes a problem-solving approach by connecting analytical thinking with an understanding of business drivers and how </span>GCA ca<span>n provide value to the organization</span></p></li><li><p><span><b>People’s Manager</b>: Manage a team of individuals and guide them on data science problem solving and storytelling.</span></p></li><li><p><span><b>Data and Information Manager</b>: Understands and uses analytical skills/tools to produce data in a clean, organized way to drive objective insights </span></p></li><li><p><span><b>Communicator</b>: Can understand, translate, and distill the complex, technical findings </span>of the data science team into commentary that facilitates e<span>ffective decision making; can readily align interpersonal style with the individual needs of others</span></p></li><li><p><span><b>Highly Collaborative</b>: Manages projects with and through others; shares responsibility and credit; develops self and others through teamwork</span></p></li><li><p><span><b>Project Manager</b>: Articulates scope and deliverables of projects and delivers analyses within timelines</span></p></li><li><p><span><b>Self-Starter</b>: Eager to take on new responsibilities and opportunities</span></p></li></ul><p></p><p><b>Technical Skills</b></p><ul><li><p>Fluent in English (written and spoken)</p></li><li><p>Strong MS Excel and PowerPoint skills</p></li><li><p>Experience with machine learning technology, such as: big data stack, Python, R, and visualization techniques</p></li><li><p>Experience in understanding brand content, strategy, and tactics</p></li><li><p>Ability to effectively utilize dashboards and data products to derive insights</p></li><li><p>Understands quantitative and qualitative research methodologies</p></li><li><p>Experience in management of secondary data with application of real-world data</p></li><li><p>Ability to partner with cross-functional teams (Commercial, Sales, Operations) to execute brand tactics</p></li><li><p>Ability to connect, integrate and synthesize analysis and data into a meaningful ‘so what’ to drive concrete strategic recommendations for brand tactics. Capable of describing relevant caveats in data or in a model and how they relate to business question</p></li></ul><p></p><p><b>Education and Experience</b></p><ul><li><p>Bachelor’s degree required, ideally in quantitative discipline like engineering or data science and 8&#43; years of work experience</p></li><li><p>Or PhD Degree in a relevant field with good publication/research record and 5&#43; years of work experience</p></li><li><p>7&#43; years&#39; experience in business analytics function, country strategy and/or strategic consulting</p></li><li><p>Experience using data science models to solve problems in a business environment setting </p></li></ul><p> <br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.<br /> </p><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><ul><li>Limited business travel required</li></ul><p></p><p></p><p>Other Job Details:</p><p>Last day to apply: May 21, 2026<br />Work Location Assignment: Hybrid</p>&amp;#xa;The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/director-data-science-pfizer/6a0743282f1861929d25327c</link><guid isPermaLink="true">http://biotechroles.com/director-data-science-pfizer/6a0743282f1861929d25327c</guid><pubDate>Fri, 15 May 2026 16:00:41 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Directeur·trice – Pharmacies et partenariats stratégiques  //Director, Pharmacy & Strategic Partnerships]]></title><description><![CDATA[<p>Date de fin d’affichage : le 28 mai 2026</p><p>Posting closing date: May 28 2026</p><p></p><p>Status : Regular, full-time  </p><p>Statut :Régulier, temps plein </p><p></p><p><b><i>(English to follow)</i></b></p><p></p><p></p><p><b>D</b><b><b>irecteur/directrice – Pharmacies et partenariats stratégiques</b></b></p><p></p><p><b><u>Aperçu du poste</u></b></p><p></p><p>Relevant du ou de la Leader – Engagement auprès des clients, la personne titulaire de ce poste sera responsable de l’harmonisation de la stratégie pharmaceutique de l’entreprise avec les principaux objectifs commerciaux d’une importante gamme de produits. Le <b>directeur ou la directrice – </b><b><b>Pharmacies et partenariats stratégiques</b></b> , Pharmacie dirigera une équipe interfonctionnelle d’envergure nationale qui se concentrera sur la création de partenariats stratégiques efficaces et sur l’optimisation des modèles de soins dirigés par des pharmaciens ou des pharmaciennes. En tant que membre de l’équipe de leadership – Engagement auprès des clients, le ou la titulaire du poste élaborera des stratégies, transformera les renseignements sur le marché en actions concrètes et assurera l’harmonisation et l’adhésion de la haute direction.</p><p></p><p>Ce poste nécessite un ou une leader qui soit très crédible au sein de l’écosystème pharmaceutique, et qui possède des relations bien établies avec les chaînes, les bannières, les associations et les principaux intervenants en pharmacie. La clé du succès pour ce poste réside dans la capacité à maîtriser des modèles d’affaires pharmaceutiques complexes, à négocier des partenariats fondés sur la valeur et à tirer parti de réseaux de confiance pour accélérer les résultats.</p><p></p><p>Si vous aimez façonner des initiatives novatrices et ouvrir de nouvelles voies qui contribuent véritablement à améliorer les soins de santé et les soins aux patients et patientes, alors ce poste est pour vous.</p><p></p><p><b><u>Fonctions principales</u></b></p><p></p><p><b>1. Stratégie pharmaceutique d’entreprise et influence</b></p><ul><li>Élaborer et affiner continuellement la stratégie de Pfizer Canada relative aux pharmacies.</li><li>Servir de porte-parole stratégique principal pour la pharmacie dans les forums d’entreprise.</li><li>Traduire les tendances et la dynamique du marché pharmaceutique en recommandations stratégiques claires et en occasions de partenariat.</li><li>Diriger les contributions de la pharmacie en matière de planification d’affaires, notamment l’élaboration de jalons, les présentations sur le leadership et le suivi des indicateurs de rendement clé.</li></ul><p></p><p><b>2. Préparation au modèle de services pharmaceutiques</b></p><ul><li>Assurer le leadership de Pfizer Canada dans les modèles de soins dirigés par les pharmaciens ou les pharmaciennes.</li><li>Diriger ou mener directement des négociations commerciales à enjeux élevés avec des partenaires pharmaceutiques.</li><li>Développer et institutionnaliser des ressources pouvant être exploitées pour de futurs lancements.</li><li>Définir et suivre les étapes clés en matière de rendement démontrant le leadership de Pfizer dans la prestation de soins de santé axés sur la pharmacie.</li></ul><p></p><p><b>3. Partenariats avec des pharmacies et excellence en commerce interentreprises</b></p><ul><li>Assurer la supervision stratégique des ententes de partenariat novatrices conclues avec des bannières nationales, des chaînes régionales, des pharmacies et des regroupements de pharmacies.</li><li>Représenter Pfizer Canada dans les discussions avec les dirigeants des pharmacies.</li><li>Adopter l’approche d’entreprise de Pfizer Canada envers les associations pharmaceutiques, les organismes professionnels et les organisations représentatives.</li></ul><p></p><p><b>4. Numérisation des pharmacies et préparation au commerce électronique</b></p><ul><li>Définir l’orientation stratégique en matière de transition numérique au sein du réseau pharmaceutique, en veillant à ce que les outils et les capacités numériques soient étroitement adaptés à la stratégie pharmaceutique et à sa mise en œuvre sur le terrain.</li><li>Veiller à ce que les stratégies des pharmacies concordent avec l’évolution de la dynamique du commerce électronique, les parcours des patients et les modèles de soins dirigés par les pharmaciens ou les pharmaciennes.</li></ul><p></p><p><b>5. Direction de l’équipe de Pharmacie</b></p><ul><li>Encadrer et perfectionner les membres de l’équipe afin de favoriser une opération efficace dans une organisation complexe et matricielle, tout en adoptant une approche axée sur l’entreprise et les comptes.</li><li>Incarner les valeurs de Pfizer et s’assurer que l’équipe de Pharmacie respecte les politiques et procédures en matière de conformité de Pfizer ainsi que le code d’éthique de Médicaments novateurs Canada.</li><li>Se présenter comme leader et membre de l’équipe de leadership de l’organisation des ventes qui pilote des initiatives se rapportant à l’amélioration de l’engagement, à la gestion de talents, au rendement et à la culture de l’organisation des ventes.</li></ul><p><b>6. Collaboration interfonctionnelle</b></p><ul><li>Travailler en étroite collaboration avec l’équipe marketing sur les stratégies de commercialisation propres aux pharmacies.</li><li>Collaborer avec les équipes des Affaires médicales, de l’Accès au marché, des Relations commerciales, des Affaires juridiques et de la Conformité afin que les stratégies soient évolutives et conformes.</li></ul><p></p><p><b><u>Aptitudes en leadership et profil de réussite</u></b></p><p>La personne retenue devra démontrer :</p><ul><li>Une connaissance approfondie des chaînes de pharmacies, des enseignes et de la dynamique des associations</li><li>Solide expérience dans la conception et la mise en œuvre de partenariats interentreprises</li><li>Prestance de chef de file et aisance dans les présentations et les négociations de haut niveau</li><li>Capacité à travailler de manière très autonome tout en faisant preuve d’un leadership fort dans la gestion d’équipes (directement ou indirectement)</li><li>Esprit stratégique associé à une discipline opérationnelle</li><li>Excellentes aptitudes pour l’évaluation des talents, des compétences et des capacités</li><li>Aptitude à gérer le changement efficacement</li></ul><p></p><p><b><u>Expérience et qualifications</u></b></p><ul><li>Diplôme universitaire en administration, en sciences de la vie ou dans un domaine connexe; maîtrise en administration des affaires (MBA) un atout</li><li>Expérience significative dans l’industrie pharmaceutique, avec une connaissance approfondie des opérations de vente au détail et de pharmacie, y compris les processus d’achat, les modèles de distribution et la dynamique du marché </li><li>Capacité avérée à mener des négociations commerciales complexes avec des partenaires en pharmacie</li><li>Réseau existant et fiable au sein de l’écosystème des pharmacies</li><li>Sens démontré du leadership au sein d’équipes nationales ou matricielles</li><li>Excellent sens de la stratégie, bonne capacité d’analyse et sens poussé des finances</li><li>Bilinguisme (français et anglais) – <i>Un niveau avancé d’anglais, tant à l’oral qu’à l’écrit, est requis afin de permettre à la personne de collaborer efficacement avec des collègues et partenaires situés ailleurs au Canada et à l’international de façon quotidienne dans le cadre de ses responsabilités<b>. </b></i></li></ul><p></p><p>Nous sommes fiers d’offrir à nos employés un modèle de travail flexible qui leur permet de planifier leurs journées afin de maximiser leur productivité, d’atteindre un meilleur équilibre entre leur vie personnelle et leur vie professionnelle et de favoriser une nouvelle façon de travailler, qui sera centrée sur les patients et stimulera l’innovation. Actuellement, nos employés sont tenus de travailler sur place 2.5 à 3 jours par semaine, en combinant la collaboration et la communication en présentiel et le télétravail, lorsque cela est approprié pour l’entreprise.</p><p></p><p><i><span>Le salaire annuel de base pour ce poste varie de 150,000<span> $ à 250,000 $</span>.</span></i></p><p><i><span>L’échelle salariale fournie s’applique seulement au Canada, et ne s’applique à aucun autre endroit à l’extérieur du Canada.</span></i></p><p>--------------------------------------------------------------------</p><p></p><p><b><b>Director, Pharmacy &amp; Strategic Partnerships</b></b></p><p><b> </b></p><p><b><u>Role Overview</u></b></p><p><b><u> </u></b></p><p>Reporting to the Customer Engagement Lead, this role is responsible for aligning enterprise pharmacy strategy with core business objectives across a vast portfolio of assets. The <b><b>Director, Pharmacy &amp; Strategic Partnerships</b></b> ,<b> </b>will lead a national, cross‑functional team, focused on delivering impactful strategic partnerships and optimizing pharmacist‑led models of care. As a member of the Customer Engagement Leadership Team, the incumbent will be accountable for developing strategies, translating market insight into execution and securing alignment and buy-in from senior executive leadership.</p><p></p><p>This role requires a leader with deep, real‑world credibility in the pharmacy ecosystem, including established relationships across chains, banners, associations, and key pharmacy stakeholders. Success in this role depends on the ability to navigate complex pharmacy business models, negotiate value‑based partnerships, and leverage trusted networks to accelerate impact.</p><p></p><p>If you enjoy shaping innovative initiatives and unlocking new pathways that truly makes a difference in healthcare and patient care, then this is the job for you.</p><p></p><p><b><u>Key Accountabilities</u></b></p><p><b> </b></p><p><b>1. Enterprise Pharmacy Strategy &amp; Influence</b></p><ul><li><p>Develop and continuously refine Pfizer Canada’s pharmacy channel strategy</p></li><li><p>Serve as the primary strategic voice for pharmacy across enterprise forums</p></li><li><p>Translate pharmacy market trends and dynamics into clear strategic recommendations and partnership opportunities</p></li><li><p>Lead pharmacy contributions to business planning including milestone development, leadership presentations, and KPI tracking</p></li></ul><p></p><p><b>2. Pharmacy Care Model Readiness</b></p><ul><li><p>Ensure Pfizer Canada leadership in pharmacist led care models</p></li><li><p>Lead or directly shaped high‑stakes commercial negotiations with pharmacy partners</p></li><li><p>Build and institutionalize capabilities that can be leveraged for future launches</p></li><li><p>Define and track performance milestones demonstrating Pfizer’s leadership in pharmacy driven healthcare delivery</p></li></ul><p></p><p><b>3. Pharmacy Partnerships &amp; B2B Excellence</b></p><ul><li><p>Provide strategic oversight for innovative partnership agreements with national banners, regional chains, pharmacies and pharmacy groups</p></li><li><p>Represent Pfizer Canada in executive level discussions with pharmacy leaders</p></li><li><p>Own Pfizer Canada’s enterprise approach to pharmacy associations, professional bodies, and representative organizations</p></li></ul><p></p><p><b>4. Digital Enablement for Pharmacy &amp; B2C Readiness</b></p><ul><li><p>Own the strategic direction for digital enablement within the pharmacy channel, ensuring that digital tools and capabilities are tightly aligned with pharmacy strategy and field execution</p></li><li><p>Ensuring pharmacy strategies are aligned with evolving B2C dynamics, patient pathways, and pharmacist‑led care models</p></li></ul><p><b> </b></p><p><b>5. Leadership of the Pharmacy Team</b></p><ul><li><p>Coach and develop team members to operate effectively with an account and business mindset in a complex, matrixed organization</p></li></ul><ul><li><p>Demonstrate Pfizer Values and ensure that the Pharmacy team adheres to Pfizer compliance policies and procedures as well as to the Innovative Medicines Canada Code of Ethical Practice</p></li><li><p>Act as a leader and member of the Sales Organization Leadership Team and leads key initiatives to improve the engagement, talent management, performance and culture of the Sales Organization</p></li></ul><p><b>6. Cross-Functional Collaboration</b></p><ul><li><p>Partner closely with Marketing on pharmacy specific go-to-market strategies.</p></li><li><p>Collaborate with Medical, Market Access, Trade, Legal, and Compliance teams to ensure strategies are scalable and compliant.</p></li></ul><p><b> </b></p><p><b><u>Leadership Capabilities &amp; Success Profile</u></b></p><p>The successful candidate will demonstrate:</p><ul><li><p>A deep understanding of pharmacy chains, banners, and association dynamics</p></li><li><p>Strong experience in B2B partnership design and execution capability</p></li><li><p>Executive presence with comfort in senior level presentations and negotiations</p></li></ul><ul><li><p>Act as a leader and member of the Sales Organization Leadership Team and leads key initiatives to improve the engagement, talent management, performance and culture of the Sales Organization</p></li></ul><ul><li><p>Strategic mindset paired with operational discipline</p></li></ul><ul><li><p>Strong talent and competency/capability assessment skills</p></li><li><p>Ability to manage change effectively</p></li><li><p>undefined</p></li></ul><p></p><p><b><u>Experience &amp; Qualifications</u></b></p><ul><li><p>University degree in Business, Life Sciences, or related field, MBA an asset</p></li><li><p>Significant pharmaceutical industry experience, with in-depth knowledge of retail and pharmacy operations, including purchasing processes, distribution models, and market dynamics </p></li><li><p>A proven track record of complex commercial negotiations with pharmacy partners</p></li><li><p>An existing, trusted network within the pharmacy ecosystem</p></li><li><p>Proven leadership of national or matrixed teams</p></li><li><p>Strong strategic, analytical, and financial acumen</p></li><li><p>Bilingualism (French and English): An advanced level of English, both spoken and written, is required to enable the individual to collaborate effectively with colleagues and partners located elsewhere in Canada and internationally daily as part of their responsibilities.</p><p></p></li></ul><p>We are proud to offer employees a flexible working model that is grounded on empowering colleagues to design their workdays so that they can maximize their productivity, enhance their work-life balance and support a way of working that fosters innovation and patient-centricity. Currently, our employees are expected to be on-site 2.5 -3 days per week blending on-site collaboration and connection with off-site remote working when it makes business sense to do so.</p><p></p><p><i><span>The annual base salary for this position ranges from <span>$150,000 to $250,000</span>.</span></i></p><p><i><span>The salary range provided applies to Canada only and does not apply to any other locations outside of Canada.</span></i></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left">At Pfizer, we embrace diversity and inclusion for innovation and growth. We are committed to building inclusive teams and an equitable workplace for our employees to bring their true selves to work.</p><p style="text-align:inherit"></p><p style="text-align:left">We also strive to provide an accessible candidate experience for our prospective employees with different abilities. Please let us know if you need any accommodations during the recruitment process. </p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left">Chez Pfizer, nous accueillons la diversité et l&#39;inclusion pour stimuler l&#39;innovation et la croissance. Nous sommes déterminés à créer des équipes inclusives et un milieu de travail équitable pour que nos employés puissent exprimer leur vraie personnalité au travail.</p><p style="text-align:inherit"></p><p style="text-align:left">Nous nous efforçons également d&#39;offrir une expérience de candidature accessible à nos employés potentiels ayant des habiletés différentes. N&#39;hésitez pas à nous faire savoir si vous avez besoin de mesures d’adaptation au cours du processus de recrutement. </p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Marketing and Market Research<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/directeurtrice-pharmacies-et-partenariats-strategiques-director-pharmacy-and-strategic-partnerships-pfizer/6a0743282f1861929d25327b</link><guid isPermaLink="true">http://biotechroles.com/directeurtrice-pharmacies-et-partenariats-strategiques-director-pharmacy-and-strategic-partnerships-pfizer/6a0743282f1861929d25327b</guid><pubDate>Fri, 15 May 2026 16:00:40 GMT</pubDate><company>Pfizer</company><location>Canada - Quebec - Kirkland</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Content Operations Specialist (Contractor)]]></title><description><![CDATA[<p>At Pfizer, we are a patient-focused company guided by our core values: Courage, Integrity and Equity, Joy, and Excellence. Our transformative culture reinforces our commitment to improving the lives of millions. We recognize that extraordinary outcomes arise wherever people unite around a shared purpose.</p><p>Pfizer, a global leader in the pharmaceutical industry, is seeking a creative, detail-oriented, and team-focused Content Operations Specialist to join its growing team. The purpose of this role is to ensure that all in-house produced promotional and non-promotional materials are accurately anchored, uploaded, version-controlled, and maintained within the Global Content Management &amp; Approval (GCMA) system, in compliance with global and local regulatory requirements.</p><h2>Key Responsibilities</h2><ul><li>Upload in-house produced materials into the GCMA system, creating placeholders or documents as required, <b>while proactively identifying opportunities to streamline submission practices and reduce rework</b>..</li><li>Apply correct GCMA anchoring and linking to ensure proper reference integrity and content traceability, <b>flagging potential risks or inconsistencies early in the process</b>..</li><li>Manage version control by uploading revisions, maintaining current approved versions, and archiving expired materials.</li><li>Complete and verify required metadata fields to support searchability, reporting, and downstream processes.</li><li>Coordinate with Marketing, Medical, Regulatory, Legal, and Digital teams to support review and approval workflows, <b>acting as a proactive point of contact and facilitate timely resolution</b>..</li><li>Ensure materials are technically ready for review, including correct formats and completeness prior to submission, <b>analyzing recurring issues and contributing to process improvement initiatives</b>..</li><li>Track submission and approval status and follow up on operational gaps or required corrections.</li><li>Maintain an organized and auditable archive of all GCMA materials, , <b>while identifying opportunities to optimize structure, accessibility, and audit readiness</b>..</li><li>Proactively identify inefficiencies, risks, or recurring challenges within GCMA processes and contribute to continuous improvement initiatives, including documentation of lessons learned and sharing best practices with relevant stakeholders.</li><li>Prepare basic operational reports on submission volumes and turnaround times.</li><li>Develop and maintain GCMA upload checklists and standard operating guides.</li><li>Provide onboarding and operational support to new team members or agency partners.</li><li>Support production kit uploads and ensure proper documentation where applicable.</li></ul><h2>Required Qualifications</h2><ul><li>Bachelor’s degree (4-year university graduate).</li><li>Fluent in Turkish; strong professional proficiency in English</li><li>Previous experience with content approval systems (e.g., Veeva Vault, PromoMats).</li><li>Familiarity with compliance-driven content review processes.</li></ul><h2>Skills &amp; Competencies</h2><ul><li>Strong communication skills and ability to work cross-functionally.</li><li>Strong attention to detail with a structured and process-driven mindset.</li><li>Ability to manage multiple submissions simultaneously and meet deadlines.</li><li>Ability to identify risks, inefficiencies, and improvement opportunities across end-to-end processes</li><li>Strong document management, file hygiene, and versioning discipline.</li><li>Basic understanding of digital asset formats (PDF, PPT, images, video).</li><li>Proficiency in MS Office applications, particularly Excel and PowerPoint.</li><li>High sense of ownership, accountability, and operational excellence.</li></ul><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p style="text-align:left"><u><span><span>Purpose</span></span></u><span><span> </span> </span></p></div><div><p style="text-align:left"><span><span><b>Breakthroughs that change patients&#39; lives...</b> At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.</span></span><span> </span></p></div><div><p style="text-align:inherit"><span><span> </span></span><span> </span></p></div><div><p style="text-align:left"><u><span><span>School of Leaders</span></span></u><span><span> </span></span></p><p style="text-align:left"><span><span>We, as Pfizer Turkey, make a difference with our visionary and pioneering approaches ranging from our concept of raising leaders through rotations, providing international career opportunities to creating a flexible, enjoyable work environment. There are no limits to what we can accomplish to touch lives here!</span></span><span> </span></p></div><div><p style="text-align:inherit"><span><span> </span></span><span> </span></p></div><div><p style="text-align:left"><u><span><span>Flexibility</span></span></u><span><span> </span></span></p><p style="text-align:left"><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!</span></span><span> </span></p></div><div><p style="text-align:inherit"><span><span> </span></span><span> </span></p></div><div><p style="text-align:left"><u><span><span>Equal Employment Opportunity</span></span></u><span><span> </span></span></p><p style="text-align:left"><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span><span> </span></p></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Marketing and Market Research<p></p><p></p>]]></description><link>http://biotechroles.com/content-operations-specialist-contractor-pfizer/6a0743272f1861929d25327a</link><guid isPermaLink="true">http://biotechroles.com/content-operations-specialist-contractor-pfizer/6a0743272f1861929d25327a</guid><pubDate>Fri, 15 May 2026 16:00:39 GMT</pubDate><company>Pfizer</company><location>Turkey - Istanbul</location><salary>$28000-45000</salary><type>Full time</type></item><item><title><![CDATA[Janitorial Services Technician (1st shift-7:00a.m-3:30p.m.)]]></title><description><![CDATA[<h1><b>Use Your Power for Purpose</b></h1><p><span><span><span>Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you&#39;ll help bring medicines to the world even faster by imagining what’s possible and taking action.</span></span></span></p><p></p><p></p><h1><span><span><b><span>What You Will Achieve</span></b></span></span></h1><p></p><p><span><span><span>Working with Pfizer’s dynamic engineering team, you will play a critical part in provides technical or business support to engineers on a variety of technical tasks. Your documentation skills will come in handy to prepare engineering documentation, reports and drawings. You will be conducting preliminary analysis of trajectory adequacy data, model dimensional consistency and quantitative judgements concerning technical data. You will also support the team by conducting tests and recording data to assist engineering evaluations.</span></span></span></p><p><span><span><span>You will be a team member who is relied to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team’s success by sharing your previously acquired knowledge.</span></span></span></p><p><span><span><span>It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.</span></span></span></p><p></p><p></p><h1><span><span><b><span>How You Will Achieve It:</span></b></span></span></h1><ul><li><p>Responsible for performing cleaning of all non-GMP areas including offices, cubicles, meeting rooms, facility main entrances &amp; corridors, cafeteria/break rooms and restrooms, locker rooms, windows, doors, walls.</p></li><li><p>Operating cleaning equipment such as floor scrubbers, buffing machines and carpet extractors.</p></li><li><p>Responsible for cleaning and storage of equipment.</p></li><li><p>Accurate and timely completing of non-GMP checklist logs.</p></li><li><p>Preparation of cleaning solutions used in the cleaning process.</p></li><li><p>Maintains supplies and work areas in a clean and orderly fashion.</p></li><li><p>Receives supplies in area and moves to designated storage area.</p></li><li><p>Checks equipment and work area to notify supervisor if repairs are needed.</p></li><li><p>Flushes, clean and documents safety showers and eye washes. Reports any malfunction to supervisor.</p></li><li><p>Disposes of trash and waste properly.</p></li><li><p>Assists in maintaining inventory and ordering of cleaning supplies.</p></li><li><p>Other duties and/or responsibilities may be assigned at the manager’s discretion.</p></li><li><p>Work in a safe manner and report all potential safety issues to leadership in a timely manner</p></li><li><p>Perform all tasks in accordance with Janitorial best practices for cleaning, vacuuming, dusting and mopping following checklist guidelines and site policies/requirements.</p></li><li><p>Dependable - Follows unit / area / facility requirements and guidelines</p></li><li><p>Perform a variety of miscellaneous tasks in support of the Rochester Site objectives</p></li></ul><p></p><h1></h1><h1><b>Here Is What You Need</b> (Minimum Requirements)</h1><ul><li><p><u><i><b>Cannot be allergic to Penicillin</b></i></u></p></li><li><p>High School Diploma or GED</p></li><li><p><span><span><span>2&#43; years of experience</span></span></span></p></li><li><p><span><span><span>Understands basic problem solving methods</span></span></span></p></li><li><p><span><span><span>Mathematics and reading skills required for SOP, Good Manufacturing Practices {also cGMP} and Batch Record comprehension</span></span></span></p></li><li><p><span><span><span>Good skills in communication and leadership</span></span></span></p></li><li><p><span><span><span>Ability to contribute to department success in a team environment</span></span></span></p></li><li><p><span><span><span>Performs tasks at a productive level under demanding conditions is mandatory</span></span></span></p></li><li><p><span><span><span>Must have basic computer knowledge as well as some of the following: Word, Excel, Outlook, Etc.</span></span></span></p></li></ul><p></p><p></p><h1><b>Bonus Points If You Have (Preferred Requirements)</b></h1><ul><li><p><span><span><span>Bachelor&#39;s Degree</span></span></span></p></li><li><p><span><span><span>GMP experience</span></span></span></p></li><li><p><span><span><span>Pharmaceutical/Manufacturing Experience</span></span></span></p></li><li><p><span>Janitorial experience</span></p></li></ul><p><span><span><span>  </span></span></span></p><p></p><h1><b>Physical/Mental requirements</b></h1><ul><li><p>This position is in a Penicillin Facility. The candidate cannot be allergic to Penicillin, and will be required to undergo Penicillin allergy testing.</p></li><li><p><span><span><span>This department requires the SMO to bend, reach, lift and stand for extended periods of time. The SMO must be able to grasp from 4 – 5 filled syringes at a time in one hand while manipulating them with the other hand for overall evaluation for defects. All SMOs must have corrected 20/20 vision and must be able to pass a routine inspection test using seeded syringes.</span></span></span></p></li><li><p><span><b>Union Hourly Rate: $26.57</b></span></p></li></ul><p></p><h1><b>Non-Standard work schedule, travel or environment requirements</b></h1><ul><li><p>The Penicillin Inspection/Packaging department is currently operating on a two-shift basis, five days per week. However, SMOs must be available for extended hours and six to seven day operations, if required. In order to maintain the required delivery schedule, overtime may be required.</p></li></ul><p><br /> </p><h1><b>Other job details</b></h1><ul><li><p>Last day to apply: May 28th, 2026</p></li><li><p><span><span><span>Work Location Assignment: On Premise</span></span></span></p></li></ul><p> <br /><br /> </p>&amp;#xa;The salary for this position ranges from $0.00 to $0.00 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Michigan - Rochester location.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Engineering&amp;#xa;]]></description><link>http://biotechroles.com/janitorial-services-technician-1st-shift-700am-330pm-pfizer/6a0743232f1861929d253279</link><guid isPermaLink="true">http://biotechroles.com/janitorial-services-technician-1st-shift-700am-330pm-pfizer/6a0743232f1861929d253279</guid><pubDate>Fri, 15 May 2026 16:00:35 GMT</pubDate><company>Pfizer</company><location>United States - Michigan - Rochester</location><salary>$35000-45000</salary><type>Full time</type></item><item><title><![CDATA[Gerente de Control de Calidad]]></title><description><![CDATA[<h1><b>Proposito General del puesto</b></h1><p></p><p>Es encargado de las operaciones analíticas del laboratorio control de calidad, de la validez de los resultados obtenidos, la seguridad e integridad del personal, el presupuesto que permite que las instalaciones, equipos e instrumentos estén disponibles para que los análisis se realicen oportunamente según la planificación que garantiza que los pacientes tengan acceso a nuestros productos.  </p><p></p><p>Las operaciones especificas que reportan al puesto abarcan desde el muestreo y análisis de las materias primas, materiales de empaque y envase, hasta el análisis de producto terminado y muestras de estabilidad.</p><p>Proporcionar información al siguiente nivel de la organización para la toma de decisiones en situaciones con impacto directo en el negocio. </p><p></p><p>Debe actuar como experto técnico, orientando a su equipo y otros en áreas de expertise, colaborar en mejorar procesos y productos existentes y optimizar el trabajo aportando capacidad analítica para lograr esto. Administrar personal y recursos para proyectos de infraestructura y eficiencia.</p><p></p><p></p><h1><b>Responsabilidades</b></h1><ul><li><p>Asegurar la eficiencia y costo competitivo de las operaciones de Control de Calidad para evitar aportar a costos prohibitivo de los productos terminados analizados en planta.</p></li><li><p>Dar cumplimiento a los métricos del área en los distintos laboratorios a su cargo coordinando el seguimiento y cierre en tiempo de las acciones relacionadas (QAR´s , CAPA´s, LIR´s, Entrenamientos). </p></li><li><p>Desarrollar y cuidar el ambiente laboral, fomentando e inspirando a cada colega a trabajar con integridad y seguridad, cuidándose entre sí para que el laboratorio pueda atraer y retener el mejor talento.</p></li><li><p>Asegurar el cumplimiento de las políticas y estándares Pfizer y mantener los indicadores operativos</p></li><li><p>Coordinación y administración de los recursos tecnológicos, materiales, de personal y financieros de los distintos laboratorios utilizados para las operaciones diarias del sitio</p></li></ul><p></p><p>  </p><h1><b>Perfil</b></h1><p></p><p><i><b><u>Escolaridad:</u></b></i></p><ul><li><p>Licenciatura y Titulados en QFB, IQ, QBP, QFI o cualquier carrera relacionada a Ciencias.</p></li></ul><p></p><p><i><b><u>Experiencia:</u></b></i></p><ul><li><p><b>Tiempo en la función / especialidad: </b>3 a 5 años</p></li><li><p><b>Experiencia total requerida:</b> 10 años en el área de calidad farmacéutica.</p></li><li><p><b>¿En qué puestos y/o roles?: </b>Jefatura o Gerencia en: Aseguramiento de Calidad, Cumplimiento de Calidad, Operaciones de Manufactura</p></li><li><p><b>Enlista las principales funciones:</b> Manejo de Personal, Análisis de PT, Material de Empaque, Buenas prácticas del laboratorio, documentación.</p></li></ul><p></p><p><i><b><u>Idiomas:</u></b></i></p><ul><li><p>Español e Inglés</p></li><li><p>Nivel: Avanzado</p></li><li><p>Aplicación: Escrito y Hablado: Avanzado en conversaciones ejecutivas y operacionales.</p></li></ul><p></p><p><i><b><u>Otros conocimientos:</u></b></i></p><ul><li><p>Manejo de Microsoft Office y Software especializado (Veeva, Trackwise, SAP, etc)</p></li><li><p>Sistemas de gestión ISO-14001 e ISO-45001. Norma NOM-59</p></li><li><p>Mejora continua</p></li></ul><p></p><p></p><h1><b>Otros detalles de la posicion</b></h1><ul><li><p>Ultimo dia para aplicar: 28 de Mayo, 2026</p></li><li><p>Work Location Assignment: On Premise</p></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>EEO (Equal Employment Opportunity) &amp; Employment Eligibility </b></p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.</p>Quality Assurance and Control<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/gerente-de-control-de-calidad-pfizer/6a0743222f1861929d253278</link><guid isPermaLink="true">http://biotechroles.com/gerente-de-control-de-calidad-pfizer/6a0743222f1861929d253278</guid><pubDate>Fri, 15 May 2026 16:00:34 GMT</pubDate><company>Pfizer</company><location>Mexico - Toluca</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Area Rare Cardiac Specialist - Detroit, MI ARCS]]></title><description><![CDATA[<div><div><p><b><span>Pfizer US</span><span>/PR</span><span><span> </span>Commercial Sales</span></b><span><span> </span></span><span> </span></p></div><div><p><span><span>Founded in 1849, Pfizer<span> </span></span><span>Inc.<span> </span></span><span>began as a small chemistry enterprise built on the belief that scientific ingenuity can improve—and protect—human life. Today, as one of the world’s leading biopharmaceutical companies, Pfizer’s purpose is<span> </span></span></span><b><span>Breakthroughs that change patients’ lives</span></b><span><span>: discovering, developing, and delivering medicines and vaccines that address unmet need, earn trust through quality and integrity, and reach patients through strong partnerships across the healthcare system. In a complex and rapidly evolving pharmaceutical landscape,<span> </span></span></span><b><span>our work is measured by one outcome</span><span><span> </span>-<span> </span></span><span>helping patients live longer, healthier lives</span></b><span><span>.</span></span><span> </span></p><p></p></div><div><p><b><span>Rare Disease<span> </span></span><span>Sales Organization Mission &amp; Impact </span></b><span> </span></p></div><div><p><span><span>Pfizer’s<span> </span></span></span><i><span>Rare Disease – Rare Cardiac Sales organization</span></i><span><span><span> </span>exists to help improve the lives of people living with serious rare cardiac conditions by connecting scientific innovation to the clinicians and systems that deliver care. We lead with integrity and patient need—</span></span><b><span>advancing disease and product education grounded in robust clinical evidence</span></b><span><span>, promoting Pfizer Rare Cardiac therapies compliantly, and supporting healthcare professionals’ understanding of appropriate patient identification and use based on approved indications.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Through evidence</span></span><span>‑</span><span><span>based scientific exchange, we help reduce access, diagnostic, and workflow barriers so more patients can start and stay on the right therapy. Our impact is<span> </span></span></span><b><span>more informed clinical decision</span></b><span>‑</span><b><span>making, improved consistency of care, and better outcomes for patients</span></b><span><span>, contributing to a higher standard of care across the rare cardiac community.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>Role Summary</span></b><span> </span></p></div><div><p><span><span>The<span> </span></span></span><i><span>Rare Disease – Rare Cardiac</span><span>, Senior Health &amp; Science Specialist<span> </span></span></i><span><span>is a field-based specialty sales role responsible for driving the growth of Rare Cardiac products through compliant, strategic relationships within assigned accounts. This role partners with Therapeutic Area Specialists and Key Opinion Leaders (KOLs) to execute effective promotional strategies, support appropriate access, and deliver high-impact customer engagement. The Rare Disease – Rare Cardiac Health &amp; Science Specialist leverages strong sales acumen, product and disease-state expertise, and a structured approach to in-person engagement while collaborating with cross-functional teams to achieve business objectives.</span></span><span> </span></p><p></p></div><div><p><b><span>Role</span><span><span> </span>Responsibilities</span></b><span> </span></p></div><div><ul><li><p><span><span>Drive customer engagement and sales performance through effective in-person interactions across rare cardiac accounts.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Build strong, compliant relationships with cardiology HCPs, multidisciplinary care teams, and office staff across assigned accounts.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Deliver approved promotional and disease-state messaging to support appropriate Rare Cardiac product use.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Leverage product, disease, and market knowledge to identify opportunities, prioritize accounts, and support patient finding and referral pathways.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Support patient access by providing information on prior authorization requirements, reimbursement support, hubs, and co-pay resources as applicable.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Collaborate with cross-functional partners to address customer needs, remove access barriers, and advance Rare Cardiac business objectives.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Use digital tools and insights to plan, execute, and optimize Rare Cardiac territory activities.</span></span><span> </span></p></li></ul></div><div><p></p><p><b><span>Basic Qualifications</span></b><span> </span></p></div></div><div><div><p><b><span>Education:</span></b><span><span><span> </span></span><span>Bachelor’s<span> </span></span><span>d</span><span>egree</span></span><span> </span></p></div><div><ul><li><p><span><span>OR an<span> </span></span><span>associate’s degree</span><span><span> </span>with 8&#43; years of<span> </span></span><span>work</span><span><span> </span>experience </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>OR a<span> </span></span><span>h</span><span>igh<span> </span></span><span>s</span><span>chool diploma (or equivalent) with 10&#43; years of<span> </span></span><span>work</span><span><span> </span>experience.  </span></span><span> </span></p></li></ul></div><div><p><b><span>Work Experience:</span></b><span><span><span> </span></span><span>Minimum of 3 years in one or more of the following:</span></span><span> </span></p></div><div><ul><li><p><span><span>Pharmaceutical, biotech, or medical device sales </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Pharmaceutical, biotech, or medical device marketing</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Aligned therapeutic specific healthcare provider experience</span></span><span> </span></p></li></ul></div><div><p><b><span>D</span><span>river’s Licensing Requirement</span><span>:<span> </span></span></b><span><span>Valid</span><span><span> </span>US driver’s license and driving record in compliance with company standards.  </span></span><span> </span></p></div><div><ul><li><p><span><span>Any DUI/DWI or other impaired driving citation within the past 7 years will disqualify you from being hired.</span></span><span> </span></p></li></ul></div><div><p><b><span>Preferred Qualifications</span></b><span><span> </span></span><span> </span></p></div><div><ul><li><p><span><span>3–5 years of specialty sales experience, preferably in<span> </span></span><span>Cardiology, Hospital</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong understanding of complex disease states, biologics, and specialty reimbursement</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience engaging key opinion leaders and high-influence accounts</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated business acumen, data-driven decision making, and strategic thinking</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong digital engagement capability (e.g., Veeva Engage, Zoom) </span></span><span> </span></p></li></ul></div><div><p><b><span>Work Location &amp; Travel Requirements  </span></b><span> </span></p></div><div><ul><li><p><span><span>This role is field based and requires the colleague to reside within a workable distance of all points of business within the assigned territory to effectively meet business needs. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Determination of workable distance will be made based on business requirements and leadership discretion</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to travel to all accounts/office locations within territory </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Depending on size of territory and business need, candidates may be required to stay overnight as necessary</span></span><span> </span></p></li></ul></div></div><div><p></p><p><b><span>Other Details</span></b><span> </span></p></div><div><p><span><span>Last Day to Apply: May 22, 2026</span></span></p><p><span><span>Territory includes but may not be limited to M</span></span><span>etro Detroit, including Henry Ford Health, Detroit Medical Center, and Corewell East.</span></p><p></p><p><span><span>The annual base salary for this position ranges from $108,600 - $250,700.<span> </span></span></span><b><span>During initial new hire sales training, you will be classified as a salary non-exempt employee which entitles you to overtime pay. Upon your training certification, you will become an overtime exempt employee.</span></b><span><span><span> </span>In addition, this position offers an additional Sales Incentive bonus. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits| (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to any location outside of the United States. </span></span><span> </span></p></div><div><p><span><span> </span></span><span> </span></p></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Sales&amp;#xa;]]></description><link>http://biotechroles.com/area-rare-cardiac-specialist-detroit-mi-arcs-pfizer/6a0743212f1861929d253277</link><guid isPermaLink="true">http://biotechroles.com/area-rare-cardiac-specialist-detroit-mi-arcs-pfizer/6a0743212f1861929d253277</guid><pubDate>Fri, 15 May 2026 16:00:33 GMT</pubDate><company>Pfizer</company><location>United States - Michigan - Remote</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Biologics & Immunogenicity Clinical Assay Lead]]></title><description><![CDATA[<p><b>Role Summary:</b></p><p>As a member of Clinical Bioanalytics within Translational Clinical Sciences, the Biologics &amp; Immunogenicity Clinical Assay Lead will play a critical role in supporting clinical strategies in all stages of drug development and post marketing activities through scientific and technical leadership, oversight and management of external and internal partners involved in delivering quality, timely, and regulatory compliant PK, PD, and/or immunogenicity bioanalytical assays and data.</p><p></p><p><b>Organizational Relationships:</b></p><ul><li><p>Reports to Biologics and Immunogenicity Group Lead or Small Molecule Clinical Assay Lead with supervisor responsibilities, Clinical Bioanalytics, within Translational Clinical Sciences.</p></li><li><p>Frequent interaction with colleagues in Translational Clinical Sciences, Clinical, Medicines or Biomedicines Design (PDM/BMD), Clinical Operations, Data Management, Statistics, Regulatory, and Finance, as appropriate.</p></li><li><p>Frequent interaction with bioanalytical Contract Research Organizations (CROs), Central Laboratories, and as appropriate external collaborators.</p></li><li><p>Member of Clinical sub-teams and study teams.</p></li></ul><p></p><p><b>Primary Responsibilities:</b></p><ul><li><p>Serves as a member of the clinical study team and bioanalytical subject matter expert for executing clinical study setup &amp; conduct, contributing to the study protocol development &amp; review, preparing submissions, addressing regulatory queries, implementing bioanalytical strategies &amp; assays, and delivering regulatory compliant data and reports within program timelines.</p></li><li><p>Leads and oversees large molecule PK, PD, and immunogenicity (ADA and Nab) assay lifecycle management from early stage to registration encompassing executing analytical strategy, development and method design, validation, data quality review, corresponding sample analyses &amp; reporting to meet evolving program objectives and regulatory expectations.  Assists CROs with effective troubleshooting of the bioanalytical assay and issue resolution.</p></li><li><p>Functions as key point of contact with external &amp; internal laboratories and supports (or leads, as appropriate) selection, qualification, performance evaluation, and periodic visits and audits of CRO laboratories conducting clinical PK, PD and immunogenicity assays (as relevant to the role).</p></li><li><p>Supports the clinical trial conduct within scope of the Clinical Bioanalytics responsibilities, including development and review of documents and processes such as CRF and data setup, clinical site lab manual, sample management &amp; reconciliation, bioanalytical study planning &amp; reporting, budgeting &amp; invoicing, compliance with clinical SOPs &amp; policies, and regulatory inspection readiness &amp; conduct.</p></li><li><p>Contributes to the development of Best Practices, processes, templates, and policies.</p></li><li><p>Maintains up-to-date knowledge of current and novel ligand binding technologies &amp; techniques, global regulatory guidance &amp; expectations, and industry best practices.</p></li><li><p>As appropriate, additional responsibilities may include the following:</p></li><li><p>Leads development of novel complex methodologies, troubleshooting &amp; resolution of complex technical &amp; logistical issues with vendors and study teams. Identifies technology/capabilities gaps and proposes mitigation strategies, including development of novel technical capabilities with vendors. Scientifically evaluates complex data (i.e., evaluates aberrant results and data trends), anticipates and corrects potential issues, and able to appropriately guide study teams through complex issues resolution.</p></li><li><p>Leads internal and cross-functional organization initiatives, best practices and demonstrates internal and external influence.</p></li><li><p>Provides subject matter expertise, guidance and mentoring to colleagues.  May have responsibility for dotted/direct line management of staff.</p></li></ul><p></p><p><b>BASIC QUALIFICATIONS:</b></p><ul><li><p>PhD or equivalent in biology or analytical chemistry/chemistry with 2 to 6 years of experience</p></li><li><p>M.S with 3 to 6 OR B.S. with 7 to 10 years of relevant industry experience.</p></li><li><p>Minimum of 5-8 years of industry or bioanalytical experience with PK and/or immunogenicity assay development, validation, and sample analyses ligand binding (ELISA and ECL) methodologies.</p></li><li><p>Working knowledge of GxP regulations governing conduct of clinical trials and regulatory guidance and expectations relevant to regulated bioanalysis.</p></li><li><p>Subject matter expert in regulated bioanalysis of Biologics and understanding of bioanalytical techniques commonly used for Biomarkers.</p></li><li><p>In depth knowledge of GxP regulations governing conduct of clinical trials and regulatory guidance and expectations relevant to regulated bioanalysis.</p></li><li><p>Demonstrated ability to think strategically, work in a highly matrixed environment, and execute multiple projects simultaneously.</p></li><li><p>Highly effective communication skills:  verbal, written, and presentation.  </p></li></ul><p></p><p><b>PREFERRED QUALIFICATIONS:</b></p><ul><li><p>Demonstrated CRO management and outsourcing experience.</p></li><li><p>Experience with regulatory inspections.</p></li><li><p>Experience preparing regulatory submissions and addressing regulatory queries.</p></li><li><p>Understanding of clinical trial design and overall principles of clinical development and related disciplines (e.g., pharmacokinetics and clinical pharmacology, statistics, ADME, formulation and drug product).</p></li><li><p>Prior experience with training, mentoring, or managing colleagues.</p></li><li><p>Hands-on experience with the development, validation and troubleshooting of the methods for PK and immunogenicity (including the determination of assay cut points, tolerance, and sensitivity along with experience implementing ACE, BEAD, and SPEAD methodologies) and clinical sample analysis.</p></li><li><p>Hands-on experience with the development, validation, and troubleshooting of LC/MS quantitation of large molecules and immunocapturing hybrid assays.</p></li><li><p>Understanding of critical reagent generation &amp; lifecycle management</p></li><li><p>Experience with biosimilars, gene therapy, multi-domain therapeutics, immunocapture, protein binding, cell-based assays and technologies such as RT-PCR, qPCR, ELISPOT, AMS and FACs.</p></li></ul><p> <br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><p></p><p><b>Additional Job Details:</b></p><ul><li><p>Work Location Assignment: On Premise</p></li><li><p>Last date to apply is May 21, 2026</p></li></ul>&amp;#xa;The annual base salary for this position ranges from $139,100.00 to $231,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Medical&amp;#xa;]]></description><link>http://biotechroles.com/biologics-and-immunogenicity-clinical-assay-lead-pfizer/6a0743202f1861929d253276</link><guid isPermaLink="true">http://biotechroles.com/biologics-and-immunogenicity-clinical-assay-lead-pfizer/6a0743202f1861929d253276</guid><pubDate>Fri, 15 May 2026 16:00:32 GMT</pubDate><company>Pfizer</company><location>United States - Connecticut - Groton</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Attendant- A1 M19]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><p>Responsible for the preparation and/or operation of various components, materials, equipment, machines including, but not limited to:  any and/or all applicable components, materials, equipment, machines in the assigned area(s). While performing all tasks in a safe manner.</p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><ul><li><p>Maintain proper documentation – batch records, check sheets, logbooks.</p></li><li><p>Perform fill room setup and perform room and equipment sanitation, including work over head.</p></li><li><p>Ensures environmental excursions are kept at an acceptable level.</p></li><li><p>Stay current with training requirements and follow SOPs, cGMPs, batch records, TCPs, BOMs and POPs.</p></li><li><p>Communicates openly and clearly with line personnel and supervision to accomplish manufacturing goals.</p></li><li><p>Promote a positive team environment.</p></li><li><p>Notifies Group Leader/Supervisor of all safety issues.</p></li></ul><p></p><p><b>QUALIFICATIONS</b></p><ul><li><p>High school diploma or equivalent (GED)</p></li><li><p>A minimum 1 year of prior work experience in a pharmaceutical, manufacturing and/or industrial type environment</p></li><li><p>Must be able to make minor mechanical machine adjustments.</p></li><li><p>Must be able to communicate and work well interdepartmentally, as well as, with all plant departments.</p></li><li><p>Must be able to read and write, as well as follow written and oral instructions.</p></li><li><p>Must be capable of performing data entry into calculators and computers.</p></li><li><p>Must be self-motivated, able to work independently and have a problem-solving mindset.</p></li></ul>&nbsp;&nbsp;<br><br><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><ul><li><p>Must be able to lift 10-20 lbs. frequently and up to 45 lbs. sporadically, including lifting above shoulders.</p></li><li><p>Must be able to withstand exposure to inks, solvents, heat, steam and liquids.</p></li><li><p>Walk and stand for up to 8 to 12 hours depending on assigned area.</p></li><li><p>Vision must be correctable to 20/20.</p></li></ul><p></p><br><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><ul><li><p>Able to work rotating shifts, holidays, nights and weekends as required</p></li><li><p>Must be able to gown aseptically and retain certification.</p></li></ul><br>Work Location Assignment:&nbsp;On Premise<br>&amp;#xa;The salary for this position ranges from $18.99 to $31.65 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Kansas - Mcpherson location.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Manufacturing&amp;#xa;]]></description><link>http://biotechroles.com/pharmaceutical-attendant-a1-m19-pfizer/6a0743202f1861929d253275</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-attendant-a1-m19-pfizer/6a0743202f1861929d253275</guid><pubDate>Fri, 15 May 2026 16:00:32 GMT</pubDate><company>Pfizer</company><location>United States - Kansas - McPherson</location><salary>$38000-52000</salary><type>Full time</type></item><item><title><![CDATA[Gastroenterology, Health & Science Specialist (SHSS) - Knoxville, TN]]></title><description><![CDATA[<div><div><p><b><span>Gastroenterology, Health &amp; Science Specialist (SHSS) - Knoxville, TN</span></b></p><p></p><p></p><p><b><span>ROLE SUMMARY</span></b><span> </span></p></div><div><p><span><span>Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is innovative and customer oriented. Whether you are involved in manufacturing, testing, or compliance, your contribution will directly<span> </span></span><span>impact</span><span><span> </span>patients.</span><span> </span></span><span> </span></p></div><div><p><span><span> </span></span><br /><span><span>All over the world, Pfizer colleagues work together to positively<span> </span></span><span>impact</span><span><span> </span>health for everyone, everywhere. Our colleagues<span> </span></span><span>have the opportunity to</span><span><span> </span>grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to<span> </span></span><span>impact</span><span><span> </span>the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.</span></span><span><span> </span></span><br /><span><span> </span></span><br /><span><span>The<span> </span></span><span>Rheumatology</span><span>/ Gastroenterology (Portfolio)<span> </span></span><span>Health &amp; Science Specialist<span> </span></span><span>is responsible for</span><span><span> </span>launching new products, deciding upon best strategies to manage business relationships, understanding formulary access, and engaging in product promotion within assigned accounts. In addition, the rep is charged with sales efforts and relationship development with assigned customers and accounts, including Therapeutic Area Specialists and Key Opinion Leaders (KOLs). </span></span><span> </span></p></div><div><p><span><span> </span></span><br /><span><span>The<span> </span></span><span>Rheumatology/ Gastroenterology (Portfolio)<span> </span></span><span>Health &amp; Science Specialist should possess customer, market and business acumen combined with strong product and disease state knowledge; demonstrate strong sales, promotional and strategic business development and management skills and in-depth customer engagement expertise in both virtual and in-person settings, utilize a systematic approach to virtual engagement (e.g., clear agenda, next steps/follow ups); have outstanding communications skills and be adept in the operation of digital and virtual tools/multi-platforms skills; with the ability to effectively work remotely in collaboration with cross-functional internal teams to address customer needs and compliantly deliver on Pfizer business objectives.<span> </span></span></span><span><span> </span></span><br /><span><span> </span></span><br /><b><span>ROLE RESPONSIBILITIES</span></b><span><span> </span></span><span> </span></p></div><div><ul><li><p><span><span>Ability to effectively<span> </span></span><span>identify</span><span><span> </span>and implement the most efficient virtual/in-person engagement strategies, by customer, to maximize overall effectiveness and impact. Develops and implements effective business and territory call plans and adapts based on self-identified opportunities and insights.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Effectively builds rapport and relationships with customers across virtual and F2F environments; maintains a methodical approach toward call objectives (e.g., clear next steps and appropriate documentation, managing to KPIs); utilizes current digital tools effectively (e.g., Veeva Engage, Zoom, Microsoft Office) as well as adapts quickly to new/beta tools (e.g., digital triage app) for successful customer engagement; leverages analytics to assist with developing insights and next best action plans.</span></span></p></li></ul></div><div><ul><li><p><span><span>Compliantly delivers relevant, targeted messaging<span> </span></span><span>utilizing</span><span><span> </span>approved materials via customer engagement to drive product demand (ask the HCP to change their prescribing behavior/close sales) and leverages account priorities to drive a positive business outcome; proactively provides insights for the development of new and innovative approved product messaging and<span> </span></span><span>resources.</span></span></p></li></ul></div><div><ul><li><p><span><span>Leverages product and disease state knowledge to appropriately educate providers on unbranded and branded product value proposition for relevant patient populations and effectively<span> </span></span><span>utilizes</span><span><span> </span>approved clinically oriented disease state information, as applicable). </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Works effectively with HCPs and directs office staff to plan for customer engagements in multiple formats (e.g., virtual and in-person).</span></span></p></li></ul></div><div><ul><li><p><span><span>Responsible for strategic deployment of approved Pfizer resources to support provider and patient’s needs (e.g., samples, vouchers, co-pay resources and patient education); works effectively across multiple virtual engagement platforms based on customer preferences/compliance guidelines; able to integrate guidance from management and other support functions (Marketing, Strategy) technical solutions (e.g., content recommendation engines) into pre-call planning; proactive planning and optimization of call environment in multiple locations; able to effectively plan day-to-day work based on personal and customer schedules; collaborate effectively with other Customer-Facing (CF) colleagues and Pfizer Connect team members.</span></span></p></li></ul></div><div><ul><li><p><span><span>Appropriately support patients’ access to Pfizer products by providing relevant information to HCPs on Reimbursement, Patient Assistant Program (PAP), Pfizer hub programs, and Co-Pay Resources. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Present terms of sale of product or existing contract terms where<span> </span></span><span>appropriate</span><span><span> </span>and with approved language; proactively answer on-label questions; proactively introduce customers to future state Pfizer on-demand portal (Galaxy) with access to appropriate targeted<span> </span></span><span>content.</span></span></p></li></ul></div><div><ul><li><p><span><span>Collaborates effectively and compliantly with cross-functional colleagues, including Field Medical, Reimbursement and Key Account Management, to address customer inquiries and advance Pfizer<span> </span></span><span>objectives</span><span>. Able to use triaging protocols and digital apps to create rapid connections with<span> </span></span><span>appropriate SMEs</span><span><span> </span>to address customer<span> </span></span><span>inquiries.</span></span></p></li><li><p><span><span>Effectively use calendaring tools, leadership goals, and personal insights to address customer priorities calls effectively; and bring insights from customer surveys to leadership to improve model.</span></span><br /><span><span> </span></span></p></li></ul></div><div><p>​</p><p><b><span>BASIC QUALIFICATIONS </span></b><span> </span></p></div><div><ul><li><p><span><span>Bachelor’s Degree.</span></span></p></li></ul></div><div><ul><li><p><span><span>Minimum of 3 years of<span> </span></span><span>previous</span><span><span> </span></span><span>Pharmaceutical</span><span><span> </span>biotech or medical marketing/promotional/sales experience, a promoted position and or developmental role with<span> </span></span><span>demonstrated</span><span><span> </span>leadership across peer groups with experienced marketing, promotional and sales in a specialized market where third-party reimbursement and service center has been utilized.</span></span></p></li></ul></div><div><ul><li><p><span><span>Have a history of marketing, promotional or sales success, strong territory management skills, outstanding communications skills, as well as<span> </span></span><span>demonstrated</span><span><span> </span>teamwork, leadership<span> </span></span><span>ability</span><span><span> </span>and<span> </span></span><span>accountability.</span></span></p></li></ul></div><div><ul><li><p><span><span>Must live within 50 miles of the<span> </span></span><span>territory.</span></span></p></li></ul></div><div><ul><li><p><span><span>Valid US driver’s license and driving record in compliance with company standards</span><span>. <span> </span></span><span>Any DUI/DWI or other impaired driving citation within the past 7 years will disqualify you from being hired.</span></span><span><span> </span></span><br /><span><span> </span></span></p></li></ul><p>​<b><span>PREFERRED QUALIFICATIONS</span></b><span> </span></p></div></div><div><div><ul><li><p><span><span>3-5 years specialty marketing/promotional/sales experience.</span></span></p></li></ul></div><div><ul><li><p><span><span>Strong knowledge of disease states, therapeutic areas, and products.</span></span></p></li></ul></div><div><ul><li><p><span><span>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/organizations).</span></span></p></li></ul></div><div><ul><li><p><span><span>S</span><span>trategic account marketing, promotional, sales and management skills. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Superior marketing, promotional, sales, technical and relationship building<span> </span></span><span>skills</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated<span> </span></span><span>track record</span><span><span> </span>of assessing account needs and bringing relevant information and resources to drive<span> </span></span><span>performance.</span></span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated<span> </span></span><span>track record</span><span><span> </span>of strong business acumen, problem solving, strategic thinking, data analytical<span> </span></span><span>skills</span><span><span> </span>and project management skills, as well as excellent planning and prioritization<span> </span></span><span>skills.</span></span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to engage, influence and support customers throughout the marketing, promotional and sales process, excellent communication, and interpersonal and leadership skills. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to quickly learn and embrace new ways of working in a rapidly changing environment.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Possess the ability to work in a matrix environment and to<span> </span></span><span>leverage</span><span><span> </span>multiple resources to meet customer needs and deliver results.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated<span> </span></span><span>track record</span><span><span> </span>of strong leadership, cross functional leadership, collaboration, and effective<span> </span></span><span>utilization</span><span><span> </span>of available resources to drive performance.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience working with key thought leaders or high influence customers in large group practices, hospitals, or managed care organizations preferred.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong organizational and analytical skills are also<span> </span></span><span>required</span><span><span> </span>and ability to analyze and draw<span> </span></span><span>appropriate conclusions</span><span><span> </span>using sales data/call reporting software/applications and able to adapt to Pfizer’s long-range technology adapting and learning to use<span> </span></span><span>new technology</span><span><span> </span>to deliver in bringing Pfizer information to<span> </span></span><span>market.</span></span></p></li></ul></div><div><ul><li><p><span><span>Change agile and able to adapt quickly to workplace<span> </span></span><span>changes.</span></span></p></li></ul></div><div><ul><li><p><span><span>Exceptional time management, and planning and organizing skills.</span></span><br /><span><span> </span></span><br /><span> </span></p></li></ul></div><div><p><b><span><span>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </span></span><span> </span></b></p></div><div><ul><li><p><span><span>Ability to travel to all accounts/office locations within<span> </span></span><span>territory.</span></span></p></li></ul></div><div><ul><li><p><span><span>Depending on size of territory and business need, candidates may<span> </span></span><span>be required</span><span><span> </span>to stay overnight as necessary.</span></span></p></li></ul><p></p><p></p><p><b>OTHER INFORMATION</b></p><ul><li><p>Last Day to Apply: May 28, 2026.</p></li><li><p>Geography includes: Knoxville to tri-cities. Not Chattanooga</p></li><li><p>Work Location Assignment: Remote - Field Based.</p></li></ul><p></p><p><span><span>The annual base salary for this position ranges from $108,600 - $250,700.<span> </span></span></span><b><span>During initial new hire sales training, you will be classified as a salary non-exempt employee which entitles you to overtime pay. Upon your training certification, you will become an overtime exempt employee.</span></b><span><span><span> </span>In addition, this position offers an additional Sales Incentive bonus. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits| (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to any location outside of the United States. </span></span><span> </span></p></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Sales&amp;#xa;]]></description><link>http://biotechroles.com/gastroenterology-health-and-science-specialist-shss-knoxville-tn-pfizer/6a07431f2f1861929d253274</link><guid isPermaLink="true">http://biotechroles.com/gastroenterology-health-and-science-specialist-shss-knoxville-tn-pfizer/6a07431f2f1861929d253274</guid><pubDate>Fri, 15 May 2026 16:00:31 GMT</pubDate><company>Pfizer</company><location>United States - Tennessee - Remote</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Commercial AI & Digital Innovation Intern EM Asia]]></title><description><![CDATA[<p><b><u>Scope &amp; Duration</u></b></p><p>·        Regional role supporting Emerging Markets Asia (EM Asia)</p><p>·        3‑month, full‑time internship with project‑based work</p><p>·        Focus on business application and learning, not coding or model building</p><p><b><u>About the Internship</u></b></p><p>This internship offers hands‑on exposure to how artificial intelligence (AI) is used in the healthcare industry to improve patient outcomes, support public health, and enable more effective engagement with healthcare professionals. As part of Pfizer’s Emerging Markets Asia (EM Asia) team, you will support regional initiatives that help commercial teams understand and apply AI responsibly in real business situations.</p><p>This is a great opportunity for students interested in healthcare, business, technology, and AI, and who want to see how digital innovation is applied across diverse markets in Asia.</p><p><b><u>What You’ll Do</u></b></p><p>·        Learn how AI is used in healthcare commercial environments, including data analytics for actionable insights, field force productivity, customer engagement, and public health initiatives</p><p>·        Support regional projects that explore AI use cases such as:</p><p>o   Understanding and segmenting healthcare customers (e.g., doctors, hospitals, healthcare systems)</p><p>o   Personalizing content and communication across digital channels</p><p>o   Analyzing market trends, demand patterns, and launch performance</p><p>o   Turning data into insights that support better decision‑making</p><p>·        Help create simple learning materials (slides, summaries, short guides) that explain AI concepts and use cases to non‑technical teams</p><p>·        Assist with presentations, dashboards, and reports to share insights with regional stakeholders</p><p>·        Collaborate with colleagues across different countries and functions, gaining exposure to how global healthcare organizations operate</p><p>·        Learn about ethical, compliant, and responsible use of AI in healthcare and life sciences</p><p><b><u>What You’ll Learn</u></b></p><p>·        How AI supports commercial strategy and public health in a regulated healthcare environment</p><p>·        How large organizations introduce new technologies and build digital skills at scale</p><p>·        How to communicate complex ideas clearly to different audiences</p><p>·        How regional teams work together across cultures and markets in Asia</p><p><b><u>Here Is What You Need (Minimum Requirements)</u></b></p><p>·        Current undergraduate or postgraduate students in Business, Life Sciences, Public Health, Data/Analytics, Technology, or related fields</p><p>·        Basic experience in healthcare, marketing, digital marketing, commercial</p><p>·        Strong interpersonal skills and comfort working with data, slides, or basic analysis</p><p>·        Ability to manage time and prioritize tasks effectively; experience with administrative tasks and process improvement</p><p>·        Ability to work under moderate supervision and follow established procedures</p><p>·        Curious about AI, digital innovation, and the future of healthcare using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.</p>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;Hybrid<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Support Services<p></p><p></p>]]></description><link>http://biotechroles.com/commercial-ai-and-digital-innovation-intern-em-asia-pfizer/6a07431d2f1861929d253273</link><guid isPermaLink="true">http://biotechroles.com/commercial-ai-and-digital-innovation-intern-em-asia-pfizer/6a07431d2f1861929d253273</guid><pubDate>Fri, 15 May 2026 16:00:29 GMT</pubDate><company>Pfizer</company><location>Singapore - Mapletree Business City</location><salary>$2000-3000</salary><type>Full time</type></item><item><title><![CDATA[Sr-Team Lead - Media and Sterilization]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. You will play a crucial role in improving patients&#39; lives by ensuring the highest standards of quality and safety in our products. Your leadership will be instrumental in driving innovation and excellence, ultimately making a global impact on patient health.</p><p></p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><ul><li><p>Lead people, technology, and financial resources.</p></li><li><p>Identify and develop innovative concepts for process or product improvements, taking calculated risks to achieve results.</p></li><li><p>Solve complex problems, leveraging experience from various areas as needed.</p></li><li><p>Recognize and address development needs, creating growth opportunities for colleagues.</p></li><li><p>Oversee and manage multiple projects and ongoing work activities, ensuring compliance with approved methodologies and cGMP documentation.</p></li><li><p>Provide technical expertise and support for laboratory and core applications, collaborating with business partners to identify and implement improvement areas.</p></li></ul><p></p><p><b>Here Is What You Need </b>(Minimum Requirements)</p><ul><li><p>MSC in microbiology / biotechnology with 10&#43; years of experience</p></li><li><p>Proven experience in leading colleagues and managing projects</p></li><li><p>A deep understanding of Good Manufacturing Practices (cGMP) compliance requirements for Quality Control Laboratories</p></li><li><p>Proficiency with Quality Control Microbiology instruments and methodologies</p></li><li><p>The Media Lead is currently accountable for managing the entire Media Management Program, which encompasses media preparation, inventory control, and execution of Growth Promotion Testing</p></li><li><p>Responsible for the management of sterilizers as part of comprehensive laboratory operations</p></li><li><p>Depp Knowledge and understanding of Microbiology Equipment Qualifications Like Steam Sterilizers, Cooling Cabinets, Incubators</p></li><li><p>Technical Expertise on USP Monographs and General Chapters</p></li><li><p></p></li></ul><p></p><p><b>Bonus Points If You Have </b>(Preferred Requirements)</p><ul><li><p>Proficiency in Laboratory Information Management Systems like GLIMS and Microsoft Office</p></li><li><p>Solid understanding of method qualification and testing of components and finished products</p></li><li><p>Experience in microbiological risk assessments</p></li><li><p>Strong problem-solving skills and the ability to think outside the box</p></li><li><p>Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use</p></li></ul><p>  <br />Work Location Assignment: On Premise</p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Quality Assurance and Control<p></p><p></p>]]></description><link>http://biotechroles.com/sr-team-lead-media-and-sterilization-pfizer/6a07431b2f1861929d253272</link><guid isPermaLink="true">http://biotechroles.com/sr-team-lead-media-and-sterilization-pfizer/6a07431b2f1861929d253272</guid><pubDate>Fri, 15 May 2026 16:00:27 GMT</pubDate><company>Pfizer</company><location>India - Vizag</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Scientist - GT&E]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>As a Senior Associate, you will play a crucial role in improving patients&#39; lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients&#39; lives.</p><p></p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><ul><li><p>Perform analytical method transfer strategies from site to site and PSci to site.</p></li><li><p>Prepare &amp; execute study protocols/reports for AMTEs</p></li><li><p>Stratification of data from engineering/EB/PVs for CQA trend analysis.</p></li><li><p>Theoretical &amp; practical knowledge on working principle of analytical instruments- FTIR, UV, IR, HPLC, GC with minimum 5 years of relevant experience.</p></li><li><p>Understanding on the purpose of different method validation parameters and ICH guideline requirements.</p></li><li><p>Reviewing/providing feedback and technical/scientific support on project deliverables, i.e. remediation initiatives, plan reports, etc.</p></li><li><p>Theoretical knowledge on titration, LOD and understanding the working principle of DSC and TGA etc.,</p></li><li><p>To be able to perform the compilation of methods and its requirements.</p></li><li><p>Ensure compliance to cGMP/ cGLP, organizations procedures and practices.</p></li><li><p>Ensure effective safety systems are implemented in the premises.</p></li><li><p>Partnering with manufacturing to meet the production schedule, ensure commercial supply and uphold quality standards.</p></li><li><p>Perform &amp; review trending and monitoring of critical quality attributes/critical process parameters to maintain product quality and to control process drift.</p></li><li><p>Identifying and implementing potential process improvements in conjunction with manufacturing operations.</p></li><li><p>Assisting in documenting changes/updates to manufacturing processes and working with manufacturing, engineering, and validation to implement those changes.</p></li></ul><p></p><p><b>Here Is What You Need </b></p><ul><li><p>M. Pharm/M.Sc with minimum 5 years of pharma experience </p></li><li><p>Experience in Analytical Development/ validation / Technology Transfer of Injectable formulations to cater regulated markets, essentially experience in Plant Technology Transfer support in Injections including process validation.</p></li><li><p><span style="color:#000000">Understanding of DMAIC methodologies (M1/M2/M3)</span></p></li><li><p><span style="color:#000000">Trained on Minitab tools</span></p></li></ul><p></p>&nbsp;&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Engineering<p></p><p></p>]]></description><link>http://biotechroles.com/scientist-gtande-pfizer/6a07431b2f1861929d253271</link><guid isPermaLink="true">http://biotechroles.com/scientist-gtande-pfizer/6a07431b2f1861929d253271</guid><pubDate>Fri, 15 May 2026 16:00:27 GMT</pubDate><company>Pfizer</company><location>India - Ahmedabad</location><salary>$12000-20000</salary><type>Full time</type></item><item><title><![CDATA[Scientist - MSAT]]></title><description><![CDATA[<p></p><p>At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your work will leverage cutting-edge design and process development capabilities to accelerate and deliver best-in-class medicines to patients globally. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, your contributions will be vital in helping Pfizer achieve new milestones and make a global impact on patient health.</p><p></p><p><b>What You Will Achieve</b></p><p></p><p>In this role, you will:</p><p></p><ul><li><p>Finalize manufacturing Process and Parameters/ CPPs for Scale up, Pre Exhibit, Exhibit, Process validation batches and Commercial batches.</p></li><li><p>Prepare and review technical data, Identifying and evaluating CPPs, Stability data, Annual Product Quality Reports, Technical documents.</p></li><li><p>Coordinate with internal departments like Purchase, Analytical R&amp;D, Production, Quality Control, Regulatory Affairs, Quality Assurance, Project Management, Engineering etc., for seamless Technology Transfer.</p></li><li><p>Plan for Technology Transfer process including various activities like procurement of API, excipients, equipment for the developmental, Optimization, Scale up, Pre Exhibit and Exhibit batches manufacturing.</p></li><li><p>Support to Regulatory Affairs for NDA/ ANDA filing activity and respond to Regulatory queries.</p></li><li><p>Prepare and review necessary guidelines/ SOPs for Developmental/ Technology Transfer activities.</p></li><li><p>Perform/execute process transfer strategies from site to site and PSci to site.</p></li><li><p>Prepare study protocols/reports for scientific studies</p></li><li><p>Stratification of data from engineering/EB/PVs for CQA trend analysis.</p></li><li><p>Technical support to Manufacturing Team for smooth launching of products.</p></li><li><p>Trouble shooting, ongoing technical support to Manufacturing team for Process validation, continuous process verification and Process improvement.</p></li><li><p>Prepare and Review of Scale up Protocols and Reports, Technology Transfer Protocols and Reports, Batch Manufacturing Records, Batch Packaging Records and Bill of Materials etc.</p></li><li><p>Ensure compliance to cGMP/ cGLP, organizations procedures and practices.</p></li><li><p>Ensure effective safety systems are implemented in the premises.</p></li><li><p>Serving as a key scientific and technical representative for process-related issues at the facility.</p></li><li><p>Partnering with manufacturing to meet the production schedule, ensure commercial supply and uphold quality standards.</p></li><li><p>Performing trending and monitoring of critical quality attributes/critical process parameters to maintain product quality and to control process drift.</p></li><li><p>Identifying and implementing potential process improvements in conjunction with manufacturing operations.</p></li><li><p>Assisting in documenting changes/updates to manufacturing processes and working with manufacturing, engineering and validation to implement those changes.</p></li><li><p>Prepare/Reviewing/providing feedback and technical/scientific support on project deliverables, i.e. remediation initiatives, plan reports, etc.</p></li><li><p>undefined</p></li></ul><p><b>Here Is What You Need</b> (Minimum Requirements)</p><p></p><ul><li><p>Ph.D./ M. Pham/M.Sc. with at least 4 years of experience </p></li><li><p>Experience in Formulation Development/Process Development/ Product Development/ Production/ Technology Transfer/Scale-up of Sterile Injectable formulations to cater regulated markets, essentially experience in Plant Technology Transfer support in Injections including process validation.</p></li><li><p><span style="color:#000000">Understanding of DMAIC methodologies (M1/M2/M3)</span></p><p><span style="color:#000000"></span></p></li><li><p><span style="color:#000000">Trained on Minitab tools/PHP/IMEx principles</span></p></li><li><p>Effective verbal and written communication skills</p></li></ul><p></p>&nbsp;&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Research and Development<p></p><p></p>]]></description><link>http://biotechroles.com/scientist-msat-pfizer/6a07431b2f1861929d253270</link><guid isPermaLink="true">http://biotechroles.com/scientist-msat-pfizer/6a07431b2f1861929d253270</guid><pubDate>Fri, 15 May 2026 16:00:27 GMT</pubDate><company>Pfizer</company><location>India - Ahmedabad</location><salary>$15000-25000</salary><type>Full time</type></item><item><title><![CDATA[Global O2C Collections Analyst & Dispute Mgt - Dutch Language (12 months fixed term)]]></title><description><![CDATA[<p>The Order to Cash Collections Analyst will form part of a virtual Global O2C Collections team reporting under the Global O2C Collections Director, Jennifer Strecker. The successful candidate will be responsible for the performance of activities such as Customer Collections and dunning, customer account management, query and dispute management. Completion of these activities will ensure that F&amp;GBS continue to support the achievement of working capital objectives and Leadership amongst other key stakeholders will have access to timely, accurate, and complete Order to Cash information. The successful candidate will receive the benefit of working for a stable and very well-established international corporation with a sonorous name and highly established organizational culture. All our colleagues become an important part of our international, friendly and dynamic team. </p><p></p><p><b>ROLE RESPONSIBILITIES </b></p><p>These responsibilities include but are not limited to the following: </p><ul><li><p>Proactively analyze AR falling due and delinquent account balances to ensure timely collection of 3rd party receivables. </p></li></ul><ul><li><p>Timely execution of customer dunning activities (e.g. outbound calls, emails, letters, etc.) </p></li></ul><ul><li><p>Coordinate customer account resolution with internal parties and execute on agreed collection strategies. </p></li></ul><ul><li><p>Timely resolution of inbound billing inquiries (calls, emails, letters, etc.,) with respective parties. </p></li></ul><ul><li><p>Maintenance of subledger. Process adjustments/write off balances (non-ADA: FX, bank charges, residuals, etc.), manage default accounts (US only) and provide guidance to Cash application on offsets and payment application where required. </p></li></ul><ul><li><p>Refund issuance (review, obtain approvals, and confirm). </p></li></ul><ul><li><p>Contribute to AR KPI reporting &amp; analysis on performance of AR ledger. </p></li></ul><ul><li><p>Research and support resolution of open disputes. Coordinate with relevant internal stakeholders and customerσ to support timely close-out of open disputes. </p></li></ul><ul><li><p>Effectively communicate to peers and management with regards to work tasks and deadlines. </p></li></ul><ul><li><p>Manage and resolve escalations in a timely manner ensuring appropriate management oversight where necessary. </p></li></ul><ul><li><p>Manage time effectively and communicate to peers and management with regards to work tasks, status and deadlines. </p></li></ul><ul><li><p>Proactively ensure hand-offs to supporting teams are timely and clearly communicated as part of a virtual Global Collections team i.e. Other regional hubs for Collections, Cash application, Credit Risk COE, AR Accounting &amp; Compliance, G2N etc. </p></li></ul><ul><li><p>Maintain receipt records, files and documentation in an organized manner. </p></li></ul><ul><li><p>Share audit documentation to support periodic SAP PC control performance and internal/external audit programs. </p></li></ul><ul><li><p>Participate in F&amp;GBS Order-to-Cash global initiatives including transformational projects as needed, as a subject matter expert for the area. </p></li></ul><ul><li><p>Ensure strong commitment to the control environment through training and review to meet all control and compliance requirements. </p></li></ul><p></p><p><b>QUALIFICATIONS </b></p><p><b>Education and Experience </b></p><ul><li><p>Bachelor&#39;s Degree, Finance or Economics or Accounting strongly preferred. </p></li></ul><ul><li><p>Fluent <b>Greek, English, and Dutch</b> language requirements to support effective engagement with Customers and colleagues/business partners as needed.</p></li></ul><ul><li><p>Up to 2 years of experience in Accounts receivable and/or broader Order to Cash function preferred.</p></li></ul><ul><li><p>Experience with financial shared services preferred. </p></li></ul><ul><li><p>Experience of working in cross-functional and multi-cultural team an advantage. </p></li></ul><ul><li><p>Ability to work in a high-performing team environment. </p></li></ul><ul><li><p>Strong interpersonal skills and ability to communicate with diverse groups and individuals. </p></li></ul><ul><li><p>Demonstrated ability to work on own initiative. </p></li></ul><ul><li><p>Strong verbal and written communication skills. </p></li></ul><ul><li><p>Strong business acumen and professionalism with the ability to interface effectively with all levels of management and operations colleagues in all applicable Pfizer Finance and business functional areas </p></li></ul><p></p><p><b>Technical Skills Requirements </b></p><ul><li><p>Proficiency in PC skills (MS Excel, Word, PowerPoint, Teams) required </p></li></ul><ul><li><p>SAP ERP system experience preferred including FSCM Collections, Dispute Mgt, S4 Hana, Power BI and ISC</p></li></ul><p></p><p>Please apply by sending your CV and a motivational letter in English</p><p><br />Work Location Assignment: Hybrid</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Finance &amp; Accounting<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/global-o2c-collections-analyst-and-dispute-mgt-dutch-language-12-months-fixed-term-pfizer/6a07431a2f1861929d25326f</link><guid isPermaLink="true">http://biotechroles.com/global-o2c-collections-analyst-and-dispute-mgt-dutch-language-12-months-fixed-term-pfizer/6a07431a2f1861929d25326f</guid><pubDate>Fri, 15 May 2026 16:00:26 GMT</pubDate><company>Pfizer</company><location>Greece-Thessaloniki Chortiatis</location><salary>$28000-42000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Statistical Analysis Platform Support Lead]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>Leads a team responsible for the reliable, compliant, and cost‑effective operation of enterprise statistical platforms <b>SAS and Posit</b>. This role owns platform support (e.g. incident management, user assistance) platform maintenance/monitoring, stakeholder engagement, while partnering with the platform engineering team to manage platform roadmap, upgrades and cloud‑native (Kubernetes‑based) deployments.</p><p></p><p><b>What You Will Achieve</b></p><ul><li>Lead and manage a platform support and operations team supporting SAS and Posit across all environments.</li><li>Own day‑to‑day platform operations, administration, incident, problem, and request management.</li><li>Serve as escalation point for major incidents and drive root‑cause analysis and continuous improvement.</li><li>Partner with Platform Engineering on platform strategy, upgrades, and enhancements, including Kubernetes‑based deployments.</li><li>Ensure platforms are performant, reliable, compliant, and cost‑effective through proactive monitoring and optimization.</li><li>Define, track, and report platform health, SLAs, and operational metrics to business and IT leadership.</li><li>Interface with end users, application teams, and dependent platforms to ensure smooth onboarding and ongoing support.</li><li>Establish operational standards, best practices, and runbooks aligned with enterprise IT and regulatory requirements.</li><li>Manage software and service vendors, including performance, contracts, and escalations.<br /> </li></ul><p><b>Minimum Requirements:</b></p><ul><li>Experience (A BA/BS degree with over 2 years of experience an MBA/MS degree with over 2 years of experience) leading enterprise platform support and operations teams with accountability for service reliability and outcomes.</li><li>Strong technical expertise in both SAS and Posit platforms.</li><li>Experience operating platforms in cloud‑native, Kubernetes‑based environments.</li><li>Proven ability to manage senior stakeholders, lead major incident response, and communicate effectively with business and IT leadership.</li><li>Experience working in regulated, compliance‑driven environments.</li></ul><ul><li>Strong people‑leadership skills, including building high‑performing teams, setting priorities, and driving disciplined execution.</li><li>Continuous‑improvement mindset with the ability to implement scalable, repeatable processes to deliver reliable outcomes.<br /> </li></ul><p><b>Preferred Requirements:</b></p><p>Experience working in a pharmaceutical organization</p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Information &amp; Business Tech<p></p><p></p>]]></description><link>http://biotechroles.com/manager-statistical-analysis-platform-support-lead-pfizer/6a0743192f1861929d25326e</link><guid isPermaLink="true">http://biotechroles.com/manager-statistical-analysis-platform-support-lead-pfizer/6a0743192f1861929d25326e</guid><pubDate>Fri, 15 May 2026 16:00:25 GMT</pubDate><company>Pfizer</company><location>India - Chennai</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Customer Facing Effectiveness Undergraduate Assistant]]></title><description><![CDATA[<p>­<b>Pfizer UK Undergraduate Programme 2026/2027</b></p><p><b>Customer Facing Effectiveness Assistant Undergraduate </b></p><p>IDM Commercial Office</p><p><b> </b></p><p><b>Department Overview</b></p><p>The field force remains our most valuable and largest channel for connecting with customers.</p><p>It is critical that we maximise engagements and continue to strengthen the value customers place on these interactions.</p><p>Newly formed Customer Facing Effectiveness Team ( CFE team) will drive the adoption, strategic direction and best practice sharing across International Developed Markets(IDM) of customer facing effectiveness initiatives. They will closely partner with Local leadership, sales leadership and key business partners such as Biopharma Ops and BIR. The role aims to support the CFE Leads to deliver with impact within their markets, across International Development Markets ( IDM)  in implementation of CFE initiatives.</p><p></p><p><b>What can I achieve and what will I be accountable for whilst completing a placement at Pfizer?</b></p><p>Pfizer provides you with the opportunity to work with experts in the pharmaceutical industry. Through working in a CFE team environment you can look forward to being exposed to one of the most critical areas of the business. The role will support  development of critical business skills , project management, cross functional partnership, communication through liaising with colleagues across multiple global markets, multi-tasking through working on a variety of projects and also leadership by owning areas of the role within role scope. We will ensure you are given the chance to direct and own key projects, which will provide invaluable strategic, leadership and project management skills.</p><p></p><p>Pfizer also offers a diverse environment which allows employees numerous opportunities to grow and develop. This is a great chance to be part of the bigger picture, and to assist in ensuring Pfizer maintains a strong and diverse workforce as well as developing a talent pipeline of future Pfizer colleagues. It is also a fantastic way to obtain a better comprehension of the pharma industry and the type of roles it has to offer.</p><p>Other tasks will include:</p><ul><li>Support and co-ordination of internal team meetings with CFE team capturing key agreements and actions</li><li>Project management support for implementation and refinement of CFE initiatives</li><li>Support facilitating and developing materials for the CFE team</li></ul><p></p><p><b>What other opportunities and benefits do Pfizer offer?</b></p><p>The role will give the candidate an opportunity to develop and demonstrate leadership within a fostering and encouraging team. The person will be given specific projects to lead on and will support different aspects of the business to ensure a diverse experience within business. Some travel could be expected few times a year.</p><p></p><p><b>When can I start?</b></p><p></p><p>Placements will start on 1st  September 2026 and will run for 12 months.</p><p></p><p><b>PERSON SPECIFICATION</b></p><p></p><p>Type of person we are looking for, in relation to ‘<b>Skills</b>’, ‘<b>Knowledge</b>’ and ‘<b>Motivation</b>’:</p><ul><li>Completing placement as part of University Degree either through Year In Industry/Industrial Placement or Gap Year</li><li>Good time/project management skills</li><li> A self-starter and able to work on own initiative as well as open to support and guidance</li><li>Strong interactive skills and a good orator</li><li>Interest in digital technology as a form of effective communication</li><li>Proficiency in Microsoft Office ( TEAMs, Word, Excel, PowerPoint)</li></ul><p></p><p><b>As a reminder…….</b></p><p></p><p><b>Who can apply?</b></p><p></p><p>Applicants must be completing placement as part of a degree course at a UK University, either through Year in Industry/Industrial Placement or Gap Year.</p><p></p><p><b>This position will close for applications at midnight on 31st May 2026. </b></p><p></p><p><b>Please note that we only accept application forms. Please do not send over your CV or cover letter as they will not be considered.</b></p><p>Please access the Word version of the Application Form here: <a href="https://www.pfizer.co.uk/careers/undergraduate-placements/undergraduate-vacancies" target="_blank">Undergraduate Vacancies | Pfizer UK </a>and find instructions as to how to complete your application and more about eligibility criteria.</p><p></p><p>#LI-PFE<span><b> </b></span></p><p><span><b> </b></span></p><p>  <br />Work Location Assignment: On Premise</p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>DisAbility Confident</u></p><p style="text-align:left">We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Support Services<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/customer-facing-effectiveness-undergraduate-assistant-pfizer/6a0743192f1861929d25326d</link><guid isPermaLink="true">http://biotechroles.com/customer-facing-effectiveness-undergraduate-assistant-pfizer/6a0743192f1861929d25326d</guid><pubDate>Fri, 15 May 2026 16:00:25 GMT</pubDate><company>Pfizer</company><location>United Kingdom - Walton Oaks</location><salary>$25000-35000</salary><type>Full time</type></item><item><title><![CDATA[​​Associate Manager, Medical Communications and Content Solutions​ -Vaccines]]></title><description><![CDATA[<p><span style="color:#000000"><span><b><span></span></b> </span></span></p><p style="color:!important"><span style="color:#000000"><span><b>ROLE SUMMARY</b> </span></span></p><p style="color:!important"><span style="color:#000000"><span>The Associate Manager, Medical Communications and Content Solutions, within the Global Medical Communications and Content Solutions (MCCS) team in the Global &amp; US Medical Communications and Content (MCC) Organization is responsible for , developing global medical content including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content under supervision.  </span></span></p><ul><li><p style="color:!important"><span style="color:#000000"><span>The Associate Manager will develop with support and supervision, relevant medical affairs content, including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content. </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Responsibilities may include researching, organizing, compiling, interpreting, and quality check of various types of technical and/or medical content. </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Provide solutions to stakeholders in alignment with manager for all projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, etc.).  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Ensure execution of all projects within expected timelines while adhering to all quality and compliance requirements for medical content. </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Ensure training on relevant tools and processes, including new generative AI technology platforms, that ensure efficient and compliant execution of all medical affairs content.  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Track the progress of projects and resolve any issues/problems with guidance from manager.  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Identify and train to become an expert on one new tool/skill for content creation representing the latest trends in the industry.  </span></span></p></li></ul><p style="color:!important"><span style="color:#000000"><span>  </span></span></p><p style="color:!important"><span style="color:#000000"><span><b>Basic Qualifications </b> </span></span></p><ul><li><p style="color:!important"><span style="color:#000000"><span>Advanced scientific degree, (eg, MS, MRes, MPharm, PhD, PharmD, MBBS/MD) </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>2&#43; years experience in pharmaceutical medicine, including medical affairs, medical compliance. </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Proven ability to take ownership of individual work and align with more experienced colleagues on scope, timelines, quality expectations, etc.  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Strong interpersonal skills to quickly build rapport and credibility with<span> </span>colleagues and key external stakeholders cross culturally/regionally.  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Experience in medical content writing /writing in academic settings/ communications experience within an agency, CRO, Pharma / Biotech Company.  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Demonstrated ability to work effectively in a team and understand the applications of technology to medical content development  </span></span></p></li></ul><p style="color:!important"><span style="color:#000000"><span><span></span> </span></span></p><p style="color:!important"><span style="color:#000000"><span><b>Preferred Qualifications</b> </span></span></p><ul><li><p style="color:!important"><span style="color:#000000"><span>Expertise in assigned therapeutic areas </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Experience in medical content creation  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Multimedia and omnichannel experience  </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Rapid adoption of new digital content, technology, and resources </span></span></p></li></ul><ul><li><p style="color:!important"><span style="color:#000000"><span>Global / international work or educational experience  </span></span></p></li></ul><p style="color:!important"><span style="color:#000000"><span><span></span> </span></span></p>&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Medical<p></p><p></p>]]></description><link>http://biotechroles.com/associate-manager-medical-communications-and-content-solutions-vaccines-pfizer/6a0743192f1861929d25326c</link><guid isPermaLink="true">http://biotechroles.com/associate-manager-medical-communications-and-content-solutions-vaccines-pfizer/6a0743192f1861929d25326c</guid><pubDate>Fri, 15 May 2026 16:00:25 GMT</pubDate><company>Pfizer</company><location>India - Remote</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Site Digital & Automation Lead, North Creek]]></title><description><![CDATA[<p><b><span>Role Summary</span></b></p><p><span>The Site Digital &amp; Automation Lead is a full member of the Site Leadership Team and a key leader within the PGS Network &amp; Automation organization. This role provides strategic direction and leadership for all digital and automation capabilities at site, serving as the primary advisor and partner to Site Leadership and above-site stakeholders. The role is accountable for shaping, owning, and executing the site’s integrated digital and automation portfolio, ensuring full alignment with site business priorities and network strategies.</span></p><p><span>This role drives long-term value creation, investment prioritization, and portfolio governance across capital and expense initiatives. The Site Digital &amp; Automation Lead leads and develops the site digital and automation team, ensuring the design, deployment, and lifecycle management of critical digital, automation, and infrastructure systems. This includes driving operational efficiency, ensuring Quality/Safety compliance, cybersecurity, business continuity and reliable system support.</span></p><p></p><p><b><span>Role Description</span></b></p><p><b><span>Core Responsibilities</span></b></p><p><b><span>Leadership and Oversight</span></b></p><ul><li><p><span>Serve as a full member of the Site Leadership Team.</span></p></li><li><p><span>Collaborate with the Site Leadership Team to ensure alignment of site and network strategies with digital and automation capabilities.</span></p></li><li><p><span>Lead teams of colleagues and contract resources to deliver digital and automation capital projects and manage expense portfolios, ensuring customer needs are met; uphold standardized platforms and oversee strategic outsourcing to key integrators.</span></p></li><li><p><span>Act as the primary contact for all digital and automation colleagues located at the site.</span></p></li><li><p><span>Build and maintain relationships with PGS Enabling Teams and Digital Organizations.</span></p></li><li><p><span>Lead and participate in network-wide digital and automation initiatives.</span></p></li><li><p><span>Lead, mentor, and develop a team of digital &amp; automation professionals</span></p></li><li><p><span>Conduct performance reviews and provide growth opportunities</span></p></li><li><p><span>Build a collaborative, innovative environment</span></p></li></ul><p></p><p><b><span>Performance Management &amp; Continuous Improvement (CI)</span></b></p><ul><li><p><span>Develop and own the site’s 3–5 year digital and automation strategy</span></p></li><li><p><span>Provide strategic direction and establish business cases for large capital, or product focused programs and technology portfolio plans; continually evaluate and deploy emerging technologies to realize value.</span></p></li><li><p><span>Implement IMEx elements, including Structured Gembas, Visual Management, and the CI Loop, to drive process improvements using digital tools.</span></p></li><li><p><span>Support site continuous improvement initiatives and share best practices and drive business adoption</span></p></li><li><p><span>Provide oversight of the site digital &amp; automation portfolio, championing AI and innovation through integrated planning and reliable project execution.</span></p></li><li><p><span>Maintain a strong awareness of automation and digitization developments in the external environment.</span></p></li><li><p><span>Oversee contract and license management for digital and automation systems, ensuring compliance and effective administration.</span></p></li><li><p><span>Ensure effective implementation and continuous oversight of lifecycle processes for all digital and automated systems and infrastructure.</span></p></li></ul><p></p><p><b><span>Operational Services</span></b></p><ul><li><p><span>Deliver dependable digital &amp; automation support services, responding quickly to real-timesystem issues while maintaining stable, high-performing digital and automation systems.</span></p></li><li><p><span>Ensure Automation Engineering support, including hardware, instrumentation, and control systems ownership.</span></p></li><li><p><span>Take responsibility for change management pertaining to digital and automation infrastructure on site, including managing outages and communicating with end users.</span></p></li><li><p><span>Serve as the primary point of contact for all digital and automation operations at the site, including escalating issues to the wider PGS Network and Automation organization.</span></p></li><li><p><span>Collaborate with the PGS Network and Automation organization to maintain service levels for crisis response, digital incident management, and service request processes.</span></p></li><li><p><span>Oversee the provision of technical support to Engineering and Operations partners for automated systems throughout the lifecycle of the equipment.</span></p></li></ul><p></p><p><b><span>Cyber Security &amp; Network</span></b></p><ul><li><p><span>Manage and coordinate cybersecurity activities and ensure compliance with digital and automation Infrastructure &amp; Architecture Standards Execution</span></p></li><li><p><span>Own change management for technology infrastructure, including outage management, end-user communications, maintenance and support</span></p></li><li><p><span>Oversee software and hardware lifecycle management and PANS Support</span></p></li></ul><p></p><p><b><span>Data Systems &amp; Integration</span></b></p><ul><li><p><span>Manage the development of the Automated System Life Cycle documents.</span></p></li><li><p><span>Ensure deployment of end-to-end data strategy for digital and automation systems.</span></p></li><li><p><span>Leverage data standards to ensure consistency and compliance.</span></p></li><li><p><span>Oversee core system integration to support seamless data flow and connectivity.</span></p></li><li><p><span>Manage the development of local applications to meet site and business needs.</span></p></li></ul><p></p><p><b><span>Computer System Assurance</span></b></p><ul><li><p><span>Proactively address business continuity risk for digital and automation assets</span></p></li><li><p><span>Maintain Quality and Safety compliance and continuous audit-readiness</span></p></li><li><p><span>Ensure adherence to system validation requirements and change control processes</span></p></li><li><p><span>Maintain up to date GMP documentation for systems and assets within the remit of the team</span></p></li></ul><p></p><p><b><span>Key Attributes, Skills &amp; Competencies</span></b></p><p><b><span>Communication &amp; Stakeholder Management</span></b></p><ul><li><p><span>Clear communicator who can translate complex technical topics to non-technical stakeholders.</span></p></li><li><p><span>Executive presence; capable of influencing across site and enterprise teams.</span></p></li></ul><p></p><p><b><span>Visionary Thinking and Technology Strategy</span></b></p><ul><li><p><span>Strong ability to design and govern reliable OT automation and site digital ecosystems (end-to-end lifecycle ownership).</span></p></li><li><p><span>Comfortable making risk-based decisions balancing production continuity, compliance, and security.</span></p></li><li><p><span>Passionate about leveraging technology to enhance operations.</span></p></li><li><p><span>Portfolio and program leadership; disciplined execution, stakeholder management, and vendor oversight.</span></p></li><li><p><span>Anticipates future digital needs and acts proactively</span></p></li></ul><p></p><p><b><span>Change and Problem Management </span></b></p><ul><li><p><span>Strong problem-solving and organizational skills</span></p></li><li><p><span>Leader of technical and organizational change</span></p></li><li><p><span>Ability to manage multiple priorities and work effectively in a dynamic environment</span></p></li></ul><p></p><p><b><span>Technical Fluency</span></b></p><ul><li><p><span>Understanding of emerging technologies, AI</span></p></li><li><p><span>Foundational digital and automation risk management</span></p></li><li><p><span>Strong grasp of integration patterns between OT systems and data platforms.</span></p></li><li><p><span>Demonstrates strong expertise in digital and automation solutions.</span></p></li></ul><p></p><p><b><span>Basic Qualifications, Experience &amp; Certifications</span></b></p><ul><li><p><span>Bachelor’s degree in engineering, Computer Science, Information Systems, business, or related technical field (Controls, Electrical, Chemical, IT/CS)</span></p></li><li><p><span>6&#43; years’ experience in information technology systems/infrastructure or specialist knowledge of process automation/process control systems</span></p></li><li><p><span>3–5 years in a regulated manufacturing environment (pharma or similar preferred)</span></p></li><li><p><span>Experience with Lean/Operational Excellence</span></p></li><li><p><span>Project/program management (PMI, Agile, SDLC) and continuous improvement (e.g., Six Sigma)</span></p></li><li><p><span>IT infrastructure management (e.g., ITIL) and GMP regulatory requirements experience preferred</span></p></li></ul><p><br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><p><br />Work Location Assignment: On Premise</p><p><b>Last day to apply :</b> May 23rd 2026</p>&amp;#xa;The annual base salary for this position ranges from $139,100.00 to $231,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Information &amp; Business Tech&amp;#xa;]]></description><link>http://biotechroles.com/site-digital-and-automation-lead-north-creek-pfizer/6a0743182f1861929d25326b</link><guid isPermaLink="true">http://biotechroles.com/site-digital-and-automation-lead-north-creek-pfizer/6a0743182f1861929d25326b</guid><pubDate>Fri, 15 May 2026 16:00:24 GMT</pubDate><company>Pfizer</company><location>United States - Washington – Bothell</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[AI Application Developer Undergraduate]]></title><description><![CDATA[<p>­­<b>Pfizer UK Undergraduate Programme 2026/2027</b></p><p><b>AI Application Developer Undergraduate Placement</b></p><p>Pfizer Digital</p><p></p><p><b>Who can apply?</b></p><p>Applicants <b>must</b> be completing a placement as part of a degree course at a UK University, either through Year in Industry/Industrial Placement or Gap Year.</p><p><b>Please note that we will only consider candidates who have applied by completing the Pfizer Placement Application Form. Candidates who do not complete and attach the application form will NOT be considered. </b>You can download the Word version of the Application Form here: <a href="https://www.pfizer.co.uk/careers/undergraduate-placements/undergraduate-vacancies" target="_blank">Undergraduate Vacancies | Pfizer UK </a>and find instructions as to how to complete your application and more about eligibility criteria. </p><p>To learn more about this exciting opportunity, please see below!!</p><p></p><p><b>Department Overview</b></p><p></p><p>Pfizer Digital is a customer-oriented, front-line organisation bringing together talent from across Pfizer into one high-performing team that works with agility, speed, and focus to create compelling experiences for our internal and external customers. With an “experience first” vision, we are here to help Pfizer ‘Win the Digital Race in Pharma’ in support of our company’s purpose: Breakthroughs that change patients’ lives.</p><p>We do this by:</p><p>•       Creating compelling and personalised digital experiences.</p><p>•       Delivering innovative digital, analytics, and technology solutions.</p><p>•       Producing powerful insights that support decisions and trigger action.</p><p>•       Digitising all aspects of our business and scaling for impact.</p><p>•       Driving a digital mindset in all that we do.</p><p></p><p><b>About the Team</b></p><p></p><p>The <b>Customer Experience, Insights &amp; AI (CXI&amp;AI)</b> organisation is accountable for creating, configuring, launching, and running digital products, services, technologies, and experiences that engage consumers and physicians while improving patient value, access, and outcomes. We also drive digital enablement internally for our colleagues and workforce.</p><p>This role sits within the <b>OSS AI Studio</b>, a multidisciplinary team inside CXI&amp;AI focused on the rapid prototyping and delivery of AI-powered internal applications and tools that improve how teams across Pfizer operate. The team takes early-stage ideas and internal process challenges and converts them into functional, validated solutions, often within days, using modern development tools, AI platforms and automation frameworks. Rather than broad external-facing development, our focus is on building internal prototypes that challenge existing ways of working: identifying where AI can replace manual effort, reduce reliance on external agencies or streamline internal workflows, and then building a working prototype to prove the concept.</p><p></p><p><b>What can I achieve and what will I be accountable for whilst completing a placement at Pfizer?</b></p><p></p><p>The <b>AI Application Developer Undergraduate</b> will play a hands-on role in supporting OSS AI Studio to deliver rapid, AI-enabled prototypes that challenge existing ways of working. You will work closely with developers, product managers, designers and AI engineers to design, build and iterate on internal tools, automations and micro-applications that demonstrably improve how teams operate. Where prototypes prove successful, you will support their transition into production-grade solutions in partnership with the wider engineering team.</p><p>This is a fast-paced, learning-rich placement that will give you exposure to the full lifecycle of internal AI product delivery, from idea through to scaled adoption, while building a strong foundation in modern software engineering and applied AI.</p><p><b>Key Tasks:</b></p><ul><li>Support the assessment of internal processes and workflows across OSS AI Studio and the wider CXI&amp;AI organisation to identify where AI-enabled prototypes could reduce manual effort, remove dependency on external suppliers or improve efficiency.</li><li>Contribute to building working prototypes of internal applications and tools using technologies such as React, NextJS, Python and Supabase, moving from concept to functional demo within days.</li><li>Help deliver AI-enabled internal solutions including automations, workflows, dashboards and micro-applications, iterating quickly based on user feedback and validation.</li><li>Explore and experiment with emerging AI capabilities, tools and methodologies, including AI platforms such as OpenAI and Anthropic, open-source models, and AI-powered development environments such as Cursor.</li><li>Collaborate with developers, engineers, designers and product managers across OSS AI Studio and the wider engineering team to transition successful prototypes into production-grade, scalable solutions.</li><li>Apply governance, compliance and security best practices throughout the build process, ensuring all work meets Pfizer standards before transitioning to production.</li><li>Produce clear documentation and support knowledge transfer so that solutions can be maintained, iterated and scaled by others across the organisation.</li><li>Stay up to date with emerging AI trends, technologies and industry best practices to drive innovation within the team.</li></ul><p></p><p><b>What other opportunities and benefits do Pfizer offer?</b></p><p></p><p>Throughout the placement, you will partner with various cross-functional teams and external delivery partners, gaining valuable insights into the pharmaceutical industry and how AI is transforming healthcare. As this is a <b>global role</b>, you will also develop strong communication skills, working across different countries, cultures, and business objectives.</p><p>This opportunity will provide hands-on experience in rapid AI prototyping and internal product delivery within a large corporate environment, helping you build a strong foundation in AI-driven digital transformation and modern software engineering practice.</p><p></p><p><b>When can I start?</b></p><p></p><p>Placements will start on 1st  September 2026 and will run for 12 months.</p><p></p><p><b>PERSON SPECIFICATION</b></p><p></p><p>Type of person we are looking for, in relation to ‘Skills’, ‘Knowledge’ and ‘Motivation’:</p><p></p><ul><li>Completing a placement as part of a University Degree, either through Year in Industry/Industrial Placement or Gap Year.</li><li>Currently pursuing a degree in Computer Science, Artificial Intelligence, Software Engineering or a related field at a UK University, with an interest in completing a year in industry placement.</li><li>A strong foundational understanding of AI technologies, machine learning concepts, and software development principles.</li><li>Experience with programming languages such as Python, JavaScript or TypeScript; familiarity with modern web frameworks such as React or NextJS is highly desirable.</li><li>Exposure to, or genuine curiosity for, AI platforms and services such as OpenAI or Anthropic, AI-powered development environments such as Cursor, and automation or backend tools such as N8N or Supabase.</li><li>A demonstrable portfolio of applications, side projects or prototypes (for example GitHub repositories or live demos) that evidence practical, hands-on delivery.</li><li>An interest in identifying internal process improvement opportunities and proposing creative, AI-driven alternatives that can be prototyped and tested quickly.</li><li>Excellent problem-solving skills and the ability to think critically and creatively when tackling technical challenges.</li><li>A genuine interest in the development and application of AI solutions to real-world problems.</li><li>Strong written and verbal communication skills, with the ability to clearly articulate technical concepts to both technical and non-technical audiences.</li><li>Demonstrated motivation and resilience to learn and adapt in a fast-paced, evolving field, and a proactive approach to personal and professional development.</li><li>Ability to work collaboratively in a team environment while also being capable of taking initiative and working independently on projects.</li></ul><p></p><p><b>As a reminder…….</b></p><p></p><p><b>Who can apply?</b></p><p></p><p>Applicants must be completing placement as part of a degree course at a UK University, either through Year in Industry/Industrial Placement or Gap Year.</p><p></p><p><b>This position will close for applications at midnight on 31st May 2026. </b></p><p></p><p><b>Please note that we only accept application forms. Please do not send over your CV or cover letter as they will not be considered.</b></p><p></p><p>Please access the Word version of the Application Form here: <a href="https://www.pfizer.co.uk/careers/undergraduate-placements/undergraduate-vacancies" target="_blank">Undergraduate Vacancies | Pfizer UK </a>and find instructions as to how to complete your application and more about eligibility criteria.</p><p></p><p>#LI-PFE</p><p></p><p></p><p>  <br />Work Location Assignment: On Premise</p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>DisAbility Confident</u></p><p style="text-align:left">We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Support Services<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/ai-application-developer-undergraduate-pfizer/6a0743182f1861929d25326a</link><guid isPermaLink="true">http://biotechroles.com/ai-application-developer-undergraduate-pfizer/6a0743182f1861929d25326a</guid><pubDate>Fri, 15 May 2026 16:00:24 GMT</pubDate><company>Pfizer</company><location>United Kingdom - Walton Oaks</location><salary>$25000-35000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Cyber Resilience]]></title><description><![CDATA[<p><span><b>ROLE SUMMARY</b></span></p><p><span> </span></p><p><span>Our Global Governance, Risk, and Compliance team provides comprehensive blueprints for cybersecurity excellence by embedding governance, risk management, and compliance into every layer. The team is responsible for ensuring risk-based decision-making is used and that security, privacy, and regulatory compliance is integrated seamlessly with Pfizer’s organization.</span></p><p><span> </span></p><p><span>We are seeking an experienced Senior Manager, Business Resilience to lead and strengthen the organization’s global resilience strategy and capabilities. This role will oversee and enhance programs that ensure continuity of operations, and provide strategic leadership in identifying, assessing, and mitigating risks that could impact business operations. The Senior Manager, Business Resilience partners closely across business units, drives governance and preparedness initiatives, and leverages established resilience and risk management frameworks to safeguard the organization’s operational stability, agility, and reputation.</span></p><p><span> </span></p><p><span><b>ROLE RESPONSIBILITIES</b></span></p><ul><li><p><span>Design, implement, and continuously enhance the enterprise business resilience framework and governance processes.</span></p></li><li><p><span>Integrate business resilience practices into enterprise risk management and corporate governance, ensuring alignment across security, operations, and compliance functions.</span></p></li><li><p><span>Lead a high‑performing team that drives an enterprise‑wide culture of preparedness and operational continuity.</span></p></li><li><p><span>Partner with key stakeholders to align resilience, continuity, and incident readiness practices across the organization.</span></p></li><li><p><span>Cultivate a culture of accountability and risk awareness across all business units, reinforcing proactive planning, and effective response to disruptive events.</span></p></li><li><p><span>Provide strategic oversight into business resilience activities.</span></p></li><li><p><span>Lead, mentor, and develop a geographically distributed team of resilience and risk professionals.</span></p></li><li><p><span>Evaluate, implement, and manage technology platforms supporting business resilience, continuity management, and incident coordination, ensuring data accuracy and strong integration with risk systems.</span></p></li><li><p><span>Define and track key performance and risk indicators (KPIs/KRIs) to monitor organizational resilience posture and deliver actionable reporting and insights to senior leadership.</span></p></li></ul><p><span> </span></p><p><span> </span></p><p><span><b>BASIC QUALIFICATIONS</b></span></p><ul><li><p><span>Bachelor’s degree required in cybersecurity, information systems, risk management, or related discipline preferred.</span></p></li><li><p><span>7&#43; years of experience in information security, risk, compliance, information protection, or related disciplines</span></p></li><li><p><span>Demonstrated success leading complex, cross‑functional security or compliance programs involving multiple stakeholder groups and competing priorities.</span></p></li><li><p><span>Strong strategic thinking and problem‑solving capabilities, with the ability to translate risk insights into actionable recommendations.</span></p></li><li><p><span>Exceptional organizational skills and a proven ability to prioritize risks and initiatives.</span></p></li><li><p><span>Excellent communication and interpersonal skills, with the ability to influence, build consensus, and collaborate effectively at all organizational levels.</span></p></li></ul><p><span> </span></p><p><span><b>PREFERRED QUALIFICATIONS</b></span></p><ul><li><p><span>Background in highly regulated industries with strong familiarity with regulatory expectations related to third‑party oversight (e.g., pharma, healthcare, financial services).</span></p></li><li><p><span>Relevant certifications such as CISSP, CISM, CRISC, CISA, PMP, or other governance/risk credentials.</span></p></li><li><p><span>Experience integrating resilience with cyber incident response and disaster recovery programs.</span></p></li><li><p><span>Familiarity with resilience standards and best practices (e.g., ISO 22301 concepts, NIST, or operational resilience frameworks).</span></p></li><li><p><span>Experience with GRC/workflow tooling (e.g., ServiceNow GRC, Archer) or continuity tools (e.g., Fusion, Castellan, Archer BCM).</span></p></li></ul><p><span><b> </b></span><span> </span></p><p>Work Location Assignment: Hybrid</p><p><span>Please apply by sending your CV and a motivational letter in English</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Information &amp; Business Tech<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/senior-manager-cyber-resilience-pfizer/6a0743182f1861929d253269</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-cyber-resilience-pfizer/6a0743182f1861929d253269</guid><pubDate>Fri, 15 May 2026 16:00:24 GMT</pubDate><company>Pfizer</company><location>Greece-Thessaloniki Chortiatis</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[Senior Associate, Cyber Resilience]]></title><description><![CDATA[<p><span><b>ROLE SUMMARY</b></span></p><p><span> </span></p><p><span>Our Global Governance, Risk, and Compliance team provides comprehensive blueprints for cybersecurity excellence by embedding governance, risk management, and compliance into every layer. The team is responsible for ensuring risk-based decision-making is used and that security, privacy, and regulatory compliance is integrated seamlessly with Pfizer’s organization.</span></p><p><span> </span></p><p><span>We are seeking an experienced Senior Associate, Resilience to support the development and execution of our cyber resilience and operational preparedness capabilities. This role will play a key part in helping ensure Pfizer can anticipate, withstand, respond to, and recover from cyber disruptions, technology failures, third‑party incidents, and operational crises—while maintaining GxP compliance, patient safety, data integrity, and regulatory continuity.</span></p><p><span> </span></p><p><span><b>ROLE RESPONSIBILITIES</b></span></p><ul><li><p><span>Support the development and maintenance of cyber resilience frameworks, playbooks, and procedures aligned to business continuity, disaster recovery, and incident response.</span></p></li><li><p><span>Contribute to cyber incident simulations, tabletop exercises, and recovery testing to validate organizational readiness.</span></p></li><li><p><span>Assist in identifying and prioritizing critical business services, systems, and dependencies to inform resilience planning.</span></p></li><li><p><span>Collaborate with GRC, Digital, Manufacturing, R&amp;D, and Business stakeholders to assess cyber resilience risks and control gaps.</span></p></li><li><p><span>Support alignment to industry frameworks and regulatory expectations (e.g., NIST CSF, GxP considerations).</span></p></li><li><p><span>Document evidence and artifacts required for audits, assessments, and regulatory inquiries.</span></p></li><li><p><span>Track remediation actions and resilience enhancements across technology, process, and third‑party dependencies.</span></p></li><li><p><span>Analyze incidents and disruption events to identify lessons learned and improvement opportunities.</span></p></li><li><p><span>Support metrics, reporting, and dashboards to communicate resilience posture to leadership.</span></p></li></ul><p><span> </span></p><p><span><b>BASIC QUALIFICATIONS</b></span></p><ul><li><p><span>Bachelor’s degree required in cybersecurity, information systems, risk management, or related discipline preferred.</span></p></li><li><p><span>3&#43; years of experience in information security, risk, compliance, information protection, or related disciplines</span></p></li><li><p><span>Foundational knowledge of cybersecurity concepts, incident response, and risk management.</span></p></li><li><p><span>Experience working in regulated industries (pharma, life sciences, healthcare, or manufacturing strongly preferred).</span></p></li><li><p><span>Strong analytical, documentation, and stakeholder communication skills.</span></p></li></ul><p><span> </span></p><p><span><b>PREFERRED QUALIFICATIONS</b></span></p><ul><li><p><span>Relevant certifications such as CISSP, CISM, CRISC, CISA, PMP, or other governance/risk credentials.</span></p></li><li><p><span>Familiarity with frameworks such as NIST CSF, NIST SP 800‑53, ISO 22301, or ISO 27001.</span></p></li><li><p><span>Exposure to GxP, validated systems, manufacturing environments, or OT/ICS risks.</span></p></li><li><p><span>Experience supporting cyber exercises, scenario testing, or recovery planning.</span></p></li></ul><p><span><b> </b></span><br />Work Location Assignment: Hybrid</p><p><span>Please apply by sending your CV and a motivational letter in English</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Information &amp; Business Tech<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/senior-associate-cyber-resilience-pfizer/6a0743172f1861929d253268</link><guid isPermaLink="true">http://biotechroles.com/senior-associate-cyber-resilience-pfizer/6a0743172f1861929d253268</guid><pubDate>Fri, 15 May 2026 16:00:23 GMT</pubDate><company>Pfizer</company><location>Greece-Thessaloniki Chortiatis</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Recruiting Onboarding Delivery Associate]]></title><description><![CDATA[<p><b>Use Your Power for Purpose </b></p><p></p><p>At Pfizer, the Associate - Regional TA &amp; Onboarding Delivery role centers around delivering an outstanding candidate experience. As part of the Candidate Experience team, you will join a dynamic team committed to attracting top talent and ensuring every candidate feels valued from the first interaction through onboarding and integration. We prioritize a welcoming and supportive environment, actively seeking ways to improve processes and resolve challenges so that candidates and new hires have a seamless, positive journey. By focusing on each individual&#39;s experience, we create a workplace that is inclusive and exceptional, ultimately advancing our mission to enhance patient care and organizational success.</p><p></p><p><b>What You Will Achieve </b></p><ul><li>Facilitate talent acquisition by attracting high-quality candidates and streamlining their onboarding process, ensuring a positive experience for all new hires from initial contact through integration.</li><li>Serve as the primary point of contact for new hires and hiring managers to resolve onboarding questions and issues, including access to relevant tools, technologies, information and events.</li><li>Execute key operational components of recruitment and onboarding, such as job postings, generating and managing offer documentation, and handling pre-boarding activities.</li><li>Take ownership of all recruitment and onboarding administration assigned tasks and tickets and make sure that they are resolved efficiently and with a superior level of quality</li><li>Manage and track pre-hire contingencies and onboarding tasks to ensure compliance, timely completion, and a positive candidate experience.</li><li>Prepare, update, and verify the accuracy of employee records and onboarding data through reliable data entry practices, supporting audit readiness and regulatory requirements.</li><li>Execute key operational components of the end to end recruitment and onboarding processes including job posting, offer documentation generation and management, and pre-boarding documentation management</li><li>Ensure process alignment with country legal and privacy-related requirements, and deliver against agreed Service Level Agreements (SLAs) and Key Performance Indicators (KPIs) for recruitment and onboarding.</li><li>Identify areas for improvement in recruitment and onboarding processes, supporting the implementation of process enhancements by collaborating with the Regional Talent Acquisition Delivery Lead.</li><li>Develop and promote effective team collaboration and communication, operate within established procedures, and seek guidance as needed to uphold best practices and support organizational goals.</li></ul><p></p><p><b>Here Is What You Need (Minimum Requirements) </b></p><ul><li>A BA/BS with at least 1 year of experience, or an associate&#39;s degree with at least 4 years of experience, or a high school diploma (or equivalent) with at least 6 years of relevant experience is required for this role. </li><li>Proficiency in MS Office to handle tasks efficiently and seamlessly. </li><li>Strong written and verbal communication skills for effective collaboration and idea articulation. </li><li>A positive and continuous improvement mindset to adapt in ever-evolving situations. </li><li>Demonstrated capability to work as a compelling team member within a matrix environment. </li><li>Ability to manage multiple tasks and prioritize effectively in a fast-paced setting. </li><li>Strong organizational skills to coordinate workflow and handle documentation logistics. </li><li>Verbal and written fluency in English to facilitate clear communication and effective collaboration across teams.</li><li>Demonstrates customer orientation and delivers excellent customer service skills to ensure satisfaction and positive experiences.</li><li>At least 1 year of experience supporting recruitment and onboarding delivery processes for North America regions, ensuring smooth transitions and compliance with regional requirements.</li><li>Proficiency in MS Office to handle tasks efficiently and seamlessly.</li><li>Experience with Workday to manage recruitment processes and support recruitment and onboarding activities.</li><li>Strong written and verbal communication skills for effective collaboration and idea articulation.</li></ul><p></p><p><b>Bonus Points If You Have (Preferred Requirements): </b></p><ul><li>Ability to utilize various analytical tools effectively for informed decision-making. </li><li>Business level fluency in French</li><li>Excellent interpersonal skills to foster collaborative relationships. </li><li>Problem-solving skills with a proactive attitude towards challenges. </li><li>Adaptability to changing environments and processes, demonstrating resilience and flexibility. </li><li>Experience in project management or coordination to support Talent acquisition initiatives. </li><li>Enthusiasm for continuous learning and professional development opportunities. </li></ul><p><br /><span>Location: <b>Escazú, Costa Rica</b>. </span></p><div>Hybrid work model, requiring 2.5 days per week in the office.</div><div></div><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>EEO (Equal Employment Opportunity) &amp; Employment Eligibility </b></p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.</p>People Experience<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/recruiting-onboarding-delivery-associate-pfizer/6a0743172f1861929d253267</link><guid isPermaLink="true">http://biotechroles.com/recruiting-onboarding-delivery-associate-pfizer/6a0743172f1861929d253267</guid><pubDate>Fri, 15 May 2026 16:00:23 GMT</pubDate><company>Pfizer</company><location>Costa Rica - Escazu</location><salary>$28000-42000</salary><type>Full time</type></item><item><title><![CDATA[Global Transparency Reporting Senior Associate]]></title><description><![CDATA[<div><div><p><b>ROLE SUMMARY</b></p><p>The Global Transparency Reporting Senior Associate will contribute to the effort to generate high quality, accurate, and consistent data incorporated into the postings, filings and reports related to Healthcare Professional (HCP), Healthcare Organization (HCO) and Patient Organization (PO) payment disclosures for the markets assigned.</p><p></p><p>The Senior Associate will utilize global transparency reporting standards, processes and the Pfizer Transparency Repository system (PTRS) to collect, monitor, reconcile and correct data from multiple financial/expense/customer engagement sources (both internal and external) throughout the year to ensure data quality and completeness.  This includes but is not limited to looking for duplicate transactions, outliers, data errors and feeding back opportunities for process improvement to source systems and business data owners.  This position is ultimately accountable for ensuring the accompanying standards, processes and data are of high quality to meet the HCP/HCO/PO transfer of value disclosure commitments in the markets assigned as required by local codes and laws. </p><p></p><p>The Senior Associate will collaborate with market implementation leads, compliance and legal stakeholders as needed to ensure timely production of transparency reports.  Additionally, this position will partner with Business Process Owners across the organization including Finance, Commercial, Legal/Compliance, Medical Evidence Development, Digital and the global transparency reporting CoE to ensure that PTRS, source systems, HCP/HCO/PO customer master and other applicable Pfizer systems evolve to meet public disclosure needs. </p><p></p><p>The Senior Associate provides key services in the execution of the operations to support the Transparency initiatives.  The Senior Associate must bring a level of rigor and consistency in providing high-level service while ensuring compliance with the established procedures.</p><p></p><p>The role will partner with the Senior Manager to ensure the processes in place are optimal and meet all internal and external reporting obligations for assigned data sources and markets.  The position requires a strong commitment to the continuous improvement vision.</p><p></p><p>The Senior Associate role contains a significant amount of work requiring judgment, decision making, limited oversight and broader knowledge of the organization</p><p></p><p><b>ROLE RESPONSIBILITIES </b></p><ul><li>Manage the data stewarding/correction process across data sources to ensure data integrity/quality including the ability to accurately associate payments with a unique HCP/HCO/PO and their respective consent (where applicable) in order to produce accurate and timely reports for publication as per market timelines</li><li>Act as a subject matter expert for the markets the role is responsible for in relation to HCP/HCO/PO transparency reporting processes</li><li>Perform all process steps necessary as required by local codes and laws (for allocated markets) to ensure that all validations are completed in a timely manner for publication.</li><li>Partner with the market stakeholders as necessary to clarify data and prepare reports to support country manager certification, publication and republication.</li><li>Monitor and feed back to markets and source systems in relation to data quality issues, to continually improve the concept of right first time capture of data.</li><li>Implement a consistent approach/processes to reporting HCP/HCO/PO Transparency Reporting data across markets allocated.</li><li>Respond to ad hoc requests for clarification, additional information and/or reports regarding HCP/HCO/PO payments/transfers of value and supporting the HCP/HCO/PO pre-disclosure &amp; dispute process.</li><li>Respond to queries from management, business unit leaders, and other stakeholders as needed in relation to transparency reporting information for markets assigned.</li><li>Contribute and adhere to Quality Assurance/Quality Control (QA/QC) and compliance standards.</li><li>Participate in Continuous Improvement projects and other system/process enhancements aimed at improving the quality of the data and associated processes.</li><li>Participate in training on an as-needed basis.</li><li>Assist in periodic audits and inspections by internal audit or external regulators.</li><li>Remediation of issues resulting from audit findings or compliance related matters.</li><li>Work with internal and external stakeholders to develop a strategy for collecting required information for disclosure.</li></ul><p></p><p><b>BASIC QUALIFICATIONS </b></p><ul><li>BA/BSc degree required.</li><li>Minimum of 3 years of professional experience is required.</li><li>Experience in finance, compliance, accounting, or management information systems in the pharmaceutical industry or related field a plus.</li><li>Fluency in oral and written English is required</li><li>Strong analytical, results oriented capabilities combined with superior organizational skills.</li><li>Experience and comfortable working in cross-functional and matrix teams.</li><li>Demonstrated skills in teamwork and customer focus.</li><li>Excellent oral and written communication skills.</li><li>Expert level working experience/ Expert knowledge of Excel is required</li><li>Fundamental understanding of analyzing and managing large sets of data via excel is required</li><li>Good oral and written communication skills in other languages is a plus</li></ul><p></p><p><b>PREFERRED QUALIFICATIONS</b></p><ul><li>Relevant experience in Transparency initiatives including the understanding of HCP/HCO/PO Transparency Disclosure policies.</li><li>Strong technical skills, including experience/ knowledge of user query tools (Excel), underlying financial &amp; reporting systems (SAP, Ariba, CVent, Concur, Business Objects) is desirable.</li></ul><p><br />Work Location Assignment: Hybrid</p></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>EEO (Equal Employment Opportunity) &amp; Employment Eligibility </b></p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.</p>Continuous Imprv and Proj Mgmt<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/global-transparency-reporting-senior-associate-pfizer/6a0743162f1861929d253266</link><guid isPermaLink="true">http://biotechroles.com/global-transparency-reporting-senior-associate-pfizer/6a0743162f1861929d253266</guid><pubDate>Fri, 15 May 2026 16:00:22 GMT</pubDate><company>Pfizer</company><location>Colombia - Bogota</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Site Digital & Automation Lead, Sanford]]></title><description><![CDATA[<div><p><b>Role Summary</b></p></div><div><div><div><div><div><div><div><div><div><p>The Site Digital &amp; Automation Lead is a full member of the Site Leadership Team and a key leader within the PGS Network &amp; Automation organization. This role provides strategic direction and leadership for all digital and automation capabilities at site, serving as the primary advisor and partner to Site Leadership and above-site stakeholders. The role is accountable for shaping, owning, and executing the site’s integrated digital and automation portfolio, ensuring full alignment with site business priorities and network strategies.</p><p>This role drives long-term value creation, investment prioritization, and portfolio governance across capital and expense initiatives. The Site Digital &amp; Automation Lead leads and develops the site digital and automation team, ensuring the design, deployment, and lifecycle management of critical digital, automation, and infrastructure systems. This includes driving operational efficiency, ensuring Quality/Safety compliance, cybersecurity, business continuity and reliable system support.</p><p></p><p><b>Role Description</b></p><p><b>Core Responsibilities</b></p><p><b>Leadership and Oversight</b></p><ul><li><p>Serve as a full member of the Site Leadership Team.</p></li><li><p>Collaborate with the Site Leadership Team to ensure alignment of site and network strategies with digital and automation capabilities.</p></li><li><p>Lead teams of colleagues and contract resources to deliver digital and automation capital projects and manage expense portfolios, ensuring customer needs are met; uphold standardized platforms and oversee strategic outsourcing to key integrators.</p></li><li><p>Act as the primary contact for all digital and automation colleagues located at the site.</p></li><li><p>Build and maintain relationships with PGS Enabling Teams and Digital Organizations.</p></li><li><p>Lead and participate in network-wide digital and automation initiatives.</p></li><li><p>Lead, mentor, and develop a team of digital &amp; automation professionals</p></li><li><p>Conduct performance reviews and provide growth opportunities</p></li><li><p>Build a collaborative, innovative environment</p></li></ul><p></p><p><b>Performance Management &amp; Continuous Improvement (CI)</b></p><ul><li><p>Develop and own the site’s 3–5 year digital and automation strategy</p></li><li><p>Provide strategic direction and establish business cases for large capital, or product focused programs and technology portfolio plans; continually evaluate and deploy emerging technologies to realize value.</p></li><li><p>Implement IMEx elements, including Structured Gembas, Visual Management, and the CI Loop, to drive process improvements using digital tools.</p></li><li><p>Support site continuous improvement initiatives and share best practices and drive business adoption</p></li><li><p>Provide oversight of the site digital &amp; automation portfolio, championing AI and innovation through integrated planning and reliable project execution.</p></li><li><p>Maintain a strong awareness of automation and digitization developments in the external environment.</p></li><li><p>Oversee contract and license management for digital and automation systems, ensuring compliance and effective administration.</p></li><li><p>Ensure effective implementation and continuous oversight of lifecycle processes for all digital and automated systems and infrastructure.</p></li></ul><p></p><p><b>Operational Services</b></p><ul><li><p>Deliver dependable digital &amp; automation support services, responding quickly to real-timesystem issues while maintaining stable, high-performing digital and automation systems.</p></li><li><p>Ensure Automation Engineering support, including hardware, instrumentation, and control systems ownership.</p></li><li><p>Take responsibility for change management pertaining to digital and automation infrastructure on site, including managing outages and communicating with end users.</p></li><li><p>Serve as the primary point of contact for all digital and automation operations at the site, including escalating issues to the wider PGS Network and Automation organization.</p></li><li><p>Collaborate with the PGS Network and Automation organization to maintain service levels for crisis response, digital incident management, and service request processes.</p></li><li><p>Oversee the provision of technical support to Engineering and Operations partners for automated systems throughout the lifecycle of the equipment.</p></li></ul><p></p><p><b>Cyber Security &amp; Network</b></p><ul><li><p>Manage and coordinate cybersecurity activities and ensure compliance with digital and automation Infrastructure &amp; Architecture Standards Execution</p></li><li><p>Own change management for technology infrastructure, including outage management, end-user communications, maintenance and support</p></li><li><p>Oversee software and hardware lifecycle management and PANS Support</p></li></ul><p></p><p><b>Data Systems &amp; Integration</b></p><ul><li><p>Manage the development of the Automated System Life Cycle documents.</p></li><li><p>Ensure deployment of end-to-end data strategy for digital and automation systems.</p></li><li><p>Leverage data standards to ensure consistency and compliance.</p></li><li><p>Oversee core system integration to support seamless data flow and connectivity.</p></li><li><p>Manage the development of local applications to meet site and business needs.</p></li></ul><p></p><p><b>Computer System Assurance</b></p><ul><li><p>Proactively address business continuity risk for digital and automation assets</p></li><li><p>Maintain Quality and Safety compliance and continuous audit-readiness</p></li><li><p>Ensure adherence to system validation requirements and change control processes</p></li><li><p>Maintain up to date GMP documentation for systems and assets within the remit of the team</p></li></ul><p></p><p><b>Key Attributes, Skills &amp; Competencies</b></p><p><b>Communication &amp; Stakeholder Management</b></p><ul><li><p>Clear communicator who can translate complex technical topics to non-technical stakeholders.</p></li><li><p>Executive presence; capable of influencing across site and enterprise teams.</p></li></ul><p></p><p><b>Visionary Thinking and Technology Strategy</b></p><ul><li><p>Strong ability to design and govern reliable OT automation and site digital ecosystems (end-to-end lifecycle ownership).</p></li><li><p>Comfortable making risk-based decisions balancing production continuity, compliance, and security.</p></li><li><p>Passionate about leveraging technology to enhance operations.</p></li><li><p>Portfolio and program leadership; disciplined execution, stakeholder management, and vendor oversight.</p></li><li><p>Anticipates future digital needs and acts proactively</p></li></ul><p></p><p><b>Change and Problem Management </b></p><ul><li><p>Strong problem-solving and organizational skills</p></li><li><p>Leader of technical and organizational change</p></li><li><p>Ability to manage multiple priorities and work effectively in a dynamic environment</p></li></ul><p></p><p><b>Technical Fluency</b></p><ul><li><p>Understanding of emerging technologies, AI</p></li><li><p>Foundational digital and automation risk management</p></li><li><p>Strong grasp of integration patterns between OT systems and data platforms.</p></li><li><p>Demonstrates strong expertise in digital and automation solutions.</p></li></ul><p></p><p><b>Basic Qualifications, Experience &amp; Certifications</b></p><ul><li><p>Bachelor’s degree in engineering, Computer Science, Information Systems, business, or related technical field (Controls, Electrical, Chemical, IT/CS)</p></li><li><p>8&#43; years’ experience in information technology systems/infrastructure or specialist knowledge of process automation/process control systems</p></li><li><p>3–5 years in a regulated manufacturing environment (pharma or similar preferred)</p></li><li><p>Experience with Lean/Operational Excellence</p></li><li><p>Project/program management (PMI, Agile, SDLC) and continuous improvement (e.g., Six Sigma)</p></li><li><p>IT infrastructure management (e.g., ITIL) and GMP regulatory requirements experience preferred</p></li></ul><p><br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><p><br />Work Location Assignment: On Premise</p><p><b>Last day to apply :</b> May 29th 2026</p></div></div></div></div></div></div></div></div></div>&amp;#xa;The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Information &amp; Business Tech&amp;#xa;]]></description><link>http://biotechroles.com/site-digital-and-automation-lead-sanford-pfizer/6a0743162f1861929d253265</link><guid isPermaLink="true">http://biotechroles.com/site-digital-and-automation-lead-sanford-pfizer/6a0743162f1861929d253265</guid><pubDate>Fri, 15 May 2026 16:00:22 GMT</pubDate><company>Pfizer</company><location>United States - North Carolina - Sanford</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Cluster HTA Hub Senior Manager]]></title><description><![CDATA[<p><b>Use Your Power for Purpose  </b></p><p></p><p>The <b>Innovating for Growth</b> organization is an agile, efficient, and innovative cluster-led model, designed to unlock growth and accelerate impact for patients. It is centered on uniting colleagues under a single cluster identity, leveraging AI and digital tools, and fostering a culture of continuous improvement. The new structure enables dynamic resource allocation, rapid learning and a start-up spirit that empowers teams to act entrepreneurially. Ultimately, I4G aims to reach more patients, faster, with greater impact and collaboration across countries where empowered teams unlock greater value than ever before.</p><p></p><p>The HTA is a technical team responsible for supporting the centralized and streamlined HTA process across the cluster, enabled by AI (where to drive efficiencies and reduce complexity in the go-to-market (GTM) model. Operating within the HTA hub established by the HTA Lead, the specialist contributes to new ways of working by generating high-quality health economic evidence, managing AI-supported workflows, and ensuring HTA submissions remain on track. The HTA specialist will have multiple market insights understanding the HTA requirements across countries within the cluster and will enable synergies across markets for HTA submissions.</p><p></p><p></p><p><b>ROLE SUMMARY</b></p><p></p><p>We are looking for a Senior Manager, Health Technology Assessment (HTA) to join the East Europe HTA Hub, covering 6 markets (Poland, Romania, Israel, Bulgaria, Slovakia, Czech Republic).</p><p></p><p>This role is part of a newly established cluster structure, designed to strengthen HTA capabilities across markets while driving new ways of working and transformation, including AI-enabled approaches.</p><p></p><p>The position combines EU-level activities (EU JCA, PICOs), HTA dossier development for countries, economic modelling and value development, and cross-functional cluster projects.</p><p></p><p></p><p><b>ROLE RESPONSIBILITIES </b></p><p></p><p>In order of importance, indicate the primary responsibilities critical to the performance of the role. It is recommended not to list actual tasks but focus on <span>5 essential responsibilities</span>. Please include:</p><p></p><ul><li><p>Country/ Cluster remit</p></li><li><p>Revenue accountability/ responsibility</p></li><li><p>TA/ Portfolio/ Product responsibility</p></li><li><p>Complexity of the role: Strategic leadership/ Operational/ Implementation management, External Engagement</p></li></ul><p></p><p></p><p><b>HTA Development &amp; Technical Execution</b></p><ul><li><p>Design and adapt health economic models (e.g., cost-utility, cost-effectiveness, budget impact) to support HTA submissions across countries within the cluster.</p></li><li><p>Generate and synthesize clinical and economic evidence, including SLRs, NMAs, and real-world data inputs.</p></li><li><p>Prepare value dossiers and submission packages aligned with national and regional HTA requirements.</p></li><li><p>Apply AI-enabled tools for literature review automation, scenario modeling, and data visualization.</p></li></ul><p></p><p></p><p><b>Submission Coordination &amp; Quality Assurance</b></p><ul><li><p>Support the end-to-end HTA submission process, ensuring accuracy, consistency, and compliance with internal and external standards.</p></li><li><p>Conduct internal review checkpoints and collaborate with cross-functional teams to address uncertainties and strengthen value propositions.</p></li><li><p>Maintain documentation and version control for all HTA deliverables across markets.</p></li></ul><p></p><p></p><p><b>Strategic Collaboration &amp; Knowledge Sharing</b></p><ul><li><p>Work closely with the HTA Lead, Medical and Commercial teams to align technical outputs with strategic objectives.</p></li><li><p>Contribute to internal knowledge sharing by documenting learnings and best practices from HTA projects.</p></li><li><p>Participate in cluster-wide HTA hub activities and support harmonization of processes across cluster.</p></li><li><p>Participate in HTA specialist community of practice across clusters and with GAV community to cross-polinate learnings and best practices.</p></li></ul><p></p><p></p><p><b>External Engagement Support</b></p><ul><li><p>Preparing materials for payer interactions, advisory boards, and external consultations.</p></li><li><p>Contribute technical input to policy shaping initiatives led by the HTA Lead or cluster teams.</p></li></ul><p></p><p></p><p></p><p></p><p><b>QUALIFICATIONS </b></p><p></p><p></p><p><b>Basic Qualifications</b></p><ul><li><p>Minimum education requirement</p></li><li><p>Area of expertise required</p></li><li><p>Years of experience.</p></li></ul><p></p><p><b>Minimum Requirements:</b></p><ul><li><p>Bachelor’s or master’s degree in natural sciences and/or public administration</p></li><li><p>Minimum 5 years of experience in HTA, market access, or health economics within pharma, biotech, or consultancy.</p></li><li><p>Strong understanding of HTA frameworks and payer requirements across cluster countries.</p></li><li><p>Hands-on experience in developing health economic models and conducting evidence synthesis</p></li><li><p>Proven track record in preparing HTA dossiers, reimbursement submissions, or value dossiers for agencies</p></li><li><p>Proficiency in modeling software (e.g., Excel, TreeAge, R, Python) and data analysis tools.</p></li><li><p>Experience collaborating with cross-functional teams (clinical, regulatory, market access, medical affairs, pricing).</p></li><li><p>Familiarity with real-world evidence (RWE) generation and use in HTA.</p></li><li><p>Strong analytical skills with a structured approach to problem solving and execution</p></li><li><p>Excellent written communication skills for developing HTA dossiers, value messages, and technical reports.</p></li><li><p>Familiarity with AI-based tools for literature review, data extraction, and scenario simulation.</p></li></ul><p></p><p></p><p><b>Preferred Requirements</b></p><ul><li><p>Master’s or PhD in Health Economics, Outcomes Research, Public Health, or a related quantitative discipline; PhD is a plus, especially in health economics, outcomes research, or epidemiology.</p></li><li><p>Experience working across countries and abiity to work in matrix organizations</p></li></ul><p></p><p></p><p><b>STAKEHOLDER MANAGEMENT</b></p><p></p><p>Provide the primary groups or key role(s) that this role will interact with as a regular part of the role responsibilities. Include any external interactions as appropriate.</p><ul><li><p>Internal connections: Cluster Commercial Lead, CMO, ICO, other cluster and country marketing and commercial teams, cluster and International commercial excellence and analytics / AI specialists, medical scientific experts, cluster leads and country medical leads, HTA and access leads, finance, business operations, regulatory, safety, legal and other enabling function.</p></li><li><p>External connections: senior HCPs / KOLs, industry associations, patient organizations, government officials, HTA authorities, regulatory authorities.</p></li></ul><p></p><p></p><p><b>Pay Transparency Note:</b><br /><br /><b>Minimal Annual Gross Base Salary: </b> 300.000 PLN<br /><b>Annual Bonus: </b>20%<br />Company car and other benefits as per Pay Policy.<br /><br />Please be kindly informed that the above salary conditions apply to Candidates based in Poland only. Applicants from other countries will be a subject to local pay policies.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u><br /><span>Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</span></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left">Pursuant to Article 24(6) of the Act of June 24, 2024 on the protection of whistleblowers, Pfizer Polska Sp. z o.o. and Pfizer Trading Polska Sp. z o.o. declare that they have adopted a joint internal reporting procedure, which, in accordance with the provisions of the aforementioned Act, is also available to persons applying for employment on the basis of an employment relationship or other legal relationship constituting the basis for providing work or services or performing functions. The content of the procedure is made available upon request sent to the contact person or to the email address <span class="WKM0">sygnalisci-px&#64;pfizer.com.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Market Access<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/cluster-hta-hub-senior-manager-pfizer/6a0743152f1861929d253264</link><guid isPermaLink="true">http://biotechroles.com/cluster-hta-hub-senior-manager-pfizer/6a0743152f1861929d253264</guid><pubDate>Fri, 15 May 2026 16:00:22 GMT</pubDate><company>Pfizer</company><location>Poland - Warsaw</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Third Party Risk Management]]></title><description><![CDATA[<h2><b>ROLE SUMMARY</b></h2><p></p><p>Our Global Governance, Risk, and Compliance (GRC) team provides comprehensive blueprints for cybersecurity excellence by embedding governance, risk management, and compliance into every layer. The team is responsible for ensuring risk-based decision-making is used and that security, privacy, and regulatory compliance is integrated seamlessly with Pfizer’s organization.</p><p></p><p>We are seeking a Manager, Third Party Risk Management, who provides direction for how the organization evaluates and oversees its external vendors. This role maintains the framework that guides third party risk decisions, ensures vendor relationships follow organizational requirements, and supports consistent oversight across all engagements. It keeps the organization focused on understanding vendor risks, applying a structured approach to assessments, and maintaining reliable documentation that supports continuity and compliance.</p><p></p><h2><b>ROLE RESPONSIBILITIES</b></h2><ul><li><p>Define and maintain third‑party risk management policies and procedures that outline how vendors are assessed, classified, and monitored.</p></li><li><p>Oversee the execution of the TPRM program.</p></li><li><p>Review inherent risk evaluations and due‑diligence assessments to confirm that relevant security, privacy, compliance, and operational risks are properly identified and documented.</p></li><li><p>Review high‑risk assessments, ensuring findings are well‑articulated, evidence‑based, and aligned with internal standards.</p></li><li><p>Lead governance for risk treatment decisions, including remediation plans, compensating controls, and formal risk acceptances/exceptions.</p></li><li><p>Ensure vendor records, assessments, contracts, and risk findings are accurate, complete, and maintained in accordance with TPRM expectations and regulatory requirements.</p></li><li><p>Coordinate communication with vendors to request clarifications, gather required evidence, and follow up on remediation activities. Prepare clear, concise reporting for leadership that summarizes third‑party risk posture, program performance, key issues, and emerging trends.</p></li><li><p>Partner with procurement, legal, security, and business stakeholders to ensure third‑party risks are understood and managed.</p></li><li><p>Partner with Legal and Procurement to ensure security and cyber requirements are embedded into contracts.</p></li><li><p>Identify opportunities to strengthen the TPRM process through improved workflow design, automation, standardization, and integration with other GRC processes.</p></li><li><p>Present on TPRM program to senior and executive leadership to provide actionable insights.</p></li></ul><p></p><h2><b>BASIC QUALIFICATIONS</b></h2><ul><li><p>Bachelor’s degree in Information Technology, Cybersecurity, Computer Science, or a related field.</p></li><li><p>5&#43; years of experience in information security, risk, compliance, information protection, or related disciplines.</p></li><li><p>Experience with frameworks and standards such as NIST Cybersecurity Framework or ISO 27001.</p></li><li><p>Experience developing and maintaining vendor risk policies, SOPs, and compliance frameworks.</p></li><li><p>Ability to manage multiple priorities, work with cross-functional teams, and deliver high-quality outputs.</p></li><li><p>Capability to align cybersecurity strategy with business objectives and operational resilience goals.</p></li><li><p>Strong leadership, communication, and presentation skills, with the ability to translate complex security concepts into business-focused insights for senior executives. </p></li><li><p>Excellent communication and interpersonal skills; ability to influence across levels and functions.</p></li><li><p>Demonstrated experience in an agile work environment possessing qualities such as a collaborative mindset, adaptability to change, and a proactive problem-solving approach.</p></li></ul><p></p><h2><b>PREFERRED QUALIFICATIONS</b></h2><ul><li><p>Demonstrated experience working in pharmaceuticals industry and large, complex, or regulated environments.</p></li><li><p>Professional certifications such as CISSP, CISM, CRISC, CISA, PMP, or similar. </p></li><li><p>Hands‑on experience with TPRM/GRC platforms (e.g., Archer).</p></li></ul><p></p><p><i>Please apply by sending your CV in English.</i></p><p><br />Work Location Assignment: Hybrid</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Information &amp; Business Tech<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/manager-third-party-risk-management-pfizer/6a0743152f1861929d253263</link><guid isPermaLink="true">http://biotechroles.com/manager-third-party-risk-management-pfizer/6a0743152f1861929d253263</guid><pubDate>Fri, 15 May 2026 16:00:21 GMT</pubDate><company>Pfizer</company><location>Greece-Thessaloniki Chortiatis</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Technical Information Security Lead]]></title><description><![CDATA[<h2><b>ROLE SUMMARY</b></h2><p></p><p>Our Global Governance, Risk, and Compliance (GRC) team provides comprehensive blueprints for cybersecurity excellence by embedding governance, risk management, and compliance into every layer. The team is responsible for ensuring risk-based decision-making is used and that security, privacy, and regulatory compliance is integrated seamlessly with Pfizer’s organization.</p><p></p><p>We are seeking a motivated Manager, Technical Information Security Lead, who will serve as a senior, business‑aligned cybersecurity leader, responsible for partnering with business and technology stakeholders, executing and overseeing technical risk assessments, and driving risk‑informed decisions across complex initiatives and platforms.</p><p></p><h2><b>ROLE RESPONSIBILITIES</b></h2><ul><li><p>Serve as the Technical Information Security Lead for assigned business units, programs, or technology domains.</p></li><li><p>Act as the primary interface between Cybersecurity/GRC and business stakeholders, ensuring security considerations are embedded early and effectively.</p></li><li><p>Build trusted relationships with Business Leaders, IT, Engineering, Cloud Services, Privacy, Legal, and other key stakeholders and teams.</p></li><li><p>Translate technical findings into clear, actionable risk statements and recommendations tailored to business audiences.</p></li><li><p>Partner with technology and business owners to define risk mitigation strategies, remediation plans, and compensating controls.</p></li><li><p>Support audit and inspection readiness by providing defensible risk narratives, assessment artifacts, and evidence.</p></li><li><p>Review and provide quality oversight of risk assessments and documentation.</p></li><li><p>Contribute to the evolution of risk assessment methodologies, standards, templates, and engagement models.</p></li><li><p>Identify opportunities to improve consistency, scalability, and efficiency across security risk engagement.</p></li><li><p>Prepare concise, executive‑level summaries for risk committees, governance forums, and senior leadership.</p></li><li><p>Provide thought leadership on emerging risks (e.g., cloud, AI, third‑party dependencies).</p></li></ul><p></p><h2><b>BASIC QUALIFICATIONS</b></h2><ul><li><p>Bachelor’s degree in Cybersecurity, Information Systems, Computer Science, Risk Management, or related field, or a related field.</p></li><li><p>5&#43; years of experience in information security, risk, compliance, information protection, or related disciplines.</p></li><li><p>Demonstrated experience leading technical risk assessments and stakeholder engagement.</p></li><li><p>Proven ability to communicate complex technical risks to senior business stakeholders.</p></li><li><p>Strong documentation, analytical, and decision‑making skills.</p></li><li><p>Experience operating in a highly regulated, matrixed enterprise environment.</p></li><li><p>Demonstrated experience in an agile work environment possessing qualities such as a collaborative mindset, adaptability to change, and a proactive problem-solving approach.</p></li></ul><p></p><p><b>PREFERRED QUALIFICATIONS</b></p><ul><li><p>Demonstrated experience working in the pharmaceuticals industry.</p></li><li><p>Professional certifications such as CISSP, CISM, CRISC, CISA, or similar.</p></li><li><p>Familiarity with GRC platforms (e.g., Archer).</p></li><li><p>Experience supporting regulatory inspections or major audits.</p></li></ul><p>  </p><p><i>Please apply by sending your CV in English.</i></p><p><br />Work Location Assignment: Hybrid</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Information &amp; Business Tech<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/manager-technical-information-security-lead-pfizer/6a0743142f1861929d253262</link><guid isPermaLink="true">http://biotechroles.com/manager-technical-information-security-lead-pfizer/6a0743142f1861929d253262</guid><pubDate>Fri, 15 May 2026 16:00:20 GMT</pubDate><company>Pfizer</company><location>Greece-Thessaloniki Chortiatis</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Director, Cloud and Infrastructure Transformation]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>At the heart of Pfizer&#39;s Digital transformation sits Infrastructure &amp; Cloud, enabling modern cloud infrastructure and engineering capabilities that influence business outcomes and provide value to our business, shareholders, and patients every day.<br /> </p><p>Pfizer is seeking an execution-focused Senior Director to lead transformational cloud and infrastructure initiatives that directly enable breakthrough science and drug discovery. You&#39;ll play a critical leadership role in developing our next-generation cloud platform for AI/ML-powered research while building and leading a high-performing technical team.<br /> </p><p>This role combines strategic thinking with hands-on delivery, technical depth with leadership impact, and the autonomy to make decisions that advance Pfizer&#39;s mission. Your work will provide the infrastructure foundation that enables our scientists to accelerate research, analyze complex data, and develop treatments that improve patients&#39; lives.<br /> </p><p>Pfizer seeks individuals that are highly self-motivated, eager to learn, and effective when working in a team environment. A strong aptitude towards self-development, continuous learning, and growth is highly desired.</p><p></p><p><span><b>What You Will Achieve</b></span></p><p><span>The Senior Director, Cloud and Infrastructure Transformation provides executive-level technical leadership and strategic direction, playing a critical role in ensuring Pfizer continues to leverage cloud-native design patterns and modern infrastructure practices at enterprise scale. This role will help ensure our Infrastructure &amp; Cloud organization delivers secure, compliant, productive, and innovative platforms that enable breakthrough science.</span><br /> </p><p><span>You will lead a team of 3-5 Directors and Senior Managers and Directors, providing strategic guidance, mentorship, and support in their professional development while driving the adoption of transformational cloud and infrastructure initiatives across the organization.</span></p><ul><li><p><span><span>Lead enterprise cloud and infrastructure transformation, including AI/ML platforms, data center migration, and network transformation</span></span></p></li><li><p><span><span>Drive multi‑cloud, data center, and network initiatives with strong execution</span></span></p></li><li><p><span><span>Make high‑impact architectural and technology decisions</span></span></p></li><li><p><span><span>Provide senior technical leadership and shape infrastructure strategy</span></span></p></li><li><p><span><span>Lead and develop senior leaders and high‑performing teams</span></span></p></li><li><p><span><span>Partner with security, digital, and business stakeholders</span></span></p></li><li><p><span><span>Operate effectively in a global, matrixed organization</span></span></p></li><li><p>Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p></li></ul><p><span> </span></p><p><b>Here Is What You Need (Minimum Requirements):</b></p><ul><li><p><span><span>Bachelor’s degree in information technology, Computer Science, Computer Engineering, or a similar discipline</span></span></p></li><li><p><span><span>12&#43; years in infrastructure, cloud, and networking with proven track record of delivering complex, multi-year transformation programs</span></span></p></li><li><p><span><span>Deep multi-cloud expertise (AWS, Azure, GCP) with hands-on experience building production platforms at scale</span></span></p></li><li><p><span><span>Comprehensive understanding of the full stack from on-premises data centers to cloud-native architectures</span></span></p></li><li><p><span><span>Demonstrated success managing and developing senior technical leaders (Senior Managers, Directors)</span></span></p></li><li><p><span><span>Extensive experience leading through influence in matrixed organizations, working across technical and business stakeholders</span></span></p></li><li><p><span><span>Strong technical judgment shaped by real-world experience delivering at scale - hands-on when needed, strategic enough to delegate and orchestrate</span></span></p></li><li><p><span><span>Expertise in modern cloud-native architectures, IaC (Terraform/OpenTofu), DevOps practices, automation, and security/compliance in regulated industries</span></span></p></li><li><p><span><span>Excellent communicator with the ability to translate technical complexity for diverse audiences and drive alignment</span></span></p></li><li><p><span><span>Proven ability to deliver results while managing multiple complex initiatives simultaneously</span></span></p></li><li><p><span><span>Pragmatic decision-maker who balances ideal solutions with practical constraints and knows when to seek input or escalate</span></span><br /> </p></li></ul><p><b>Bonus Points If You Have (Preferred Qualifications):</b><span> </span></p><ul><li><p><span><span>AI/ML infrastructure experience, especially supporting research and data science workloads</span></span></p></li><li><p><span><span>Background in pharma, biotech, or highly regulated industries</span></span></p></li><li><p><span><span>Cloud certifications demonstrating depth of expertise</span></span></p></li><li><p><span><span>Experience with large-scale migrations, datacenter exits, or M&amp;A integrations</span></span></p></li><li><p><span><span>Global team management across time zones and cultures</span></span></p></li></ul><p></p><p><b>Other Job Details</b></p><ul><li><p>Last day to apply: May 28, 2026</p></li><li><p>Work location assignment: Hybrid - onsite at NY Headquarters an average of 2.5 days per week or as the business requires</p></li><li><p>10-20% Travel</p></li></ul>&amp;#xa;The annual base salary for this position ranges from $214,900.00 to $358,100.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 22.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Information &amp; Business Tech&amp;#xa;]]></description><link>http://biotechroles.com/sr-director-cloud-and-infrastructure-transformation-pfizer/6a0743132f1861929d253261</link><guid isPermaLink="true">http://biotechroles.com/sr-director-cloud-and-infrastructure-transformation-pfizer/6a0743132f1861929d253261</guid><pubDate>Fri, 15 May 2026 16:00:19 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$220000-320000</salary><type>Full time</type></item><item><title><![CDATA[Product Specialist Hemato-Oncology (filed based)]]></title><description><![CDATA[<p>Purpose:<br>
• Execution of marketing and sales strategies to optimize brand performance based on market needs.<br>
• Leading the In-Field Teams’ to execute marketing &amp; sales initiatives, coordinating all activities related to marketing materials, and supporting other In-Field Teams’ related processes placing the patients' needs at the center of any efforts and operating within AbbVie&#xa0;business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities:</p><p>• Actively engage with multiple stakeholders to foster gathering of insights.</p><p>• Support implementation of Marketing-led initiatives including supporting coordination with partner agencies to deliver appropriate and multi-channel and digital campaigns.</p><p>• Share In-Field best practices, and support In-Field Teams in their tactical executions to align In-Field Team activities.</p><p>• Support marketing colleagues in the development of marketing materials, in gathering information for forecasting and KPI monitoring.</p><p>• Organize and coordinate symposiums, congresses on national &amp; international levels.</p><p>• Collect feedback about market condition changes, competitor activities, etc., and forward this&#xa0;information to the management and the team.</p><p>• Execute digital transformation and support IFT in implantation.• Differentiate AbbVie’s value proposition with health providers assigned and identify, develop and maintain disease state experts and speakers/advocates in order to maximize brand performance.</p>]]></description><link>http://biotechroles.com/product-specialist-hemato-oncology-(filed-based)-abbvie/6a06ef382f1861929d253259</link><guid isPermaLink="true">http://biotechroles.com/product-specialist-hemato-oncology-(filed-based)-abbvie/6a06ef382f1861929d253259</guid><pubDate>Fri, 15 May 2026 10:02:32 GMT</pubDate><company>AbbVie</company><location>Hod Hasharon, Hod Hasharon</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Government Affairs Manager - Fixed Term Contract]]></title><description><![CDATA[<p>We are seeking a Government Affairs Manager for a fixed-term contract covering AbbVie's external communication towards policymakers and other key stakeholders related to corporate communication and defined brands.</p><p>In this position you will develop policy input, collect information about ongoing processes and help AbbVie communicate clearly to stakeholders and secure favorable environment for our company. The position will also contribute to develop executing the developed strategy for AbbVie’s external engagements and priorities and secure that these are executed in a good way.</p><p>The position also supports all AbbVie’s patient engagement managers on questions related to government affairs.</p><p>Major Responsibilities:</p><ul><li>Develop and implement strategies to build strong and trusted relationships with policy makers to shape a favorable environment for our brands and guarantee our freedom to operate.</li><li>Continuously deepen understanding of healthcare environment, map relevant stakeholders (e.g., Politicians, agencies, patient and physician Associations and trade bodies), understand their role in future healthcare policies and identify key challenges and opportunities for the Affiliate and specific brands.</li><li>Write and develop briefs/executive summaries for management.</li><li>Proactively identify opportunities for&#xa0;AbbVie and create favorable environment to achieve&#xa0;business objectives and defend&#xa0;AbbVie&#xa0;vs. government policies that could harm the organization.</li><li>Work cross functionally with Market Access, Corporate Affairs, HEOR, and Commercial teams to develop and align the GA strategy across the Scandinavian Affiliate.</li><li>Participate in Area GA network, share best practices and key learning and identify possible synergies or common projects to work on.&#xa0;</li><li>Ensure internal alignment across Scandinavia and support team members in external engagements.</li></ul>]]></description><link>http://biotechroles.com/government-affairs-manager-fixed-term-contract-abbvie/6a06ef362f1861929d253258</link><guid isPermaLink="true">http://biotechroles.com/government-affairs-manager-fixed-term-contract-abbvie/6a06ef362f1861929d253258</guid><pubDate>Fri, 15 May 2026 10:02:30 GMT</pubDate><company>AbbVie</company><location>Copenhagen, Copenhagen</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Spécialiste Contrôle Qualité (QC) (F/H/X)]]></title><description><![CDATA[<p><strong>Description : </strong></p><p>En tant que Spécialiste Contrôle Qualité, vous serez chargé d'effectuer des analyses routine et hors routine de produits selon les normes GMP au sein d’un laboratoire QC soutenant le réseau de fabrication d’AbbVie. Vous contribuerez à valider les méthodes, à garantir la conformité des produits intermédiaires et finis, ainsi qu’à vérifier leurs stabilités de manière autonome. Le spécialiste contrôle qualité est un élément moteur dans la gestion des événements techniques ou instrumentaux ainsi que la formation de l’équipe.</p><p><strong>Missions principales :</strong></p><ul><li>Réaliser les analyses de routine et hors routine selon les méthodes établies (DS/DP&#xa0;; HPLC, ELISA, etc.),</li><li>Maitriser plusieurs techniques de laboratoire et les exécuter avec un minimum d’erreurs, avec une spécialisation possible en chimie ou biologie.</li><li>Comprendre, appliquer et maintenir les normes cGMP liées aux procédures et aux systèmes conformément aux exigences locales, globales et règlementaires.</li><li>Enregistrer et vérifier les résultats des analyses dont leur conformité aux spécifications produits.</li><li>Assurer la traçabilité et l’intégrité des données de toutes les activités réalisées (DI, LIMS, maintenance, actions correctives/préventives)</li><li>Rédiger des procédures de laboratoire avec une guidance minimale.</li><li>Respecter toutes les procédures et politiques EHS, y compris la déclaration des incidents, l’utilisation des EPI, la gestion et l’élimination des déchets, ainsi que tout autre programme applicable aux missions du poste.</li><li>Maintenir le laboratoire assurant un environnement de travail sûr et respectant les exigences réglementaires</li><li>Gérer le suivi des tendances analytiques pour assurer la performance des essais</li><li>Reconnaître et résoudre des problèmes techniques simples à modérément complexes (techniques ou instrumentaux). Rédiger les enquêtes et participer aux investigations de laboratoire</li><li>Suivre les équipements dont la responsabilité a été définie dans l’équipe</li><li>Maintenir ses certifications nécessaires aux tâches assignées et former d’autres membres du personnel de laboratoire à toute technique figurant dans son plan de formation.</li></ul>]]></description><link>http://biotechroles.com/specialiste-controle-qualite-(qc)-(fhx)-abbvie/6a06ef352f1861929d253257</link><guid isPermaLink="true">http://biotechroles.com/specialiste-controle-qualite-(qc)-(fhx)-abbvie/6a06ef352f1861929d253257</guid><pubDate>Fri, 15 May 2026 10:02:29 GMT</pubDate><company>AbbVie</company><location>Martillac, Martillac</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Manufacturing Technician]]></title><description><![CDATA[<p><strong>There are many ways to be a difference maker. Find yours. At AbbVie.</strong></p><p>We are now recruiting&#xa0;<strong>Manufacturing Operator&#xa0;</strong> to join our diverse team in Westport.</p><p><strong>Flexibility around shifts is</strong><strong> <em>essential</em></strong><strong> for these roles as it will include 12hour shift support over weekends.</strong>&#xa0;</p><p>The&#xa0;<strong>Manufacturing Operator&#xa0;</strong>&#xa0;is responsible in providing support to maintain cGMP standards in the Multidose department by performing his duties as per EM100. Ensure that cGMP standards are met in the Multidose department.&#xa0;Attend all department meetings and Tier 1 meetings. Good documentation skills.</p>]]></description><link>http://biotechroles.com/manufacturing-technician-abbvie/6a06ef332f1861929d253256</link><guid isPermaLink="true">http://biotechroles.com/manufacturing-technician-abbvie/6a06ef332f1861929d253256</guid><pubDate>Fri, 15 May 2026 10:02:27 GMT</pubDate><company>AbbVie</company><location>Westport, Westport</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager - Sales Analytics]]></title><description><![CDATA[<p>The&#xa0;<strong>Senior Manager/Head - Sales Analytics</strong>, serves as a strategic analytics partner to field sales leadership. This role is responsible for delivering sub-national insights and performance analytics that drive data-informed decision making, optimize resource allocation, and enhance field force effectiveness. The Head will collaborate closely with Commercial and Marketing teams to ensure alignment on methodologies and a unified view of performance across geographies. This role is critical in translating data into actionable strategies that enable sales teams to execute with precision and maximize impact in the field.&#xa0;This position will report to the Head – Commercial Excellence and will be based in Bangalore.</p><p><strong><u>Main Responsibilities:</u></strong></p><ul><li><strong>Strategic partner to Field Sales leadership</strong>&#xa0;within a designated Therapeutic Area, supporting territory- and region-level planning, opportunity analysis, performance reviews, resource optimization, and new indication launches with actionable, sub-national analytics.</li><li><strong>Single point of contact for Customer Facing Capabilities for the Field</strong> – Triage and manage multiple questions around Field Effectiveness</li><li><strong>Develop, track, and refine KPIs</strong>&#xa0;that measure field sales execution and effectiveness, ensuring alignment with national brand strategy supporting marketing teams.</li><li><strong>Co-Lead the creation and delivery of sub-national performance insights</strong>, translating data into strategic recommendations that inform field resource allocation, incentive design, pull-through strategies, and performance optimization.</li><li><strong>Co-lead ad-hoc and recurring sub-national analyses</strong>, identifying trends and opportunities across geographies and customer segments using metrics such as call activity, HCP engagement, territory coverage, and pull-through effectiveness.</li><li><strong>Develop and manage field-facing dashboards and reporting tools</strong>&#xa0;that synthesize key sales metrics and enable real-time decision-making for field leaders and senior commercial stakeholders.</li><li><strong>Liaise with external vendors and internal partners</strong>&#xa0;to ensure delivery of high-quality, timely sub-national Sales Force Effectiveness (SFE) reports that are fit-for-purpose and actionable.</li><li><strong>Co-lead and Field Collaborate in the design and measurement of field tactics</strong>, including targeting effectiveness, sales cadence, pull-through initiatives, and deployment optimization strategies.</li><li><strong>Ensure data integrity and reliability</strong>&#xa0;by working closely with data governance and commercial data management teams to validate sources, define metrics, and troubleshoot inconsistencies.</li><li><strong>Mentor junior analysts or matrixed team members</strong>&#xa0;by sharing therapeutic-area-specific knowledge, analytics best practices, and business acumen to drive team effectiveness and career growth.</li></ul>]]></description><link>http://biotechroles.com/senior-manager-sales-analytics-abbvie/6a06ef322f1861929d253255</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-sales-analytics-abbvie/6a06ef322f1861929d253255</guid><pubDate>Fri, 15 May 2026 10:02:26 GMT</pubDate><company>AbbVie</company><location>Bengaluru, Bangalore</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Payroll Specialist, Belgian Market]]></title><description><![CDATA[<p>Remote working is an option and could be considered for candidates - non-locals.</p><p><strong>The role purpose:</strong></p><p>Payroll Specialist is responsible for processing and correcting payroll transactions for specific countries as assigned (generally larger, more complex countries). The activities include supporting pre-payroll activities time and absence processes, reviewing and verifying files generated internally for monthly payroll run, enforcing key payroll deadlines, as well as answering employee/manager/HR queries and year-end payroll activities. This position requires both payroll experience and expertise to be able to deal with complex issues and escalations and act as SME for both internal and external stakeholders.</p><p><strong>Responsibilities:</strong></p><p>• Partner with internal stakeholders and with Payroll Vendor to process payroll and resolve payroll transactions that are in error.</p><p>• Review and validate payroll files (eg. Payroll Reconciliation File, Bank File) and reports generated internally or by the GPV and approve for processing.</p><p>• Lead pre-payroll activities (eg. finalize data entry, review master data file quality, and confirm time/payroll data completeness).</p><p>• T&amp;A process support.</p><p>• Handle input errors (and other errors) from the third-party vendors or internal AbbVie stakeholders and drive it to the resolution. Plan and lead improvements based on root causes identified.</p><p>• Take care of resolving bank errors (with AbbVie Treasury’s support), coordinate communication with stakeholders and implement preventive actions.</p><p>• Manage Year-End Payroll processing activities (eg. develop and provide payroll calendar, review year-end tax reports and notify AbbVie employees of availability of tax information).</p><p>• Respond to internal AbbVie stakeholders (Tax, Treasury, Finance and BHR) with regards to questions or issues they have raised around payroll data and/or payroll reports.</p><p>• Lead smaller global, regional and country specific projects and participate on global project teams.</p><p>• Some travel may be required.</p>]]></description><link>http://biotechroles.com/payroll-specialist-belgian-market-abbvie/6a06ef302f1861929d253254</link><guid isPermaLink="true">http://biotechroles.com/payroll-specialist-belgian-market-abbvie/6a06ef302f1861929d253254</guid><pubDate>Fri, 15 May 2026 10:02:24 GMT</pubDate><company>AbbVie</company><location>Kraków, Krakow</location><salary>$35000-50000</salary><type>Full-time</type></item><item><title><![CDATA[Customer Operations & Logistics Analyst – Medical Device (1 Year Temporary Contract)]]></title><description><![CDATA[<ul><li>Gestione dei resi delle pompe Vyafuser e Cadd Legacy</li><li>Evasione giornaliera ordini Duodopa intradigiunale e vaporizzatori con attività di affidamento, per la consegna, a DHL</li><li>Gestione spedizioni pompe reclamate ai siti di investigazione</li><li>Gestione vaporizzatori per riparazione a aziende esterne quando necessari con compilazione documenti come per pompe.</li><li>Ricezione vaporizzatori, pompe 951 e intradigiunali e loro collocazione in magazzino</li><li>Preparazione device (vapor, 951 e Duo) da spedire in riparazione</li><li>Assicurare aggiornamenti delle movimentazioni con le relative transazioni in SAP</li><li>Controllo e spunta dei nuovi prodotti quando ricevuti e carico a sistema</li><li>Gestione del magazzino e del magazzino elettronico</li><li>Aggiornamento dati dispositivi in DT+ e relative transazioni</li><li>Drenaggio Vaporizzatori</li><li>Gestire i resi dei vaporizzatori, le calibrazioni scadute, contratti scaduti</li><li>Gestire lo smaltimento dei dispositivi obsoleti e relativa distruzione</li><li>Supportare il manager nella conta fisica annuale presso Campoverde per la parte accessori</li><li>Inspection Test sui dispositivi ricevuti</li><li>Aggiornamento DT+ Vaporizzatori</li></ul>]]></description><link>http://biotechroles.com/customer-operations-and-logistics-analyst-medical-device-(1-year-temporary-contract)-abbvie/6a06ef2e2f1861929d253253</link><guid isPermaLink="true">http://biotechroles.com/customer-operations-and-logistics-analyst-medical-device-(1-year-temporary-contract)-abbvie/6a06ef2e2f1861929d253253</guid><pubDate>Fri, 15 May 2026 10:02:22 GMT</pubDate><company>AbbVie</company><location>Campoverde, Campoverde di Aprilia</location><salary>$28000-38000</salary><type>Full-time</type></item><item><title><![CDATA[Intern - Estagiário (a)]]></title><description><![CDATA[<p><strong>Cargo: Estagiário(a) de Tecnologia Farmacêutica</strong></p><p>&#xa0;</p><p>Descrição do Cargo e principais atribuições: Dar suporte à área de Tecnologia Farmacêutica executando atividades relacionadas a validação de processos, qualificação de equipamentos, validação de sistemas computadorizados, abrangendo elaboração de documentos e acompanhamento prático, a fim de garantir a qualidade dos produtos e a robustez dos processos atendendo aos padrões e normas de boas práticas de fabricação nacionais e internacionais.</p><p>Principais atividades relacionadas</p><p>· Elaboração de protocolos e relatórios</p><p>· Execução de validações e qualificações in loco</p><p>· Vivência da rotina do plano de qualificação e validação da fábrica</p><p>· Vivência da rotina de operações de uma indústria farmacêutica multinacional</p><p>· Suporte na organização de documentos para auditorias nacionais e internacionais</p>]]></description><link>http://biotechroles.com/intern-estagiario-(a)-abbvie/6a06ef2c2f1861929d253252</link><guid isPermaLink="true">http://biotechroles.com/intern-estagiario-(a)-abbvie/6a06ef2c2f1861929d253252</guid><pubDate>Fri, 15 May 2026 10:02:20 GMT</pubDate><company>AbbVie</company><location>Guarulhos, Guarulhos</location><salary>$1000-2000</salary><type>Part-time</type></item><item><title><![CDATA[Associate Director, Product Quality]]></title><description><![CDATA[<p>Responsible for quality of assigned products which may include small molecule pharmaceuticals and/or biologics products, combination products, and medical devices to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by AbbVie plants or by third-party manufacturers, In Licensing relationships, or Co-Marketing relationships. Acts as the primary quality representative for the global supply chain pertaining to external manufacturing business relationships and builds and maintains relationships with TPM Operations, Supplier Quality Management, TPM Business Alliance, Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs, R&amp;D, and S&amp;T to ensure alignment on strategic in</p><p>Responsibilities</p><ul><li>Lead a team of Quality professionals for product transfer activities and direct cross-functional team members to achieve on-time quality deliverables, high customer value, and profitable results. Ensures delivery of all quality elements needed to facilitate new product launches including Third Party Manufacturer’s that provide products directly to distribution centres, or to AbbVie domestic and International plants for further packaging and/or testing. Primary driver for the quality and complian</li><li>Develops Global Product Quality Assurance strategy and implements agreed strategy to support pharmaceuticals, biologics, device and combination products produced at AbbVie plants as well as third party manufacturing (TPM) facilities.</li><li>Primary Quality contact between third party manufacturers, R&amp;D and AbbVie Operations in support of commercial operations, New Product Introductions and product transfers. Supports the regulatory filings and marketing authorization dossiers by developing and/or reviewing of chemistry, manufacturing and controls documents and Drug Master files/Certificate if suitability of monographs of the Ph. Eur. Documents. Lead QA contact with AbbVie Affiliates and Regulatory to prepare submissions and partic</li><li>Makes key decisions on product quality, compliance and regulatory conformance issues for sterile, biological, liquid, solids, and/or device products and elevates medium and high risk events to AbbVie management. Leads the collection, verification and improvement of Quality metrics used for management review in partnership with senior leadership to develop a clear picture of overall compliance state and linking this to local / global project implementation.</li><li>Leads product quality team to support development of the legal supply agreements, contractors or letters of intent to ensure that the appropriate quality, compliance and regulatory aspects are met for the products and services covered and manage the organisation’s actions within the legal boundaries of these documents. Ensures alignment of Quality and Technical Agreements with the legal contracts and that the commitments of the quality and technical agreements are being fulfilled. Helps facilita</li><li>Establishes and maintains relationships and open communication with Third Party Manufacturers, AbbVie plants, affiliates and other functional groups to maintain roles and responsibilities, identify potential projects and issues, obtain an in-depth understanding of the quality, compliance, and resource needs at each site and provide guidance on quality concerns. Supports the management of exception documents and CAPA.</li><li>Communicates and negotiates with external companies’ quality organization to maintain a consistent level of quality and a level of expectation that will minimize compliance risks but also balance the cost of operating to provide AbbVie with the agreed service. Prioritizes programs, initiatives, and problem solving with consideration for impact to timelines, resources and conflicting priorities.</li><li>Manages team interfaces with Quality Assurance audit team to develop audit plans, due diligence plans, and inspection readiness plans, review audit observations and responses, and maintain corrective action timetable. Provides support for quality audits, initial site approvals and due diligence activities. Leads and manages pre-approval inspection readiness as related to the third party manufacturers to ensure regulatory approvals are obtained, with no delays to market entries.</li><li>Core team member or lead of strategic programs; including Brand Teams, New Product Introductions, Product Transfers, Global Strategic Sourcing, Due Diligence, Site Selection, and Approvals and Continuous Improvement. Provides support and interfaces directly/indirectly with the FDA, EMA, MHRA, ANVISA, MoH, etc. for pre-approval inspections.</li><li>Responsible for the strategic leadership of one or more division level quality systems to include SOP Development, Maintenance and Training. Develops, and/or implements the systems across AbbVie operations to assure consistent, high quality products and compliance with worldwide regulatory requirements. Develops new and improved Quality systems within Operations. Influences the decision making process to ensure quality requirements are included when improvement initiatives take place.</li></ul>]]></description><link>http://biotechroles.com/associate-director-product-quality-abbvie/6a06ef2a2f1861929d253251</link><guid isPermaLink="true">http://biotechroles.com/associate-director-product-quality-abbvie/6a06ef2a2f1861929d253251</guid><pubDate>Fri, 15 May 2026 10:02:18 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Parkinson's - Oakland, CA]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.<br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-parkinson&apos;s-oakland-ca-abbvie/6a06ef292f1861929d253250</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-parkinson&apos;s-oakland-ca-abbvie/6a06ef292f1861929d253250</guid><pubDate>Fri, 15 May 2026 10:02:17 GMT</pubDate><company>AbbVie</company><location>Oakland, US-Virtual Office</location><salary>$95000-140000</salary><type>Full-time</type></item><item><title><![CDATA[Sales Data Analyst]]></title><description><![CDATA[<p>We are looking for&#xa0;a skilled Sales Data Analyst to join our&#xa0;Business Excellence team&#xa0;where we cover our&#xa0;Central Southern Eastern Europe&#xa0;(CSEE)&#xa0;organisation, with 9 countries in scope.&#xa0;</p><p>In this&#xa0;position,&#xa0;you will report to&#xa0;CSEE&#xa0;Business Excellence&#xa0;(BE)&#xa0;Manager.&#xa0;&#xa0;</p><p>The Sales Data Analyst is responsible for&#xa0;high-level analysis&#xa0;of the&#xa0;reports and&#xa0;sales figures&#xa0;provided by our distribution partners&#xa0;located&#xa0;in&#xa0;different&#xa0;markets where&#xa0;our&#xa0;products are sold.&#xa0;&#xa0;Ultimately,&#xa0;your&#xa0;role is to provide&#xa0;relevant and useful&#xa0;insights&#xa0;regarding&#xa0;our products&#xa0;and&#xa0;customers’ performance, as well as&#xa0;to support our commercial&#xa0;organisation&#xa0;by highlighting business opportunities.&#xa0;This role is highly involved in tracking our&#xa0;Sales Force Effectiveness KPIs&#xa0;and providing solutions to reach our business priorities.&#xa0;You are therefore&#xa0;a&#xa0;key&#xa0;partner&#xa0;and work closely with&#xa0;the sales managers in each country&#xa0;as well as the in-field teams.&#xa0;</p><p><strong>Some of your responsibilities&#xa0;include:&#xa0;</strong></p><p>Master Data Management</p><ul><li>Maintain master database such as customer profile, territory, employee, and target information and continuously seek ways for enhancement&#xa0;</li><li>Conduct routine customer data matching and mapping validation&#xa0;</li><li>Routinely&#xa0;monitor&#xa0;data accuracy and system usage&#xa0;</li></ul><p>Engagement</p><ul><li>Regularly work&#xa0;with commercial and sales team to improve data collection, validation, and reporting process to drive both speed and&#xa0;accurate&#xa0;delivery&#xa0;</li><li>Work with BE Manager to process quarterly territory and&#xa0;healthcare professional (HCP)&#xa0;target group setting information in the system&#xa0;</li><li>Track KPIs related to Sales Force&#xa0;Effectiveness&#xa0;&#xa0;</li><li>Super user of BI and CRM able to answer queries and questions&#xa0;regarding&#xa0;system use&#xa0;</li><li>Be point of contact and expert on Veeva/BI for the other BE Managers and Veeva/SOA.&#xa0;</li></ul><p>Customer Segmentation/Profiling</p><ul><li>Customer Profiling Management for CRM. Ensuring data is collected to allow segmentation and targeting strategies&#xa0;to be&#xa0;implemented.&#xa0;</li><li>Track sales force performance&#xa0;</li></ul>]]></description><link>http://biotechroles.com/sales-data-analyst-abbvie/6a06ef272f1861929d25324d</link><guid isPermaLink="true">http://biotechroles.com/sales-data-analyst-abbvie/6a06ef272f1861929d25324d</guid><pubDate>Fri, 15 May 2026 10:02:15 GMT</pubDate><company>AbbVie</company><location>Bucharest, Praha 5, Stodůlky</location><salary>$45000-65000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - Idaho Falls, ID]]></title><description><![CDATA[<p><strong><em>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.</em></strong><br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-idaho-falls-id-abbvie/6a06ef252f1861929d25324c</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-idaho-falls-id-abbvie/6a06ef252f1861929d25324c</guid><pubDate>Fri, 15 May 2026 10:02:13 GMT</pubDate><company>AbbVie</company><location>Idaho Falls, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Allergan Aesthetics Clinical Specialist]]></title><description><![CDATA[<p>Role Summary</p><p>The Clinical Specialist will play a key role in supporting the delivery of Allergan Aesthetics’ AMI educational strategy across Ireland. This field-based role is focused on providing in-clinic educational support, developing tailored facilitation pathways for healthcare professionals, and supporting the delivery of affiliate-level AMI events and digital education initiatives.</p><p>The role is primarily educational and facilitative in nature, supporting HCP development through a bespoke, hands-off approach that respects clinical autonomy while helping to improve knowledge, confidence, and patient outcomes. The Clinical Specialist will work closely with beginner and intermediate HCPs, supporting them through structured educational journeys aligned to the AMI Infinity curriculum.</p><p>Key Responsibilities</p><p>1. Deliver In-Clinic Services (70%)</p><ul><li>Identify educational needs and develop recommendations to enhance clinical practice within aesthetic clinics.</li><li>Deliver bespoke educational journeys for HCPs enrolled on a Facilitation Pathway, based on self-assessment of knowledge, skills, and confidence.</li><li>Establish and maintain tailored AMI Infinity curriculum-aligned Facilitation Pathways with HCPs to support improved patient outcomes.</li><li>Deliver facilitation in a hands-off manner, ensuring the HCP retains full clinical judgement and responsibility for patient treatment.</li><li>Support primarily beginner and intermediate HCPs through structured, high-quality clinical education.</li><li>Maintain a high standard of service through timely and reliable follow-up after each HCP interaction.</li><li>Record all activity accurately in Veeva CRM to support KPI monitoring, reporting, and business insights.</li></ul><p>2. Support Education via AMI Digital World (15%)</p><ul><li>Guide HCPs through the AMI Digital World educational pathway as a core part of the Facilitation Pathway.</li><li>Use AMI Digital World to support the development of clinical knowledge and confidence around Allergan Aesthetics products and treatment approaches.</li><li>Ensure digital education is integrated appropriately to meet the needs of beginner injectors, while also providing value to more experienced HCPs where relevant.</li><li>Reinforce learning through ongoing education and follow-up, ensuring a seamless and supportive learner experience.</li></ul><p>3. Support the AMI Lead in Event Delivery (15%)</p><ul><li>Support the delivery of affiliate-level AMI events as requested by the AMI Lead.</li><li>Attend industry conferences, AMI meetings, workshops, and the MD Codes™ Mentee Program to engage with customers and support educational excellence.</li><li>Contribute to personal development and upskilling through participation in events and workshops.</li><li>Where clinically qualified and appropriately insured, assist faculty during live technical workshops as required.</li><li>Support the overall delivery of high-quality educational experiences that reflect the standards of Allergan Aesthetics.</li></ul>]]></description><link>http://biotechroles.com/allergan-aesthetics-clinical-specialist-abbvie/6a06ef232f1861929d25324b</link><guid isPermaLink="true">http://biotechroles.com/allergan-aesthetics-clinical-specialist-abbvie/6a06ef232f1861929d25324b</guid><pubDate>Fri, 15 May 2026 10:02:11 GMT</pubDate><company>AbbVie</company><location>Dublin, Dublin</location><salary>$65000-90000</salary><type>Full-time</type></item><item><title><![CDATA[Intern Talent Acquisition]]></title><description><![CDATA[<ul><li>Gestionarás y darás seguimiento al Programa de Becas, participando en el <strong>proceso de selección y siendo el punto de contacto </strong>con todos los becarios de la compañía y sus tutores.</li><li>Colaborarás en la <strong>creación, modificación y gestión de los materiales de Employer Branding</strong>.</li><li>Organizarás <strong>Mesas Redondas</strong> entre los <strong>becarios</strong> de los diferentes departamentos.</li><li>Coordinarás el <strong>Onboarding de los nuevos becarios.</strong></li><li>Revisarás y gestionarás <strong>los convenios</strong> con escuelas y universidades.</li><li>Gestionarás altas y bajas en la <strong>Seguridad Social </strong>de los becarios</li><li>Captación y contacto de posibles candidatos por <strong>Linkedin.</strong></li><li>Participaciparás en el <strong>plan táctico de RRHH</strong>.</li><li>Darás apoyo en la <strong>herramienta de Selección</strong> (SR).</li><li>Colaborarás en los <strong>diferentes proyectos de Talent Acquisition, así como otras áreas del departamento de RRHH</strong></li></ul>]]></description><link>http://biotechroles.com/intern-talent-acquisition-abbvie/6a06ef212f1861929d25324a</link><guid isPermaLink="true">http://biotechroles.com/intern-talent-acquisition-abbvie/6a06ef212f1861929d25324a</guid><pubDate>Fri, 15 May 2026 10:02:09 GMT</pubDate><company>AbbVie</company><location>Madrid, Madrid</location><salary>$15000-22000</salary><type>Full-time</type></item><item><title><![CDATA[Business Development Manager (Facial Aesthetics)]]></title><description><![CDATA[<p>Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma.&#xa0;Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world.</p><p>Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective&#xa0;therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around the world live longer, healthier lives every day.</p><p>Allergan is a company that will inspire you to aim high with your ambition. Where you can build bridges all over the world. Where you can power ideas that drive change. And where you will act fast and drive results for customers and patients. &#xa0;Power your future &amp;&#xa0;join our bold team.</p><p><strong>Position Overview:</strong></p><p>This is Territory Sales role working towards a sales quota with a robust sales incentive plan.&#xa0;</p><p>Business Development Manager represents the Facial Aesthetics product portfolio to targeted aesthetic customers within a designated geographical area. Responsible for creating product acceptance and enhancing portfolio growth through business development activities. The BDM provides technical product and procedure expertise as well as competitive product differentiation. Assigned sales goals are obtained through creative, consultative selling and implementation of the U.S. Sales/Marketing plan.&#xa0;The company offers flexible career paths with a strong emphasis on opportunity for internal mobility.</p><p><strong><em>Main Areas of Responsibilities</em></strong></p><p>The Business Development Manager (BDM) leverages Allergan Medical resources to enhance adoption of the Facial Aesthetics Portfolio.&#xa0;Synergistically works and coordinates activities with other Allergan sales personnel and support teams (include, but are not limited to, facial aesthetics, breast aesthetic, APCs, neurology, topical aesthetics, medical dermatology, marketing, and other Allergan sales forces).&#xa0;Complies with required reports, requests, and compliance policies.&#xa0;Effectively manages field assets and resources to include, but not limited to, expense management, computer and other allocated equipment.</p><ul></ul><p>#LI-AL1</p>]]></description><link>http://biotechroles.com/business-development-manager-(facial-aesthetics)-abbvie/6a06ef202f1861929d253247</link><guid isPermaLink="true">http://biotechroles.com/business-development-manager-(facial-aesthetics)-abbvie/6a06ef202f1861929d253247</guid><pubDate>Fri, 15 May 2026 10:02:08 GMT</pubDate><company>AbbVie</company><location>Bentonville, US-Virtual Office</location><salary>$95000-140000</salary><type>Full-time</type></item><item><title><![CDATA[Site Management Lead]]></title><description><![CDATA[<p>The SML provides direction and operational expertise for all Clinical Site Management (CSM) integrity, quality, and timeliness of activities in assigned studies. The position can be assigned to serve as the overall CSM functional study strategy leader and/or can be assigned to manage area site execution activities in collaboration with other assigned SMLs dependent on size, complexity, and geographic scope of assigned studies.<br>
Influences and aligns within Clinical Development Operations, with other assigned Site Management leaders, and key stakeholders in assigned studies. If assigned as the study strategy leader, is a key member of the Clinical Study Team representing CSM globally from study planning to close out. If assigned to area site execution activities, responsible and accountable for directing site monitors in a matrix environment and serve as a liaison and primary contact between site monitors, the study strategy leader, and the Clinical Study Team.</p><p>Responsibilities</p><ul><li>Accountable for driving study level global and/or area level CSM deliverables by targeted timelines with allocated resources for their assigned studies.</li><li>Analyze study timelines and overall study assumptions to confirm deliverables are feasible for CSM.<br>
Support and communicate CSM resource needs with Country Leaders in alignment with study deliverables and milestones.<br>
Accountable for study level site monitoring strategy, documented in Site Monitoring Plan.<br>
Accountable to set and lead Site Engagement Strategy.</li><li>Ensure study-level and/or area-level timelines are maintained across the study lifecycle.<br>
Provide timely and essential study information for country-level teams to execute milestones.<br>
Drive site-level activities at study level and/or area level, including site selection, activation, site engagement, protocol adherence and close out.</li><li>Oversee monitoring activities at study and/or area level in collaboration with other assigned SMLs as applicable, ensuring quality deliverables, status tracking, and milestone adherence and acceleration if applicable.<br>
Drives CSM deliverables during data snapshots and database locks, aligned to Data Cleaning Plan.<br>
Ensure sites are closed per Site Closure Plan.</li><li>Proactively identify, evaluate, and mitigate risks, ensuring effective action plans; key contributor to Risk Assessment and Mitigation Plan (RAMP).<br>
&#xa0;</li><li>Collaborate with other assigned SMLs and stakeholders in the Clinical Study Team to address and manage risks to align with overall study execution.<br>
Ensure site compliance, escalate issues, and analyze trends for continuous improvement.</li><li>Responsible for providing inputs on expected CSM documents at the study level and driving TMF completeness for CSM artifacts</li><li>Responsible from study start to close for ensuring that on-going CSM Inspection Readiness activities are completed at the study level</li></ul>]]></description><link>http://biotechroles.com/site-management-lead-abbvie/6a06ef1e2f1861929d253246</link><guid isPermaLink="true">http://biotechroles.com/site-management-lead-abbvie/6a06ef1e2f1861929d253246</guid><pubDate>Fri, 15 May 2026 10:02:06 GMT</pubDate><company>AbbVie</company><location>Irvine, North Chicago</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Gerente Comercial & Marketing Oncologia Sólidos (Pulmão)]]></title><description><![CDATA[<p><strong>Seu papel será:</strong></p><p>Responsável por liderar a estratégia integrada de marca, a execução em campo e as iniciativas comerciais e de marketing, assegurando o alcance dos resultados de negócio, o fortalecimento da marca e a geração de valor para pacientes, clientes e stakeholders. Esta é uma posição que alia o Marketing à Gestão do time de Demanda.</p><p>&#xa0;</p><p><strong>Você será responsável por:</strong></p><ul><li>Liderar a construção, adaptação e implementação do plano estratégico e tático da marca, garantindo alinhamento com as diretrizes globais e a realidade do mercado local.</li><li>Traduzir prioridades estratégicas em planos de ação claros para equipes de campo, marketing e demais áreas envolvidas.</li><li>Conduzir análises de mercado, concorrência, tendências, comportamento de stakeholders e oportunidades de crescimento, identificando riscos e oportunidades de negócio.</li><li>Monitorar e analisar KPIs, market share, demanda, produtividade e performance de execução, propondo planos de ação corretivos quando necessário.</li><li>Elaborar, acompanhar e revisar forecast, budget e ROI das iniciativas sob sua responsabilidade, assegurando eficiência na alocação de recursos.</li><li>Liderar o lançamento de um novo produto em câncer de pulmão, incluindo preparação estratégica, integração cross-functional e suporte à execução em campo.</li><li>Garantir a execução coordenada das iniciativas com áreas multifuncionais, incluindo Força de Vendas (sob sua gestão), Acesso, Medical Affairs, Regulatório, Treinamento, Finanças e demais parceiros internos.</li><li>Liderar e desenvolver uma equipe de 3 posições de campo por meio de coaching, feedback, acompanhamento de performance e construção de planos de desenvolvimento individual.</li><li>Representar a marca em reuniões estratégicas, congressos, eventos médicos e fóruns com stakeholders internos e externos.</li><li>Garantir a conformidade com políticas internas, normas de ética, compliance e regulamentações aplicáveis à indústria farmacêutica.</li><li>Estar disponível para viagens frequentes em território nacional, conforme necessidade do negócio.</li></ul><p>&#xa0;</p><p>&#xa0;</p><ul></ul>]]></description><link>http://biotechroles.com/gerente-comercial-and-marketing-oncologia-solidos-(pulmao)-abbvie/6a06ef1c2f1861929d253245</link><guid isPermaLink="true">http://biotechroles.com/gerente-comercial-and-marketing-oncologia-solidos-(pulmao)-abbvie/6a06ef1c2f1861929d253245</guid><pubDate>Fri, 15 May 2026 10:02:04 GMT</pubDate><company>AbbVie</company><location>Sao Paulo, Sao Paulo</location><salary>$85000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Customer Solutions Specialist - Orlando, FL]]></title><description><![CDATA[<p><strong>This role is field-based, and candidates should live within a reasonable distance from the primary city.</strong></p><p>&#xa0;</p><p><u>Candidates may live in the following cities:</u></p><ul><li>Orlando, FL</li><li>North Tampa, FL</li></ul><p>&#xa0;</p><p>The Customer Solutions Specialist (CSS) is a key member of the Access and Reimbursement team within AbbVie Patient Services. The CSS calls on HCP offices in their assigned territory to represent and serve as a subject matter expert on AbbVie’s in-office portals and access related solutions. The CSS also partners closely with other AbbVie field stakeholders to offer the right solutions to offices that create the best possible patient prescription experience possible.</p><p><strong>Responsibilities:</strong></p><ul><li>Understand HCP office process and offer electronic solutions (i.e. portals) that will improve the patient Rx experience.</li><li>Thoroughly understand and represent AbbVie’s HCP facing portals and other electronic solutions serving as a subject matter expert.</li><li>Partner with AbbVie field teams to implement and offer solutions to HCPs in assigned territory. Working with an HCP office, evaluate and diagnose areas of delay and disruption that may occur for patients in their Rx experience to determine if an AbbVie digital solution may be helpful for the patient.</li><li>Develop relationship with HCP offices using a portal/solution and provide regular updates on new functionality matching new or unused features with patient needs.</li><li>Communicate with AbbVie field teams in a compliant manner.</li></ul>]]></description><link>http://biotechroles.com/customer-solutions-specialist-orlando-fl-abbvie/6a06ef192f1861929d253244</link><guid isPermaLink="true">http://biotechroles.com/customer-solutions-specialist-orlando-fl-abbvie/6a06ef192f1861929d253244</guid><pubDate>Fri, 15 May 2026 10:02:01 GMT</pubDate><company>AbbVie</company><location>Orlando, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, Business Analytics]]></title><description><![CDATA[<p><strong>Purpose</strong><br>
The Manager, Business/Data Analytics, is responsible for being a hands-on data and business analyst, working with and eventually managing the data analyst within the AbbVie Complete Access function. This role is tasked with enhancing the team's capabilities in data storytelling, business alignment, and insights delivery. Additionally, the role ensures that business operations are synchronized with data-driven processes and business objectives.</p><p><strong>Responsibilities</strong></p><ul><li>Manages a team of Data Analysts, including selecting and hiring, guiding performance expectations, and developing staff by coaching and elevating the team to enhance analytical skills that drive business goals.</li><li>Collaborates cross-functionally with business partners and internal teams to drive meaningful, data-driven business outcomes and insights.</li><li>Drives the overall development and implementation of the organization using advanced data analytics techniques to set PM goals and optimize data-driven projects, ensuring accurate and insightful reporting of activities and outcomes.</li><li>Leads projects centered around complex data models, ensuring comprehensive reporting of activities and outcomes using predictive analytics by translating complex data into clear, actionable business insights.</li><li>Directs data-related investigations by employing analytical frameworks to validate data by designing and building dashboards, visualizations, and reports to support strategy and operations.</li><li>Provides oversight for accuracy and quality assurance, leveraging data mining techniques to identify improvements and address emerging data trends.</li><li>Oversees the management of reporting systems and performance metrics, utilizing sophisticated analytics tools to track Key Performance Indicators (KPIs) and extract actionable insights to drive operational improvements.</li><li>Develops and supports other functional analytics-driven initiatives, programs, and systems that enhance operational efficiency and data utilization.</li><li>Acts as a mentor and quality reviewer for Data Analysts, responsible for selecting and hiring, guiding them with performance expectations, and developing staff by coaching and elevating the team to enhance analytical skills that drive business goals.</li></ul>]]></description><link>http://biotechroles.com/manager-business-analytics-abbvie/6a06ef182f1861929d253243</link><guid isPermaLink="true">http://biotechroles.com/manager-business-analytics-abbvie/6a06ef182f1861929d253243</guid><pubDate>Fri, 15 May 2026 10:02:00 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist I/Senior Scientist II - Preclinical Primate Immunology]]></title><description><![CDATA[<p>AbbVie’s Immunology Discovery Research group is&#xa0;seeking&#xa0;a highly motivated and experienced in vivo and in vitro&#xa0;cellular&#xa0;immunologist&#xa0;to&#xa0;lead&#xa0;development of pharmacodynamic endpoints in&#xa0;non-human primate&#xa0;(NHP)&#xa0;preclinical pharmacology studies. This position offers an opportunity to&#xa0;test&#xa0;and&#xa0;preclinically&#xa0;validate&#xa0;mechanistic and translationally&#xa0;relevant endpoints to support experimental medicine studies as well as&#xa0;gain an&#xa0;understanding&#xa0;of drug MOAs.&#xa0;You will&#xa0;be exposed to&#xa0;AbbVie’s diverse immunology pipeline, and you&#xa0;will have&#xa0;the ability to influence&#xa0;the&#xa0;development&#xa0;strategy&#xa0;of&#xa0;high value programs.&#xa0;&#xa0;&#xa0;&#xa0;</p><p>The candidate&#xa0;will&#xa0;work within an existing, highly&#xa0;matrixed&#xa0;and collaborative team to deliver rigorous and detailed data packages from in vivo pharmacology studies in non-human primates, including ex vivo endpoints.&#xa0;As a Senior&#xa0;II&#xa0;Scientist you will&#xa0;directly&#xa0;conduct benchwork, design in vivo studies,&#xa0;expand upon existing&#xa0;partnerships,&#xa0;and serve as a subject matter expert for non-human primate immunology&#xa0;studies&#xa0;across the R&amp;D organization.&#xa0;You&#xa0;will&#xa0;ultimately&#xa0;be&#xa0;responsible for&#xa0;both&#xa0;identifying&#xa0;innovative, yet&#xa0;feasible&#xa0;opportunities to&#xa0;impact&#xa0;the Immunology&#xa0;portfolio using NHP models&#xa0;and&#xa0;developing&#xa0;a highly functioning team focused on NHP&#xa0;pharmacology.&#xa0;&#xa0;</p><p>Key&#xa0;responsibilities:&#xa0;&#xa0;</p><ul><li><p>Leverage&#xa0;deep&#xa0;non-human primate immunology&#xa0;expertise&#xa0;and current literature&#xa0;to&#xa0;advise&#xa0;project teams&#xa0;</p></li></ul><ul><li><p>Communicate&#xa0;and coordinate&#xa0;study&#xa0;logistics&#xa0;within the existing team and across other stakeholders in Discovery&#xa0;Immunology.&#xa0;</p></li></ul><ul><li><p>Coordinate&#xa0;with&#xa0;the team&#xa0;colony and study coordinator&#xa0;and supervisor&#xa0;regarding&#xa0;budget and colony maintenance&#xa0;whole&#xa0;maintaining&#xa0;a&#xa0;high level&#xa0;of productivity&#xa0;</p></li></ul><ul><li><p>Mentor and coach&#xa0;others&#xa0;while driving innovative science from the bench.&#xa0;</p></li></ul><ul><li><p>Co-develop fit-for-purpose models to address specific program&#xa0;questions&#xa0;through networking with project relevant leads in&#xa0;the global organization.&#xa0;</p></li></ul><ul><li><p>Directly develop&#xa0;translational immune-profiling assays.&#xa0;</p></li></ul><ul><li><p>Establish&#xa0;translational rationale for&#xa0;utilizing&#xa0;primate&#xa0;models.&#xa0;</p></li></ul><ul><li><p>Establish a&#xa0;tissue repository for rapid test article screening.&#xa0;</p></li></ul><ul><li><p>Present results&#xa0;at&#xa0;project&#xa0;team&#xa0;meetings&#xa0;and internal/external science meetings.&#xa0;</p></li></ul>]]></description><link>http://biotechroles.com/principal-scientist-isenior-scientist-ii-preclinical-primate-immunology-abbvie/6a06ef162f1861929d253242</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-isenior-scientist-ii-preclinical-primate-immunology-abbvie/6a06ef162f1861929d253242</guid><pubDate>Fri, 15 May 2026 10:01:58 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$130000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Geopolitical Analyst, Business Risk Intelligence]]></title><description><![CDATA[<p>The Geopolitical Analyst, Business Risk Intelligence (BRI) provides global security intelligence and risk analysis for AbbVie stakeholders, including senior leaders, assessing and analyzing threats to AbbVie’s people, assets, and operations around the world, helping to mitigate risks and to reduce uncertainty in decision making. The Analyst is an expert in advanced methods such as structured analytical techniques. The role involves monitoring and evaluating the changing security environment relating to risk trends and geopolitical developments in different countries and regions around the world. Deliverables include global/regional/country risk assessments, risk trend analyses, situational and topical intelligence reports, forward-looking reporting including scenario forecasts, newsletter articles, security advice, and verbal briefings.</p><p>&#xa0;</p><p><strong>Responsibilities</strong></p><ul><li>Create intelligence reports for audiences including senior company leaders to support decision making and risk mitigation / management. Products include country risk assessments, regional risk trend analyses, BRI newsletter articles, threat assessments, situational and topical reports and presentations, and forward-looking intelligence including scenario analyses.</li><li>Continuously monitor the worldwide security environment, identifying and analyzing risk trends and geopolitical events that could impact AbbVie people, assets, or business continuity.</li><li>Provide subject matter expertise as appropriate in regard to risks posed by geopolitical developments, crime, terrorism, social unrest, armed conflict, epidemics, natural disasters, and other threats.</li><li>Provide decision support for leadership, such as short- and long-term planning strategies and implementation of proactive security recommendations and risk mitigation measures.</li><li>Participate in other BRI projects, including support for Crisis Management &amp; Business Resiliency with both situational reporting and forward-looking intelligence.</li><li>Build and maintain strong working partnerships within Global Security, other AbbVie functions, as well as liaising with external stakeholders such as government intelligence agencies and private-sector benchmarking groups.</li></ul>]]></description><link>http://biotechroles.com/geopolitical-analyst-business-risk-intelligence-abbvie/6a06ef142f1861929d253241</link><guid isPermaLink="true">http://biotechroles.com/geopolitical-analyst-business-risk-intelligence-abbvie/6a06ef142f1861929d253241</guid><pubDate>Fri, 15 May 2026 10:01:56 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$95000-140000</salary><type>Full-time</type></item><item><title><![CDATA[COOP Student (Commercial)]]></title><description><![CDATA[<p>Purpose</p><p>As an AbbVie COOP, the student participates in a paid program that is focused on providing students with robust projects and with the opportunity to work with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. As an Intern/COOP, the student will be located at one of our Operations sites at Barceloneta or at our Commercial Affiliate at San Juan, Puerto Rico. AbbVie’s worldwide business offers an opportunity for a variety of potential work experiences that are aligned to a variety of functional areas, including (but not limited to):<br>
- Manufacturing<br>
- Engineering<br>
- Quality<br>
- Science &amp; Technology<br>
- Central Services – Facilities Engineering<br>
- BTS (Business technology Solutions)<br>
- Commercial Affiliate: Marketing, Medical Affairs, Market Access, Communications, Finance, Ethics and Compliance, etc.</p><p>Responsibilities</p><ul><li>Perform various projects as assigned.</li><li>Participate in social/networking and learning &amp; development activities.</li><li>Willingness to do meaningful work that has a real impact on our business and patients worldwide.</li><li>Present to the staff leaders, managers, and mentors the achievements of the assigned projects as well as the main learnings gained during the program.</li><li>Provide assistance to operations in accordance with environmental management, occupational health and safety (EH&amp;S) systems and promote continuous improvement. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.</li></ul>]]></description><link>http://biotechroles.com/coop-student-(commercial)-abbvie/6a06ef112f1861929d253240</link><guid isPermaLink="true">http://biotechroles.com/coop-student-(commercial)-abbvie/6a06ef112f1861929d253240</guid><pubDate>Fri, 15 May 2026 10:01:53 GMT</pubDate><company>AbbVie</company><location>San Juan, San Juan</location><salary>$2000-4000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Analyst, Finance]]></title><description><![CDATA[<p><strong>Purpose</strong></p><p>The primary objective of this position is to support the reporting and planning for Balance Sheet actuals and forecasts as well as the cross functional processes and planning to ensure timeliness and accuracy of financials. This role will also be responsible for specific P&amp;L actuals reporting and forecasts for budgets such as AbbVie Incentive Plan (AIP), Bad Debt, and IT Project Expense budgeting for Actuals Reporting, Latest Best Estimates (LBEs), annual Plans, and Annual Long-Range Plan (LRP).</p><p><strong>Responsibilities</strong></p><ul><li>Lead the US Tx cross-functional balance sheet processes across actuals and forecasts ensuring a clear calendar, timely reviews, and accurate financials.</li><li>Report and forecast key balance sheet accounts across all cycles (actuals, LBE, LRP, and Plan).</li><li>Provide clear and concise commentary for balance sheet accounts vs. applicable benchmarks.</li><li>Prepare, forecast, analyze, and report on multiple US Tx budgets such as AIP, Bad Debt, and IT Project Expense.</li><li>Collaborate on US Tx capital plans and LRPs ensuring an understanding of projects and impacts to the business and financials.</li><li>Support the US Tx Reporting team on ad hoc requests, data loads, data pulls, and analytics.</li></ul>]]></description><link>http://biotechroles.com/senior-analyst-finance-abbvie/6a06ef0f2f1861929d25323f</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-finance-abbvie/6a06ef0f2f1861929d25323f</guid><pubDate>Fri, 15 May 2026 10:01:51 GMT</pubDate><company>AbbVie</company><location>Mettawa, Mettawa</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Inside Sales Rep I, Pharma]]></title><description><![CDATA[<p>AbbVie’s Austin-based Inside Sales is a professional team of inside sales personnel that supports existing field sales, operational, and marketing initiatives utilizing a set of approved best practices, job aides, and quality metrics to build lasting relationships with Healthcare Practices across the nation.&#xa0;</p><p>Our team is searching for high energy, self-motivated, dynamic individuals wishing to join a team environment that values individual achievement in a quota driven/incentivized role. Candidates must be able to work in a fast-paced environment with a continued focus on utilizing phone and other channels to create, nurture, and expand relationships with healthcare professionals to achieve brand objectives.&#xa0;</p><p>Successful candidates will possess strong verbal communication skills, be highly organized, flexible, self-starter and can articulate value on a consistent basis to foster growth of an expanding customer base by creating positive customer interactions and lasting relationships.&#xa0;</p><p>Core responsibilities include:</p><ul><li>Ability to use inside sales techniques to ensure positive results to a highly targeted, assigned list of healthcare professionals. &#xa0;</li><li>Ability to apply account management skills such as call planning, customer education, reporting and follow-up to maximize territory performance potential.</li><li>Comfortable establishing a commanding and engaging phone presence with an ability to build rapport and engage in clinical/promotional conversations to maintain productive business relationships.</li><li>Manage daily sales call activity to optimize time and maximize the achievement of sales and market share objectives.</li><li>Profile and manage targeted list of healthcare professionals and provide value-added benefits to grow product volume.</li><li>Maintain the required product expertise including competitive product knowledge.</li><li>Demonstrate thorough knowledge of products and ensure clear, concise and accurate communication of product information with target audiences using proper medical terminology.</li><li>Successfully complete product training (self-study, testing, field work and classroom training or virtually) and meet training expectations.</li><li>Demonstrate effectiveness working independently and in a team environment.</li><li>Introduce, establish, grow relationships, and retain an expanding group of healthcare professionals from all levels – including office staff, Medical Assistants, nurses, and doctors.</li><li>Must safeguard patient privacy and confidentiality by following the guidelines set forth in the Privacy and Security Rules of the Health Insurance Portability and Accountability Act (HIPAA)</li></ul><p>&#xa0;</p><ul></ul>]]></description><link>http://biotechroles.com/inside-sales-rep-i-pharma-abbvie/6a06ef0d2f1861929d25323e</link><guid isPermaLink="true">http://biotechroles.com/inside-sales-rep-i-pharma-abbvie/6a06ef0d2f1861929d25323e</guid><pubDate>Fri, 15 May 2026 10:01:49 GMT</pubDate><company>AbbVie</company><location>Austin, Austin</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, Material Review and Promotion]]></title><description><![CDATA[<p>The&#xa0;Manager Material Review, Marketing Operations&#xa0;facilitates&#xa0;the management of&#xa0;Advertising &amp;&#xa0;Promotional materials&#xa0;as they pertain to the U.S.&#xa0;Commercial&#xa0;MRP&#xa0;(Material Review&#xa0;Process).&#xa0;&#xa0;</p><p><strong>The&#xa0;Manager&#xa0;Material Review, Marketing Operations&#xa0;ensures:&#xa0;&#xa0;</strong></p><ul><li>Facilitation of&#xa0;cross-functional team (Medical, Regulatory,&#xa0;Commercial,&#xa0;Legal,&#xa0;Compliance,&#xa0;others) review and approval of:&#xa0;&#xa0;</li><li>Advertising materials&#xa0;</li><li>Promotional materials&#xa0;</li><li>Sales Training materials&#xa0;&#xa0;</li><li>Promotional Labeling materials&#xa0;&#xa0;</li><li>Leads management of cross functional team members and advertising agencies&#xa0;</li><li>Open communication of material status with cross-functional team members and advertising agencies&#xa0;</li><li>Tactical support and project timeline oversight of materials through MRP&#xa0;&#xa0;</li><li>Lead consultant and trainer on the MRP, supporting to all team members responsible for uploading and approving materials&#xa0;</li><li>Timely review of all promotional, non-promotional materials through U.S. Commercial, Medical reviewers, Regulatory reviewers, and other key stakeholders&#xa0;&#xa0;</li></ul><p><strong>Additionally, provides&#xa0;key leadership for:&#xa0;</strong></p><ul><li>Management and development a staff of project managers&#xa0;</li><li>Solutions and contingency plans to facilitate business success&#xa0;</li><li>Holds self and team accountable for results&#xa0;</li><li>Serves as a mentor and coaches others on the MRP&#xa0;&#xa0;</li><li>Proactively provides consulting, expertise and MRP process training to cross-functional team members&#xa0;</li><li>Evaluates and updates processes to adapt to a changing environment and to optimize efficiencies&#xa0;</li><li>Coordinating logistics to ensure timely production,&#xa0;fulfillment&#xa0;and shipment of materials&#xa0;</li><li>Provides Leadership for innovative solutions to project hurdles&#xa0;</li><li>Develops a strong knowledge of customers’ goals and priorities, partners to support those objectives&#xa0;</li></ul><p><strong>Process&#xa0;Management:&#xa0;</strong></p><ul><li>Leads the review process for promotional and non-promotional materials that are routed through the MRP&#xa0;</li><li>Perform “Final Sign-off” on material submissions uploaded into Veeva&#xa0;</li><li>Validate that the metadata / review tier aligns with the submitted materials&#xa0;&#xa0;</li><li>Determine if legal/compliance is required&#xa0;</li><li>Determine if Editorial Quality Check is required&#xa0;</li><li>If additional reviewers are not aligned with the selected review tier, tag additional reviewers and update review tier as necessary&#xa0;</li><li>Ensure sources files are uploaded into the Veeva for production vendors&#xa0;</li><li>Validate all back-end approvals prior to routing material to Regulatory Affairs for Office of Prescription Drug Promotion (OPDP) submission&#xa0;&#xa0;</li><li>Oversee release of approved material for distribution&#xa0;&#xa0;</li><li>When material withdrawal is required, inform inventory vendors&#xa0;</li><li>Initiate production of updated package inserts&#xa0;</li><li>Identify promotional material that needs inventory updates and Initiate inventory update process&#xa0;</li><li>Proactively looks for and leads ways to improve agility by streamlining and simplifying internal processes and drives implementation of process changes&#xa0;</li><li>Strong understanding of Agency and Printer process. Offering guidance and leadership to commercial team members and agencies as it relates to printing processes&#xa0;</li></ul><p><strong>Cross-functional team meetings:</strong></p><ul><li>Project manages&#xa0;a team of&#xa0;10&#xa0;to&#xa0;20&#xa0;cross-functional team members&#xa0;</li><li>Schedule, manage and facilitate formal concept review requests, schedules live review meetings to resolve and discuss reviewer comments (i.e., Tier 1 reviews, Formal Concept Reviews)&#xa0;</li><li>Creates and communicates weekly review team meeting agendas&#xa0;&#xa0;</li><li>Prioritize and schedule any additional live meeting requests (e.g., exceptions, revise &amp; resubmits) as needed&#xa0;&#xa0;</li><li>Schedule and facilitate weekly live prioritization meetings with business owners&#xa0;&#xa0;</li><li>Review dashboard within Veeva to understand upcoming volume of materials being planned for submission&#xa0;&#xa0;</li><li>Act as a neutral facilitator in project discussions, summarizes team agreements and maintains required documentation of discussion outcomes.&#xa0;&#xa0;</li><li>Leads discussion on projects that didn’t go well to identify learnings and improvement opportunities&#xa0;</li><li>Leads team discussion on metrics; evaluates and provides opportunities for improved agility&#xa0;&#xa0;</li><li>Maintain a positive, energetic, and engaged attitude and approach to work under times of stress&#xa0;</li><li>Demonstrates strong good understanding of the brand(s) supported&#xa0;</li></ul><p><strong>Communication:</strong></p><ul><li>Attend brand and tactical planning meetings to understand upcoming workload&#xa0;&#xa0;</li><li>Send material status notifications through MRP&#xa0;</li><li>Work closely with Compliance to address identified issues, as needed.&#xa0;&#xa0;</li><li>Notify Fulfillment Center, Business&#xa0;Owner&#xa0;or Interactive Agency of material status&#xa0;&#xa0;</li><li>Develop, maintain, and track process metrics, communicating results to all stakeholders.&#xa0;&#xa0;</li><li>Provide regular updates to relevant stakeholders on the health of the advertising and promotional review and approval process.&#xa0;&#xa0;</li><li>When an existing piece is updated / changed, run report to identify in-market materials that are impacted and need to be updated / expired – alert Business Owners&#xa0;</li><li>Consistently communicates timely and accurate information and project progress to project owners&#xa0;</li><li>Identifies project bottlenecks and brings cross-functional team members together to resolve issues&#xa0;</li><li>Leads the development of solutions and contingency plans to facilitate business success&#xa0;</li><li>Develops best practices/lessons learned and shares with the business to enhance team success&#xa0;</li><li>Proactively leads ongoing communication with project owners / vendors to ensure that project timelines are aligned with business needs and expectations&#xa0;</li></ul><p><strong>Key Skills:&#xa0;</strong></p><ul><li>Advanced project management skills, highly proficient at balancing competing priorities&#xa0;</li><li>Ability to forecast, prioritize, multitask, and manage multiple jobs in a fast-paced, rapidly changing environment&#xa0;</li><li>Capable of making informed, data-driven decisions under tight deadlines&#xa0;</li><li>Advanced understanding of data analytics, and measurement&#xa0;</li><li>Strong interpersonal skills with the ability to collaborate well with others&#xa0;&#xa0;</li><li>Ability to quickly learn, adapt to, and comply with business needs, policies, and guidelines&#xa0;&#xa0;</li><li>Experienced in risk mitigation, issue resolution, and seeing the big picture&#xa0;</li><li>Demonstrated leadership for identifying, applying, and socializing lessons learned&#xa0;</li></ul>]]></description><link>http://biotechroles.com/manager-material-review-and-promotion-abbvie/6a06ef0c2f1861929d25323d</link><guid isPermaLink="true">http://biotechroles.com/manager-material-review-and-promotion-abbvie/6a06ef0c2f1861929d25323d</guid><pubDate>Fri, 15 May 2026 10:01:48 GMT</pubDate><company>AbbVie</company><location>Mettawa, Mettawa</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Executive Medical Director, Medical Affairs - Precision Medicine]]></title><description><![CDATA[<p>Oncology remains a core therapeutic area at AbbVie, featuring a robust portfolio of marketed products and a promising oncology pipeline. AbbVie is currently seeking a dynamic Executive Medial Director/Sr. Scientific Director for Medical Affairs, Precision Medicine, to lead US CDx strategy in oncology. This role requires a strong background in cancer diagnostics, pathology, biomarkers, and cancer therapeutics, as well as a demonstrated commitment to precision medicine.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Lead and deliver a comprehensive, US focused medical strategy for upcoming CDx launches, overseeing execution of key deliverables.</li><li>Develop and implement the medical affairs strategy for upcoming CDx launches.</li><li>Build and maintain key external relationships with diagnostic partners, academic and community labs, and reference labs.</li><li>Cultivate relationships with expert pathologists and key opinion leaders.</li><li>Forge strong partnerships with leading pathology societies and develop EQA/PT programs.</li><li>Represent Medical Affairs in cross-functional Oncology Precision Medicine teams across the organization.</li><li>Act as the medical affairs lead on the integrated brand team and medical affairs team.</li><li>Develop and execute a biomarker and CDx evidence generation plan in collaboration with precision medicine, HEOR, and TA teams.</li><li>Execute key functional deliverables aligned with the CDx medical strategy, including:<ul><li>Evidence generation to address biomarker and testing gaps.</li><li>Medical review of scientific publications.</li><li>Educational initiatives for both internal and external audiences on biomarkers and testing.</li><li>Review of medical promotional materials for biomarker and testing content.</li><li>Collaboration with Value and Evidence teams on guideline strategies for biomarkers and testing.</li><li>Insight generation via advisory boards and engagements with external experts.</li><li>Develop and implement a congress strategy for pathologists, including EE engagements and digital initiatives.</li><li>Support oncology congresses with biomarker and testing materials in partnership with the TA team.</li></ul></li></ul>]]></description><link>http://biotechroles.com/executive-medical-director-medical-affairs-precision-medicine-abbvie/6a06ef0a2f1861929d25323c</link><guid isPermaLink="true">http://biotechroles.com/executive-medical-director-medical-affairs-precision-medicine-abbvie/6a06ef0a2f1861929d25323c</guid><pubDate>Fri, 15 May 2026 10:01:46 GMT</pubDate><company>AbbVie</company><location>Mettawa, Mettawa</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientific Director, Medical Affairs - Precision Medicine]]></title><description><![CDATA[<p>Oncology remains a core therapeutic area at AbbVie, featuring a robust portfolio of marketed products and a promising oncology pipeline. AbbVie is currently seeking a dynamic Executive Medial Director/Sr. Scientific Director for Medical Affairs, Precision Medicine, to lead US CDx strategy in oncology. This role requires a strong background in cancer diagnostics, pathology, biomarkers, and cancer therapeutics, as well as a demonstrated commitment to precision medicine.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Lead and deliver a comprehensive, US focused medical strategy for upcoming CDx launches, overseeing execution of key deliverables.</li><li>Develop and implement the medical affairs strategy for upcoming CDx launches.</li><li>Build and maintain key external relationships with diagnostic partners, academic and community labs, and reference labs.</li><li>Cultivate relationships with expert pathologists and key opinion leaders.</li><li>Forge strong partnerships with leading pathology societies and develop EQA/PT programs.</li><li>Represent Medical Affairs in cross-functional Oncology Precision Medicine teams across the organization.</li><li>Act as the medical affairs lead on the integrated brand team and medical affairs team.</li><li>Develop and execute a biomarker and CDx evidence generation plan in collaboration with precision medicine, HEOR, and TA teams.</li><li>Execute key functional deliverables aligned with the CDx medical strategy, including:<ul><li>Evidence generation to address biomarker and testing gaps.</li><li>Medical review of scientific publications.</li><li>Educational initiatives for both internal and external audiences on biomarkers and testing.</li><li>Review of medical promotional materials for biomarker and testing content.</li><li>Collaboration with Value and Evidence teams on guideline strategies for biomarkers and testing.</li><li>Insight generation via advisory boards and engagements with external experts.</li><li>Develop and implement a congress strategy for pathologists, including EE engagements and digital initiatives.</li><li>Support oncology congresses with biomarker and testing materials in partnership with the TA team.</li></ul></li></ul>]]></description><link>http://biotechroles.com/senior-scientific-director-medical-affairs-precision-medicine-abbvie/6a06ef082f1861929d25323b</link><guid isPermaLink="true">http://biotechroles.com/senior-scientific-director-medical-affairs-precision-medicine-abbvie/6a06ef082f1861929d25323b</guid><pubDate>Fri, 15 May 2026 10:01:44 GMT</pubDate><company>AbbVie</company><location>Mettawa, Mettawa</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist II or Senior Scientist I, Multi-specific Biologics]]></title><description><![CDATA[<p>Discovery Biotherapeutics at AbbVie is seeking a highly skilled and self-motivated scientist to join a dynamic team supporting design, engineering, and manufacturing of multispecifics. This position will impact projects through engineering, production, and characterization of multispecific biopharmaceutical products. The ideal candidate should have extensive experience with biologics and multispecifics production platforms, analytical characterization, and a proven track record implementing multispecific engineering and production strategies to advance early- and late-stage discovery programs. The applicant should be an enthusiastic, creative scientist who will make tangible contributions to the continuous improvement and innovation within the organization.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Responsible for design, engineering and production of multispecific biologics to support oncology</li><li>Evaluate and integrate state-of-the-art technology to improve therapeutic production platforms, and demonstrate creative “out-of-the-box” thinking to solve difficult problems</li><li>Serve as a Multispecifics Engineering representative for cross-functional teams, and contribute scientific insights into multiple projects across various therapeutic areas; recognized expert in multispecifics design and production</li><li>Serve as the Biologics lead on projects to coordinate activities and transitions from hit generation through candidate nomination</li><li>Identify and solve technical problems independently, conceive and implement innovative process research ideas</li><li>Ensure consistency and quality of technical reports</li><li>Provide project update, analysis and advice to cross-functional teams and senior management</li><li>Present original work internally across departments and at internal and external scientific conferences; may author or co-author peer-reviewed scientific papers or patents</li></ul>]]></description><link>http://biotechroles.com/scientist-ii-or-senior-scientist-i-multi-specific-biologics-abbvie/6a06ef062f1861929d25323a</link><guid isPermaLink="true">http://biotechroles.com/scientist-ii-or-senior-scientist-i-multi-specific-biologics-abbvie/6a06ef062f1861929d25323a</guid><pubDate>Fri, 15 May 2026 10:01:42 GMT</pubDate><company>AbbVie</company><location>Worcester, Worcester</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Oncology Specialist - Seattle, WA]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city, Seattle. This geography covers Washington and Alaska.&#xa0;</p><p>Reporting into the District Manager (DM), the Oncology Specialist (OS) will build and implement territory business plans that align with overall brand objectives and business goals. The Oncology Specialist must demonstrate clear and thorough disease state understanding, have established strong and professional relationships with oncologists (in private, group practice and hospital settings), nursing and office staff, and all others involved in the oncology patient care continuum. This individual fosters robust collaboration with peers and the entire extended team network. They contribute to the accomplishments of team goals by sharing knowledge, experience, and information. He or she drives results aligned with brand expectations and AbbVie’s mission for the betterment of patients. Responsibilities include building a comprehensive strategic business plan with specific, measurable objectives and action-oriented strategies in accordance with regional and national goals. This includes responsible resource allocation, a commitment to good operating principles and compliant, high ethical standards.</p><p><strong>Key Accountabilities/Core Job Responsibilities:</strong></p><ul><li>Responsible for meeting/exceeding assigned sales goal.&#xa0;</li><li>Presents approved disease state and product information to customers, utilizing persuasive selling skills -- all within the boundaries of AbbVie Promotional Policy.</li><li>Leverages sales analytics and customer intelligence to create high-impact, strategic plans that align with our brand objectives.</li><li>Execute sales and marketing strategies within the territory, leveraging our cross functional partners and all approved resources.</li><li>Continuously build knowledge of an evolving marketplace, territory changes, and disease state knowledge &amp; product expertise.</li><li>Collaborate effectively with all territory partners and external counterpart(s).</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize sales opportunities.</li><li>Complies with all laws, regulations, and policies that govern the conduct of AbbVie activities.</li></ul>]]></description><link>http://biotechroles.com/oncology-specialist-seattle-wa-abbvie/6a06ef052f1861929d253239</link><guid isPermaLink="true">http://biotechroles.com/oncology-specialist-seattle-wa-abbvie/6a06ef052f1861929d253239</guid><pubDate>Fri, 15 May 2026 10:01:41 GMT</pubDate><company>AbbVie</company><location>Seattle, US-Virtual Office</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Finance]]></title><description><![CDATA[<p><strong><u>Position Overview</u></strong></p><p>The primary objective of this position is to provide financial leadership and business support for R&amp;D Finance. Specifically, this position is responsible for all consolidated financial planning and reporting, internal controls, and leadership. In addition, this position provides strategic business partnership to the Vice President Controller or R&amp;D Finance.</p><p><strong><u>Core Responsibilities</u></strong></p><ol><li><strong>Financial Reporting and Internal Control</strong>:<ul><li>Lead the monthly, quarterly and annual close / reporting processes ensuring accurate and timely reporting of monthly financial results in accordance with GAAP and reporting requirements from Division, Global and Corporate requirements.</li><li>Develop effective reporting, monitor performance and support development of contingency plans as necessary to deliver results with clear and concise commentary.</li><li>Work closely with the external and internal audit teams to complete all audit cycles effectively and implementing any audit recommendations according to due dates as applicable.</li><li>Drive to continue to enhance internal controls and ensure financial results are recorded in compliance with AbbVie financial policies, SOX and GAAP.</li></ul></li><li><strong>Financial Planning and Analysis</strong>:<ul><li>Proactively lead the planning processes [Plan, UPD, LBE and LRP] ensuring accurate and timely integration of sales forecast, pricing and investment resourcing, ensuring senior management input to meet overall Division / Global / Corporate deadlines and deliverables.</li><li>Coordinate across the division timelines, requirements, targets, financial presentations, and financial results for all Corporate planning requirements.&#xa0;</li><li>Lead the finance team that provides direct financial support to all of the support organizations within the division.</li><li>Ensure financial planning and reporting deliverables are accurate, clear and concise for Executive level review and approval.</li></ul></li><li><strong>Strategic Business Partnership:</strong><ul><li>Provide proactive leadership across overall Financial Planning and Reporting function by effectively communicating / interfacing with Senior management, business unit controllers and other cross functional teams with R&amp;D Finance as well as all external customers encompassing Global and Corporate FP&amp;A communities.&#xa0;&#xa0;</li><li>Be a strategic partner to the Vice President – R&amp;D Finance and provide clear and concise output deliverables that are Executive management ready.</li><li>Decision Support / Special Projects -- Provide analyses for ad hoc or other business presentations that lend insight into key business drivers enabling senior management to adapt more appropriate tactics / strategy to meet both short- and long-term objectives.</li></ul></li><li><strong><u>Leadership</u></strong><ul><li>Build an effective network within the R&amp;D Finance teams to facilitate navigation and alignment throughout the complex matrix environment.</li><li>Identify, nurture and develop key talent with an eye towards future leadership roles within various areas of the organization.</li><li>Acclimate to US forecasting cycles and consider areas for future process improvements as part of a key member of the planning processes, along with DHQ and members of the extended finance leadership team.</li></ul></li><li><strong><u>Demand Management &amp; Pricing (as applicable):</u></strong>&#xa0; Partner with Demand Planning/Pricing teams to monitor and maintain the stability of AbbVie product in the U.S. supply channel, ensure the equitable allocation of product to customers and provide business insights on purchase and pricing trends across AbbVie’s key brands.&#xa0;</li><li>Effectively lead and develop a team of professionals with direct reports.</li></ol>]]></description><link>http://biotechroles.com/senior-director-finance-abbvie/6a06ef032f1861929d253238</link><guid isPermaLink="true">http://biotechroles.com/senior-director-finance-abbvie/6a06ef032f1861929d253238</guid><pubDate>Fri, 15 May 2026 10:01:39 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Process Safety and Design]]></title><description><![CDATA[<p>Reporting directly to the Vice President of Global Engineering, this role will have high visibility to the Operations executive leadership team as a key leader and globally recognized Subject Matter Expert - sharing your knowledge and expertise to ensure that we deliver best-in-class process design in the projects that we execute and throughout our global manufacturing network. In this role, you will be expected to bring new ideas, industry best practices and innovative solutions so that we are continuously ensuring our manufacturing facilities operate at the highest standards of engineering design and process safety.</p><p>Responsibilities:</p><ul><li>You will be a trusted partner and establish process safety strategy for the global manufacturing network, providing Leadership with regular updates on the manufacturing sites and continuous improvement initiatives related to Process Safety Management (PSM).</li><li>Successfully engaging globally across all manufacturing sites, collaborating with site leadership to create defined timelines for the implementation of process safety recommendations and continuous improvement goals. You will have joint responsibility with Site Directors to ensure that timelines are achieved.</li><li>With your team of SMEs, you will be accountable to drive global network Process Hazard Analysis (PHA) efforts, capital project design reviews, process safety training and other process safety initiatives.</li><li>Design, develop, implement and monitor the process safety roadmap for the global network with an overarching focus to drive standardized processes, reduce risk, eliminate failure modes and ensure global compliance.</li><li>Leveraging your background in Chemical Engineering, Chemistry or related technical field, provide technical support to global network of sites on design and process safety related issues.</li><li>Drive continuous improvement process safety culture across the network. Be a visible leader for AbbVie’s Zero. Believe it. Achieve it.(ZBA) philosophy.</li><li>Lead process safety reviews, during design and start-up for major capital projects across the global network. Provide technical input for Requests for Capital Expenditure (RCE) to ensure that significant safety and environmental aspects are properly integrated during the Front-End Planning design process for new product introduction, product-transfer between sites, and changes to existing processes and equipment. Lead the hazard screening process for Tech Transfers and New Product Introductions.</li><li>Develop network dashboard of process safety related KPIs to measure continuous improvement progress. Maintain currency with industry best practices, Best Available Technologies (BAT), and trends. Share this knowledge with peers and leadership.</li><li>With your team, support the process safety element of internal EHS audits to ensure compliance with applicable standards and policies, adoption of best practices to identify and manage risk, and conformance to company directives.</li><li>Experienced people leader with proven responsibility for talent selection, talent development and performance management.</li></ul>]]></description><link>http://biotechroles.com/director-process-safety-and-design-abbvie/6a06ef012f1861929d253236</link><guid isPermaLink="true">http://biotechroles.com/director-process-safety-and-design-abbvie/6a06ef012f1861929d253236</guid><pubDate>Fri, 15 May 2026 10:01:37 GMT</pubDate><company>AbbVie</company><location>Worcester, North Chicago</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - St. Petersburg, FL]]></title><description><![CDATA[<p><em><strong>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.</strong></em><br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-st.-petersburg-fl-abbvie/6a06eeff2f1861929d253235</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-st.-petersburg-fl-abbvie/6a06eeff2f1861929d253235</guid><pubDate>Fri, 15 May 2026 10:01:35 GMT</pubDate><company>AbbVie</company><location>St. Petersburg, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Account Specialist, Chronic Migraine - Boston East, MA]]></title><description><![CDATA[<p>The Account Specialist role promotes a product to community practices and health systems. Customer accounts may include community/private practices, community-based hospitals, academic medical centers, and government accounts (military treatment facilities and/or Veteran’s Affairs Medical Centers). The Account Specialist develops and maintains relationships with various accounts/departments such as neurology, pain medicine, physical medicine and rehabilitation, primary care, and pharmacy. Or in Urology, specialists such as urology, urogynecology, obstetrics and gynecology, female pelvic medicine, ambulatory surgical centers, and reconstructive surgery.</p><p>Responsibilities</p><ul><li>Promote a product to meet/exceed sales goals in community/private practices as well as hospitals/health systems.</li><li>Identify/uncover customer needs (training, clinical, operational, reimbursement) and address with appropriate AbbVie resources</li><li>Provide education and clinical/injection training for residents, fellows, and other key hospital personnel.</li><li>Expert delivery of anatomical/procedural information and training, including the appropriate use of anatomical terminology to train injection paradigms/postures while highlighting various anatomical and injection insights and considerations.</li><li>Effectively utilize AbbVie's sales and data resources to enhance productivity and growth of AbbVie products while implementing U.S. Marketing Plan.</li><li>Collaborate with other Account Specialist to promote the product for approved indications and execute individual, department, or group resident/fellow trainings within hospital/health system accounts.</li></ul>]]></description><link>http://biotechroles.com/account-specialist-chronic-migraine-boston-east-ma-abbvie/6a06eefd2f1861929d253234</link><guid isPermaLink="true">http://biotechroles.com/account-specialist-chronic-migraine-boston-east-ma-abbvie/6a06eefd2f1861929d253234</guid><pubDate>Fri, 15 May 2026 10:01:33 GMT</pubDate><company>AbbVie</company><location>Boston, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Digestive Account Executive - Florida]]></title><description><![CDATA[<p><strong><em>This role is field-based and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.</em></strong></p><p>Perform all aspects of account management, including developing and maintaining strategic business relationships with corporate/senior management staff in key accounts with the goal of establishing multi-level relationships to increase representative access, develop new business, maximize resource utilization, and increase sales and market share of the assigned product.</p><p>Responsibilities</p><ul><li>Work with internal teams to manage and identify key target account opportunities. Develop product strategies to fully and consistently penetrate these accounts.</li><li>Provide strategic and tactical direction regarding target accounts to regional and district teams.</li><li>Advise sales and marketing management with appropriate direction on challenges and opportunities within key target accounts. Analyze and supports channel specific training needs within the Region.</li><li>Develop an annual business plan with goals and objectives to increase sales volume and market share in target accounts across all FDA approved indications. Routinely identify local opportunities and threats and develop/modify business plans accordingly. Anticipate change and take proactive measures to address.</li><li>Understand and effectively utilize a broad range of financial and quantitative data and analyses. Assess business impact of target account opportunities to include overall profitability and impact on sales.</li><li>Partner with Field Sales Managers to evaluate and penetrate non-retail account drivers within MSAs.</li><li>Drive target account volume and share growth through detailed analysis, providing recommendations and driving execution and pull through of District Managers and representatives.</li></ul>]]></description><link>http://biotechroles.com/digestive-account-executive-florida-abbvie/6a06eefb2f1861929d253233</link><guid isPermaLink="true">http://biotechroles.com/digestive-account-executive-florida-abbvie/6a06eefb2f1861929d253233</guid><pubDate>Fri, 15 May 2026 10:01:31 GMT</pubDate><company>AbbVie</company><location>Florida City, US-Virtual Office</location><salary>$120000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Field Reimbursement Manager, Oncology - Northeast Region]]></title><description><![CDATA[<p><strong>This role is field-based, and candidates should live within a reasonable distance of the primary city. Talent will be hired at a level commensurate with experience.</strong></p><p><u>Candidates may live in the following cities:</u></p><ul><li>Hartford, CT</li><li>Stamford, CT</li><li>Albany, NY&#xa0;</li><li>Concord, NH</li><li>Portland, ME</li></ul><p>&#xa0;</p><p>The Field Reimbursement Manager (FRM) acts as an alternative in-office resource that is available to address HCP questions about patient access.&#xa0; The FRM calls directly on HCP offices in their assigned, specific geography to answer questions about patient access &amp; reimbursement in support of the AbbVie Oncology portfolio.&#xa0; The FRM provides expertise on coverage and common access and reimbursement challenges affecting AbbVie Oncology products.&#xa0; The FRM responsibilities include educating on the access and reimbursement support tools available from AbbVie, advising HCPs on patient prescription status and program eligibility, and educating HCP offices on payer processes and procedures.&#xa0;</p><p><strong>Responsibilities:</strong></p><ul><li>Educate HCPs on patient support programs, including access and reimbursement support tools and services</li><li>Educate on product-specific acquisition and access options such as specialty pharmacy networks and specialty distribution</li><li>Educate on resources available to address access issues</li><li>Provide local expertise in regards to national/regional payor policies in order to educate providers on payer issues, coding changes, and appropriate claims submission processes</li><li>Liaise with AbbVie’s Access and Reimbursement support center to update HCPs on Rx status and program eligibility</li><li>Report back payer trends related for approved products to Patient Services and MHC account management teams</li><li>Establish and maintain relationships with appropriate providers within territory</li><li>Remain current on key managed care, reimbursement, and policy activities</li></ul>]]></description><link>http://biotechroles.com/field-reimbursement-manager-oncology-northeast-region-abbvie/6a06eef92f1861929d253232</link><guid isPermaLink="true">http://biotechroles.com/field-reimbursement-manager-oncology-northeast-region-abbvie/6a06eef92f1861929d253232</guid><pubDate>Fri, 15 May 2026 10:01:29 GMT</pubDate><company>AbbVie</company><location>Hartford, US-Virtual Office</location><salary>$95000-135000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Parkinson's - Austin, TX]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.&#xa0;&#xa0;<strong>This territory includes Austin, El Paso and Lubbock</strong><br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-parkinson&apos;s-austin-tx-abbvie/6a06eef82f1861929d253231</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-parkinson&apos;s-austin-tx-abbvie/6a06eef82f1861929d253231</guid><pubDate>Fri, 15 May 2026 10:01:28 GMT</pubDate><company>AbbVie</company><location>Austin, US-Virtual Office</location><salary>$85000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Financial process and systems, Business Planning and Consolidation (SAP BPC) & SAC Analytics]]></title><description><![CDATA[<p>Key areas of Focus</p><ul><li>Key support lead for the corporate planning models in the BPC environment including problem resolution break fix support, enhancements and optimization.&#xa0; Requires strong understanding of the corporate consolidation planning process, and requirements for management reporting.</li><li>Manage and ensure that actuals loaded into BPC tie to reported results monthly.&#xa0; Ensure that monthly financial data is loaded to BPC is complete and that all validation checks are performed.</li><li>Provide the Corporate finance team with support for ad-hoc reports.&#xa0; Ensure forecast tie to final monthly, quarterly reported results.&#xa0; Coordinate with finance collection of forecasts from 100+ users regarding system readiness. Finally, coordinate the submission of forecasts with other system administrators to corporate.&#xa0;&#xa0;</li><li>Act as BPC subject matter expert for the Corporate FP&amp;A finance planning organization.&#xa0; Continuously and proactively improve the environment to enrich experience by promoting and developing the automation of processes with current and future application flows, enhancing existing reports, along with making metadata suggestions to optimize management reporting. &#xa0;Develop, maintain and improve documentation on key business processes and procedures in compliance with internal control policies as well as provide training documentation and support for end users.</li><li>Maintain production and development databases, including data management, hierarchy updates, calculation script logic updates, data backups, and user security. Design, develop and troubleshoot load rules, Business Rules and Calculation Scripts. Assist with technical patches, upgrades and system/application migrations.</li><li>Lead project team in development of SAC Analytics build for Corporate FP&amp;A, Balance Sheet and Entity Plan.</li></ul>]]></description><link>http://biotechroles.com/senior-manager-financial-process-and-systems-business-planning-and-consolidation-(sap-bpc)-and-sac-analytics-abbvie/6a06eef62f1861929d253230</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-financial-process-and-systems-business-planning-and-consolidation-(sap-bpc)-and-sac-analytics-abbvie/6a06eef62f1861929d253230</guid><pubDate>Fri, 15 May 2026 10:01:26 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Software / Control Engineer]]></title><description><![CDATA[<p>•As&#xa0;<strong>Software / Control Engineer,&#xa0;</strong>you are responsible for basic configuration and programming per AbbVie’s change management procedures for the manufacturing process, utilities and facilities control systems. This position performs system troubleshooting during and outside business hours as necessary. Responsible for the maintenance of assigned site operations technologies (OT) systems per applicable departmental procedures.</p><p><strong>Responsibilities</strong></p><ul><li>Develop basic control configuration or programming in accordance with the design documents to meet the functional requirements.</li><li>Provide first line technical support to Project Engineers, Maintenance, Production and Technical Operation personnel in automation related problems as need arises. Provides training for OT Systems users in automation technologies and process control applications.</li><li>Diagnose and troubleshooting Control System hardware, software, and networking issues, replace defective components as needed.</li><li>Perform site OT systems (PLC’s, SCADA, and Data Historian) upgrades and data migrations activities.</li><li>Develop and execute qualification protocols plus associated technical documentation like System’s Functional and\or Design Specifications following OT Systems lifecycle validation activities.</li><li>Perform scheduled OT Systems administration and maintenance tasks such as operating systems (OS) and anti-virus updates, users accounts managements, critical data back-up and others.</li><li>Evaluate and provide input and recommendations regarding control system improvements. Establish monitoring and reporting project techniques to support equipment performance reliability.</li><li>Provide production support during off-peak hours. This might require working overtime, overnight or on weekends.</li><li>Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.</li></ul>]]></description><link>http://biotechroles.com/software-control-engineer-abbvie/6a06eef42f1861929d25322f</link><guid isPermaLink="true">http://biotechroles.com/software-control-engineer-abbvie/6a06eef42f1861929d25322f</guid><pubDate>Fri, 15 May 2026 10:01:24 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Partnership and Program Management, Device & Combination Product Development]]></title><description><![CDATA[<p>The Director of Partnership and Program Management is accountable for leading the global team of program and partnership managers who co-lead cross functional teams focused on the development of drug-device combination products and medical devices. The Director ensures that the strategy and plans defined for assigned programs are aligned with the needs of the patient and customer and the business objectives of the CMC and Asset team.&#xa0; This position reports to the Senior Director of Device Technology and Program Management, Device and Combination Product Development.</p><p><em>Summary of Responsibilities and Accountabilities: </em></p><p>The Director will be accountable to functional leadership under the Device &amp; Combination Product Development organization.&#xa0; Team members are accountable to the CMC team, the CMC Product Development Director and departmental senior leadership to deliver on the development strategy, plans and budget defined for the project portfolio. &#xa0;</p><p>Responsibilities include:</p><ul><li>Establishing and maintaining robust and consistent external and internal collaborations.</li><li>Providing guidance on project management principles, strategies, and best practices to the PM team:<ul><li>Co-leadership of drug delivery system product development projects</li><li>Tactical and strategic management of external device partners including acting as a key interface, managing the project governance process and forward-looking evaluation of potential partners</li><li>Representing the R&amp;D organization to cross functional leadership through effective and timely communication</li><li>Ensuring effective use of meetings by clearly defining objectives, agendas, and attendees, and capturing minutes, decisions and action items for dissemination.</li></ul></li><li>Effective and efficient resource allocation and forecasting for future growth</li><li>Driving continuous improvement on program/project management processes and tools</li></ul><p>&#xa0;</p><p><em>External Partnerships</em>: The Director ensures Program Managers lead the team in managing the relationship and performance of key external device development partners.&#xa0; This includes establishing an effective and efficient governance process, such as defining key interfaces, establishing meeting cadences, performance monitoring, project scope/change control, issue escalation, risk management, and financial tracking.&#xa0; The Director will ensure timely and efficient communication regarding partner performance to the broader AbbVie organization as required. The Director will provide accurate and timely estimates for resourcing, budgeting, and forecasting. &#xa0;</p><p><em>Functional Management: </em>The Director directly manages a global group of Program Managers through efficient assignment and distribution of project responsibilities, establishing team norms and best practices, support of opportunities for professional development, and actionable and timely feedback on performance.&#xa0; This includes a focus on continuous improvement of the group’s competency in project and program management and product development related processes.&#xa0;&#xa0;</p><p><em>Impact on AbbVie</em>: This role has broad influence and impact on the development of AbbVie assets. Devices and combination products are often technically complex, involve multiple sub-systems, and must meet global industry and regulatory requirements.&#xa0; The Director must frequently interact with cross functional senior leadership and key internal stakeholders through effective communication and influence.</p>]]></description><link>http://biotechroles.com/director-partnership-and-program-management-device-and-combination-product-development-abbvie/6a06eef22f1861929d25322e</link><guid isPermaLink="true">http://biotechroles.com/director-partnership-and-program-management-device-and-combination-product-development-abbvie/6a06eef22f1861929d25322e</guid><pubDate>Fri, 15 May 2026 10:01:22 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Associate General Counsel]]></title><description><![CDATA[<p>The role of Associate General Counsel, Global Commercial Legal, Aesthetics is responsible for developing legal strategy for AbbVie’s U.S. aesthetics products, including neurotoxins (BOTOX®) and dermal fillers (JUVÉDERM®). The role requires leading with influence and legal depth at the intersection of strategy and execution. As an Associate General Counsel, you will serve as a trusted advisor to senior leaders, guiding high-impact decisions across complex operational and commercial environments. This role combines legal mastery, leadership, and enterprise thinking, empowering you to shape business outcomes, mentor legal talent, and drive initiatives that safeguard the company while enabling innovation.</p><p><strong>Key Responsibilities Include</strong><strong>:</strong></p><ul><li>Serve as lead counsel to executive and senior leaders in AbbVie’s aesthetics business unit, providing legal advice that drives both compliance and growth. Legal advice will be given on topics such as new product launches, patient programs, marketing strategies, promotion, customer contracting, scientific exchange and regulatory submissions.</li></ul><ul><li>Provide substantive advice across departments including Marketing, Sales, Medical Affairs, Regulatory Affairs and others concerning a broad range of legal, regulatory and compliance issues. These include FDA regulations, False Claims Act, Anti-Kickback Statute, OIG guidance, the PhRMA &amp; AdvaMed Codes, the Sunshine Act, Foreign Corrupt Practices Act and competition law.</li><li>Lead cross-functional legal projects aligned to enterprise strategic priorities.</li><li>Anticipate and navigate legal risks across business models, operations, and stakeholder relationships.</li><li>Mentor, coach and direct multiple attorneys; contribute to talent development and succession planning to shape leadership pipeline.</li><li>Influence strategic direction by translating legal, regulatory and industry shifts into actionable guidance.</li><li>Oversee outside counsel engagements, manage and develop budgets for assigned legal matters.</li><li>Serve as a thought partner within the Legal function, helping to shape legal frameworks, policies and priorities.</li></ul>]]></description><link>http://biotechroles.com/associate-general-counsel-abbvie/6a06eef12f1861929d25322d</link><guid isPermaLink="true">http://biotechroles.com/associate-general-counsel-abbvie/6a06eef12f1861929d25322d</guid><pubDate>Fri, 15 May 2026 10:01:21 GMT</pubDate><company>AbbVie</company><location>Irvine, Irvine</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director, RA-CMC PAC DM]]></title><description><![CDATA[<p>The Director Regulatory Affairs for Chemistry, Manufacturing and Controls Post Approval Change Dossier Management (CMC PAC DM) combines scientific, regulatory and business knowledge with superior leadership skills to lead the PAC DM team responsible for ensuring&#xa0;RA-CMC post approval change&#xa0;objectives&#xa0;are met.&#xa0; Builds and maintains partnerships within the Regulatory Affairs functional areas and the Operations and Research &amp; Development (R&amp;D) organizations. Provides an environment for staff members to develop their careers and take their own leadership positions throughout AbbVie.</p><p><strong>Responsibilities</strong></p><ul><li>Leads a global RA CMC PAC DM team who project manages marketed product variations including authoring and compilation of chemistry,&#xa0;manufacturing,&#xa0;and control (CMC) sections to ensure timely preparation of submission documents.</li><li>Devises (or advises their team on) tactical strategies for executing post approval changes with complicated scenarios (e.g., complex dosage form or multiple operational changes, aggressive timelines).</li><li>Provides leadership to PAC-DM staff to ensure consistency in the execution of post approval changes across all global programs.&#xa0;</li><li>Provides direction and guidance to direct reports and their teams, as applicable, who exercise significant latitude and independence in their assignments.</li><li>Designs initiatives to drive business efficiencies across the organization (within or outside of the regulatory groups). Identifies opportunities for process improvements, identifies/solicits solutions and drives for implementation. Ensures enterprise culture initiatives are implemented across the PAC-DM team.&#xa0;</li><li>Effectively mentors staff to achieve business objectives and staff member personal growth. Reviews and provides feedback on RA training programs.</li><li>Provides leadership to PAC-DM staff by communicating and providing guidance towards achieving department objectives. Identifies engagement needs and partners with stakeholders to implement action plans accordingly.&#xa0;</li><li>Trains, develops and mentors individuals; includes formal supervisory responsibilities.&#xa0;Evaluates performance of and assists in career development planning for PAC-DM staff.</li></ul>]]></description><link>http://biotechroles.com/director-ra-cmc-pac-dm-abbvie/6a06eeef2f1861929d25322c</link><guid isPermaLink="true">http://biotechroles.com/director-ra-cmc-pac-dm-abbvie/6a06eeef2f1861929d25322c</guid><pubDate>Fri, 15 May 2026 10:01:19 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Commissioning and Start-Up Engineering]]></title><description><![CDATA[<p>This position has responsibility for managing and leading AbbVie's Global energy management programs. Global energy spend is approximately $100 million per year, which includes purchased electricity and fuel. AbbVie's total CO2 emissions are well over 1 billion pounds annually. This position will have overall responsibility and accountability to lead and manage all energy related initiatives such as cost reductions and CO2 emissions reductions within AbbVie. Energy related cost savings and cost avoidance initiatives are critical to the success of this position. CO2 emissions and other energy related greenhouse gas emissions are being scrutinized by both regulatory authorities around the World, as well as the public sector. This position will focus on minimizing AbbVie's overall carbon footprint and achieving challenging energy and environmental targets. This is a very strategic function in AbbVie, and this position must proactively influence Global Leaders and Site Directors.</p><p>Responsibilities</p><ul><li>Strategic planning and program development for energy related issues.</li><li>Provide leadership and support to all AbbVie sites in negotiating cost effective energy contracts with energy suppliers.</li><li>Ensure we achieve our internal and external energy &amp; CO2 reduction targets.</li><li>Provide leadership to site directors and facility energy managers in the development, approval and implementation of multi-million dollar energy projects and programs.</li><li>Fulfill the role of company-wide energy expert.</li><li>Develop AbbVie energy LRP, energy related KPIs, and ensure that detailed energy surveys, assessments, and audits are accomplished.</li><li>Pursue measures to optimize the existing facilities infrastructure and be responsible for tracking and creating reports and data for ongoing energy performance improvement.</li></ul>]]></description><link>http://biotechroles.com/director-commissioning-and-start-up-engineering-abbvie/6a06eeed2f1861929d25322b</link><guid isPermaLink="true">http://biotechroles.com/director-commissioning-and-start-up-engineering-abbvie/6a06eeed2f1861929d25322b</guid><pubDate>Fri, 15 May 2026 10:01:17 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, People Support - HRConnect People Solutions]]></title><description><![CDATA[<p><strong>Purpose</strong></p><p>Associate Director, HRConnect People Support is responsible for leading a team dedicated to delivering excellent and efficient employee experience as the first point of contact for all HR-related matters within AbbVie’s global HR operations shared service center. Collaborates closely with cross-functional partners (e.g. Employees at globally diverse locations, Business HR, Total Rewards, Payroll, Finance, Digital and Data strategy, Business Technology Solution and vendor partners) to deliver on the AbbVie HR Strategic Choices, HR Operation’s Strategic Priorities and meet business needs. This role has responsibility for managing multiple geographies and working cross functionally with global teams. Must have the ability to effectively interact and manage stakeholder relationships, identify/ translate business requirements, and transform those requirements into system and HR services solutions.</p><p><strong>Responsibilities</strong></p><ul><li>Champion the services and content available to employees and ensure HR Operations deliver excellent employee experience.</li><li>Build and sustain a high-performing, highly engaged team of HR Operations Consultants.</li><li>Identify, sponsor and deliver process optimization efforts, including but not limited to technology&#xa0;enhancements, to reduce resolution time and manual effort on the team and improve the employee experience.</li><li>Serve as a liaison to our HR business partners globally to support alignment of HR Operations People Experience support to business HR strategies, identifying ways to increase employee and manager self-service, and reduce risk of human errors, administrative effort to affiliate HR teams and COE partners.</li><li>Effectively engage with stakeholders (internal and external) to meet or exceed key service level agreements, quality targets and key performance indicators.</li></ul>]]></description><link>http://biotechroles.com/associate-director-people-support-hrconnect-people-solutions-abbvie/6a06eeeb2f1861929d25322a</link><guid isPermaLink="true">http://biotechroles.com/associate-director-people-support-hrconnect-people-solutions-abbvie/6a06eeeb2f1861929d25322a</guid><pubDate>Fri, 15 May 2026 10:01:16 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Hospital Surgical Rep (HS), Allergan Aesthetics, Orlando S. FL]]></title><description><![CDATA[<p>The Hospital Surgical Representative is responsible for providing sales and promotion of Allergan Medical plastic surgery products, maintaining customer base, developing new markets, and obtaining new customers</p><p>Responsibilities</p><ul><li>Meet or exceed sales targets on an ongoing basis and has the capability of selling targeted products to targeted accounts.</li><li>Conduct excellent product in-servicing and product evaluations that lead to customer conversions. </li><li>Prospect and develop relationships with prospective customers, converting them to Allergan customers (primary customers include the physician, materials manager and the purchasing administrator).</li><li>Increase account penetration with orders for Allergan Tissue Matrices for new surgical procedures.</li></ul>]]></description><link>http://biotechroles.com/hospital-surgical-rep-(hs)-allergan-aesthetics-orlando-s.-fl-abbvie/6a06eeea2f1861929d253229</link><guid isPermaLink="true">http://biotechroles.com/hospital-surgical-rep-(hs)-allergan-aesthetics-orlando-s.-fl-abbvie/6a06eeea2f1861929d253229</guid><pubDate>Fri, 15 May 2026 10:01:14 GMT</pubDate><company>AbbVie</company><location>Orlando, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Emerging Channel Insights & Analytics -Market Access & Patient Services]]></title><description><![CDATA[<p>AbbVie’s Analytics and Performance Excellence (APEX) function is seeking a highly strategic, analytical, and collaborative Associate Director to provide analytics leadership for the Business Evolution Strategic Development (BESD) Team. This role will drive impactful business analytics and insights to help AbbVie anticipate and navigate evolving healthcare environments, especially focusing on market access and policy disruptors.</p><p>The Associate Director will bridge <strong>Market Access and Patient Services (MAPS)</strong> Team within APEX and BESD (Business Evolution Strategic Development) team objectives by leading modelling, advanced insights and analytics supporting forward-looking strategies, enabling enterprise readiness, and shaping market access policies and outcomes for AbbVie’s diverse U.S. portfolio. This role requires a strong grasp of healthcare policy, payer analytics, and strategy formulation within a collaborative, cross-functional environment.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Lead the planning and execution (hands-on performing) of analytics to inform market access strategies, price reform and policy analysis, with actionable recommendations for AbbVie leadership.</li><li>Identify payer opportunities/threats through deep dive analytics ('Follow the Dollar', claims analysis, and scenario modeling).</li><li>Foster positive relationships and close collaboration with teams including Government Affairs, Finance, Legal, Corporate Affairs, Brand, and Market Access.</li><li>Communicate complex findings and insight-driven narratives to senior leadership and cross-functional teams, enabling improved payer knowledge and strategic decision-making.</li><li>Monitor external environment and translate emerging trends (political, regulatory, legislative, commercial) into strategic recommendations for AbbVie’s business evolution.</li><li>Advise on analytics infrastructure enhancements to drive business impact.</li></ul><p><strong>Skills</strong></p><ul><li>Action and Accountability: Own responsibility for activities within relevant workstreams, and engage and inspire cross functional stakeholders to advance towards clear objectives and strategies; make quick, but informed decisions, as appropriate, to ensure best paths forward in the midst of change market and policy dynamics.&#xa0; Constantly engage, guide, and support cross-functional team to address roadblocks, challenges, resourcing constraints and other dynamics.</li><li>Leadership and Influence: Influence and persuade across multiple external and internal stakeholders.</li><li>Collaboration and Teamwork: Work effectively with internal stakeholders, external market experts and partners.</li></ul>]]></description><link>http://biotechroles.com/associate-director-emerging-channel-insights-and-analytics-market-access-and-patient-services-abbvie/6a06eee82f1861929d253227</link><guid isPermaLink="true">http://biotechroles.com/associate-director-emerging-channel-insights-and-analytics-market-access-and-patient-services-abbvie/6a06eee82f1861929d253227</guid><pubDate>Fri, 15 May 2026 10:01:12 GMT</pubDate><company>AbbVie</company><location>San Francisco, Mettawa</location><salary>$165000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Marketing Analytics - Derm Atopic Dermatitis]]></title><description><![CDATA[<p>AbbVie’s Dermatology Franchise is seeking Senior Manager to support Sales and Marketing initiatives by delivering end-to-end analysis, insights, and recommendations that shape brand strategy and drive measurable business performance. This role translates complex physician, patient, account, and competitive data into clear narratives and actionable strategic and tactical adjustments. A successful candidate will proactively define business questions, apply rigorous analytical and modeling methodologies, and communicate concise, decision-ready insights to a broad set of stakeholders. Success requires strong business acumen, strong people and influencing skills, and close partnership with Brand and Sales Leadership to align priorities and support the current and future dermatology portfolio.</p><p><strong>Major Responsibilities: </strong></p><ul><li>Analyze physician, account, patient, and competitive data at national and sub-national levels to strengthen the brand team’s understanding of market dynamics and opportunities</li><li>Lead fast-paced ad-hoc analytics projects, including taking initiative to identify the key business questions relative to product performance, that inform strategical and tactical decision-making, as well as brand planning process, ensuring multiple stakeholders’ perspectives are considered and integrated where relevant.</li><li>Strengthen the organization’s understanding of marketplace performance and opportunities through tracking, modeling, and analysis of physician- and patient-level dynamics within quickly evolving competitive landscape.</li><li>Develop fact-based promotional investment strategies and guide investment decisions from marketing mix/business optimization and other analysis to optimize performance, influence business growth &amp; inform continuous financial forecasting cycles and brand planning process</li><li>Develop near-term KPIs and longer-term ROI measurements that will inform recommendations to optimize personal and non-personal promotional channels</li><li>Closely involved with financial planning process, responsible for input into financial planning process &amp; key conduit to Forecasting for all monthly estimates, annual plan and long-range plan deliverables</li><li>Understand sub-national drivers of cross-brand performance, providing more granularity to performance dynamics across distribution channels and customers</li><li>Leverage innovative, sophisticated analytic models that address critical issues but also meet key business criteria (e.g. cost, risk, business impact) and key technical criteria (e.g. reliability, validity, and predictability)</li><li>Effectively work with cross-functional partners to deliver integrated analytics reflecting the diverse contributions across the functions</li><li>Lead contract support, and external suppliers to increase and enhance the use of advanced modeling and analytic methods and produce results that fully leverage available data and analytics</li></ul>]]></description><link>http://biotechroles.com/senior-manager-marketing-analytics-derm-atopic-dermatitis-abbvie/6a06eee72f1861929d253226</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-marketing-analytics-derm-atopic-dermatitis-abbvie/6a06eee72f1861929d253226</guid><pubDate>Fri, 15 May 2026 10:01:11 GMT</pubDate><company>AbbVie</company><location>Mettawa, Mettawa</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Specialist, Regulatory Strategic Planning]]></title><description><![CDATA[<p>The <strong>Senior Associate, Regulatory Strategic Planning</strong>, is responsible for successfully delivering project management capabilities for cross-functional teams within the Regulatory Affairs organization. The individual combines knowledge of scientific, regulatory, and business processes to properly drive the execution of AbbVie’s regulatory strategies. Responsibilities include developing and managing the schedules, activities, and deliverables for the Global Regulatory Product Teams (GRPTs), interacting with key stakeholders, and supporting process improvement efforts to help achieve business performance goals for regulatory compliance and productivity.</p><p><u><strong>Responsibilities:</strong></u></p><ul><li>Provides project management leadership in support of GRPTs; develops schedules and wave plans to ensure regulatory milestones are adequately planned and tracked, and works with Regulatory staff across the globe to drive the execution of GRPT-related activities and deliverables.</li><li>Works independently to plan and facilitate GRPT and related meetings (e.g., Dossier Kick-off Meetings, Regulatory Strategic Reviews, Rapid Response Teams, and Regulatory Advisory Panels); ensures action items are assigned and completed; periodically summarizes and shares team highlights with stakeholders as necessary.</li><li>Interacts with ADTs and other key stakeholders across the enterprise to ensure regulatory milestones are properly communicated; periodically communicates with Regulatory management to provide timely updates on progress and/or issues that may impact the global program.</li><li>Drives GRPT operations in support of the Global Regulatory Lead (GRL); ensures GRPT-related information and tools (e.g., team sites, rosters, charters, schedules) are kept up to date. Executes process improvement initiatives of low- to medium-complexity; demonstrates effective change leadership, and is able to move ideas from concept to implementation.</li><li>Possesses working knowledge of the regulatory product lifecycle, business processes, and regulations across Regulatory sub-functions; is able to provide business subject matter knowledge on assigned initiatives, and demonstrates effective problem solving &amp; decision making, learning and adjusting behaviors based on prior results/experience.</li><li>Leads team meetings effectively; uses the project governance process to effectively escalate and drive resolution of issues; demonstrates effective group facilitation skills and ability to drive consensus among team members regarding process changes.Develops effective working relationships with project team members; prepares and delivers clear, relevant, and influential written reports and presentations for a variety of audiences.</li><li>Develops effective working relationships with project team members; prepares and delivers clear, relevant, and influential written reports and presentations for a variety of audiences.Coordinates and drives deliverable preparation; develops and maintains process models using standard methods and tools; manages and tracks budgets, contracts, communications, metrics, and reporting-related processes.</li><li>Supports mechanisms to identify, capture, and report business performance metrics. Analyzes metrics with subject matter experts in an effort to drive increase compliance, quality, and productivity across the organization.Incorporates diverse, cross-functional, and global perspectives into strategies &amp; tactics that consistently enhance the ability to improve outcomes for the Regulatory Affairs organization.</li><li>This position will work a hybrid work schedule (3 days in office) from our Lake County, IL AbbVie headquarters.&#xa0;</li></ul><p>Significant Work Activities:&#xa0;Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required</p>]]></description><link>http://biotechroles.com/senior-specialist-regulatory-strategic-planning-abbvie/6a06eee52f1861929d253225</link><guid isPermaLink="true">http://biotechroles.com/senior-specialist-regulatory-strategic-planning-abbvie/6a06eee52f1861929d253225</guid><pubDate>Fri, 15 May 2026 10:01:09 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Account Specialist, AI - Riverside, CA]]></title><description><![CDATA[<p><strong><em>This role is field-based and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.</em></strong></p><ul><li>Advances hospital and specialty customers along the sales continuum and gains prescriber commitments through effective questioning, active listening, and utilization of approved data and resources. Delivers on-label presentations/sales calls to appropriately highlight the benefits and risks of the product portfolio to create awareness of product solutions and address gaps in therapeutic areas, resulting in sales goal achievement.</li><li>Develops professional relationships and differentiates the Anti-Infective portfolio’s value proposition at all levels (C-Suite, Physicians, Hospital Staff, Support Personnel) within accounts and departments to further the use of the product portfolio.</li><li>Strong understanding and ability to problem solve product and patient flow through Specialty Pharmacy, Specialty Distribution, and Buy and Bill channels. Ability to coordinate and mobilize key stakeholders across multiple departments with competing goals to align individuals on patient focused solutions.</li><li>Uses opportunities to understand and address customer needs. Builds strong relationships that provide market intelligence and support development of compliant and innovative programs and initiatives. Builds and maintains relationships across accounts that result in opportunities to benefit patients, physicians, and other HCPs within the geography.</li><li>Ability to achieve success in a complex, matrixed, account-based selling environment in which the need for collaboration and cross functional discipline is critical. Consistently partners with AbbVie in-field (MSLs, National Director of Accounts and Key Account Directors) to and in-house teams to identify, design, and/or adapt appropriate approaches and tactics.</li><li>Creates, develops, executes, and monitors strategic geography business plans. Determines appropriate department, channel, HCP focus and frequency by account to deliver on sales objectives. Aligns appropriate resources to support tactic execution and adjusts as needed.</li><li>Sources, interprets and utilizes key data by account to develop and maintain working account profiles and relationship maps for all territory accounts to maximize call continuum and communication. Consistently targets key stakeholders and decision makers within each hospital/institution/outpatient setting to expand physician usage and customer base.</li><li>Attend and actively participate in local boards, societies, conventions, and other HCP meetings when appropriate. Represent AbbVie and assigned products at such venues, build/improve new/existing relationships. Channel key information, developments, or findings to internal partners/stakeholders. All communications in these forums are on-label.</li><li>Complete all AbbVie required training and maintain adherence to all company policies and OEC/Legal procedures.<br>
Meet health care industry representative credentialing requirements to gain entry into facilities and organizations that are in assigned territory. These HCIR credentialing requirements may include, but are not limited to, background checks, drug screens, and proof of immunization/vaccination for various diseases.</li><li>Proactively collaborates across multiple departments within healthcare institutions and across organizations. Seamlessly works with cross-functional partners including National Director of Accounts and Key Account Directors to develop processes within the account base while working with Medical Science Liaisons to develop compliant communication strategies.</li></ul>]]></description><link>http://biotechroles.com/account-specialist-ai-riverside-ca-abbvie/6a06eee32f1861929d253224</link><guid isPermaLink="true">http://biotechroles.com/account-specialist-ai-riverside-ca-abbvie/6a06eee32f1861929d253224</guid><pubDate>Fri, 15 May 2026 10:01:07 GMT</pubDate><company>AbbVie</company><location>Riverside, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Medical Infocomm Mgr - Medical Aesth]]></title><description><![CDATA[<ol><li>执行公司既定的销售策略、计划、目标和预算，挖掘业务机会，并完成公司产品在指定区域、目标医院/机构的推广；</li><li>洞察客户机会，挖掘并掌握客户需求，能够为客户赋能，提供专业的支持和培训等；</li><li>建立、完善和维护良好的目标客户群网络；</li><li>协助地区经理和市场部等跨部门人员，落实执行公司的各类项目；根据所负责机构/医院特性定制化调整，使执行效果最优；</li><li>遵循商业行为准则，合法合理开展业务活动 ；</li><li>上级主管安排的其他任务。</li></ol>]]></description><link>http://biotechroles.com/medical-infocomm-mgr-medical-aesth-abbvie/6a06eee22f1861929d253223</link><guid isPermaLink="true">http://biotechroles.com/medical-infocomm-mgr-medical-aesth-abbvie/6a06eee22f1861929d253223</guid><pubDate>Fri, 15 May 2026 10:01:06 GMT</pubDate><company>AbbVie</company><location>Shenyang, Shenyang</location><salary>$35000-60000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Security Analyst I, Identity & Access Management]]></title><description><![CDATA[<p>This position is part of the Information Security &amp; Risk Management (ISRM) team. We are here to put our partners in a position to succeed — providing the knowledge, tools, and governance frameworks they need to use data and technology securely while managing risk at enterprise scale.</p><p>We are looking for a highly motivated, technically skilled identity professional to join our Identity and Access Management (IAM) team. This role is critical in safeguarding the enterprise by ensuring that user access is accurate, compliant, and aligned with global security standards. <strong>The IAM Senior Security Analyst I will drive the full lifecycle of identity governance across OIM, Saviynt, Ping, Active Directory, and other enterprise identity systems</strong> — enabling secure, seamless access for employees, contractors, and partners worldwide.</p><p>The ideal candidate brings deep hands-on expertise in identity administration and governance, a strong understanding of compliance frameworks, and the ability to work independently to drive improvements across people, processes, and technology.</p><p><strong>Key Responsibilities</strong></p><ul><li>Act as a subject matter expert for identity lifecycle events — joiner, mover, and leaver — across global user populations, ensuring timely and accurate execution within established SLAs</li><li>Drive access provisioning and governance activities in accordance with least-privilege and Segregation of Duties (SoD) principles, validating approvals against business rules and compliance requirements</li><li>Lead and support periodic access certification and recertification campaigns within Saviynt, identifying anomalies and driving remediation</li><li>Create, modify, and maintain federation and SSO application integrations, resolving identity-related incidents including login failures, MFA issues, and provisioning errors</li><li>Identify process improvement opportunities and develop plans of action with minimal management intervention or direction</li><li>Collaborate cross-functionally with IT support teams, application owners, and security engineers to remediate access issues and reduce manual workload through automation</li><li>Maintain documentation and audit evidence to support internal and external audits, ensuring adherence to SOX, GDPR, and ISO 27001 requirements</li><li>Contribute to enhancements in Saviynt workflows, access request forms, and role models; support rollout of new IAM capabilities and governance policies</li><li>Monitor automated provisioning workflows, escalate failures, and drive continuous improvement in IAM operational reliability</li></ul>]]></description><link>http://biotechroles.com/senior-security-analyst-i-identity-and-access-management-abbvie/6a06eee02f1861929d253222</link><guid isPermaLink="true">http://biotechroles.com/senior-security-analyst-i-identity-and-access-management-abbvie/6a06eee02f1861929d253222</guid><pubDate>Fri, 15 May 2026 10:01:04 GMT</pubDate><company>AbbVie</company><location>Singapore, Singapore</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Consumer & Customer Engagement Manager, Allergan Aesthetics]]></title><description><![CDATA[<p>The <strong>Consumer and Customer Engagement Manager</strong> is responsible for developing and executing consumer-focused marketing strategies that drive brand awareness, customer acquisition, and long-term loyalty within the aesthetic, beauty, or wellness sector. This role bridges <strong>aesthetic marketing</strong>, <strong>customer experience</strong>, and <strong>data-driven engagement</strong>, ensuring consistent, personalized, and compelling interactions across all consumer touchpoints.</p><p><strong>Key Responsibilities</strong></p><p><strong>Consumer &amp; Customer Engagement Strategy</strong></p><ul><li>Develop and lead integrated <strong>consumer and customer engagement strategies</strong> aligned with brand positioning and business objectives.</li><li>Design and manage <strong>end-to-end customer journeys</strong> across online, in-clinic, and offline channels.</li><li>Identify key consumer insights and translate them into effective marketing initiatives that enhance emotional connection and trust with the brand.</li><li>Work closely with our key account stakeholders to understand their need then develop a strategic DTC campaign with excellent in execution to help them in recruiting and maintaining their patients.</li></ul><p><strong>Aesthetic Marketing &amp; Brand Experience</strong></p><ul><li>Plan and execute <strong>aesthetic marketing campaigns</strong> across digital, social media, CRM, events, and partnerships.</li><li>Ensure all consumer-facing content reflects <strong>premium aesthetics, clinical credibility, and brand consistency</strong>.</li><li>Collaborate with creative, medical, and sales teams to develop campaigns that highlight treatments, products, and customer success stories.</li></ul><p><strong>Customer Relationship Management (CRM)</strong></p><ul><li>Own and optimize CRM programs including <strong>loyalty programs, customer retention initiatives, and lifecycle communication</strong>.</li><li>Segment customer databases based on behavior, preferences, and lifecycle stages.</li><li>Drive personalization strategies to improve engagement, repeat visits, and customer lifetime value.</li></ul><p><strong>Digital &amp; Social Engagement</strong></p><ul><li>Oversee social media and digital platforms with a focus on <strong>community building, education, and engagement</strong>, not just promotion.</li><li>Work closely with digital marketing teams to leverage paid media, influencer marketing, and social listening.</li><li>Monitor and respond to customer feedback, reviews, and conversations to protect and enhance brand reputation.</li></ul><p><strong>Data, Insights &amp; Performance Tracking</strong></p><ul><li>Track and analyze engagement KPIs</li><li>Use consumer data and market trends to continuously optimize campaign performance and customer experiences.</li><li>Prepare regular reports and actionable insights for senior management.</li></ul><p><strong>Cross-Functional Collaboration</strong></p><ul><li>Partner with sales, business excellence, clinical specialists, medical, and customer service teams to ensure seamless customer experience.</li><li>Train internal teams on customer-centric engagement practices and brand communication guidelines.</li><li>Manage external agencies and vendors, including creative, CRM, and digital partners.</li></ul>]]></description><link>http://biotechroles.com/consumer-and-customer-engagement-manager-allergan-aesthetics-abbvie/6a06eede2f1861929d253221</link><guid isPermaLink="true">http://biotechroles.com/consumer-and-customer-engagement-manager-allergan-aesthetics-abbvie/6a06eede2f1861929d253221</guid><pubDate>Fri, 15 May 2026 10:01:02 GMT</pubDate><company>AbbVie</company><location>Pathum Wan, Pathumwan</location><salary>$95000-140000</salary><type>Full-time</type></item><item><title><![CDATA[MSL]]></title><description><![CDATA[<p>• Maintain updated medical knowledge of assigned therapeutic are • Create and update medical training and communication material and deliver the training/communication efficiently • Participate proactively in PPD medical projects and events, including study operation, meeting organization, etc. as coordinator • Develop advocacy for company and product by sustained KOL and prescriber liaison • Provide medical advice on PPD product medical communication, under the guidance from medical advisors</p>]]></description><link>http://biotechroles.com/msl-abbvie/6a06eedd2f1861929d253220</link><guid isPermaLink="true">http://biotechroles.com/msl-abbvie/6a06eedd2f1861929d253220</guid><pubDate>Fri, 15 May 2026 10:01:01 GMT</pubDate><company>AbbVie</company><location>Wuhan, Wuhan</location><salary>$45000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Project Manager, Evidence Solutions]]></title><description><![CDATA[<p>JOB SUMMARY Project Manager is responsible for executing clinical studies (including but not limited to Phase IV clinical trials, epidemiology studies, Patient Report Outcome study, product registry, disease registry, data extraction and management of Investigator initiated studies) in compliance with relevant quality standards. Project Manager also takes the responsibility of clinical trial disclosure process, study drug management, sourcing process, budget management, and payment process, as well as be responsible for auditing and archiving per requirements. CORE RESPONSIBILITIES: Phase IV clinical trial Responsible for execution and management for Phase IV clinical trials which include Post-approval commitment study (PAC), Post Marketing Observational study (PMOS) and interventional studies using AbbVie product as an investigational drug. - Site selection and management: screening and selection of sites and investigators, and work within teams to provide scientific and technical support and leadership for feasibility of conducting the trial. - Develop site patient recruitment strategies. - Database and data management: establish database and Electronic Data Capture (EDC). - Budget planning and management: responsible for budget planning, phasing, daily management, and relevant financial communication. - Contract management: responsible for contract preparation, negotiation, finalization, and signature with hospitals, institutions, and vendors. - Insurance and subjects AE compensation in clinical trial as needed. - Investigational drug packaging and distribution as needed. - Responsible for regular update to cross-functional team and stakeholders on study status. - Ensure our clinical trial management system is up to date. - Support communication with biostatistics and cycle analysis/research report. Investigator initiated studies and other programs - Responsible for sponsorship qualification, contract negotiation, signature, payment, and investigational drug packaging and shipment scheduled for Investigator Initiated Studies. - Provide proper advice/support to sponsor on EC process and regulatory submission as needed. - Responsible for other data generation projects from qualification assessment to contract process and payment schedule. - Work with stakeholders to facilitate research grant, third party studies, In vivo/in vitro assessment, contract process and payment schedule if needed. Vendor management and sourcing - Responsible for vendor selection, project scope development, and oversight of vendors in compliance with AbbVie processes, procedures, and applicable regulations. - Responsible for quality control of the service provided by vendor according to AbbVie standards. People and performance management - Lead contract CRAs on site identification, qualification, initiation, monitor and study close-out visits. - Lead contract CRAs on conducting quality patient recruitment per plan, and other operational tasks in a highly efficient way. Documentation, system, and compliance - Archive all the essential documents across the project life cycle in required systems and format. Ensure the access control, version control, and information security. - Ensure all the AbbVie information assets, including electronic database on service provider side, are compliant and secured. Archive the database within AbbVie when the project is completed. Quality assurance, audit, and inspection - Ensure that all activities and interactions are conducted with due regard to all applicable industrial, global, and national laws, regulations, guidelines, codes of conduct, company policies and accepted standards of best practice. - Ensure adherence to regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), monitoring plans, and quality standards in conducting clinical research. - Monitor regulatory reforms and industry trends within country. Conduct and/or implement impact analysis of all significant changes to conform with updated regulatory/industrial regulations. - Work with relevant functions to ensure the project quality control, and no critical findings from internal audit. - Always ensure audit-readiness and inspection-readiness. Plan and conduct self-inspection working plan if needed. - Serve as a country contact for regulatory questions related to monitoring processes and procedures.</p>]]></description><link>http://biotechroles.com/project-manager-evidence-solutions-abbvie/6a06eedb2f1861929d25321f</link><guid isPermaLink="true">http://biotechroles.com/project-manager-evidence-solutions-abbvie/6a06eedb2f1861929d25321f</guid><pubDate>Fri, 15 May 2026 10:00:59 GMT</pubDate><company>AbbVie</company><location>Shanghai, Shanghai</location><salary>$45000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Account Specialist (Dermatology) - South Central]]></title><description><![CDATA[<p>Be the direct contact for key stakeholders to communicate the value proposition; be the main executor of the infield brand strategy. Develop customer relationships whilst maximising opportunities based on strong account plans.</p><p><strong>Customer selling and relationship management:</strong></p><ul><li>Drive Sales – Own the customer engagement for target HCPs across channels, to reflect customer preferences, leveraging available content and multiple engagement channels</li><li>Develops SMART pre call objectives in line with territory plans and aligned to brand strategy.</li><li>Effectively handles objections or concerns. Consistently gains a logical, reasonable call to action/close on every sales call.</li><li>Educates medical providers, other relevant decision makers and affiliated healthcare professionals.</li><li>Identifies &amp; develops disease state experts building advocacy aligned to territory plan.</li></ul><p><strong>Continuously strive to gain market intelligence:</strong></p><ul><li>Organise and manage stakeholder meetings</li><li>Differentiates AbbVie's value proposition to physicians or other stakeholders assigned from any competitors</li><li>Strong communication skills, ability to flex style based on customer insights</li></ul><p><strong>Clinical and Market Knowledge Development:</strong></p><ul><li>Deep understanding of the product and its place within the local NHS healthcare economy</li><li>Ability to navigate NHS ecosystem barriers &amp; identify opportunities to deliver collaborative results</li><li>Shares best practice to enhance our business success</li><li>Proactively initiates, develops and implements a growth plan to develop in current position and prepare for future opportunities</li><li>Demonstrates in depth disease, product, market and competitive intelligence expertise</li><li>Has a deep understanding of the multi-stakeholder environment</li></ul><p><strong>Territory Management:</strong></p><ul><li>Continuously analyses sales reports (CRM etc.) and overlays field intelligence to adapt the territory plan</li><li>Collaborates closely with medical colleagues to support customer needs and implement regional/national programs</li><li>Develops a business plan for own territory in line with brand strategy</li><li>Effectively targets and tracks resources to maximise sales opportunities.</li><li>Adheres to industry and AbbVie compliance requirements.</li></ul>]]></description><link>http://biotechroles.com/account-specialist-(dermatology)-south-central-abbvie/6a06eed92f1861929d25321e</link><guid isPermaLink="true">http://biotechroles.com/account-specialist-(dermatology)-south-central-abbvie/6a06eed92f1861929d25321e</guid><pubDate>Fri, 15 May 2026 10:00:57 GMT</pubDate><company>AbbVie</company><location>Winchester, Maidenhead</location><salary>$65000-95000</salary><type>Full-time</type></item><item><title><![CDATA[Spécialiste Senior, Communication et Formation Médicale et Scientifique]]></title><description><![CDATA[<p>AbbVie France recrute&#xa0;<strong>un.e Spécialiste Senior, Information et Communication Médicale et Scientifique&#xa0;</strong>rattaché.e au Responsable de la Division Information Médicale et Scientifique pour notre Filiale France.  &#xa0;</p><p> <u>A&#xa0;ce titre, vos principales missions seront de</u> : &#xa0;</p><ul><li> Définir, proposer et mettre en œuvre une stratégie de formation visant à développer les connaissances médicales et scientifiques des collaborateurs du Département Médical.&#xa0;</li><li>Accompagner les équipes médicales dans le processus de validation des documents initiées par le Département Médical&#xa0;</li><li>Gérer une personne, et éventuellement des étudiants en stage/alternance</li></ul><p><br>
<u>Activité Formation</u> :&#xa0;</p><ul><li>Définir la stratégie de formation des équipes médicales.&#xa0;</li><li>Être responsable de la création/validation des supports de formation sur les produits, les pathologies, la concurrence et l’environnement à destination des équipes médicales.&#xa0;</li><li>Être responsable de la mise à jour/validation des supports de formation des équipes médicales en fonction de l’évolution du contexte scientifique, médical, réglementaire, pharmaco-économique….&#xa0;</li><li>Coordonner et/ou animer des sessions de formations à destination des équipes médicales&#xa0;</li><li>En partenariat avec les Responsables des Unités Médicales, analyser les besoins individuels de formation et proposer des actions de formation adaptées&#xa0;</li></ul><p><br>
<u>Activité communication scientifique et médicale</u> :&#xa0;</p><ul><li>Coordonner et participer au circuit de validation locale des supports de présentation utilisés par les équipes médicale via l’outil informatique dédié&#xa0;</li><li>Être à jour des dernières données scientifiques sur l’aire thérapeutique dont il est responsable&#xa0;</li><li>Participer au plan de publication locale et accompagner les équipes médicales dans le suivi des étapes des soumissions dans le respect des procédures&#xa0;&#xa0;</li></ul><p><br>
<u>Activité information médicale et scientifique</u><u> :</u>&#xa0;</p><ul><li>Elaborer du contenu scientifique et médical en support des chargés d’information médicale et scientifique&#xa0;</li><li>Elaborer des réponses spécifiques non prises en charge par les chargés d’information médicale et scientifique&#xa0;</li><li>Relecture et validation des réponses spécifiques ponctuelles élaborées par les chargés d’information médicale et scientifique&#xa0;</li><li>Réaliser la veille médicale et scientifique sur les produits AbbVie dont il est responsable et partager avec les équipes médico-marketing&#xa0;</li><li>Réaliser des recherches bibliographiques sur des sujets spécifiques et en faire une synthèse&#xa0;</li></ul>]]></description><link>http://biotechroles.com/specialiste-senior-communication-et-formation-medicale-et-scientifique-abbvie/6a06eed72f1861929d25321b</link><guid isPermaLink="true">http://biotechroles.com/specialiste-senior-communication-et-formation-medicale-et-scientifique-abbvie/6a06eed72f1861929d25321b</guid><pubDate>Fri, 15 May 2026 10:00:55 GMT</pubDate><company>AbbVie</company><location>Boulogne-Billancourt, Boulogne-Billancourt</location><salary>$75000-105000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Enablement (CX)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;About Hello Heart:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Hello Heart is on a mission to make heart attacks a thing of the past.&lt;/p&gt;
&lt;p&gt;We’re an AI company focused exclusively on heart health, building a platform that predicts and prevents cardiac events before they happen—identifying risk up to 10 days in advance versus 10 years in traditional clinical models.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;This is already working at scale. Hello Heart has been shown to reduce inpatient hospital days by 47% and deliver ~$1,800 in annual savings per member.&amp;nbsp;Hello Heart is the cardiac prevention partner to over 80% of large U.S. health plans and serves hundreds of public and private employers.&lt;br&gt;&lt;br&gt;We’re defining how the #1 cause of death—heart disease—is managed in the AI era. Join us.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We&#39;re seeking a &lt;strong&gt;Senior Manager, CX Enablement&lt;/strong&gt; to help take our Customer Success team to the next stage of its evolution.&amp;nbsp; You’ll serve as a trusted operational partner to the Customer Success team’s leadership, and be a force multiplier by documenting “what good looks like” and giving the team the tools and training to execute it at scale.&amp;nbsp; If you have expertise in Customer Success enablement and are passionate about standardization, optimization and scale (while also being a fun and encouraging partner in team development), then this role is for you.&lt;/p&gt;
&lt;p&gt;This role reports to our VP of Revenue Operations &amp;amp; will play a key part in our next stage of growth.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Own, Write &amp;amp; Evolve the CS Playbook&lt;/strong&gt; - Document &amp;amp; evolve the playbook for how the CS team operates - ranging from daily activities (e.g. how to use key Salesforce reports) to macro strategy (e.g. how to design an account plan that mitigates risk).&amp;nbsp; Synthesize inputs from leadership across CS, Marketing, Product to create the source of truth “how to” document for CS.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Talk Tracks &amp;amp; Template Creation &lt;/strong&gt;- Write content for the team to execute at scale.&amp;nbsp; Examples include scripts for EBR slides, objection handling answers &amp;amp; email templates.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Synthesizing GTM Insights&lt;/strong&gt; - Monitor campaigns (e.g. EBR’s, new product launches) and bubble up themes including customer feedback, which parts of materials are/aren’t resonating &amp;amp; training needs. Be fluent in the details (e.g. based on review of Gong, internal interviews), while also being able to package up insights/recommendations to the executive audience.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Asset Management&lt;/strong&gt; - Maintain the database of GTM assets and information in Highspot. Thoughtfully organize to optimize usage, and rigorously update/prune content.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Information Funnel &lt;/strong&gt;-&amp;nbsp; Streamline the high-volume &amp;amp; diverse flow of information (GTM campaigns, operational best practices, technical product details) into digestible format &amp;amp; language.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Training&lt;/strong&gt; - Design &amp;amp; conduct engaging training &amp;amp; maintain a 3-6 month training roadmap &amp;amp; in partnership with leadership.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The ideal candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experienced using AI tools in your daily workflow&lt;/li&gt;
&lt;li&gt;7+ years of professional experience, with at least 3 years in GTM Enablement&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Expertise in enablement with Customer Success is required - you bring expertise and best practices from your experience and can help uplevel our team right away. Strong preference for specialized experience in CS, but will consider candidates with broader coverage, provided they have extensive CS experience&lt;/li&gt;
&lt;li&gt;Background in digital health, SaaS, or health tech strongly preferred&lt;/li&gt;
&lt;li&gt;Able to operate with a high degree of autonomy&lt;/li&gt;
&lt;li&gt;Exceptional organizational skills, with proven ability to manage and prioritize a high volume of projects/tasks while keeping multiple stakeholders happy&lt;/li&gt;
&lt;li&gt;Strong written skills required - extensive experience writing slide scripts, talking points, and email templates&lt;/li&gt;
&lt;li&gt;Familiarity with GTM tools such as Salesforce, Highspot, Gong, Salesloft&lt;/li&gt;
&lt;li&gt;Ability to travel up to 20% annually as needed.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;The US base salary range for this full-time position is $145,000.00 to $155,000.00. Salary ranges are determined by role and level. Compensation is determined by additional factors, including job-related skills, experience, and relevant education or training. Please note that the compensation details listed in US role postings reflect the annual salary and bonus only, and do not include equity or benefits&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Hello Heart has a positive, diverse, and supportive culture - we look for people who are collaborative, creative, and courageous. Oh, and if you want to see some recent evidence of the fun things we do at Hello Heart, check out our &lt;a href=&quot;https://www.instagram.com/helloheartapp/&quot; target=&quot;_blank&quot;&gt;Instagram page&lt;/a&gt;.&amp;nbsp;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-enablement-(cx)-hello-heart/6a069aef2f1861929d253218</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-enablement-(cx)-hello-heart/6a069aef2f1861929d253218</guid><pubDate>Fri, 15 May 2026 04:02:55 GMT</pubDate><company>Hello Heart</company><location>Remote US</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Health Plan Growth]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;About Hello Heart:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Hello Heart is on a mission to make heart attacks a thing of the past.&lt;/p&gt;
&lt;p&gt;We’re an AI company focused exclusively on heart health, building a platform that predicts and prevents cardiac events before they happen—identifying risk up to 10 days in advance versus 10 years in traditional clinical models.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;This is already working at scale. Hello Heart has been shown to reduce inpatient hospital days by 47% and deliver ~$1,800 in annual savings per member.&amp;nbsp;Hello Heart is the cardiac prevention partner to over 80% of large U.S. health plans and serves hundreds of public and private employers.&lt;br&gt;&lt;br&gt;We’re defining how the #1 cause of death—heart disease—is managed in the AI era. Join us.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;About the Role&lt;/strong&gt;:&lt;/p&gt;
&lt;p&gt;Reporting to our Chief Growth Officer, as&lt;strong&gt; Director, Health Plan Growth&lt;/strong&gt;, you are responsible for national business development/sales activities across &lt;strong&gt;targeted National Payers in the Medicare space&lt;/strong&gt;. This position develops and executes strategic approaches for new business development with both established pipeline opportunities and new targeted opportunities, working closely with the Hello Heart Health Plan Business Development team. You should be an expert at building deep relationships with large, complex partners. With excellent communication skills, you will work cross-functionally with our internal customer success, business development, and sales teams to increase care access for our members.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as a Business Development Leader for the company.&amp;nbsp; Become a deep subject matter expert in all aspects related to Hello Heart and how we can work with targeted national payers.&lt;/li&gt;
&lt;li&gt;Lead prospecting, pitching, and contracting for strategic partnerships in the &lt;strong&gt;Health Plan/Medicare &lt;/strong&gt;space.&lt;/li&gt;
&lt;li&gt;Manage and develop the Health Plan pipeline with accountability for strategic partnership targets.&lt;/li&gt;
&lt;li&gt;Negotiate and manage the execution of channel partnership agreements with Health Plans.&lt;/li&gt;
&lt;li&gt;Identify and execute partnership expansion opportunities.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;5+ years of demonstrated &lt;strong&gt;Business Development or Management Consulting experience in the Health Plan /Medicare space&lt;/strong&gt;.&lt;/li&gt;
&lt;li&gt;Experience and success in end-to-end partnerships by developing an overall strategy to build/maintain pipelines and executing through prospecting, relationship building, pitching, and contracting.&lt;/li&gt;
&lt;li&gt;100% independent with a demonstrated strong problem-solving skill set.&lt;/li&gt;
&lt;li&gt;A strong team player who can work with multiple functions within the company.&lt;/li&gt;
&lt;li&gt;Ability to effectively escalate to leadership matters that have a strategic impact&lt;/li&gt;
&lt;li&gt;Go-getter who operates with a sense of urgency in a fast-paced environment.&lt;/li&gt;
&lt;li&gt;Prior experience in a startup.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Stellar written and verbal communication and presentation skills.&lt;/li&gt;
&lt;li&gt;Highly organized, able to multitask, and easily adaptable to change.&lt;/li&gt;
&lt;li&gt;Happy to always roll up your sleeves to help and get things done.&lt;/li&gt;
&lt;li&gt;Ability to&lt;strong&gt; travel 50%&lt;/strong&gt;. Preference for candidates currently based in the Midwest or the West Coast.&lt;br&gt;&lt;br&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;The US base salary range for this full-time position is $175,000.00 to $200,000.00. Salary ranges are determined by role and level. Compensation is determined by additional factors, including job-related skills, experience, and relevant education or training. Please note that the compensation details listed in US role postings reflect the annual salary and bonus only, and do not include equity or benefits.&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Hello Heart has a positive, diverse, and supportive culture - we look for people who are collaborative, creative, and courageous. Oh, and if you want to see some recent evidence of the fun things we do at Hello Heart, check out our &lt;a href=&quot;https://www.instagram.com/helloheartapp/&quot; target=&quot;_blank&quot;&gt;Instagram page&lt;/a&gt;.&amp;nbsp;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-health-plan-growth-hello-heart/6a069aee2f1861929d253217</link><guid isPermaLink="true">http://biotechroles.com/director-health-plan-growth-hello-heart/6a069aee2f1861929d253217</guid><pubDate>Fri, 15 May 2026 04:02:54 GMT</pubDate><company>Hello Heart</company><location>Remote US</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Process Engineering Associate II]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Ready to redefine what&#39;s possible in molecular diagnostics?&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Join a team of brilliant, passionate innovators determined to transform healthcare. At BillionToOne, we&#39;ve built a category-defining, publicly traded company on Nasdaq where transparency fuels trust, collaboration drives breakthroughs, and every contribution moves the needle on our mission to make life-changing diagnostics accessible to all. We don&#39;t just aim for incremental improvements; we build products that are 10x better than anything that exists today.&lt;/p&gt;
&lt;p&gt;Our scientists, engineers, sales executives, and visionaries are united by an unwavering commitment to changing the standard of care in prenatal and cancer diagnostics. This is where cutting-edge science meets human compassion, and every innovation you contribute helps remove the fear of the unknown from some of life&#39;s most critical medical moments.&lt;/p&gt;
&lt;p&gt;If you&#39;re driven by purpose, energized by innovation, and ready to help shape the future of precision medicine at scale, this is where you belong.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;We seek a &lt;strong&gt;Process Engineering Associate II&lt;/strong&gt; whose interests span molecular diagnostics, process optimization, and quantitative problem solving. In this role you will (1) drive process improvement and development to enhance clinical assay performance, (2) support technology transfer from R&amp;amp;D into our high-throughput CLIA lab, and (3) troubleshoot and identify root causes of recurring errors to enable long-term corrective actions. You will also play a key role in standing up our newly built lab in Austin, TX. You will leverage and deepen your expertise across molecular techniques, laboratory automation, and data analysis while contributing directly to category-defining NIPT assays that transform patient lives one molecule at a time. This onsite position starts at our Union City, CA laboratory and will relocate to Austin, TX in summer 2027. The Process Engineering Associate II reports to the Senior Development Scientist.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, execute, and analyze wet lab experiments to improve process efficiency and assay reliability.&lt;/li&gt;
&lt;li&gt;Evaluate new molecular biology techniques and technologies to enhance assay performance.&lt;/li&gt;
&lt;li&gt;Perform complex manual and automated laboratory procedures (e.g. nucleic acid extraction, PCR, sequencing, reagent preparation).&lt;/li&gt;
&lt;li&gt;Conduct assay validation studies to qualify new and improved assays for clinical use at both sites.&lt;/li&gt;
&lt;li&gt;Build data analysis and software tools to monitor process health, surface sources of error, and accelerate troubleshooting.&lt;/li&gt;
&lt;li&gt;Collaborate with the team to analyze complex data, diagnose issues, and implement solutions.&lt;/li&gt;
&lt;li&gt;Support technology transfer to our new Austin, TX CLIA lab to bring the new site online.&lt;/li&gt;
&lt;li&gt;Present project progress, data, and technical insights to the team and department.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS or MS in a relevant scientific or engineering discipline (e.g., Bioengineering, Chemical Engineering, Molecular Biology, Biochemistry, Chemistry, or Physics).&lt;/li&gt;
&lt;li&gt;At least 1 year of hands-on lab research experience, including core molecular biology techniques (e.g., PCR, DNA/RNA extraction, sequencing).&lt;/li&gt;
&lt;li&gt;Exceptional analytical reasoning and troubleshooting skills, with experience in data analysis (bioinformatics, statistical analysis, or similar) and comfort using modern AI tools.&lt;/li&gt;
&lt;li&gt;Strong mathematical and statistical aptitude, with a process- and systems-level mindset.&lt;/li&gt;
&lt;li&gt;Excellent attention to detail and clear written and verbal communication.&lt;/li&gt;
&lt;li&gt;Driven, creative, and persistent, with a willingness to go above and beyond and to work both independently and collaboratively in a fast-paced environment.&lt;/li&gt;
&lt;li&gt;Willingness to relocate from Union City, CA to Austin, TX in summer 2027.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Nice-to-haves:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Start-up experience.&lt;/li&gt;
&lt;li&gt;Previous automation or clinical laboratory experience.&lt;/li&gt;
&lt;li&gt;Experience with next-generation sequencing (NGS) and library preparation.&lt;/li&gt;
&lt;li&gt;Experience in a cell-free DNA setting.&lt;/li&gt;
&lt;li&gt;Prior experience with technology transfer, assay validation, or new lab/site standup.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Benefits And Perks:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients&lt;/li&gt;
&lt;li&gt;Open, transparent culture that includes weekly Town Hall meetings&lt;/li&gt;
&lt;li&gt;The ability to indirectly or directly change the lives of hundreds of thousands patients&lt;/li&gt;
&lt;li&gt;Multiple medical benefit options; employee premiums paid 100% of select plans, dependents covered up to 80%&lt;/li&gt;
&lt;li&gt;Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)&lt;/li&gt;
&lt;li&gt;Free UNITY Complete NIPT testing for employees &amp;amp; spouses&lt;/li&gt;
&lt;li&gt;Supplemental fertility benefits coverage&lt;/li&gt;
&lt;li&gt;Retirement savings program including a 4% Company match&lt;/li&gt;
&lt;li&gt;Increase paid time off with increased tenure&lt;/li&gt;
&lt;li&gt;Latest and greatest hardware (laptop, lab equipment, facilities)&lt;/li&gt;
&lt;li&gt;Free daily on-site lunches provided from top eateries&lt;/li&gt;
&lt;li&gt;A variety of perks on campus (state of the art gym, restaurant)&lt;/li&gt;
&lt;li&gt;Free on-site EV charging (compatible with all EVs, including Tesla)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At BillionToOne, we are proud to offer a combination of a (1) base pay range (actual amount offered is based on experience and salary/equity options split that the candidate chooses), (2) generous equity options offering, (3) corporate bonus program, on top of (4) industry leading company benefits (free healthcare options, 401k match, very generous fully paid parental leave, etc.).&lt;/p&gt;
&lt;p&gt;For this position, we offer a total compensation package of &lt;span data-sheets-root=&quot;1&quot;&gt;$104,322 &lt;/span&gt;per year, including a base pay range of &lt;span data-sheets-root=&quot;1&quot;&gt;$75,029 &lt;/span&gt;- &lt;span data-sheets-root=&quot;1&quot;&gt;$85,748&lt;/span&gt;&lt;span data-sheets-root=&quot;1&quot;&gt;&amp;nbsp;&lt;/span&gt;per year.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;BillionToOne is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;For more information about how we protect your information, we encourage you to review our &lt;a href=&quot;https://billiontoone.com/privacy-policy/&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;BillionToOne is a next-generation molecular diagnostics company on a mission to make powerful, accurate diagnostic tests accessible to everyone. Our revolutionary QCT molecular counting technology enhances disease detection resolution by over a thousandfold using cell-free DNA,a breakthrough that has already transformed the lives of over half a million patients worldwide.&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;Our Impact&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;&lt;a href=&quot;https://www.unityscreen.com/&quot;&gt;&lt;strong&gt;Unity Complete™&lt;/strong&gt;&lt;/a&gt; is the only non-invasive prenatal screen capable of assessing fetal risk for both common recessive conditions and aneuploidies from a single maternal blood sample. Our &lt;a href=&quot;https://www.northstaronc.com/&quot;&gt;&lt;strong&gt;Northstar®&lt;/strong&gt;&lt;/a&gt; liquid biopsy test uniquely combines treatment selection with real-time monitoring, giving oncologists unprecedented precision in cancer care.&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;Our Growth&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;From $0 to $150M+ in Annual Recurring Revenue in just five years. In 2025, we completed one of the most successful IPOs for a medical diagnostics company, building on nearly $400M in private funding,including our $130M Series D in 2024 and backed by world-class investors including Hummingbird, Adams Street Partners, Neuberger Berman, Baillie Gifford, and Premji Invest.&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;Our Recognition&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;Forbes named us one of &lt;strong&gt;America&#39;s Best Startup Employers for 2025&lt;/strong&gt; and we&#39;re &lt;strong&gt;Great Place to Work certified&lt;/strong&gt;, with 100% of our people willing to go the extra mile, even as we&#39;ve scaled to over 700 employees.&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;Our Future&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;Headquartered in Menlo Park with facilities in Union City, CA, and a new lab opening in Austin, TX in 2027, we&#39;re continuing to push the boundaries of what&#39;s possible in molecular diagnostics. We&#39;re just getting started.&lt;/p&gt;
&lt;hr&gt;
&lt;p&gt;Ready to help us change the world, one molecule at a time? Learn more at&lt;a href=&quot;https://www.billiontoone.com&quot;&gt; billiontoone.com&lt;/a&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/process-engineering-associate-ii-billion-to-one/6a069aee2f1861929d253215</link><guid isPermaLink="true">http://biotechroles.com/process-engineering-associate-ii-billion-to-one/6a069aee2f1861929d253215</guid><pubDate>Fri, 15 May 2026 04:02:54 GMT</pubDate><company>Billion To One</company><location>Union City, CA</location><salary>$75000-95000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Credentialing, Licensing & Provider Operations Coordinator - Remote]]></title><description><![CDATA[&lt;h2 data-section-id=&quot;1jjwpys&quot; data-start=&quot;513&quot; data-end=&quot;525&quot;&gt;About Tia&lt;/h2&gt;
&lt;p data-start=&quot;527&quot; data-end=&quot;931&quot;&gt;Tia is building a new model for women’s healthcare, one that treats women as whole people, not separate conditions or life stages. By integrating primary care, mental health, gynecology, dermatology, and wellness across both in-person and virtual settings, Tia is improving outcomes, lowering costs, and creating a better experience for patients and providers alike.&lt;/p&gt;
&lt;h2 data-section-id=&quot;v4pco1&quot; data-start=&quot;435&quot; data-end=&quot;511&quot;&gt;Senior Credentialing, Licensing &amp;amp; Provider Operations Coordinator - Remote&lt;/h2&gt;
&lt;p data-start=&quot;952&quot; data-end=&quot;1138&quot;&gt;We’re hiring a &lt;strong data-start=&quot;967&quot; data-end=&quot;1036&quot;&gt;Senior Credentialing, Licensing &amp;amp; Provider Operations Coordinator&lt;/strong&gt; to manage credentialing, licensing, and provider readiness workflows across Tia’s growing care model.&lt;/p&gt;
&lt;p data-start=&quot;1140&quot; data-end=&quot;1455&quot;&gt;In this role, you will help ensure providers are licensed, credentialed, enrolled, compliant, and ready to see patients on time. You will manage complex trackers, monitor expirables, coordinate with providers and external partners, and support Clinical Operations with high-priority provider operations initiatives.&lt;/p&gt;
&lt;p data-start=&quot;1457&quot; data-end=&quot;1660&quot;&gt;This role is a great fit for someone with strong credentialing and licensing experience who is highly organized, detail-oriented, proactive, and comfortable owning complex workflows from start to finish.&lt;/p&gt;
&lt;hr&gt;
&lt;h2 data-section-id=&quot;1irn8v3&quot; data-start=&quot;1662&quot; data-end=&quot;1672&quot;&gt;Why Tia&lt;/h2&gt;
&lt;ul data-start=&quot;1674&quot; data-end=&quot;2098&quot;&gt;
&lt;li data-section-id=&quot;1u0z0rm&quot; data-start=&quot;1674&quot; data-end=&quot;1735&quot;&gt;Opportunity to help scale a new model of women’s healthcare&lt;/li&gt;
&lt;li data-section-id=&quot;13um4ya&quot; data-start=&quot;1736&quot; data-end=&quot;1808&quot;&gt;Mission-driven team focused on access, quality, and patient experience&lt;/li&gt;
&lt;li data-section-id=&quot;19zfdfu&quot; data-start=&quot;1809&quot; data-end=&quot;1896&quot;&gt;High-impact role supporting provider readiness and compliance across multiple markets&lt;/li&gt;
&lt;li data-section-id=&quot;7zzqku&quot; data-start=&quot;1897&quot; data-end=&quot;1998&quot;&gt;Cross-functional partnership with Clinical Operations, People Ops, providers, and external partners&lt;/li&gt;
&lt;li data-section-id=&quot;l3emp7&quot; data-start=&quot;1999&quot; data-end=&quot;2098&quot;&gt;Opportunity to strengthen and improve credentialing, licensing, and provider operations workflows&lt;/li&gt;
&lt;/ul&gt;
&lt;hr&gt;
&lt;h2 data-section-id=&quot;1wajri6&quot; data-start=&quot;2100&quot; data-end=&quot;2117&quot;&gt;What You’ll Do&lt;/h2&gt;
&lt;ul data-start=&quot;2119&quot; data-end=&quot;3519&quot;&gt;
&lt;li data-section-id=&quot;1hqhzi6&quot; data-start=&quot;2119&quot; data-end=&quot;2249&quot;&gt;&lt;strong data-start=&quot;2121&quot; data-end=&quot;2158&quot;&gt;Credentialing &amp;amp; Re-Credentialing:&lt;/strong&gt; Manage day-to-day credentialing and re-credentialing workflows for Tia’s provider network.&lt;/li&gt;
&lt;li data-section-id=&quot;axmpiy&quot; data-start=&quot;2251&quot; data-end=&quot;2450&quot;&gt;&lt;strong data-start=&quot;2253&quot; data-end=&quot;2280&quot;&gt;Licensing Coordination:&lt;/strong&gt; Support medical licensing workflows for MDs, DOs, NPs, PAs, and RNs across multiple states, including tracking requirements, deadlines, renewals, and application status.&lt;/li&gt;
&lt;li data-section-id=&quot;wrtzrb&quot; data-start=&quot;2452&quot; data-end=&quot;2597&quot;&gt;&lt;strong data-start=&quot;2454&quot; data-end=&quot;2477&quot;&gt;Provider Readiness:&lt;/strong&gt; Track onboarding progress and help ensure providers are licensed, credentialed, enrolled, and compliant before go-live.&lt;/li&gt;
&lt;li data-section-id=&quot;boot2g&quot; data-start=&quot;2599&quot; data-end=&quot;2753&quot;&gt;&lt;strong data-start=&quot;2601&quot; data-end=&quot;2630&quot;&gt;APP Supervision Tracking:&lt;/strong&gt; Maintain tracking for APP supervision agreements, collaborative practice filings, and related state-specific requirements.&lt;/li&gt;
&lt;li data-section-id=&quot;1qg3ebz&quot; data-start=&quot;2755&quot; data-end=&quot;2946&quot;&gt;&lt;strong data-start=&quot;2757&quot; data-end=&quot;2790&quot;&gt;Compliance &amp;amp; Audit Readiness:&lt;/strong&gt; Maintain accurate, audit-ready provider files and monitor expirables such as licenses, DEA registrations, certifications, and other required documentation.&lt;/li&gt;
&lt;li data-section-id=&quot;1agvdd8&quot; data-start=&quot;2948&quot; data-end=&quot;3142&quot;&gt;&lt;strong data-start=&quot;2950&quot; data-end=&quot;2983&quot;&gt;Partner &amp;amp; Provider Follow-Up:&lt;/strong&gt; Communicate with providers, internal teams, health system partners, credentialing teams, and licensing entities to move open items forward and resolve delays.&lt;/li&gt;
&lt;li data-section-id=&quot;1uniszx&quot; data-start=&quot;3144&quot; data-end=&quot;3344&quot;&gt;&lt;strong data-start=&quot;3146&quot; data-end=&quot;3183&quot;&gt;Operational Tracking &amp;amp; Reporting:&lt;/strong&gt; Maintain trackers, update status reports, flag risks early, and communicate timelines, blockers, and next steps to Clinical Operations and physician leadership.&lt;/li&gt;
&lt;li data-section-id=&quot;n1vyev&quot; data-start=&quot;3346&quot; data-end=&quot;3519&quot;&gt;&lt;strong data-start=&quot;3348&quot; data-end=&quot;3377&quot;&gt;Cross-Functional Support:&lt;/strong&gt; Partner with People Ops, Clinical Ops, and other internal teams to support provider onboarding, compliance, and provider operations projects.&lt;/li&gt;
&lt;/ul&gt;
&lt;hr&gt;
&lt;h2 data-section-id=&quot;1lpl61x&quot; data-start=&quot;3521&quot; data-end=&quot;3541&quot;&gt;What You’ll Bring&lt;/h2&gt;
&lt;h3 data-section-id=&quot;14esvje&quot; data-start=&quot;3543&quot; data-end=&quot;3559&quot;&gt;Requirements&lt;/h3&gt;
&lt;ul data-start=&quot;3561&quot; data-end=&quot;4578&quot;&gt;
&lt;li data-section-id=&quot;9xty5p&quot; data-start=&quot;3561&quot; data-end=&quot;3707&quot;&gt;3+ years of experience in healthcare operations, credentialing, licensing, provider enrollment, provider onboarding, or provider data management&lt;/li&gt;
&lt;li data-section-id=&quot;1nmzcr&quot; data-start=&quot;3708&quot; data-end=&quot;3821&quot;&gt;Experience supporting credentialing and/or licensing workflows for providers such as MDs, DOs, NPs, PAs, or RNs&lt;/li&gt;
&lt;li data-section-id=&quot;7v24mm&quot; data-start=&quot;3822&quot; data-end=&quot;3942&quot;&gt;Familiarity with medical licensing boards, CAQH, payer enrollment, provider documentation, and credentialing processes&lt;/li&gt;
&lt;li data-section-id=&quot;ckgncx&quot; data-start=&quot;3943&quot; data-end=&quot;4026&quot;&gt;Strong attention to detail and ability to manage complex provider data accurately&lt;/li&gt;
&lt;li data-section-id=&quot;cgora1&quot; data-start=&quot;4027&quot; data-end=&quot;4150&quot;&gt;Strong organizational skills with the ability to manage multiple providers, deadlines, applications, and renewals at once&lt;/li&gt;
&lt;li data-section-id=&quot;1n9qpq2&quot; data-start=&quot;4151&quot; data-end=&quot;4262&quot;&gt;Comfort working in Google Sheets, Microsoft Excel, trackers, and credentialing or provider operations systems&lt;/li&gt;
&lt;li data-section-id=&quot;5ogk14&quot; data-start=&quot;4263&quot; data-end=&quot;4342&quot;&gt;Clear, proactive communication style with strong follow-up and follow-through&lt;/li&gt;
&lt;li data-section-id=&quot;1bfo04f&quot; data-start=&quot;4343&quot; data-end=&quot;4505&quot;&gt;Ability to partner professionally with providers, physician leadership, internal teams, health system partners, and external credentialing or licensing entities&lt;/li&gt;
&lt;li data-section-id=&quot;gs86yp&quot; data-start=&quot;4506&quot; data-end=&quot;4578&quot;&gt;Comfort working in a fast-paced environment where priorities may shift&lt;/li&gt;
&lt;/ul&gt;
&lt;h3 data-section-id=&quot;gxq2rq&quot; data-start=&quot;4580&quot; data-end=&quot;4596&quot;&gt;Nice to Have&lt;/h3&gt;
&lt;ul data-start=&quot;4598&quot; data-end=&quot;4943&quot;&gt;
&lt;li data-section-id=&quot;szozji&quot; data-start=&quot;4598&quot; data-end=&quot;4688&quot;&gt;Experience in digital health, telehealth, startup, or high-growth healthcare environment&lt;/li&gt;
&lt;li data-section-id=&quot;dfh49w&quot; data-start=&quot;4689&quot; data-end=&quot;4760&quot;&gt;Experience supporting multi-state provider licensing or credentialing&lt;/li&gt;
&lt;li data-section-id=&quot;1ubsjg5&quot; data-start=&quot;4761&quot; data-end=&quot;4844&quot;&gt;Experience with APP supervision agreements or collaborative practice requirements&lt;/li&gt;
&lt;li data-section-id=&quot;198hllg&quot; data-start=&quot;4845&quot; data-end=&quot;4943&quot;&gt;Experience building, improving, or standardizing trackers, workflows, or documentation processes&lt;/li&gt;
&lt;/ul&gt;
&lt;hr&gt;
&lt;h2 data-section-id=&quot;maw0ah&quot; data-start=&quot;4945&quot; data-end=&quot;4961&quot;&gt;Work Location&lt;/h2&gt;
&lt;p data-start=&quot;4963&quot; data-end=&quot;5063&quot;&gt;This is a remote role. This position may require occasional attendance at company or team off-sites.&lt;/p&gt;
&lt;hr&gt;
&lt;h2 data-section-id=&quot;sov3bn&quot; data-start=&quot;5065&quot; data-end=&quot;5091&quot;&gt;Compensation &amp;amp; Benefits&lt;/h2&gt;
&lt;p data-start=&quot;5093&quot; data-end=&quot;5331&quot;&gt;Tia is committed to pay equity and pay transparency. Compensation for this role will be determined based on job-related factors, including experience, skills, qualifications, location, role leveling, business needs, and market conditions.&lt;/p&gt;
&lt;p data-start=&quot;5333&quot; data-end=&quot;5382&quot;&gt;The expected compensation range for this role is: &lt;strong data-start=&quot;5384&quot; data-end=&quot;5412&quot;&gt;$70,000 - $9&lt;/strong&gt;&lt;strong data-start=&quot;5384&quot; data-end=&quot;5412&quot;&gt;0,000 per year&lt;/strong&gt;&lt;/p&gt;
&lt;p data-start=&quot;5414&quot; data-end=&quot;5443&quot;&gt;You may also be eligible for:&lt;/p&gt;
&lt;ul data-start=&quot;5445&quot; data-end=&quot;5628&quot;&gt;
&lt;li data-section-id=&quot;tdi03w&quot; data-start=&quot;5445&quot; data-end=&quot;5501&quot;&gt;Medical, dental, and vision benefits effective day one&lt;/li&gt;
&lt;li data-section-id=&quot;1i4yz26&quot; data-start=&quot;5502&quot; data-end=&quot;5562&quot;&gt;Paid time off, sick leave, and dedicated learning time off&lt;/li&gt;
&lt;li data-section-id=&quot;bpvg8o&quot; data-start=&quot;5563&quot; data-end=&quot;5597&quot;&gt;Professional development support&lt;/li&gt;
&lt;li data-section-id=&quot;1fyx2ba&quot; data-start=&quot;5598&quot; data-end=&quot;5628&quot;&gt;Other role-specific benefits&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-credentialing-licensing-and-provider-operations-coordinator-remote-tia/6a069aeb2f1861929d253214</link><guid isPermaLink="true">http://biotechroles.com/senior-credentialing-licensing-and-provider-operations-coordinator-remote-tia/6a069aeb2f1861929d253214</guid><pubDate>Fri, 15 May 2026 04:02:51 GMT</pubDate><company>Tia</company><location>Corporate (Remote)</location><salary>$75000-95000</salary><type>Full-time</type></item><item><title><![CDATA[Physician - Full-Spectrum Primary Care  - NYC - Talent Community]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Talent Community: Physician (MD/DO): Primary Care &amp;amp; Gynecology&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is on a mission to transform healthcare for women by increasing access to and improving the experience of key preventive healthcare services. Known as the best and only way to both transform outcomes and reduce cost, Tia’s preventive care model focuses on integrating key services across primary care, mental health, gynecology, dermatology and other wellness services. Tia is trailblazing a new paradigm for women’s healthcare that treats women as whole people vs. parts or life stages.&amp;nbsp; Blending in-person and virtual care services, Tia’s “Whole Woman, Whole Life” care model is a unique and “life-long” model for women’s care. By making women’s health higher quality and lower cost, Tia makes women healthier, providers happier, and the business of care delivery stronger — setting a new standard of care for women everywhere.&lt;/p&gt;
&lt;p&gt;Read more about Tia’s:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Products:&amp;nbsp;&lt;a href=&quot;https://asktia.com/article/what-is-product-at-tia&quot;&gt;https://asktia.com/article/what-is-product-at-tia&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Services:&amp;nbsp;&lt;a href=&quot;https://asktia.com/&quot;&gt;https://asktia.com/&lt;/a&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Care principles:&amp;nbsp;&lt;a href=&quot;https://www.asktia.com/care-philosophy/&quot;&gt;https://www.asktia.com/care-philosophy/&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are constantly building our talent pipeline and welcome conversations with physicians for both current openings and future roles as Tia grows. We’re looking to connect with physicians passionate about providing comprehensive primary care to women for Tia’s&lt;strong&gt; New York City&lt;/strong&gt; area clinics. We are interested in connecting with &lt;strong&gt;part time&lt;/strong&gt;&amp;nbsp;and&amp;nbsp;&lt;strong&gt;full time interested providers.&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;As a Physician (MD/DO) at Tia you’ll be integral to the excellent care we provide. Your clinical expertise related to the full spectrum of providing affirming primary care for women including: preventative care, holistic primary care and acute and chronic disease management and your desire to teach and collaborate plays an integral part of our clinical team. Board certification or board eligible in Family Medicine or Internal Medicine is preferred but we will consider other relevant specialties.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Physicians are a critical member of our interdisciplinary care team - and this role affords you the opportunity to provide direct patient care but also engage in teaching and collaboration as well as the unique opportunity to partner with the Tia technical teams to contribute to the technology life cycle of the products and tools you will use to care for patients.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;A bit about you:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Values and abilities you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re motivated to elevate women’s care by bringing a shared-decision making approach to women’s health.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You are comfortable managing a variety of clinical cases that may come your way - and approach clinical care with curiosity, warmth and collaboration.&lt;/li&gt;
&lt;li&gt;You’re facile with technology and interested in the process of developing new technology to support high quality clinical care.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re data driven and consistently incorporate new and evolving research into your day-to-day practice&lt;/li&gt;
&lt;li&gt;You are excited about teaching and collaborating with an interdisciplinary team - including nurse practitioners, acupuncture providers and support staff.&lt;/li&gt;
&lt;li&gt;You are a tolerant and inclusive thinker.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Skills and assets you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re a board certified or board eligible Physician (Family Medicine, Internal Medicine, and Gynecology preferred), in the state of&amp;nbsp;&lt;strong&gt;New York&lt;/strong&gt;, with an unrestricted license, able to provide primary care and support of all aspects of women’s health with compassion and empathy&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re adept at providing primary care services to women including: preventative care, hypertension management, diabetes management, urgent care concerns (coughs, sore throat, abdominal pain, etc), basic dermatological condition management, STD screens, UTI &amp;amp; vaginal infections consults, pelvic pain, vaginal bleeding, birth control counseling, etc and are motivated to deliver this care and collaborate with other members of the care team to ensure every Tia patient receives excellent care.&lt;/li&gt;
&lt;li&gt;You’re highly tech savvy&lt;/li&gt;
&lt;li&gt;You’re willing to work evenings + weekends as needed by schedule.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re authorized to work in the US&lt;/li&gt;
&lt;li&gt;You’re willing and eligible to be credentialed with our academic partners&lt;/li&gt;
&lt;li&gt;You’re able to serve as a collaborating physician for our NY nurse practitioners&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other “nice to have” skills:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;As an organization that seeks to create an environment for all women to feel safe, heard, recognized and avowed in their health, bodies and lives, we are consistently seeking providers with backgrounds that are meaningfully different from those already forming our team. You bring a diverse background, a range of care experiences in different communities or various modalities.&lt;/li&gt;
&lt;li&gt;Experience or formal training weaving integrative medicine practices into your care plan development.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Tia requires that Physicians complete credentialing with specified payors and that you authorize Tia to complete this credentialing through our preferred vendors.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Benefits&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Talented and collaborative team who will support and collaborate with you&lt;/li&gt;
&lt;li&gt;Competitive salary with quarterly bonus program in place for clinicians&lt;/li&gt;
&lt;li&gt;Paid time off, paid sick leave, paid learning time off&lt;/li&gt;
&lt;li&gt;Comprehensive benefits package effective day one, including medical, dental &amp;amp; vision&lt;/li&gt;
&lt;li&gt;Medical malpractice coverage&lt;/li&gt;
&lt;li&gt;Reimbursed for state licenses, Board Certification, and BLS certification. DEA will be reimbursed where it is required for practice.&lt;/li&gt;
&lt;li&gt;Complimentary subscriptions to educational tools such as UptoDate along with extensive internal educational resources and monthly clinical training opportunities&lt;/li&gt;
&lt;li&gt;Access to AI documentation software drastically reducing administrative burden of clinical documentation&lt;/li&gt;
&lt;li&gt;10-40 hour/week role depending on your preference (benefits start at 30 hours)&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Us:&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Tia is on a mission to transform healthcare for women. We are building a high-quality, multi-specialty medical home designed specifically for women — integrating primary care, gynecology, mental health, dermatology and evidence-based wellness into one coordinated experience across in-person centers and a robust virtual platform.&lt;/p&gt;
&lt;p&gt;Tia is technology-enabled, advancing and scaling excellent care through a proprietary clinical and operational platform that supports clinicians, strengthens care continuity, and improves outcomes.&lt;/p&gt;
&lt;p&gt;We are deepening and expanding one of the most comprehensive preventive care models for women on the market — with a growing focus on cardiometabolic health, longitudinal data, and earlier risk detection across the lifespan. By integrating technology, structured clinical pathways, and mission-aligned interdisciplinary teams, Tia delivers consistently strong clinical outcomes and a differentiated care experience for women.&lt;/p&gt;
&lt;p&gt;Tia is a Series D, venture-backed company with more than 120,000 women who trust Tia for their care, across four markets, supported by a national virtual platform. In each market, we partner with leading health systems to expand access, strengthen primary care, and improve quality for women at scale.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Tia’s Culture:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is building a culture of excellence — in people, process and product. This is our northstar value;&lt;/p&gt;
&lt;p&gt;What is excellence, exactly?&lt;/p&gt;
&lt;p&gt;Excellence about constantly elevating yourself, it is the process of constantly striving to perform to the best of your abilities, and identifying your top potential through constant learning, experimentation and evolution. Excellence is not about achieving perfection, as that insinuates a pinnacle. Instead, in our terms, excellence is about the pursuit of constant improvement. We’re looking for people who want to go on that hard journey of constantly setting new personal records, and organizational records.&lt;/p&gt;
&lt;p&gt;We practice excellence at Tia by demonstrating the following types of behaviors: We chose (and actively choose) excellence as Tia’s highest order value because it crystalizes into one word several behaviors that we hold dear, specifically:&lt;/p&gt;
&lt;p&gt;A drive to constantly improve through experimentation, reflection. and an insatiable growth mindset — said another way, we’re energized by the possibility of invention, innovation, and iteration&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Being present in and grateful for the journey — not just the goal line. Perfection is static. Excellence is a process (more on this important distinction below)&lt;/li&gt;
&lt;li&gt;Asking why, then why again — because accepting “this is just the way it is” is not good enough&lt;/li&gt;
&lt;li&gt;Grit &amp;amp; perseverance — a maker mentality that involves “rolling up your sleeves”, but also deep care for oneself and for others&lt;/li&gt;
&lt;li&gt;A commitment to uncovering talents to unlock “rock star” potential across every individual&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Furthermore, excellence reflects the “bigness” and the “boldness” of Tia’s mission and vision — a world in which every woman can achieve optimal health, as defined by herself.&lt;/p&gt;
&lt;p&gt;Said another way, Tia’s mission is NOT to make healthcare incrementally better for women. Instead, we’ve intentionally set out to create a fundamentally new paradigm for modern women’s healthcare that’s truly excellent. We believe that creating a company that operates in a culture of excellence will manifest in our product. Reaching this goal is not an overnight pursuit or a “one and done.” We have not and will not “get it right” with the first swing. Rather, this higher order goal is a moving target — one we have not and will not ever fully “achieve.” By design, we will never be “done” with this work, but instead, we will be continuously in pursuit of our mission. It is this continuous pursuit — the journey, not the finish line — that truly embodies excellence.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;This position may require attendance at company and team off-sites.&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;Unfortunately, scams targeting job seekers are on the rise. To protect yourself, know that we will never ask for payment, gift cards, or sensitive financial information during our hiring process. All communication from our team will come from an official company email address (@asktia.com). If something feels off, trust your instincts and reach out to us directly at &lt;/em&gt;&lt;em&gt;peopleservices@asktia.com&lt;/em&gt;&lt;em&gt;.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Tia is an equal opportunity employer. We believe that diversity of experience, perspectives, and background will lead to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are committed to collaborative problem solving, creating high-quality and user-centric products, and want to make waves in women&#39;s healthcare, join us!&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;br&gt;&lt;br&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/physician-full-spectrum-primary-care-nyc-talent-community-tia/6a069ae92f1861929d253213</link><guid isPermaLink="true">http://biotechroles.com/physician-full-spectrum-primary-care-nyc-talent-community-tia/6a069ae92f1861929d253213</guid><pubDate>Fri, 15 May 2026 04:02:49 GMT</pubDate><company>Tia</company><location>Brooklyn, New York, United States; Manhattan, New York, United States</location><salary>$220000-320000</salary><type>Full-time</type></item><item><title><![CDATA[Physician - Full-Spectrum Primary Care  - Los Angeles - Talent Community]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Talent Community: Physician (MD/DO): Primary Care &amp;amp; Gynecology&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is on a mission to transform healthcare for women by increasing access to and improving the experience of key preventive healthcare services. Known as the best and only way to both transform outcomes and reduce cost, Tia’s preventive care model focuses on integrating key services across primary care, mental health, gynecology, dermatology and other wellness services. Tia is trailblazing a new paradigm for women’s healthcare that treats women as whole people vs. parts or life stages.&amp;nbsp; Blending in-person and virtual care services, Tia’s “Whole Woman, Whole Life” care model is a unique and “life-long” model for women’s care. By making women’s health higher quality and lower cost, Tia makes women healthier, providers happier, and the business of care delivery stronger — setting a new standard of care for women everywhere.&lt;/p&gt;
&lt;p&gt;Read more about Tia’s:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Products: &lt;a href=&quot;https://asktia.com/article/what-is-product-at-tia&quot;&gt;https://asktia.com/article/what-is-product-at-tia&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Services: &lt;a href=&quot;https://asktia.com/&quot;&gt;https://asktia.com/&lt;/a&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Care principles: &lt;a href=&quot;https://www.asktia.com/care-philosophy/&quot;&gt;https://www.asktia.com/care-philosophy/&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are constantly building our talent pipeline and welcome conversations with physicians for both current openings and future roles as Tia grows. We’re looking to connect with physicians passionate about providing comprehensive primary care to women for Tia’s&lt;strong&gt; Los Angeles&lt;/strong&gt; area clinics (Both east and west LA). We are interested in connecting with &lt;strong&gt;part time&lt;/strong&gt; and &lt;strong&gt;full time interested providers.&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;As a Physician (MD/DO) at Tia you’ll be integral to the excellent care we provide. Your clinical expertise related to the full spectrum of providing affirming primary care for women including: preventative care, holistic primary care and acute and chronic disease management and your desire to teach and collaborate plays an integral part of our clinical team. Board certification or board eligible in Family Medicine or Internal Medicine is preferred but we will consider other relevant specialties.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Physicians are a critical member of our interdisciplinary care team - and this role affords you the opportunity to provide direct patient care but also engage in teaching and collaboration as well as the unique opportunity to partner with the Tia technical teams to contribute to the technology life cycle of the products and tools you will use to care for patients.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;A bit about you:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Values and abilities you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re motivated to elevate women’s care by bringing a shared-decision making approach to women’s health.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You are comfortable managing a variety of clinical cases that may come your way - and approach clinical care with curiosity, warmth and collaboration.&lt;/li&gt;
&lt;li&gt;You’re facile with technology and interested in the process of developing new technology to support high quality clinical care.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re data driven and consistently incorporate new and evolving research into your day-to-day practice&lt;/li&gt;
&lt;li&gt;You are excited about teaching and collaborating with an interdisciplinary team - including nurse practitioners, acupuncture providers and support staff.&lt;/li&gt;
&lt;li&gt;You are a tolerant and inclusive thinker.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Skills and assets you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re a board certified or board eligible Physician (Family Medicine, Internal Medicine, and Gynecology preferred), in the state of &lt;strong&gt;California&lt;/strong&gt;, with an unrestricted license, able to provide primary care and support of all aspects of women’s health with compassion and empathy&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re adept at providing primary care services to women including: preventative care, hypertension management, diabetes management, urgent care concerns (coughs, sore throat, abdominal pain, etc), basic dermatological condition management, STD screens, UTI &amp;amp; vaginal infections consults, pelvic pain, vaginal bleeding, birth control counseling, etc and are motivated to deliver this care and collaborate with other members of the care team to ensure every Tia patient receives excellent care.&lt;/li&gt;
&lt;li&gt;You’re highly tech savvy&lt;/li&gt;
&lt;li&gt;You’re willing to work evenings + weekends as needed by schedule.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re authorized to work in the US&lt;/li&gt;
&lt;li&gt;You’re willing and eligible to be credentialed with our academic partners&lt;/li&gt;
&lt;li&gt;You’re able to serve as a collaborating physician for our CA nurse practitioners&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other “nice to have” skills:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;As an organization that seeks to create an environment for all women to feel safe, heard, recognized and avowed in their health, bodies and lives, we are consistently seeking providers with backgrounds that are meaningfully different from those already forming our team. You bring a diverse background, a range of care experiences in different communities or various modalities.&lt;/li&gt;
&lt;li&gt;Experience or formal training weaving integrative medicine practices into your care plan development.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Tia requires that Physicians complete credentialing with specified payors and that you authorize Tia to complete this credentialing through our preferred vendors.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Benefits&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Talented and collaborative team who will support and collaborate with you&lt;/li&gt;
&lt;li&gt;Competitive salary with quarterly bonus program in place for clinicians&lt;/li&gt;
&lt;li&gt;Paid time off, paid sick leave, paid learning time off&lt;/li&gt;
&lt;li&gt;Comprehensive benefits package effective day one, including medical, dental &amp;amp; vision&lt;/li&gt;
&lt;li&gt;Medical malpractice coverage&lt;/li&gt;
&lt;li&gt;Reimbursed for state licenses, Board Certification, and BLS certification. DEA will be reimbursed where it is required for practice.&lt;/li&gt;
&lt;li&gt;Complimentary subscriptions to educational tools such as UptoDate along with extensive internal educational resources and monthly clinical training opportunities&lt;/li&gt;
&lt;li&gt;Access to AI documentation software drastically reducing administrative burden of clinical documentation&lt;/li&gt;
&lt;li&gt;10-40 hour/week role depending on your preference (benefits start at 30 hours)&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Compensation&lt;/strong&gt;: $250,000 - $300,000 for a full-time position. Part-time positions are compensated proportionally based off this range.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Us:&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Tia is on a mission to transform healthcare for women. We are building a high-quality, multi-specialty medical home designed specifically for women — integrating primary care, gynecology, mental health, dermatology and evidence-based wellness into one coordinated experience across in-person centers and a robust virtual platform.&lt;/p&gt;
&lt;p&gt;Tia is technology-enabled, advancing and scaling excellent care through a proprietary clinical and operational platform that supports clinicians, strengthens care continuity, and improves outcomes.&lt;/p&gt;
&lt;p&gt;We are deepening and expanding one of the most comprehensive preventive care models for women on the market — with a growing focus on cardiometabolic health, longitudinal data, and earlier risk detection across the lifespan. By integrating technology, structured clinical pathways, and mission-aligned interdisciplinary teams, Tia delivers consistently strong clinical outcomes and a differentiated care experience for women.&lt;/p&gt;
&lt;p&gt;Tia is a Series D, venture-backed company with more than 120,000 women who trust Tia for their care, across four markets, supported by a national virtual platform. In each market, we partner with leading health systems to expand access, strengthen primary care, and improve quality for women at scale.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Tia’s Culture:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is building a culture of excellence — in people, process and product. This is our northstar value;&lt;/p&gt;
&lt;p&gt;What is excellence, exactly?&lt;/p&gt;
&lt;p&gt;Excellence about constantly elevating yourself, it is the process of constantly striving to perform to the best of your abilities, and identifying your top potential through constant learning, experimentation and evolution. Excellence is not about achieving perfection, as that insinuates a pinnacle. Instead, in our terms, excellence is about the pursuit of constant improvement. We’re looking for people who want to go on that hard journey of constantly setting new personal records, and organizational records.&lt;/p&gt;
&lt;p&gt;We practice excellence at Tia by demonstrating the following types of behaviors: We chose (and actively choose) excellence as Tia’s highest order value because it crystalizes into one word several behaviors that we hold dear, specifically:&lt;/p&gt;
&lt;p&gt;A drive to constantly improve through experimentation, reflection. and an insatiable growth mindset — said another way, we’re energized by the possibility of invention, innovation, and iteration&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Being present in and grateful for the journey — not just the goal line. Perfection is static. Excellence is a process (more on this important distinction below)&lt;/li&gt;
&lt;li&gt;Asking why, then why again — because accepting “this is just the way it is” is not good enough&lt;/li&gt;
&lt;li&gt;Grit &amp;amp; perseverance — a maker mentality that involves “rolling up your sleeves”, but also deep care for oneself and for others&lt;/li&gt;
&lt;li&gt;A commitment to uncovering talents to unlock “rock star” potential across every individual&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Furthermore, excellence reflects the “bigness” and the “boldness” of Tia’s mission and vision — a world in which every woman can achieve optimal health, as defined by herself.&lt;/p&gt;
&lt;p&gt;Said another way, Tia’s mission is NOT to make healthcare incrementally better for women. Instead, we’ve intentionally set out to create a fundamentally new paradigm for modern women’s healthcare that’s truly excellent. We believe that creating a company that operates in a culture of excellence will manifest in our product. Reaching this goal is not an overnight pursuit or a “one and done.” We have not and will not “get it right” with the first swing. Rather, this higher order goal is a moving target — one we have not and will not ever fully “achieve.” By design, we will never be “done” with this work, but instead, we will be continuously in pursuit of our mission. It is this continuous pursuit — the journey, not the finish line — that truly embodies excellence.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;This position may require attendance at company and team off-sites.&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;Unfortunately, scams targeting job seekers are on the rise. To protect yourself, know that we will never ask for payment, gift cards, or sensitive financial information during our hiring process. All communication from our team will come from an official company email address (@asktia.com). If something feels off, trust your instincts and reach out to us directly at &lt;/em&gt;&lt;em&gt;peopleservices@asktia.com&lt;/em&gt;&lt;em&gt;.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Tia is an equal opportunity employer. We believe that diversity of experience, perspectives, and background will lead to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are committed to collaborative problem solving, creating high-quality and user-centric products, and want to make waves in women&#39;s healthcare, join us!&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;br&gt;&lt;br&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/physician-full-spectrum-primary-care-los-angeles-talent-community-tia/6a069ae72f1861929d253212</link><guid isPermaLink="true">http://biotechroles.com/physician-full-spectrum-primary-care-los-angeles-talent-community-tia/6a069ae72f1861929d253212</guid><pubDate>Fri, 15 May 2026 04:02:47 GMT</pubDate><company>Tia</company><location>Culver City, California, United States; Los Angeles, California, United States; Pasadena, California, United States; Playa Vista, California, United States; Studio City, California, United States</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Physician - Full-Spectrum Primary Care  - Arizona - Talent Community]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Talent Community: Physician (MD/DO): Primary Care &amp;amp; Gynecology&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is on a mission to transform healthcare for women by increasing access to and improving the experience of key preventive healthcare services. Known as the best and only way to both transform outcomes and reduce cost, Tia’s preventive care model focuses on integrating key services across primary care, mental health, gynecology, dermatology and other wellness services. Tia is trailblazing a new paradigm for women’s healthcare that treats women as whole people vs. parts or life stages.&amp;nbsp; Blending in-person and virtual care services, Tia’s “Whole Woman, Whole Life” care model is a unique and “life-long” model for women’s care. By making women’s health higher quality and lower cost, Tia makes women healthier, providers happier, and the business of care delivery stronger — setting a new standard of care for women everywhere.&lt;/p&gt;
&lt;p&gt;Read more about Tia’s:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Products:&amp;nbsp;&lt;a href=&quot;https://asktia.com/article/what-is-product-at-tia&quot;&gt;https://asktia.com/article/what-is-product-at-tia&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Services:&amp;nbsp;&lt;a href=&quot;https://asktia.com/&quot;&gt;https://asktia.com/&lt;/a&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Care principles:&amp;nbsp;&lt;a href=&quot;https://www.asktia.com/care-philosophy/&quot;&gt;https://www.asktia.com/care-philosophy/&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are constantly building our talent pipeline and welcome conversations with physicians for both current openings and future roles as Tia grows. We’re looking to connect with physicians passionate about providing comprehensive primary care to women for Tia’s&lt;strong&gt; Arizona&lt;/strong&gt; area clinic. We are interested in connecting with&amp;nbsp;&lt;strong&gt;part time&lt;/strong&gt;&amp;nbsp;and&amp;nbsp;&lt;strong&gt;full time interested providers.&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;As a Physician (MD/DO) at Tia you’ll be integral to the excellent care we provide. Your clinical expertise related to the full spectrum of providing affirming primary care for women including: preventative care, holistic primary care and acute and chronic disease management and your desire to teach and collaborate plays an integral part of our clinical team. Board certification or board eligible in Family Medicine or Internal Medicine is preferred but we will consider other relevant specialties.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Physicians are a critical member of our interdisciplinary care team - and this role affords you the opportunity to provide direct patient care but also engage in teaching and collaboration as well as the unique opportunity to partner with the Tia technical teams to contribute to the technology life cycle of the products and tools you will use to care for patients.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;A bit about you:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Values and abilities you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re motivated to elevate women’s care by bringing a shared-decision making approach to women’s health.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You are comfortable managing a variety of clinical cases that may come your way - and approach clinical care with curiosity, warmth and collaboration.&lt;/li&gt;
&lt;li&gt;You’re facile with technology and interested in the process of developing new technology to support high quality clinical care.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re data driven and consistently incorporate new and evolving research into your day-to-day practice&lt;/li&gt;
&lt;li&gt;You are excited about teaching and collaborating with an interdisciplinary team - including nurse practitioners, acupuncture providers and support staff.&lt;/li&gt;
&lt;li&gt;You are a tolerant and inclusive thinker.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Skills and assets you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re a board certified or board eligible Physician (Family Medicine, Internal Medicine, and Gynecology preferred), in the state of&amp;nbsp;&lt;strong&gt;Arizona&lt;/strong&gt;, with an unrestricted license, able to provide primary care and support of all aspects of women’s health with compassion and empathy&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re adept at providing primary care services to women including: preventative care, hypertension management, diabetes management, urgent care concerns (coughs, sore throat, abdominal pain, etc), basic dermatological condition management, STD screens, UTI &amp;amp; vaginal infections consults, pelvic pain, vaginal bleeding, birth control counseling, etc and are motivated to deliver this care and collaborate with other members of the care team to ensure every Tia patient receives excellent care.&lt;/li&gt;
&lt;li&gt;You’re highly tech savvy&lt;/li&gt;
&lt;li&gt;You’re willing to work evenings + weekends as needed by schedule.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re authorized to work in the US&lt;/li&gt;
&lt;li&gt;You’re willing and eligible to be credentialed with our academic partners&lt;/li&gt;
&lt;li&gt;You’re able to serve as a collaborating physician for our AZ nurse practitioners&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other “nice to have” skills:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;As an organization that seeks to create an environment for all women to feel safe, heard, recognized and avowed in their health, bodies and lives, we are consistently seeking providers with backgrounds that are meaningfully different from those already forming our team. You bring a diverse background, a range of care experiences in different communities or various modalities.&lt;/li&gt;
&lt;li&gt;Experience or formal training weaving integrative medicine practices into your care plan development.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Tia requires that Physicians complete credentialing with specified payors and that you authorize Tia to complete this credentialing through our preferred vendors.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Benefits&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Talented and collaborative team who will support and collaborate with you&lt;/li&gt;
&lt;li&gt;Competitive salary with quarterly bonus program in place for clinicians&lt;/li&gt;
&lt;li&gt;Paid time off, paid sick leave, paid learning time off&lt;/li&gt;
&lt;li&gt;Comprehensive benefits package effective day one, including medical, dental &amp;amp; vision&lt;/li&gt;
&lt;li&gt;Medical malpractice coverage&lt;/li&gt;
&lt;li&gt;Reimbursed for state licenses, Board Certification, and BLS certification. DEA will be reimbursed where it is required for practice.&lt;/li&gt;
&lt;li&gt;Complimentary subscriptions to educational tools such as UptoDate along with extensive internal educational resources and monthly clinical training opportunities&lt;/li&gt;
&lt;li&gt;Access to AI documentation software drastically reducing administrative burden of clinical documentation&lt;/li&gt;
&lt;li&gt;10-40 hour/week role depending on your preference (benefits start at 30 hours)&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Us:&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Tia is on a mission to transform healthcare for women. We are building a high-quality, multi-specialty medical home designed specifically for women — integrating primary care, gynecology, mental health, dermatology and evidence-based wellness into one coordinated experience across in-person centers and a robust virtual platform.&lt;/p&gt;
&lt;p&gt;Tia is technology-enabled, advancing and scaling excellent care through a proprietary clinical and operational platform that supports clinicians, strengthens care continuity, and improves outcomes.&lt;/p&gt;
&lt;p&gt;We are deepening and expanding one of the most comprehensive preventive care models for women on the market — with a growing focus on cardiometabolic health, longitudinal data, and earlier risk detection across the lifespan. By integrating technology, structured clinical pathways, and mission-aligned interdisciplinary teams, Tia delivers consistently strong clinical outcomes and a differentiated care experience for women.&lt;/p&gt;
&lt;p&gt;Tia is a Series D, venture-backed company with more than 120,000 women who trust Tia for their care, across four markets, supported by a national virtual platform. In each market, we partner with leading health systems to expand access, strengthen primary care, and improve quality for women at scale.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Tia’s Culture:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is building a culture of excellence — in people, process and product. This is our northstar value;&lt;/p&gt;
&lt;p&gt;What is excellence, exactly?&lt;/p&gt;
&lt;p&gt;Excellence about constantly elevating yourself, it is the process of constantly striving to perform to the best of your abilities, and identifying your top potential through constant learning, experimentation and evolution. Excellence is not about achieving perfection, as that insinuates a pinnacle. Instead, in our terms, excellence is about the pursuit of constant improvement. We’re looking for people who want to go on that hard journey of constantly setting new personal records, and organizational records.&lt;/p&gt;
&lt;p&gt;We practice excellence at Tia by demonstrating the following types of behaviors: We chose (and actively choose) excellence as Tia’s highest order value because it crystalizes into one word several behaviors that we hold dear, specifically:&lt;/p&gt;
&lt;p&gt;A drive to constantly improve through experimentation, reflection. and an insatiable growth mindset — said another way, we’re energized by the possibility of invention, innovation, and iteration&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Being present in and grateful for the journey — not just the goal line. Perfection is static. Excellence is a process (more on this important distinction below)&lt;/li&gt;
&lt;li&gt;Asking why, then why again — because accepting “this is just the way it is” is not good enough&lt;/li&gt;
&lt;li&gt;Grit &amp;amp; perseverance — a maker mentality that involves “rolling up your sleeves”, but also deep care for oneself and for others&lt;/li&gt;
&lt;li&gt;A commitment to uncovering talents to unlock “rock star” potential across every individual&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Furthermore, excellence reflects the “bigness” and the “boldness” of Tia’s mission and vision — a world in which every woman can achieve optimal health, as defined by herself.&lt;/p&gt;
&lt;p&gt;Said another way, Tia’s mission is NOT to make healthcare incrementally better for women. Instead, we’ve intentionally set out to create a fundamentally new paradigm for modern women’s healthcare that’s truly excellent. We believe that creating a company that operates in a culture of excellence will manifest in our product. Reaching this goal is not an overnight pursuit or a “one and done.” We have not and will not “get it right” with the first swing. Rather, this higher order goal is a moving target — one we have not and will not ever fully “achieve.” By design, we will never be “done” with this work, but instead, we will be continuously in pursuit of our mission. It is this continuous pursuit — the journey, not the finish line — that truly embodies excellence.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;This position may require attendance at company and team off-sites.&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;Unfortunately, scams targeting job seekers are on the rise. To protect yourself, know that we will never ask for payment, gift cards, or sensitive financial information during our hiring process. All communication from our team will come from an official company email address (@asktia.com). If something feels off, trust your instincts and reach out to us directly at &lt;/em&gt;&lt;em&gt;peopleservices@asktia.com&lt;/em&gt;&lt;em&gt;.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Tia is an equal opportunity employer. We believe that diversity of experience, perspectives, and background will lead to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are committed to collaborative problem solving, creating high-quality and user-centric products, and want to make waves in women&#39;s healthcare, join us!&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/physician-full-spectrum-primary-care-arizona-talent-community-tia/6a069ae62f1861929d253211</link><guid isPermaLink="true">http://biotechroles.com/physician-full-spectrum-primary-care-arizona-talent-community-tia/6a069ae62f1861929d253211</guid><pubDate>Fri, 15 May 2026 04:02:46 GMT</pubDate><company>Tia</company><location>Phoenix, Arizona, United States</location><salary>$220000-320000</salary><type>Full-time</type></item><item><title><![CDATA[Nurse Practitioner / Physician Assistant, Per Diem - Los Angeles (West Side) - Onsite]]></title><description><![CDATA[&lt;h3&gt;&lt;strong&gt;On Call / Per Diem - Nurse Practitioners &amp;amp; Physician Assistants&lt;/strong&gt;&lt;/h3&gt;
&lt;h3&gt;&lt;strong&gt;About Tia&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;&lt;a href=&quot;https://asktia.com/&quot;&gt;Tia&lt;/a&gt; is a full-stack women&#39;s healthcare business that builds products, tools and clinical services virtually and in person to help every woman be her own patient advocate and get meaningfully better healthcare. We’re putting the soul back in medicine, one patient and one provider at a time through a &lt;a href=&quot;https://asktia.com/care-philosophy&quot;&gt;care philosophy &lt;/a&gt;that is reimagined to listen to and empower women to actively take control of their healthcare. The care philosophy that supports our patients is also built to support clinicians who are the heart and soul of the care Tia is able to provide. In order to do that - we need YOU!&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;About the role&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;We’re looking for experienced Nurse Practitioners/Physician Assistants to provide on-call / per diem coverage across Tia’s Westside Los Angeles clinics (West Hollywood, Culver City, Playa Vista). This is a high-autonomy role for clinicians who can step into any clinic, quickly integrate into the flow, and deliver high-quality, whole-person care from day one.&lt;/p&gt;
&lt;p&gt;You’ll support continuity of care during same-day callouts, high-volume periods, and planned coverage gaps — ensuring patients receive timely, thoughtful, and clinically excellent care no matter where they’re seen. This is not a “ramp over time” role; it’s for providers who are confident, adaptable, and ready to operate across a broad scope of primary and women’s health immediately.&lt;/p&gt;
&lt;p&gt;Beyond direct care, you’ll contribute to evolving Tia’s care model through collaboration with interdisciplinary teams, clinical feedback loops, and ongoing innovation in how care is delivered.&lt;/p&gt;
&lt;h4&gt;&lt;strong&gt;Schedule&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;On-call providers serve as standby coverage for urgent clinic needs. Shifts are 8 hours (between 8:00am–7:00pm), and providers must be able to report onsite within two hours if activated. You’ll indicate your availability (minimum one day per week, weekdays or weekends). During downtime, you may support virtual care, inbox coverage, or care team workflows.&lt;/h4&gt;
&lt;p&gt;We believe in setting our on-call providers up for success from day one. To ensure you are fully integrated into our systems and clinical culture, we require a comprehensive &lt;strong&gt;40-hour onboarding program&lt;/strong&gt;.&lt;/p&gt;
&lt;p&gt;While we offer flexibility, this is ideally completed within &lt;strong&gt;1–2 weeks&lt;/strong&gt; of your start date and includes:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;IT &amp;amp; Systems Integration:&lt;/strong&gt; One full day dedicated to virtual IT setup, credentialing, and software access to ensure your digital toolkit is ready to go.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Core Training Modules:&lt;/strong&gt; Completion of specialized training modules covering our internal protocols, safety standards, and operational workflows.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Mentor Shadowing:&lt;/strong&gt; Four full days of immersive shadowing with a dedicated mentor. Depending on your specific role and location, this may take place in-person (IRL), virtually (URL), or a hybrid of both.&lt;/p&gt;
&lt;h4&gt;&lt;strong&gt;What you bring (must-haves)&lt;/strong&gt;&lt;/h4&gt;
&lt;p&gt;Day 1 clinical readiness:&amp;nbsp; You’re able to independently assess, diagnose, and manage a wide range of visits without ramp time, including:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;New patient visits and annual preventive exams&lt;/li&gt;
&lt;li&gt;Contraception and all-options pregnancy consults&lt;/li&gt;
&lt;li&gt;Vaginal, vulvar, urinary, and pelvic concerns&lt;/li&gt;
&lt;li&gt;STI evaluation and treatment&lt;/li&gt;
&lt;li&gt;Cough, cold, flu, and other urgent care presentations&lt;/li&gt;
&lt;li&gt;Abdominal and digestive concerns&lt;/li&gt;
&lt;li&gt;Mental health assessments (anxiety, depression, mood, stress) and follow-ups&lt;/li&gt;
&lt;li&gt;Sleep concerns&lt;/li&gt;
&lt;li&gt;Lab review and care plan development&lt;/li&gt;
&lt;li&gt;Cervical cancer screening follow-up&lt;/li&gt;
&lt;li&gt;Pregnancy confirmation&lt;/li&gt;
&lt;li&gt;Vaccines and injections&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Procedural competency&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Confident performing high-volume procedures, including IUD insertions and basic dermatologic procedures&lt;/li&gt;
&lt;li&gt;Experience with — or willingness to train and map to — expanded specialties (e.g., weight management, menopause care, advanced dermatology)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Clinical scope and approach&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Board-certified Nurse Practitioner with an active, unrestricted California license&lt;/li&gt;
&lt;li&gt;Proven ability to deliver both primary care and gynecologic care across a broad spectrum of women’s health needs&lt;/li&gt;
&lt;li&gt;Comfortable operating independently in a fast-paced, multi-site environment with minimal oversight&lt;/li&gt;
&lt;li&gt;Strong clinical judgment with the ability to triage, prioritize, and adapt quickly&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;How you show up&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You practice shared decision-making and treat patients as true partners in their care&lt;/li&gt;
&lt;li&gt;You listen first, then act — grounding your care in curiosity, respect, and clinical rigor&lt;/li&gt;
&lt;li&gt;You’re inclusive, sex-positive, and committed to delivering care that is affirming for all patients&lt;/li&gt;
&lt;li&gt;You’re tech-forward and comfortable navigating EMRs, virtual care, and evolving care delivery models&lt;/li&gt;
&lt;li&gt;You’re flexible and reliable — when you’re on call, the team can count on you to show up and deliver&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;strong&gt;Nice to have (but not required)&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Experience with Nexplanon insertions, colposcopy, or interest in expanding procedural skills&lt;/li&gt;
&lt;li&gt;Background in trauma-informed care, LGBTQ+ care (including gender-affirming hormone management), or behavioral health integration&lt;/li&gt;
&lt;li&gt;Experience in high-growth, interdisciplinary, or non-traditional care models&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;strong&gt;Benefits&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Talented and collaborative team who will support and collaborate with you&lt;/li&gt;
&lt;li&gt;Competitive salary of $96/hour with mileage reimbursement&lt;/li&gt;
&lt;li&gt;Medical malpractice coverage&lt;/li&gt;
&lt;li&gt;Reimbursed for state licenses, board certification, and BLS certification.&amp;nbsp;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;DEA will be reimbursed where it is required for practice.&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;Complimentary subscriptions to educational tools such as UptoDate along with extensive internal educational resources and monthly clinical training opportunities&lt;/li&gt;
&lt;li&gt;Access to AI documentation software drastically reducing administrative burden of clinical documentation&lt;/li&gt;
&lt;/ul&gt;
&lt;h4&gt;&lt;strong&gt;More about Tia&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Tia is on a mission to transform healthcare for women. We are building a high-quality, multi-specialty medical home designed specifically for women — integrating primary care, gynecology, mental health, dermatology and evidence-based wellness into one coordinated experience across in-person centers and a robust virtual platform.&lt;/h4&gt;
&lt;p&gt;Read more about Tia’s:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Products: &lt;a href=&quot;https://asktia.com/article/what-is-product-at-tia&quot;&gt;https://asktia.com/article/what-is-product-at-tia&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Services: &lt;a href=&quot;https://asktia.com/&quot;&gt;https://asktia.com/&lt;/a&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Care principles: &lt;a href=&quot;https://www.asktia.com/care-philosophy/&quot;&gt;https://www.asktia.com/care-philosophy/&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Tia is technology-enabled, advancing and scaling excellent care through a proprietary clinical and operational platform that supports clinicians, strengthens care continuity, and improves outcomes.&lt;/p&gt;
&lt;p&gt;We are deepening and expanding one of the most comprehensive preventive care models for women on the market — with a growing focus on cardiometabolic health, longitudinal data, and earlier risk detection across the lifespan. By integrating technology, structured clinical pathways, and mission-aligned interdisciplinary teams, Tia delivers consistently strong clinical outcomes and a differentiated care experience for women.&lt;/p&gt;
&lt;p&gt;Tia is a Series D, venture-backed company with more than 120,000 women who trust Tia for their care, across four markets, supported by a national virtual platform. In each market, we partner with leading health systems to expand access, strengthen primary care, and improve quality for women at scale.&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;About Tia’s Culture&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;Tia is building a culture of excellence — in people, process and product. This is our northstar value;&lt;/p&gt;
&lt;p&gt;What is excellence, exactly?&lt;/p&gt;
&lt;p&gt;Excellence about constantly elevating yourself, it is the process of constantly striving to perform to the best of your abilities, and identifying your top potential through constant learning, experimentation and evolution. Excellence is not about achieving perfection, as that insinuates a pinnacle. Instead, in our terms, excellence is about the pursuit of constant improvement. We’re looking for people who want to go on that hard journey of constantly setting new personal records, and organizational records.&lt;/p&gt;
&lt;p&gt;We practice excellence at Tia by demonstrating the following types of behaviors: We chose (and actively choose) excellence as Tia’s highest order value because it crystalizes into one word several behaviors that we hold dear, specifically:&lt;/p&gt;
&lt;p&gt;A drive to constantly improve through experimentation, reflection. and an insatiable growth mindset — said another way, we’re energized by the possibility of invention, innovation, and iteration&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Being present in and grateful for the journey — not just the goal line. Perfection is static. Excellence is a process (more on this important distinction below)&lt;/li&gt;
&lt;li&gt;Asking why, then why again — because accepting “this is just the way it is” is not good enough&lt;/li&gt;
&lt;li&gt;Grit &amp;amp; perseverance — a maker mentality that involves “rolling up your sleeves”, but also deep care for oneself and for others&lt;/li&gt;
&lt;li&gt;A commitment to uncovering talents to unlock “rock star” potential across every individual&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Furthermore, excellence reflects the “bigness” and the “boldness” of Tia’s mission and vision — a world in which every woman can achieve optimal health, as defined by herself.&lt;/p&gt;
&lt;p&gt;Said another way, Tia’s mission is NOT to make healthcare incrementally better for women. Instead, we’ve intentionally set out to create a fundamentally new paradigm for modern women’s healthcare that’s truly excellent. We believe that creating a company that operates in a culture of excellence will manifest in our product. Reaching this goal is not an overnight pursuit or a “one and done.” We have not and will not “get it right” with the first swing. Rather, this higher order goal is a moving target — one we have not and will not ever fully “achieve.” By design, we will never be “done” with this work, but instead, we will be continuously in pursuit of our mission. It is this continuous pursuit — the journey, not the finish line — that truly embodies excellence.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;This position may require attendance at company and team off-sites.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Unfortunately, scams targeting job seekers are on the rise. To protect yourself, know that we will never ask for payment, gift cards, or sensitive financial information during our hiring process. All communication from our team will come from an official company email address (@asktia.com). If something feels off, trust your instincts and reach out to us directly at peopleservices@asktia.com.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Tia is an equal opportunity employer. We believe that diversity of experience, perspectives, and background will lead to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are committed to collaborative problem solving, creating high-quality and user-centric products, and want to make waves in women&#39;s healthcare, join us!&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/nurse-practitioner-physician-assistant-per-diem-los-angeles-(west-side)-onsite-tia/6a069ae42f1861929d253210</link><guid isPermaLink="true">http://biotechroles.com/nurse-practitioner-physician-assistant-per-diem-los-angeles-(west-side)-onsite-tia/6a069ae42f1861929d253210</guid><pubDate>Fri, 15 May 2026 04:02:44 GMT</pubDate><company>Tia</company><location>Los Angeles, California, United States</location><salary>$0-0</salary><type>Full-time</type></item><item><title><![CDATA[Nurse Practitioner / Physician Assistant, Per Diem - Los Angeles (East Side) - Onsite]]></title><description><![CDATA[&lt;h3&gt;&lt;strong&gt;On Call / Per Diem - Nurse Practitioners &amp;amp; Physician Assistants&lt;/strong&gt;&lt;/h3&gt;
&lt;h3&gt;&lt;strong&gt;About Tia&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;&lt;a href=&quot;https://asktia.com/&quot;&gt;Tia&lt;/a&gt; is a full-stack women&#39;s healthcare business that builds products, tools and clinical services virtually and in person to help every woman be her own patient advocate and get meaningfully better healthcare. We’re putting the soul back in medicine, one patient and one provider at a time through a &lt;a href=&quot;https://asktia.com/care-philosophy&quot;&gt;care philosophy &lt;/a&gt;that is reimagined to listen to and empower women to actively take control of their healthcare. The care philosophy that supports our patients is also built to support clinicians who are the heart and soul of the care Tia is able to provide. In order to do that - we need YOU!&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;About the role&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;We’re looking for experienced Nurse Practitioners/Physician Assistants to provide on-call / per diem coverage across Tia’s Eastside Los Angeles clinics (Pasadena, Silver Lake, Studio City). This is a high-autonomy role for clinicians who can step into any clinic, quickly integrate into the flow, and deliver high-quality, whole-person care from day one.&lt;/p&gt;
&lt;p&gt;You’ll support continuity of care during same-day callouts, high-volume periods, and planned coverage gaps — ensuring patients receive timely, thoughtful, and clinically excellent care no matter where they’re seen. This is not a “ramp over time” role; it’s for providers who are confident, adaptable, and ready to operate across a broad scope of primary and women’s health immediately.&lt;/p&gt;
&lt;p&gt;Beyond direct care, you’ll contribute to evolving Tia’s care model through collaboration with interdisciplinary teams, clinical feedback loops, and ongoing innovation in how care is delivered.&lt;/p&gt;
&lt;h4&gt;&lt;strong&gt;Schedule&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;On-call providers serve as standby coverage for urgent clinic needs. Shifts are 8 hours (between 8:00am–7:00pm), and providers must be able to report onsite within two hours if activated. You’ll indicate your availability (minimum one day per week, weekdays or weekends). During downtime, you may support virtual care, inbox coverage, or care team workflows.&lt;/h4&gt;
&lt;p&gt;We believe in setting our on-call providers up for success from day one. To ensure you are fully integrated into our systems and clinical culture, we require a comprehensive &lt;strong&gt;40-hour onboarding program&lt;/strong&gt;.&lt;/p&gt;
&lt;p&gt;While we offer flexibility, this is ideally completed within &lt;strong&gt;1–2 weeks&lt;/strong&gt; of your start date and includes:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;IT &amp;amp; Systems Integration:&lt;/strong&gt; One full day dedicated to virtual IT setup, credentialing, and software access to ensure your digital toolkit is ready to go.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Core Training Modules:&lt;/strong&gt; Completion of specialized training modules covering our internal protocols, safety standards, and operational workflows.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Mentor Shadowing:&lt;/strong&gt; Four full days of immersive shadowing with a dedicated mentor. Depending on your specific role and location, this may take place in-person (IRL), virtually (URL), or a hybrid of both.&lt;/p&gt;
&lt;h4&gt;&lt;strong&gt;What you bring (must-haves)&lt;/strong&gt;&lt;/h4&gt;
&lt;p&gt;Day 1 clinical readiness:&amp;nbsp; You’re able to independently assess, diagnose, and manage a wide range of visits without ramp time, including:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;New patient visits and annual preventive exams&lt;/li&gt;
&lt;li&gt;Contraception and all-options pregnancy consults&lt;/li&gt;
&lt;li&gt;Vaginal, vulvar, urinary, and pelvic concerns&lt;/li&gt;
&lt;li&gt;STI evaluation and treatment&lt;/li&gt;
&lt;li&gt;Cough, cold, flu, and other urgent care presentations&lt;/li&gt;
&lt;li&gt;Abdominal and digestive concerns&lt;/li&gt;
&lt;li&gt;Mental health assessments (anxiety, depression, mood, stress) and follow-ups&lt;/li&gt;
&lt;li&gt;Sleep concerns&lt;/li&gt;
&lt;li&gt;Lab review and care plan development&lt;/li&gt;
&lt;li&gt;Cervical cancer screening follow-up&lt;/li&gt;
&lt;li&gt;Pregnancy confirmation&lt;/li&gt;
&lt;li&gt;Vaccines and injections&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Procedural competency&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Confident performing high-volume procedures, including IUD insertions and basic dermatologic procedures&lt;/li&gt;
&lt;li&gt;Experience with — or willingness to train and map to — expanded specialties (e.g., weight management, menopause care, advanced dermatology)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Clinical scope and approach&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Board-certified Nurse Practitioner with an active, unrestricted California license&lt;/li&gt;
&lt;li&gt;Proven ability to deliver both primary care and gynecologic care across a broad spectrum of women’s health needs&lt;/li&gt;
&lt;li&gt;Comfortable operating independently in a fast-paced, multi-site environment with minimal oversight&lt;/li&gt;
&lt;li&gt;Strong clinical judgment with the ability to triage, prioritize, and adapt quickly&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;How you show up&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You practice shared decision-making and treat patients as true partners in their care&lt;/li&gt;
&lt;li&gt;You listen first, then act — grounding your care in curiosity, respect, and clinical rigor&lt;/li&gt;
&lt;li&gt;You’re inclusive, sex-positive, and committed to delivering care that is affirming for all patients&lt;/li&gt;
&lt;li&gt;You’re tech-forward and comfortable navigating EMRs, virtual care, and evolving care delivery models&lt;/li&gt;
&lt;li&gt;You’re flexible and reliable — when you’re on call, the team can count on you to show up and deliver&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;strong&gt;Nice to have (but not required)&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Experience with Nexplanon insertions, colposcopy, or interest in expanding procedural skills&lt;/li&gt;
&lt;li&gt;Background in trauma-informed care, LGBTQ+ care (including gender-affirming hormone management), or behavioral health integration&lt;/li&gt;
&lt;li&gt;Experience in high-growth, interdisciplinary, or non-traditional care models&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;strong&gt;Benefits&lt;/strong&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Talented and collaborative team who will support and collaborate with you&lt;/li&gt;
&lt;li&gt;Competitive salary of $96/hour with mileage reimbursement&lt;/li&gt;
&lt;li&gt;Medical malpractice coverage&lt;/li&gt;
&lt;li&gt;Reimbursed for state licenses, board certification, and BLS certification.&amp;nbsp;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;DEA will be reimbursed where it is required for practice.&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;Complimentary subscriptions to educational tools such as UptoDate along with extensive internal educational resources and monthly clinical training opportunities&lt;/li&gt;
&lt;li&gt;Access to AI documentation software drastically reducing administrative burden of clinical documentation&lt;/li&gt;
&lt;/ul&gt;
&lt;h4&gt;&lt;strong&gt;More about Tia&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Tia is on a mission to transform healthcare for women. We are building a high-quality, multi-specialty medical home designed specifically for women — integrating primary care, gynecology, mental health, dermatology and evidence-based wellness into one coordinated experience across in-person centers and a robust virtual platform.&lt;/h4&gt;
&lt;p&gt;Read more about Tia’s:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Products: &lt;a href=&quot;https://asktia.com/article/what-is-product-at-tia&quot;&gt;https://asktia.com/article/what-is-product-at-tia&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Services: &lt;a href=&quot;https://asktia.com/&quot;&gt;https://asktia.com/&lt;/a&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Care principles: &lt;a href=&quot;https://www.asktia.com/care-philosophy/&quot;&gt;https://www.asktia.com/care-philosophy/&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Tia is technology-enabled, advancing and scaling excellent care through a proprietary clinical and operational platform that supports clinicians, strengthens care continuity, and improves outcomes.&lt;/p&gt;
&lt;p&gt;We are deepening and expanding one of the most comprehensive preventive care models for women on the market — with a growing focus on cardiometabolic health, longitudinal data, and earlier risk detection across the lifespan. By integrating technology, structured clinical pathways, and mission-aligned interdisciplinary teams, Tia delivers consistently strong clinical outcomes and a differentiated care experience for women.&lt;/p&gt;
&lt;p&gt;Tia is a Series D, venture-backed company with more than 120,000 women who trust Tia for their care, across four markets, supported by a national virtual platform. In each market, we partner with leading health systems to expand access, strengthen primary care, and improve quality for women at scale.&lt;/p&gt;
&lt;h3&gt;&lt;strong&gt;About Tia’s Culture&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;Tia is building a culture of excellence — in people, process and product. This is our northstar value;&lt;/p&gt;
&lt;p&gt;What is excellence, exactly?&lt;/p&gt;
&lt;p&gt;Excellence about constantly elevating yourself, it is the process of constantly striving to perform to the best of your abilities, and identifying your top potential through constant learning, experimentation and evolution. Excellence is not about achieving perfection, as that insinuates a pinnacle. Instead, in our terms, excellence is about the pursuit of constant improvement. We’re looking for people who want to go on that hard journey of constantly setting new personal records, and organizational records.&lt;/p&gt;
&lt;p&gt;We practice excellence at Tia by demonstrating the following types of behaviors: We chose (and actively choose) excellence as Tia’s highest order value because it crystalizes into one word several behaviors that we hold dear, specifically:&lt;/p&gt;
&lt;p&gt;A drive to constantly improve through experimentation, reflection. and an insatiable growth mindset — said another way, we’re energized by the possibility of invention, innovation, and iteration&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Being present in and grateful for the journey — not just the goal line. Perfection is static. Excellence is a process (more on this important distinction below)&lt;/li&gt;
&lt;li&gt;Asking why, then why again — because accepting “this is just the way it is” is not good enough&lt;/li&gt;
&lt;li&gt;Grit &amp;amp; perseverance — a maker mentality that involves “rolling up your sleeves”, but also deep care for oneself and for others&lt;/li&gt;
&lt;li&gt;A commitment to uncovering talents to unlock “rock star” potential across every individual&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Furthermore, excellence reflects the “bigness” and the “boldness” of Tia’s mission and vision — a world in which every woman can achieve optimal health, as defined by herself.&lt;/p&gt;
&lt;p&gt;Said another way, Tia’s mission is NOT to make healthcare incrementally better for women. Instead, we’ve intentionally set out to create a fundamentally new paradigm for modern women’s healthcare that’s truly excellent. We believe that creating a company that operates in a culture of excellence will manifest in our product. Reaching this goal is not an overnight pursuit or a “one and done.” We have not and will not “get it right” with the first swing. Rather, this higher order goal is a moving target — one we have not and will not ever fully “achieve.” By design, we will never be “done” with this work, but instead, we will be continuously in pursuit of our mission. It is this continuous pursuit — the journey, not the finish line — that truly embodies excellence.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;This position may require attendance at company and team off-sites.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Unfortunately, scams targeting job seekers are on the rise. To protect yourself, know that we will never ask for payment, gift cards, or sensitive financial information during our hiring process. All communication from our team will come from an official company email address (@asktia.com). If something feels off, trust your instincts and reach out to us directly at peopleservices@asktia.com.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Tia is an equal opportunity employer. We believe that diversity of experience, perspectives, and background will lead to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are committed to collaborative problem solving, creating high-quality and user-centric products, and want to make waves in women&#39;s healthcare, join us!&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/nurse-practitioner-physician-assistant-per-diem-los-angeles-(east-side)-onsite-tia/6a069ae22f1861929d25320f</link><guid isPermaLink="true">http://biotechroles.com/nurse-practitioner-physician-assistant-per-diem-los-angeles-(east-side)-onsite-tia/6a069ae22f1861929d25320f</guid><pubDate>Fri, 15 May 2026 04:02:42 GMT</pubDate><company>Tia</company><location>Los Angeles, California, United States</location><salary>$0-0</salary><type>Full-time</type></item><item><title><![CDATA[Nurse Practitioner / Physician Assistant - Full Spectrum Primary Care - Remote - Talent Community]]></title><description><![CDATA[&lt;div class=&quot;job__description body&quot;&gt;
&lt;h4&gt;&lt;strong&gt;Talent Community: Virtual Nurse Practitioners &amp;amp; Physician Assistants (FNPs/WHNPs/PAs)&lt;/strong&gt;&lt;/h4&gt;
&lt;p&gt;Tia is on a mission to transform healthcare for women by increasing access to and improving the experience of key preventive healthcare services. Known as the best and only way to both transform outcomes and reduce cost, Tia’s preventive care model focuses on integrating key services across primary care, mental health, gynecology, dermatology and other wellness services. Tia is trailblazing a new paradigm for women’s healthcare that treats women as whole people vs. parts or life stages.&amp;nbsp; Blending in-person and virtual care services, Tia’s “Whole Woman, Whole Life” care model is a unique and “life-long” model for women’s care. By making women’s health higher quality and lower cost, Tia makes women healthier, providers happier, and the business of care delivery stronger — setting a new standard of care for women everywhere.&lt;/p&gt;
&lt;p&gt;Read more about Tia’s:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Products:&amp;nbsp;&lt;a href=&quot;https://asktia.com/article/what-is-product-at-tia&quot;&gt;https://asktia.com/article/what-is-product-at-tia&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Services:&amp;nbsp;&lt;a href=&quot;https://asktia.com/&quot;&gt;https://asktia.com/&lt;/a&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Care principles:&amp;nbsp;&lt;a href=&quot;https://www.asktia.com/care-philosophy/&quot;&gt;https://www.asktia.com/care-philosophy/&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We’re looking to connect with&amp;nbsp;&lt;strong&gt;Nurse Practitioners &amp;amp; Physician Assistants&amp;nbsp;&lt;/strong&gt;passionate about women’s health for&amp;nbsp;&lt;strong&gt;Tia’s Virtual Care Team&lt;/strong&gt;. As a Nurse Practitioner, you will be an integral part of the care delivery system. Your clinical expertise related to the full spectrum of providing affirming primary care for women including: gynecological services, primary care, procedures and holistic whole person care is welcome!&lt;/p&gt;
&lt;p&gt;Nurse Practitioners are integral to the formation and iteration of our care model - with opportunities to provide direct patient care but also participate in technology development, interdisciplinary case studies, protocol development and innovation.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Schedule&lt;/strong&gt;&amp;nbsp;is set with some flexibility. We are open to part-time and full-time employment&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;We offer 10 hr or 8 hr days. Start times are 7a-9a for early shifts and or 10a-12p for later shifts.&amp;nbsp; Expectation is that you take one evening shift per week.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;A bit about you:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Values and abilities you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re motivated to elevate women’s care by bringing a shared-decision making approach to women’s health.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You believe that each woman knows her body best. Your mission as a healthcare provider is to listen to patients and find ways to help them achieve their optimal health.&amp;nbsp; You practice this by being a true partner on a patient’s health journey.&lt;/li&gt;
&lt;li&gt;You’re facile with technology&lt;/li&gt;
&lt;li&gt;You are a tolerant and inclusive thinker. You believe in sex-positive, no judgment and radically inclusive healthcare for every person, and espouse these values in your everyday life.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Skills and assets you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re a board certified Nurse Practitioner in the state of California, with an unrestricted license, able to provide primary and gynecology care and support of all aspects of women’s health with compassion and empathy&lt;/li&gt;
&lt;li&gt;You’re adept at providing primary care services including: annual exams and pap smears, hypertension management, diabetes management, anxiety and depression management, urgent care concerns (coughs, sore throat, abdominal pain, etc), basic dermatological condition management, STD screens, UTI &amp;amp; Vaginal infections consults etc&lt;/li&gt;
&lt;li&gt;You’re highly tech savvy&lt;/li&gt;
&lt;li&gt;You’re willing to work some (but not all) evenings + weekends as needed by schedule.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re authorized to work in the US&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other “nice to have” skills:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You have procedural skills to perform: IUD insertions, nexplanon insertion and colposcopies or a desire to learn.&lt;/li&gt;
&lt;li&gt;As an organization that seeks to create an environment for all women to feel safe, heard, recognized and avowed in their health, bodies and lives, we are consistently seeking providers with backgrounds that are meaningfully different from those already forming our team. You bring a diverse background, a range of care experiences in different communities or various modalities.&lt;/li&gt;
&lt;li&gt;Formal professional training in the following areas is highly valued: care delivery for women who have experienced trauma, care delivery for LGBTQ identified folks including gender affirming hormone management, outpatient primary care depression and anxiety management.&lt;/li&gt;
&lt;li&gt;Experience or formal training weaving integrative medicine practices into your care plan development&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Benefits&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Talented and collaborative team who will support and collaborate with you&lt;/li&gt;
&lt;li&gt;Competitive salary with quarterly bonus program in place for full time clinicians&lt;/li&gt;
&lt;li&gt;Paid time off, paid sick leave, paid learning time off&lt;/li&gt;
&lt;li&gt;Comprehensive benefits package effective day one, including medical, dental &amp;amp; vision&lt;/li&gt;
&lt;li&gt;Medical malpractice coverage&lt;/li&gt;
&lt;li&gt;Reimbursed for state licenses, board certification, and BLS certification.&amp;nbsp;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;DEA will be reimbursed where it is required for practice.&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;Complimentary subscriptions to educational tools such as UptoDate along with extensive internal educational resources and monthly clinical training opportunities&lt;/li&gt;
&lt;li&gt;Access to AI documentation software drastically reducing administrative burden of clinical documentation&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Us:&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Tia is on a mission to transform healthcare for women. We are building a high-quality, multi-specialty medical home designed specifically for women — integrating primary care, gynecology, mental health, dermatology and evidence-based wellness into one coordinated experience across in-person centers and a robust virtual platform.&lt;/p&gt;
&lt;p&gt;Tia is technology-enabled, advancing and scaling excellent care through a proprietary clinical and operational platform that supports clinicians, strengthens care continuity, and improves outcomes.&lt;/p&gt;
&lt;p&gt;We are deepening and expanding one of the most comprehensive preventive care models for women on the market — with a growing focus on cardiometabolic health, longitudinal data, and earlier risk detection across the lifespan. By integrating technology, structured clinical pathways, and mission-aligned interdisciplinary teams, Tia delivers consistently strong clinical outcomes and a differentiated care experience for women.&lt;/p&gt;
&lt;p&gt;Tia is a Series D, venture-backed company with more than 120,000 women who trust Tia for their care, across four markets, supported by a national virtual platform. In each market, we partner with leading health systems to expand access, strengthen primary care, and improve quality for women at scale.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Tia’s Culture:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is building a culture of excellence — in people, process and product. This is our northstar value;&lt;/p&gt;
&lt;p&gt;What is excellence, exactly?&lt;/p&gt;
&lt;p&gt;Excellence about constantly elevating yourself, it is the process of constantly striving to perform to the best of your abilities, and identifying your top potential through constant learning, experimentation and evolution. Excellence is not about achieving perfection, as that insinuates a pinnacle. Instead, in our terms, excellence is about the pursuit of constant improvement. We’re looking for people who want to go on that hard journey of constantly setting new personal records, and organizational records.&lt;/p&gt;
&lt;p&gt;We practice excellence at Tia by demonstrating the following types of behaviors: We chose (and actively choose) excellence as Tia’s highest order value because it crystalizes into one word several behaviors that we hold dear, specifically:&lt;/p&gt;
&lt;p&gt;A drive to constantly improve through experimentation, reflection. and an insatiable growth mindset — said another way, we’re energized by the possibility of invention, innovation, and iteration&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Being present in and grateful for the journey — not just the goal line. Perfection is static. Excellence is a process (more on this important distinction below)&lt;/li&gt;
&lt;li&gt;Asking why, then why again — because accepting “this is just the way it is” is not good enough&lt;/li&gt;
&lt;li&gt;Grit &amp;amp; perseverance — a maker mentality that involves “rolling up your sleeves”, but also deep care for oneself and for others&lt;/li&gt;
&lt;li&gt;A commitment to uncovering talents to unlock “rock star” potential across every individual&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Furthermore, excellence reflects the “bigness” and the “boldness” of Tia’s mission and vision — a world in which every woman can achieve optimal health, as defined by herself.&lt;/p&gt;
&lt;p&gt;Said another way, Tia’s mission is NOT to make healthcare incrementally better for women. Instead, we’ve intentionally set out to create a fundamentally new paradigm for modern women’s healthcare that’s truly excellent. We believe that creating a company that operates in a culture of excellence will manifest in our product. Reaching this goal is not an overnight pursuit or a “one and done.” We have not and will not “get it right” with the first swing. Rather, this higher order goal is a moving target — one we have not and will not ever fully “achieve.” By design, we will never be “done” with this work, but instead, we will be continuously in pursuit of our mission. It is this continuous pursuit — the journey, not the finish line — that truly embodies excellence.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;This position may require attendance at company and team off-sites.&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;Unfortunately, scams targeting job seekers are on the rise. To protect yourself, know that we will never ask for payment, gift cards, or sensitive financial information during our hiring process. All communication from our team will come from an official company email address (@asktia.com). If something feels off, trust your instincts and reach out to us directly at &lt;/em&gt;&lt;em&gt;peopleservices@asktia.com&lt;/em&gt;&lt;em&gt;.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Tia is an equal opportunity employer. We believe that diversity of experience, perspectives, and background will lead to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are committed to collaborative problem solving, creating high-quality and user-centric products, and want to make waves in women&#39;s healthcare, join us!&lt;/em&gt;&lt;/p&gt;
&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/nurse-practitioner-physician-assistant-full-spectrum-primary-care-remote-talent-community-tia/6a069ae12f1861929d25320e</link><guid isPermaLink="true">http://biotechroles.com/nurse-practitioner-physician-assistant-full-spectrum-primary-care-remote-talent-community-tia/6a069ae12f1861929d25320e</guid><pubDate>Fri, 15 May 2026 04:02:41 GMT</pubDate><company>Tia</company><location>Remote</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Nurse Practitioner / Physician Assistant - Full-Spectrum Primary Care  - Los Angeles- Talent Community]]></title><description><![CDATA[&lt;h4&gt;&lt;strong&gt;Talent Community: Nurse Practitioners &amp;amp; Physician Assistants&lt;/strong&gt;&lt;/h4&gt;
&lt;p&gt;Tia is on a mission to transform healthcare for women by increasing access to and improving the experience of key preventive healthcare services. Known as the best and only way to both transform outcomes and reduce cost, Tia’s preventive care model focuses on integrating key services across primary care, mental health, gynecology, dermatology and other wellness services. Tia is trailblazing a new paradigm for women’s healthcare that treats women as whole people vs. parts or life stages.&amp;nbsp; Blending in-person and virtual care services, Tia’s “Whole Woman, Whole Life” care model is a unique and “life-long” model for women’s care. By making women’s health higher quality and lower cost, Tia makes women healthier, providers happier, and the business of care delivery stronger — setting a new standard of care for women everywhere.&lt;/p&gt;
&lt;p&gt;Read more about Tia’s:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Products:&amp;nbsp;&lt;a href=&quot;https://asktia.com/article/what-is-product-at-tia&quot;&gt;https://asktia.com/article/what-is-product-at-tia&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Services:&amp;nbsp;&lt;a href=&quot;https://asktia.com/&quot;&gt;https://asktia.com/&lt;/a&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Care principles:&amp;nbsp;&lt;a href=&quot;https://www.asktia.com/care-philosophy/&quot;&gt;https://www.asktia.com/care-philosophy/&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We’re looking to connect with &lt;strong&gt;Nurse Practitioners &lt;/strong&gt;passionate about women’s health for&amp;nbsp;&lt;strong&gt;Tia’s East and West LA Clinics&lt;/strong&gt;. As a Nurse Practitioner, you will be an integral part of the care delivery system. Your clinical expertise related to the full spectrum of providing affirming primary care for women including: gynecological services, primary care, procedures and holistic whole person care is welcome!&lt;/p&gt;
&lt;p&gt;Nurse Practitioners are integral to the formation and iteration of our care model - with opportunities to provide direct patient care but also participate in technology development, interdisciplinary case studies, protocol development and innovation.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Schedule&lt;/strong&gt; is set with some flexibility. We are open to part-time and full-time employment&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;We offer 10 hr or 8 hr days. Start times are 7a-9a for early shifts and or 10a-12p for later shifts.&amp;nbsp; Expectation is that you take one evening shift per week.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;A bit about you:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Values and abilities you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re motivated to elevate women’s care by bringing a shared-decision making approach to women’s health.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You believe that each woman knows her body best. Your mission as a healthcare provider is to listen to patients and find ways to help them achieve their optimal health.&amp;nbsp; You practice this by being a true partner on a patient’s health journey.&lt;/li&gt;
&lt;li&gt;You’re facile with technology&lt;/li&gt;
&lt;li&gt;You are a tolerant and inclusive thinker. You believe in sex-positive, no judgment and radically inclusive healthcare for every person, and espouse these values in your everyday life.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Skills and assets you’ll bring to Tia:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You’re a board certified Nurse Practitioner in the state of California, with an unrestricted license, able to provide primary and gynecology care and support of all aspects of women’s health with compassion and empathy&lt;/li&gt;
&lt;li&gt;You’re adept at providing primary care services including: annual exams and pap smears, hypertension management, diabetes management, anxiety and depression management, urgent care concerns (coughs, sore throat, abdominal pain, etc), basic dermatological condition management, STD screens, UTI &amp;amp; Vaginal infections consults etc&lt;/li&gt;
&lt;li&gt;You’re highly tech savvy&lt;/li&gt;
&lt;li&gt;You’re willing to work some (but not all) evenings + weekends as needed by schedule.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You’re authorized to work in the US&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other “nice to have” skills:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You have procedural skills to perform: IUD insertions, nexplanon insertion and colposcopies or a desire to learn.&lt;/li&gt;
&lt;li&gt;As an organization that seeks to create an environment for all women to feel safe, heard, recognized and avowed in their health, bodies and lives, we are consistently seeking providers with backgrounds that are meaningfully different from those already forming our team. You bring a diverse background, a range of care experiences in different communities or various modalities.&lt;/li&gt;
&lt;li&gt;Formal professional training in the following areas is highly valued: care delivery for women who have experienced trauma, care delivery for LGBTQ identified folks including gender affirming hormone management, outpatient primary care depression and anxiety management.&lt;/li&gt;
&lt;li&gt;Experience or formal training weaving integrative medicine practices into your care plan development&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Benefits&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Talented and collaborative team who will support and collaborate with you&lt;/li&gt;
&lt;li&gt;Competitive salary with quarterly bonus program in place for full time clinicians&lt;/li&gt;
&lt;li&gt;Paid time off, paid sick leave, paid learning time off&lt;/li&gt;
&lt;li&gt;Comprehensive benefits package effective day one, including medical, dental &amp;amp; vision&lt;/li&gt;
&lt;li&gt;Medical malpractice coverage&lt;/li&gt;
&lt;li&gt;Reimbursed for state licenses, board certification, and BLS certification.&amp;nbsp;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;DEA will be reimbursed where it is required for practice.&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;Complimentary subscriptions to educational tools such as UptoDate along with extensive internal educational resources and monthly clinical training opportunities&lt;/li&gt;
&lt;li&gt;Access to AI documentation software drastically reducing administrative burden of clinical documentation&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Compensation:&amp;nbsp;&lt;/strong&gt;$140,000 - $160,000 for full-time positions. Part-time positions are compensated proportionally based of this range.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Us:&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Tia is on a mission to transform healthcare for women. We are building a high-quality, multi-specialty medical home designed specifically for women — integrating primary care, gynecology, mental health, dermatology and evidence-based wellness into one coordinated experience across in-person centers and a robust virtual platform.&lt;/p&gt;
&lt;p&gt;Tia is technology-enabled, advancing and scaling excellent care through a proprietary clinical and operational platform that supports clinicians, strengthens care continuity, and improves outcomes.&lt;/p&gt;
&lt;p&gt;We are deepening and expanding one of the most comprehensive preventive care models for women on the market — with a growing focus on cardiometabolic health, longitudinal data, and earlier risk detection across the lifespan. By integrating technology, structured clinical pathways, and mission-aligned interdisciplinary teams, Tia delivers consistently strong clinical outcomes and a differentiated care experience for women.&lt;/p&gt;
&lt;p&gt;Tia is a Series D, venture-backed company with more than 120,000 women who trust Tia for their care, across four markets, supported by a national virtual platform. In each market, we partner with leading health systems to expand access, strengthen primary care, and improve quality for women at scale.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Tia’s Culture:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tia is building a culture of excellence — in people, process and product. This is our northstar value;&lt;/p&gt;
&lt;p&gt;What is excellence, exactly?&lt;/p&gt;
&lt;p&gt;Excellence about constantly elevating yourself, it is the process of constantly striving to perform to the best of your abilities, and identifying your top potential through constant learning, experimentation and evolution. Excellence is not about achieving perfection, as that insinuates a pinnacle. Instead, in our terms, excellence is about the pursuit of constant improvement. We’re looking for people who want to go on that hard journey of constantly setting new personal records, and organizational records.&lt;/p&gt;
&lt;p&gt;We practice excellence at Tia by demonstrating the following types of behaviors: We chose (and actively choose) excellence as Tia’s highest order value because it crystalizes into one word several behaviors that we hold dear, specifically:&lt;/p&gt;
&lt;p&gt;A drive to constantly improve through experimentation, reflection. and an insatiable growth mindset — said another way, we’re energized by the possibility of invention, innovation, and iteration&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Being present in and grateful for the journey — not just the goal line. Perfection is static. Excellence is a process (more on this important distinction below)&lt;/li&gt;
&lt;li&gt;Asking why, then why again — because accepting “this is just the way it is” is not good enough&lt;/li&gt;
&lt;li&gt;Grit &amp;amp; perseverance — a maker mentality that involves “rolling up your sleeves”, but also deep care for oneself and for others&lt;/li&gt;
&lt;li&gt;A commitment to uncovering talents to unlock “rock star” potential across every individual&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Furthermore, excellence reflects the “bigness” and the “boldness” of Tia’s mission and vision — a world in which every woman can achieve optimal health, as defined by herself.&lt;/p&gt;
&lt;p&gt;Said another way, Tia’s mission is NOT to make healthcare incrementally better for women. Instead, we’ve intentionally set out to create a fundamentally new paradigm for modern women’s healthcare that’s truly excellent. We believe that creating a company that operates in a culture of excellence will manifest in our product. Reaching this goal is not an overnight pursuit or a “one and done.” We have not and will not “get it right” with the first swing. Rather, this higher order goal is a moving target — one we have not and will not ever fully “achieve.” By design, we will never be “done” with this work, but instead, we will be continuously in pursuit of our mission. It is this continuous pursuit — the journey, not the finish line — that truly embodies excellence.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;This position may require attendance at company and team off-sites.&lt;/em&gt;&lt;em&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;Unfortunately, scams targeting job seekers are on the rise. To protect yourself, know that we will never ask for payment, gift cards, or sensitive financial information during our hiring process. All communication from our team will come from an official company email address (@asktia.com). If something feels off, trust your instincts and reach out to us directly at &lt;/em&gt;&lt;em&gt;peopleservices@asktia.com&lt;/em&gt;&lt;em&gt;.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Tia is an equal opportunity employer. We believe that diversity of experience, perspectives, and background will lead to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are committed to collaborative problem solving, creating high-quality and user-centric products, and want to make waves in women&#39;s healthcare, join us!&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1jjwpys&quot; data-start=&quot;66&quot; data-end=&quot;78&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;80&quot; data-end=&quot;385&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is on a mission to transform healthcare for women by increasing access, improving outcomes, and delivering a better care experience. Our “Whole Woman, Whole Life” model integrates primary care, gynecology, mental health, dermatology, and wellness across in-person care and a national virtual platform.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;387&quot; data-end=&quot;652&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;We are a Series D, venture-backed company trusted by more than 120,000 women across four markets. Through our technology-enabled care model and partnerships with leading health systems, Tia is building one of the most comprehensive preventive care models for women.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;1x8x4he&quot; data-start=&quot;654&quot; data-end=&quot;676&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;About Tia’s Culture&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;678&quot; data-end=&quot;1083&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is building a culture of excellence in people, process, and product. For us, excellence is not perfection. It is the ongoing pursuit of improvement through learning, reflection, experimentation, curiosity, grit, and care for ourselves and others. We are looking for people who are energized by building, iterating, asking why, and helping create a fundamentally better healthcare experience for women.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1085&quot; data-end=&quot;1152&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;This position may require attendance at company and team off-sites.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;11qu7cz&quot; data-start=&quot;1154&quot; data-end=&quot;1168&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Scam Notice&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1170&quot; data-end=&quot;1453&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia will never ask for payment, gift cards, or sensitive financial information during the hiring process. All communication from our team will come from an official company email address ending in @asktia.com. If something feels off, please contact &lt;a style=&quot;color: rgb(126, 140, 141);&quot; data-start=&quot;1425&quot; data-end=&quot;1450&quot;&gt;peopleservices@asktia.com&lt;/a&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;h4 style=&quot;line-height: 1;&quot; data-section-id=&quot;l5aaog&quot; data-start=&quot;1455&quot; data-end=&quot;1475&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Equal Opportunity&lt;/span&gt;&lt;/h4&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1477&quot; data-end=&quot;1760&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;Tia is an equal opportunity employer. We believe diversity of experience, perspectives, and background leads to a better environment for our employees and a better product for our users and patients. We strongly encourage people of color and members of the LGBTQ+ community to apply.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;line-height: 1;&quot; data-start=&quot;1762&quot; data-end=&quot;1903&quot; data-is-last-node=&quot;&quot; data-is-only-node=&quot;&quot;&gt;&lt;span style=&quot;color: rgb(126, 140, 141);&quot;&gt;If you are committed to collaborative problem solving, high-quality work, and making waves in women’s healthcare, we’d love to hear from you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/nurse-practitioner-physician-assistant-full-spectrum-primary-care-los-angeles-talent-community-tia/6a069adf2f1861929d25320d</link><guid isPermaLink="true">http://biotechroles.com/nurse-practitioner-physician-assistant-full-spectrum-primary-care-los-angeles-talent-community-tia/6a069adf2f1861929d25320d</guid><pubDate>Fri, 15 May 2026 04:02:39 GMT</pubDate><company>Tia</company><location>Culver City, California, United States; Los Angeles, California, United States; Pasadena, California, United States; Playa Vista, California, United States; Studio City, California, United States</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Senior IT Systems Engineer]]></title><description><![CDATA[<div>Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.</div>
<div>&nbsp;</div>
<div>At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a&nbsp;<a href="https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6">public benefit corporation</a>&nbsp;(PBC), legally bound to balancing the interests of customers, employees, society, and investors.</div>
<div>&nbsp;</div>
<div>As a&nbsp;<a href="https://careers.veeva.com/work-anywhere/">Work Anywhere</a>&nbsp;company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.</div>
<div>&nbsp;</div>
<div>Join us in&nbsp;<a href="https://www.youtube.com/watch?v=TaPSP8cCSKY&amp;ab_channel=Forbes">transforming the life sciences industry</a>, committed to making a positive impact on its customers, employees, and communities.</div><div><br></div><div>
<h3>The Role</h3>
<div>This is both a <strong>‘build’ and ‘run’</strong> role. You will be responsible for the day-to-day operation of our enterprise systems while also working on projects to design and implement user-centric solutions. We are seeking a resourceful, technically-adept professional who thrives in fast-paced environments and takes full ownership of end-to-end delivery. The ideal candidate combines a customer-first mentality with a passion for problem-solving and continuous technical growth.</div>
</div></br><b>What You'll Do</b></br><div>

<li>Provide operational support (ex: troubleshooting user issues, configuration changes, feature releases) across our enterprise collaboration systems (Zoom, Google Workspace, Microsoft 365, etc.)</li>
<li>Maintain internal documentation, knowledge articles, and operating procedures</li>
<li>Work closely with first level end user support teams for incident and problem resolution, training of support team</li>
<li>Work with Veeva Security teams for incident investigations and implementation of security changes</li>
<li>Support the onboarding or rationalization of internal systems as required</li>
<li>Design, build, and maintain custom tooling and solutions as required</li>
<li>Proactively identify opportunities for internal improvements and deliver on those projects</li>

</div></br><b>Requirements</b></br><div>

<li>Bachelor’s degree in IT, Computer Science, or related field or other related experience</li>
<li>3+ years experience administrating enterprise systems such as Google Workspace, Zoom, or other equivalent IT systems</li>
<li>Experience managing vendor relationships</li>
<li>Demonstrated history of learning and adopting new technology and tools quickly</li>
<li>Strong analytical skills: able to listen and elicit business requirements and translate into technical solutions</li>
<li>Strong communication skills: written, verbal, and presentation</li>
<li>Ability to work independently in a fast paced environment with little direct supervision</li>
<li>Commitment to excellent customer service</li>
<li>Must be legally eligible to work in the US</li>

</div></br><h6>#LI-Remote</h6>
<h6>#LI-MidSenior</h6><div><br></div><div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>]]></description><link>http://biotechroles.com/senior-it-systems-engineer-veeva/6a069a702f1861929d25320a</link><guid isPermaLink="true">http://biotechroles.com/senior-it-systems-engineer-veeva/6a069a702f1861929d25320a</guid><pubDate>Fri, 15 May 2026 04:00:47 GMT</pubDate><company>Veeva</company><location>Ohio - Columbus</location><salary>$120000-160000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Business Consultant - EU Analytics]]></title><description><![CDATA[<div>
<div><span style="font-size: 16px;">Veeva is building the industry cloud for Life Sciences through software, data, AI, and Business Consulting working together. Learn more about our products, vision and values, and status as a public benefit corporation on our </span><a rel="noopener noreferrer" href="http://veeva.com/" style="font-size: 16px;" class="postings-link">website</a><span style="font-size: 16px;">.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">Consulting is changing, and we’re not like other firms. </span><a rel="noopener noreferrer" href="https://www.veeva.com/services/business-consulting-services/" style="font-size: 16px;" class="postings-link">Veeva Business Consulting</a><span style="font-size: 16px;"> was launched in 2019 and has grown quickly and organically to a global organization of over 400 people. Our team is focused on making the life sciences industry more efficient and effective through software, data, and consulting working together.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">We expect significant growth in Business Consulting as we look towards 2030, and are looking for great people to make it happen.</span></div>
</div><div><br></div><div>
<h3><span style="font-size: 18px;">The Role</span></h3>
<div>As a <strong>Senior Consultant</strong> in our <strong>EU Analytics Practice</strong>, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI. You will focus on reshaping operating models, driving organizational change, and measuring tangible business value.</div>
<div>&nbsp;</div>
<div>This is an opportunity to build your career in a multidisciplinary team of consultants and data scientists, participating in the delivery of large-scale analytics transformations and leveraging Veeva’s unique position to help our customers extract maximum value from their data assets. In this role, you will lead specific project workstreams from end-to-end, ensuring high-quality design and delivery.</div>
</div></br><b>What You'll Do</b></br><div>

<li><strong>Project Leadership:</strong> Act as the Lead for small-scale projects, managing end-to-end design and delivery of high-quality customer solutions</li>
<li><strong>Team Management:</strong> Lead project teams of 2–3 consultants and data scientists, developing your people leadership skills in a project setting</li>
<li><strong>Business Development:</strong> Drive practice growth by leading proposal development and identifying new opportunities within your engagements</li>
<li><strong>Strategic Problem Solving:</strong> Solve complex challenges for Life Sciences leaders by leveraging Veeva’s unique data, software, and AI insights</li>
<li><strong>Subject Matter Expertise:</strong> Support multiple projects across the <strong>EU Analytics Practice</strong> while developing deep expertise in 1–2 specific functional areas</li>

</div></br><b>Requirements</b></br><div>

<li><strong>Experience:</strong> 4+ years in Life Sciences Consulting (Business or Management Consulting preferred)</li>
<li><strong>Domain Knowledge:</strong> Proven expertise in Commercial Analytics/Excellence and/or Medical Strategy, with a solid understanding of the Life Sciences industry, as well as a good understanding of statistics and analytical techniques, with the ability to generate insights from data through metrics and visual reports</li>
<li><strong>Analytical Rigor:</strong> A strong mindset for both quantitative and qualitative reasoning</li>
<li><strong>Communication:</strong> Ability to articulate complex ideas clearly to senior and non-technical stakeholders</li>
<li><strong>Education:</strong> Bachelor’s degree or higher</li>

</div></br><div>
<h6><span style="font-size: 10px;">#RemoteSpain</span></h6>
<h6><span style="font-size: 10px;">#LI-MidSenior</span></h6>
</div><div><br></div><div>
<div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.</div>
<div>&nbsp;</div>
<div>If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>
</div>]]></description><link>http://biotechroles.com/senior-business-consultant-eu-analytics-veeva/6a069a702f1861929d253209</link><guid isPermaLink="true">http://biotechroles.com/senior-business-consultant-eu-analytics-veeva/6a069a702f1861929d253209</guid><pubDate>Fri, 15 May 2026 04:00:47 GMT</pubDate><company>Veeva</company><location>Spain - Barcelona</location><salary>$120000-180000</salary><type>Full-Time</type></item><item><title><![CDATA[Principal Software Engineer - AI Application]]></title><description><![CDATA[<div>Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.</div>
<div>&nbsp;</div>
<div>At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a&nbsp;<a href="https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6">public benefit corporation</a>&nbsp;(PBC), legally bound to balancing the interests of customers, employees, society, and investors.</div>
<div>&nbsp;</div>
<div>Join us in&nbsp;<a href="https://www.youtube.com/watch?v=TaPSP8cCSKY&amp;ab_channel=Forbes">transforming the life sciences industry</a>, committed to making a positive impact on its customers, employees, and communities.</div><div><br></div><h3><strong style="font-size: 18px;">The Role</strong></h3>
<div><strong>Veeva </strong>is seeking a <strong>Principal Backend Engineer</strong> to join our dynamic team in <strong>Beijing</strong>.</div>
<div>&nbsp;</div>
<div>In this role, you will lead the <strong>development of China CRM applications</strong> on our industry <strong>SaaS cloud platform</strong>, shaping the future of enterprise solutions for the Life Sciences industry. You’ll work alongside top engineers, solving complex challenges, optimizing performance, and ensuring reliability at scale.</div></br><b>What You'll Do</b></br>
<li><strong>Architect &amp; Design</strong> enterprise-grade SaaS solutions for China CRM applications</li>
<li><strong>Lead &amp; Mentor</strong> a talented team of engineers, fostering best practices in backend development</li>
<li><strong>Design and implement </strong>AI application features based on LLM</li>
<li><strong>Collaborate</strong> with cross-functional teams to deliver seamless, high-quality solutions</li>
<li><strong>Resolve </strong>the technical challenges and power the business by technical innovations</li>
<li><strong>Drive Innovation</strong> by leveraging modern cloud technologies to enhance system performance and scalability</li>
<li><strong>Develop</strong> the codes with Python skillsets</li>
</br><b>Requirements</b></br>
<li>Bachelor degree or above in computer related field</li>
<li>7+ years of development experience</li>
<li>Familiar with ToB SaaS application software design and development, with practical experience</li>
<li>Expert in common data structures and algorithms, mainstream relational database and NoSQL database</li>
<li>In-depth understanding of object-oriented design, clean coding style</li>
<li>Familiar with at least one major programming language, such as Python, Java, C++, etc</li>
<li>Familiar with web development technology and framework, such as Django/Flask/Spring, etc</li>
<li>Familiar with cloud native technologies, AWS Cloud, Docker, K8S, CI/CD, etc</li>
<li>Continuous enthusiasm for technology, optimistic personality, logical, good at working with people of all backgrounds</li>
</br><h6><span style="font-size: 10px;">#LI-MidSenior</span></h6><div><br></div><div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.</div>]]></description><link>http://biotechroles.com/principal-software-engineer-ai-application-veeva/6a069a702f1861929d253208</link><guid isPermaLink="true">http://biotechroles.com/principal-software-engineer-ai-application-veeva/6a069a702f1861929d253208</guid><pubDate>Fri, 15 May 2026 04:00:47 GMT</pubDate><company>Veeva</company><location>China - Beijing</location><salary>$120000-200000</salary><type>Full-Time</type></item><item><title><![CDATA[Principal Business Consultant - EU Analytics]]></title><description><![CDATA[<div>
<div><span style="font-size: 16px;">Veeva is building the industry cloud for Life Sciences through software, data, AI, and Business Consulting working together. Learn more about our products, vision and values, and status as a public benefit corporation on our </span><a rel="noopener noreferrer" href="http://veeva.com/" style="font-size: 16px;" class="postings-link">website</a><span style="font-size: 16px;">.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">Consulting is changing, and we’re not like other firms. </span><a rel="noopener noreferrer" href="https://www.veeva.com/services/business-consulting-services/" style="font-size: 16px;" class="postings-link">Veeva Business Consulting</a><span style="font-size: 16px;"> was launched in 2019 and has grown quickly and organically to a global organization of over 400 people. Our team is focused on making the life sciences industry more efficient and effective through software, data, and consulting working together.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">We expect significant growth in Business Consulting as we look towards 2030, and are looking for great people to make it happen.</span></div>
</div><div><br></div><div>
<h3><span style="font-size: 18px;">The Role</span></h3>
<div>As a <strong>Principal Consultant</strong> in our <strong>EU Analytics practice</strong>, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI. You will focus on reshaping operating models, driving organizational change, and measuring tangible business value.</div>
<div>&nbsp;</div>
<div>You will play a pivotal role in scaling our EU Analytics practice, directing integrated teams of consultants and data scientists to deliver business value. You will drive innovation across our service offerings, ensuring Veeva remains at the forefront of the shift toward data-led, tech-enabled Life Science commercial models. You will also collaborate closely with Veeva’s Product and Sales leadership to ensure a unified approach to large-scale data-driven transformations.</div>
</div></br><b>What You'll Do</b></br><div>

<li><strong>Project Mastery:</strong> Act as the Lead for Veeva BC’s largest and most complex global projects, maintaining full accountability for excellence across multiple teams</li>
<li><strong>Strategic Growth:</strong> Lead and own Business Development for EU Analytics practice, focusing on architecting and winning key deals exceeding $1M+</li>
<li><strong>People Leadership: </strong>Manage and mentor high-performing consulting teams, taking responsibility for the professional growth and delivery standards of the practice while developing a strong team spirit and leading community initiatives</li>
<li><strong>Thought Leadership:</strong> Develop and champion industry-leading thought leadership in Analytics and AI to keep Veeva at the cutting edge of Life Sciences</li>
<li><strong>Customer Success:</strong> Serve as a trusted advisor to C-suite stakeholders, leveraging Veeva’s data and software to solve their most critical challenges</li>

</div></br><b>Requirements</b></br><div>

<li><strong>Experience:</strong> 8+ years of Life Sciences Consulting experience (Management Consulting preferred)</li>
<li><strong>Track Record:</strong> Proven ability to win and deliver $1M+ consulting engagements</li>
<li><strong>Expertise:</strong> Deep domain knowledge and proven experience in Commercial Excellence, Pharma Operating Models, Advanced Analytics, Large-scale Data Strategy, and AI/Machine Learning applications and a comprehensive understanding of the Life Sciences landscape</li>
<li><strong>Leadership:</strong> Extensive experience managing multiple project teams and senior-level customer relationships</li>
<li><strong>Education:</strong> Bachelor’s degree or higher</li>

</div></br><div>
<h6><span style="font-size: 10px;">#RemoteGermany</span></h6>
<h6><span style="font-size: 10px;">#LI-Principal</span></h6>
</div><div><br></div><div>
<div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.</div>
<div>&nbsp;</div>
<div>If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>
</div>]]></description><link>http://biotechroles.com/principal-business-consultant-eu-analytics-veeva/6a069a702f1861929d253207</link><guid isPermaLink="true">http://biotechroles.com/principal-business-consultant-eu-analytics-veeva/6a069a702f1861929d253207</guid><pubDate>Fri, 15 May 2026 04:00:47 GMT</pubDate><company>Veeva</company><location>Germany - Berlin</location><salary>$120000-180000</salary><type>Full-Time</type></item><item><title><![CDATA[Engagement Manager - EU Analytics Business Consulting]]></title><description><![CDATA[<div>
<div><span style="font-size: 16px;">Veeva is building the industry cloud for Life Sciences through software, data, AI, and Business Consulting working together. Learn more about our products, vision and values, and status as a public benefit corporation on our </span><a rel="noopener noreferrer" href="http://veeva.com/" style="font-size: 16px;" class="postings-link">website</a><span style="font-size: 16px;">.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">Consulting is changing, and we’re not like other firms. </span><a rel="noopener noreferrer" href="https://www.veeva.com/services/business-consulting-services/" style="font-size: 16px;" class="postings-link">Veeva Business Consulting</a><span style="font-size: 16px;"> was launched in 2019 and has grown quickly and organically to a global organization of over 400 people. Our team is focused on making the life sciences industry more efficient and effective through software, data, and consulting working together.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">We expect significant growth in Business Consulting as we look towards 2030, and are looking for great people to make it happen.</span></div>
</div><div><br></div><h3><span style="font-size: 18px;">The Role</span></h3>
<div>As an <strong>Engagement Manager</strong> in our <strong>EU Analytics practice</strong>, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI. You will focus on reshaping operating models, driving organizational change, and measuring tangible business value.</div>
<div>&nbsp;</div>
<div>This is an opportunity to build your career in a multidisciplinary team of consultants and data scientists, leading the delivery of large-scale analytics transformations and leveraging Veeva’s unique position to help our customers extract maximum value from their data assets. In this role, you will lead our most complex analytics projects from end-to-end, acting as a strategic partner to our clients and a mentor to our growing team.</div></br><b>What You'll Do</b></br><div>

<li><strong>Strategic Delivery:</strong> Act as the end-to-end lead on Veeva’s most complex, large-scale, and global engagements</li>
<li><strong>Account Leadership:</strong> Build and navigate senior customer relationships, leading proposals for significant project wins and driving long-term account strategy</li>
<li><strong>People Leadership:</strong> Lead and inspire teams of 4+ consultants and data scientists across multiple projects simultaneously, fostering a culture of excellence</li>
<li><strong>Financial Oversight:</strong> Manage project budgets of $1M+, acting as the primary point of contact for project health and commercial success</li>
<li><strong>Practice Building: </strong>Support brand-building activities and the development of internal IP to keep Veeva Business Consulting at the forefront of the industry</li>

</div></br><b>Requirements</b></br><div>

<li><strong>Experience:</strong> 6+ years in Life Sciences Consulting (Business or Management Consulting preferred)</li>
<li><strong>Leadership:</strong> Proven track record of managing large project teams and $1M+ engagements, demonstrating the ability to drive projects to success and make critical decisions in the face of uncertainty</li>
<li><strong>Domain Knowledge:</strong> Proven expertise in Commercial Excellence, Analytics, Go-to-Market Strategies and the broader Life Sciences industry. You must demonstrate proven project management skills in organizing and prioritizing day-to-day team tasks and customer interactions, alongside a mastery of end-to-end data management, analytics and governance frameworks</li>
<li><strong>Mindset:</strong> A highly analytical approach to problem-solving with the ability to influence C-suite stakeholders and to translate customer needs into solutions</li>
<li><strong>Education:</strong> Bachelor’s degree or higher</li>

</div></br><div>
<h6><span style="font-size: 10px;">#RemoteUK</span></h6>
<h6><span style="font-size: 10px;">#LI-MidSenior</span></h6>
</div><div><br></div><div>
<div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.</div>
<div>&nbsp;</div>
<div>If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>
</div>]]></description><link>http://biotechroles.com/engagement-manager-eu-analytics-business-consulting-veeva/6a069a702f1861929d253204</link><guid isPermaLink="true">http://biotechroles.com/engagement-manager-eu-analytics-business-consulting-veeva/6a069a702f1861929d253204</guid><pubDate>Fri, 15 May 2026 04:00:47 GMT</pubDate><company>Veeva</company><location>United Kingdom - London</location><salary>$110000-160000</salary><type>Full-Time</type></item><item><title><![CDATA[Business Consultant - EU Analytics]]></title><description><![CDATA[<div>
<div><span style="font-size: 16px;">Veeva is building the industry cloud for Life Sciences through software, data, AI, and Business Consulting working together. Learn more about our products, vision and values, and status as a public benefit corporation on our </span><a rel="noopener noreferrer" href="http://veeva.com/" style="font-size: 16px;" class="postings-link">website</a><span style="font-size: 16px;">.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">Consulting is changing, and we’re not like other firms. </span><a rel="noopener noreferrer" href="https://www.veeva.com/services/business-consulting-services/" style="font-size: 16px;" class="postings-link">Veeva Business Consulting</a><span style="font-size: 16px;"> was launched in 2019 and has grown quickly and organically to a global organization of over 400 people. Our team is focused on making the life sciences industry more efficient and effective through software, data, and consulting working together.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">We expect significant growth in Business Consulting as we look towards 2030, and are looking for great people to make it happen.</span></div>
</div><div><br></div><div>
<h3><span style="font-size: 18px;">The Role</span></h3>
<div>As a <strong>Consultant </strong>in our <strong>EU Analytics Practice</strong>, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI. You will focus on reshaping operating models, driving organizational change, and measuring tangible business value.</div>
<div>&nbsp;</div>
<div>This is an opportunity to build your career in a multidisciplinary team of consultants and data scientists, participating in the delivery of large-scale analytics transformations and leveraging Veeva’s unique position to help our customers extract maximum value from their data assets. In this role, you will lead specific project workstreams from end-to-end, ensuring high-quality design and delivery.</div>
</div></br><b>What You'll Do</b></br><div>

<li><strong>Lead project workstreams</strong> from end-to-end, ensuring the high-quality design and delivery of customer solutions</li>
<li><strong>Solve complex problems</strong> for Life Sciences leaders, leveraging Veeva’s unique data and software insights</li>
<li><strong>Mentor and manage </strong>Associate Consultants, overseeing their work and professional development within your workstream</li>
<li><strong>Drive practice growth</strong> by contributing to business development and internal IP creation</li>

</div></br><b>Requirements</b></br><div>

<li><strong>Experience:</strong> 2+ years in Life Sciences Consulting (Business or Management Consulting preferred)</li>
<li><strong>Domain Knowledge:</strong> Proven expertise in Commercial Analytics/Excellence and/or Medical Strategy, with a solid understanding of the Life Sciences industry, as well as a good understanding of statistics and analytical techniques, with the ability to generate insights from data through metrics and visual reports</li>
<li><strong>Analytical Rigor:</strong> A strong mindset for quantitative and logical reasoning</li>
<li><strong>Communication:</strong> Ability to articulate complex ideas clearly to senior and non-technical stakeholders</li>
<li><strong>Education:</strong> Bachelor’s degree or higher</li>

</div></br><div>
<h6><span style="font-size: 10px;">#RemoteGermany</span></h6>
<h6><span style="font-size: 10px;">#LI-Associate</span></h6>
</div><div><br></div><div>
<div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.</div>
<div>&nbsp;</div>
<div>If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>
</div>]]></description><link>http://biotechroles.com/business-consultant-eu-analytics-veeva/6a069a6f2f1861929d253201</link><guid isPermaLink="true">http://biotechroles.com/business-consultant-eu-analytics-veeva/6a069a6f2f1861929d253201</guid><pubDate>Fri, 15 May 2026 04:00:47 GMT</pubDate><company>Veeva</company><location>Germany - Berlin</location><salary>$65000-95000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Manager / Associate Director, Cost Accounting]]></title><description><![CDATA[<div>More than one million people in the United States today are fighting blood cancer. While a traditional <a href="https://www.mayoclinic.org/tests-procedures/allogeneic-stem-cell-transplant/pyc-20384863" class="postings-link">allogeneic stem cell transplant</a> has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.<strong>&nbsp;</strong><span style="font-size: inherit;">With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.</span></div><div><br></div><div>The Senior Manager / Associate Director, Cost Accounting will lead cost accounting activities for manufacturing and operational functions within a biotechnology or pharmaceutical organization. This role is responsible for overseeing product costing, inventory valuation, COGS reporting, and cost-related controls, while supporting business scaling from clinical-stage through commercialization. The position requires strong leadership, cross-functional partnership, and deep expertise in manufacturing cost structures.</div></br><b>Essential Duties & Key Responsibilities</b></br>
<li><strong>Cost Accounting &amp; Analysis</strong></li>
<li>Develop, own and oversee standard costing, variance analysis, and cost allocations across manufacturing operations</li>
<li>Establish and maintain cost accounting policies, procedures, and internal controls</li>
<li>Lead and review monthly close activities related to inventory, COGS, and manufacturing variances</li>
<li>Support cost-of-goods-sold (COGS) analysis for clinical and commercial products</li>

<div>&nbsp;</div>

<li><strong>Inventory &amp; Manufacturing Accounting</strong></li>
<li>Maintain accurate inventory valuation for raw materials, WIP, and finished goods</li>
<li>Account for complex manufacturing processes, including batch-based and patient-specific production, where applicable</li>
<li>Partner with Manufacturing, Supply Chain, and R&amp;D to understand cost drivers and improve cost accuracy</li>
<li>Lead physical inventory counts and cycle count programs</li>
<li>Ensure proper capitalization and expensing of manufacturing-related costs</li>

<div>&nbsp;</div>

<li><strong>Financial Reporting &amp; Compliance</strong></li>
<li>Support monthly close activities related to inventory, COGS, and manufacturing variances</li>
<li>Ensure compliance with GAAP, SOX (if applicable), and internal controls</li>
<li>Assist with audit requests related to inventory, cost accounting, and manufacturing transactions</li>
<li>Support implementation and maintenance of ERP and cost accounting systems</li>
<li>Serve as a primary point of contact for auditors on cost accounting and inventory-related matters</li>

<div>&nbsp;</div>

<li><strong>Budgeting &amp; Forecasting</strong></li>
<li>Assist in manufacturing cost forecasts and annual budgets</li>
<li>Monitor actual costs versus budget and provide variance analysis</li>
<li>Support long-range planning related to scale-up, tech transfer, and commercialization</li>
</br><b>Minimum Experience, Education, Certifications, Licenses</b></br>
<li>Bachelor’s degree in accounting, Finance, or related field</li>
<li>5+ years of progressive cost accounting experience in a manufacturing, biotech, or pharmaceutical environment</li>
<li>Strong understanding of standard costing, inventory accounting, and variance analysis</li>
<li>Experience working with ERP systems – NetSuite is highly desirable</li>
<li>Strong Excel skills and data analysis capabilities</li>
<li>Strong analytical and problem-solving skills</li>
<li>Ability to work cross-functionally with manufacturing and operations teams</li>
<li>High attention to detail and accuracy</li>
<li>Ability to manage multiple priorities in a fast-paced environment</li>
</br><div>The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Who we are</strong></div>
<div>&nbsp;</div>
<div>We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.</div>
<div>&nbsp;</div>
<div>We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.</div>
<div>&nbsp;</div>
<div>We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.</div>
<div>&nbsp;</div>
<div>We maintain a start-up culture of camaraderie and leadership by example, regardless of title.</div>
<div>&nbsp;</div>
<div>We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Notice to staffing firms</strong></div>
<div>&nbsp;</div>
<div>Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.</div>]]></description><link>http://biotechroles.com/senior-manager-associate-director-cost-accounting-orca-bio/6a069a692f1861929d2531ff</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-associate-director-cost-accounting-orca-bio/6a069a692f1861929d2531ff</guid><pubDate>Fri, 15 May 2026 04:00:41 GMT</pubDate><company>Orca Bio</company><location>Menlo Park, CA</location><salary>$150000-190000</salary><type>Regular, Full-Time Employee</type></item><item><title><![CDATA[Manager, Accounting]]></title><description><![CDATA[<div>More than one million people in the United States today are fighting blood cancer. While a traditional <a href="https://www.mayoclinic.org/tests-procedures/allogeneic-stem-cell-transplant/pyc-20384863" class="postings-link">allogeneic stem cell transplant</a> has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.<strong>&nbsp;</strong><span style="font-size: inherit;">With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.</span></div><div><br></div><div>As<em><strong> </strong></em><strong>Manager, Accounting</strong> you will oversee the daily operations of the company’s accounting function, ensuring accurate, timely, and compliant financial reporting and accounting operations in a fast-paced, high-growth environment. You will lead and develop the accounting team, manage high-volume transactional processes and month-end close activities, maintain strong internal controls, and partner cross-functionally to support the company’s continued growth and operational execution.</div></br><b>Essential Duties & Key Responsibilities</b></br>
<li>Oversee all aspects of the accounting function, ensuring accurate, timely, and compliant financial reporting while supporting the organization’s strategic and operational objectives.</li>
<li>Manage and maintain the general ledger, including preparing and reviewing journal entries within assigned areas of responsibility.</li>
<li>Develop and maintain a comprehensive understanding of the company’s financial reporting processes and general ledger structure.</li>
<li>Ensure compliance with internal accounting policies, procedures, GAAP standards, and applicable regulatory requirements.</li>
<li>Lead, mentor, and supervise accounting staff, while driving improvements and enhancing operational efficiency.</li>
<li>Coordinate and support external audit activities, including annual financial statement audits, quarterly reviews, and internal control testing.</li>
<li>Oversee statutory and regulatory filings in accordance with local jurisdiction requirements, including but not limited to 1099 reporting, sales and use tax, property tax, and census reporting.</li>
<li>Experience with clinical trial accounting and accrual management is preferred but not required.</li>
<li>Proficiency with ERP systems, preferably NetSuite and strong knowledge of accounting software and financial reporting tools.</li>
</br><b>Minimum Experience, Education, Certifications, Licenses</b></br>
<li>Bachelor’s degree in Accounting, Finance, or related field; CPA preferred.</li>
<li>5+ years of progressive accounting experience within biotechnology or life sciences.</li>
<li>Prior people management experience required, including leading and developing accounting staff and driving accountability/performance.</li>
<li>Strong knowledge of day-to-day accounting operations, including accounts payable, general ledger, monthly close, accruals, and statutory/compliance filings.</li>
<li>Experience managing high-volume AP and operational accounting workflows in a fast-paced environment.</li>
<li>Demonstrated ability to operate with firmness and accountability while building effective cross-functional relationships.</li>
<li>Strong organizational skills, attention to detail, and ability to prioritize across competing deadlines.</li>
<li>Experience with ERP/accounting systems and Microsoft Excel.</li>
</br><div>The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Who we are</strong></div>
<div>&nbsp;</div>
<div>We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.</div>
<div>&nbsp;</div>
<div>We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.</div>
<div>&nbsp;</div>
<div>We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.</div>
<div>&nbsp;</div>
<div>We maintain a start-up culture of camaraderie and leadership by example, regardless of title.</div>
<div>&nbsp;</div>
<div>We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Notice to staffing firms</strong></div>
<div>&nbsp;</div>
<div>Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.</div>]]></description><link>http://biotechroles.com/manager-accounting-orca-bio/6a069a692f1861929d2531fe</link><guid isPermaLink="true">http://biotechroles.com/manager-accounting-orca-bio/6a069a692f1861929d2531fe</guid><pubDate>Fri, 15 May 2026 04:00:41 GMT</pubDate><company>Orca Bio</company><location>Menlo Park, CA</location><salary>$140000-180000</salary><type>Regular, Full-Time Employee</type></item><item><title><![CDATA[Director, Device Development]]></title><description><![CDATA[<div>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11.0pt; line-height: 115%;">As part of BlueRock Therapeutics vision to change the future of medicine by enabling ground-breaking cell therapies, the candidate will be a leader in the combination device development and manufacturing team responsible for ensuring that the company’s leading cell product candidates have an appropriately designed, tested and implemented combination device.&nbsp; Key elements include procedures to prepare and administer cell products compatible with current clinical technologies and practice of medicine, and medical device systems that safely, and accurately deliver these products to meet the unmet needs of patients with intractable diseases.&nbsp; The Device Development team works with leading physicians and other experts to develop clinical product procedures, delivery systems and other technologies in close partnership with our cell product development colleagues.&nbsp; The successful candidate is a proven team leader in the development and manufacturing of cutting-edge medical product technologies including combination medical devices and ancillary products.&nbsp; The ideal candidate has a deep understanding of medical device development processes and regulations, is comfortable working directly with world-renowned physicians, is highly familiar with design and manufacturing technologies and has a demonstrated track record of leading product development teams that have taken concepts and advanced them into clinical evaluation and commercial launch utilizing internal and external capabilities.&nbsp; Collaboration with a highly motivated, world-class team of engineers and scientists promises an exciting and engaging work environment for motivated, self-starting candidates.&nbsp; Proven history in developing drug delivery device development is required; experience in combination product development and surgical device development is strongly preferred.</span></p>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11.0pt; line-height: 115%;">The <strong>Director, Device Development </strong>serves as a <strong>global technical and organizational leader</strong> responsible for the <strong>end‑to‑end design, development, transfer, and clinical readiness of complex medical devices and combination products</strong> for BRT’s Cell Therapy portfolio. </span></p>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11.0pt; line-height: 115%;">This role operates <strong>beyond individual project execution</strong>, providing <strong>strategic technical leadership</strong>, <strong>cross‑functional alignment</strong>, and <strong>governance‑level decision support</strong> across Device Development, TechOps, Quality, Regulatory, Clinical, and New Product Planning organizations.</span></p>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11.0pt; line-height: 115%;">The role is a <strong>recognized authority</strong> in device design, design control, and industrialization, and functions as a <strong>primary integrator between BRT internal teams and external device partners</strong> (e.g., CDMOs, suppliers, analytical labs), ensuring clinic readiness and compliance from development through clinical studies and eventual handoff to parties responsible for commercialization.</span></p>
</div></br><b>Responsibilities:</b></br><div>
<p><strong>1. Technical Leadership</strong></p>

<li>Acts as technical representative on project teams for complex delivery and preparation device systems, spanning system, device, and component levels.</li>
<li>Defines and maintains technical strategy, design intent, and risk profile across development phases, from early development through clinical phases and handoff to those with ownership for launch and commercial sustainment.</li>
<li>Provides expert judgment on material selection, key quality target product profile, usability, manufacturability, and design trade‑offs, particularly for cell therapy combination products (drug delivery, dose preparation, accessories, etc.).</li>

<p><strong>2. Cross‑Functional &amp; Matrix Leadership (No Formal Direct Reports Required)</strong></p>

<li>Leads cross‑functional collaboration across Device Development, TDT, Quality, Regulatory, Supply Chain, Commercial and Bayer stakeholders.</li>
<li>Serves as primary escalation point for device‑related technical and executional issues, resolving ambiguity and enabling timely decision‑making.</li>
<li>Coaches and mentors senior and mid‑level engineers, strengthening technical depth, decision quality, and design control rigor across the organization.</li>
<li>Liaises with Bayer Device stakeholders to align approaches and maintain a network of internal and external device technical SMEs.</li>

<p><strong>3. Governance, Decision‑Making &amp; Executive Interface</strong></p>

<li>Represents device engineering at program governance forums, steering committees, and executive reviews (e.g., Board, TechOps, CMC).</li>
<li>Shapes device strategy narratives for leadership audiences, translating technical complexity into clear risk, readiness, and decision frameworks.</li>
<li>Drives alignment on what BRT must own internally vs. leverage externally, enabling scalable development and industrialization models.</li>

<p><strong>4. Design Control &amp; Regulatory Stewardship</strong></p>

<li>Accountable for design control strategy and execution in accordance with BRT QMS and global regulatory expectations for combination products.</li>
<li>Ensures design history file (DHF) integrity, robust V&amp;V planning, and traceability across user needs, risk management, and performance requirements.</li>
<li>Partners closely with Regulatory Affairs and Quality to support global submissions and associated efforts related to pre-clinical and clinical phases of development.</li>

<p><strong>5. Industrialization, Transfer &amp; Commercial Readiness Leadership</strong></p>

<li>Key contributor to design transfer to Bayer Product Supply, ensuring manufacturability, scalability, and global supply robustness.</li>
<li>Shapes early phase clinical device strategy with commercial goals in mind, including supplier selection, design development and manufacturing site readiness to support clinical phases.</li>
<li>Drives alignment across clinical, open‑label, and commercial device configurations, ensuring continuity and long‑term sustainability.</li>

<p><strong>Impact Indicators</strong></p>

<li>Recognized internally as the go‑to authority for cell therapy device design and device strategy.</li>
<li>Influences multiple programs and organizational capabilities, not just a single asset.</li>
<li>Independently sets direction in areas of technical ambiguity, with decisions shaping program outcomes.</li>
<li>Elevates the effectiveness of the broader device organization through mentorship, standards, and governance leadership.</li>

</div></br><b>Minimum Requirements: </b></br>
<li>Bachelor’s or Master’s degree or equivalent, or PhD with 10+ years of experience</li>
<li>B.S. or M.S. in Biomedical, Materials engineering, or related and a minimum of ten years of medical product (preferably medical device or biologics) development and manufacturing experience.&nbsp; An equivalent combination of education and experience sufficient to successfully perform the job duties as listed above may be considered.</li>
<li>Thorough understanding of Design Controls and cGMP requirements compliant with ISO 13485 and the QSR (21 CFR Part 820)</li>
<li>Significant experience in development and validation of medical device manufacturing processes and technologies is required</li>
<li>Demonstrated cross functional leader with successful track record of delivering projects on time and within budget</li>
<li>Experience with biologic product delivery (delivery media, bio-polymers, delivery technologies, micro-fluidic control, anatomy) is a strong plus.</li>
<li>Experience leader in delivering products through IND</li>
<li>Competency in computer skills and familiarity with Microsoft Office (Word, Excel, PowerPoint, Project)</li>

<div>&nbsp;</div>
<div>Salary Range: $<span data-teams="true">230,000 - 260,000</span>&nbsp;</div></br><div>#LI-AL1</div>]]></description><link>http://biotechroles.com/director-device-development-bluerock/6a069a642f1861929d2531fd</link><guid isPermaLink="true">http://biotechroles.com/director-device-development-bluerock/6a069a642f1861929d2531fd</guid><pubDate>Fri, 15 May 2026 04:00:36 GMT</pubDate><company>BlueRock</company><location>Toronto, Ontario</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Sr. Director, Quality Systems]]></title><description><![CDATA[<p>Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.</p>
<p><strong>Title</strong>: Sr. Director, Quality Systems</p>
<p><strong>Reports to</strong>: VP, Quality</p>
<p><strong>Location</strong>: Emeryville, CA (Hybrid onsite twice a week)</p>
<p><strong>Summary</strong></p>
<p>Kyverna is seeking a highly motivated Sr. Director, Quality Systems to join our Quality organization. This role will provide leadership across core quality systems and ensure compliance with global GXP requirements while enabling rapid organizational growth and operational execution in a highly complex, patient-centric environment.&nbsp; The ideal candidate is a strategic and operational quality leader responsible for establishing, scaling, and managing a phase-appropriate Quality Management System (QMS) to support late-stage clinical development, Biologics License Application (BLA) readiness, and commercial launch for Kyverna’s cell therapy program(s).</p>
<p>The Sr. Director, Quality Systems will partner cross-functionally with Manufacturing, Quality Control, Regulatory Affairs, Technical Development, Supply Chain, Patient Operations, IT, Clinical Operations, Clinical Development, Data Management, Biostats, and PV/Safety to ensure alignment and effectiveness of Kyverna’s QMS.</p></br><b>Responsibilities</b></br><div>

<li>Develop, implement, and manage Kyverna’s Quality Management System.</li>
<li>In close collaboration with Technical Operations and Clinical Functions, define the requirements for a late phase and commercial lifecycle stage-appropriate quality system.&nbsp;</li>
<li>Drive the maturation and continuous improvement of the QMS to support clinical development through commercialization.</li>
<li>Represent Quality and provide Quality leadership on cross-functional project and program teams, as required.</li>
<li>Ensure compliance with all applicable regulations, industry best practices, and standards related to Kyverna products. Adapt the QMS per region-specific requirements as required.</li>
<li>Serve as the Quality business process owner (BPO) and provide oversight for Change Management, Deviation/CAPA Management, Document Lifecycle Management, Records Management, Training Program, Quality Risk Management, Computer Systems Quality Assurance, Quality Management Review, and Quality Governance Boards.</li>
<li>Lead Quality Management Review and Quality Governance Board (such as Material Review Boards, Specification Review Boards, Change Control Review Boards, etc.) meetings and monitor the state of control of Kyverna’s QMS.</li>
<li>Set and/or facilitate establishment of key performance indicators and metrics. Perform trend analysis and assess QMS processes for potential gaps to ensure compliance and to monitor the health of the QMS. Ensure proper communication and escalation to peers, senior, and executive management as required.</li>
<li>Assist in the development and deployment of quality systems in accordance with ICH Q 8,9,10 model, PDA TR 56, and other industry best practices.</li>
<li>Ensure that quality systems are designed and operate as appropriate to provide support in development and commercialization for GXP areas.</li>
<li>Evaluate, identify, and drive continuous improvement opportunities to maintain product quality and improve process effectiveness in the overall QMS lifecycle.</li>
<li>Oversee and manage the electronic Quality Management System (eQMS), including workflow configuration and the continued validation of the system.</li>
<li>Support inspection readiness activities including assessment and oversight of Kyverna records, storyboard, and inspection logistics.</li>
<li>Participate in audits and inspections representing Quality Systems</li>
<li>Support Regulatory Filings as required.</li>
<li>Manage a budget for implementation of quality tools and training</li>
<li>Support processes and work with contract service providers providing manufacturing and testing and clinical services.</li>
<li>Manages and mentors a team of highly performing individuals</li>

</div></br><b>Qualifications</b></br>
<li>Bachelor's degree and 10+ years’ experience in a biopharmaceutical, pharmaceutical, biologics, or related life sciences area and relevant Quality Systems experience, ATMP experience preferred.</li>
<li>4+ years’ personnel management experience</li>
<li>In-depth knowledge of cGMPs, FDA regulations (21 CFR Parts 210, 211, 11), EudraLex, ICH Guidelines, etc.</li>
<li>Working knowledge of GXP regulations and guidelines, as it pertains to Quality Systems</li>
<li>Experience with implementation and qualification of an eQMS</li>
<li>Ability to work with ambiguity, creative approach to problem solving and ability to define a clear path forward with emphasis on compliance and efficiency</li>
<li>Ability to work effectively with various technical groups</li>
<li>Ability to work in a collaborative team environment is essential, with a customer-focused approach</li>
<li>Strong decision maker with the ability to utilize critical thinking to problem-solve</li>
<li>Must have strong interpersonal and communication skills</li>
<li>Expert level experience writing, reviewing and editing SOPs, as well as other document types</li>
</br><div>
<p>The San Francisco Bay Area salary range for this position is $255K to $280K USD annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on factors including experience, education, geographic location, internal equity, and market data. This position is also eligible for annual bonus, equity, benefits, and participation in the Company’s stock plan.</p>
</div>]]></description><link>http://biotechroles.com/sr.-director-quality-systems-kyverna/6a069a622f1861929d2531fb</link><guid isPermaLink="true">http://biotechroles.com/sr.-director-quality-systems-kyverna/6a069a622f1861929d2531fb</guid><pubDate>Fri, 15 May 2026 04:00:34 GMT</pubDate><company>Kyverna</company><location>Emeryville, CA</location><salary>$180000-240000</salary><type>Full Time</type></item><item><title><![CDATA[Paralegal, Contract Management & Legal Operations]]></title><description><![CDATA[<div>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">&nbsp;</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;"><strong>Title</strong>: Paralegal, Contract Management &amp; Legal Operations</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;"><strong>Reports to</strong>: Associate General Counsel</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;"><strong>Location</strong>: Remote (West coast hours preferred)</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">&nbsp;</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;"><strong>Summary</strong></p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">The Paralegal will provide a diverse range of legal and contract management support within the Legal Department, managing a high volume of documents, including end-to-end contract administration, ensuring contracts are accurately formatted, properly routed, and efficiently executed. This role will be responsible for tracking and organizing agreements, maintaining contract records, and supporting workflow optimization using tools such as SharePoint and Ironclad.</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">&nbsp;</p>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">This is a highly detail-oriented role focused on process, coordination, and operational excellence, enabling timely contract execution across the organization.</p>
</div></br><b>Responsibilities</b></br><div>
<ul type="disc" style="margin-top: 0in; margin-bottom: 0in;">
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Serve as the primary administrator for the Legal Department systems (e.g., document management, specifically IronClad, and the department Sharepoint pages)</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Act as a central point of coordination for contract-related inquiries and status updates</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Maintain a centralized contract tracking system (e.g., SharePoint, Ironclad, or CLM tool)</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Own triage and assignment of legal matters as a bridge between business requesters and the Legal Department, including ensuring a clear understanding and training of the processes and procedures</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Assist with training internal stakeholders on contracting processes and tools</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Manage the lifecycle of all contracts using CLM (IronClad) and assist with ongoing optimization</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Coordinate the intake, routing, and execution of contracts across internal stakeholders</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Track contract status and follow up with stakeholders to ensure timely completion</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Review contracts for formatting, completeness, and consistency with company templates</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Ensure proper use of templates, clause libraries, and version control</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Identify and flag inconsistencies or missing information for attorney review</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Maintain high standards for document accuracy and professionalism</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Route agreements for review and signature using e-signature platforms (e.g., Adobe Sign), ensuring all required approvals are obtained prior to execution</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Ensure all executed agreements are properly stored, indexed, and easily retrievable</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Track key contract metadata, including effective dates, expiration/renewal dates, and contract owners</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Generate reports and dashboards to provide visibility into contract status and obligations</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Identify opportunities to improve efficiency, reduce cycle times, and standardize processes</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Support implementation of contract templates, playbooks, and intake forms</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Assist with calendar and travel management, and submission of invoices and expenses</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Prepare and maintain department meeting agendas and minutes</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Monitor Legal Department performance based on articulated goals and provide data-driven insights to inform department decision-making</li>

</ul></div></br><b>Qualifications</b></br><div>
<ul type="disc" style="margin-top: 0in; margin-bottom: 0in;">
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Bachelor’s degree required and/or Paralegal Certificate</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">7+ years of experience as paralegal, contract administration, legal operations, or similar legal support role</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Experience working with contract lifecycle management (CLM) systems, preferably Ironclad</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Strong working knowledge of Microsoft SharePoint for document management and tracking</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Experience with e-signature tools (e.g., Adobe Sign)</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Both In-house and law firm paralegal experience highly desired</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Excellent written and verbal communication skills with strong client focus</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Extremely strong attention to detail, particularly in document formatting and version control; must be able to perform final QC of documents</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Handles confidential matters with discretion and judgment.</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Demonstrate nimbleness with challenges and resilience with setbacks; embraces a growth mindset and welcomes opportunities to learn and take stretch assignments.&nbsp;</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Highly collaborative with excellent organizational and time management skills</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Ability to manage multiple contracts and priorities simultaneously, and multi-task across projects to prioritize and manage timelines effectively</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Experience in biotech, pharmaceutical, highly preferred</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Ability to sustain high levels of performance in a constantly changing environment</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Familiarity with contract templates, clause libraries, and basic legal terminology</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Experience building or improving contract tracking systems or dashboards&nbsp;</li>
<li style="margin-bottom: 0in; margin-top: 0in; margin-right: 0in; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;">Other duties as assigned, including management of documents related to or arising from litigation or disputes, document collections responsive to risk management renewal efforts, projects related to document retention efforts, etc.</li>

</ul></div></br><div>
<p style="margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">The national salary range for this position is $125K to $140K USD annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on factors including experience, education, geographic location, internal equity, and market data. This position is also eligible for annual bonus, equity, benefits, and participation in the Company’s stock plan.</p>
</div>]]></description><link>http://biotechroles.com/paralegal-contract-management-and-legal-operations-kyverna/6a069a622f1861929d2531fc</link><guid isPermaLink="true">http://biotechroles.com/paralegal-contract-management-and-legal-operations-kyverna/6a069a622f1861929d2531fc</guid><pubDate>Fri, 15 May 2026 04:00:34 GMT</pubDate><company>Kyverna</company><location>Remote</location><salary>$85000-120000</salary><type>Full Time</type></item><item><title><![CDATA[Research Associate, Platform Technology]]></title><description><![CDATA[<div>
<h3><strong>About Us</strong></h3>
<div>Deep Genomics is at the forefront of using artificial intelligence to transform drug discovery. Our proprietary AI platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms, and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, bioinformatics, data science, engineering, and drug development, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how new medicines are created.</div>
<div>&nbsp;</div>
<div>
<h3><strong>Opportunity&nbsp;</strong></h3>
<div>We are looking for a passionate and detail-oriented Research Associate to become an integral part of our Platform Technology team. This is an opportunity to contribute hands-on to an AI-driven drug discovery platform, generating the experimental data that directly informs the biological models powering our therapeutic pipeline. You will bring scientific curiosity and rigor to the bench, supporting the execution of molecular and sequencing-based assays that our computational and therapeutic teams rely on to advance program goals.</div>
<div>&nbsp;</div>
<div>This role offers early-career professionals a meaningful foothold in a cross functional discovery environment, with exposure to cutting-edge technologies spanning NGS workflows, liquid handling automation, and diverse RNA therapeutic modalities including ADAR editing, ASOs, siRNAs, and mRNAs. If you are eager to develop technical breadth while contributing to work that has real therapeutic impact, we encourage you to apply.</div>
</div>
</div></br><b>Key Responsibilities</b></br>
<li>Execute amplicon sequencing workflows, including NGS library preparation and targeted sequencing, under the guidance of senior team members, to support the evaluation of RNA therapeutic candidates.</li>
<li>Carry out library QC using tools such as TapeStation, Qubit and qPCR, flagging workflow bottlenecks to ensure high-quality datasets for downstream computational analysis.</li>
<li>Operate sequencing instruments such as the Illumina NextSeq, including run setup and routine troubleshooting, with increasing independence over time.</li>
<li>Perform routine molecular biology techniques including PCR, qPCR/ddPCR, and nucleic acid extractions from a variety of cell types and tissues.</li>
<li>Assist in running automated workflows on liquid handling platforms (e.g., Hamilton STAR, Agilent Bravo, Beckman Echo) to support scaling of discovery and screening activities.</li>
<li>Maintain accurate and thorough documentation of experimental plans, results, SOPs, and troubleshooting steps within an electronic lab notebook (ELN).</li>
<li>Contribute to team meetings and share experimental results and assay updates with immediate project collaborators.</li>
</br><b>Basic Qualifications </b></br>
<li>BS in Molecular Biology, Genetics, Genomics, Biotechnology, Biochemistry, or a related discipline with 1–3 years of relevant industry or research experience (including internships or postgraduate research).</li>
<li>Foundational knowledge of molecular and cell biology principles.</li>
<li>Some hands-on exposure to amplicon sequencing or other targeted NGS workflows; broader NGS experience is also welcomed.</li>
<li>Experience with nucleic acid extraction, quantitation, and standard molecular biology techniques such as PCR, qPCR or d(d)PCR, gel electrophoresis.</li>
<li>Strong attention to detail and commitment to rigorous, reproducible lab work.&nbsp;</li>
<li>Ability to work both independently and collaboratively in a team-oriented environment.</li>
</br><div>Deep Genomics encourages applications from all backgrounds who seek the opportunity to build the world's leading AI-driven genetic medicine company.&nbsp;</div>
<div>&nbsp;</div>
<div>If you have a disability or special need, accommodation is available on request for candidates taking part in all aspects of the selection process.</div>
<div>&nbsp;</div>
<div>&nbsp;</div>
<div>*This posting reflects a current vacancy.&nbsp;</div>
<div>&nbsp;</div>
<div><span style="font-size: 11pt;">We offer competitive compensation aligned with local market benchmarks. The salary range for this role is $75,000 - $90,000, and reflects Cambridge, USA-based roles; compensation may differ for Canada-based candidates.</span></div>]]></description><link>http://biotechroles.com/research-associate-platform-technology-deep-genomics/6a069a5e2f1861929d2531f9</link><guid isPermaLink="true">http://biotechroles.com/research-associate-platform-technology-deep-genomics/6a069a5e2f1861929d2531f9</guid><pubDate>Fri, 15 May 2026 04:00:30 GMT</pubDate><company>Deep Genomics</company><location>Cambridge, MA</location><salary>$75000-105000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, in vitro Pharmacology]]></title><description><![CDATA[<h3><strong>About Us</strong></h3>
<div>Deep Genomics is at the forefront of using artificial intelligence to transform drug discovery. Our proprietary AI platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms, and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, bioinformatics, data science, engineering, and drug development, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how new medicines are created.</div>
<div>&nbsp;</div>
<div>
<h3><strong>Opportunity</strong></h3>
<p>The Associate Director, in vitro pharmacology will be responsible for leading the target validation function at Deep Genomics with the goal of advancing our RNA editing therapeutics portfolio. This is a leadership role with the opportunity to make a significant impact on Deep Genomics’ therapeutic pipeline. Success in this role requires the ability to lead strategically, execute tactically, and influence others in a highly matrixed and multidisciplinary team.&nbsp;</p>
<p>The ideal candidate will have direct experience in designing, executing and interpreting target validation studies for a variety of liver disease indications. Deep knowledge of a variety of in vitro liver models, relevant functional assays and genome engineering methods is essential. Direct experience with ADAR or other oligonucleotide therapeutics is highly beneficial as is experience with pooled screening approaches and laboratory automation. This role requires leadership from the bench as well as experience supervising junior scientists directly and indirectly. In addition to working closely with the therapeutic program teams, the candidate is expected to work closely with our Target Identification team to translate AI-derived target nominations into a clear action plan leading to go/no-go decisions.&nbsp;</p>
<p>As a key member of an early stage discovery team, this individual must demonstrate initiative and ownership in both scientific and strategic decisions and have an entrepreneurial mindset. Ability to pro-actively anticipate needs and independently seek solutions is a key skill, together with effective communication in all directions. This role may lead to the opportunity to manage and mentor direct reports in the future. Please note that the title is commensurate with prior experience.</p>
</div></br><b>Key Responsibilities</b></br><div>

<li>Lead all aspects of liver biology target validation from strategy, execution and interpretation, working with direct and indirect reports.</li>
<li>Serve as the senior liver biology subject matter expert, leading in vitro pharmacology strategy and collaborating closely with the in vivo pharmacology team to advance therapeutic programs.</li>
<li>Collaborate closely with the Target Identification team on availability, feasibility and predictive power of in vitro models and assays for new targets.</li>
<li>Present clear, data-driven go/no-go decisions on novel targets.&nbsp;</li>
<li>Demonstrate strong leadership, personal accountability and interpersonal skills, and capability for mentoring (direct reports and others).</li>
<li>Analyze, interpret and present data to scientists and management in internal and external venues and publish in peer-reviewed journals as appropriate</li>

</div></br><b>Basic Qualifications</b></br><div>

<li>PhD in biological sciences with 6+ years of post-graduate experience in relevant roles (or equivalent) in in vitro pharmacology for the development of genetic medicines.</li>
<li>3+ years building, managing, and leading teams to meet therapeutic program goals.</li>
<li>Direct, hands-on experience with in vitro models of liver disease and a wide array of functional assays including steatosis, inflammation and fibrosis.</li>
<li>Direct, hands-on experience with gene editing or oligonucleotide therapeutics.</li>
<li>Proven ability to work independently and cross-functionally in a fast-paced environment.</li>
<li>Ability to communicate complex data sets to key stakeholders from diverse backgrounds.</li>
<li>Strong personal qualities, including attention to detail, emotional intelligence, integrity, creativity, and a willingness to have ideas challenged by team members and to challenge them.</li>

</div></br><div>Deep Genomics encourages applications from all backgrounds who seek the opportunity to build the world's leading AI-driven genetic medicine company.&nbsp;</div>
<div>&nbsp;</div>
<div>If you have a disability or special need, accommodation is available on request for candidates taking part in all aspects of the selection process.</div>
<div>&nbsp;</div>
<div>&nbsp;</div>
<div>*This posting reflects a current vacancy.&nbsp;</div>
<div>&nbsp;</div>
<div><span style="font-size: 11pt;">We offer competitive compensation aligned with local market benchmarks. The salary range for this role is $195,000 - $230,000, and reflects Cambridge, USA-based roles; compensation may differ for Canada-based candidates.</span></div>]]></description><link>http://biotechroles.com/associate-director-in-vitro-pharmacology-deep-genomics/6a069a5e2f1861929d2531fa</link><guid isPermaLink="true">http://biotechroles.com/associate-director-in-vitro-pharmacology-deep-genomics/6a069a5e2f1861929d2531fa</guid><pubDate>Fri, 15 May 2026 04:00:30 GMT</pubDate><company>Deep Genomics</company><location>Cambridge, MA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Sales Manager / Director of Sales]]></title><description><![CDATA[<div><a data-token-index="0" rel="noopener noreferrer" href="https://osmind.org/" tabindex="0">Osmind</a>&nbsp;is a public benefit corporation advancing psychiatry through technology, services, and real-world evidence to bring innovative mental health treatments to patients in need. Osmind’s psychiatry-tailored software and services, used by leading psychiatry practices across the U.S., help improve patient outcomes while driving practice success. Osmind's network of over 1000 clinics comprises the country's largest network of interventional psychiatry practices. Simultaneously, Osmind's clinic network, point-of-care software, and real-world data support life sciences companies in developing and scaling access to cutting-edge treatments. Osmind is a 50-person, Series B-stage company and has raised funding from top investors such as DFJ Growth, Y Combinator, and General Catalyst.</div></br><b>The Opportunity</b></br><p>We're hiring a Sales Manager to lead our sales team and sales motion end-to-end. This is a player-coach role for the first 6–12 months before evolving into full-time manager. For the player-coach time period, you'll contribute to the team’s quota and close your own deals while building the systems, playbooks, and coaching cadence that help level up our current two-person AE team. You’ll then transition to full time management and continue to level up &amp; grow the team.</p>
<p>You'll report to our VP Growth and manage our two AEs from day one. You'll have real authority: over deal strategy, pipeline accountability, close methodology, and how we evolve the motion across our Software and Software + Services pipelines.</p>
<p>We’re growing rapidly as a company with market leadership, strong market pull, and a massive and growing opportunity ahead of us, and have consistently outpaced goal. This is an opportunity to help level up our processes and fully tap the strong potential our GTM motion shows, while making an impact on clinician, researcher, and patient lives.</p>
</br><b>What You'll Do</b></br><div>

<li>Own revenue targets. In the first 6-12 months as player coach, you’ll personally contribute a book of business to best learn our ICP, market, and products.</li>
<li>Build and run the sales coaching infrastructure from scratch: pipeline and demo reviews, deal strategy sessions, close methodology, CRM discipline/pipeline hygiene, and the playbooks our AEs run on every deal. Tailor this to our various products and ICPs. Leverage data-driven analysis to identify pipeline and process gaps and quickly address them.</li>
<li>Provide strong mentorship to our high-performing sales team, helping them confidently beat goal every quarter</li>
<li>Partner with the VP of Growth on team quota-setting, forecasting, and how the sales motion evolves as we scale.</li>
<li>Be the connective tissue between marketing and sales — ensuring inbound volume is followed up with the right urgency, motion, and sequencing.</li>
<li>Represent the voice of sales in cross-functional conversations: surfacing product gaps, ICP refinement, pricing feedback, and what's actually happening in the field</li>
<li>Represent Osmind at various industry conferences and events (quarterly travel).</li>
<li>Use AI to increase selling and coaching effectiveness: Leverage Gong, Claude Skills, and other AI insights, e.g. call summarization, automated follow-ups, demo prep to reduce manual admin so the team spends more time on high-quality prospecting and deal execution.</li>

</div></br><div>
<div data-qa="salary-range">
<div>Depending on experience. This role includes equity package. Actual compensation will be commensurate with the candidate’s experience and local cost of labor. In addition, Osmind offers a wide range of comprehensive and inclusive employee benefits, including healthcare, dental, vision, generous family leave, FSA/DCFSA, mental health benefits, a 401(k) plan, and flexible paid time off.</div>
</div>
<div data-qa="closing-description">
<div data-qa="salary-range">
<p>Some candidates may see the list above and feel discouraged because they don't match all the items. Please apply anyway: there's a good chance you also have important skills we’ve missed! We are committed to diversity and building an equitable and inclusive environment for people of all backgrounds and experiences, and we're taking steps to meet that commitment. We especially encourage members of traditionally underrepresented communities to apply, including women, underrepresented people of color, LGBTQ+ people, veterans, and people with disabilities.</p>
</div>
<div data-qa="ai-disclaimer">
<div>We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.</div>
</div>
</div>
<div data-qa="ai-disclaimer">
<div>We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.</div>
</div>
</div>]]></description><link>http://biotechroles.com/senior-sales-manager-director-of-sales-osmind/6a069a512f1861929d2531f8</link><guid isPermaLink="true">http://biotechroles.com/senior-sales-manager-director-of-sales-osmind/6a069a512f1861929d2531f8</guid><pubDate>Fri, 15 May 2026 04:00:17 GMT</pubDate><company>Osmind</company><location>United States</location><salary>$140000-220000</salary><type></type></item><item><title><![CDATA[Senior Manager, Patient Safety, Epidemiology Science and Execution]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Your science could change what doctors know. Your work could change what patients experience.</b></p><p></p><p>At Bristol Myers Squibb, we believe that understanding risk is just as important as discovering opportunity. And right now, we&#39;re looking for someone like you, a curious, driven scientist who wants their career to mean something beyond the data.</p><p></p><p>This isn&#39;t a role where you&#39;ll sit in the background quietly checking boxes. This is a role where your scientific judgement shapes how BMS medicines are understood, used, and kept safe, for real patients, in the real world.</p><p></p><p><b>So, what will you actually be doing?</b></p><p>Think of yourself as the person who connects the dots between cutting-edge science, regulatory reality, and patient safety. You&#39;ll own end-to-end execution of <b>post-marketing safety studies (PASS/PMR)</b> and real-world data analyses, from developing the protocol to delivering inspection-ready outputs. That means your name is on work that goes to regulators, shapes drug labelling, and ultimately informs how clinicians manage risk on behalf of their patients.</p><p></p><p>You&#39;ll be the trusted scientific partner that <b>Safety Management Teams</b> turn to when a safety signal needs context. You&#39;ll lead literature reviews and secondary analyses that don&#39;t just sit in a report, they actively influence benefit-risk decisions on medicines that patients depend on every day.</p><p></p><p>You&#39;ll collaborate across functions, internally across BMS matrix teams, and externally with partners and study vendors, bringing people together and keeping complex, multi-threaded workstreams on track. You&#39;ll also have a genuine voice in <b>continuous improvement initiatives</b>, helping to shape how epidemiology is <i>done</i> at BMS, not just executed.</p><p></p><p><b>What&#39;s in it for you?</b></p><ul><li><b>Scientific ownership that&#39;s real, not theoretical</b> You won&#39;t be just supporting someone else&#39;s vision. Operating with limited supervision, you&#39;ll <i>translate strategy into delivery</i>, making meaningful scientific and operational decisions that carry your fingerprint from start to finish.</li><li><b>A springboard for your career</b> This is an early-to-mid career role by design, meaning there is <i>deliberate space for you to grow</i>. You&#39;ll build safety and regulatory expertise, deepen your epidemiology toolkit, and expand your cross-functional leadership skills, all within a globally recognised biopharma company. The exposure you&#39;ll gain here, regulatory submissions, benefit-risk assessments, real-world evidence generation, is the kind that opens doors.</li><li><b>Work that genuinely matters</b> BMS medicines treat serious diseases, cancers, autoimmune conditions, cardiovascular disease. When you assess adverse events or characterise disease background rates, you&#39;re contributing to a body of knowledge that keeps patients safer. It&#39;s hard to overstate how meaningful that is, day in, day out.</li><li><b>A collaborative culture, not a siloed one</b> You&#39;ll work within a matrix environment that values your perspective. Whether you&#39;re aligning with clinical teams, regulatory affairs, or external academic collaborators, you&#39;ll be surrounded by people who take science seriously and who genuinely want to solve hard problems together.</li><li><b>Just enough travel to keep it interesting</b> With approximately 5% business travel, you&#39;ll attend key scientific congresses and regulatory meetings, keeping you connected to the wider scientific community and the latest thinking in your field, without the exhaustion of constant time away from home.</li></ul><p></p><p><b>You&#39;ll thrive here if you...</b></p><ul><li>Have a <b>scientific or biomedical degree</b> (MPH, PharmD, PhD, MD, MSc, or similar) and at least <b>3 years of relevant experience</b> in epidemiology, drug safety, real-world evidence, or clinical research</li><li>Are comfortable navigating <b>regulatory frameworks</b> and writing correspondence that holds up to scrutiny</li><li>Can <b>hold multiple workstreams</b> in your head at once and still deliver quality outputs on time</li><li>Communicate clearly — in writing and in conversation — especially when the audience is technical or regulatory</li><li>Are the kind of person who notices when a process could be better, and does something about it</li></ul><p></p><p><b>Why BMS?</b></p><p>Because here, patient safety isn&#39;t a compliance exercise — it&#39;s a commitment. We invest in the science behind safety because we believe our responsibility to patients doesn&#39;t end at approval. It continues across the entire lifecycle of every medicine we develop.</p><p>You&#39;d be joining a team that takes that responsibility seriously, and a company that takes <i>you</i> seriously — giving you the tools, the scope, and the support to do some of the most impactful work of your career.</p><p></p><p><b>Ready to make your science matter?</b> <i>Apply now and tell us what drives you.</i></p><p>#LI-Hybrid</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Warsaw - PL: zł227,340 - zł275,484&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601880 : Senior Manager, Patient Safety, Epidemiology Science and Execution]]></description><link>http://biotechroles.com/senior-manager-patient-safety-epidemiology-science-and-execution-bristol-myers-squibb/6a05f7182f1861929d2531f7</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-patient-safety-epidemiology-science-and-execution-bristol-myers-squibb/6a05f7182f1861929d2531f7</guid><pubDate>Thu, 14 May 2026 16:23:52 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Warsaw - PL</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Patient Safety, Epidemiology Science and Execution]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Have you ever wondered what happens after a medicine reaches a patient?</b></p><p>Behind every approved therapy, there&#39;s a team asking the hard questions — <i>Is it safe? For whom? Under what conditions?</i> At Bristol Myers Squibb, that team is us. And we&#39;re looking for someone like you to help answer them.</p><p></p><p><b>Your Work Will Reach Further Than You Think</b></p><p><b>As a Manager in Patient Safety / Epidemiology Science and Execution</b>, you won&#39;t just be pushing papers or ticking compliance boxes. You&#39;ll be part of the scientific machinery that ensures BMS medicines are as safe as they are transformative.</p><p></p><p>Think about it: the data you analyze, the protocols you help draft, the literature you review — these feed directly into benefit-risk decisions that shape how doctors prescribe, how regulators approve, and ultimately, how patients live. That&#39;s not abstract. <i>That&#39;s real impact</i>.</p><p></p><p><b>What You&#39;ll Actually Be Doing</b></p><p>You&#39;ll work within a collaborative, senior-led epidemiology team, which means you&#39;ll be supported and mentored but you&#39;ll also be genuinely <i>trusted</i> with meaningful work from day one:</p><ul><li><b>Own your deliverables </b>- You&#39;ll be accountable for executing assigned epidemiology study components, from literature reviews and data source assessments to contributing directly to study protocols, analysis plans, and regulatory documents. Your fingerprints will be on science that matters.</li><li><b>Contribute to regulatory-grade science </b>- You&#39;ll draft sections of safety study protocols and study reports, risk management plans, aggregate safety reports,  learning firsthand how rigorous, audit-ready science is built. If you&#39;ve ever wanted to understand how pharma regulatory submissions come together, you&#39;re about to find out<b>.</b></li><li><b>Work across the organisation </b>- You&#39;ll coordinate with cross-functional teams, manage timelines, and navigate dependencies. You&#39;ll grow your stakeholder management skills in an environment where collaboration is the norm, not the exception.</li><li><b>Spot problems before they become problems </b>- By identifying execution-level risks and escalating with proposed solutions, you&#39;ll quickly develop a professional instinct that&#39;s invaluable in any scientific career.</li><li><b>Help shape how we work </b>- You&#39;ll actively contribute to continuous improvement initiatives, meaning your ideas about quality and efficiency won&#39;t disappear into a suggestion box, they&#39;ll be heard.</li></ul><p></p><p><b>What You&#39;ll Gain (Beyond the Job Title)</b></p><p><b>Execute post marketing safety study components - </b>A portfolio of real-world evidence work in a globally recognised pharma company</p><p><b>Draft regulatory documents </b>- Deep expertise in the language and standards of international drug regulation</p><p><b>Work with senior epidemiologists - </b>A mentorship network and scientific foundation you can&#39;t get from a textbook</p><p><b>Coordinate cross-functional activities</b> - Project management skills that travel with you across your entire career</p><p><b>Support inspection-ready documentation </b>- A reputation for quality and precision, the gold standard in science</p><p><b>Contribute to CI initiatives </b>- A voice in how science gets done at BMS</p><p></p><p><b>You Might Be Exactly Who We&#39;re Looking For If…</b></p><p>You have a<b> scientific or biomedical degree </b>- whether that&#39;s a BS, MPH, PharmD, RN, MD, PhD or equivalent and at least 2 years of relevant experience (yes, that can include hands-on work from your training).</p><p></p><p><b>You&#39;re the kind of person who:</b></p><ul><li>Reads the details others miss</li><li>Juggles multiple priorities without dropping the scientific thread</li><li>Communicates clearly — whether you&#39;re writing a regulatory document or explaining a finding to a cross-functional colleague</li><li>Thrives in a structured environment while still bringing your own thinking to the table</li><li>Is curious about how AI tools are shaping modern scientific work <i>(a bonus if you&#39;ve already started exploring this)</i></li></ul><p></p><p><b>A Little About Where You&#39;d Be Working</b></p><p>BMS&#39;s Patient Safety Epidemiology team designs and conducts scientifically rigorous, observational research, assessing adverse events, studying disease natural history, evaluating background rates, and contextualising safety signals across both approved and pipeline products. In short, we exist to make sure patients get the best possible version of each medicine we bring to the world.</p><p></p><p>You&#39;ll join a team that collaborates across drug development and lifecycle management, meaning your exposure won&#39;t be siloed. You&#39;ll see the science from multiple angles.</p><p></p><p>And yes, there&#39;s some travel involved (~5%), think key scientific congresses, regulatory meetings, and engagements where you&#39;ll represent BMS and continue to grow your professional profile on a global stage.</p><p></p><p><b>Ready to Do Science That Reaches Patients?</b></p><p>If you&#39;re an early-career epidemiologist or scientist ready to move from learning the ropes to <i>pulling them</i>, this is your opportunity to grow inside one of the world&#39;s leading biopharma companies — with the mentorship, the mandate, and the meaningful work to match.</p><p></p><p><b>Apply today. Your science has somewhere to go.</b></p><p>#LI-Hybrid</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Warsaw - PL: zł154,275 - zł186,945&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601882 : Manager, Patient Safety, Epidemiology Science and Execution]]></description><link>http://biotechroles.com/manager-patient-safety-epidemiology-science-and-execution-bristol-myers-squibb/6a05f7162f1861929d2531f6</link><guid isPermaLink="true">http://biotechroles.com/manager-patient-safety-epidemiology-science-and-execution-bristol-myers-squibb/6a05f7162f1861929d2531f6</guid><pubDate>Thu, 14 May 2026 16:23:50 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Warsaw - PL</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[EG-90 – Senior Therapeutic Area Specialist, Oncology (San Francisco, CA)]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary:</b></p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.  </p><p></p><p>The TAS role is field based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b></p><p><i>Portfolio Promotion </i></p><ul><li>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </li><li>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </li><li>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </li><li>Prepares and successfully implements comprehensive territory and account plans. </li><li>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </li></ul><p><b>Fair &amp; Balanced Scientific Dialogue:</b></p><ul><li>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </li><li>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </li><li>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </li><li>Maintains a high level of working expertise on emerging data for approved indications. </li><li>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries.  </li></ul><p><b>Cross-Functional Collaboration:</b></p><ul><li>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </li><li>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </li><li>Complies with all laws, regulations, and policies that govern the conduct of BMS. </li></ul><p><b>Required Qualifications &amp; Experience:</b></p><ul><li>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </li><li>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </li><li>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </li><li>Experience in Oncology is preferred. </li><li>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </li><li>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </li><li>Strong selling and promotional skills proven through a track record of performance. </li></ul><p><b>Key Competencies Desired:</b></p><ul><li>Customer/commercial mindset </li><li>Demonstrated ability to drive business results. </li><li>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </li><li>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </li><li>Demonstrated resourcefulness and ability to connect with customers. </li></ul><p><b>Patient Centricity:</b></p><ul><li>Understands the patient journey and experience. </li><li>Has a patient-focused mindset. </li></ul><p><b>Scientific Agility: </b></p><ul><li>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </li><li>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </li></ul><p><b>Analytical Capability: </b></p><ul><li>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </li><li>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </li><li>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </li><li>Ability to use CE^3 to generate insights and do dynamic call planning. </li></ul><p><b>Technological Agility:</b> </p><ul><li>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </li><li>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </li><li>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </li><li>Ability to use the Medical on Call technology effectively. </li><li>Being able to navigate and utilize the internet and online resources effectively. </li><li>Keeping up to date with technological advancements and changes. </li></ul><p><b>Teamwork/Enterprise Mindset:</b></p><ul><li>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </li><li>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </li><li>Track record of balancing individual drive and collaborative attitude. </li><li>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </li><li>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </li></ul><p><b>#LinkedIn Remote</b></p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602375 : EG-90 – Senior Therapeutic Area Specialist, Oncology (San Francisco, CA)]]></description><link>http://biotechroles.com/eg-90-senior-therapeutic-area-specialist-oncology-san-francisco-ca-bristol-myers-squibb/6a05f7152f1861929d2531f5</link><guid isPermaLink="true">http://biotechroles.com/eg-90-senior-therapeutic-area-specialist-oncology-san-francisco-ca-bristol-myers-squibb/6a05f7152f1861929d2531f5</guid><pubDate>Thu, 14 May 2026 16:23:49 GMT</pubDate><company>Bristol-Myers Squibb</company><location>San Francisco - CA - US</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Director, HRBP - Neurology and Strategy & Innovation]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>The Sr. Director, HRBP for Neurology and Strategy &amp; Innovation in Drug Development plays a pivotal role in providing strategic partnership to the Senior Leaders for the Therapeutic Areas within the function. This position is responsible for aligning the Research, Development, and Commercial HRBP team in support of the Neurology and ICV people strategy. The role demands HR leadership in driving the people strategy, workforce planning, organizational design, talent management, team effectiveness, and change management. Given the global presence of the client group across multiple BMS locations and geographies, close alignment with the People Org and function leadership is essential to ensure the seamless execution of workforce planning and talent strategy.</p><p></p><p></p><p><b><u>Key Responsibilities</u></b></p><ul><li>Provides strategic HR Business Partner expertise to the Therapeutic Areas Leadership in function to maximize organizational performance. </li><li>Leverages business strategy, people strategy, external best practices and organizational insights to deliver bold and innovative organizational and talent solutions, including organizational design, workforce planning, talent management, and culture change. </li><li>Aligns corporate and functional strategies with BMS people strategy, monitoring the effectiveness of organizational performance programs through metrics and analytics to bring value through the business. </li><li>Collaborates with Centers of Excellence (COE’s) to monitor external environment (e.g., job market, technology, demographic development) and define future workforce requirements (quantitative and qualitative) as well as identifying and articulating the People needs of the business to the COE’s and deploys their programs and processes in ways that bring value to the business. </li><li>Drives the ONE People team across the region and provides guidance and collaborates with therapeutic area HR Business Partners, COEs and People Services leaders for effective global deployment of People activities. </li><li>Analyzes key data and trends to drive organizational effectiveness and the development of a workforce plan aligned with business strategy and objectives. </li><li>Supports succession planning, talent retention efforts and pipelining, as necessary, for external talent. </li><li>Leads a team of functional HRBPs ensuring continuous performance, engagement and development of all team members. </li></ul><p></p><p></p><p><b><u>Additional Responsibilities </u></b></p><ul><li>Role Model our BMS Values of Integrity, Innovation, Urgency, Passion, Accountability, and Inclusion. </li><li>Ensures end-to-end org design, encompassing communication and effective change management. </li><li>Translate business strategy and organizational needs into contemporary organizational solutions including organizational design, inclusion and diversity, succession &amp; talent management, and culture change. </li><li>Collaborate across the People OP Model (COE’s, People Services) to articulate business needs and partners in delivering solutions in ways that bring value across the enterprise. </li><li>Applies judgment to data insights and trends to support business talent and organization decisions that drives organizational effectiveness and innovative and robust workforce planning, engagement strategies, and succession management  </li><li>Shape and lead change management efforts to ensure delivery of organizational solutions, programs, and deliverables. </li></ul><p></p><p><b><u>Qualifications</u></b></p><ul><li>BA/BS Degree, Advanced Degree preferred, and 15&#43; years of HR relevant business experience </li><li>Proven leadership effectiveness in followership, innovation, people program/project management, and executive coaching, demonstrating the ability to inspire and guide teams, foster a culture of creativity and continuous improvement, manage complex projects and programs efficiently, and provide strategic coaching to senior executives to enhance their leadership capabilities.  </li><li>Expertise in talent management, including end-to-end talent acquisition, performance management, engagement, and diversity, equity, and inclusion.  </li><li>Demonstrated experience utilizing data and analytics to drive business and talent decisions, including data analysis, insights generation, data visualization, data integrity, and diagnostic capabilities.  </li><li>Demonstrated behavioral skills in curiosity, learning agility, and growth mindset.  </li><li>Exhibit understanding of regulatory compliance, including the human elements and implications to enterprise and business.  </li><li>Demonstrated strength in strategy and business acumen by influencing and shaping business strategy through people strategy, anticipating external trends, providing context and influence for organizational effectiveness, applying systems thinking, and using a diagnostic mindset to improve talent and business outcomes.  </li><li>Extensive experience in business partnering, including organizational savvy and influence, consulting, performance management, organizational design, change management, and significant leadership skills in building and leading global, diverse teams of People professionals.  </li><li>Extensive experience as an HR business partner with significant leadership skills leading and working across global, diverse teams of HR professionals. </li><li>Proven success in working effectively at senior management levels to impact and influence decision-making. </li><li>Experience working with global teams. </li><li>Experience in leading change management efforts, including defining change and communication plans. </li><li>Experience in the use of metrics and analytics in a way that drives business performance. </li><li>Demonstrated experience in applying workforce planning knowledge, engagement strategies, and succession management. </li><li>Proven experience in working effectively within a matrixed environment and building alignment in a cross-functional and team environment. </li><li>Knowledge of external trends and factors that influence human behaviors and decision-making at the individual, group, and organizational level.  </li></ul><p></p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $221,430 - $268,315 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602407 : Sr. Director, HRBP - Neurology and Strategy &amp; Innovation]]></description><link>http://biotechroles.com/sr-director-hrbp-neurology-and-strategy-and-innovation-bristol-myers-squibb/6a05f7152f1861929d2531f4</link><guid isPermaLink="true">http://biotechroles.com/sr-director-hrbp-neurology-and-strategy-and-innovation-bristol-myers-squibb/6a05f7152f1861929d2531f4</guid><pubDate>Thu, 14 May 2026 16:23:49 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Senior Analyst, Financial Risk Management]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Title: Senior Analyst, Financial Risk Management</b></p><p><b>Department: Global Business Operations</b></p><p><b>Location:       Princeton, NJ</b></p><p><b>Summary:</b></p><p>Working within Corporate Treasury and reporting to the Senior Director of Financial Risk Management, this role supports the execution of the foreign exchange hedging programs, investing the BMS cash portfolio, pension and benefits plan, and will participate in various projects across the broader Treasury organization.</p><p></p><p><b>Key responsibilities include:</b></p><p>·       Balance Sheet FX Hedging Program</p><p>o   Aggregate and validate balance sheet FX exposure from ERP systems</p><p>o   Execute hedges on 360T and ensure appropriate legal entity allocation</p><p>o   Identify and analyze drivers of variance between actual P&amp;L and forecast</p><p>·       Daily management &gt;$10B investment portfolio</p><p>o   Partner cross-functionally to ensure sufficient daily cash and liquidity</p><p>o   Manage portfolio based on daily cash position and market opportunities</p><p>·       Pensions and 401k Benefits</p><p>o   Monitor and report on the performance of retirement plan investments</p><p>o   Assist with audits of pension and savings plans, and SOX control requirements</p><p>·       Support Financial Risk Management colleagues with interest rate hedging, cash flow FX hedging, commercial paper issuance, and net investment hedging</p><p>·       Partner with technology for improvements/implementations </p><p><b> </b></p><p> <b>Skills, Competencies and Knowledge:</b> </p><p>·       Strong analytical and technical skills</p><p>·       External focus, strategic perspective, attention to details</p><ul><li><p><span>Adheres to highest ethical standards and values</span></p></li></ul><p>·       Proactive approach and ability to partner with internal and external stakeholders, including corporate accounting, technology, tax, banks, European Treasury Center, CFA, Atlas, and Quantum</p><p></p><p><b>Education / Experience</b></p><p>·       Bachelor&#39;s degree in Finance, Business, Computer Science or a related discipline</p><p><span><span>·<span>       </span></span></span><span>Finance interest or experience in treasury, financial analysis, audit, or accounting in a corporate setting</span></p><p>·       The individual should possess strong oral and written communication, problem solving, and organization skills. In addition, the ability to learn new concepts quickly and work with internal and external business partners with collaboration mindset</p><p></p><p><b> </b></p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $73,610 - $89,198 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602420 : Senior Analyst, Financial Risk Management]]></description><link>http://biotechroles.com/senior-analyst-financial-risk-management-bristol-myers-squibb/6a05f7142f1861929d2531f3</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-financial-risk-management-bristol-myers-squibb/6a05f7142f1861929d2531f3</guid><pubDate>Thu, 14 May 2026 16:23:48 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Oncology/Hematology - San Francisco, CA]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3.</p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact.</p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values. </p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers.</p><p></p><p><b>Key Responsibilities:</b></p><p><b>Portfolio Promotion</b></p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner.</p></li><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients.</p></li><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas.</p></li><li><p>Prepares and successfully implements comprehensive territory and account plans.</p></li><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement.</p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b></p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy.</p></li><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label.</p></li><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics.</p></li><li><p>Maintains a high level of working expertise on emerging data for approved indications.</p></li><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries.</p></li></ul><p><b>Cross-functional collaboration</b></p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs. </p></li><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers.</p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b></p></li></ul><p></p><p><b>Required Qualifications &amp; Experience</b></p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.</p></li><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients.</p></li><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx).</p></li><li><p>Experience in Hematology/Oncology required.</p></li><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals.</p></li><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. </p></li><li><p>Strong selling and promotional skills proven through a track record of performance.</p></li></ul><p><b>Key Competencies Desired</b></p><p><b>Customer/commercial mindset</b></p><ul><li><p>Demonstrated ability to drive business results.</p></li><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey.</p></li><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages.</p></li><li><p>Demonstrated resourcefulness and ability to connect with customers.</p></li></ul><p><b>Patient centricity </b></p><ul><li><p>Understands the patient journey and experience.</p></li><li><p>Has a patient-focused mindset.</p></li></ul><p><b>Scientific Agility </b></p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.</p></li><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data.</p></li></ul><p><b>Analytical Capability:</b></p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively.</p></li><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs.</p></li><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data.</p></li><li><p>Ability to use CE^3 to generate insights and do dynamic call planning.</p></li></ul><p><b>Technological Agility:</b></p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs.</p></li><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication.</p></li><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals.</p></li><li><p>Ability to use the Medical on Call technology effectively.</p></li><li><p>Keeping up to date with technological advancements and changes.</p></li></ul><p></p><p><b>Teamwork/Enterprise mindset</b></p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans.</p></li><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations.</p></li><li><p>Track record of balancing individual drive and collaborative attitude.</p></li><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures.</p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company.</p></li></ul><p>#LI-Remote</p><p></p><p></p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602413 : Senior Therapeutic Area Specialist, Oncology/Hematology - San Francisco, CA]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-san-francisco-ca-bristol-myers-squibb/6a05f7132f1861929d2531f2</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-san-francisco-ca-bristol-myers-squibb/6a05f7132f1861929d2531f2</guid><pubDate>Thu, 14 May 2026 16:23:47 GMT</pubDate><company>Bristol-Myers Squibb</company><location>San Francisco - CA - US</location><salary>$145000-190000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, CMC Project Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p><b>Job Description</b></p><p></p><p>Senior Project Manager (PM) will sit within the Cell Therapy Development (CTD) Project and Portfolio Management Office (PMO). This individual will be responsible for overseeing the planning, execution, and delivery of project(s) in alignment with the company&#39;s strategy, commitments, and goals. The project(s) will be technical in nature and will be supporting an individual product program(s) or the development portfolio as a whole.  The primary assignment for this role is supporting a complex late stage autologous asset through registrational enabling activities and submission preparation.</p><p></p><p>The Senior CMC PM will work with stakeholders to identify project scope and strategy, develop and maintain detailed project plans, and collaborate with functional leads and network project managers to coordinate project deliverables. The Senior PM will manage project timelines, risk, budgets, and resources; communicate project status and be accountable for project outcomes. They will use CTD PMO best practices, tools, and templates, and work with internal and external partners to implement effective project management plans. The ideal candidate will have strong cross-functional experience, able to work under tight deadlines with world-class partners, suppliers, and business leaders.</p><p></p><p><b><span>Primary Responsibilities:</span></b></p><ul><li><p>Partner with project, functional and work stream leads to successfully achieve project objectives inclusive of program assets as well as strategic initiatives.</p></li><li><p>Apply project management expertise across the portfolio for standard and complex projects, managing multiple projects in parallel.</p></li><li><p>Provide strong team leadership and drive to ensure projects are executed on-time and within budget</p></li><li><p>Facilitate the definition of project scope, goals and deliverables</p></li><li><p>Create project plans; scope, work, resources, scheduling, etc.</p></li><li><p>Maintain and update project objectives through project lifecycle</p></li><li><p>Monitor execution and quality to customer/stakeholder/sponsor standards</p></li><li><p>Proactive risk management to identify, assess, collaborate on mitigation plans and resolve issues</p></li><li><p>Report on project progress, offer viable solutions and opportunities as they arise</p></li><li><p>Implement appropriate project change control</p></li><li><p>Facilitate project team meetings; attend related project meetings as necessary to ensure alignment</p></li><li><p>Evaluate and assess result of the project through regular after-action reviews</p></li><li><p>Provide structure and leadership across departments to ensure team meets project objectives</p></li><li><p>Work with internal and external stakeholders to manage project deliverables</p></li><li><p>Develop and communicate status to organizational leadership</p></li></ul><p><br /><span>Compet<b>encies &amp; Experiences</b></span></p></div><ul><li><p>5&#43; years’ experience in bio tech/life sciences project management; Cell Therapy experience preferred</p></li><li><p>Bachelor’s degree in STEM/Life Sciences-related discipline</p></li><li><p>PMP qualification preferred</p></li><li><p>Proficiency with related software tools such as: MS Project, Office Timeline Pro, MS PPT, MS Excel, SharePoint, etc.</p></li><li><p>Strong knowledge of biopharma industry. Familiarity/experience with end-to-end CMC drug development.</p></li><li><p>Excellent interpersonal, communication, and presentation skills</p></li><li><p>Ability to work cross-functionally, with matrixed teams; maintaining strong business partner relationships</p></li><li><p>Strong leadership skills and executive presence; ability to positively influence outcomes</p></li><li><p>Excellent conflict resolution, critical thinking and problem-solving skills</p></li><li><p>Ability to navigate and bring clarity to areas of uncertainty in a dynamic environment</p></li></ul><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Seattle - WA: $158,580 - $192,157&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602388 : Senior Manager, CMC Project Manager]]></description><link>http://biotechroles.com/senior-manager-cmc-project-manager-bristol-myers-squibb/6a05f7132f1861929d2531f1</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-cmc-project-manager-bristol-myers-squibb/6a05f7132f1861929d2531f1</guid><pubDate>Thu, 14 May 2026 16:23:47 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Seattle 400 Dexter - WA - US</location><salary>$145000-190000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Customer Insights & Engagement]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b><span>Position Summary:</span></b></p><p><span>The Senior Manager, Business Insights &amp; Analytics supports the development and execution of analytics-driven insight generation that informs strategic and tactical decision-making for the Neuroscience business. Working alongside the Director, this role contributes to the design and delivery of analytics initiatives, synthesizes insights across data sources, and communicates clear, objective findings that guide brand strategy, execution, and customer engagement.<span> </span></span></p><p><span><span> </span></span></p><p><span>This role is accountable for executing end-to-end analytics-based insights and supporting analyses, ensuring alignment with brand objectives and enterprise commercial strategies. As a Senior Manager, this role collaborates closely with cross-functional partners—including Brand, Medical, Sales, and Access teams—to enable data-informed decision-making across the Neuroscience portfolio. The role operates under the guidance of the Director while taking ownership of defined analytics workstreams and contributing to the adoption of advanced analytics capabilities, including AI and machine learning.<span> </span></span></p><p><span><span> </span></span></p><p><b><span>Key Responsibilities:</span></b></p><p><span>Business Analytics &amp; Insights<span> </span></span></p><p><span>• Support the Neuroscience Commercial team in addressing priority business questions through analytics-driven insights, identifying brand opportunities and performance levers.<span> </span></span></p><p><span>• Execute defined analytics workstreams aligned to brand strategy, including performance diagnostics, customer behavior analyses, and market dynamics assessments.<span> </span></span></p><p><span>• Synthesize insights across multiple data sources (e.g., IQVIA, SHS, claims, patient chart data, brand performance and promotional data) to support learning agendas and pull-through actions.<span> </span></span></p><p><span>• Prepare clear, concise analytical readouts and presentations that translate data into actionable business implications.<span> </span></span></p><p><span><span> </span></span></p><p><span>Cross-Functional Partnership<span> </span></span></p><p><span>• Partner with Brand team members to provide data-based inputs into strategic choices and support senior leader presentations.<span> </span></span></p><p><span>• Collaborate with Insights &amp; Engagement Centers of Excellence to contribute to a unified, integrated approach to analytics and insight generation across Neuroscience.<span> </span></span></p><p><span><span> </span></span></p><p><span>Innovation &amp; Advanced Analytics<span> </span></span></p><p><span>• Partner with the Director to identify opportunities to apply innovative analytics approaches that reflect best practices and evolving industry standards.<span> </span></span></p><p><span>• Drive adoption and application of advanced analytics capabilities, including AI, machine learning, and predictive approaches, to enhance insight generation and decision support.<span> </span></span></p><p><span>• Contribute to continuous improvement of analytics processes by identifying operational efficiencies and participating in capability-building initiatives.<span> </span></span></p><p><span><span> </span></span></p><p><span>Strategic Enablement<span> </span></span></p><p><span>• Maintain a continuous improvement mindset and stay informed on emerging analytics trends and methodologies to help elevate the organization’s Neuroscience insights capabilities.<span> </span></span></p><p><span>• Support Business Insights &amp; Analytics representation in BU-level forums as directed, contributing analytical perspectives to cross-functional discussions.<span> </span></span></p><p><span>• Guide integration of advanced analytics outputs into broader brand and commercial decision-making.<span> </span></span></p><p><span><span> </span></span></p><p><span>Leadership &amp; Governance<span> </span></span></p><p><span>• This role does not have direct people management responsibilities but may provide direction to peers, offshore teams, and vendors on project-based activities.<span> </span></span></p><p><span>• Ensure adherence to all company operating policies, governance standards, and quality control processes.<span> </span></span></p><p><span><span> </span></span></p><p><b><span>Key Qualifications, Skills &amp; Experience:</span></b></p><p><span>• Minimum 3 years of experience in pharmaceutical commercial analytics, business insights, or related analytical roles; Neuroscience or CNS experience preferred.<span> </span></span></p><p><span>• Bachelor’s degree required; advanced degree (Master’s, MBA, or PhD) a plus.<span> </span></span></p><p><span>• Demonstrated ability to work with complex data sources and translate analyses into clear, business-relevant insights.<span> </span></span></p><p><span>• Developing stakeholder management skills with a collaborative, cross-functional mindset.<span> </span></span></p><p><span>• Strong communication and presentation skills, with the ability to clearly convey analytical findings.<span> </span></span></p><p><span>• Familiarity with industry-standard data sources and analytics tools (e.g., IQVIA, SHS, analytics platforms).<span> </span></span></p><p><span>• Strategic Contributor: Builds productive relationships with brand teams and supports translation of analytics into strategy.<span> </span></span></p><p><span>• Customer-Focused Mindset: Uses data to deepen understanding of HCP and patient behavior to inform Neuroscience engagement.<span> </span></span></p><p><span>• Enterprise Awareness: Understands how analytics efforts support both brand and broader enterprise objectives.<span> </span></span></p><p><span>• Curious &amp; Developing Thinker: Demonstrates enthusiasm for advanced analytics tools and emerging methodologies.<span> </span></span><br /> </p><p>#CASA</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $133,710 - $162,019 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601543 : Senior Manager, Customer Insights &amp; Engagement]]></description><link>http://biotechroles.com/senior-manager-customer-insights-and-engagement-bristol-myers-squibb/6a05f7122f1861929d2531f0</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-customer-insights-and-engagement-bristol-myers-squibb/6a05f7122f1861929d2531f0</guid><pubDate>Thu, 14 May 2026 16:23:46 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$150000-200000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist - Oncology/Hematology- Tampa, FL]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p>This territory includes: <span>Naples, Fort Myers, Port Charlotte, Sarasota, Bradenton, Sun City, Brandon, Tampa, and Sebring. </span></p><p></p><p><b><span>Position Summary</span></b><span> </span></p></div><div><p><span><span>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for<span> </span></span><span>appropriate patients</span><span>. </span></span><span> </span></p><p></p></div><div><p><span><span>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the<span> </span></span><span>appropriate patients</span><span>. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (</span><span>Cx</span><span>) through deeper scientific dialogue on and consistent with label,<span> </span></span><span>leveraging</span><span><span> </span>new ways of working and CE^3.</span></span><span> </span></p><p></p></div><div><p><span><span>The role builds and<span> </span></span><span>maintains</span><span><span> </span>strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact.</span></span><span> </span></p><p></p></div><div><p><span><span>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (</span><span>Cx</span><span>) – by meeting HCP needs in<span> </span></span><span>a timely</span><span><span> </span>and scientific manner. This role will prioritize the safe and<span> </span></span><span>appropriate use</span><span><span> </span>of BMS products while also focusing on overall business results and performance<span> </span></span><span>objectives</span><span><span> </span>while exemplifying BMS values.</span></span></p></div><div><p></p><p><span><span>The TAS role is<span> </span></span><span>field-based</span><span>. A TAS is<span> </span></span><span>anticipated</span><span><span> </span>to spend 100% of their time in the field with external customers.</span></span><span> </span></p></div><div><p><b><span>Key Responsibilities:</span></b><span> </span></p></div><div><p><b><span>Portfolio Promotion</span></b><span> </span></p></div><div><ul><li><p><span><span>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in<span> </span></span><span>appropriate patients</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages with and continuously<span> </span></span><span>maintains</span><span>/grows<span> </span></span><span>a high level</span><span><span> </span>of scientific<span> </span></span><span>expertise</span><span><span> </span>in all assigned products and therapeutic areas.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Prepares and successfully implements comprehensive territory and account plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement.</span></span><span> </span></p></li></ul></div><div><p><b><span>Fair &amp; Balanced Scientific Dialogue</span></b><span> </span></p></div><div><ul><li><p><span><span>Demonstrates scientific<span> </span></span><span>expertise</span><span><span> </span>and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with<span> </span></span><span>label</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and<span> </span></span><span>facilitating</span><span><span> </span>scheduling and<span> </span></span><span>logistics</span><span>.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Maintains<span> </span></span><span>a high level</span><span><span> </span>of working<span> </span></span><span>expertise</span><span><span> </span>on emerging data for approved indications.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages real-time medical support through<span> </span></span><span>Medical on</span><span><span> </span>Call to reactively answer unsolicited questions and complex technical inquiries.</span></span><span> </span></p></li></ul></div><div><p><b><span>Cross-functional collaboration</span></b><span> </span></p></div><div><ul><li><p><span><span>Proactively collaborates with other field teams to ensure the best Customer Experience (</span><span>Cx</span><span>) for HCPs. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Gathers and shares relevant insights and information internally with the<span> </span></span><span>appropriate stakeholders</span><span><span> </span>to enable BMS to better serve its customers.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Complies with</span><span><span> </span>all laws, regulations, and policies that govern the conduct of BMS.</span></b><span> </span></p></li></ul></div><div><p><b><span>Required Qualifications &amp; Experience</span></b><span> </span></p></div><div><ul><li><p><span><span>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated experience building and<span> </span></span><span>maintaining</span><span><span> </span>strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (</span><span>Cx</span><span>).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in Hematology/Oncology<span> </span></span><span>required</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance<span> </span></span><span>track record</span><span><span> </span>of meeting or exceeding goals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong selling and promotional skills proven through<span> </span></span><span>a track record</span><span><span> </span>of performance.</span></span><span> </span></p></li></ul></div><div><p><b><span>Key Competencies Desired</span></b><span> </span></p></div><div><p><b><span>Customer/commercial mindset</span></b><span> </span></p></div><div><ul><li><p><span><span>Demonstrated ability to drive business results.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience<span> </span></span><span>identifying</span><span>, engaging, and cultivating credibility with customers across the patient care journey.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated resourcefulness and ability to connect with customers.</span></span><span> </span></p></li></ul></div></div><div><div><p><b><span>Patient centricity </span></b><span> </span></p></div><div><ul><li><p><span><span>Understands the<span> </span></span><span>patient</span><span><span> </span>journey and experience.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a patient-focused mindset.</span></span><span> </span></p></li></ul></div><div><p><b><span>Scientific Agility </span></b><span> </span></p></div><div><ul><li><p><span><span>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data.</span></span><span> </span></p></li></ul></div><div><p><b><span>Analytical Capability:</span></b><span> </span></p></div><div><ul><li><p><span><span>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understanding how to interpret and analyze data related to BMS products, customer preferences</span><span>, clinical</span><span><span> </span>data.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use CE^3 to generate insights<span> </span></span><span>and do</span><span><span> </span>dynamic call planning.</span></span><span> </span></p></li></ul></div><div><p><b><span>Technological Agility:</span></b><span> </span></p></div><div><ul><li><p><span><span>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and<span> </span></span><span>maintain</span><span><span> </span>effective communication.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in<span> </span></span><span>a timely</span><span><span> </span>and compliant manner, track interactions, and plan future engagements with healthcare professionals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use the Medical on Call technology effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Keeping up to date with technological advancements and changes.</span></span><span> </span></p></li></ul></div><div><p><b><span>Teamwork/Enterprise mindset</span></b><span> </span></p></div><div><ul><li><p><span><span>Strong business acumen to understand and<span> </span></span><span>analyze business and market drivers</span><span><span> </span>and develop, execute, and adjust business plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrates<span> </span></span><span>a strong sense</span><span><span> </span>of learning agility. Seeks out and learns from unfamiliar<span> </span></span><span>experiences, and</span><span><span> </span>then applies those lessons to achieve better results in<span> </span></span><span>subsequent</span><span><span> </span>situations.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Track record</span><span><span> </span>of balancing individual drive and collaborative attitude.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Holds<span> </span></span><span>a high level</span><span><span> </span>of integrity and good judgment,<span> </span></span><span>in order to</span><span><span> </span>navigate the requirements of the role effectively and compliantly<span> </span></span><span>in accordance with</span><span><span> </span>BMS policies and procedures.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company.</span></span><span> </span></p></li></ul></div><div><p><span><span>#LI-Remote</span></span><span> </span></p></div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602404 : Senior Therapeutic Area Specialist - Oncology/Hematology- Tampa, FL]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-tampa-fl-bristol-myers-squibb/6a05f7122f1861929d2531ef</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-tampa-fl-bristol-myers-squibb/6a05f7122f1861929d2531ef</guid><pubDate>Thu, 14 May 2026 16:23:46 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Tampa - FL - US</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Cardiovascular Community - Spring Hill, FL]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p></p><p><b>Position Summary:</b></p><p></p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.  </p><p></p><p>The TAS role is field based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p></p><p><b>Key Responsibilities:</b></p><p><i>Portfolio Promotion </i></p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li><li><p>Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p></p><p><b>Fair &amp; Balanced Scientific Dialogue:</b></p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries.  </p></li></ul><p></p><p><b>Cross-Functional Collaboration:</b></p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><p></p><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p><p></p><p><b>Required Qualifications &amp; Experience:</b></p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li><li><p>Experience in cardiovascular preferred. </p></li><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p></p><p><b>Key Competencies Desired:</b></p><ul><li><p>Customer/commercial mindset </p></li><li><p>Demonstrated ability to drive business results. </p></li><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p></p><p><b>Patient Centricity:</b></p><ul><li><p>Understands the patient journey and experience. </p></li><li><p>Has a patient-focused mindset. </p></li></ul><p></p><p><b>Scientific Agility: </b></p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p></p><p><b>Analytical Capability: </b></p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p></p><p><b>Digital Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li><li><p>Ability to use the Medical on Call technology effectively. </p></li><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p></p><p><b>Teamwork/Enterprise Mindset:</b></p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li><li><p>Track record of balancing individual drive and collaborative attitude. </p></li><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><p></p><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p><p></p><p><b>#LinkedIn Remote</b></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $124,090 - $150,370&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602419 : Senior Therapeutic Area Specialist, Cardiovascular Community - Spring Hill, FL]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-cardiovascular-community-spring-hill-fl-bristol-myers-squibb/6a05f7112f1861929d2531ee</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-cardiovascular-community-spring-hill-fl-bristol-myers-squibb/6a05f7112f1861929d2531ee</guid><pubDate>Thu, 14 May 2026 16:23:45 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Spring Hill - FL - US</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Full Stack Engineer, Clinical Engineering & Operations]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><u>Position Summary: </u></p><p>We are seeking a Manager, Full Stack Engineer to serve <b>in an AI‑first, agile product team</b> supporting Global Development Operations (GDO). This role is accountable for designing, building, and operating <b>AI‑native products</b> where large language models, agentic workflows, and data‑driven intelligence are the <i>default</i> approach to solving business problems—not an add‑on.</p><p>The ideal candidate brings hands‑on engineering expertise and proven experience delivering <b>production‑grade Generative and Agentic AI solutions</b> in a regulated environment. This individual will help shape how products are designed, developed, delivered, and continuously improved, embedding AI into core workflows to augment decision‑making, automate execution, and scale impact across GDO.</p><p></p><p><u>Specific responsibilities: </u></p><ul><li>Accountable for the build, operation, and continuous improvement of <b>AI‑native applications and platforms</b>, including bespoke solutions and AI‑enabled SaaS, with AI as the default design paradigm.</li><li>Partner with product managers and GDO stakeholders to identify opportunities where AI can augment human decision‑making, automate execution, and create step‑change improvements in clinical and operational workflows.</li><li>Design, develop, and maintain secure, scalable applications using Python/Java/Node JS/React JS.</li><li>Build applications on the Salesforce platform.</li><li>Design and operate <b>LLM‑native and agentic systems</b> as long‑lived products, incorporating human‑in‑the‑loop patterns, continuous learning, monitoring, and governance as part of the standard operating model. Frameworks include OpenAI, AWS Bedrock, and LangChain.</li><li>Incorporate microservices, APIs, MCPs, event-driven processes, and middleware within enterprise systems.</li><li>Use critical thinking to investigate issues with systems and data, and identify solutions for short-term remediation and long-term strategy.</li><li>Implement CI/CD practices for software applications.</li><li>Monitor model performance in production and manage model drift, retraining, and rollback strategies.</li><li>Ensure compliance with data governance, privacy, and security standards.</li></ul><p></p><p><u>Requirements:</u></p><ul><li>Must have a minimum of 8 years of strong experience in software engineering; Pharma/Life Sciences experience is a plus.</li><li>Bachelor’s degree in Computer Science, Software Engineering, or related field.</li><li>Must have experience in developing applications on <b>Salesforce platform</b>.</li><li>Should have a demonstrated track record implementing moderately complex technical solutions, developing software applications following SDLC processes in a regulated environment. </li><li>Practical experience building Generative AI and Agentic AI applications using tools like LangChain, LlamaIndex, Google ADK, etc.</li><li>Strong proficiency in Python and React; Java or TypeScript familiarity.</li><li>Solid grasp of REST APIs, MCPs, FastAPI, and JSON/XML and knowledge about TensorFlow or PyTorch.</li><li>Experience with AWS Cloud services such as Lambda, S3, DynamoDB, Bedrock, SageMaker.</li><li>Strong data analytics skills - SQL/NoSQL databases, able to write efficient queries.</li><li>Excellent problem-solving and analytical skills.</li><li>Must be a relationship builder and capable of working effectively in a highly matrix organization with strong communication, planning, and collaboration skills.</li><li>Strong technical expertise, leadership skills, and a passion for delivering high-quality, reliable solutions.</li><li>Must possess excellent written and verbal skills and demonstrate an ability to effectively communicate at all levels of the organization.</li></ul><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $108,970 - $132,046 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1600805 : Manager, Full Stack Engineer, Clinical Engineering &amp; Operations]]></description><link>http://biotechroles.com/manager-full-stack-engineer-clinical-engineering-and-operations-bristol-myers-squibb/6a05f7102f1861929d2531ed</link><guid isPermaLink="true">http://biotechroles.com/manager-full-stack-engineer-clinical-engineering-and-operations-bristol-myers-squibb/6a05f7102f1861929d2531ed</guid><pubDate>Thu, 14 May 2026 16:23:44 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Senior Medical Science Liaison, Oncology, International Markets (Argentina, Chile, Colombia, and Peru)]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><i>Bristol Myers Squibb es un empleador que brinda igualdad de oportunidades. Las personas que apliquen para cualquier vacante, y que estén calificadas para la misma recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, nacionalidad, edad, discapacidad, condición de veterano protegido, embarazo, ciudadanía, estado civil, expresión de género, información genética, afiliación política o cualquier otra característica protegida por la ley.</i></p><p></p><p><span><span><b><span>External Description</span></b></span></span></p><h1><span><span><span>Role Summary</span></span></span></h1><p><span><span><span>The Senior Medical Science Liaison (MSL) advances the BMS medical mission by building trusted, peer-to-peer scientific partnerships and delivering timely data and actionable insights that support appropriate use of BMS medicines and improve patient care.</span></span></span></p><p><span><span><span>This is a field-based role. The Senior MSL is expected to spend approximately 80–90% of their time with external stakeholders (e.g., investigators and clinical thought leaders), while maintaining strong therapeutic-area expertise and supporting internal stakeholders. Field time may vary based on asset life cycle, therapeutic area, and geographic scope. </span><b><span>Travel is required</span></b><span> and may include international travel.</span></span></span></p><p><span><span><span>The Senior MSL will act as the country field medical lead, engaging clinical investigators and TLs, serving as the therapeutic resource for external and internal stakeholders. A key differentiator of this senior role is a strong focus on clinical trial engagement, including leading investigator relationships, supporting site feasibility, enabling patient recruitment, and facilitating evidence-generation activities in close collaboration with Regional Clinical Operations (RCO). The Senior MSL also develops and executes a territory plan that supports medical education and disease-landscape shaping, aligned with the local Oncology Medical Affairs strategy. This role reports to the Regional Medical Market Lead.</span></span></span></p><p><span><span><span>All activities are performed in an ethical and compliant manner, in full adherence with all applicable BMS policies, local laws, and external regulations.</span></span></span></p><p></p><h1><span><span><span>Key Responsibilities</span></span></span></h1><p><span><span><b><span>1. External Engagement and Customer Focus</span></b></span></span></p><ul><li><p><span><span><span>Develop, maintain, and deepen trusted peer-to-peer relationships with National and Regional (above market) Thought Leaders (NTLs/RTLs), HCPs, patient advocacy groups (PAGs), medical societies, and payer stakeholders within a defined geographic scope.</span></span></span></p></li><li><p><span><span><span>Engage with TLs/HCPs through multiple channels (e.g., 1:1 meetings, group presentations, virtual/remote interactions).</span></span></span></p></li><li><p><span><span><span>Continuously profile and assess the medical landscape within the therapeutic area, maintaining up-to-date knowledge of treatment strategies, clinical trial activities, unmet medical needs, competitive landscape, and scientific developments.</span></span></span></p></li><li><p><span><span><span>Effectively present scientific and clinical information to HCPs, ensuring medical accuracy and full compliance with local procedures, ethical guidelines, and legal and regulatory directives.</span></span></span></p></li><li><p><span><span><span>Identify and engage potential speakers for BMS educational programs, ensuring all speakers receive appropriate product and disease-state training.</span></span></span></p></li><li><p><span><span><span>Engage strategically with payers during pre- and peri-launch phases in collaboration with Field HEOR and Account Executives where applicable.</span></span></span></p></li><li><p><span><span><span>Support acceleration of pipeline impact and launch readiness through HCP engagement, medical education, advisory boards, and scientific exchange.</span></span></span></p></li><li><p><span><span><span>Leverage digital tools and capabilities — including AI — to enhance the quality, reach, and efficiency of medical engagement.</span></span></span></p></li></ul><p></p><p><span><span><b><span>2. Clinical Trial Support and Evidence Generation </span></b></span></span></p><ul><li><p><span><span><span>Serve as the primary point of contact between clinical trial investigators and the BMS Medical/Global Development Operations (GDO) team, as aligned with local medical leadership.</span></span></span></p></li><li><p><span><span><span>Support Interventional and Non-Interventional Research (NIR) studies by identifying and assessing potential study sites, facilitating patient recruitment, and supporting discussions around the safe and effective use of BMS investigational products — in accordance with local medical management direction and the relevant study scope document.</span></span></span></p></li><li><p><span><span><span>Provide feasibility insights to the clinical development team (study and site), based on field knowledge and investigator relationships.</span></span></span></p></li><li><p><span><span><span>Actively support CRO/RCO-sponsored studies as agreed with local medical management and as defined by the applicable study scope document.</span></span></span></p></li><li><p><span><span><span>Support Investigator-Sponsored Research (ISR) and collaborative study submissions and execution processes, including follow-up, in accordance with BMS guidance.</span></span></span></p></li><li><p><span><span><span>Liaise with key accounts to understand clinical barriers to patient access and promote equity in access to clinical trials.</span></span></span></p></li><li><p><span><span><span>Lead or support investigator meetings, as agreed with local and regional medical management.</span></span></span></p></li><li><p><span><span><span>Contribute to the involvement of TLs in local and/or GDO-driven studies, Managed Access Protocols (MAP), and other scientific activities.</span></span></span></p></li><li><p><span><span><span>Ensure that BMS Pharmacovigilance procedural documents are understood and applied by all investigators in local studies; promptly alert appropriate BMS personnel to any identified Adverse Events (AEs).</span></span></span></p></li></ul><p></p><p><span><span><span>3. </span><b><span>Medical Planning and Execution</span></b></span></span></p><ul><li><p><span><span><span>Contribute to the Local/Regional Medical Plan (e.g., clinical trial support, ISR strategy, and medical-insight priorities).</span></span></span></p></li><li><p><span><span><span>Develop and execute a Scientific engagement plan aligned with therapeutic area objectives and stakeholder needs.</span></span></span></p></li></ul><ul><li><p><span><span><span>Use an institution/account planning approach and contribute to cross-functional institution and account plans.</span></span></span></p></li><li><p><span><span><span>Contribute to medical strategy by sharing medical insights and disease-area knowledge, grounded in patient needs and treatment trends.</span></span></span></p></li></ul><ul><li><p><span><span><span>Lead/ support the execution of regional advisory board meetings, satellite symposia, expert exchange meetings, and other strategic tactics.</span></span></span></p></li><li><p><span><span><span>Contribute to the medical/scientific sections of pricing and reimbursement files where applicable.</span></span></span></p></li></ul><p></p><p><span><span><b><span>4. Medical Insights Capture and Communication</span></b></span></span></p><ul><li><p><span><span><span>Systematically collect and communicate meaningful medical insights from the field back to internal stakeholders to inform strategy development, medical plans, and pipeline decisions.</span></span></span></p></li><li><p><span><span><span>Gather and share intelligence on the competitive landscape and clinical practice trends to support strategic decision-making.</span></span></span></p></li><li><p><span><span><span>Appropriately document all activities and achieve annual goals in accordance with BMS performance and reporting requirements.</span></span></span></p></li></ul><ul><li><p><span><span><span>Contribute to medical strategy by sharing medical insights and disease-area knowledge, grounded in patient needs and treatment trends.</span></span></span></p></li></ul><p></p><p><span><span><b><span>5. Internal Medical Support</span></b></span></span></p><ul><li><p><span><span><span>Provide scientific support at medical meetings, including presenting unbiased data, evaluating speakers, and supporting BMS-contracted speakers.</span></span></span></p></li><li><p><span><span><span>Support the initial and ongoing product and disease-area training of investigational site staff, site managers, and monitors involved in BMS studies.</span></span></span></p></li><li><p><span><span><span>Provide scientific training and medical updates to internal stakeholders including Commercial, Regional Clinical Operations (RCO), Regional Delivery Leads (RDL), Regulatory Affairs, Pharmacovigilance, Legal, HEOR, and Market Access teams, as appropriate.</span></span></span></p></li></ul><p></p><p><span><span><b><span>6. Compliance and Ethics</span></b></span></span></p><ul><li><p><span><span><span>Endorse and actively model a culture of compliance and integrity, adhering to all applicable internal BMS policies and external laws and regulations.</span></span></span></p></li><li><p><span><span><span>Act as a role model demonstrating consistent ethical and professional behaviour at all times.</span></span></span></p></li><li><p><span><span><span>Alert management or the Compliance Department promptly to any potential compliance issues identified in the field.</span></span></span></p></li><li><p><span><span><span>Work with the local Pharmacovigilance-responsible colleague to ensure all AE information identified in the field is correctly and transparently collected and reported to relevant Health Authorities.</span></span></span></p></li></ul><p></p><h1><span><span><span>Required Qualifications &amp; Experience</span></span></span></h1><ul><li><p><span><span><b><span>Advanced scientific or medical degree required:</span></b><span> MD, PharmD, or PhD with experience in Oncology, or with a broad medical background.</span></span></span></p><ul><li><p><span><span><span>Science Graduate with substantial and relevant pharmaceutical/industry experience may also be considered.</span></span></span></p></li></ul></li></ul><ul><li><p><span><span><span>Contribute to medical strategy by sharing medical insights and disease-area knowledge, grounded in patient needs and treatment trends.</span></span></span></p></li></ul><ul><li><p><span><span><span>Demonstrated experience working in a scientific and/or clinical research environment in Oncology.</span></span></span></p></li><li><p><span><span><span>Robust experience in clinical trial support, including site identification, investigator engagement, patient recruitment facilitation, and ISR/collaborative study processes.</span></span></span></p></li><li><p><span><span><span>Experience in translating and communicating complex scientific or clinical data in a clear, accurate, and valuable manner to support HCPs in best serving their patients.</span></span></span></p></li><li><p><span><span><span>Proven ability to develop and maintain effective peer-to-peer relationships with investigators, TLs, and other healthcare professionals.</span></span></span></p></li><li><p><span><span><span>Experience with investigator-sponsored research, non-registrational studies, and early patient access programmes.</span></span></span></p></li><li><p><span><span><span>Experience working effectively with cross-functional teams including Clinical, Commercial, Regulatory, Pharmacovigilance, and Health Outcomes colleagues.</span></span></span></p></li></ul><ul><li><p><span><span><span>Contribute to medical strategy by sharing medical insights and disease-area knowledge, grounded in patient needs and treatment trends.</span></span></span></p></li></ul><ul><li><p><span><span><span>Language requirement: English &amp; French working proficiency required, Spanish a strong asset</span></span></span></p></li></ul><p><span><span><span> </span></span></span></p><h1><span><span><span>Key competencies desired</span></span></span></h1><ul><li><p><span><span><b><span>Change agility - </span></b><span>The ability of individuals, teams, and organizations to adapt, respond, and thrive in the face of change and ambiguity.</span></span></span></p></li><li><p><span><span><b><span>Scientific agility</span></b><span> - Ability to understand the application of science to the business by staying up-to-date in the rapidly changing landscape of scientific advancement to address the needs and challenges of healthcare professionals and organizations.</span></span></span></p></li><li><p><span><span><b><span>Scientific communication/Customer engagement</span></b><span> - Effectively engage and partner with HCPs, utilising all communication channels, to drive scientific exchange, enhance medical education, data generation and collect quality insights that inform strategic decisions to deliver more medicines to more patients faster.</span></span></span></p></li><li><p><span><span><b><span>Customer mindset</span></b><span> - Adopting a strategic and customer-focused perspective to facilitate scientific exchange and increase patient access to BMS medicines.</span></span></span></p></li><li><p><span><span><b><span>Teamwork/Enterprise mindset</span></b><span> - An approach that prioritizes collaboration, shared goals, and collective success within a team or organization to deliver an exceptional customer experience.</span></span></span></p></li><li><p><span><span><b><span>Digital agility</span></b><span> - The ability to adapt, thrive, and excel in the rapidly evolving digital landscape harnessing digital technologies to increase customer engagement and overall competitiveness.</span></span></span></p></li><li><p><span><span><b><span>Analytical mindset</span></b><span> - An approach with a strong emphasis on critical thinking, logical reasoning, and data-driven decision-making to identify and capitalise on the best opportunities for BMS.</span></span></span></p></li></ul><p></p><p></p><p><span>#LI-REMOTE </span></p><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602180 : Senior Medical Science Liaison, Oncology, International Markets (Argentina, Chile, Colombia, and Peru)]]></description><link>http://biotechroles.com/senior-medical-science-liaison-oncology-international-markets-argentina-chile-colombia-and-peru-bristol-myers-squibb/6a05f7102f1861929d2531ec</link><guid isPermaLink="true">http://biotechroles.com/senior-medical-science-liaison-oncology-international-markets-argentina-chile-colombia-and-peru-bristol-myers-squibb/6a05f7102f1861929d2531ec</guid><pubDate>Thu, 14 May 2026 16:23:44 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Field - Argentina - AR</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Clinical Research Associate (Colombia Remote)]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><i>Bristol Myers Squibb es un empleador que brinda igualdad de oportunidades. Las personas que apliquen para cualquier vacante, y que estén calificadas para la misma recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, nacionalidad, edad, discapacidad, condición de veterano protegido, embarazo, ciudadanía, estado civil, expresión de género, información genética, afiliación política o cualquier otra característica protegida por la ley.</i></p><p></p><p></p><p>Responsable de la supervisión del progreso de un ensayo clínico y de garantizar que se realice, registre e informe de acuerdo con el<br />protocolo, los procedimientos operativos estándar (SOP), las buenas prácticas clínicas (BPC) y los requisitos reglamentarios aplicables ( s).<br />Actuar como uno de los puntos de contacto a nivel de Hub para las partes interesadas internas y externas.<br />• Contribuir significativamente al equipo de estudio y al personal del sitio de entrenadores para mejorar el rendimiento del sitio y del centro.<br />• Servir como un recurso clave para los colegas, proporcionando orientación, capacitación líder y tutoría a otros miembros del equipo a<br />través de un proceso de tutoría mediante presentaciones formales e informales.<br />• Ayudar a la gerencia en diversas tareas, según se le asigne o solicite.<br />Busque de manera proactiva mejorar las habilidades de comunicación tanto con las partes internas (nivel global) como con todas las partes<br />externas relevantes y entrene a otros para que hagan lo mismo.<br />• Identifica nuevos investigadores potenciales, a través de colaboraciones continuas con partes interesadas internas y externas. Evalúa<br />investigadores potenciales y sus sitios para asegurarse de que tengan los recursos y las capacidades para realizar ensayos clínicos.<br />Documenta la visita y comunica los hallazgos. Proporciona comentarios sobre los hallazgos de la Evaluación potencial del sitio a los<br />colaboradores. Recomienda sitios durante el proceso de viabilidad y / o selección del sitio.<br />• Desarrolla nuevos sitios, que tienen una experiencia mínima en investigación, brindando apoyo para comprender los requisitos para<br />ejecutar ensayos clínicos (es decir, SOP, capacitación, recursos de personal, etc.)<br />• Determina la necesidad y / o el tipo de visita previa al estudio que se requiere según la experiencia previa del sitio con la ejecución de<br />ensayos clínicos de BMS.<br />• Realiza visitas de iniciación en colaboración con otros miembros del equipo de estudio y grupos funcionales auxiliares. Proporciona<br />capacitación individualizada y específica del protocolo basada en la experiencia del investigador y del personal del sitio, antes de la<br />activación del sitio.<br />• Revisa las actividades y la calidad del sitio a través de visitas al sitio y fuera del sitio. Realiza actividades de monitoreo y garantiza la<br />seguridad y protección de los sujetos del estudio de acuerdo con el plan de monitoreo, los PBPD de BMS y las mejores prácticas, el<br />protocolo, las Directrices ICH / GCP y otras regulaciones locales según corresponda.<br />• Realice actividades de Monitoreo de sitio no cegado para proteger a los ciegos del estudio actuando como una fuente de monitoreo<br />secundaria separada del monitor ciego. Incluye actividades de monitoreo del sitio para farmacia, revisión de aleatorización, responsabilidad<br />de medicamentos y conciliación de los productos de investigación cegados. Trabajar con el personal del estudio no ciego, incluidos<br />farmacéuticos o preparadores de medicamentos no ciegos, y comunicarse solo con el personal interno del estudio BMS no ciego durante la<br />realización del estudio.<br />• Si bien el monitoreo demuestra la capacidad de usar datos para evaluar riesgos, identificar problemas y tomar decisiones apropiadas.<br />Identifica los factores clave y la importancia relativa de un problema. Analice la causa raíz y el sesgo potencial. Busca información adecuada<br />y crea un plan de acción correctivo o preventivo y comunica el proceso de manera lógica y oportuna.<br />• Realiza actividades de cierre del sitio cuando se completan todas las visitas de protocolo requeridas y el seguimiento.<br />• Administra múltiples protocolos, en múltiples áreas terapéuticas, que pueden requerir viajes, según la ubicación del sitio asignado y / o el<br />territorio geográfico.<br />• Asegura la calidad de los datos enviados desde los sitios de estudio y asegura la vigencia de los datos mediante el uso de los sistemas<br />disponibles para seguir las actividades del sitio.<br />• La revisión del listado de datos clínicos se realiza en los puntos de tiempo asignados de acuerdo con el plan de revisión de datos y / o SMP<br />• Supervisa las actividades generales del personal del sitio sobre el que no hay autoridad directa.<br />• Motiva / influye en el sitio para cumplir con los objetivos del estudio, incluidas las metas de inscripción y retención. Demuestra flexibilidad y<br />adaptabilidad al comunicarse con diferentes partes interesadas utilizando el método de comunicación más apropiado.<br />• Anticipa, identifica y apoya proactivamente al sitio en la resolución de problemas a medida que ocurren. Documenta de manera adecuada y<br />escala de manera oportuna los problemas pendientes graves o persistentes a la administración y al equipo del proyecto. Inicia, recomienda,<br />documenta y comunica acciones correctivas según sea necesario y realiza un seguimiento para garantizar que se implementen las acciones<br />correctivas / preventivas basadas en el análisis de la causa raíz.<br />• Participación en el proceso de auditoría / inspección de Cumplimiento Normativo, según sea necesario. Esto incluye el desarrollo e<br />implementación de acciones correctivas y preventivas en el sitio.<br />• Prepara y presenta informes escritos, tanto de seguimiento como administrativos, de manera oportuna, precisa, concisa, profesional y<br />objetiva.<br />• Construye, cultiva y mantiene relaciones con los clientes e identifica sinergias entre las necesidades del cliente y los intereses de la<br />empresa.<br />• Genera confianza con los clientes sirviendo como un recurso consistente y preciso.</p><p></p><p><u>D<span>egree Requirements</span></u><span> </span></p><p><span>Bachelors degree required. </span></p><p><span>Field of study within life sciences or </span><span>equivalent</span><br /><u><span>Experience Requirements</span></u></p><p><span>1</span><span> </span><span>y</span><span>e</span><span>a</span><span>r</span><span> </span><span>o</span><span>f</span><span> </span><span>r</span><span>e</span><span>l</span><span>e</span><span>v</span><span>a</span><span>n</span><span>t</span><span> </span><span>c</span><span>l</span><span>i</span><span>n</span><span>i</span><span>c</span><span>a</span><span>l</span><span> </span><span>r</span><span>e</span><span>s</span><span>e</span><span>a</span><span>r</span><span>c</span><span>h</span><span> </span><span>e</span><span>x</span><span>p</span><span>e</span><span>r</span><span>i</span><span>e</span><span>n</span><span>c</span><span>e</span><span> </span><span>a</span><span>n</span><span>d</span><span>/</span><span>o</span><span>r</span><span> </span><span>r</span><span>e</span><span>l</span><span>e</span><span>v</span><span>a</span><span>n</span><span>t</span><span> </span><span>e</span><span>d</span><span>u</span><span>c</span><span>a</span><span>t</span><span>i</span><span>o</span><span>n</span><span>a</span><span>l</span><span> </span><span>e</span><span>x</span><span>p</span><span>e</span><span>r</span><span>i</span><span>e</span><span>n</span><span>c</span><span>e</span></p><p><u><span>English intermediate </span></u></p><p></p><p></p><p></p><p><span>#LI-REMOTE </span></p><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601610 : Clinical Research Associate (Colombia Remote)]]></description><link>http://biotechroles.com/clinical-research-associate-colombia-remote-bristol-myers-squibb/6a05f70f2f1861929d2531eb</link><guid isPermaLink="true">http://biotechroles.com/clinical-research-associate-colombia-remote-bristol-myers-squibb/6a05f70f2f1861929d2531eb</guid><pubDate>Thu, 14 May 2026 16:23:43 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Field - Colombia - CO</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Sterility Assurance]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p></p><p>The Sr. Manager, Sterility Assurance, is a highly critical role and is responsible for managing Sterility Assurance which provides support to the CAR T manufacturing site. This role is responsible for supporting facility design/modifications, the aseptic process validation program, operator qualification/requalification, the gowning certification/recertification program, critical utilities sampling and testing, and overall contamination control program for the site. The Sr. Manager Sterility Assurance is responsible to act as the SME during regulatory inspections.</p><p></p><p><b>Duties/Responsibilities</b></p><ul><li><p>To support final product testing and release, incoming components and materials testing and release and monitoring of the critical utilities systems.</p></li><li><p>Development and management of SOPs, forms, and methods required to support the compliant operation.</p></li><li><p>The Senior Manager, Sterility Assurance plays a critical role in ensuring the execution and support of the contamination control strategy for the facility including, but not limited to aseptic process validation, facility design and modification, gowning, critical utilities, and EMPQs. Generates, owns, and/or supports change controls, deviations, CAPAs within the eQMS system.</p></li><li><p>Support equipment, facility, and microbiological method qualifications.</p></li><li><p>Ensure the site and department objectives are met.</p></li><li><p>Manage and develop direct reports.</p></li><li><p>Onboard new materials required to support manufacturing operations.</p></li><li><p>Support manufacturing schedule and needs.</p></li><li><p>Ensure employees are properly trained and qualified to perform assigned tasks, provide performance evaluations, and support career development of direct reports.</p></li><li><p>The incumbent will be required to gown for entry into Aseptic core and supporting areas, on an as-needed basis.</p></li><li><p>The management incumbent (or designee) will be expected to be on call, to support manufacturing issues involving sampling and/or test excursions or questions during shift operations.</p></li><li><p>This job description is intended to describe the general nature and level of work being performed by the person assigned to this position.</p></li><li><p>The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.</p></li><li><p>Occasional travel may be required.</p></li><li><p>Perform other tasks as assigned.</p></li></ul><p></p><p><b>Qualifications</b></p><ul><li><p>Advanced knowledge of cGMP&#39;s, FDA, USP, MHRA, BP, EP, JP, PMDA, and DEA regulations and guidelines, as related to manufacture of cell therapy products.</p></li><li><p>Advanced data integrity knowledge and practices.</p></li><li><p>Intermediate understanding of statistics, control charts, action and alert limits and data trending.</p></li><li><p>Advanced knowledge of Microbiology.</p></li><li><p>Intermediate knowledge of Good Engineering Practices and Validation Principles: URS, IQ, OQ, PQ, PVs, etc.</p></li><li><p>Advanced verbal and written communication skills.</p></li><li><p>Demonstrated critical reasoning, problem solving, troubleshooting, investigation, and decision-making skills.</p></li><li><p>Must be team-oriented and has the demonstrated ability to work cross[1]departmentally throughout the manufacturing site.</p></li><li><p>Demonstrated leadership and management skills, including establishing direction and goals, and guiding execution while fostering a team-based environment.</p></li><li><p>Advanced mentoring and coaching, influencing, negotiating and personal interaction skills.</p></li><li><p>Demonstrated resource management and planning skills.</p></li><li><p>Must be flexible and adaptable, and able to work under pressure, while meeting designated timelines.</p></li><li><p>Advanced knowledge of safety, OSHA, and EPA regulations, electrical and energized equipment (lockout/tag out), fall safety, HAZCOM, MSDS sheets, etc.</p></li><li><p>Advanced of Microsoft Word, Outlook, Excel, PowerPoint, etc.</p></li><li><p>Microbiology laboratory and/or Environmental Monitoring setting.</p></li><li><p>Experience working with cell therapy products is preferred.</p></li><li><p>2-3 years of leadership/managerial experience required.</p></li><li><p>Experience in participating and supporting regulatory audits preferred: FDA, MHRA, PMDA, etc.</p></li><li><p>Experience in working with Quality Systems preferred: SOPs, Change Control, Deviations, CAPAs, and Risk Assessments.</p></li><li><p> An equivalent combination of education and experience may substitute</p></li></ul><p></p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Summit West - NJ - US: $121,070 - $146,703&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1596592 : Senior Manager, Sterility Assurance]]></description><link>http://biotechroles.com/senior-manager-sterility-assurance-bristol-myers-squibb/6a05f70f2f1861929d2531ea</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-sterility-assurance-bristol-myers-squibb/6a05f70f2f1861929d2531ea</guid><pubDate>Thu, 14 May 2026 16:23:43 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Summit West - NJ - US</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Oncology/Hematology -Harrisburg, PA]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>This territory includes: <span>Harrisburg, Hershey, State College, Duboise, Lancaster, York</span></p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602415 : Senior Therapeutic Area Specialist, Oncology/Hematology -Harrisburg, PA]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-harrisburg-pa-bristol-myers-squibb/6a05f70e2f1861929d2531e9</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-harrisburg-pa-bristol-myers-squibb/6a05f70e2f1861929d2531e9</guid><pubDate>Thu, 14 May 2026 16:23:42 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Harrisburg - PA - US</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Translational Program Manager (Immunology, Cardiovascular, and Neuroscience)]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p><span>We are searching for a highly motivated Program Manager to support Translational Medicine Leaders in the Immunology, Cardiovascular and Neurology (ICN) Disease Team to enable the effective &amp; efficient execution of our translational development plans. The Translational Program Manager, as part of the Translational Development team in Research, would manage multiple complex high-profile late phase portfolio assets and facilitate broad, integrated biomarker plans to enable the delivery of our translational medicine portfolio.</span></p><p></p><p><b>Key Responsibilities:</b></p><ul><li><p><span>Collaborate with the ICN Translational Medicine Lead to design and execute comprehensive program timelines, integrating scientific and operational expertise to deliver translational biomarker strategies. Oversee key activities, including data delivery, contracting, data transfers, regulatory submissions, and internal/external collaborations</span></p></li><li><p>Provide strong collaboration, coordination, and communication skills to support cross-functional interactions and <span>prioritization of activities outside of TM such as assay development, outsourcing, vendor management, biospecimen, data management, biostatistics, and operations teams to align with ICN and strategic stakeholder priorities</span></p></li><li><p>Establish, manage, and maintain cross-functional relationships in coordination with BMS biomarker leads, supporting teams, and relevant stakeholders/technical experts. This includes conducting meetings, organizing agendas, preparing meeting minutes, and following up on action items. Meetings may include translational sub-teams, vendor meetings, other internal meetings with translational focus or components</p></li><li><p>Proactively manage project risks with a robust understanding of scientific and operational challenges, developing and implementing effective mitigation strategies. Escalate significant</p><p>issues to the Translational Medicine Lead and senior management, as needed</p></li><li><p>Establish and maintain a book of work for relevant assets, creating visibility and maintaining transparency into translational activities to key stakeholders that contribute to the overall translational plan for a defined portfolio of assets using effective visualization tools (e.g., Smartsheet, PowerPoint, Office Timeline)</p></li><li><p>Oversee the end-to-end ICN budgeted contracts, ensuring alignment with scientific and operational goals. Coordinate with vendor management, alliance management, finance, and global procurement to streamline contract execution and delivery, global procurement and outsourcing management as appropriate to drive from initial draft contract through issuing of purchase orders</p></li><li><p>Support the preparation of biomarker study reports and related documentation. Coordinate reviews with biomarker leads and appropriate stakeholders of documents which may</p><p>support the final clinical study report in relevant SharePoint sites and/or repositories (Verity)</p></li><li><p>Coordinate review with biomarker lead and appropriate stakeholders of documents from vendors (e.g., contracts, contract amendments, reports, data transfer agreements) and storage of appropriate final documents in relevant SharePoint sites and/or repositories</p></li><li><p>Facilitate publication planning and ensure data delivery for internal/external presentations, publications and conferences, ensuring alignment with strategic timelines</p></li><li><p>Support transition of programs internally from early-stage translational team, as needed per program</p></li><li><p>Support continuous evolution and measurement of processes and tools to drive efficiency and enhance business value across Translational Development. Proactively seek opportunities to leverage and streamline processes and tools to drive improved engagement and program management support. Develop and implement agile, creative solutions to solve business challenges within the line organization, across the company, and in partnership with external collaborators</p></li></ul><p></p><p><b>Qualifications &amp; Experience:</b></p><ul><li><p>B.S., M.S. in a scientific discipline; PMP or equivalent project management experience is desirable</p></li><li><p>5&#43; years pharmaceutical, or related, industry experience in a variety of operational/scientific roles in a highly matrixed environment (level of role dependent on experience)</p></li><li><p>Strong communicator experienced with influencing and interacting at all levels including with senior scientific, operational, or external thought leaders to drive connectivity and efficiency of collaborative research</p></li><li><p>Works with a sense of urgency and experience managing multiple projects, building structure from ambiguity, and helping teams to develop priorities</p></li><li><p>Experience designing and leading complex projects comprised of virtual team members of diverse styles, driving to successful outcomes with and without direct management responsibilities</p></li><li><p>Skilled listener with ability to manage complex internal – up, across, and down the hierarchy - and external relationships through constructive conflict management; experience with third party governance oversight desirable</p></li><li><p>Experience with vendor management</p></li><li><p>Experience with various project management tools (i.e., Smartsheet, SharePoint, Office Timeline)</p></li><li><p>Shapes strategic approaches to scientific delivery, utilizing sophisticated negotiation and scenario planning</p></li></ul><p>#LI-Hybrid</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Cambridge Crossing: $180,430 - $218,638 &amp;#xa;Madison - Giralda - NJ - US: $156,890 - $190,117&amp;#xa;San Diego - CA - US: $167,560 - $203,044&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602382 : Associate Director, Translational Program Manager (Immunology, Cardiovascular, and Neuroscience)]]></description><link>http://biotechroles.com/associate-director-translational-program-manager-immunology-cardiovascular-and-neuroscience-bristol-myers-squibb/6a05f70e2f1861929d2531e8</link><guid isPermaLink="true">http://biotechroles.com/associate-director-translational-program-manager-immunology-cardiovascular-and-neuroscience-bristol-myers-squibb/6a05f70e2f1861929d2531e8</guid><pubDate>Thu, 14 May 2026 16:23:42 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Madison - Giralda - NJ - US</location><salary>$150000-200000</salary><type>Full time</type></item><item><title><![CDATA[Senior Specialist, Associate Process Engineer II]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>1.         PURPOSE AND SCOPE OF POSITION:</b></p><p>Process Engineers provide technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. Process Engineers work closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. Process engineers work to identify and drive continuous improvements to the manufacturing process.</p><p></p><p><b>2.         REQUIRED COMPETENCIES:  Knowledge, Skills, and Abilities</b></p><p>·         Senior Specialist, Associate Process Engineer II: Minimum 2.5&#43; years of industry experience with a minimum of 1 year of relevant experience in GMP biologic/cell therapy manufacturing technical or process support. cGMP and/or Cell Therapy manufacturing experience preferred.</p><p></p><p><b>3.         DUTIES AND RESPONSIBILITIES</b></p><p><span>·         Provides on-the-floor and on-site troubleshooting and technical support to Manufacturing</span></p><p><span>·         Facilitates deviation prevention and deviation closure through site quality systems</span></p><p><span>·         Analyze and summarize manufacturing data to support impact assessments and investigations</span></p><p><span>·         Owner of change controls for routine process and procedure changes</span></p><p><span>·         CAPA owner for Manufacturing improvements</span></p><p><span>·         Author and revise manufacturing SOPs and provide technical content and direction for electronic batch records</span></p><p><span>·         Participates in technology transfer efforts for new processes and product implementation</span></p><p><span>·         Train and support GMP operators on new procedures, processes, and changes</span></p><p><span>·         Applies continuous improvement tools to identify and close procedural and compliance gaps</span></p><p><span>·         Identify opportunities for process improvements and operational efficiencies, and lead implementation efforts.</span></p><p><span>·         Interfaces with other functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities &amp; Engineering</span></p><p><span>·         Support equipment and systems validation activities, including review of equipment qualification documents, drafting user requirements, and participating on impact assessments</span></p><p><span>·         Ability to perform gowning activities and enter the manufacturing plant. Exposure to strong magnetic fields is commonplace in the manufacturing areas.</span></p><p></p><p><b>4.         EDUCATION AND EXPERIENCE</b></p><p>·          BSc and/or MSc degree in Science or Chem/Bio Engineering</p><p><b> </b></p><p>This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.</p><p>This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Devens - MA - US: $87,660 - $106,224&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602437 : Senior Specialist, Associate Process Engineer II]]></description><link>http://biotechroles.com/senior-specialist-associate-process-engineer-ii-bristol-myers-squibb/6a05f70d2f1861929d2531e7</link><guid isPermaLink="true">http://biotechroles.com/senior-specialist-associate-process-engineer-ii-bristol-myers-squibb/6a05f70d2f1861929d2531e7</guid><pubDate>Thu, 14 May 2026 16:23:41 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Devens - MA - US</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Cardiovascular Specialty - West Palm Beach, FL]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p></p><p><b><span>Job<span> </span></span><span>Pos</span><span>ting Title</span><span>:</span></b><span><span><span> </span></span><span>Senior<span> </span></span><span>Therapeutic Area Specialist, C</span><span>ardiovascular<span> </span></span><span>Specialty - West Palm Beach, FL</span></span></p></div><div><p><b><span>Therapeutic Area (TA):</span></b><span><span><span> </span>Cardiovascular</span></span><span> </span></p></div><div><p><b><span>Primary<span> </span></span><span>Location</span></b><span><span>:<span> </span></span><span>Field – United States</span></span><span> </span></p></div><div><p><b><span>Primary Job Posting<span> </span></span><span>Location</span></b><span><span>:<span> West Palm Beach, FL</span></span></span></p></div><div><p><span> </span></p></div><div><p><span><span>At Bristol Myers Squibb, we<span> </span></span><span>are inspired</span><span><span> </span>by a single vision – transforming patients’ lives through science. The BMS Mission is to discover,<span> </span></span><span>develop</span><span><span> </span>and deliver innovative medicines that help patients prevail over serious diseases. In oncology, hematology,<span> </span></span><span>immunology</span><span><span> </span>and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues<span> </span></span><span>contribute</span><span><span> </span>to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Join us, build your professional career within one of the most innovative bio-pharma companies, and<span> </span></span><span>make a difference</span><span>.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><u><span>Position Summary</span></u><span> </span></p></div><div><p><span><span>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for<span> </span></span><span>appropriate patients</span><span>. </span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the<span> </span></span><span>appropriate patients</span><span>. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (</span><span>Cx</span><span>) through deeper scientific dialogue on and consistent with label,<span> </span></span><span>leveraging</span><span><span> </span>new ways of working and CE^3.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The role builds and<span> </span></span><span>maintains</span><span><span> </span>strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The TAS<span> </span></span><span>liaises</span><span><span> </span>with other BMS functions as needed to deliver an overall higher Customer Experience (</span><span>Cx</span><span>) – by meeting HCP needs in<span> </span></span><span>a timely</span><span><span> </span>and scientific manner. This role will prioritize the safe and<span> </span></span><span>appropriate use</span><span><span> </span>of BMS products while also focusing on overall business results and performance<span> </span></span><span>objectives</span><span><span> </span>while exemplifying BMS values. </span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The TAS role is<span> </span></span><span>field-based</span><span>. A TAS<span> </span></span><span>is<span> </span></span><span>anticipated</span><span><span> </span>to spend much of their time spent field with external customers.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><div><p><u><span>Key Responsibilities</span></u><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Portfolio Promotion</span></span><span> </span></p></div><div><ul><li><p><span><span>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in<span> </span></span><span>appropriate patients</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages with and continuously<span> </span></span><span>maintains</span><span>/grows<span> </span></span><span>a high level</span><span><span> </span>of scientific<span> </span></span><span>expertise</span><span><span> </span>in all assigned products and therapeutic areas.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Prepares and successfully implements comprehensive territory and account plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proactively uses available tools such as SOPHIA to derive insights and to dynamically inform call plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Provides feedback on experience using these tools to leadership to enable continuous improvement.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Fair &amp; Balanced Scientific Dialogue</span></span><span> </span></p></div><div><ul><li><p><span><span>Demonstrates scientific<span> </span></span><span>expertise</span><span><span> </span>and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with<span> </span></span><span>label</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and<span> </span></span><span>facilitating</span><span><span> </span>scheduling and<span> </span></span><span>logistics</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Maintains<span> </span></span><span>a high level</span><span><span> </span>of working<span> </span></span><span>expertise</span><span><span> </span>on emerging data for approved indications.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages real-time medical support through<span> </span></span><span>Medical on</span><span><span> </span>Call to reactively answer unsolicited questions and complex technical inquiries. </span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Cross-functional collaboration</span></span><span> </span></p></div><div><ul><li><p><span><span>Proactively collaborates with other field teams to ensure the best Customer Experience (</span><span>Cx</span><span>) for HCPs. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Gathers and shares relevant insights and information internally with the<span> </span></span><span>appropriate stakeholders</span><span><span> </span>to enable BMS to better serve its customers.</span></span><span> </span></p></li></ul></div></div><div><div><p><span> </span></p></div><div><p><span><span>Complies with</span><span><span> </span>all laws, regulations, and policies that govern the conduct of BMS.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><u><span>Required Qualifications &amp; Experience</span></u><span> </span></p></div><div><ul><li><p><span><span>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated experience building and<span> </span></span><span>maintaining</span><span><span> </span>strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (</span><span>Cx</span><span>).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in cardiovascular preferred.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance<span> </span></span><span>track record</span><span><span> </span>of meeting or exceeding goals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong selling and promotional skills proven through<span> </span></span><span>a<span> </span></span><span>track record</span><span><span> </span>of performance.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><u><span>Key competencies desired</span></u><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Customer/commercial mindset</span></span><span> </span></p></div><div><ul><li><p><span><span>Demonstrated ability to drive business results.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience<span> </span></span><span>identifying</span><span>, engaging, and cultivating credibility with customers across the patient care journey.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated resourcefulness and ability to connect with customers.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div></div><div><div><p><span><span>Patient centricity </span></span><span> </span></p></div><div><ul><li><p><span><span>Understands the<span> </span></span><span>patient</span><span><span> </span>journey and experience.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a patient-focused mindset.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Scientific Agility </span></span><span> </span></p></div><div><ul><li><p><span><span>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Analytical Capability:</span></span><span> </span></p></div><div><ul><li><p><span><span>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understanding how to interpret and analyze data related to BMS products, customer preferences</span><span>, clinical</span><span><span> </span>data.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use CE^3 to generate insights<span> </span></span><span>and do</span><span><span> </span>dynamic call planning.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Digital Agility:</span></span><span> </span></p></div><div><ul><li><p><span><span>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and<span> </span></span><span>maintain</span><span><span> </span>effective communication.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in<span> </span></span><span>a timely</span><span><span> </span>and compliant manner, track interactions, and plan future engagements with healthcare professionals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use the Medical on Call technology effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Keeping up to date with technological advancements and changes.</span></span><span> </span></p></li></ul></div></div><div><div><p><span> </span></p></div><div><p><span><span>Teamwork/Enterprise mindset</span></span><span> </span></p></div><div><ul><li><p><span><span>Strong business acumen to understand and analyze business, market drivers, and develop, execute, and adjust business plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrates<span> </span></span><span>a strong sense</span><span><span> </span>of learning agility. Seeks out and learns from unfamiliar<span> </span></span><span>experiences, and</span><span><span> </span>then applies those lessons to achieve better results in<span> </span></span><span>subsequent</span><span><span> </span>situations.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Track record</span><span><span> </span>of balancing individual drive and collaborative attitude.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Holds<span> </span></span><span>a high level</span><span><span> </span>of integrity and good judgment to navigate the<span> </span></span><span>role&#39;s</span><span><span> </span>requirements effectively and compliantly<span> </span></span><span>in accordance with</span><span><span> </span>BMS policies and procedures.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company.</span></span><span> </span></p></div></div><p></p><p></p><p></p></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $134,390 - $162,843&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602427 : Senior Therapeutic Area Specialist, Cardiovascular Specialty - West Palm Beach, FL]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-cardiovascular-specialty-west-palm-beach-fl-bristol-myers-squibb/6a05f70a2f1861929d2531e6</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-cardiovascular-specialty-west-palm-beach-fl-bristol-myers-squibb/6a05f70a2f1861929d2531e6</guid><pubDate>Thu, 14 May 2026 16:23:38 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Field - United States - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Cardiovascular Specialty - Lexington, KY]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p></p><p><b><span>Job<span> </span></span><span>Pos</span><span>ting Title</span><span>:</span></b><span><span><span> </span></span><span>Senior<span> </span></span><span>Therapeutic Area Specialist, C</span><span>ardiovascular<span> </span></span><span>Specialty - Lexington, KY</span></span></p></div><div><p><b><span>Therapeutic Area (TA):</span></b><span><span><span> </span>Cardiovascular</span></span><span> </span></p></div><div><p><b><span>Primary<span> </span></span><span>Location</span></b><span><span>:<span> </span></span><span>Field – United States</span></span><span> </span></p></div><div><p><b><span>Primary Job Posting<span> </span></span><span>Location</span></b><span><span>:<span> Lexington, KY</span></span></span></p></div><div><p><span> </span></p></div><div><p><span><span>At Bristol Myers Squibb, we<span> </span></span><span>are inspired</span><span><span> </span>by a single vision – transforming patients’ lives through science. The BMS Mission is to discover,<span> </span></span><span>develop</span><span><span> </span>and deliver innovative medicines that help patients prevail over serious diseases. In oncology, hematology,<span> </span></span><span>immunology</span><span><span> </span>and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues<span> </span></span><span>contribute</span><span><span> </span>to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Join us, build your professional career within one of the most innovative bio-pharma companies, and<span> </span></span><span>make a difference</span><span>.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><u><span>Position Summary</span></u><span> </span></p></div><div><p><span><span>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for<span> </span></span><span>appropriate patients</span><span>. </span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the<span> </span></span><span>appropriate patients</span><span>. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (</span><span>Cx</span><span>) through deeper scientific dialogue on and consistent with label,<span> </span></span><span>leveraging</span><span><span> </span>new ways of working and CE^3.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The role builds and<span> </span></span><span>maintains</span><span><span> </span>strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The TAS<span> </span></span><span>liaises</span><span><span> </span>with other BMS functions as needed to deliver an overall higher Customer Experience (</span><span>Cx</span><span>) – by meeting HCP needs in<span> </span></span><span>a timely</span><span><span> </span>and scientific manner. This role will prioritize the safe and<span> </span></span><span>appropriate use</span><span><span> </span>of BMS products while also focusing on overall business results and performance<span> </span></span><span>objectives</span><span><span> </span>while exemplifying BMS values. </span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>The TAS role is<span> </span></span><span>field-based</span><span>. A TAS<span> </span></span><span>is<span> </span></span><span>anticipated</span><span><span> </span>to spend much of their time spent field with external customers.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><div><p><u><span>Key Responsibilities</span></u><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Portfolio Promotion</span></span><span> </span></p></div><div><ul><li><p><span><span>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in<span> </span></span><span>appropriate patients</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages with and continuously<span> </span></span><span>maintains</span><span>/grows<span> </span></span><span>a high level</span><span><span> </span>of scientific<span> </span></span><span>expertise</span><span><span> </span>in all assigned products and therapeutic areas.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Prepares and successfully implements comprehensive territory and account plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proactively uses available tools such as SOPHIA to derive insights and to dynamically inform call plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Provides feedback on experience using these tools to leadership to enable continuous improvement.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Fair &amp; Balanced Scientific Dialogue</span></span><span> </span></p></div><div><ul><li><p><span><span>Demonstrates scientific<span> </span></span><span>expertise</span><span><span> </span>and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with<span> </span></span><span>label</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and<span> </span></span><span>facilitating</span><span><span> </span>scheduling and<span> </span></span><span>logistics</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Maintains<span> </span></span><span>a high level</span><span><span> </span>of working<span> </span></span><span>expertise</span><span><span> </span>on emerging data for approved indications.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Engages real-time medical support through<span> </span></span><span>Medical on</span><span><span> </span>Call to reactively answer unsolicited questions and complex technical inquiries. </span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Cross-functional collaboration</span></span><span> </span></p></div><div><ul><li><p><span><span>Proactively collaborates with other field teams to ensure the best Customer Experience (</span><span>Cx</span><span>) for HCPs. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Gathers and shares relevant insights and information internally with the<span> </span></span><span>appropriate stakeholders</span><span><span> </span>to enable BMS to better serve its customers.</span></span><span> </span></p></li></ul></div></div><div><div><p><span> </span></p></div><div><p><span><span>Complies with</span><span><span> </span>all laws, regulations, and policies that govern the conduct of BMS.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><u><span>Required Qualifications &amp; Experience</span></u><span> </span></p></div><div><ul><li><p><span><span>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated experience building and<span> </span></span><span>maintaining</span><span><span> </span>strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (</span><span>Cx</span><span>).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in cardiovascular preferred.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance<span> </span></span><span>track record</span><span><span> </span>of meeting or exceeding goals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong selling and promotional skills proven through<span> </span></span><span>a<span> </span></span><span>track record</span><span><span> </span>of performance.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><u><span>Key competencies desired</span></u><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Customer/commercial mindset</span></span><span> </span></p></div><div><ul><li><p><span><span>Demonstrated ability to drive business results.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience<span> </span></span><span>identifying</span><span>, engaging, and cultivating credibility with customers across the patient care journey.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated resourcefulness and ability to connect with customers.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div></div><div><div><p><span><span>Patient centricity </span></span><span> </span></p></div><div><ul><li><p><span><span>Understands the<span> </span></span><span>patient</span><span><span> </span>journey and experience.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a patient-focused mindset.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Scientific Agility </span></span><span> </span></p></div><div><ul><li><p><span><span>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Analytical Capability:</span></span><span> </span></p></div><div><ul><li><p><span><span>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understanding how to interpret and analyze data related to BMS products, customer preferences</span><span>, clinical</span><span><span> </span>data.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use CE^3 to generate insights<span> </span></span><span>and do</span><span><span> </span>dynamic call planning.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>Digital Agility:</span></span><span> </span></p></div><div><ul><li><p><span><span>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and<span> </span></span><span>maintain</span><span><span> </span>effective communication.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in<span> </span></span><span>a timely</span><span><span> </span>and compliant manner, track interactions, and plan future engagements with healthcare professionals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to use the Medical on Call technology effectively.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Keeping up to date with technological advancements and changes.</span></span><span> </span></p></li></ul></div></div><div><div><p><span> </span></p></div><div><p><span><span>Teamwork/Enterprise mindset</span></span><span> </span></p></div><div><ul><li><p><span><span>Strong business acumen to understand and analyze business, market drivers, and develop, execute, and adjust business plans.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrates<span> </span></span><span>a strong sense</span><span><span> </span>of learning agility. Seeks out and learns from unfamiliar<span> </span></span><span>experiences, and</span><span><span> </span>then applies those lessons to achieve better results in<span> </span></span><span>subsequent</span><span><span> </span>situations.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Track record</span><span><span> </span>of balancing individual drive and collaborative attitude.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Holds<span> </span></span><span>a high level</span><span><span> </span>of integrity and good judgment to navigate the<span> </span></span><span>role&#39;s</span><span><span> </span>requirements effectively and compliantly<span> </span></span><span>in accordance with</span><span><span> </span>BMS policies and procedures.</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><span><span>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company.</span></span><span> </span></p></div></div><p></p><p></p><p></p></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $134,390 - $162,843&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602422 : Senior Therapeutic Area Specialist, Cardiovascular Specialty - Lexington, KY]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-cardiovascular-specialty-lexington-ky-bristol-myers-squibb/6a05f7092f1861929d2531e5</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-cardiovascular-specialty-lexington-ky-bristol-myers-squibb/6a05f7092f1861929d2531e5</guid><pubDate>Thu, 14 May 2026 16:23:37 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Field - United States - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Director, Enterprise Employer Access - Cell Therapy]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b> SUMMARY:</b><br />The Director, Enterprise Employer Access - Cell Therapy is responsible for establishing early, upstream engagement across the employer benefit decision landscape to influence benefit design decisions for CAR-T and future cell and gene therapies both directly with employers and indirectly through the consultants, TPAs, and specialty vendors that shape those decisions, before carve-outs, COE mandates, or restrictive site-of-care requirements are finalized.</p><p></p><p>This role addresses a critical access gap created by the shift of benefit decision-making authority from payers to employers by proactively engaging the stakeholders who define benefit philosophy upstream. The objective is to protect patient access, preserve provider flexibility, and support long-term enterprise value before coverage parameters are locked in.</p><p></p><p>As employers increasingly serve as the ultimate decision-makers for high-cost therapies, often delegating execution to intermediaries, downstream payer influence becomes limited or nonexistent once benefit design decisions are finalized. This role ensures the organization is present where and when influence is exerted, shaping benefit strategy early rather than relying on reactive, exception-based access remediation later.<b> </b></p><p></p><p><b>RESPONSIBILITIES:</b></p><p></p><h3><b>Employer &amp; Benefit-Decision Influencer Engagement:</b></h3><ul><li><p>Lead upstream engagement with the decision networks that shape employer coverage and utilization decisions for cell and gene therapies, including:</p><ul><li><p>Large self-insured employers (where direct engagement is feasible)</p></li><li><p>National and regional benefits consultants</p></li><li><p>Third-party administrators (TPAs)</p></li><li><p>Specialty benefit managers and cell carve-out vendors</p></li><li><p>Employer-facing clinical, navigation, and care management partners</p></li></ul></li><li><p>Build and manage a prioritized portfolio of employer decision networks, recognizing that:</p><ul><li><p>Employers often delegate benefit authority to consultants or vendors</p></li><li><p>Direct employer access may be limited, episodic, or mediated</p></li><li><p>Influence is frequently exerted through trusted advisors rather than employers themselves</p></li></ul></li><li><p>Establish sustained educational relationships with key decision influencers within each network, focused on:</p><ul><li><p>Benefit design philosophy for high-cost, high-impact therapies</p></li><li><p>Total cost of care and episode-of-care economics</p></li><li><p>Workforce productivity, disability avoidance, and long-term value—not drug acquisition cost alone</p></li></ul></li><li><p>Engage stakeholders ahead of annual benefit cycles to inform:</p><ul><li><p>Cell therapy drug carve-out strategies</p></li><li><p>COE and site-of-care frameworks</p></li><li><p>Utilization management approaches for cell and gene therapies</p></li></ul></li><li><p>Tailor messaging based on stakeholder role, ensuring relevance to:</p><ul><li><p>HR and benefits leaders</p></li><li><p>Finance and CFO-aligned decision-makers</p></li><li><p>Consultant-led benefit committees and advisory councils</p></li></ul></li><li><p>Position the organization as a credible, non-promotional thought partner in employer benefit strategy, filling the upstream education gap that otherwise defaults to cost-only narratives.</p></li></ul><p></p><h3><b>Benefit Design Influence:</b></h3><ul><li><p>Engage employers prior to annual benefit design finalization</p></li><li><p>Influence employer philosophy related to:</p><ul><li><p>Cell therapy drug carve-outs</p></li><li><p>COE requirements</p></li><li><p>Site-of-care restrictions</p></li></ul></li><li><p>Help prevent access barriers that cannot be mitigated once embedded in benefit design</p></li></ul><h3><b> </b></h3><h3><b>Key Stakeholders and Call Points:</b></h3><ul><li><p>Coordinate closely with:</p><ul><li><p>Payer and regional market access teams</p></li><li><p>Provider and community oncology partnerships</p></li><li><p>Employer consultants, TPAs, and specialty vendors (as appropriate)</p></li></ul></li><li><p>Support aligned employer-provider discussions where relevant (e.g., site-of-care strategy, community access)</p></li></ul><h3></h3><p></p><h3><b>Market Intelligence &amp; Feedback Loop:</b></h3><ul><li><p>Capture and synthesize employer insights to inform:</p><ul><li><p>Market access strategy</p></li><li><p>Contracting and value frameworks</p></li><li><p>Policy and advocacy priorities</p></li></ul></li><li><p>Identify emerging trends in employer carve-outs, vendor models, and utilization controls</p></li></ul><h3></h3><p></p><h3><b>Measurement &amp; Impact Tracking:</b></h3><ul><li><p>Track leading indicators of success, including:</p><ul><li><p>Avoided or modified carve-outs</p></li><li><p>Improved alignment on site of care</p></li><li><p>Earlier employer engagement relative to benefit cycles</p></li></ul></li><li><p>Partner with leadership to assess impact and inform future scaling decisions</p></li></ul><p></p><p><br /><b>Scope &amp; Coverage:</b></p><ul><li><p>Regional alignment: East or West</p></li><li><p>Employer coverage: 30–40 priority employers per role</p></li><li><p>National coordination<b>:</b> Collaborates across regions to ensure consistent strategy and messaging</p></li></ul><h2></h2><p></p><h2><b>QUALIFICATIONS:</b></h2><p></p><h3><b>Required:</b></h3><ul><li><p>Bachelor’s degree in a relevant field; advanced degree preferred</p></li><li><p>10&#43; years of experience in Market Access, Employer Benefits, Payer Strategy, or related roles</p></li><li><p>Deep understanding of:</p><ul><li><p>Self-insured employer benefit design</p></li><li><p>Specialty drug economics and medical benefit dynamics</p></li><li><p>Payer vs employer decision authority</p></li></ul></li><li><p>Proven ability to engage senior, non-clinical stakeholders (HR, Finance, Benefits)</p></li><li><p>Experience with complex, high-cost therapies preferred (oncology, specialty, rare disease, cell/gene therapy)</p></li></ul><h3></h3><p></p><h3><b>Preferred:</b></h3><ul><li><p>Experience working with:</p><ul><li><p>Employer consultants or TPAs</p></li><li><p>Episode-of-care or total cost of care frameworks</p></li></ul></li><li><p>Strong executive presence and ability to translate clinical value into business impact</p></li><li><p>Comfort operating in white-space roles with high strategic visibility</p></li></ul><p></p><h2></h2><h2><b>Work Location &amp; Travel Requirements:</b></h2><ul><li><p>This position is fully remote within the United States, with flexibility to work from a home-based office.</p></li><li><p>Expected travel is approximately 50%, primarily to support:</p><ul><li><p>In-person meetings with employer benefit decision influencers (e.g., consultants, TPAs, specialty vendors)</p></li><li><p>Select employer and provider partner engagements</p></li><li><p>Internal planning sessions, leadership meetings, and key industry conferences</p></li></ul></li><li><p>Travel requirements may vary seasonally and align with employer benefit design cycles and strategic priorities</p></li></ul><p></p><p></p><p>#LI-Field</p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $196,390 - $237,982&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602372 : Director, Enterprise Employer Access - Cell Therapy]]></description><link>http://biotechroles.com/director-enterprise-employer-access-cell-therapy-bristol-myers-squibb/6a05f7092f1861929d2531e4</link><guid isPermaLink="true">http://biotechroles.com/director-enterprise-employer-access-cell-therapy-bristol-myers-squibb/6a05f7092f1861929d2531e4</guid><pubDate>Thu, 14 May 2026 16:23:37 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Field - United States</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Cardiovascular Accounts & Customer Engagement - Chicago, IL]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p></p><p>The Associate Director, CV Accounts &amp; Customer Engagement, reports to the Director, CV Accounts &amp; Customer Engagement and will work cross-functionally with matrix teams, both in the field and at the home office, to ensure tactical execution aligns with the overall brand strategy. By collaborating with teams focused on reimbursement, REMS, access, brand, and field operations, the Associate Director will support business goals and drive the effective implementation of strategic initiatives to achieve organizational objectives.</p><p></p><p><b><u>KEY RESPONSIBILITIES</u></b></p><p></p><p><b>Key Account Management</b> </p><ul><li><p>Deliver all access, value, PHM, quality, and unbranded messages and tools with population health decision makers or C-suite individuals. </p></li></ul><ul><li><p>Support safe and appropriate use of BMS CV products through education on treatment protocols, order sets and other clinical management tools with formulary committee members.</p></li></ul><ul><li><p>Support onboarding and ongoing management to LDN operations at SPs to support REMS and access. </p></li></ul><ul><li><p>Education around EHRs through approved resources and referral to the HIT specialist </p></li></ul><ul><li><p>Collaborate cross-functionally with Sales, Medical, Marketing, Market Access, Patient Services, BI&amp;A, and other matrix teams to support strategic initiatives. </p></li></ul><p></p><p><b>KOL Strategic Development</b> </p><ul><li><p>Establish BMS as a credible and trusted partner amongst the thought leaders in Cardiology. </p></li></ul><ul><li><p>Support the brand’s commercial efforts at conferences (National and Regional Level) </p></li></ul><ul><li><p>Support content development of Speaker Programs and training of Speakers. </p></li></ul><ul><li><p>Gather local and national insights to inform brand strategy through KOL engagement.</p></li></ul><ul><li><p>Support advisory boards by providing input on content development (e.g., discussion guides) for non-access related advisory boards.</p></li></ul><ul><li><p>Develop regional/local expertise in HCM care pathways and identify key opinion leaders. </p></li></ul><p>  </p><p><b>Compliance &amp; Operational Excellence</b> </p><ul><li><p>Ensure all activities are conducted in full compliance with applicable laws, regulations, and BMS policies. </p></li></ul><ul><li><p>Uphold high ethical standards while driving business success and fostering a customer-centric approach. </p></li></ul><p></p><p><b>Qualifications &amp; Experience</b> </p><ul><li><p>Field Based Role. Minimum 5 years of experience in marketing, access, account management, business development, or sales leadership within the pharmaceutical or healthcare industry. Cardiovascular experience strongly preferred. </p></li></ul><ul><li><p>Must possess a bachelor&#39;s degree; an advanced degree is strongly preferred. </p></li></ul><ul><li><p>Deep understanding of the U.S. healthcare system, including hospitals and acute care, integrated delivery networks (IDNs), limited distribution networks (LDNs), organizer provider networks, and payer dynamics </p></li></ul><ul><li><p>Experience with hospital payment models and metrics, formulary access and reimbursement dynamics, pathways and protocol development, EMR/EHR systems, pharmacy planning and operations strongly preferred. </p></li></ul><ul><li><p>Track record of driving revenue growth and / or achieving field execution targets in the pharmaceutical industry and consistently exceeding expectations </p></li></ul><ul><li><p>Strong strategic thinking skills with the ability to structure complex challenges and translate them into actionable plans. </p></li></ul><ul><li><p>Strong ability to interface with stakeholders both internally and externally. </p></li></ul><ul><li><p>Excellent communication skills, both written and oral </p></li></ul><ul><li><p>Experience in the pharmaceutical or healthcare industry with a strong focus on hospital-based sales and market access </p></li></ul><p></p><p></p><p></p><p></p><p></p></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $166,350 - $201,571&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602412 : Associate Director, Cardiovascular Accounts &amp; Customer Engagement - Chicago, IL]]></description><link>http://biotechroles.com/associate-director-cardiovascular-accounts-and-customer-engagement-chicago-il-bristol-myers-squibb/6a05f7082f1861929d2531e3</link><guid isPermaLink="true">http://biotechroles.com/associate-director-cardiovascular-accounts-and-customer-engagement-chicago-il-bristol-myers-squibb/6a05f7082f1861929d2531e3</guid><pubDate>Thu, 14 May 2026 16:23:36 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Field - United States - US</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Executive Assistant, Deven's Cell Therapy]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>At <b>Bristol Myers Squibb</b> we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.</p><p></p><p>The primary focus of the <b>Executive Assistant, Deven&#39;s Cell Therapy</b> role will be to provide administrative and executive support at the BMS Cell Therapy Facility in Devens, MA and to assist with all aspects of daily administrative management at a detailed level.</p><p></p><p>The Executive Assistant will be proficient in all aspects of corporate administration, executive calendar, email, and conference room management, arrange travel itineraries and process expense reports, PowerPoint preparation, meeting and event coordination. This role will also process, track, reconcile, update invoices for office and misc. supplies.</p><p></p><p>Critical to this role are exceptional interpersonal, communication and time management skills. The successful candidate has a sense of humor, works autonomously, welcomes and accepts direction and thrives in a fast paced, occasionally ambiguous startup environment. This person will take ownership over their area of responsibility while noticing and supporting other opportunities for growth.</p><p></p><p><b>Shifts Available:</b></p><p>M – F, Standard Working Hours</p><p></p><p><b>Responsibilities will include, but are not limited to the following:</b></p><ul><li><span>Assist with all aspects of daily management at a detailed level for your own charges, as well as assisting with basic administration. Partner with the larger organization and other administrative personnel to provide the highest level of support for the Devens Cell Therapy Facility.</span></li><li><span>Adapt and adjust to a rapidly changing environment where priorities shift daily. Complete a broad variety of administrative tasks including managing extremely active calendars; expense reports; correspondence; arranging detailed travel plans and expense reports, itineraries, and agendas.</span></li><li><span>Ensure a high standard of service and confidentiality is maintained and enhanced. Provide a bridge for smooth communication between departments and functions. Develop cross-functional professional alliances.</span></li><li><span>Prioritize conflicting needs; handle matters expeditiously and proactively. Follow-through on projects to successful completion, often with deadline pressures. Ability to discern between urgent and important, and to ask for help when needed.</span></li><li><span>Attend staff and department meetings and assist in administrative management of these meetings as required; this includes arranging and establishing video conference connections, support in preparing agendas, and generation of meeting summaries as required.</span></li><li><span>Disclaimer: This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.</span></li></ul><p></p><p><b><span>Minimum Requirements:</span></b></p><ul><li><span>Diploma or Degree in Business Administration or equivalent qualifications</span></li><li><span>10&#43; years Administrative experience with progressive responsibilities. 3&#43; yrs supporting VP level or above preferred</span></li><li><span>Experience in providing support and assistance at corporate level at large or fast paced growing organizations.</span></li><li><span>Demonstrated relevant experience with Microsoft Office, an Outlook “Ninja” and a general understanding of IT technology including SharePoint.</span></li><li><span>Excellent organizational, record keeping and communication skills (oral and written).</span></li><li><span>A strong work ethic to generate high quality work under tight deadlines.</span></li><li><span>Must have a can-do attitude, be resourceful, and have an approachable demeanor.</span></li><li><span>Ability to anticipate and be proactive is critical.</span></li><li><span>Experience working within the fields of biotechnology, life science or project management sectors preferred.</span></li></ul><p></p><p><b>BMSCART</b></p><p><b>#LI-ONSITE</b></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Devens - MA - US: $82,090 - $99,477&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602330 : Executive Assistant, Deven's Cell Therapy]]></description><link>http://biotechroles.com/executive-assistant-devens-cell-therapy-bristol-myers-squibb/6a05f7082f1861929d2531e2</link><guid isPermaLink="true">http://biotechroles.com/executive-assistant-devens-cell-therapy-bristol-myers-squibb/6a05f7082f1861929d2531e2</guid><pubDate>Thu, 14 May 2026 16:23:36 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Devens - MA - US</location><salary>$70000-95000</salary><type>Full time</type></item><item><title><![CDATA[Senior District Sales Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><h1>主要职责 (岗位相关):</h1><ul><li>充分了解公司战略并能运用到工作中</li><li>分配年度、季度、月度的资源和活动(人员/预算/活动)</li><li>管理和辅导销售代表实现共同目标</li><li>符合BMS 生物制药行为和合规政策方面的所有要求</li><li>通过不同的沟通工具, 建立和维护与医生和KOL的持续的联系和沟通.</li><li>提供卓越的客户服务&#xff0c;建立稳固的、长期的客户关系&#xff0c;以快速和专业的态度平衡多方需求</li><li>深入收集客户信息&#xff0c;充分理解客户需求特别是在疾病管理方面的需求。和经理分享信息并寻求有效的方式去处理客户的反馈。</li><li>分析客户类型和业务机会&#xff0c;并把这些信息转化为业务计划</li><li>密切跟踪/了解竞争对手的市场活动&#xff0c;和经理、团队分享自己创新的想法&#xff0c;从而获得竞争优势。</li><li>和不同部门维护好牢固的工作关系&#xff0c;特别是在专业领域的疾病教育方面&#xff0c;如市场部、医学和注册部、市场准入部、商务部、企业事务部, 免疫肿瘤战略合作部等&#xff0c;获得在本地区决策和执行上的支持&#xff0c;驱动业务绩效。</li><li>管理和监控好关键的活动 – IHM(作为现场观察员覆盖50%)/RTM(作为现场观察员覆盖80%), 管理和监控好医院相关项目</li><li>展示出快速理解和学习科学信息的能力&#xff0c;不断自学公开发布的科学文献&#xff0c;参加相关的专题讨论会和学术会议。</li><li>在多样化的情境中清晰地、逻辑性地、简洁地沟通&#xff0c;包括1&#xff1a;1会谈&#xff0c;正式小组简报和书面沟通中</li><li>通过成熟的沟通技巧和专业能力赢得KOL的信任</li></ul><p></p><p></p><p>岗位要求</p><p></p><p>具备医药&#xff0c;生命科学相关本科以上学历 熟悉当地及周边地区医院的推广工作 4-5 年销售经验 至少2-3 年带团队经验 有肿瘤经验者优先考虑 具备良好的人际沟通技巧&#xff0c;团队合作精神&#xff0c;能独立分析解决问题并在压力下工作。</p><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601108 : Senior District Sales Manager]]></description><link>http://biotechroles.com/senior-district-sales-manager-bristol-myers-squibb/6a05f7072f1861929d2531e1</link><guid isPermaLink="true">http://biotechroles.com/senior-district-sales-manager-bristol-myers-squibb/6a05f7072f1861929d2531e1</guid><pubDate>Thu, 14 May 2026 16:23:35 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Chengdu</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Principal Solution Engineer]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><u><b>Position Summary:</b></u></p><p>At BMS, digital innovation and Information Technology are central to our vision of transforming patients’ lives through science. To accelerate our ability to serve patients around the world, we must unleash the power of technology.  We are committed to being at the forefront of transforming the way medicine is made and delivered by harnessing the power of computer and data science, artificial intelligence, and other technologies to promote scientific discovery, faster decision making, and enhanced patient care.   </p><p>If you want an exciting and rewarding career that is meaningful, consider joining our diverse team!</p><p></p><p>As a Principal Solution Engineer for Business Insights &amp; Technology (BI&amp;T) based out of our BMS Hyderabad you are part of the Research and Development BI&amp;T team that delivers platform, data and intelligent insights driven analytics capabilities for Trial Optimization and Clinical Modeling (TOCM) and Document Automation Product lines.</p><p></p><p>The incumbent plays a pivotal techno‑functional role within R&amp;D BI&amp;T, driving the design, analysis, and delivery of digital, data, and AI‑enabled solutions that accelerate clinical development. This role bridges business strategy and technology execution—partnering deeply with Global Clinical Operations, GBDS, Regulatory, Patient Safety, Portfolio Operations, and other stakeholders to transform protocol design, trial execution, and decision‑making. The incumbent will define solution requirements, assess business needs, translate them into functional/technical specifications, support engineering teams, and ensure scalable, compliant, and high‑quality products.</p><p>This role requires expertise in clinical development workflows, data and analytics platforms, AI/ML‑supported decision tools, and strong cross‑functional leadership.</p><p>This role is core to BMS’ vision of transforming the way clinical trials are designed through data and technology translating into robust, scalable, AI enabled digital solutions—directly accelerating the speed, quality, and success of bringing medicines to patients.</p><p></p><p><u><b>Key Responsibilities</b></u></p><ul><li><p>Accountable for leading and delivering high quality solutions for capabilities such as Trial Design and Optimization, Trial Operations and Trial Acceleration, Trial Success prediction and Document Automation.</p></li><li><p>Lead the end-to-end business analysis process partnering with R&amp;D stakeholders to understand scientific, clinical, and operational needs — current state assessment, gap analysis, future state solution design, and requirement elicitation; and translate them into high‑value digital and analytical capabilities.</p></li><li><p>Define functional requirements, design requirements, data requirements, system interactions, and business process flows to support Trial Design, Optimization, Operations, and Success Prediction capabilities.</p></li><li><p>Provide techno-functional leadership for solution discovery, prototyping, and feasibility assessments across AI/ML, analytics, and workflow automation.</p></li><li><p>Translate business requirements into detailed solution specifications consumable by engineering, data, and platform teams.</p></li><li><p>Work closely with Product Managers, Solution Architects, Platform Engineers, Data Engineers, and UX designers to develop scalable design options.</p></li><li><p>Ensure alignment to R&amp;D BI&amp;T architectural standards, patterns, integration guidelines, and enterprise data governance.</p></li><li><p>Support development, testing, validation, and release management activities; ensure that solutions meet quality, security, and compliance standards.</p></li><li><p>Collaborate with engineering teams to ensure proper integration of ML models, LLMs, and data pipelines into production systems.</p></li><li><p>Drive continuous improvement in requirements of quality, solution documentation, and delivery processes.</p></li><li><p>Monitor solution performance, user adoption, production issues, and enhancements, collaborating with engineering and operations teams for issue resolution.</p></li><li><p>Up to date on evolving trends in Clinical Trial Design and Acceleration (i.e. application of AI/ ML and GenAI towards accelerating clinical trial execution)</p></li><li><p>Has End to End ownership mindset in driving initiatives through completion</p></li><li><p>Comfortable working in a fast-paced environment with minimal oversight</p></li><li><p>Mentors other team members effectively to unlock full potential</p></li><li><p>Prior experience working in an Agile/Product based environment</p></li><li><p>Stays current with emerging trends. Identifies future state and dimensions of change (org, tech, cultural) to deliver outcomes.</p></li></ul><p></p><p><u><b>Qualifications &amp; Experience</b></u></p><ul><li><p>10&#43; years of experience in solution analysis, business analysis, or techno-functional roles within data/analytics or digital product teams.</p></li><li><p>8&#43; years of demonstrable experience in pharmaceutical industry with proven expertise in data acquisition, clinical trial execution, and analysis reporting on a global scale.</p></li><li><p>Bachelor&#39;s degree in computer science, Information Technology, Life Sciences, or related fields. Advanced degree preferred.</p></li><li><p>Experience with clinical development systems, data standards, GCP, and regulatory frameworks.</p></li><li><p>Hands-on exposure to AI/ML enabled solutions, data engineering pipelines, cloud platforms (AWS/Azure), and modern software architectures.</p></li><li><p>Strong knowledge of SDLC, Agile, DevOps, and product-based delivery methodologies.</p></li><li><p>Understanding data modeling, SQL/NoSQL databases, APIs, cloud services (AWS/GCP/Azure).</p></li><li><p>Familiarity with ML model lifecycle, MLOps processes, and analytical toolsets.</p></li><li><p>Ability to translate complex technical concepts into business-friendly language and vice versa.</p></li><li><p>Proven track record of delivering complex software products in Agile environments.</p></li><li><p>Exhibit influential leadership and communication capabilities with a proven ability to engage, develop and inspire a diverse geographical team.</p></li><li><p>Expertise in defining product vision, market positioning, and competitive strategy.</p></li><li><p>Strong communication, stakeholder management, and negotiation skills.</p></li><li><p>Demonstrated ability to work in global, matrixed environments and influence business partners.</p></li><li><p>Experience with vendor coordination, service delivery oversight, and outcome driven execution.</p></li></ul><p></p><p><b>Why You Should Apply</b></p><p>Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of our colleagues.</p><p>Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.</p><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1599316 : Senior Manager, Principal Solution Engineer]]></description><link>http://biotechroles.com/senior-manager-principal-solution-engineer-bristol-myers-squibb/6a05f7072f1861929d2531e0</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-principal-solution-engineer-bristol-myers-squibb/6a05f7072f1861929d2531e0</guid><pubDate>Thu, 14 May 2026 16:23:35 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Hyderabad - TS - IN</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Manager, Submission Management Clinical Trials]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p>The  Senior Specialist, Submission Management Clinical Trials supports end-to-end regulatory activities for assigned projects, including executing the preparation and compilation of compliant clinical trial maintenance submissions for global health authorities.</p><p><br /><b>Position Responsibilities</b></p><p><b><span>Regulatory (CTA) Management</span></b></p><ul><li><span>Collaborate with stakeholders to define clinical trial submission strategies and document requirements, ensuring alignment with regulatory standards and project timelines. </span></li><li><span>Assess core submission deliverables to ensure compliance, prepare and distribute global CTA dossiers, and manage data required for EU CTIS and substantial modifications.<b> </b></span></li><li><span>Monitor and influence the regulatory assessment process, drive negotiations with stakeholders to resolve information requests, and communicate regulatory changes to ensure ongoing compliance. </span></li><li><span>Manage and track queries, commitments, and submissions with health authorities, collaborate with subject matter experts for responses, and provide periodic status updates on commitments.</span></li><li><span>Prepare and distribute the global Clinical Trial Application dossier to country applicants and CROs for submission to ECs and HAs. </span></li><li><span>Prepare the data required in CTIS for CTA dossiers and their subsequent substantial modifications. </span></li><li><span>Execute required activities in RIM systems (Veeva RIM) and use available tools to generate reports and track submission content. </span></li></ul><p></p><p><b><span>Continuous Improvement Initiatives</span></b></p><ul><li><span><span>·</span></span><span>Support initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams. </span></li><li><span>Contribute to the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information. </span></li><li><span>Ensure consistency of Clinical Trial Applications across projects, studies, and countries, aligning with regulatory standards and best practices. </span></li></ul><p><br /><b>Degree Requirements</b><br /><span>BA/BS degree, science / technology field preferred</span></p><p><br /><b>Experience Requirements</b></p><ul><li><span>3&#43; years relevant regulatory submission experience</span></li><li>Foundational knowledge of global regulatory practices, submission guidelines, and requirements</li><li>Strong critical thinking and problem-solving skills; proposes alternative solutions for submission-related and project situations</li><li>Effective stakeholder engagement and communication, including proficiency in English (written and oral) and ability to communicate with non-English speakers</li><li>Ability to execute and prioritize non-complex projects with attention to detail; communicates project status and updates to relevant stakeholders</li><li>Demonstrates basic presentation skills and adapts content for diverse audiences</li><li>Proficiency with desktop software and regulatory systems with the ability to instruct others; understand how non-regulatory systems interact with regulatory systems.  Embrace the use of artificial intelligence and automation tools.</li></ul><div></div><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Warsaw - PL: zł174,980 - zł212,026&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601868 : Manager, Submission Management Clinical Trials]]></description><link>http://biotechroles.com/manager-submission-management-clinical-trials-bristol-myers-squibb/6a05f7062f1861929d2531df</link><guid isPermaLink="true">http://biotechroles.com/manager-submission-management-clinical-trials-bristol-myers-squibb/6a05f7062f1861929d2531df</guid><pubDate>Thu, 14 May 2026 16:23:34 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Warsaw - PL</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Clinical Data Management]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary</b></p><p></p><p>The Associate Director, Clinical Data Management is a leadership role considered essential to the sustainability and success of the BMS R&amp;D pipeline. </p><p></p><p><b>Position Responsibilities </b></p><h3>(include, but are not limited to)</h3><p></p><p><b><u>Program Management</u></b></p><ul><li>Act as a Program Lead to provide oversight of a program within the organization providing oversight to a group of studies and Data Management Leads ensuring that the studies within the program are delivered per corporate goals and objectives</li><li>Establish a governance framework for a program or asset to ensure monitoring of risks and mitigation strategies across different studies within the program</li><li>Developing strong and productive working relationships with cross functional stakeholders responsible to provide strategic support to project team</li><li>Responsible for attending program level strategic meetings</li><li>May act as a driver to set program level data collection and review standards with cross functional team in partnership with global standards</li></ul><p></p><p><b><u>Line Management</u></b></p><ul><li>Line management responsibility of Data Management Leads based on business requirements</li><li>Manages the resource assignments ensuring appropriate support is in place to provide data quality oversight for clinical trials</li><li>Forecast’s future resource needs based on the book of work and initiatives; proposing solutions to meet potential resource constraints</li><li>Assigns resources to initiatives in line with their development plans and providing appropriate guidance to staff to influence results and drive to completion</li><li>Works proactively with staff to understand individual strengths, opportunities, and career goals; supporting development of plans that capitalize on strengths and address opportunities; providing regular feedback to promote development.</li><li>Effectively coaches and mentors’ staff, seeking out training opportunities where needed, to develop the next generation leaders. </li><li>Develops and promotes a workplace culture that values diversity of thought, promotes integrity, creates accountability, supports effective decision making, and provides opportunities to grow.</li></ul><p></p><p><b><u>Project Management and Leadership</u></b></p><ul><li>Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects</li><li>Provides clinical data management leadership within the study team to align on and drive data collection requirements for one or more complex clinical development projects</li><li>Responsible for end-to-end clinical data management activities and may serves as a primary point of contact for internal and external study team members</li><li>Provides strong quality and project oversight over third party vendor responsible for data management deliverables</li><li>Takes a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (eCOA, External Data, Safety Gateway). Enforces data standard conventions and quality expectations for clinical data per defined processes</li><li>May author, review/revise DM related study plans including Data Quality Management Plan, Data Validation Plans, Data Review Plan, eCRF Completion Guidelines and other study documents to ensure quality and standardization</li><li>Participate in Data Quality Review meetings with cross functional study team members to ensure on-going review of trial data currency, quality and completeness</li><li>Represents DM on cross-functional project teams, portfolio review meetings &amp; Submission Teams</li><li>Lead or support the Health Authority inspections and audits</li></ul><p></p><p><b><u>FSP/CRO/Vendor Oversight</u></b></p><ul><li>May act as core member of the study team and provides FSP/CRO/Vendor oversight for end-to-end Data Management activities, manages data currency throughout the trial, and overall monitoring DM deliverables according to the Service Level Agreement (SLA)</li></ul><p></p><p><b><u>Continuous improvement initiatives </u></b></p><ul><li>Supports change management initiatives with broad impact as a lead or participant in initiatives, and/or authors (or participates in) functional SOPs/WP/GD</li><li>Utilizes knowledge of data management processes to evaluate and recommend new technologies and systems for improved data management functionality</li><li>May mentor new or existing team members, as applicable</li><li>Lead CAPA management activities and ensure timely closure of CAPA action items</li><li>Holds accountability to resolve complex issues and proactively develop solutions, within the function and across functions. Leveraging technical/functional expertise to develop solutions.  Using clear communications and collaborative strategies to drive to resolution</li><li>Authors procedural documents (SOPs, work instructions, job aids) and coordinating reviews/approvals.  Ensuring procedural documents are reflective of industry standards and regulatory requirements, include optimal processes and are regularly maintained. </li></ul><p></p><p><b>Key Requirements</b></p><p></p><p><b>Degree</b></p><p>Bachelor’s Degree required with an advanced degree preferred.</p><p></p><p><b>Experience</b></p><ul><li>At least 7 years of relevant industry experience.</li><li>Project management certification (e.g. PMP) is desirable.</li><li>Experience in managing late phase studies and portfolio for Data Management is highly preferred</li></ul><p></p><p><b>Key Competency Requirements</b></p><ul><li>Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors</li><li>Sound knowledge of Clinical Drug Development Process, regulatory and ICH guidelines (e.g. EMEA, FDA) and industry standard practices regarding data management</li><li>Strong knowledge and experience of EDC systems (Medidata RAVE preferred); demonstrated knowledge of Microsoft Office skills and well versed in industry trends and emerging technologies supporting data collection</li><li>Strong project management; Exhibits expertise in metrics analysis and reporting methodologies</li><li>Excellent oral and written communication skills</li><li>Communicate effectively with senior management and cross-functional teams</li><li>Solid knowledge of submission requirements, [e.g. New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA)]</li><li>Solution oriented mindset and ability to drive change</li></ul><p></p><p><span>#LI-Hybrid</span></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Warsaw - PL: zł325,830 - zł394,830&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1601827 : Associate Director, Clinical Data Management]]></description><link>http://biotechroles.com/associate-director-clinical-data-management-bristol-myers-squibb/6a05f7042f1861929d2531de</link><guid isPermaLink="true">http://biotechroles.com/associate-director-clinical-data-management-bristol-myers-squibb/6a05f7042f1861929d2531de</guid><pubDate>Thu, 14 May 2026 16:23:32 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Warsaw - PL</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Learning Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Primary responsibilities:</b></p><ul><li>To develop strategic learning plans for respective business units or brand field force.</li><li>Deliver and/or support all training initiatives for commercial sales teams; to include disease state, clinical, competitor &amp; product knowledge, product launches, selling skills, coaching &amp; functional skills and capability building.</li><li>Partner with stakeholders at all levels to ensure business priorities are achieved and align learning solutions where appropriate.</li><li>Establish a robust model for how learning supports the functional skills and capability development for the field roles (including first line managers) across our commercialisation model (initial and advanced training curricula).</li><li>Identify, recommend, and execute learning programs that leverage resources from the WW Commercialisation Learning Centre of Excellence (COE) to evolve training strategies to deliver integrated training curriculums with minimal adaptation.</li><li>Share learnings with colleagues and with the COE to drive efficiencies and innovation.</li><li>Act as a strategic business partner to advise and provide input on the strategic direction of the Commercial Training strategy to organise and deliver innovative and flexible training solutions (curriculum &amp; pathways) that drive an evolving and agile business centric organisation.</li><li>Develop &amp; design innovative learning solutions, to include disease state, clinical, product <span>knowledge,</span> selling skills &amp; capability upskilling, that demonstrate value and leverage technology, platforms and processes to meet the needs of the business and the learner.</li><li>Develop, update and execute the learning strategy for First- and Second-Line Sales leaders for the region.</li><li>Assess and analyse the effectiveness training programs and initiatives utilizing Kirkpatrick Model </li><li>Continuously seek to identify and leverage state-of-the-art adult learning methodologies that can accelerate skill and knowledge development of field teams.</li><li>Project manage key WW Commercialisation Learning initiatives at the brand or market level and collaborate with Learning Managers across brands.</li></ul><p></p><p>(Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned)</p><p></p><p><b>Qualifications:</b></p><ul><li><span>Bachelor’s degree or equivalent required;</span> Advanced degree preferred: MBA, PharmD, or other graduate experience; Proficient English skills in both speaking and writing</li></ul><ul><li>3&#43; years healthcare industry experience, including professional work experience in commercial learning development and execution.</li><li>Must have experience in developing and executing learning strategies, sales/marketing experience in Hematology is an advantage.</li><li>Intermediate knowledge of adult learning principles, good at learning design and familiar with widely adopted methodology and framework in training sales, marketing, management, coaching and leadership</li><li>Strong analytical skills and experience using and presenting data to make decisions; including learning evaluations and people analytics</li><li>Effective facilitation and presentation skills, excellent MS office skills including ppt, excel,etc</li><li>Strong communication, organisational and interpersonal skills, and proven project management experience</li></ul><p></p><ul><li>Influential individual contributor with credibility and track record of establishing strong collaboration across matrix organisations, including senior leadership, to prioritize business objectives and drive actions to meet business requirements.</li></ul><ul><li>Ability to prioritize, manage and execute on multiple projects simultaneously.</li><li>Diligent attention to detail, accuracy, timeliness, and follow-up</li><li><span>Curiosity &amp; innovative thinking to generate new ideas and approaches to respond to the evolving environment.</span></li></ul><ul><li>Experience in partnering and collaborating with external vendors/agencies. </li><li>Ability to travel less than 20% of time.</li><li>This position will be based in Shanghai</li></ul><p style="text-align:inherit"></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span class="WIN0">accommodations/adjustments</span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span class="WIN0">accommodation/adjustment</span></span> prior to accepting a job offer. If you require reasonable <span><span class="WIN0">accommodations/adjustments</span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span class="WIN0">https://careers.bms.com/fraud-protection</span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602445 : Learning Manager]]></description><link>http://biotechroles.com/learning-manager-bristol-myers-squibb/6a05f7032f1861929d2531dd</link><guid isPermaLink="true">http://biotechroles.com/learning-manager-bristol-myers-squibb/6a05f7032f1861929d2531dd</guid><pubDate>Thu, 14 May 2026 16:23:31 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Shanghai - CN</location><salary>$65000-110000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist , Oncology/Hematology- Oklahoma]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>This territory includes: <span>Oklahoma City, Tulsa, Ardmore, Muskogee.</span></p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602387 : Senior Therapeutic Area Specialist , Oncology/Hematology- Oklahoma]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-oklahoma-bristol-myers-squibb/6a05f7032f1861929d2531dc</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-oncologyhematology-oklahoma-bristol-myers-squibb/6a05f7032f1861929d2531dc</guid><pubDate>Thu, 14 May 2026 16:23:31 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Tulsa - OK - US</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Senior Therapeutic Area Specialist, Hematology -Brooklyn/Queens, NY]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>This territory includes: Brooklyn, Queens, Staten Island, Brooklyn Heights, Bushwick, Midwood, Astoria, Jamaica, Flushing, Bayside</p><p></p><p><b>Position Summary</b> </p><p>The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.  </p><p></p><p>The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. </p><p></p><p>The role builds and maintains strong professional credibility with regional thought leaders (RTLs) and community-based physicians/HCPs in private practice, medical groups practices, office staff, and other stakeholders in the patient care continuum as their primary point of contact. </p><p></p><p>The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. This role will prioritize the safe and appropriate use of BMS products while also focusing on overall business results and performance objectives while exemplifying BMS values.</p><p></p><p>The TAS role is field-based. A TAS is anticipated to spend 100% of their time in the field with external customers. </p><p><b>Key Responsibilities:</b> </p><p><b>Portfolio Promotion</b> </p><ul><li><p>Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. </p></li></ul><ul><li><p>Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. </p></li></ul><ul><li><p>Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. </p></li></ul><ul><li><p>Prepares and successfully implements comprehensive territory and account plans. </p></li></ul><ul><li><p>Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. </p></li></ul><p><b>Fair &amp; Balanced Scientific Dialogue</b> </p><ul><li><p>Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. </p></li></ul><ul><li><p>Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. </p></li></ul><ul><li><p>Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. </p></li></ul><ul><li><p>Maintains a high level of working expertise on emerging data for approved indications. </p></li></ul><ul><li><p>Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. </p></li></ul><p><b>Cross-functional collaboration</b> </p><ul><li><p>Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.  </p></li></ul><ul><li><p>Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. </p></li></ul><ul><li><p><b>Complies with all laws, regulations, and policies that govern the conduct of BMS.</b> </p></li></ul><p><b>Required Qualifications &amp; Experience</b> </p><ul><li><p>Advanced scientific degree and/or preferred 5&#43; years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. </p></li></ul><ul><li><p>Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. </p></li></ul><ul><li><p>Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). </p></li></ul><ul><li><p>Experience in Hematology/Oncology required. </p></li></ul><ul><li><p>Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. </p></li></ul><ul><li><p>Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude.  </p></li></ul><ul><li><p>Strong selling and promotional skills proven through a track record of performance. </p></li></ul><p><b>Key Competencies Desired</b> </p><p><b>Customer/commercial mindset</b> </p><ul><li><p>Demonstrated ability to drive business results. </p></li></ul><ul><li><p>Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. </p></li></ul><ul><li><p>Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. </p></li></ul><ul><li><p>Demonstrated resourcefulness and ability to connect with customers. </p></li></ul><p><b>Patient centricity </b> </p><ul><li><p>Understands the patient journey and experience. </p></li></ul><ul><li><p>Has a patient-focused mindset. </p></li></ul><p><b>Scientific Agility </b> </p><ul><li><p>Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. </p></li></ul><ul><li><p>Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. </p></li></ul><p><b>Analytical Capability:</b> </p><ul><li><p>Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. </p></li></ul><ul><li><p>Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. </p></li></ul><ul><li><p>Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. </p></li></ul><ul><li><p>Ability to use CE^3 to generate insights and do dynamic call planning. </p></li></ul><p><b>Technological Agility:</b> </p><ul><li><p>Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. </p></li></ul><ul><li><p>Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. </p></li></ul><ul><li><p>Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. </p></li></ul><ul><li><p>Ability to use the Medical on Call technology effectively. </p></li></ul><ul><li><p>Keeping up to date with technological advancements and changes. </p></li></ul><p><b>Teamwork/Enterprise mindset</b> </p><ul><li><p>Strong business acumen to understand and analyze business and market drivers and develop, execute, and adjust business plans. </p></li></ul><ul><li><p>Demonstrates a strong sense of learning agility. Seeks out and learns from unfamiliar experiences, and then applies those lessons to achieve better results in subsequent situations. </p></li></ul><ul><li><p>Track record of balancing individual drive and collaborative attitude. </p></li></ul><ul><li><p>Holds a high level of integrity and good judgment, in order to navigate the requirements of the role effectively and compliantly in accordance with BMS policies and procedures. </p></li></ul><ul><li><p>As this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of “Qualified Driver,” as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver’s license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. </p></li></ul><p>#LI-Remote </p><p></p><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Field - United States - US: $144,500 - $175,100&amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602464 : Senior Therapeutic Area Specialist, Hematology -Brooklyn/Queens, NY]]></description><link>http://biotechroles.com/senior-therapeutic-area-specialist-hematology-brooklynqueens-ny-bristol-myers-squibb/6a05f7022f1861929d2531db</link><guid isPermaLink="true">http://biotechroles.com/senior-therapeutic-area-specialist-hematology-brooklynqueens-ny-bristol-myers-squibb/6a05f7022f1861929d2531db</guid><pubDate>Thu, 14 May 2026 16:23:30 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Brooklyn - NY - US</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Contract Management]]></title><description><![CDATA[<p style="text-align:left"><b>Working with Us</b><br />Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.</p><p style="text-align:inherit"></p><p style="text-align:left">Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" target="_blank"><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">careers.bms.com/working-with-us</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>Position Summary:</b></p><p></p><p>The Associate Director, Office Contract Management position will act as the site-level single point of governance accountability for the IFM Service Provider scope of work at our Princeton Pike and Lawrenceville NJ locations. This position will oversee all facilities services and develop annual budgets for all services such as maintenance (hard services), hospitality (cafeteria, catering, office coffee, vending, special events, reception, etc.) housekeeping, pest control, mail, shipping and receiving, space planning and lab services (where appropriate). Through the development of mutually beneficial relationships (partnerships) and the execution of governance processes with the IFM Service Provider and internal BMS stakeholders such as BMS facilities operations, site customers, local and regional Finance, EHS, Quality, Procurement, Human Resources, Global Facilities Services and Global Energy departments, the Associate Director, Contract Management is responsible for the governance, monitoring and assurance of all aspects of the facilities management scope of services to ensure a consistent and cost effective service delivery that meets the service delivery needs of the facility and the IFM Service Provider.  This will be achieved by developing aligned objectives on service delivery and performance expectations between site leadership and the Service Provider.</p><p></p><p>The position will report to the Senior Regional Director, Facilities Operations, LVL/PPK.</p><p></p><div><p><b>Key Focus:</b></p><p></p></div><p>Key focus is the successful governance and implementation of the IFM contract at the site level, acting as the single point of contact to govern, develop and maintain positive relationships with the Service Provider for all facilities management services at the facility.  Furthermore, it is expected that consistency will be achieved across all sites through the use of matrix management and standardized governance processes within BMS.  In this capacity the Associate Director, Contract Management will be responsible for developing and monitoring yearly budgets in conjunction with the Service Provider and will facilitate/resolve site-specific governance issues with the IFM Service Provider and use good judgment when escalating issues throughout BMS’s matrix organization.</p><p></p><div><p><b>Key Responsibilities:</b></p></div><ul><li>Primary operational responsibility for the Princeton Pike site, and Office buildings of the Lawrenceville Campus.</li><li>Demonstrates tangible leadership and relationship management skills both across primary BMS stakeholders and Service Provider’s Account team.</li><li>Interact with corporate level executives and enable service levels supportive of their needs.  Support large scale meetings and events supporting corporate functions.</li><li>Aligns objectives of BMS and the Service Provider to ensure the service delivery model meets the needs of the facility and is mutually beneficial to BMS and Service Provider.</li><li>Represents BMS’s interests while overseeing service delivery and maintaining and growing relationships with the Service Provider utilizing both informal and standardized local and regional governance processes and partnerships with BMS stakeholders such as BMS facilities operations, site customers, local and regional Finance, EHS, Quality, Procurement, Human Resources, Global Facilities Services and Global Energy departments</li><li>Responds to problems and concerns; oversees the implementation of BMS policies, rules and regulations as they relate to the IFM Service Provider to minimize BMS risk.</li><li>Partners with the Service Provider Representative to assure excellent service delivery to the facility; reviews and monitors performance in line with agreed SLAs.</li><li>Approval of service provider monthly and quarterly KPI metric results</li><li>Reviews Service Provider’s procedure manuals that demonstrate performance is being consistently delivered.</li><li>Reviews and manages contract documents to ensure consistency and adherence with master contract and BMS’s corporate standards</li><li>Ensures superior delivery of all contract deliverables, including measurable value-add, innovation, and continuous improvement.</li><li>Works with Service Provider’s account management team and internal BMS stakeholders to monitor and modify the service deliverables in accordance with the changing business needs of the facility.</li><li>Develops site budget baseline and annual budget and assumptions with Service Provider</li><li>Controls and is accountable for the annual site IFM services facility budget, including direct Controllable and indirect Non-Controllable contract service expenses, preventative maintenance costs, project costs, rental expenses, energy management expenses and project/capital items. Accountable for and participates in site invoice reconciliation process (in a pass-through commercial model) and shared savings financial management.</li></ul><p></p><div><p><b>Qualifications &amp; Experience:</b></p></div><ul><li>Bachelor’s degree in Business Administration, Engineering, Finance, Planning or related field or equivalent work experience may substitute</li><li>5&#43; years operational experience with emphasis on integrated facility services. A core competency in the Hard Services and the management skills to oversee a portfolio of facilities services such as hospitality (cafeteria, catering, office coffee, vending, special events, reception, etc.) housekeeping, pest control, mail, shipping and receiving, space planning and lab services</li><li>Strong leader with a management style that exhibits high energy, collaboration, candor, openness, results orientation and an ability to manage and resolve issues.</li><li>Demonstrated experience in contract negotiation for facilities related services.</li><li>Extensive contract management experience, preferably experience managing a performance based IFM contract.</li><li>Strong financial management skills, including budgeting, forecasting, and analysis of variances.</li><li>Experience in managing the financial aspects of facility operations and services.  Accounting and budget process knowledge.</li><li>Development of executive level presentations.</li><li>Experience working in a pharmaceutical R&amp;D or laboratory environment or equivalent regulated industry.</li><li>Demonstrated leadership/management skills to deal with and resolve issues ranging from senior level, to administrative, to maintenance/engineering and soft services</li><li>Strong communication, negotiation and analytical skills.</li><li>Excellent interpersonal skills.</li><li>Ability to manage to multi-million dollar budgets.</li><li>Demonstrable Health &amp; Safety knowledge and/or experience (IOSH minimum).</li><li>Proven record of providing excellent internal and external customer service.</li><li>Ability to comprehend, analyze and interpret complex business documents.</li><li>Ability to respond effectively to highly sensitive issues.</li><li>Ability to write reports, manuals, presentations and articles using distinctive style.</li><li>Strong experience managing external business partners and vendors across various disciplines and geographies.</li><li>Demonstrated ability to manage across functional lines and deliver results in a matrix organization</li></ul><ul></ul><p style="text-align:left"><i>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.</i></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><b><b><b>Compensation Overview:</b></b></b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Princeton - NJ - US: $161,250 - $195,391 &amp;#xa;<p style="text-align:inherit"></p><p style="text-align:left"><span>The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. </span><br /><br /><span>Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit </span><a href="https://careers.bms.com/life-at-bms/" target="_blank"> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span class="WIN0">https://careers.bms.com/life-at-bms/.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></a><br /> </p><p style="text-align:left"><span>Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:</span></p><ul><li><p style="text-align:left"><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</p></li><li><p style="text-align:left"><span><b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).</span></p></li><li><p style="text-align:left"><span><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><b><span>​</span><span>Work-life benefits include:</span></b></p><p style="text-align:left"><span>Paid Time Off</span></p><ul><li><p style="text-align:left"><span>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)</span></p></li><li><p style="text-align:left"><span>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.</span></p><p style="text-align:inherit"></p><p style="text-align:left">All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.</p><p style="text-align:inherit"></p><p style="text-align:left"><i><b>*Eligibility Disclosure: </b><i>T</i>he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.</i></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Uniquely Interesting Work, Life-changing Careers</b><br />With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting <span>global participation </span>in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>On-site Protocol</b></p><p style="text-align:left"><span>BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Supporting People with Disabilities</b></p><p style="text-align:left"><span>BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> and ongoing support in their roles. Applicants can request a reasonable workplace <span><span><span><span><span><span class="WIN0">accommodation/adjustment</span></span></span></span></span></span> prior to accepting a job offer. If you require reasonable <span><span><span><span><span><span class="WIN0">accommodations/adjustments</span></span></span></span></span></span> in completing this application, or in any part of the recruitment process, direct your inquiries to </span><span><a href="mailto:adastaffingsupport&#64;bms.com" target="_blank"><span><span><span><span><span><span class="WIN0">adastaffingsupport&#64;bms.com</span></span></span></span></span></span></a></span><span>. Visit </span><span><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>careers.bms.com/</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>eeo</span></a><a href="https://careers.bms.com/eeo-accessibility" target="_blank"><span>-accessibility</span></a></span><span> to access our complete Equal Employment Opportunity statement.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Candidate Rights</b></p><p style="text-align:left"><span>BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: </span><span><a href="https://careers.bms.com/california-residents/" target="_blank"><span><span><span><span><span><span class="WIN0">https://careers.bms.com/california-residents/</span></span></span></span></span></span></a></span></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Data Protection</b></p><p style="text-align:left">We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at <a href="http://careers.bms.com/fraud-protection" target="_blank"><span><span><span><span><span class="WIN0">https://careers.bms.com/fraud-protection</span></span></span></span></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left">Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</p><p></p><p><span>If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at </span><a href="mailto:TAEnablement&#64;bms.com" target="_blank">TAEnablement&#64;bms.com</a><span>. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.</span></p><p></p><p></p>R1602463 : Associate Director, Contract Management]]></description><link>http://biotechroles.com/associate-director-contract-management-bristol-myers-squibb/6a05f7012f1861929d2531da</link><guid isPermaLink="true">http://biotechroles.com/associate-director-contract-management-bristol-myers-squibb/6a05f7012f1861929d2531da</guid><pubDate>Thu, 14 May 2026 16:23:29 GMT</pubDate><company>Bristol-Myers Squibb</company><location>Princeton - NJ - US</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Biostatistics Manager, Centralized Statistical Monitoring (CSM)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Research<h2></h2><h2><b>Job Description</b></h2><p><b>Biostatistics Manager, Centralized Statistical Monitoring (CSM)</b></p><p></p><p><b>What you will do:</b></p><p>Amgen’s Center for Design and Analysis Organization has a new opportunity for a <b>Biostatistics Manager</b> to provide statistical expertise in support of <b>Centralized Statistical Monitoring (CSM)</b> across clinical development programs.</p><p>The ideal candidate will build machine learning models and other statistical models, as well as support their implementation and deployment through a good understanding of the Software Development Life Cycle (SDLC).  Develop business requirements through collaborations with cross-functional stakeholders and the use of excellent communication skills.  Experience with clinical trials and their data collection process, storage, quality, and use would be looked for.  The latter will be particularly critical in a regulated environment.</p><p>In this role, you will leverage your experience as a biostatistician to contribute to the design, application, and continuous improvement of data-driven monitoring methods that support risk-based quality management (RBQM). You will apply your ML and AI skills to detect atypical data patterns, identify emerging quality risks, and enhance proactive oversight of clinical trials.</p><p>Functional requirements, prototype code, good documentation, testing, and relevant visualizations will be expected as deliverables when producing new algorithms as required by the stakeholders.</p><p>Key responsibilities include:</p><ul><li><p>Provide statistical and data science expertise to support CSM activities across multiple studies and therapeutic areas.</p></li><li><p>Develop and enhance statistical, machine learning, and AI-guided methodologies, to strengthen CSM signal detection and site-level risk assessment.</p></li><li><p>Perform detailed statistical review and quality control of CSM outputs, signals, and study-level metrics to ensure accuracy, consistency, and appropriate interpretation prior to stakeholder communication.</p></li><li><p>Collaborate with cross-functional partners (e.g., Clinical, Operations, Data Management, RBQM, Quality, Digital/Technology teams) to translate critical-to-quality (CTQ) factors into analytically robust and scalable monitoring solutions.</p></li><li><p>Contribute to validation, documentation, and controlled deployment of analytical methodologies and tools within regulated environments, ensuring reproducibility and adherence to internal standards.</p></li><li><p>Develop clear visualizations, dashboards, and analytical applications to enhance transparency and facilitate interpretation of monitoring outputs.</p></li><li><p>Stay current with evolving developments in data science, machine learning, and AI relevant to clinical trial monitoring.</p></li><li><p>Adhere to all Amgen policies and Standard Operating Procedures (SOPs).</p></li></ul><p></p><p><b>What we expect of you:</b></p><p>The statistical professional we seek is strong in the following qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>MSc or PhD in Statistics, Biostatistics, or related field with 8years of Industrial experience.                </p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Proficiency in statistical programming (e.g., R, SAS, or Python) with demonstrated experience applying machine learning and advanced analytical methods in practice.</p></li><li><p>Clinical trial experience within a pharmaceutical or medical research environment.</p></li><li><p>Prior experience serving as a study statistician for clinical trials, with responsibility for study-level statistical analysis and reporting.</p></li><li><p>Experience working effectively in a globally dispersed team environment with cross-cultural partners.</p></li><li><p>Demonstrable strategic thinking skills, originality, and creativity.</p></li><li><p>Writing skills with samples of technical writing (papers, reports, or project descriptions).</p></li><li><p>Self-directed, and well organized.</p></li></ul><p></p><p><b>What you can expect of us:</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.</p><p>Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models, including remote work arrangements, where possible</p></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/biostatistics-manager-centralized-statistical-monitoring-csm-amgen/6a05f6152f1861929d2531d9</link><guid isPermaLink="true">http://biotechroles.com/biostatistics-manager-centralized-statistical-monitoring-csm-amgen/6a05f6152f1861929d2531d9</guid><pubDate>Thu, 14 May 2026 16:19:33 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Safety Statistician, Manager]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Research<h2></h2><h2><b>Job Description</b></h2><p><b>Safety Statistician, Manager</b></p><p><b>What you will do</b></p><p>Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN) playing a key role in integrated delivery and functional leadership. Amgen’s Center for Design and Analysis Organization has a new opportunity for a <b>Safety Statistician, Manager</b> to provide statistical expertise in support of safety assessment activities across clinical development programs. In this role, you will contribute to the assessment and interpretation of aggregate safety data across multiple studies and products, working closely with Safety Assessment Teams and cross-functional partners. You will apply sound statistical judgment to support safety evaluation and reporting throughout the clinical trial lifecycle.</p><p></p><p><b>Responsibilities:</b></p><ul><li><p>Provide statistical expertise to support the assessment and interpretation of aggregate safety data across multiple studies and programs.</p></li><li><p>Contribute to the development and execution of aggregated safety analysis plans and related safety assessment and reporting activities.</p></li><li><p>Perform statistical analyses of safety data, including exploratory analyses, and contribute to the interpretation of results and formulation of conclusions.</p></li><li><p>Collaborate with cross-functional partners to provide statistical input into safety assessment discussions and deliverables.</p></li><li><p>Support the development and application of statistical methods, tools, and analyses for safety assessment, including data visualizations and advanced analytical approaches where appropriate.</p></li><li><p>Apply knowledge of statistical principles, regulatory guidance, and internal standards to ensure quality and consistency of safety analyses.</p></li><li><p>Stay current with developments in statistical methodology and analytical innovation relevant to safety assessment.</p></li><li><p>Adhere to all Amgen policies and Standard Operating Procedures (SOPs).</p></li></ul><p></p><p>This position is currently located at Amgen India (Hyderabad).</p><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The statistical professional we seek is strong in the following qualifications.</p><p></p><p><u>Basic Qualifications:</u></p><ul><li><p>MSc or PhD in Statistics, Biostatistics, or related field with 8years of Industrial experience</p></li><li><p>Proficient in an analytical application (e.g., R or SAS).</p></li></ul><p></p><p><u>Preferred Qualifications:</u></p><ul><li><p>Hands-on experience in statistical design and analysis, and machine learning</p></li><li><p>Clinical trial experience within a pharmaceutical or medical research environment.</p></li><li><p>Experience in statistical analyses of safety data in a clinical trials setting.</p></li><li><p>Experience working effectively in a globally dispersed team environment with cross-cultural partners.</p></li><li><p>Proficiency in developing, or supervising the development of, data visualization tools and analytical applications (e.g., R/Shiny) is highly desirable.</p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.</p><p>Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models, including remote work arrangements, where possible</p></li></ul><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/safety-statistician-manager-amgen/6a05f6102f1861929d2531d8</link><guid isPermaLink="true">http://biotechroles.com/safety-statistician-manager-amgen/6a05f6102f1861929d2531d8</guid><pubDate>Thu, 14 May 2026 16:19:28 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison, Uncontrolled Gout - Rare Disease - NC/SC/East TN]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Medical Affairs<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><div><div><div><div><div><div><div><div><div><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Medical Science Liaison, Uncontrolled Gout - Rare Disease - NC/SC/East TN</b></p><p><b>Territory to include Charlotte NC/SC/Eastern TN</b></p><p></p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will serve as a scientific liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with prominent experts and clinicians throughout the US.</p><ul><li><p>Network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors, managed care decision makers, and pharmacy directors in alignment with applicable compliance, legal, and regulatory guidelines.</p></li><li><p>Understand, integrate and effectively communicate scientific/medical information and commercial value of products to the medical community and other key internal and external audiences.</p></li><li><p>Prioritize and work effectively in a self-directed manner in a constantly changing environment, including ability to obtain, integrate, and communicate customer feedback.</p></li><li><p>Pair customers’ unmet needs with available internal resources.</p></li><li><p>Collaborate effectively with all functional areas to identify opportunities and needs that can be addressed via communication of scientific, medical, and health economic information.</p></li><li><p>Identify potential new speakers and train on scientific content for sponsored external speaker programs.</p></li><li><p>Participate in national and regional conferences, meetings, and other scientific venues as appropriate to support the Medical/Clinical strategy and to obtain new competitive information, keep abreast of clinical trends, and support and maintain relationships with key investigators and scientific research.</p></li><li><p>Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.</p></li><li><p>Monitor the competitive environment for advances and trends in our therapeutic areas, including new treatment management and new therapies, as well as competitive products and features and provide feedback to the senior leadership team on specific initiatives of competitors.</p></li></ul><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a self starter with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree</p></li></ul><p>OR</p><ul><li><p>Master’s degree &amp; 3 years of Medical Affairs experience</p></li></ul><p>OR</p><ul><li><p>Bachelor’s degree &amp; 5 years of Medical Affairs experience</p></li></ul><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered)</p></li><li><p>2 years of proven experience in scientific or medical affairs at a biotech or pharmaceutical company</p></li><li><p>Exceptional oral and written communication and interpersonal skills (including strong demonstration of ability to network) required.</p></li><li><p>Ability to travel up to 60% for territory management, attendance at regional and national conferences/workshops, and attendance at company meetings.</p></li><li><p>There may be a need to work up to 15-hour days due to travel</p></li><li><p>Must have ability to learn to use new business applications across hardware tools (e.g., PC, iPad).</p></li><li><p>Proficient in Microsoft Office.</p></li><li><p>Professional, proactive demeanor.</p></li><li><p>Strong interpersonal skills.</p></li><li><p>Excellent written and verbal communication skills.</p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models, including remote and hybrid work arrangements, where possible</p></li></ul><p></p><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p></p><p><b>Application deadline</b></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>156,998.40USD -212,409.60 USD]]></description><link>http://biotechroles.com/medical-science-liaison-uncontrolled-gout-rare-disease-ncsceast-tn-amgen/6a05f6102f1861929d2531d7</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-uncontrolled-gout-rare-disease-ncsceast-tn-amgen/6a05f6102f1861929d2531d7</guid><pubDate>Thu, 14 May 2026 16:19:28 GMT</pubDate><company>Amgen</company><location>US - North Carolina - Charlotte</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[Executive Director Marketing Repatha Brand Lead]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Marketing<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients </b></p><p>At Amgen, if you feel like you are a part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the future of cardiovascular disease.In this vital role for Amgen, the Executive Director, Repatha Brand Lead will help shape the future growth trajectory of one of the company’s most strategically important franchises. Repatha is a market-leading Lipid lowering inhibitor with proven cardiovascular outcomes benefits and a significant opportunity to transform LDL-C management across the U.S. healthcare system.The lipid-management landscape is entering a period of unprecedented change. Emerging therapies, evolving treatment guidelines, new quality measures, expanding cardiometabolic screening infrastructure, and increasing focus on preventive care are poised to dramatically expand the category and redefine how patients are identified, treated, and managed.The Executive Director will lead the Repatha brand through this next era of growth — helping accelerate earlier LDL-C intervention, broaden appropriate adoption, and accelerate Repatha’s leadership in a rapidly evolving marketplace.This role has leadership responsibility for driving all aspects of U.S. brand strategy and execution while leading a high-performing cross-functional marketing organization. The Executive Director will work closely with Commercial, Medical, Market Access, Value &amp; Access, Digital, Data &amp; Analytics, Sales, and R&amp;D leadership to deliver against ambitious growth objectives and unlock the next wave of category expansion.</p><p></p><p><b>Key responsibilities include:</b></p><ul><li><p>Lead the development and execution of bold, future-oriented strategies that drive sustainable revenue growth, market leadership, and long-term franchise profitability</p></li><li><p>Shape the future vision for Repatha within an evolving lipid-management ecosystem that includes new entrants, earlier treatment intensification, quality measure evolution, and expanding preventive cardiology pathways</p></li><li><p>Drive growth across strategically important patient segments including ASCVD, familial hypercholesterolemia, statin-intolerant patients, diabetes populations, and other high-risk cardiometabolic groups by accelerating patient identification, treatment intensification, and appropriate PCSK9 adoption</p></li><li><p>Develop and execute integrated brand strategies spanning positioning, messaging, omnichannel engagement, forecasting, lifecycle planning, market access, and healthcare economics initiatives</p></li><li><p>Lead development of breakthrough multichannel marketing campaigns and next-generation customer engagement strategies that leverage AI, advanced analytics, personalization, and emerging digital technologies to improve HCP engagement, patient activation, and commercial effectiveness at scale</p></li><li><p>Partner closely with Market Access, Medical Affairs, R&amp;D, Digital, Data &amp; Analytics, and Commercial Excellence teams to strengthen evidence generation, expand patient access, and identify innovative engagement models that create competitive advantage</p></li><li><p>Collaborate with U.S. and global leadership teams to inform franchise strategy, lifecycle opportunities, and long-term growth priorities</p></li><li><p>Build and lead a high-performing marketing organization that fosters accountability, innovation, collaboration, talent development, and strategic thinking</p></li><li><p>Ensure all commercial strategies and operational plans comply with applicable regulatory, legal, and ethical standards while promoting a highly compliant operating environment</p></li><li><p>Requires approximately 25% travel, including some overnight and weekend commitments</p></li></ul><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree &amp; 6 years of Marketing experience OR</p></li><li><p>Master’s degree &amp; 10 years of Marketing experience OR</p></li><li><p>Bachelor’s degree &amp; 12 years of Marketing experience AND</p></li><li><p>6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Minimum eight years of experience in a series of commercial roles of increasing scope, scale, and complexity, with leading companies in the bio-pharmaceutical or health and wellness industry</p></li><li><p>Experience developing and implementing innovative commercial strategies within highly competitive markets where innovation and marketing prowess are a key factor of success</p></li><li><p>Consumer and Healthcare Provider marketing, strategic and tactical implementation roles, with an emphasis on uncovering novel and motivating customer insights and executing integrated multi-touch point initiatives to move an apathetic market</p></li><li><p>Understanding of US market access, pricing, and reimbursement environment</p></li><li><p>Experience leading cross-functional teams in a matrix environment; managing projects involving multiple functions and shared accountabilities</p></li><li><p>Cardiovascular therapeutic area is preferred</p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $262,534 to $355,194. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies</p></li></ul><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p>Sponsorship for this role is not guaranteed.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>262,534.40USD -355,193.60 USD]]></description><link>http://biotechroles.com/executive-director-marketing-repatha-brand-lead-amgen/6a05f6102f1861929d2531d6</link><guid isPermaLink="true">http://biotechroles.com/executive-director-marketing-repatha-brand-lead-amgen/6a05f6102f1861929d2531d6</guid><pubDate>Thu, 14 May 2026 16:19:28 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Associate Plant QA 12 Day Shift (6am- 6pm)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Quality<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><h2>Sr. Associate Plant QA Day Shift</h2><p></p><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this role As Senior Associate Plant QA, you will be working in a shift system; you will be mainly responsible for providing QA guidance and support to AOH production, and you will be performing Quality Batch Record Review of all commercial batches labelled and packed at AOH. Next to that, you will provide support in different QA related projects/systems.</p><p></p><p>In this role, you will be in direct contact with a wide range of stakeholders, and you will be responsible for establishing effective working relationships with production operators, production line leads, production shift supervisors, warehouse, facilities, maintenance and engineering.</p><p></p><h2><b>Responsibilities</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will:</p><ul><li><p>Provide daily guidance and support to Production staff regarding compliance with Standard Operating Procedures and Work Instructions.</p></li><li><p>Ensure regular presence in device assembly and packaging areas to monitor GMP operations and quality systems.</p></li><li><p>Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations.</p></li><li><p>Lead, mentor, and coach Operations and support personnel on quality matters, while driving the site Quality culture.</p></li><li><p>Review and approve batch production record and other GMP documentation in support of daily operations. data entries before production activities take place</p></li><li><p>Perform finished product checks during (commercial) production runs</p></li><li><p>Compile and review batch records for lots assembled, packaged and labeled at AOH in preparation for batch disposition.</p></li><li><p>Own, review, and approve controlled documents, including Standard Operating Procedures (SOPs), Work Instructions and Forms.</p></li><li><p>Review and approve Deviation, CAPA, and Change Control records.</p></li><li><p>Participate in self-led inspections and provide support during internal / external regulatory inspections.</p></li><li><p>Support Lean Transformation and Operational Excellence initiatives</p></li><li><p>Adhering to safety rules and maintaining a safe work environment for both yourself and others by supporting EHSS corporate and site goals.</p></li></ul><p></p><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The Quality professional we seek is a dynamic, flexible and driven individual with any of these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><p>High school/GED &#43; 4 years of Quality and/or GMP Manufacturing experience</p><p>OR</p><p>Associate’s &#43; 2 years of Quality and/or GMP Manufacturing experience</p><p>OR</p><p>Bachelor’s &#43; 6 months of Quality and/or GMP Manufacturing experience</p><p>OR</p><p>Master&#39;s</p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Scientific degree in Life Sciences, Physical Sciences, Applied Engineering or Manufacturing Technologies</p></li><li><p>Experience in and knowledge of GMP/GCP operations or similarly regulated industry</p></li><li><p>Affinity with digital innovation, data sciences and Quality engineering</p></li><li><p>Experience with raw material receipt, inspection &amp; sampling</p></li><li><p>Highly effective verbal and written communication skills, strong interpersonal skills</p></li><li><p>Great attention to detail and high degree of accuracy in task execution and GMP documentation</p></li><li><p>Ability to complete tasks autonomously, providing updates to senior management, and identifying potential issues</p></li><li><p>Strong organizational skills, including ability to follow assignments through to completion</p></li><li><p>Direct experience with Enterprise Resource Management software (SAP), TrackWise, CDOCS etc.</p></li></ul><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models, including remote and hybrid work arrangements, where possible</p></li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>82,081.95USD -111,052.05 USD]]></description><link>http://biotechroles.com/sr-associate-plant-qa-12-day-shift-6am-6pm-amgen/6a05f60f2f1861929d2531d5</link><guid isPermaLink="true">http://biotechroles.com/sr-associate-plant-qa-12-day-shift-6am-6pm-amgen/6a05f60f2f1861929d2531d5</guid><pubDate>Thu, 14 May 2026 16:19:27 GMT</pubDate><company>Amgen</company><location>US - Ohio - New Albany</location><salary>$75000-95000</salary><type>Full time</type></item><item><title><![CDATA[Scientist - Molecular Immunology]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Scientist – Molecular Immunology</b></p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. Amgen’s Immunoengineering organization is seeking an experienced, enthusiastic, and collaborative Scientist to join the Experimental Immunology Team at our Amgen British Columbia site.</p><p></p><p>This is a laboratory-focused position involving the design, development, and execution of molecular and cellular biology research platforms to support immunology and therapeutic discovery programs. The ideal candidate will possess a strong foundation in molecular biology and protein biochemistry combined with broad hands-on technical expertise across multiple experimental systems and technologies. This role will contribute directly to the development of novel technologies, molecular tools, and next-generation research platforms within a highly collaborative and fast-paced research environment.</p><p></p><p>The successful candidate will have experience spanning protein engineering and characterization, bio-conjugation strategies, and molecular construct design. The position will involve work with protein expression systems, engineered fusion proteins, and molecular tagging approaches including SNAP/CLIP technologies, as well as analytical characterization techniques such as Western blotting, HPLC, and mass spectrometry. Experience designing and generating lentiviral, AAV, and plasmid-based systems is highly desired, along with expertise in primary cell culture and cellular assay development.</p><p></p><p>Additional experience working with RNA biology, RNA-protein immune complexes, and related molecular interrogation techniques will be valuable for success in this role. Well-suited applicants will demonstrate scientific curiosity, adaptability, and enthusiasm for learning and applying a wide range of experimental approaches. We are particularly interested in candidates with a broad and versatile technical skill set who are excited to work across disciplines and contribute to the development of innovative experimental capabilities and enabling technologies.</p><p></p><p>This individual will thrive in a team-oriented environment and will bring strong experimental rigor, creativity, and problem-solving skills to challenging scientific questions. The candidate should also possess excellent communication skills and a demonstrated ability to work collaboratively across cross-functional research teams.</p><p><br /><b>What we expect of you</b><br />We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a candidate with these qualifications.</p><p></p><p><b>Basic Qualifications:</b><br />PhD in a related discipline with 0-2 years of experience<br />MSc with 3-4 years of experience.<br />BSc with 5&#43; years of experience.</p><p></p><p><b>Preferred Qualifications:</b><br />• Strong foundation in molecular biology, protein biochemistry, and cellular biology.<br />• Hands-on experience with protein design, engineering, expression, purification, and characterization workflows.<br />• Experience with bio-conjugation strategies and engineered protein systems including fusion proteins and SNAP/CLIP tag technologies.<br />• Experience using analytical and characterization techniques including Western blotting, HPLC, and mass spectrometry.<br />• Experience designing and generating lentiviral, AAV, and plasmid-based expression systems.<br />• Experience with primary cell culture and cell-based assay development.<br />• Experience working with RNA biology and RNA/protein immune complexes.<br />• Broad laboratory training with the flexibility and curiosity to work across multiple technology areas and experimental platforms.<br />• Strong written and verbal communication and interpersonal skills.<br />• Desire to be a team player in a dynamic, cross-functional environment.<br />• Demonstrated scientific analysis and problem-solving skills.</p><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>Amgen is proud to have been recognized as one of LinkedIn Top 25 Companies in Canada for career growth. Click <a href="https://nam11.safelinks.protection.outlook.com/?url&#61;https%3A%2F%2Fwww.linkedin.com%2Fpulse%2Flinkedin-top-companies-2025-25-best-workplaces-grow-your-3mgie&amp;data&#61;05%7C02%7Ctbrawner%40amgen.com%7C17817f6f28cb428f95f308ddb59cbc92%7C4b4266a6136841afad5a59eb634f7ad8%7C0%7C0%7C638866406959632854%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;sdata&#61;%2BtQzUlrLG%2B%2FddGYWmwrOg7DQ9mMamH%2Bo%2BEiO7MMHsow%3D&amp;reserved&#61;0" target="_blank">HERE</a> for more details.</p><p></p><p>The salary for this position in Canada is $109,255 - $147,815.</p><p></p><p>In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>109,254.75 CAD - 147,815.25 CAD]]></description><link>http://biotechroles.com/scientist-molecular-immunology-amgen/6a05f60f2f1861929d2531d4</link><guid isPermaLink="true">http://biotechroles.com/scientist-molecular-immunology-amgen/6a05f60f2f1861929d2531d4</guid><pubDate>Thu, 14 May 2026 16:19:27 GMT</pubDate><company>Amgen</company><location>Canada - Burnaby</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[Senior Director, Global Forecasting, Obesity]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales &amp; Marketing Operations<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><h2><b>Senior Director, Global Forecasting, Obesity</b></h2><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. Amgen is committed to transforming the lives of patients by advancing science, delivering innovative medicines, and creating sustainable value for healthcare systems worldwide. Obesity represents one of the most pressing global health challenges of our time, with rapidly evolving science, treatment paradigms, competitive dynamics, access considerations, and patient needs shaping the future of care.</p><p>To support this important therapeutic area, we are seeking a Senior Director, Global Forecasting, Obesity to lead forecasting strategy and execution for Amgen’s global obesity portfolio. This leader will be responsible for developing robust, evidence-based forecasts that inform portfolio strategy, investment decisions, launch planning, lifecycle management, resource allocation, and long-range business planning.</p><p>The Senior Director will partner closely with Global Commercial, U.S. Commercial, Regional Commercial, Finance, Medical, Market Access, R&amp;D, Business Development, Market Research, Analytics, and Competitive Intelligence teams to ensure forecasts reflect aligned assumptions, rigorous methodology, and a forward-looking view of market evolution. The role requires a strategic forecasting leader who can operate in ambiguity, influence senior stakeholders, build organizational confidence in forecast outputs, and translate complex market dynamics into clear business implications.</p><p><b>This role requires at least 3 days on campus in Thousand Oaks, CA.</b></p><p><b>Global Forecasting Leadership</b></p><ul><li>Lead global forecasting for Amgen’s obesity portfolio, including pipeline assets, launch brands, lifecycle opportunities, and long-range therapeutic area planning.</li><li>Develop and maintain short-term, mid-term, and long-range forecasts that support strategic planning, investment decisions, portfolio prioritization, and performance expectations.</li><li>Establish clear forecasting frameworks, methodologies, governance, and assumptions across global, regional, and U.S. stakeholders.</li><li>Translate forecast outputs into actionable strategic recommendations for senior leadership.</li><li>Serve as a trusted forecasting advisor to Global Commercial, Finance, R&amp;D, Medical, Market Access, and regional leadership teams.</li><li>Ensure forecasts are credible, transparent, and grounded in robust data, business logic, and cross-functional alignment.</li></ul><p><b>Obesity Market and Portfolio Forecasting</b></p><ul><li>Build forecasts that reflect the complexity of the global obesity market, including treatment adoption, patient flow, diagnosis and treatment rates, payer dynamics, adherence, persistence, capacity constraints, competitor entry, and evolving standards of care.</li><li>Incorporate global and local market dynamics, including epidemiology, pricing and reimbursement, access restrictions, regional launch sequencing, promotional investment, and healthcare system differences.</li><li>Evaluate key forecast drivers such as patient segmentation, demand generation, product profile, differentiation, market expansion, switching, discontinuation, and competitive response.</li><li>Develop scenarios to assess upside and downside risks across major markets and regions.</li><li>Partner with cross-functional teams to assess commercial implications of clinical data, label scenarios, indication expansion, device or formulation changes, and lifecycle opportunities.</li><li>Support business development, licensing, and external innovation assessments as needed through objective commercial forecasting.</li></ul><p><b>Strategic Planning and Decision Support</b></p><ul><li>Ensure forecasts directly inform global brand strategy, launch planning, annual operating plans, long-range planning, portfolio reviews, and investment trade-off decisions.</li><li>Partner with Finance to align forecast outputs with financial planning cycles, revenue expectations, and business performance management.</li><li>Collaborate with Market Access and Pricing teams to reflect reimbursement scenarios, access timing, net price assumptions, payer restrictions, and affordability considerations.</li><li>Partner with Market Research, Analytics, and Competitive Intelligence to ensure forecasts are informed by the best available evidence and updated as new insights emerge.</li><li>Develop clear narratives that explain forecast movement, key assumptions, risks, sensitivities, and strategic implications.</li><li>Prepare executive-ready materials for senior leadership discussions, governance forums, portfolio reviews, and business planning meetings.</li></ul><p><b>Forecast Governance and Excellence</b></p><ul><li>Lead cross-functional forecast alignment processes across global, regional, and U.S. teams.</li><li>Ensure seamless forecast transitions from global strategy to regional and U.S. execution, with consistent assumptions, transparent methodology, and clear ownership.</li><li>Drive forecast quality through disciplined model design, assumption documentation, sensitivity analysis, version control, and governance.</li><li>Establish best practices for obesity forecasting, including launch curve development, analog selection, patient-based modeling, scenario planning, and competitive event modeling.</li><li>Identify opportunities to enhance forecasting capabilities through advanced analytics, automation, real-world evidence, and improved data integration.</li><li>Maintain a clear view of forecast risks and opportunities, proactively advising leadership on changes in market outlook.</li></ul><p><b>Cross-Functional and Global Collaboration</b></p><ul><li>Partner with Global General Managers, regional commercial leaders, U.S. leadership, Finance, R&amp;D, Medical, Market Access, Supply, Manufacturing, and Strategy teams to align around forecast assumptions and business implications.</li><li>Influence senior stakeholders in a highly matrixed global organization.</li><li>Facilitate productive debate around key assumptions while driving alignment and decision-making.</li><li>Ensure global forecasts reflect local market realities while maintaining enterprise-level consistency.</li><li>Build strong relationships across functions to ensure forecasting is embedded into strategic decision-making, not treated as a standalone exercise.</li></ul><p><b>People Leadership</b></p><ul><li>Lead, develop, and mentor forecasting talent supporting the obesity portfolio.</li><li>Foster a culture of analytical rigor, transparency, accountability, curiosity, and business partnership.</li><li>Champion diversity, equity, and inclusion within the team and across forecasting processes.</li><li>Build forecasting capability across the organization by coaching teams on methodology, assumptions, scenario planning, and interpretation of forecast outputs.</li><li>Encourage innovation while maintaining disciplined forecasting standards.</li></ul><p></p><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a collaborative leader with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 5 years of experience in forecasting, analytics, market insights, finance, strategy, or commercial planning</p><p>OR</p><p>Master’s degree and 9 years of experience in forecasting, analytics, market insights, finance, strategy, or commercial planning  </p><p>OR</p><p>Bachelor’s degree and 11 years of experience in forecasting, analytics, market insights, finance, strategy, or commercial planning</p><p></p><p>In addition to meeting at least one of the above requirements, you must have at least 5 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.  Your managerial experience may run concurrently with the required technical experience referenced above</p><p><b>Preferred Qualifications:</b></p><ul><li>Deep biopharmaceutical forecasting expertise, ideally with experience in obesity, metabolic disease, diabetes, cardiovascular disease, or other large primary care or specialty markets.</li><li>Strong understanding of global pharmaceutical markets, including launch dynamics, pricing and reimbursement, market access, regional variation, and competitive strategy.</li><li>Experience developing patient-based forecasts, epidemiology-driven models, analog-based launch forecasts, scenario analyses, and long-range portfolio forecasts.</li><li>Ability to integrate inputs from market research, secondary analytics, competitive intelligence, clinical development, medical, access, and finance into cohesive forecast recommendations.</li><li>Strong executive communication skills, with the ability to distill complex models and assumptions into clear strategic narratives.</li><li>Proven ability to challenge assumptions constructively, manage ambiguity, and make sound recommendations with incomplete information.</li><li>Experience supporting major investment decisions, launch planning, lifecycle planning, business development assessments, or portfolio prioritization.</li><li>Strong business acumen and ability to connect forecast implications to strategy, resource allocation, and enterprise value.</li><li>High adaptability and comfort operating in a fast-moving therapeutic area with rapidly evolving competitive dynamics.</li></ul><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>216,632.70USD -293,091.30 USD]]></description><link>http://biotechroles.com/senior-director-global-forecasting-obesity-amgen/6a05f60e2f1861929d2531d3</link><guid isPermaLink="true">http://biotechroles.com/senior-director-global-forecasting-obesity-amgen/6a05f60e2f1861929d2531d3</guid><pubDate>Thu, 14 May 2026 16:19:26 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Vice President, Regulatory Affairs – ELMAC]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Regulatory<h2></h2><h2><b>Job Description</b></h2><h2><b>Join Amgen’s Mission of Serving Patients </b><br /> </h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.<br /> </p><h2><b>Vice President, Regulatory Affairs – ELMAC  </b></h2><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role as Vice President, Regulatory Affairs ELMAC, (Europe, Latin America, Middle East, Africa &amp; Canada) you will set the strategic direction for Regulatory Affairs across ELMAC, ensuring the organization delivers compliant, innovative, and forward-looking regulatory strategies that accelerate patient access and support enterprise growth. You will operate as a key member of the global regulatory leadership team, shaping both regional execution and the future of the regulatory function. This role defines and drives the regional regulatory strategy, shaping submissions, health authority engagement, and portfolio execution to enable compliant development, accelerate patient access, and support enterprise growth.<br /> </p><p><b>Set and lead the regional regulatory strategy</b><br />Define and drive a cohesive regulatory strategy across ELMAC that aligns with global priorities and enables timely, efficient product development and market access. Ensure regional strategies are integrated, forward-looking, and responsive to an evolving regulatory landscape.<br /> </p><p><b>Lead and evolve a high-performing organization</b><br />Build and lead a modern regulatory organization equipped to meet future demands. Establish a clear vision, operating model, and workforce strategy. Drive strong engagement, develop leadership bench strength, and ensure effective resource allocation and prioritization across the region.<br /> </p><p><b>Drive enterprise alignment and decision-making</b><br />Serve as a strategic advisor to senior leadership, providing clear visibility into risks, tradeoffs, and opportunities. Influence enterprise decisions by connecting regional insights with global priorities and ensuring regulatory considerations are embedded early in development and commercialization strategies.<br /> </p><p><b>Enable affiliate and market success</b><br />Partner closely with country leadership to ensure regulatory strategies enable local business objectives and patient access. Strengthen alignment between regional priorities and affiliate execution, with particular focus on key markets and growth regions.<br /> </p><p><b>Accelerate innovation and transformation</b><br />Champion new ways of working across Regulatory Affairs, including automation, advanced analytics, and the use of emerging technologies. Lead initiatives that improve speed, quality, and scalability of regulatory processes while reducing complexity and cost.<br /> </p><p><b>Strengthen quality and operational excellence</b><br />Ensure consistent, high-quality regulatory submissions and labeling practices across the region. Establish clear performance metrics and continuously improve processes to enhance reliability, compliance, and efficiency.<br /> </p><p><b>Shape the external regulatory environment</b><br />Represent the organization with global and regional health authorities, industry groups, and policy forums. Build strong external relationships that enhance credibility, influence regulatory policy, and enable more predictable and efficient pathways for product approval and access.<br /> </p><p><b>Define the future of the regulatory function</b><br />Anticipate and help lead the evolution of Regulatory Affairs, including increased use of real-world evidence, digital data exchange, and global regulatory collaboration. Position the organization to lead in a more connected, data-driven, and technology-enabled regulatory environment.<br /> </p><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an experienced leader with the following qualifications. They will also embody the Amgen leadership attributes which are:</p><ul><li><b>Inspire:</b> Create a connected, inclusive, and inspiring work environment that empowers talent to thrive</li><li><b>Accelerate:</b> Enable speed that matches the urgency of patient needs by encouraging progress over perfection</li><li><b>Integrate:</b> Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholders</li><li><b>Adapt:</b> Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver results</li></ul><p><b>Basic Qualifications:</b></p><ul><li>Doctorate degree &amp; 8 years of directly related experience OR</li><li>Master’s degree &amp; 10 years of directly related experience OR</li><li>Bachelor’s degree &amp; 12 years of directly related experience AND</li><li>8 years of direct managerial experience. Previous experience managing other managers</li></ul><p><b>Preferred Qualifications:</b></p><ul><li>Advanced degrees (e.g., Ph.D. or PharmD) preferred</li><li>A minimum of eight years of industry experience, including direct leadership of highly skilled teams composed of senior professionals.</li><li>Extensive knowledge of regulatory requirements and strategies in relevant therapeutic areas.</li><li>Regulatory Leadership in a Matrix Organization: Proven ability to lead, manage, and inspire teams within a complex, multi-functional, multi-national matrix structure.</li><li>Regional Regulatory and Healthcare Ecosystem Expertise: Experience navigating regional, and local regulatory landscapes and healthcare systems.</li><li>Strategic External Engagement: Strong ability to engage with regulatory authorities, industry bodies, and key external stakeholders, with an established network within the regulatory community.</li><li>Pharmaceutical Industry and Compliance Expertise: Strong understanding of the pharmaceutical industry, including legal, ethical, and health system considerations impacting regulatory decisions.</li><li>Financial and Resource Management: Experience in budgeting, resource allocation, and operational efficiency within regulatory functions.</li><li>Effective Communication and Problem Solving: Skilled in articulating complex regulatory and scientific concepts in both written and verbal formats, with a track record of sound decision-making and strategic problem-solving.</li></ul><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.<br />Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans and bi-annual company-wide shutdowns</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.<br /> </li></ul><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/vice-president-regulatory-affairs-elmac-amgen/6a05f60e2f1861929d2531d2</link><guid isPermaLink="true">http://biotechroles.com/vice-president-regulatory-affairs-elmac-amgen/6a05f60e2f1861929d2531d2</guid><pubDate>Thu, 14 May 2026 16:19:26 GMT</pubDate><company>Amgen</company><location>United Kingdom - Uxbridge</location><salary>$180000-280000</salary><type>Full time</type></item><item><title><![CDATA[Intern, Medical Operations - Oncology]]></title><description><![CDATA[<h2><b>Career Category</b></h2>College Job<h2></h2><h2><b>Job Description</b></h2><p>Join Amgen’s Mission of Serving Patients</p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b><span>Intern, Medical Operations - Oncology </span></b></p><p><span>Duration: ~</span><b><span> 6 months</span></b></p><p>Reports to: Medical Director, Oncology</p><p>Location: Mississauga Flexible Commuter (Hybrid Work)</p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will support the Medical Advisor in the responsibilities associated with the implementation and follow up of all planned medical activities.</p><p></p><p><b>Key Responsibilities:</b></p><ul><li>Support the Medical Affairs team in the strategic development and execution of the Medical tactics.</li><li>Operational support with budget, contracting and payments for medical tactics.</li><li>Ensure quality and compliance in all activities.</li><li>Be involved in the scientific content of all activities i.e. getting necessary approval of slides decks etc.</li><li>Be the point of contact for partnership with Strategic Meeting Management (SMM) &amp; Centre of Excellence (COE) for all activities.</li><li>Assist in coordinating accredited continuing medical education and learning activities with Medical Advisor.</li><li>Support the development of scientific advisory boards and speaker programs.</li><li>Plan and coordinate Scientific Affairs activities at key scientific congresses.</li><li>Manage vendors and consultants and project budgets.</li><li>Takes independent action on handling requests; determines the appropriate course of action while informing the medical advisor always.</li><li>Take on ad-hoc projects/tasks</li></ul><p></p><p></p><p><b>What we expect of you</b></p><p></p><p><b>Basic qualifications</b></p><ul><li>Currently enrolled in (or recently graduated from within the last 3 years) an undergraduate or graduate program in Life Sciences, Business/Marketing, Computer Science, Instructional Design, or a related field.</li><li>Strong research and writing skills; ability to simplify complex concepts clearly.</li><li>High attention to detail and comfort working through iterative testing and feedback cycles.</li><li>Strong collaboration skills and curiosity to learn in a fast-moving environment.</li></ul><p></p><p><b>Preferred qualifications</b></p><ul><li>An understanding of the pharmaceutical commercialization process, and knowledge of the legal and regulatory guidelines affecting promotion of prescription products</li><li>Familiarity with processes for accreditation of CME materials/programs</li><li>Familiarity with Innovative Medicines Canada Code of Ethical Practice</li></ul><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The salary for this position in Canada is <span>58000 – 72000 CAD. </span></p><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/intern-medical-operations-oncology-amgen/6a05f60d2f1861929d2531d1</link><guid isPermaLink="true">http://biotechroles.com/intern-medical-operations-oncology-amgen/6a05f60d2f1861929d2531d1</guid><pubDate>Thu, 14 May 2026 16:19:25 GMT</pubDate><company>Amgen</company><location>Canada - Mississauga</location><salary>$35000-45000</salary><type>Full time</type></item><item><title><![CDATA[Associate Scientist – In Vivo Pharmacology, Cardiometabolic Disorders]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases.</p><p></p><p>With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year.</p><p></p><p>Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions.</p><p></p><p>As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><h2><b>Associate Scientist – In Vivo Pharmacology</b></h2><h2></h2><h2><b>What you will do</b></h2><p></p><p>Let’s do this. Let’s change the world. In this vital role you will work onsite at Amgen’s South San Francisco campus as part of a collaborative in vivo research team advancing discovery biology and the therapeutic development of the next generation of cardiovascular medicines. You will contribute to studies that deepen our understanding of cardiovascular disease and help push the boundaries of cardiovascular science in support of innovative drug discovery.</p><p></p><p>Key Responsibilities:</p><ul><li>Carry out hands-on in vivo work in mice, including dosing, handling, health monitoring, and blood collection.</li><li>Support in vivo cardiovascular models and related study procedures.</li><li>Apply mouse surgical and microsurgical techniques, including Alzet pump implantation and other in vivo procedures.</li><li>Perform necropsies and support ex vivo tissue activities, including dissection, processing, sample preparation, and experimental readouts.</li><li>Partner with scientists to support study execution, communicate results, and maintain accurate study records.</li><li>Participate in dosing and monitoring rotations, including occasional evening or weekend work.</li></ul><p></p><h2><b>What we expect of you</b></h2><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The Associate Scientist we seek is a highly motivated researcher with these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><p></p><p>Master’s degree and 1 year of experience in <i>in-vivo</i> work with rodents</p><p>OR</p><p>Bachelor’s degree and 3 years of experience in <i>in-vivo</i> work with rodents</p><p></p><p><b>Preferred Qualifications:</b></p><ul><li>Hands-on experience in <i>in-vivo</i> rodent studies in an academic or industry setting.</li><li>Proficiency in mouse techniques such as dosing, blood collection, and health monitoring.</li><li>Experience performing necropsy and collecting tissues for downstream analyses.</li><li>Familiarity with cardiovascular in vivo studies and ex vivo tissue workflows.</li><li>Experience with mouse surgical or microsurgical techniques, or other technically demanding rodent procedures requiring strong manual dexterity.</li><li>Familiarity with mouse husbandry and vivarium-based study support.</li><li>Cardiovascular research background is a plus.</li></ul><p></p><h2><b>What you can expect of us</b></h2><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>This role is paid hourly. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Application deadline</h2><p></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p></p><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Amgen will consider for employment qualified applicants with criminal histories in a manner consistent with the San Francisco Fair Chance Ordinance.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/associate-scientist-in-vivo-pharmacology-cardiometabolic-disorders-amgen/6a05f60c2f1861929d2531d0</link><guid isPermaLink="true">http://biotechroles.com/associate-scientist-in-vivo-pharmacology-cardiometabolic-disorders-amgen/6a05f60c2f1861929d2531d0</guid><pubDate>Thu, 14 May 2026 16:19:25 GMT</pubDate><company>Amgen</company><location>US - California - South San Francisco</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Scientist – In Vivo Pharmacology, Cardiometabolic Disorders]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year.</p><p></p><p>Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions.</p><p></p><p>As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><h2>Scientist – In Vivo Pharmacology – Cardiometabolic Disorders</h2><p></p><h2><b>What you will do</b></h2><p></p><p>Let’s do this. Let’s change the world. In this vital role, you will work onsite at Amgen’s South San Francisco campus as part of a collaborative in vivo research team advancing discovery biology and the therapeutic development of the next generation of cardiovascular medicines.</p><p></p><p>You will contribute to studies that deepen our understanding of cardiovascular disease and help push the boundaries of cardiovascular science in support of innovative drug discovery.</p><p></p><p>Key Responsibilities:</p><p></p><ul><li>Conduct hands-on in vivo work in mice, including dosing, handling, health monitoring, and blood collection.</li><li>Perform necropsies and collect tissues to support downstream workflows.</li><li>Conduct tissue workflow activities, including tissue fixation, trimming, embedding, cry sectioning and/or FFPE sectioning, slide preparation, and sample tracking to ensure high-quality samples are delivered to downstream groups for analysis.</li><li>Maintain tissue and slide quality through proper specimen orientation, labeling, handling, and section QC.</li><li>Partner with scientists to execute study plans, communicate progress, and present data and results to study teams.</li><li>Maintain accurate experimental records and coordinate sample flow from collection through slide preparation and handoff to downstream groups for analysis.</li><li>Participate in dosing and husbandry, including occasional evening or weekend work.</li></ul><p></p><h2><b>What we expect of you</b></h2><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The Scientist we seek is a seasoned professional with these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><p></p><p>Doctorate degree<br /> </p><p>OR<br /> </p><p>Master’s degree and 2 years of In Vivo Pharmacology experience<br /> </p><p>OR<br /> </p><p>Bachelor’s degree and 4 years of In Vivo Pharmacology experience</p><p></p><p><b>Preferred Qualifications:</b></p><p></p><ul><li>Hands-on experience on in vivo rodent studies in an academic or industry setting.</li><li>Proficiency in mouse techniques such as dosing, blood collection, and health monitoring.</li><li>Demonstrated skill in necropsy and in the collection, dissection, and preservation of tissues for histologic and other downstream analyses.</li><li>Familiarity with histology workflows, including tissue fixation, processing, embedding, cryosectioning, microtomy, FFPE preparation, slide preparation, and staining methods.</li><li>Ability to manage sectioning workflows and prepare high-quality slides for downstream analysis.</li><li>Familiarity with mouse husbandry and vivarium-based study support.</li><li>Cardiovascular in vivo background is a plus.</li></ul><p></p><h2>What you can expect from us</h2><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><p></p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><p></p><p><b>careers.amgen.com</b></p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Application deadline</h2><p></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p></p><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Amgen will consider for employment qualified applicants with criminal histories in a manner consistent with the San Francisco Fair Chance Ordinance.<p><b>Salary Range</b></p>123,052.80USD -166,483.20 USD]]></description><link>http://biotechroles.com/scientist-in-vivo-pharmacology-cardiometabolic-disorders-amgen/6a05f60c2f1861929d2531cf</link><guid isPermaLink="true">http://biotechroles.com/scientist-in-vivo-pharmacology-cardiometabolic-disorders-amgen/6a05f60c2f1861929d2531cf</guid><pubDate>Thu, 14 May 2026 16:19:24 GMT</pubDate><company>Amgen</company><location>US - California - South San Francisco</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Liaison, Uncontrolled Gout - Rare Disease - PA/South Jersey]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Medical Affairs<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><div><div><div><div><div><div><div><div><div><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Medical Science Liaison, Uncontrolled Gout - Rare Disease - PA/South Jersey</b></p><p><b>Territory to include All of PA and Southern NJ</b></p><p></p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will serve as a scientific liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with prominent experts and clinicians throughout the US.</p><ul><li><p>Network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors, managed care decision makers, and pharmacy directors in alignment with applicable compliance, legal, and regulatory guidelines.</p></li><li><p>Understand, integrate and effectively communicate scientific/medical information and commercial value of products to the medical community and other key internal and external audiences.</p></li><li><p>Prioritize and work effectively in a self-directed manner in a constantly changing environment, including ability to obtain, integrate, and communicate customer feedback.</p></li><li><p>Pair customers’ unmet needs with available internal resources.</p></li><li><p>Collaborate effectively with all functional areas to identify opportunities and needs that can be addressed via communication of scientific, medical, and health economic information.</p></li><li><p>Identify potential new speakers and train on scientific content for sponsored external speaker programs.</p></li><li><p>Participate in national and regional conferences, meetings, and other scientific venues as appropriate to support the Medical/Clinical strategy and to obtain new competitive information, keep abreast of clinical trends, and support and maintain relationships with key investigators and scientific research.</p></li><li><p>Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.</p></li><li><p>Monitor the competitive environment for advances and trends in our therapeutic areas, including new treatment management and new therapies, as well as competitive products and features and provide feedback to the senior leadership team on specific initiatives of competitors.</p></li></ul><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a self starter with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications:</b></p><ul><li><p>Doctorate degree</p></li></ul><p>OR</p><ul><li><p>Master’s degree &amp; 3 years of Medical Affairs experience</p></li></ul><p>OR</p><ul><li><p>Bachelor’s degree &amp; 5 years of Medical Affairs experience</p></li></ul><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered)</p></li><li><p>2 years of proven experience in scientific or medical affairs at a biotech or pharmaceutical company</p></li><li><p>Exceptional oral and written communication and interpersonal skills (including strong demonstration of ability to network) required.</p></li><li><p>Ability to travel up to 60% for territory management, attendance at regional and national conferences/workshops, and attendance at company meetings.</p></li><li><p>There may be a need to work up to 15-hour days due to travel</p></li><li><p>Must have ability to learn to use new business applications across hardware tools (e.g., PC, iPad).</p></li><li><p>Proficient in Microsoft Office.</p></li><li><p>Professional, proactive demeanor.</p></li><li><p>Strong interpersonal skills.</p></li><li><p>Excellent written and verbal communication skills.</p></li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models, including remote and hybrid work arrangements, where possible</p></li></ul><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p></p><p><b>Application deadline</b></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>156,998.40USD -212,409.60 USD]]></description><link>http://biotechroles.com/medical-science-liaison-uncontrolled-gout-rare-disease-pasouth-jersey-amgen/6a05f60c2f1861929d2531ce</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-uncontrolled-gout-rare-disease-pasouth-jersey-amgen/6a05f60c2f1861929d2531ce</guid><pubDate>Thu, 14 May 2026 16:19:24 GMT</pubDate><company>Amgen</company><location>US - Pennsylvania - Philadelphia</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Scientist - Systems Immunology]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Sr. Scientist - Systems Immunology</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. Amgen’s Immunoengineering organization is seeking an experienced, enthusiastic, and collaborative Scientist to join the Experimental Immunology Team at our Amgen British Columbia site.</p><p></p><p>This is a systems immunology-focused position involving the integration, analysis, and interpretation of high-dimensional immune profiling datasets to support discovery and translational research efforts. The ideal candidate will possess deep foundational expertise in immunology combined with strong computational and quantitative biology skills. This role will focus on the integration of multimodal datasets including high-dimensional spectral cytometry, secretomics, and transcriptomics to uncover immune mechanisms, characterize complex cellular phenotypes, and identify biomarkers and therapeutic hypotheses.</p><p></p><p>The successful candidate will work closely within cross-functional research teams to design studies, develop analytical workflows, and generate biologically meaningful insights from complex datasets. Experience with systems-level analysis approaches, data visualization, statistical modeling, and multi-omics integration is highly desired. Well-suited applicants will demonstrate scientific creativity, intellectual curiosity, strong communication skills, and the ability to thrive in a collaborative, interdisciplinary environment. This individual will also have a track record of high-quality research, innovative problem-solving, and enthusiasm for addressing challenging questions in immunology and translational science.</p><p><br /><b>What we expect of you:</b><br />We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a candidate with these qualifications.</p><p></p><p><b>Basic Qualifications:</b><br />PhD in a related discipline with 2&#43; years of experience<br />MSc with 5&#43; years of experience.<br />BSc with 8&#43; years of experience.</p><p></p><p><b>Preferred Qualifications:</b><br />• Deep understanding of immunology with expertise in systems immunology approaches and quantitative data analysis.<br />• Experience integrating and analyzing high-dimensional immune profiling datasets including spectral cytometry, secretomics, and transcriptomics.<br />• Strong computational and statistical analysis skills with experience using bioinformatics tools and programming languages such as R and/or Python.<br />• Experience with dimensionality reduction, clustering, and visualization approaches for high-dimensional datasets.<br />• Experience working with multi-omics datasets and developing biologically meaningful interpretations from complex data.<br />• Strong written and verbal communication and interpersonal skills.<br />• Desire to be a team player in a dynamic, cross-functional environment.<br />• Demonstrated scientific analysis and problem-solving skills.<br /> </p><p><b>What you can expect of us</b><br />As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.</p><p></p><p>Amgen is proud to have been recognized as one of LinkedIn Top 25 Companies in Canada for career growth. Click <a href="https://nam11.safelinks.protection.outlook.com/?url&#61;https%3A%2F%2Fwww.linkedin.com%2Fpulse%2Flinkedin-top-companies-2025-25-best-workplaces-grow-your-3mgie&amp;data&#61;05%7C02%7Ctbrawner%40amgen.com%7C17817f6f28cb428f95f308ddb59cbc92%7C4b4266a6136841afad5a59eb634f7ad8%7C0%7C0%7C638866406959632854%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;sdata&#61;%2BtQzUlrLG%2B%2FddGYWmwrOg7DQ9mMamH%2Bo%2BEiO7MMHsow%3D&amp;reserved&#61;0" target="_blank">HERE</a> for more details.</p><p><br />The salary range for this position in Canada is $115,503 - $156,269 CAD.</p><p><br />In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.<br /> </p><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>115,503.10 CAD - 156,268.90 CAD]]></description><link>http://biotechroles.com/sr-scientist-systems-immunology-amgen/6a05f60b2f1861929d2531cd</link><guid isPermaLink="true">http://biotechroles.com/sr-scientist-systems-immunology-amgen/6a05f60b2f1861929d2531cd</guid><pubDate>Thu, 14 May 2026 16:19:23 GMT</pubDate><company>Amgen</company><location>Canada - Burnaby</location><salary>$140000-200000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager Manufacturing Systems Engineering ​- Automation]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Engineering<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b> </p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. </p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. </p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lie within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. </p><p></p><p>Be part of Amgen&#39;s newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen&#39;s plan to be a carbon-neutral company by 2027. </p><p></p><p><b>Senior Manager Manufacturing Systems Engineering</b><b> ​- Automation</b></p><p></p><div><div><p><b><span>What You Will Do</span></b><span> </span></p></div><div><p><span><span>Let’s</span><span><span> </span>do this.<span> </span></span><span>Let’s</span><span><span> </span>change the world. In this role The Senior Manager<span> </span></span><span>is responsible for</span><span><span> </span>providing technical and administrative leadership to a group of Automation Engineers accountable for administrating and<span> </span></span><span>maintaining</span><span><span> </span>automation systems for Drug Substance manufacturing at Amgen<span> </span></span><span>North Carolina</span><span><span> </span>(</span><span>ANC</span><span>). Responsibilities include meeting key performance metrics, leading and technically developing reports, and ensuring all targets and turning points are completed on time. The Sr. Manager also ensures that the automation team<span> </span></span><span>applies</span><span><span> </span>the Corporate Automation Business Processes and drivers to deliver the automation services to the<span> </span></span><span>organization.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>As part of the Facilities&amp; Engineering (F&amp;E) group, the Senior Manager will work with the Director of Engineering at<span> </span></span><span>Amgen</span><span><span> </span></span><span>North Carolina</span><span>. This role is expected to provide leadership as follows:</span></span><span> </span></p></div><div><ul><li><p><span><span>Lead a team of Automation Engineers and serve as the main point of contact for automation function for<span> </span></span><span>ANC</span><span><span> </span></span><span>1<span> </span></span><span>manufacturing</span><span>.</span><span> <span> </span></span><span>Systems including Allen Bradley PLCs, Siemens<span> </span></span><span>D</span><span>esi</span><span>go</span><span><span> </span>CC</span><span><span> </span>for<span> </span></span><span>b</span><span>uilding<span> </span></span><span>a</span><span>utomation, and Emerson<span> </span></span><span>DeltaV</span><span><span> </span>for process control</span><span>.  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Define, drive, and deliver the automation and process control strategy within Drug substance manufacturin</span><span>g</span><span>.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Serve as an experienced advisor to senior level management and ensure the automation development strategy aligns with Amgen Process Development strategy.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strategic and tactical management and leadership in providing 24x7 day-to-day operational support, mentoring, staff development, team productivity, and efficient use of available resources.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Develop support structures with internal/multi-functional teams for capital projects, plant support, and Amgen network-level initiatives&#39; execution.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Provid</span><span><span> </span>input into department<span> </span></span><span>objectives</span><span><span> </span>and<span> </span></span><span>establishing</span><span><span> </span>strategic direction within the Drug Substance Network for the F&amp;E automation team.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Maintain and improve capabilities and automation systems reliability in partnership with F&amp;E and plant leadership, and other technical staff in the network, focusing on “</span><span>Maintenance Excellence</span><span>” systems failures and recurrence avoidance.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Work with diverse groups (Manufacturing, Quality, PD, Automation,<span> </span></span><span>Technology</span><span>, EHSS, Global Engineering) and drive new business processes to ensure continuous and sustained improvements. Translate business needs into engineering technology solutions. Lead analysis of alternatives and recommendations for technical/business proposals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Identify</span><span><span> </span>areas of potential improvement, conduct analysis, recommend solutions, sponsor improvement projects, and implement.</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Ensure site readiness and compliance for internal audits, external agency audits, and partner audits. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensure the safety of all personnel during plant operations and engineering activities.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Develop expense budget<span> </span></span><span>forecast</span><span><span> </span>and adhere to department budgets and spend<span> </span></span><span>for</span><span><span> </span>operational and capital expenses, holding 100% accountability.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Be knowledgeable about compliance and regulatory aspects for operation and maintenance, equipment validation, and support regulatory inspections and audits.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensure Amgen Enterprise cyber resiliency compliance is<span> </span></span><span>maintained</span><span><span> </span>at 100%.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensure the right processes/systems are in place to capture 100% quality compliance for the right-</span><span>first-time</span><span><span> </span>(RFT) delivery of automation solutions.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensure that reporting functionality is incorporated for all unit operations for<span> </span></span><span>production</span><span><span> </span>Batch records, cleaning, and sterilization systems, including Audit trail and version control.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Responsible for ensuring that service contracts with all OEMs for systems are<span> </span></span><span>established</span><span><span> </span>for service and support needs, including service banked hours for specialized support needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensure that all automation staff are adequately trained and follow all GMP standards and procedures by managing the team&#39;s internal and external training needs.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensure the automation staff are fully aware and confident to work on all automation systems, process equipment, and<span> </span></span><span>facility</span><span><span> </span>to provide 24x7 reliable plant automation support.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Responsible for ensuring that the automation team actively<span> </span></span><span>participates</span><span><span> </span>in daily/weekly<span> </span></span><span>Work Center Team (</span><span>WCT</span><span>)</span><span><span> </span>meetings – Manufacturing area</span><span><span> </span></span><span>&amp; plant WCTs, Automation WCT, Automation leadership WCT, etc. to address day-to-day topics and discuss issues with multi-functional teams to resolve.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Responsible for ensuring the automation team provides the required support to implement expense, department capital, construction, and GLAM-DTI projects.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Provide active leadership such that proactive feedback is<span> </span></span><span>solicited</span><span><span> </span>from the automation staff and actions are taken to<span> </span></span><span>maintain</span><span><span> </span>proper work-life balance.</span></span><span> </span></p></li></ul></div><div><p><b><span>What We Expect<span> </span></span><span>Of</span><span><span> </span>You</span></b><span> </span></p></div><div><p><span><span>We are all different, yet we all use our unique contributions to serve patients. The engineering management professional we<span> </span></span><span>seek</span><span><span> </span>will<span> </span></span><span>possess</span><span><span> </span>these qualifications.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>Basic Qualifications:</span></b><span> </span></p></div><div><ul><li><p>High school diploma / GED and 12 years of Engineering and/or Project Management experience OR </p></li></ul><ul><li><p>Associate’s degree and 10 years of Engineering and/or Project Management experience OR </p></li></ul><ul><li><p>Bachelor’s degree and 8 years of Engineering and/or Project Management experience OR </p></li></ul><ul><li><p>Master’s degree and 6 years of Engineering and/or Project Management experience OR </p></li></ul><ul><li><p>Doctorate degree and 2 years of Engineering and/or Project Management experience </p></li></ul><ul><li><p>Additionally: In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above </p></li></ul></div></div><div><div><p><span> </span></p></div><div><p><b><span>Preferred Qualifications:</span></b><span> </span></p></div><div><ul><li><p><span><span>Degree in Electrical Engineering, Computer Science, Chemical Engineering, Biotech Engineering, or related field </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience with Emerson<span> </span></span><span>DeltaV</span><span><span> </span>DCS system</span><span>, Siemens<span> </span></span><span>D</span><span>esigo</span><span><span> </span>CC, Allen Bradley<span> </span></span><span>PLC</span><span><span> </span></span><span>and ability to perform advanced troubleshooting, and system integration using OPC, Foundation Fieldbus, and Profibus technologies</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Direct knowledge of automation system design</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in programming, installation and lifecycle management of automation and field instrumentation technologies</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in automation of GMP biopharmaceutical equipment and systems such as buffer prep and hold, chromatography,<span> </span></span><span>single use</span><span><span> </span>mixing vessels, depth filtration, and solution prep</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in integrating various OEM automation software</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in programming, design, installation and lifecycle management of manufacturing process controls, and automation and field instrumentation technologies. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span> Fieldbus, and Profibus technologies</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to interpret and apply GAMPs and GMPs, and familiarity with documentation in a highly regulated environment with requirements such as 21 CFR Part 11, ASTM 2500, S88 and S95</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Self-directed team player able to work cross-functionally </span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Strong leadership, technical writing, and communication skills</span></span><span> </span></p></li></ul><p></p><p><b>Thrive</b> </p><p><b>What you can expect of us</b> </p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.  </p><p>Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:  </p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.  </p></li></ul><ul><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan </p></li></ul><ul><li><p>Stock-based long-term incentives  </p></li></ul><ul><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns  </p></li></ul><ul><li><p>Flexible work models, including remote work arrangements, where possible </p></li></ul><p></p><p><b>Apply now</b> <b>for a career that defies imagination</b> </p><p>Objects in your future are closer than they appear. Join us. </p><p></p><p><b>careers.amgen.com</b> </p><p></p><p>#AmgenNorthCarolina  </p><p></p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. </p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. </p></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>163,288.40USD -220,919.60 USD]]></description><link>http://biotechroles.com/senior-manager-manufacturing-systems-engineering-automation-amgen/6a05f60b2f1861929d2531cc</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-manufacturing-systems-engineering-automation-amgen/6a05f60b2f1861929d2531cc</guid><pubDate>Thu, 14 May 2026 16:19:23 GMT</pubDate><company>Amgen</company><location>US - North Carolina - Holly Springs</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, US Forecasting]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales &amp; Marketing Operations<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p><b>Senior Manager, US Forecasting</b></p><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. The Forecasting team at Amgen plays a pivotal role as a strategic partner to Commercial leadership, offering data-backed insights crucial for driving commercial success. As a Forecasting Senior Manager, you will contribute significantly to our inline brand strategy, executing and managing discussions with brand leads and commercial leaders.</p><p>The individual in this role will need to strategically influence and challenge a diverse set of collaborators from Commercial, R&amp;D, Medical, Finance, Manufacturing, Access, and Pricing/Contracting, while proficiently understanding the nuances of the particular disease area of interest and markets they support.</p><p>This role reports to the Director of Forecasting and operates within the broader framework of Business Analytics and Insights (BAI).</p><p><b>Flexible Commuter role to Thousand Oaks office. You will work on-site 2-3 days a week.</b></p><h2>Advanced Forecasting Techniques:</h2><ul><li>Ability to build detailed and advanced forecast model (patient, Rx, sales, Rx Based, etc.) projecting units and revenue for our inline products by indication/regions</li><li>Use advanced simulation models (e.g., Monte Carlo analysis, statistical trending) to quantify uncertainty</li><li>Leverage diverse pharmaceutical data sources and their nuances to enhance forecasting approaches and methodologies</li><li>Leads methodology development and ensures consistency across multiple brand forecasts</li><li>Designs forecasting frameworks adaptable for &#39;what-if&#39; and scenario planning</li></ul><h2>Market Analysis and Competitor Intelligence:</h2><ul><li>Analyze competitors and market dynamics to inform forecasting models and strategic decisions</li><li>Develop an objective brand strategy by integrating insights across multiple functions and capability areas</li><li>Interprets policy and pricing changes (e.g., IRA, access shifts) and quantifies their impact</li></ul><h2>Collaboration and Stakeholder Engagement:</h2><ul><li>Act as the key point of contact for global brand leads, engaging them in forecasting deliverables</li><li>Facilitate discussions and build consensus among partners to establish clear and rigorous worldwide sales expectations for pipeline assets</li><li>Advises cross-functional teams on implications of clinical milestones and competitive events</li><li>Owns multi-brand forecasts; challenges entrenched assumptions; drives process improvements across cycles</li></ul><h2>Strategic Insights and Recommendations:</h2><ul><li>Support leadership in identifying actionable strategies to improve Commercial potential, prioritizing risks and opportunities</li><li>Provide informed recommendations on product development continuation or discontinuation based on market conditions, financial projections, and strategic goals</li><li>Maintains awareness of broader market dynamics and integrates them into TA-level forecasts</li></ul><h2>Communication and Presentation:</h2><ul><li>Develop and deliver transparent presentations that articulate key variables in the forecast, ensuring comprehensive understanding for decision-makers</li><li>Use communication and interpersonal skills to influence leadership on recommended courses of action</li><li>Narrates drivers of forecast change; frames forecasts in terms of strategic risks and opportunities</li></ul><h2>Collaboration with BAI:</h2><ul><li>Collaborate with the broader BAI organization to integrate comprehensive insights and analytics knowledge into forecast development</li><li>Improve the depth and accuracy of forecasts by leveraging a broad spectrum of insights across the organization</li><li>Explores AI/ML and automation; identifies team capability gaps and builds skills.</li></ul><h2>Process Optimization:</h2><ul><li>Drive productivity and efficiency by streamlining forecasting processes where possible</li><li>Oversees deliverables across brands/assets; ensures forecasts are auditable and scalable</li></ul><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The forecasting professional we seek is a leader with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 2 years of Pharma/Biotech forecasting, demand planning, or supply chain management experience</p><p>OR</p><p>Master’s degree and 4 years of Pharma/Biotech forecasting, demand planning, or supply chain management experience</p><p>OR</p><p>Bachelor’s degree and 6 years of Pharma/Biotech forecasting, demand planning, or supply chain management experience</p><p>OR</p><p>Associate’s degree and 10 years of Pharma/Biotech forecasting, demand planning, or supply chain management experience</p><p>OR</p><p>High school diploma / GED and 12 years of Pharma/Biotech forecasting, demand planning, or supply chain management experience</p><p><b>Preferred Qualifications:</b></p><ul><li>Ability to quickly establish credibility with and influence ED/VP level staff</li><li>Knowledge and experience working with industry internal and secondary data sources; experience doing analog and uptake curve analysis</li><li>Proficiency in advanced forecasting techniques, statistical modeling, and data analysis.</li><li>Highly skilled in working collaboratively in a team-based environment and gaining alignment across an organization</li><li>High level of proficiency in Excel, PowerPoint, Word</li><li>Excellent communication skills with the ability to present complex data and insights to both technical and non-technical partners</li><li>Ability to interpret and analyze data trends, identify patterns, and make data-driven decisions</li><li>Experience in contributing to the development of long-term business plans based on forecasting insights</li></ul><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models, including remote and hybrid work arrangements, where possible</li></ul><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>141,736.65USD -191,761.35 USD]]></description><link>http://biotechroles.com/senior-manager-us-forecasting-amgen/6a05f60a2f1861929d2531cb</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-us-forecasting-amgen/6a05f60a2f1861929d2531cb</guid><pubDate>Thu, 14 May 2026 16:19:22 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[CDnA - Competitive Intelligence Manager, R&D Competitive Intelligence and AI Innovation]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales &amp; Marketing Operations<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>CDnA - Competitive Intelligence Manager, R&amp;D Competitive Intelligence and AI Innovation</b></p><p></p><p><b>What you will do</b></p><p></p><p>In this vital role you will serve as a Competitive Intelligence Manager with a focus on identifying, developing, and deploying AI/ML-enabled solutions that improve how Business Analytics and Insights teams generate, synthesize, and activate competitive intelligence. This role will report directly to the Director/Sr Director, Competitive Intelligence.</p><p></p><p><b>Responsibilities</b></p><ul><li><p>Act as the primary bridge between Business Analytics and Insights stakeholders and technology stakeholders, translating business needs across Competitive Intelligence, Forecasting, Marketing, Medical, R&amp;D, and Commercial teams into actionable AI/ML and digital product requirements</p></li><li><p>Identify high-friction competitive intelligence and analytics workflows that can be solved or improved through agentic AI, large language models, machine learning, automation, and advanced knowledge-management solutions</p></li><li><p>Partner with cross-functional business teams to define key intelligence questions, user needs, success criteria, and adoption requirements for CI-focused AI/ML tools and internal capabilities</p></li><li><p>Lead hands-on development of functional MVPs, prototypes, and internal tools using modern technology stacks such as workflow orchestration platforms, Python/TypeScript, LLM APIs, vector databases, knowledge graphs, and structured/unstructured data sources</p></li><li><p>Leverage AI-assisted coding and development tools such as Codex, Claude Code, Cursor, Replit, and similar platforms to accelerate development velocity from idea to deployed internal tool</p></li><li><p>Serve as technical product owner for successful CI prototypes, including defining product requirements, user workflows, testing plans, governance considerations, and value measurement</p></li><li><p>Once a tool is proven valuable, define the target architecture and hand-off approach for Enterprise IT, DevOps, vendors, or other technology partners to support long-term maintenance, scaling, and operationalization</p></li><li><p>Synthesize competitive intelligence, market events, scientific and medical developments, clinical trial updates, and other external signals into actionable insights for internal stakeholders</p></li><li><p>Leverage secondary research resources and internal/external data sources to support hypothesis-driven competitive intelligence, opportunity assessment, scenario planning, and business decision-making</p></li><li><p>Manage multiple simultaneous initiatives across competitive intelligence, AI/ML enablement, business analytics and insights (BAI), and digital product development</p></li><li><p>Abide by and strictly enforce Amgen’s CI Legal and Ethical Guidelines with internal colleagues and agencies.</p></li><li><p>Some travel (&lt;10%) required.</p></li></ul><p></p><p><b>What we expect of you</b></p><p></p><p>We are all different, yet we all use our unique contributions to serve patients. The competitive intelligence professional we seek is a collaborator, builder, and digital product owner with these qualifications.</p><p></p><p></p><p><b>Basic Qualifications:</b></p><p></p><p>Doctorate degree<br />OR<br />Master’s degree and 2 years of Competitive Intelligence, Business Development, Tech Transfer, Equity Research, Consulting, Patent Law, Business Analytics, Data Science, Digital Product Management, or AI/ML solution development experience<br />OR<br />Bachelor’s degree and 4 years of Competitive Intelligence, Business Development, Tech Transfer, Equity Research, Consulting, Patent Law, Business Analytics, Data Science, Digital Product Management, or AI/ML solution development experience<br />OR<br />Associate’s degree and 8 years of Competitive Intelligence, Business Development, Tech Transfer, Equity Research, Consulting, Patent Law, Business Analytics, Data Science, Digital Product Management, or AI/ML solution development experience<br />OR<br />High school diploma / GED and 10 years of Competitive Intelligence, Business Development, Tech Transfer, Equity Research, Consulting, Patent Law, Business Analytics, Data Science, Digital Product Management, or AI/ML solution development experience</p><p></p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Strong communicator with proven ability to generate succinct insights from complex scientific, clinical, market, technical, and business data for diverse stakeholders of various functions and levels</p></li><li><p>Experience in competitive intelligence, business analytics, forecasting, marketing, R&amp;D, medical, commercial strategy, business development, consulting, equity research, tech transfer, patent law, digital product ownership, or similar roles</p></li><li><p>Knowledge of basic principles of functions across the pharmaceutical value chain, including drug discovery and development, clinical trials, FDA / EMA regulation, commercialization, forecasting, and lifecycle planning</p></li><li><p>Proven track record managing multiple, simultaneous projects and working with proprietary technical, regulatory, competitive, financial, and business data sources</p></li><li><p>Experience supporting insight generation by coordinating with cross-functional R&amp;D, commercial, medical, scientific, forecasting, marketing, technology, and analytics teams to inform therapeutic area strategy</p></li><li><p>Ability to analyze competitive events, ongoing clinical trials, global regulatory considerations, market dynamics, and competitor behavior to develop scenarios for launch timing, market share, and strategic implications</p></li><li><p>Understanding of pharmaceutical forecasting models and ability to provide competitor-focused assumptions in support of long-range planning scenarios, go/no-go decisions, opportunity assessments, and business development activities</p></li><li><p>Hands-on fluency with workflow orchestration and automation tools such as n8n, LangChain, Zapier, or similar platforms</p></li><li><p>Proficiency in scripting, preferably Python or TypeScript, for API integrations, data processing, prototyping, and internal tool development</p></li><li><p>Deep understanding of LLM capabilities and solution patterns, including retrieval-augmented generation, function calling, agents, prompt engineering, evaluation, and responsible deployment considerations</p></li><li><p>Experience using AI-assisted coding and development tools such as Codex, Claude Code, Cursor, Replit, or similar platforms</p></li><li><p>Ability to navigate a cross-functional, matrixed organization and translate effectively between business stakeholders and technology, developer, vendor, or enterprise IT teams</p></li><li><p>Self-starter mentality with an engineering mindset, comfort operating in ambiguity, and ability to move from business problem definition to prototype, testing, refinement, deployment, and scale-up planning</p></li><li><p>Passion for learning emerging AI/ML capabilities and applying that knowledge to create practical, high-impact competitive intelligence solutions that help teams make faster, better-informed decisions</p></li></ul><p></p><p></p><p><b><span>LOCATION: </span></b><span>This role is for a Hybrid Position, with a requirement to be on-site in Thousand Oaks, CA or Deerfield, IL Tuesday and Wednesday each week, and rarely additional days when required (e.g., for workshops, stakeholder meetings). </span></p><p></p><p><b>What you can expect of us</b></p><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><p></p><ul><li><p>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans</p></li><li><p>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</p></li></ul><p></p><p></p><p>Apply now and make a lasting impact with the Amgen team.</p><p></p><p>careers.amgen.com</p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p>Application deadline</p><p></p><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p>Sponsorship</p><p></p><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>124,295.50USD -168,164.50 USD]]></description><link>http://biotechroles.com/cdna-competitive-intelligence-manager-randd-competitive-intelligence-and-ai-innovation-amgen/6a05f60a2f1861929d2531ca</link><guid isPermaLink="true">http://biotechroles.com/cdna-competitive-intelligence-manager-randd-competitive-intelligence-and-ai-innovation-amgen/6a05f60a2f1861929d2531ca</guid><pubDate>Thu, 14 May 2026 16:19:22 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$135000-185000</salary><type>Full time</type></item><item><title><![CDATA[Senior Scientist: Synthetic Biology, Molecular engineering, and NGS]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Scientific<h2></h2><h2><b>Job Description</b></h2><p>Senior Scientist (5-2) – Synthetic Biology, Molecular Engineering and NGS</p><p>Thousand Oaks, CA</p><div></div><h2>Join Amgen’s Mission of Serving Patients</h2><p></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Synthetic Biology, Molecular Engineering and NGS</b></p><p></p><h2><b>What you will do</b></h2><p></p><h2>What you can expect from us</h2><p>Let’s change the world.</p><p>Amgen Protein Therapeutics is seeking a highly motivated Scientist to join our multidisciplinary team in Thousand Oaks, CA. Our group integrates protein engineering and design, synthetic biology, protein chemistry and advanced analytics to develop next-generation biologic therapeutics.</p><p>You are a creative, critical thinker with a passion for innovation, with strengths in synthetic biology and molecular engineering.  In this role, you will help develop and deploy novel synthetic biology and sequencing workflows that enable rapid and scalable realization of complex protein designs, central to advancing the frontier of therapeutic biologic development in the service of patients.</p><p><b>At Amgen, you will: </b></p><ul><li>Deploy and execute innovative, integrated synthetic biology and NGS capabilities to advance programs in Amgen’s large molecule portfolio.</li><li>Partner with cross-functional teams to enable seamless design-build-test cycles at speed to drive iterative learning at scale.</li><li>Collaborate to translate early-stage ideas into robust, high-throughput experimental workflows, including opportunities to contribute to automation-enabled pipelines.</li><li>Work within and contribute towards the success of a supportive, collaborative team engaging with a deep commitment to excellence in scientific rigor and inquiry, high-quality data generation and documentation, and clear, timely and considerate communication.</li></ul><p><b>What we expect of you:</b></p><p>We recognize that strong candidates may bring different combinations of skills and experiences. The scientific professional we seek is curious, resilient, and motivated to tackle complex biological problems, and will have the experience that aligns with many of these qualifications.  If you are excited about this role, we encourage you to apply - even if you don’t meet every qualification listed.</p><p><b>Basic Qualifications</b></p><p>Doctorate degree (PhD) in Molecular Biology, Synthetic Biology, Biochemistry, or a related field<br />OR<br />Master’s degree and 2 years of scientific experience<br />OR<br />Bachelor’s degree and 4 years of scientific experience</p><p><b>Required Qualifications</b></p><ul><li>Strong practical and theoretical experience in molecular/synthetic biology.</li><li>Experience in Next Generation Sequencing.</li><li>Demonstrated ability to optimize experiments and troubleshoot molecular biology workflows with a detail-oriented and thoughtful approach.  </li><li>Clear communicator and collegial collaborator who can work in teams to achieve excellence in fast-paced, cutting-edge laboratory environment.</li></ul><p><b>Preferred Qualifications</b></p><ul><li>Experience or exposure to laboratory automation and scripting.</li><li>Laboratory management experience, that may include equipment maintenance, reagent supply, Laboratory Information Management Systems and capacity planning.</li><li>Experience with NGS data analysis, or high-throughput sample management and large volume data analysis and documentation. </li></ul><p></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><p></p><h2>Apply now and make a lasting impact with the Amgen team.</h2><p><b>careers.amgen.com</b></p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><h2>Application deadline</h2><p></p><h2><b>External/Internal postings: </b></h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><h2><b>Internal only posting (or Pre-ID candidate): </b></h2><p>Amgen anticipates accepting applications however, we may continue accepting applications beyond this date if we do not receive a sufficient number of candidates.</p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p></p><h2></h2><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>127,121.75USD -171,988.25 USD]]></description><link>http://biotechroles.com/senior-scientist-synthetic-biology-molecular-engineering-and-ngs-amgen/6a05f6092f1861929d2531c9</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-synthetic-biology-molecular-engineering-and-ngs-amgen/6a05f6092f1861929d2531c9</guid><pubDate>Thu, 14 May 2026 16:19:21 GMT</pubDate><company>Amgen</company><location>US - California - Thousand Oaks</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Dir Observational Research]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Clinical<h2></h2><h2><b>Job Description</b></h2><h2>Join Amgen’s Mission of Serving Patients</h2><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><h2><b>Dir Observational Research</b></h2><h2><b>What you will do</b></h2><p>Let’s do this. Let’s change the world. In this vital role you will leads the company&#39;s strategic planning initiatives and oversees its operational performance, working with leaders across the organization to implement the strategic vision.</p><p>Do you want an exciting position working with multiple teams to generate real-world evidence supporting a wide variety of business needs?</p><p>The growing demand for real-world evidence (RWE) from regulatory and reimbursement authorities makes observational research a key component of drug development and commercialization. Amgen&#39;s Center for Observational Research (CfOR) is a global organization with an industry-leading analytical capability that generates RWE to support business needs across a product’s lifecycle. CfOR scientists partner with internal collaborators and industry experts to craft, conduct, interpret, and publish observational research that advises decision-making from the early development of a molecule to the design of clinical trials and the safety and efficacy of Amgen medicines. CfOR studies include but are not limited to evidence generation regarding the frequency and distribution of disease, the clinical burden of disease, the natural history or clinical course of the disease, the design of clinical trials, treatment cost, and utilization patterns, and the safety and efficiency of therapeutic interventions.</p><p><b>Job Description</b></p><p>Amgen is searching for a Director of Observational Research, who will lead an asset in the Oncology therapeutic area. A CfOR director is recognized as a strong scientific contributor and is a first or contributing author for papers in peer-reviewed journals or for internal reports that enhance the company’s mission. Working with the cross-functional teams, the Director will be responsible for establishing strategic direction, and providing technical and managerial leadership through:</p><ul><li>Designing and executing studies to support evidence generation such as identifying appropriate patient populations, assessing disease burden and resource utilization, obtaining product registrations and label-expansions, meeting post-marketing requirements/commitments and product differentiation.</li><li>Finding opportunities to substitute for and/or complement interventional studies to reduce time and cost of drug development.</li><li>Influencing cross-functional stakeholders in the utilization and timing of non-interventional research to answer high-priority strategic business questions.</li><li>Leveraging real-world data and CfOR analytic approaches to inform high-value business decisions for multiple partners.</li><li>Tracking business and functional priorities and aligning resources for those priorities.</li><li>Contributing to the mission of the CfOR including progressing innovative epidemiological methods and analytical capabilities to support the CfOR’s leadership role within Amgen and the industry.</li><li>Effectively leading, developing and mentoring staff and teams.</li><li>Participating in initiatives to improve capabilities within the CfOR and providing input.</li><li>Supporting the development of product and CfOR strategies.</li><li>Developing and maintaining relationships with organizational leaders.</li></ul><p></p><h2><b>What we expect of you</b></h2><p>We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a leader with these qualifications.</p><p><b>Basic Qualifications:</b></p><p>Doctorate degree and 4 years of scientific experience OR</p><p>Master&#39;s degree and 7 years of scientific experience  OR</p><p>Bachelor&#39;s Degree and 9 years of scientific experience OR</p><p>Associate’s degree and 10 years of scientific experience OR</p><p>High school diploma / GED &amp; 12 years of scientific experience</p><p><b>Preferred Qualifications:</b></p><h2>•Doctorate in Epidemiology or other subject with high observational research content</h2><h2>•Experience in the design, execution, and analysis of observational research studies within Pharmaceutical or Public Health setting</h2><h2>•Experience in research to support drug development</h2><h2>•Experience in observational research project planning and management</h2><h2>•Excellent verbal and writing communication and interpersonal skills</h2><h2>•Experience working in multi-disciplinary teams</h2><p></p><h2><b>What you can expect of us</b></h2><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.</li></ul><h2>Apply now and make a lasting impact with the Amgen team.</h2><h2><b>careers.amgen.com</b></h2><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><h2>Application deadline</h2><p>Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>202,250.70USD -273,633.30 USD]]></description><link>http://biotechroles.com/dir-observational-research-amgen/6a05f6092f1861929d2531c8</link><guid isPermaLink="true">http://biotechroles.com/dir-observational-research-amgen/6a05f6092f1861929d2531c8</guid><pubDate>Thu, 14 May 2026 16:19:21 GMT</pubDate><company>Amgen</company><location>United States - Remote</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Sr Biopharmaceutical Rep (General Medicine)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p></p><p><b><span>HOW MIGHT YOU DEFY IMAGINATION?</span></b></p><p>Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but has also invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a Biopharmaceutical Account Executive/Manager in Singapore<i><span>.</span></i></p><p></p><p><b><span>Live</span></b></p><p><b><span>What you will do:</span></b></p><p></p><p>Reporting to the Sales Manager, you will maximize sales of Amgen’s products in territory, achieve sales targets, collaborate with the team to implement agreed plan of action (POA) in line with marketing strategy. You will also identify and establish high quality customer relationships and internal collaboration. You must possess in depth knowledge of the product, market, stakeholders and competition.</p><p></p><p>Main Responsibilities</p><ul><li>Collaborates with manager to develop and implement territory POA and key account plans. Achieve POA.</li><li>Evaluates progress vs. plan monthly and agrees to course corrections with manager</li><li>Contributes to Cluster/Territory Teams Collaborates (Medical Affairs/Key Account Manager, etc.) to agree on key account plan <span>objectives/responsibilities</span></li><li>Engages with peers and manager to learn best practices</li><li>Demonstrates an understanding of industry and healthcare trends, of how retail practices, clinics and hospitals operate.</li><li>Identifies and gathers competitive information</li><li>Follows through on customer commitments and requests in a timely fashion</li><li>Reports customer activity in the CRM system and ensures customer profiles are kept up to date</li><li>Demonstrates an understanding of Amgen Performance 4 selling platform to satisfy customer and Amgen needs</li><li>Operates within the agreed expense budget aligned with POA priorities</li><li>Seeks advice and assistance to organize activities</li><li>Continuously develops and improves product knowledge, communication and selling skills through self-learning and active participation in agreed training programs. Drives own development</li></ul><p></p><p><b><span>Win</span></b></p><p><b><span>What we expect of you:</span></b></p><p></p><p>Minimum Requirements</p><ul><li>Minimum 2 to 5 years of experience in the orthopedic, endocrinology and general medicine</li><li>Knowledge of and experience in a hospital environment</li><li>Basic exposure to marketing project will be an advantage</li><li>Some experience with computer systems (CRM databases and MS Office)</li><li>Relevant local legal qualification</li></ul><p></p><p>Preferred Requirements</p><ul><li>Bachelor’s degree in life science or (bio) medical sciences</li><li>Knowledge of Customer <span>Relation Management</span> principles</li><li>Exposure to interactions with various disciplines and organizational levels</li><li>Exposure to project management principles</li></ul><p></p><p><b><span>Thrive</span></b></p><p><b><span>What you can expect of us:</span></b></p><p>As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.</p><ul><li>Vast opportunities to learn and move up and across our global organization</li><li>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul><p></p><p><b><span>Apply now for a career that defies imagination.</span></b></p><p>In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.</p><p></p><p>careers.amgen.com</p><p></p><p><b><span>Equal Opportunity Statement</span></b></p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-biopharmaceutical-rep-general-medicine-amgen/6a05f6082f1861929d2531c7</link><guid isPermaLink="true">http://biotechroles.com/sr-biopharmaceutical-rep-general-medicine-amgen/6a05f6082f1861929d2531c7</guid><pubDate>Thu, 14 May 2026 16:19:20 GMT</pubDate><company>Amgen</company><location>Singapore Affiliate - Duo Tower</location><salary>$80000-120000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Biopharmaceutical Rep, CV]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p><b>MAIN RESPONSIBILITIES: </b></p><ul><li>Achieves sales target</li><li>Deliver scientific information and key message on the product including therapeutic indication, disease states and latest clinical data</li><li>Collaborates with manager to implement agreed POA in line with marketing strategy</li><li>Identifies and establishes high quality customer relationships and internal collaboration</li><li>Organize and implement scientific events to efficiently deliver product information</li><li>Knows in-depth knowledge of the product(s), market, stakeholders and competitors</li><li>Works within agreed budgets</li><li>Lives the Amgen Values</li></ul><p> <b>REQUIREMENTS:</b></p><ul><li>University degree</li><li>Minimum 3 years of sales experience in university hospital channel</li><li><b>Experience in market</b><b> </b><b>preferred </b></li><li>Skill and knowledge of territory planning, sales analysis and sales excellence.</li><li>Possess a high level of business ethics, integrity and professionalism and the ability to ensure those standards  </li><li>Excellent communication skill and interpersonal skill</li><li>Good command of written and spoken English is preferred</li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-biopharmaceutical-rep-cv-amgen/6a05f6082f1861929d2531c6</link><guid isPermaLink="true">http://biotechroles.com/sr-biopharmaceutical-rep-cv-amgen/6a05f6082f1861929d2531c6</guid><pubDate>Thu, 14 May 2026 16:19:20 GMT</pubDate><company>Amgen</company><location>South Korea - Seoul</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Biopharmaceutical Rep, bone]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p><b>MAIN RESPONSIBILITIES:</b><br />• Achieves sales target<br />• Deliver scientific information and key message on the product including therapeutic indication, disease states and latest clinical data<br />• Collaborates with manager to implement agreed POA in line with marketing strategy<br />• Identifies and establishes high quality customer relationships and internal collaboration<br />• Organize and implement scientific events to efficiently deliver product information<br />• Knows in-depth knowledge of the product(s), market, stakeholders and competitors<br />• Works within agreed budgets<br />• Lives the Amgen Values</p><p></p><p><b>REQUIREMENTS:</b><br />• University degree<br />• Minimum 3 years of sales experience in university hospital channel<br />• Experience in related therapeutic market preferred<br />• Skill and knowledge of territory planning, sales analysis and sales excellence.<br />• Possess a high level of business ethics, integrity and professionalism and the ability to ensure those standards<br />• Excellent communication skill and interpersonal skill<br />• Good command of written and spoken English is preferred</p><p></p><p><b>Location/Territory: </b>Seoul, Gyeonggi-do, and Gangwon-do</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-biopharmaceutical-rep-bone-amgen/6a05f6082f1861929d2531c5</link><guid isPermaLink="true">http://biotechroles.com/sr-biopharmaceutical-rep-bone-amgen/6a05f6082f1861929d2531c5</guid><pubDate>Thu, 14 May 2026 16:19:20 GMT</pubDate><company>Amgen</company><location>South Korea - Seoul</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Specialty Account Manager - UPLIZNA -Rare Disease- Nashville, TN]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p>Join Amgen’s Mission of Serving Patients</p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p><b>Account Manager/Specialty Account Manager - Rare Disease </b></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will be responsible for representing UPLIZNA to physicians and health care professionals, establishing product sales, and performing total territory account management.</p><p>The Specialty Account Manager is responsible for providing account management support to accounts within a specific geography in the designated marketplace with a focus on issues specific to their designated accounts. The SAM acts as central account manager; responsible for driving product demand and coordinating relevant field teams to address account needs.</p><ul><li><p>Develops a comprehensive and effective territory business plan aimed at achieving and exceeding annual sales goals established by sales and business unit leadership.</p></li><li><p>Promotes UPLIZNA within approved labeling in a comprehensive, fair and ethical manner that is consistent with industry specific and corporate legal and regulatory guidelines.</p></li><li><p>Addresses issues related to access, pull-through, and reimbursement by coordinating with key stakeholders and matrix team members.</p></li><li><p>Develops strong customer relationships by better understanding the customer’s needs and goals and communicating those needs and goals to other team members.</p></li><li><p>Consistently meets or exceeds corporate sales goals.</p></li><li><p>Communicates territory activity in an accurate and timely manner as directed by management.</p></li><li><p>Drive product demand among targets through education on disease state and product information.</p></li><li><p>Provides feedback to sales and business unit leadership, colleagues, and other internal departments about changing environment and results.</p></li><li><p>Adheres to the Company’s compliance policies and guidelines as well as any other applicable guidelines, including but not limited to the PhRMA code.</p></li><li><p>Must be able to work closely with patient services and market access team members, and understand their roles, to achieve overall business goals,</p></li><li><p>Coordinate between accounts and relevant Amgen field teams to support full range of account needs,</p></li><li><p>Educate healthcare professionals and office staff on site of care options.</p></li><li><p>Attends medical congresses and society meetings as needed.</p></li><li><p>Manages efforts within assigned promotional and operational budget.</p></li><li><p>Maximizes use of approved resources to achieve territory and account level goals</p></li><li><p>Successfully completes all Company training classes.</p></li><li><p>Completes administrative duties in an accurate and timely fashion.</p></li><li><p>Functions as a contributing member of a high-performance team.</p></li><li><p>Perform such other tasks and responsibilities as requested by the Company.</p></li></ul><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The Specialty Account Manager we seek is a motivated professional with these qualifications.</p><p><b>Basic Qualifications (Account Manager – Level 4)</b></p><p>Bachelor&#39;s Degree and 3 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />Associate degree and 6 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />High school diploma/GED and 8 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience</p><p></p><p><b>Basic Qualifications (Specialty Account Manager – Level 5)</b></p><p>Doctorate degree &amp; 2 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Master’s degree &amp; 6 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Bachelor’s degree &amp; 8 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Associate degree &amp; 10 years of collective account management experience, sales, &amp; commercial experience</p><p><b>Preferred Qualifications:</b></p><ul><li><p>Demonstrated success in a role involving reimbursement navigation, site of care education, and/or patient access coordination.</p></li><li><p>Experience promoting a product that requires extensive coordination with office staff, infusion centers, and patient services teams.</p></li><li><p>Proven ability to build strong customer relationships, educate on complex disease states, and adapt communication to diverse audiences.</p></li><li><p>Buy-and-bill experience with documented success and/or biologic/infusion experience strongly preferred.</p></li><li><p>Sales experience in Rheumatology, Gastroenterology, Nephrology, Hematology, Neurology, and/or rare/specialty disease states preferred.</p></li><li><p>Site of care and reimbursement experience strongly preferred.</p></li><li><p>Experience working with institutions and integrated delivery networks preferred.</p></li><li><p>Pharma account management selling experience essential; must be able to coordinate across field teams to address full range of account needs.</p></li><li><p>Approximately 80% travel (may vary by territory), including some overnight and weekend commitments.</p></li><li><p>Proficient in Microsoft Office.</p></li><li><p>Professional, proactive demeanor.</p></li><li><p>Strong interpersonal skills.</p></li><li><p>Excellent written and verbal communication skills.</p></li></ul><p></p><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is (Account Manager – Level 4) $154,736 - $183,900 (Specialty Account Manager – Level 5) $160,397 - $190,628. In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models, including remote work arrangements, where possible</p></li></ul><p><b>Apply now </b> </p><p><b>For a career that defies imagination</b> </p><p>Objects in your future are closer than they appear. Join us.<b>careers.amgen.com</b> </p><p></p><p><b>Application deadline</b></p><p><b>External/Internal postings: </b></p><p>Amgen&#39;s application deadline is 5/30/2026 for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p>accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/specialty-account-manager-uplizna-rare-disease-nashville-tn-amgen/6a05f6062f1861929d2531c4</link><guid isPermaLink="true">http://biotechroles.com/specialty-account-manager-uplizna-rare-disease-nashville-tn-amgen/6a05f6062f1861929d2531c4</guid><pubDate>Thu, 14 May 2026 16:19:18 GMT</pubDate><company>Amgen</company><location>US - Tennessee - Nashville-Davidson</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Account Manager/Specialty Account Manager, Rheumatology (Rare Disease) Kansas City, MO]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p>Join Amgen’s Mission of Serving Patients</p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role In this vital role you will be responsible for representing KRYSTEXXA to physicians and health care professionals, establishing product sales, and performing total territory account management.</p><p>The Specialty Account Manager, Rheumatology is responsible for representing Amgen products to physicians and healthcare professionals, establishing Biotech/Infusion product sales, and performing total territory account management. The NSAM is also responsible for providing account management support to Rheumatology accounts within a specific geography.</p><ul><li><p>Develops a comprehensive and effective territory business plan aimed at achieving and exceeding annual sales goals established by commercial leadership.</p></li><li><p>Promotes KRYSTEXXA within approved labeling in a comprehensive, fair and ethical manner that is consistent with industry specific and corporate legal and regulatory guidelines.</p></li><li><p>Develops strong customer relationships by better understanding the customer’s needs and goals and communicating those needs and goals to other Amgen team members.</p></li><li><p>Serves as a resource/consultant to customers and Amgen staff regarding local, regional and national payer policies, reimbursement regulations and processes (i.e., eligibility and benefit verification, prior-authorization, billing, coding, claims, and appeals/denials), Medicare and Medicaid rules and regulations, and OSHA and HIPAA compliance as related to Amgen products.</p></li><li><p>Consistently meets or exceeds corporate sales goals.</p></li><li><p>Communicates territory activity in an accurate and timely manner as directed by management.</p></li><li><p>Provides feedback to sales and commercial leadership, colleagues, marketing, and other internal departments about changing environment and results.</p></li><li><p>Adheres to the Amgen’s compliance policies and guidelines as well as any other applicable guidelines, including but not limited to the PhRMA code.</p></li><li><p>Successfully completes all Amgen training classes.</p></li><li><p>Completes administrative duties in an accurate and timely fashion.</p></li><li><p>Manages efforts within assigned promotional and operational budget.</p></li><li><p>Maximizes use of approved resources to achieve territory and account level goals.</p></li><li><p>Must be able to work closely with and effectively collaborate across all divisions within the GBU to achieve business objectives.</p></li><li><p>Attends medical congresses and society meetings as needed.</p></li><li><p>Perform such other tasks and responsibilities as requested by management from time to time.</p></li></ul><p></p><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The Specialty Account Manager we seek is a motivated professional with these qualifications.</p><p></p><p><b>Basic Qualifications (Account Manager – Level 4)</b></p><p>Bachelor&#39;s Degree and 3 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />Associate degree and 6 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />High school diploma/GED and 8 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience</p><p></p><p><b>Basic Qualifications (Specialty Account Manager – Level 5)</b></p><p>Doctorate degree &amp; 2 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Master’s degree &amp; 6 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Bachelor’s degree &amp; 8 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Associate degree &amp; 10 years of collective account management experience, sales, &amp; commercial experience</p><p><b>Preferred Qualifications:</b></p><ul><li><p>Minimum of 2 years’ sales experience in Rheumatology therapeutic area.</p></li><li><p>Buy and bill experience and success strongly preferred.</p></li><li><p>Biologic/biotech sales and reimbursement experience strongly preferred.</p></li><li><p>Rheumatology therapeutic area experience strongly preferred.</p></li><li><p>Experience working with institutions and integrated delivery networks preferred.</p></li><li><p>Experience working in a team environment which successfully partners with all Commercial Operations functions.</p></li><li><p>Proficient in Microsoft Office.</p></li><li><p>Professional, proactive demeanor.</p></li><li><p>Strong interpersonal skills.</p></li><li><p>Excellent written and verbal communication skills.</p></li><li><p>Strong organizational, analytical and computer skills.</p></li><li><p>Requires approximately 20-30% travel, including some overnight and weekend commitments.</p></li></ul><p></p><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is (Account Manager – Level 4) $145,311 - $196,597 (Specialty Account Manager – Level 5) $158,931 - $215,025. In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models, including remote work arrangements, where possible</p></li></ul><p></p><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p></p><p>Application deadline</p><p>Amgen&#39;s application deadline is 6/8 for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p>#CLOLI</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/account-managerspecialty-account-manager-rheumatology-rare-disease-kansas-city-mo-amgen/6a05f6062f1861929d2531c3</link><guid isPermaLink="true">http://biotechroles.com/account-managerspecialty-account-manager-rheumatology-rare-disease-kansas-city-mo-amgen/6a05f6062f1861929d2531c3</guid><pubDate>Thu, 14 May 2026 16:19:18 GMT</pubDate><company>Amgen</company><location>US - Missouri - Kansas City</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Account Manager/Specialty Account Manager, Endocrinology (Rare Disease) Atlanta West, GA]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Sales<h2></h2><h2><b>Job Description</b></h2><p></p><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>Account Manager/Specialty Account Manager - TEPEZZA</b></p><p></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role you will be responsible for representing TEPEZZA to physicians and health care professionals, establishing product sales, and performing total territory account management.</p><p>The Specialty Account Manager is responsible for providing account management support to accounts within a specific geography in the designated marketplace with a focus on issues specific to their designated accounts. The SAM acts as central account manager; responsible for driving product demand and coordinating relevant field teams to address account needs.</p><p><b>Responsibilities</b></p><ul><li><p>Develops a comprehensive and effective territory business plan aimed at achieving and exceeding annual sales goals established by sales and business unit leadership.</p></li><li><p>Promotes TEPEZZA within approved labeling in a comprehensive, fair and ethical manner that is consistent with industry specific and corporate legal and regulatory guidelines.</p></li><li><p>Addresses issues related to access, pull-through, and reimbursement by coordinating with key stakeholders and matrix team members.</p></li><li><p>Develops strong customer relationships by better understanding the customer’s needs and goals and communicating those needs and goals to other team members.</p></li><li><p>Consistently meets or exceeds corporate sales goals.</p></li><li><p>Communicates territory activity in an accurate and timely manner as directed by management.</p></li><li><p>Drive product demand among targets through education on disease state and product information.</p></li><li><p>Provides feedback to sales and business unit leadership, colleagues, and other internal departments about changing environment and results.</p></li><li><p>Adheres to the Company’s compliance policies and guidelines as well as any other applicable guidelines, including but not limited to the PhRMA code.</p></li><li><p>Must be able to work closely with patient services and market access team members, and understand their roles, to achieve overall business goals,</p></li><li><p>Coordinate between accounts and relevant Amgen field teams to support full range of account needs,</p></li><li><p>Educate healthcare professionals and office staff on site of care options.</p></li><li><p>Attends medical congresses and society meetings as needed.</p></li><li><p>Manages efforts within assigned promotional and operational budget.</p></li><li><p>Maximizes use of approved resources to achieve territory and account level goals</p></li><li><p>Successfully completes all Company training classes.</p></li><li><p>Completes administrative duties in an accurate and timely fashion.</p></li><li><p>Functions as a contributing member of a high-performance team.</p></li><li><p>Perform such other tasks and responsibilities as requested by the Company.</p></li></ul><p><b>Win</b></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The Specialty Account Manager we seek is a motivated professional with these qualifications.</p><p></p><p><b>Basic Qualifications (Account Manager – Level 4)</b></p><p>Bachelor&#39;s Degree and 3 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />Associate degree and 6 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience<br />OR<br />High school diploma/GED and 8 years of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experience</p><p></p><p><b>Basic Qualifications (Specialty Account Manager – Level 5)</b></p><p>Doctorate degree &amp; 2 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Master’s degree &amp; 6 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Bachelor’s degree &amp; 8 years of collective account management experience, sales, &amp; commercial experience</p><p>OR</p><p>Associate degree &amp; 10 years of collective account management experience, sales, &amp; commercial experience</p><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Buy-and-bill experience with documented success and/or biologic/infusion experience strongly preferred.</p></li><li><p>Sales experience in Endocrinology, Ophthalmology, and/or rare/specialty disease states preferred.</p></li><li><p>Site of care and reimbursement experience strongly preferred.</p></li><li><p>Experience working with institutions and integrated delivery networks preferred.</p></li><li><p>Pharma account management selling experience essential; must be able to coordinate across field teams to address full range of account needs.</p></li><li><p>Approximately 80% travel (may vary by territory), including some overnight and weekend commitments.</p></li><li><p>Proficient in Microsoft Office.</p></li><li><p>Professional, proactive demeanor.</p></li><li><p>Strong interpersonal skills.</p></li><li><p>Excellent written and verbal communication skills.</p></li></ul><p></p><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is (Account Manager – Level 4) $154,736 - $183,900 (Specialty Account Manager – Level 5) $160,000 - $190,000. In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:</p><ul><li><p>Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.</p></li><li><p>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</p></li><li><p>Stock-based long-term incentives</p></li><li><p>Award-winning time-off plans and bi-annual company-wide shutdowns</p></li><li><p>Flexible work models, including remote work arrangements, where possible</p></li></ul><p></p><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p></p><p>Application deadline</p><p>Amgen&#39;s application deadline is 5/30 for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.</p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p></p><p>#CLOLI</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>USD - USD]]></description><link>http://biotechroles.com/account-managerspecialty-account-manager-endocrinology-rare-disease-atlanta-west-ga-amgen/6a05f6052f1861929d2531c2</link><guid isPermaLink="true">http://biotechroles.com/account-managerspecialty-account-manager-endocrinology-rare-disease-atlanta-west-ga-amgen/6a05f6052f1861929d2531c2</guid><pubDate>Thu, 14 May 2026 16:19:17 GMT</pubDate><company>Amgen</company><location>US - Georgia - Atlanta</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Senior Associate -  Talent Panning]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Human Resources<h2></h2><h2><b>Job Description</b></h2><p><b>Job Description</b></p><p>Join Amgen’s Mission of Serving Patients</p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas - Oncology, Inflammation, General Medicine, and Rare Disease - we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller, happier lives.</p><p>Our award-winning culture is collaborative, innovative, and science-based. If you have a passion for challenges and the opportunities that lie within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this vital role, you will support hiring plan maintenance and help drive talent planning services across geographies. You will actively partner with HRBPs, Workforce Planning, and Talent Acquisition teams to enable timely recruitment activation for the right roles at the right time.</p><p><b>Responsibilities:</b></p><ul><li>Maintain a consolidated hiring plan dataset, including records management and the development of rolling global workforce plans.</li><li>Reconcile and report hiring plan data, and communicate planned vs. actual requisition status to Hiring Managers and HR Business Partners.</li><li>Support the rollout of a continuous recruitment process and related enhancements to hiring plan administration workflows.</li><li>Partner with the analytics lead to ensure hiring plan data supports recruitment process dashboards.</li><li>Lead data reconciliation with Organizational Design and Talent Acquisition teams to ensure hiring plan data aligns with organizational design plans of record and TA activity.</li><li>Partner with hiring leads to provide hiring process guidance, support required actions, and serve as a point of contact for issue resolution and key deliverables.</li><li>Support analytics dashboard and source data refinement while maintaining reports and dashboards for organizational design workflows.</li><li>Handle sensitive and confidential information with discretion.</li><li>Collaborate with team members and support ongoing process improvements as needed.</li></ul><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients.</p><p><b>Basic Qualifications:</b></p><ul><li>Bachelor’s degree and 7&#43; years of experience in Talent Planning, Workforce Planning, HR Operations, Recruitment Operations, or a related HR function</li></ul><p>OR</p><ul><li>Master’s degree and 6&#43; years of relevant experience</li><li>Experience supporting hiring plan management, workforce data reconciliation, reporting, and recruitment coordination.</li><li>Experience partnering with HRBPs, Workforce Planning, Talent Acquisition, and cross-functional stakeholders in a global environment.</li><li>Strong project coordination, stakeholder management, data accuracy, and analytical skills.</li></ul><p></p><p><b>Must-Have Skills:</b></p><ul><li>Proficiency in Microsoft Office Suite and HR/workforce planning tools.</li><li>Experience in hiring plan management, reporting, and data reconciliation.</li><li>Understanding of workforce planning, recruitment operations, and organizational design workflows.</li></ul><p></p><p><b>Soft Skills:</b></p><ul><li>Effective stakeholder management and collaboration skills.</li><li>Analytical thinking and problem-solving capability.</li><li>Strong attention to detail and process orientation.</li><li>Ability to manage multiple priorities in a dynamic environment.</li><li>Sound judgment when handling confidential data.</li><li>Agile mindset and continuous learning orientation.</li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p>In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/senior-associate-talent-panning-amgen/6a05f6052f1861929d2531c1</link><guid isPermaLink="true">http://biotechroles.com/senior-associate-talent-panning-amgen/6a05f6052f1861929d2531c1</guid><pubDate>Thu, 14 May 2026 16:19:17 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Senior Associate, Manufacturing]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Manufacturing<h2></h2><h2><b>Job Description</b></h2><p><b>Manufacturing Senior </b><b>Associate – L4</b></p><p><b>Amgen Dun Laoghaire</b></p><p></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. As part of Amgen’s Operations organization, Manufacturing continuously strives to be a differentiated leader in the manufacture of complex, high-quality therapeutics for our patients.</p><p><span>The Senior Associate reports</span> to the Manager Manufacturing. The ideal candidate will provide strong leadership to the Manufacturing teams. They will have strong GMP and quality system knowledge and the ability coach/mentor a team on the quality system requirements as well as maintaining a strong culture of safety within their shift team and in the manufacturing area in general. The candidate will have excellent troubleshooting skills using standard industry problem solving techniques. The successful candidate will build on a culture of diversity, inclusion and belonging in fast-paced and evolving environment. The candidate will have a continuous improvement mindset to drive changes in efficiency, safety, compliance, and quality.</p><p></p><p>The successful candidate will be required to work a shift pattern. This role will begin as a days position, moving to 24/5 shift pattern in the future.</p><p></p><p><b><span>Key Responsibilities:</span></b></p><ul><li>Responsible for leading the shift in conjunction with FLM. Responsible for outlining roles for the day, ensuring schedule is on track, triaging events, writing deviations, Batch Record Review. Running MDI’s.</li><li>Oversees opportunities from project from training perspective in project phase.</li><li>Support development of SOPs/job-aids/guidance.</li><li><span>Support the Manufacturing Manager in leading a shift of Process Technicians to achieve production targets efficiently in line with GMP, safety and regulatory standards.</span></li><li>Ensure shift Process Technicians are given clear direction and information to perform daily tasks as per the production schedule.</li><li>Lead an assigned process area Work Centre Team (WCT) to ensure cross functional alignment on objectives and action plans.</li><li>Maintain an accurate, up-to-date manufacturing schedule reflecting current status of production and plan critical path activities.</li><li>Foster a good safety culture in our team and act as a safety role model.</li></ul><ul><li>Oversee completion and review of documentation (batch records, EBRs) using relevant software systems and Standard Operating Procedures (SOPs).</li></ul><ul><li><span>Proactively identify training needs and facilitate completion of training to meet the area resource and cross training models.</span></li></ul><ul><li>Assist, plan and implement continuous improvement initiatives using lean principles.</li><li>Proactively identify and resolve process issues (including escalation and follow up) to minimize production disruptions.</li><li><span>Support and assist with corporate, FDA, HPRA and other regulatory bodies during company audits.</span></li></ul><ul><li>Lead on shift team in the absence of the Manufacturing Manager.</li></ul><p></p><p></p><p><b>Win</b></p><p><b>What we expect of you</b></p><p>The successful candidate for this role will bring the following education, skills and experience</p><p></p><ul><li>Educated to pass Leaving Certificate standard or equivalent</li><li>A third level qualification in a relevant subject area would be an advantage.</li><li>Applicants should have relevant experience of operations of a manufacturing function in a sterile pharmaceutical manufacturing or similar environment. Aseptic experience preferred.</li><li>Significant experience in a GMP/other regulated environment.</li><li>Demonstrated knowledge of GMP principles.</li><li>Demonstrated aseptic knowledge in GMP areas.</li><li>Drug product manufacturing experience.</li><li>Experience working with equipment utilized in the manufacture of parenteral products such as autoclaves, filling lines and formulation vessels.</li><li>Demonstrated ability to deliver to team, site and personal objectives.</li></ul><ul><li>Demonstrated understanding and use of right first-time techniques and lean manufacturing concepts.</li></ul><ul><li>Results-oriented.</li><li>Demonstrated ability to work within an AI Mindset</li><li>Excellent organizational, communicational and team development skills.</li><li>Strong understanding of the quality system requirements and regulations for working in an aseptic drug product facility.</li><li>Excellent communication skills.</li></ul><ul><li>Team leadership experience (preferred).</li><li>Excellent computer skills - knowledge of Electronic Batch Records, Quality Management Systems and Performance management Systems.</li><li>Fluent English required.</li></ul><p></p><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan designed to support your health, financial wellbeing, work/life balance, and long-term career growth. Comprehensive employee benefits package, including health and welfare plans for staff and eligible dependents, retirement and savings plan with generous company contributions, group medical, life and disability insurance. Discretionary annual bonus program. Exceptional learning, development, and career advancement opportunities, empowering employees to grow and build long-term careers. At Amgen, we are committed to nurturing talent and providing meaningful pathways for professional development.</p><p><i>Amgen is an equal opportunity employer.</i></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/senior-associate-manufacturing-amgen/6a05f6052f1861929d2531c0</link><guid isPermaLink="true">http://biotechroles.com/senior-associate-manufacturing-amgen/6a05f6052f1861929d2531c0</guid><pubDate>Thu, 14 May 2026 16:19:17 GMT</pubDate><company>Amgen</company><location>Ireland - Dublin</location><salary>$75000-105000</salary><type>Full time</type></item><item><title><![CDATA[Manufacturing Manager]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Manufacturing<h2></h2><h2><b>Job Description</b></h2><p><b>Manufacturing Front Line Manager </b></p><p><b>Amgen Dun Laoghaire</b></p><p></p><p><b>Live</b></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. As part of Amgen’s Operations organization, Manufacturing continuously strives to be a differentiated leader in the manufacture of complex, high-quality therapeutics for our patients.</p><p>The Manufacturing Front Line Manager (FLM) at Amgen Dun Laoghaire is a key member of the Operations Leadership Team. They oversee formulation and aseptic filling of Amgen’s drug products (syringes), in compliance with Good Manufacturing Practices.</p><p></p><p>The FLM oversees shift operations to ensure adherence to the production schedule, collaborating with support functions (Maintenance, Engineering, Quality, Planning). They maintain a strong culture of Safety and Quality within their team and in the manufacturing area overall.</p><p></p><p>The FLM develops and coaches a high-performing team of Manufacturing Process <span>Technicians/Associates,</span> fostering a culture aligned with Amgen values and leadership attributes that supports team growth while delivering exceptional results in a leading biotechnology business.</p><p></p><p><span>The successful candidate will be required to work a shift pattern. This role will begin as a days position, moving to 24/5 shift pattern in the future.</span></p><p></p><p><b><span>Key Responsibilities:</span></b></p><ul><li>Model Amgen’s values and leadership attributes, ensuring all cleanroom activities meet the highest standards of quality and safety while adhering to the manufacturing schedule.</li><li>Manage a shift of Process Technicians to achieve production targets efficiently in accordance with GMP, safety, and other regulatory standards.</li><li>Facilitate daily scheduling and team meetings to align all groups on critical activities to meet the manufacturing plan.</li><li>Support the commissioning, qualification, and product transfer of Amgen’s drug products to the new filling line.</li><li>Drive problem-solving efforts on the shift, working with cross-functional teams to minimize schedule disruptions.</li><li>Act as Aseptic Coach by observing and advising on aseptic practices in the manufacturing clean rooms.</li><li>Ensure the team compiles, maintains, and reviews all necessary reports and documentation, including batch records/EBRs, using appropriate systems and SOPs.</li><li>Collaborate with Quality groups (QCC/QCM/QCI and QA), Materials Management, Maintenance, Technical Services, and Human Resources to achieve department objectives.</li><li>People management, including team development, engagement and ongoing performance reviews via the Maximizing Amgen’s Performance (MAP) process, ensuring clarity and accountability for expected performance levels.</li><li>Identify training needs and facilitate completion per Amgen’s Learning Management System and production requirements.</li><li>Implement lean practices and supports continuous improvement opportunities using lean principles.</li><li>Assist with audits from corporate, FDA, HPRA, and other regulatory bodies.</li><li>Capable to work in high-pressure and fast paced environment that are inherent to large-scale project.</li></ul><p></p><p><b>Win</b></p><p><b>What we expect of you</b></p><p>The successful candidate for this role will bring the following education, skills and experience</p><ul><li>Bachelor’s degree in engineering or science.</li><li>Knowledge of relevant regulations and regulatory requirements (GMP, EH&amp;S).</li><li>5&#43; years’ experience in Syringe aseptic manufacturing operations or demonstrated capacity to learn quickly and adapt to new technology.</li><li>Previous experience in managing and leading teams.</li></ul><ul><li>Understanding and use of RFT techniques and lean manufacturing concepts.</li><li>Excellent people management skills, including performance management, coaching, mentoring, and team development.</li><li>Ability to lead, challenge, and positively influence in a team environment.</li><li>Proficient computer skills - knowledge of Electronic Batch Records (PAS/X), Quality tracking system (QMTS), and personnel performance tracking (MAPs).</li><li><span>Demonstrated ability to work within an AI Mindset</span></li><li>Fluent English required.</li></ul><p></p><p><b>Thrive</b></p><p><b>What you can expect of us</b></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan designed to support your health, financial wellbeing, work/life balance, and long-term career growth. Comprehensive employee benefits package, including health and welfare plans for staff and eligible dependents, retirement and savings plan with generous company contributions, group medical, life and disability insurance. Discretionary annual bonus program. Exceptional learning, development, and career advancement opportunities, empowering employees to grow and build long-term careers. At Amgen, we are committed to nurturing talent and providing meaningful pathways for professional development.</p><p></p><p><i>Amgen is an equal opportunity employer.</i></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/manufacturing-manager-amgen/6a05f6042f1861929d2531bf</link><guid isPermaLink="true">http://biotechroles.com/manufacturing-manager-amgen/6a05f6042f1861929d2531bf</guid><pubDate>Thu, 14 May 2026 16:19:16 GMT</pubDate><company>Amgen</company><location>Ireland - Dublin</location><salary>$85000-115000</salary><type>Full time</type></item><item><title><![CDATA[Sr Associate Data Visualization]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p>As a Senior Associate IS Business Systems Analyst at Amgen, you will support the analysis, design, and implementation of information systems solutions to meet business requirements. You will collaborate with cross-functional teams to gather and document system requirements, perform system testing, troubleshoot issues, and provide end-user support. Your attention to detail, analytical skills, and strong technical acumen will contribute to the successful delivery of IT projects and the continuous improvement of business processes. This is a Reporting engineer role on the Data Visualization Team and report into the Senior Manager, Value Management Agile Solutions. This individual will join the team that manages Amgen’s Value Management Office reporting (e.g., portfolio data, financial data, productivity metrics) and partner with other colleagues across the globe. This includes executing solutions to compliantly connect data assets from sources to that include Enterprise Data Fabric, Jira, Jira Align, Anaplan, Smartsheets and others that will serve as the foundation for driving Agile Lean Portfolio analytics that inform enhanced portfolio management and execution. This position includes the responsible for developing the reporting visualizations in connection with AI capabilities. This individual will partner with Value Management Office and Client Facing product teams on the data aggregation, integration, and ongoing operations.</p><p></p><p><b><u>Roles &amp; Responsibilities:</u></b></p><ul><li><p>Develop and maintain interactive dashboards and reports using <b>Power BI</b> and <b>Tableau</b>.</p></li><li><p>Collaborate with stakeholders to gather reporting requirements and translate them into technical solutions.</p></li><li><p>Perform data validation and ensure accuracy and consistency across reports.</p></li><li><p>Assist in optimizing data models and queries for performance and scalability.</p></li><li><p>Support ad-hoc reporting needs and data analysis requests.</p></li><li><p>Document reporting processes and maintain version control of reporting assets.</p></li><li><p>Stay current with BI trends and tools to continuously improve reporting capabilities.</p></li><li><p>Enforce data governance for data assets through data access management and business approval processes</p></li></ul><p><b><u>Basic Qualifications and Experience:</u></b></p><ul><li><p>Bachelor’s or Master&#39;s degree with 5 - 9 years</p></li><li><p>Proven experience in working in global teams and across time zones and cultures</p></li><li><p>Proven experience in working in Product teams and delivering high quality solution in adherence with established processes</p></li><li><p>Strong stakeholder management and communication skills.</p></li><li><p>Excellent English oral and written communication.<br /> </p></li></ul><p><b><u>Functional Skills:</u></b></p><p><b>Must-Have Skills:</b></p><ul><li><p>Hands-on experience with <b>Power BI</b> and <b>Tableau</b> (academic, internship, or project-based).</p></li><li><p>Strong understanding of data visualization principles and best practices.</p></li><li><p>Experience with AI Bot/n8n etc.</p></li><li><p>Basic knowledge of SQL and data modeling concepts.</p></li><li><p>Excellent analytical and problem-solving skills.</p></li><li><p>Strong communication and collaboration abilities.</p></li><li><p>Ability to effectively translate business stakeholder requirements to IT partners to ensure high quality, timely, integrated data assets</p></li><li><p>Deliver prioritized data deliverables through agile execution and continuous improvement</p></li><li><p>Demonstrated self-starter, ability to work under limited supervision</p></li><li><p>Strong interpersonal skills, active listening, and relationship management skills</p></li><li><p>Strong vendor management skills</p></li></ul><p><b>Good-to-Have Skills:</b></p><ul><li><p>Exposure to <b>AI/ML concepts</b> or tools (e.g., Azure ML, Python, AutoML).</p></li><li><p>Experience with cloud platforms (e.g., Azure, AWS, GCP).</p></li><li><p>Familiarity with version control systems like Git.</p></li><li><p>Familiarity with and application of Scaled Agile Framework (SAFe).<br /> </p></li></ul><p><b><u>Soft Skills:</u></b></p><ul><li><p>Exceptional collaboration and communication skills.</p></li><li><p>Strong data &amp; analytics/critical-thinking and decision-making abilities.</p></li><li><p>Able to perform well in a fast-paced, changing environment.</p></li></ul><p>Strong oral, written, and presentation skills, with the ability to articulate complex concepts and controversial findings clearly and compellingly.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-associate-data-visualization-amgen/6a05f6042f1861929d2531be</link><guid isPermaLink="true">http://biotechroles.com/sr-associate-data-visualization-amgen/6a05f6042f1861929d2531be</guid><pubDate>Thu, 14 May 2026 16:19:16 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Director, Centralized Study Support]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Clinical Development<h2></h2><h2><b>Job Description</b></h2><p><b>Director, Centralized Study Support (CSS)</b> </p><p><b>Location: Hyderabad, India</b> </p><p></p><p><u>ABOUT AMGEN</u> </p><p>Amgen harnesses the best of biology and technology to fight the world&#39;s toughest diseases, and make people&#39;s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what&#39;s known today. </p><p><u>ABOUT THE ROLE</u> </p><p><u>Role Description:</u> </p><p></p><p>The Director, CSS is responsible for building &amp; leading a large Centralized Study Support team, and for shaping an inclusive, high-performing organization grounded in clear accountability and consistent delivery excellence.  This role also oversees complex, resourcing across global portfolios, optimising capacity, capability, and deployment to support study delivery.  </p><p></p><p><u>Roles &amp; Responsibilities:</u>          </p><p><b>Global CSS Leadership</b> </p><ul><li><p>Provide strategic and operational leadership to a large, multi-layered CSS organization through senior managers and managers, ensuring consistent delivery, quality, and employee engagement across the function. </p></li></ul><ul><li><p>Set the vision, priorities, and long-term operating model for centralized study support in alignment with Global Development Operations objectives and evolving portfolio needs.          </p></li></ul><ul><li><p>Establish clear performance expectations, governance, and decision-making frameworks that drive accountability, consistency, and operational excellence across the organization. </p></li></ul><ul><li><p>Monitor functional performance through KPIs, capacity indicators, and quality metrics, proactively addressing risks and identifying opportunities to improve service delivery. </p></li></ul><p></p><p><b>Leadership Team Development</b> </p><ul><li><p>Lead, coach, and develop senior managers and managers to strengthen leadership capability, succession readiness, and organizational resilience. </p></li></ul><ul><li><p>Guide leaders through complex people, performance, and organizational design decisions while fostering a culture of inclusion, transparency, and continuous learning. </p></li></ul><ul><li><p>Build a high-performing leadership community that models collaboration, change agility, and strong talent stewardship across teams and geographies. </p></li></ul><p><b>Culture, Engagement &amp; Performance Excellence</b> </p><ul><li><p>Build and sustain a culture of delivery, accountability, belonging, and performance excellence across the CSS organization, ensuring employees are connected to the mission and clear on expectations. </p></li></ul><ul><li><p>Create an environment where diverse perspectives are valued, inclusion is intentional, and leaders foster strong engagement, development, and retention across teams and geographies. </p></li></ul><ul><li><p>Model and reinforce high standards for execution, collaboration, and people leadership while recognizing performance, addressing gaps, and promoting continuous improvement at every level. </p></li></ul><p></p><p></p><p><b>Resource Strategy, Allocation &amp; FSP Oversight</b> </p><ul><li><p>Provide strategic oversight of resource forecasting, allocation, and capacity planning for CSS roles across clinical programs, ensuring alignment with portfolio priorities, study demand, and budget considerations. </p></li></ul><ul><li><p>Oversee resource allocation governance and scenario planning, anticipating supply-demand gaps and driving timely mitigation plans, hiring strategies, and deployment decisions.          </p></li></ul><ul><li><p>Lead oversight of FSP partnerships supporting CSS, ensuring external capacity, performance, and capabilities align with business needs. </p></li></ul><p></p><p><b>Stakeholder Partnership &amp; Governance</b> </p><ul><li><p>Build trusted relationships with senior stakeholders across Global Development Operations and serve as the senior escalation point.</p></li></ul><ul><li><p>Communicate strategic updates, resource insights, risks, and recommendations clearly and persuasively to senior leadership, enabling informed portfolio and operational decisions. </p></li></ul><p></p><p><b>Quality, Compliance &amp; Risk Management</b> </p><ul><li><p>Ensure teams and partners operate in accordance with SOPs, regulatory requirements, quality standards, and internal controls, while proactively identifying and mitigating operational and resourcing risks. </p></li></ul><p></p><p><b>Operational Excellence &amp; Capability Building</b> </p><ul><li><p>Identify organizational capability gaps and define strategies to strengthen functional expertise, leadership depth, and scalable ways of working across CSS.          </p></li></ul><ul><li><p>Lead continuous improvement initiatives across processes, tools, systems, and reporting to improve efficiency, visibility, and consistency, including thoughtful use of AI and automation where appropriate. </p></li></ul><p></p><p><b>Enterprise Planning Support</b> </p><ul><li><p>Partner across GDO to support workforce planning, hiring strategies, forecasting analysis for CSS. </p></li></ul><p></p><p><u>Basic Qualifications and Experience:</u> </p><ul><li><p><b>Doctorate degree, Master&#39;s degree, OR Bachelor&#39;s degree with over 18 years of experience.</b></p></li><li><p>In addition to meeting at least one of the above requirements, you must have a minimum of 5 years of experience directly managing people and/or leadership experience leading teams, programs, organizational change, or directing the allocation of resources. This should include practical experience managing resourcing decisions such as capacity forecasting, prioritization of demand, and allocation trade-offs across a global portfolio of studies, programs, and geographies. Leadership experience may run concurrently with the required technical experience referenced above.                            </p></li></ul><p><u>Preferred Qualifications and Experience: </u> </p><ul><li><p>10&#43; years of work experience in the life sciences industry, including significant biopharmaceutical clinical research experience within a biotech, pharmaceutical, or CRO environment.          </p></li></ul><ul><li><p>Experience building teams from inception, fostering an inclusive, high-performance culture with a strong emphasis on delivery and continuous improvement </p></li></ul><ul><li><p>Experience overseeing complex resourcing across global portfolios, optimising capacity, capability, and deployment to deliver against shifting strategic priorities </p></li></ul><ul><li><p>Experience leading continuous improvement initiatives and delivering positive, sustainable change across complex organisations. </p></li></ul><p></p><p><u>Competencies:</u> </p><ul><li><p>Ability to translate portfolio and operational complexity into scalable organizational strategies, resource models, and practical execution plans. </p></li></ul><ul><li><p>Strong executive presence, communication, and influencing skills with the ability to engage senior leaders, cross-functional partners, and external stakeholders. </p></li></ul><ul><li><p>Uses data, trends, and scenario analysis to guide decisions, surface risks early, and drive clear business recommendations.                   </p></li></ul><ul><li><p>Demonstrated ability to lead, develop, and inspire leaders and large teams across functions, cultures, geographies, and time zones. </p></li></ul><ul><li><p>Experience balancing quality, compliance, financial discipline, and resource efficiency in a complex global clinical development environment.          </p></li></ul><ul><li><p>Track record of leading continuous improvement, simplification, and change initiatives that strengthen organizational effectiveness.          </p></li></ul><ul><li><p>Strong understanding of the clinical development lifecycle, study delivery principles, and the operational interdependencies across Global Development Operations. </p></li></ul><ul><li><p>Experience overseeing external partners, including FSP and vendor governance, performance management, and issue escalation to deliver high-quality outcomes. </p></li></ul><ul><li><p>Ability to navigate ambiguity, manage competing priorities, and build durable partnerships across diverse regulatory, cultural, and operational environments.          </p></li></ul><ul><li><p>Demonstrated capability to build organizational talent pipelines, strengthen leadership capability, and evolve operating models to meet future business needs. </p></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/director-centralized-study-support-amgen/6a05f6032f1861929d2531bd</link><guid isPermaLink="true">http://biotechroles.com/director-centralized-study-support-amgen/6a05f6032f1861929d2531bd</guid><pubDate>Thu, 14 May 2026 16:19:15 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$140000-210000</salary><type>Full time</type></item><item><title><![CDATA[Senior Associate Solutions Engineer – Automation & AI]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p><b><u>ABOUT AMGEN</u></b></p><p>Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.</p><h1><u>ABOUT THE ROLE</u></h1><p><b><u>Role Description:</u></b></p><p>In this role, you will build and implement Automation and AI-enabled solutions that support Contracting Operations and Revenue Management platforms within Amgen’s Global Commercial Operations and Corporate Functions Technology organization.</p><p>You will work across systems including Salesforce, Conga CLM and CPQ, Model N, MuleSoft, Databricks and Anaplan to support improvements in contracting and pricing workflows. Your work will focus on integrating AI capabilities and delivering AI driven automation solutions that reduce manual effort, improve data quality and increase process efficiency.</p><p>You will contribute to implementing solutions designed by senior engineers, working on assigned features, configurations, integrations and data flows within a defined scope. You will operate with guidance on design and priorities. This is a hands-on role suited for detail-oriented individuals eager to learn across enterprise platforms and progressively take on more complex work while delivering high-quality components.</p><h1><u>Roles &amp; Responsibilities:</u></h1><ul><li>Build and configure intelligent, AI-driven automation solutions using Python across enterprise platforms, aligned with established designs and patterns.</li><li>Drive automation of pricing, revenue and forecasting workflows across CPQ, Model N, and Anaplan within the defined scope.</li><li>Support the automation of end‑to‑end contract lifecycle processes, including creation, approvals, amendments and renewals, through system configuration.</li><li>Develop and support integrations using APIs and Middleware following standard patterns.</li><li>Contribute to AI‑driven use cases, including workflow automation and development of lightweight assistant capabilities to enhance user productivity.</li><li>Execute development tasks such as configuration, scripting, data mapping, and workflow orchestration, with a strong focus on quality, scalability and maintainability.</li><li>Perform assigned tasks and collaborate with engineers and cross-functional teams to deliver against priorities.</li><li>Participate in testing (unit, integration) and support defect resolution, data fixes and issue troubleshooting within scope.</li><li>Ensure adherence to design standards, best practices and documentation for maintainability and consistency.</li><li>Escalate risks, dependencies, or design issues beyond scope and continuously expand skills across platforms and technologies</li></ul><h1><u>Technology Focus Areas:</u></h1><ul><li>Experience in AI-driven automation using Python, enabling efficient workflow orchestration and process optimization across business systems.</li><li>Strong understanding of Generative AI concepts, AI orchestration frameworks and machine learning libraries to apply them effectively in real-world business workflows.</li><li>Exposure to AI assistants/copilots, vector search (embeddings-based retrieval) and prompt-driven workflows within enterprise platforms.</li><li>Experience in workflow and rules‑based automation, system configuration, and business process execution using tools like Salesforce Flow and similar frameworks.</li><li>Enterprise SaaS platforms like Salesforce, Conga CLM and CPQ, Model N, MuleSoft, Databricks and Anaplan is good to have.</li><li>System integration fundamentals including APIs, data exchange and middleware tools.</li><li>Data structures and models supporting contract lifecycle, pricing and revenue workflows.</li></ul><h1><u>Basic Qualifications and Experience:</u></h1><p>Bachelor’s degree or master’s degree and 4-8 years of experience and</p><ul><li>2&#43; years of experience in development of AI-powered automation workflows using Python, driving efficiency across enterprise processes and systems preferably across CRM/CPQ, Data &amp; Analytics.</li><li>Familiar with AI orchestration frameworks, APIs and ML libraries, along with hands‑on experience with automation tools, workflows and scripting to build intelligent, scalable solutions.</li><li>Experience with API integrations and data exchange across systems.</li><li>Good to have experience in Salesforce/Conga CPQ and data integrations using MuleSoft/Databricks.</li><li>Experience working in a team environment with engineers, product managers or business stakeholders.</li><li>Demonstrated ability to execute defined tasks with guidance and follow established implementation approaches while delivering consistent, high-quality results</li></ul><p><b><u>Preferred Qualifications:</u></b></p><ul><li>Experience with AI orchestration frameworks (LangChain/LangGraph), APIs (OpenAI/Anthropic/Hugging Face) and ML libraries (TensorFlow/PyTorch).</li><li>Familiar with AI/ML CI/CD pipelines (MLOps/AIOps) to enable continuous development, deployment and monitoring of AI-driven workflows.</li><li>Exposure to Salesforce, MuleSoft, Databricks.</li><li>Experience configuring workflows, rules or automation within enterprise platforms.</li><li>Experience supporting system integrations or data synchronization processes.</li><li>Familiarity with contract lifecycle management or pricing systems.</li><li>Experience working in Agile or iterative development environments.</li><li>Demonstrated progression in taking on increasingly complex technical tasks within a team setting.</li></ul><h1><u>Soft Skills:</u></h1><ul><li>Strong attention to detail and commitment to quality</li><li>Problem-solving mindset with the ability to follow structured approaches and escalate when needed</li><li>Clear and concise communication within teams and with cross-functional stakeholders.</li><li>Ability to take direction, ask clarifying questions, and execute tasks reliably</li><li>Strong organizational skills and ability to manage assigned work effectively</li><li>Curiosity and willingness to learn new systems and technologies</li><li>Collaborative mindset and openness to feedback</li></ul><h1><u>EQUAL OPPORTUNITY STATEMENT</u></h1><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/senior-associate-solutions-engineer-automation-and-ai-amgen/6a05f6032f1861929d2531bc</link><guid isPermaLink="true">http://biotechroles.com/senior-associate-solutions-engineer-automation-and-ai-amgen/6a05f6032f1861929d2531bc</guid><pubDate>Thu, 14 May 2026 16:19:15 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$18000-35000</salary><type>Full time</type></item><item><title><![CDATA[Solutions Engineer – Automation & AI]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p><b><u>ABOUT AMGEN</u></b></p><p>Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.</p><h1><u>ABOUT THE ROLE</u></h1><p><b><u>Role Description:</u></b></p><p>In this role, you will design, build and deliver Automation and AI-enabled solutions that support Contracting Operations and Revenue Management platforms within Amgen’s Global Commercial Operations and Corporate Functions Technology organization.</p><p>You will work across systems including Salesforce, Conga CLM and CPQ, Model N, MuleSoft, Databricks and Anaplan improving contracting and pricing workflows operate end to end. Your work will focus on designing &amp; integrating AI capabilities, delivering AI driven automation solutions that reduce manual effort, improve data quality and increase process efficiency.</p><p>You will partner with business, product, and engineering teams to turn operational problems into practical, scalable solutions. This role is for engineers who are comfortable working across multiple systems and learning new ones over time. You are not expected to have deep expertise in every platform on day one.<br /><span>You will operate within a defined problem space, partnering with senior leaders to shape solution approaches and guide implementation across a small team. You will make design and implementation decisions within your scope, aligned to broader architectural direction. This is a hands-on role with end-to-end ownership from design through delivery while actively building and implementing solutions</span></p><h1><u>Roles &amp; Responsibilities:</u></h1><ul><li>Design, Build and Configure intelligent, AI-driven automation solutions using Python across enterprise platforms, aligned with established designs and patterns.</li><li>Translate business requirements for automation into technical designs and implement solution components across Salesforce, Conga CLM/CPQ, Model N and related systems based on defined specifications.</li><li>Automation of end‑to‑end contract lifecycle processes, including creation, approvals, amendments and renewals, through system configuration.</li><li>Drive automation of pricing, revenue and forecasting workflows across CPQ, Model N, and Anaplan within the defined scope.</li><li>Develop and support integrations using APIs and Middleware.</li><li>Contribute to AI‑driven use cases, including workflow automation and development of lightweight assistant capabilities to enhance user productivity.</li><li>Apply AI where it adds value (e.g., contract summarization, insights, workflow automation) and support embedded assistants/copilots.</li><li>Prototype AI Automation and iterate rapidly, prioritizing simple, maintainable and platform-first solutions.</li><li>Collaborate with architecture, AI platform teams and cross-functional partners to align with enterprise standards.</li><li>Provide technical guidance to engineers through design alignment, reviews and implementation support.</li><li>Break down solutions into clear components and ensure quality through best practices and reviews.</li><li>Own end-to-end delivery of AI automation solutions from design to stabilization, driving measurable improvements in cycle time, data quality and operational efficiency.</li></ul><h1><u>Technology Focus Areas:</u></h1><ul><li>Design and implement Generative AI solutions and AI‑driven automation using Python to enable efficient workflow orchestration and process optimization.</li><li>Leverage AI orchestration frameworks, APIs and machine learning libraries to build intelligent and scalable solutions.</li><li>Work with AI assistants/copilots, vector search (embeddings-based retrieval), and prompt-driven workflows within enterprise platforms.</li><li>Build and configure workflow and rules‑based automation to support business process execution using tools like Salesforce Flow and similar frameworks.</li><li>Utilize enterprise platforms such as Salesforce, Conga CLM/CPQ, Model N, MuleSoft, Databricks and Anaplan to deliver integrated solutions.</li><li>Apply knowledge of data structures and models supporting contract lifecycle, pricing, and revenue management processes.</li><li>Integrate with enterprise AI services such as Azure OpenAI or similar platforms to enable advanced AI capabilities.</li></ul><h1><u>Basic Qualifications and Experience:</u></h1><ul><li>Bachelor’s degree or master’s degree and 8-12 years of experience</li><li>4&#43; years of experience in design &amp; development of AI-powered automation workflows using Python, driving efficiency across enterprise processes and systems preferably across CRM/CPQ, Data &amp; Analytics.</li><li>Experience with with AI orchestration frameworks, APIs, ML libraries and automation tools, workflows and scripting to build intelligent, scalable solutions.</li><li>Experience developing integrations using APIs, middleware or event-driven architectures building scalable and intelligent solutions.</li><li>Good to have experience in Salesforce/Conga CPQ and data integrations using MuleSoft/Databricks.</li><li>Ability to evaluate when AI-driven approaches are appropriate versus deterministic automation.</li><li>Experience working with cross-functional teams across product, engineering, and business functions.</li></ul><p></p><p><b><u>Preferred Qualifications:</u></b></p><ul><li>Experience with AI orchestration frameworks (LangChain/LangGraph), APIs (OpenAI/Anthropic/Hugging Face) and ML libraries (TensorFlow/PyTorch).</li><li>Familiar with AI/ML CI/CD pipelines (MLOps/AIOps) to enable continuous development, deployment and monitoring of AI-driven workflows.</li><li>Exposure to Salesforce, Conga CLM/CPQ, Model N, MuleSoft, Databricks or Anaplan.</li><li>Experience configuring workflows, rules or automation within enterprise platforms.</li><li>Experience supporting system integrations or data synchronization processes.</li><li>Familiarity with contract lifecycle management or pricing systems.</li><li>Experience working in Agile or iterative development environments.</li><li>Demonstrated progression in taking on increasingly complex technical tasks within a team setting.</li></ul><h1><u>Soft Skills:</u></h1><ul><li>Strong problem-solving and systems thinking</li><li>Ability to translate business needs into scalable technical solutions</li><li>Clear communication across technical and non-technical stakeholders</li><li>Ability to manage multiple priorities in a fast-paced environment</li><li>Ownership mindset with a focus on delivering results</li><li>Curiosity and willingness to learn new technologies</li></ul><h1><u>EQUAL OPPORTUNITY STATEMENT</u></h1><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/solutions-engineer-automation-and-ai-amgen/6a05f6022f1861929d2531bb</link><guid isPermaLink="true">http://biotechroles.com/solutions-engineer-automation-and-ai-amgen/6a05f6022f1861929d2531bb</guid><pubDate>Thu, 14 May 2026 16:19:14 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$12000-25000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manufacturing Process Technician -  Night Shift (12 Hour)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Manufacturing<h2></h2><h2><b>Job Description</b></h2><p><b>Join Amgen’s Mission of Serving Patients</b></p><p>At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.</p><p></p><p>Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p></p><p>Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p>Sr Mfg Process Technician I</p><p></p><p><b>What you will do</b></p><p>Let’s do this. Let’s change the world. In this role you will be operating an automated and innovative manufacturing equipment for the packaging operations of our products. This individual will be trained and cross-trained to both operate and troubleshoot issues (in the event of faults and machine stops) across a variety of equipment such as: automated, assembly, labeling, printing and robotic automation. In addition to equipment operation and troubleshooting, the technician will ensure product quality as a result of the performance of the equipment. Based on their mechanical proficiency, the process technician will conduct machine troubleshooting and problem-solving skills in a fast paced manufacturing environment.</p><p></p><p>Specific responsibilities include but are not limited to:</p><ul><li>Under limited supervision, perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency.</li><li>Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment.</li><li>Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions</li><li>Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)</li><li>Assist as training resource on manufacturing tasks and equipment use</li><li>Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.</li><li>Ensures components and products are available for a continuous operation.</li><li>Carries out equipment inspections and generates emergency, corrective, or preventative work orders as needed in the Maximo system.</li><li>Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes.</li><li>Partner with cross-functional teams to help drive improvement opportunities.</li><li>Able to use computer systems to support material inventory system (SAP transactions) and electronic batch records.</li><li>Oversight of equipment/process validation protocols independently.</li><li>Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging. Must follow Good Manufacturing Practices (GMPs).</li><li>Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained.</li><li>Train fellow staff on the manufacturing processes, equipment, and general</li><li>Available to support Operation in Non-Standard shift that includes weekends and /or holidays as determined by business skills.</li></ul><p></p><p><b>What we expect of you</b></p><p>We are all different, yet we all use our unique contributions to serve patients. The Sr Mfg. Process Technician professional we seek is an individual contributor with these qualifications.</p><p></p><p><b>Basic Qualifications:</b></p><p>High school diploma and 2 years of technical experience in Pharmaceutical, Manufacturing, or Packaging environment</p><p>Or</p><p>Associate’s degree and 6 months of technical experience in Pharmaceutical, Manufacturing, or Packaging environment</p><p></p><p><b>Preferred Qualifications:</b></p><ul><li>Ability to follow written procedures.</li><li>Capability to diagnose malfunctions and perform equipment setup.</li><li>Educational Background in Mechanical, Electronic Engineering Technology or Industrial Mechanics.</li><li>Working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment.</li><li>Ability to use computer systems to support the material inventory system (SAP transactions) and electronic batch records.</li><li>Excellent attention to detail, good organization, and capable of working independently..</li><li>Able to work in small groups and cross functional teams to troubleshoot issues, identify and implement collective corrective actions.</li><li>Experience working with highly automated equipment.</li><li>Experience working with Human Machine Interfaces (HMIs).</li><li>Experience working with discrete component assembly.</li><li>Good documentation planning and inventory skills.</li><li>Ideal candidate will have keen eye for quality, is self motivated, and will work collaboratively within a team, and possess a positive demeanor.</li><li>Knowledgeable of the following technical areas: Packaging or Process Equipment/System Maintenance</li></ul><p></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.</p><p></p><p>The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.</p><p></p><p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:</p><ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models, including remote and hybrid work arrangements, where possible</li></ul><p></p><p><b>Apply now</b></p><p><b>for a career that defies imagination</b></p><p>Objects in your future are closer than they appear. Join us.</p><p><b>careers.amgen.com</b></p><p></p><h2>Sponsorship</h2><p>Sponsorship for this role is not guaranteed.</p><p></p><p>In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.</p><p></p><p>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p></p><p>Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p></p><p>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.<p><b>Salary Range</b></p>62,731.70USD -84,872.30 USD]]></description><link>http://biotechroles.com/senior-manufacturing-process-technician-night-shift-12-hour-amgen/6a05f6012f1861929d2531ba</link><guid isPermaLink="true">http://biotechroles.com/senior-manufacturing-process-technician-night-shift-12-hour-amgen/6a05f6012f1861929d2531ba</guid><pubDate>Thu, 14 May 2026 16:19:13 GMT</pubDate><company>Amgen</company><location>US - Ohio - New Albany</location><salary>$75000-95000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Associate Healthcare Community Contracting]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><div><div>Job Description</div></div><div><div><div><div><div><div><div><div><div><p><u>L4 Health Care Community Contracting Senior Associate</u> </p><p></p><p>Amgen’s Research and Development (R&amp;D) Business Operations organization addresses complex business challenges with outstanding people, tools, and processes. The team delivers on key initiatives and capabilities to support R&amp;D. This position is primarily responsible for overseeing and processing healthcare compliance related contracting and payments of proposed arrangements by Amgen staff with Members of the U.S. Healthcare Community. We are looking for talent who have play a key role in supporting the healthcare contracting process and ensuring accurate and timely payments to members of the health care community. The senior associate requires a solid understanding of contracting as well as SAP software and its functionalities. The senior associate will collaborate with cross-functional teams, including legal, sourcing, accounts payable, and finance, to ensure smooth and seamless contract management and payment operations. We are a team that delivers for our partners! </p><p></p><p>Required Competencies and Skills:  </p><p></p><p>Key Responsibilities:  </p><p></p><p>Lead the review, drafting, and negotiation of contracts for members of the healthcare community (Fee for Service, Consulting, Sponsorship, Donation, Exhibits or other similar engagements).  </p><p>Maintain contract documentation and ensure compliance with contractual terms and conditions. </p><p>Coordinate contract execution and distribution.  </p><p>Triage intake from Amgen R&amp;D or other supported functions to appropriate contract managers, as needed.  </p><p>Cross-Functional Collaboration: Collaborate with sourcing, accounts payable, and other relevant teams to streamline financial processes and resolve any issues or discrepancies.  </p><p>Ensure effective communication and foster positive working relationships. </p><p>Process invoices, reimbursements, and payments related to healthcare contracts. </p><p>Verify accuracy of invoices and resolve discrepancies with suppliers and providers. </p><p>Ensure timely payments and adherence to payment terms. </p><p>Ensure compliance with internal controls, policies, and regulations.  </p><p>Develop and enforce policies and procedures related to contracting and payment operations. </p><p>Participate in audits and assist with compliance-related activities as required. </p><p>Contribute to the development and implementation of strategic initiatives to optimize contracting and payment processes. </p><p></p><p>Knowledge:  </p><ul><li><p>Excellent computer and MS Office skills </p></li></ul><ul><li><p>Excellent writing skills; detail-oriented </p></li></ul><ul><li><p>Communicates effectively within and outside department </p></li></ul><ul><li><p>Familiarity with SAP </p></li></ul><ul><li><p>Knowledge of current and legally binding contractual language and terminology. </p></li></ul><ul><li><p>Solid understanding of purchasing and supply chain procedures. </p></li></ul><ul><li><p>Solid understanding of standard operating procedures (SOPs) and healthcare regulations. </p></li></ul><ul><li><p>Solid understanding of standard contracting legal principles.   </p></li></ul><p></p><p>Problem Solving: </p><ul><li><p>Ability to process simple transactions from end to end, engaging business partners where appropriate.  </p></li></ul><ul><li><p>Identify and escalate business issues needing resolution, as well as identifying potential process improvements and manage multiple assignments at one time. </p></li></ul><ul><li><p>Review and either approve payments or triage errors to the appropriate Amgen staff member.  </p></li></ul><ul><li><p>Review invoice/expenses related to Fee for Service Arrangements (i.e. CARFs) and triage any issues. </p></li></ul><ul><li><p>Review invoice/expenses related to Advisory Board Arrangements (i.e. ABCARFs) and triage any issues.  </p></li></ul><ul><li><p>Communicate and escalate contractual and/or payment challenges to leadership team. </p></li></ul><ul><li><p>Exercises good judgment. </p></li></ul><ul><li><p>Interact with business partners to ensure compliance processes and standards are understood and followed. </p></li></ul><p></p><p>Contribution:  </p><ul><li><p>Consistent with Amgen’s Healthcare Compliance Policy and Standard Operating Procedures: </p></li></ul><ul><li><p>Review proposed arrangements via Amgen’s healthcare compliance operations system of record (C3). </p></li></ul><ul><li><p>Support Amgen staff members with any related questions and/or concerns such as C3 system support,  </p></li></ul><ul><li><p>Ability to read legal documents and facilitate legal review, interpret financial reports and technical documents. </p></li></ul><ul><li><p>Manage payment inquiries that are received via the <a href="http://HCCPaymentRequests&#64;amgen.com/" target="_blank">HCC Payment Requests</a> mailbox from RAEs, Service Providers etc. Outcome may include further reviews, research and/or triage. </p></li></ul><ul><li><p>Proofread, edit and fact-check legal documents for accuracy and consistency.  </p></li></ul><ul><li><p>Time management and problem-solving skills. </p></li></ul><ul><li><p>Other duties as assigned. </p></li></ul><p></p><p>Bachelor’s degree or Master&#39;s degree with 5-8 years of related resource management, paralegal, contracting and/or financial accounting experience.</p><p></p><p>Preferred Requirements </p><p>Familiarity with research and clinical development in biopharmaceutical industry as well as medical and scientific terminology. </p><p>Finance, resource, and budget management experience including cost analysis and reporting. </p><p>Experience with analytics software (Microsoft Access, Spotfire, Tableau, Smartsheet), document management applications, portfolio planning tools, supply chain and financial systems (Planisware, Veeva, SAP, Ariba). </p><p>Intermediate Microsoft Office user (Excel, Word, PowerPoint, Outlook). </p><p>Experience working with virtual teams and using collaborative tools and platforms. </p><p>Exceptional interpersonal, organizational, critical thinking and verbal/written communication skills </p><p>Ability to work in a highly cross matrixed environment </p><p>Strong planning and project management skills with the demonstrated ability to work effectively in a fast-paced environment with multiple high priority projects and minimal supervision. </p><p></p></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-associate-healthcare-community-contracting-amgen/6a05f6002f1861929d2531b9</link><guid isPermaLink="true">http://biotechroles.com/sr-associate-healthcare-community-contracting-amgen/6a05f6002f1861929d2531b9</guid><pubDate>Thu, 14 May 2026 16:19:12 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Sr Associate Software Engineer - Full Stack]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Engineering<h2></h2><h2><b>Job Description</b></h2><h2></h2><h2><u>ABOUT AMGEN</u></h2><h2>Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.</h2><h2></h2><h2><u>ABOUT THE ROLE</u></h2><h2><u>Role Description:</u></h2><h2>Amgen is seeking a Sr Software Engineer - Full Stack to design, develop, and support modern AI-enabled web applications that power Insights and Field Intelligence capabilities.</h2><h2>This role focuses on building scalable, responsive, and intelligent full-stack applications using React, Next.js, Node.js, and cloud-native technologies while integrating AI/ML capabilities such as Large Language Models (LLMs), Retrieval-Augmented Generation (RAG), AI agents, and intelligent workflow automation.</h2><h2>The ideal candidate combines strong front-end and back-end engineering expertise with hands-on experience integrating AI services and APIs into enterprise applications. The successful candidate should have a passion for modern application development, AI innovation, and building intelligent systems that improve business productivity and decision-making.</h2><h2><u>Roles &amp; Responsibilities:</u></h2><ul><li><h2>Design, develop, and maintain scalable full-stack web applications using React.js, Next.js, Node.js, Typescript</h2></li><li><h2>Build responsive, mobile-first, and user-centric interfaces that support enterprise Insights and Field Intelligence use cases.</h2></li><li><h2>Develop reusable UI components, application frameworks, and shared libraries following modern front-end engineering best practices.</h2></li><li><h2>Design and develop secure and scalable backend services, APIs, and microservices using Node.js and REST/GraphQL architectures.</h2></li><li><h2>Implement server-side rendering (SSR), static site generation (SSG), and modern web optimization techniques using Next.js.</h2></li><li><h2>Ensure application scalability, performance optimization, accessibility, and cross-browser compatibility.</h2></li><li><h2>Design and develop AI-enabled applications leveraging Large Language Models (LLMs) such as OpenAI models and enterprise AI services.</h2></li><li><h2>Develop Retrieval-Augmented Generation (RAG) solutions using vector databases and enterprise knowledge sources.</h2></li><li><h2>Design and implement AI agent workflows and orchestration frameworks to automate business processes and insight generation.</h2></li><li><h2>Integrate AI capabilities into enterprise web applications, APIs, and workflows for real-time intelligence and automation.</h2></li><li><h2>Implement context management approaches such as Model Context Protocol (MCP) or similar AI orchestration frameworks.</h2></li><li><h2>Evaluate and adopt emerging AI technologies, frameworks, and engineering best practices.</h2></li><li><h2>Design, build, and maintain scalable APIs and backend integration services supporting enterprise and AI-driven applications.</h2></li><li><h2>Develop integrations with enterprise platforms including CRM, analytics, and business intelligence systems.</h2></li><li><h2>Build secure and reusable API services enabling AI-driven workflows and data access patterns.</h2></li><li><h2>Implement monitoring, logging, observability, and error handling across APIs and application services.</h2></li><li><h2>Leverage AWS cloud services to build scalable, resilient, and secure application platforms.</h2></li><li><h2>Implement CI/CD pipelines and DevOps best practices for application deployment and lifecycle management.</h2></li><li><h2>Support containerized application deployment using Docker and cloud-native deployment approaches.</h2></li><li><h2>Optimize application performance, scalability, and operational reliability in cloud environments.</h2></li><li><h2>Participate in agile ceremonies including sprint planning, backlog refinement, estimation, and retrospectives.</h2></li></ul><ul><li><h2>Create and maintain technical documentation including architecture diagrams, API specifications, deployment procedures, and operational guides.</h2></li></ul><h2></h2><h2><u>Basic Qualifications and Experience:</u></h2><ul><li><h2>Master’s / Bachelor’s degree with 5 - 8 years of experience in Computer Science, IT or related field</h2></li></ul><h2></h2><h2><u>Functional Skills:</u></h2><h2></h2><h2>Must-Have Skills</h2><ul><li><h2>Strong hands-on experience developing full-stack applications using React.js, Next.js, Node.js, Typescript, Javascript</h2></li><li><h2>Strong experience building scalable RESTful APIs and backend services</h2></li><li><h2>Hands-on experience building Retrieval-Augmented Generation (RAG) pipelines and integrating vector databases.</h2></li><li><h2>Understanding of AI agent architectures, orchestration frameworks, and context-aware AI systems.</h2></li><li><h2>Experience integrating AI capabilities into web applications, APIs, and enterprise workflows.</h2></li><li><h2>Experience with AWS cloud data platforms</h2></li></ul><h2></h2><h2>Good-to-Have Skills:</h2><ul><li><h2>Experience with machine learning workflows (Databricks ML, or similar)</h2></li><li><h2>Familiarity with Model Context Protocol (MCP) or similar AI context management approaches.</h2></li><li><h2>Knowledge of real-time/streaming architectures</h2></li><li><h2>Understanding of field analytics, CRM data models, or commercial insights use cases</h2></li></ul><h2></h2><h2><u>Professional Certifications </u></h2><ul><li><h2>Certified AWS Professional or Associate certification (Required)</h2></li><li><h2>OpenAI, Generative AI, or Cloud AI-related certification (Preferred)</h2></li></ul><h2></h2><h2><u>Soft Skills:</u></h2><ul><li><h2>Excellent critical-thinking and problem-solving skills</h2></li><li><h2>Strong communication and collaboration skills</h2></li><li><h2>Demonstrated awareness of how to function in a team setting</h2></li><li><h2>Demonstrated presentation skills</h2></li></ul><h2></h2><h2></h2><h2><u>EQUAL OPPORTUNITY STATEMENT</u></h2><h2>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</h2><h2>We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</h2><h2></h2><h2></h2><h2></h2><h2></h2><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/sr-associate-software-engineer-full-stack-amgen/6a05f5ff2f1861929d2531b8</link><guid isPermaLink="true">http://biotechroles.com/sr-associate-software-engineer-full-stack-amgen/6a05f5ff2f1861929d2531b8</guid><pubDate>Thu, 14 May 2026 16:19:11 GMT</pubDate><company>Amgen</company><location>India - Hyderabad</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Lead Data & Analytics Engineer]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Information Systems<h2></h2><h2><b>Job Description</b></h2><p>Join our team at AMGEN Capability Center Portugal, consistently recognized among the top companies in the Best Workplaces™ ranking by Great Place to Work® in Portugal. In 2026, we were once again distinguished as one of the top Best Workplaces in the country (category 201–500 employees), reinforcing our commitment to an exceptional employee experience and workplace culture.</p><p></p><p>We are a team of over 500 talented individuals, spanning more than 30 functions and areas of expertise, and representing over 40 nationalities. Together, we bring diverse perspectives and professional backgrounds to help shape the future of healthcare through innovation and technology.</p><p>This is your opportunity to explore a world of possibilities across areas such as Data &amp; Analytics, Digital, Technology &amp; Innovation, Cybersecurity, R&amp;D Operations, Global Distribution, Finance, Regulatory Affairs, General &amp; Administrative, Human Resources, and many more.</p><p></p><p>Located in the heart of Lisbon, our AMGEN office fosters a culture of innovation, excellence, and purpose. Come thrive with us at AMGEN, supporting our mission To Serve Patients.</p><p></p><p>What we do at AMGEN matters in people’s lives.</p><p></p><p></p><p></p><p><span class="emphasis-3"><b>LEAD DATA &amp; ANALYTICS ENGINEER</b></span></p><p></p><p></p><p></p><h2><span class="emphasis-3"><b>LIVE</b></span></h2><p><span class="emphasis-3"><b>WHAT YOU WILL DO</b></span></p><p></p><p></p><p></p><p>We are seeking a highly skilled Lead Data &amp; Analytics Engineer with 10&#43; years of experience to support web and data-driven applications across Global Medical Data and Analytics team.</p><p></p><p>This role is suited for professionals with Technical Lead experience and partner with business on requirements, develop Prototype, proof of concepts,  design and develop integration and data pipelines, analytics solutions and engage with validation engineers, product owner, architects and the members of the development team.  </p><p></p><p>The ideal candidate will have innovative mindset and experience in software development using python, Databricks, React js frameworks, data analysis and familiarity of Agile practices, along with a strong willingness to learn and take on additional responsibilities like leading proof of concepts with advanced technology and AI.   </p><p></p><p>This role will be part of Medical Data Analytics and Insights Global Product Team and primarily focus on delivering Analytics and Strategic Insights capabilities across Global Medical business organization.</p><p></p><p></p><p><b>Key Responsibilities:</b></p><p></p><ul><li><p>As a Lead Data &amp; Analytics Engineer lead the design, aid development, and deployment of advanced data integration solutions for Global Medical teams, enabling actionable insights across diverse business capabilities. </p></li></ul><ul><li><p>Colaborate closely with business partners to understand requirements and gaps and Design integrated solutions, Quick POCs, adhoc data analysis using  analytical summarized dimensional data models and datasets  </p></li></ul><ul><li><p>Aid Development platform team with design, development of backend infrastructure and integrated views using AWS,  Databricks notebooks with Python, sql, node.js  </p></li></ul><ul><li><p>Drive innovation in data analytics by introducing advanced techniques (e.g., AI, predictive analytics, dynamic storytelling) to highlight trends and opportunities. </p></li><li><p>Drive cross-functional collaboration with engineering, data science, and business teams to streamline workflows and enhance efficiency. </p></li><li><p>Stay updated with emerging trends and tools in data and analytics, incorporating innovative solutions into the team&#39;s workflows. </p></li><li><p>Advocate for the adoption of cutting-edge tools and methodologies</p></li><li><p>Ensure adherence to Agile principles and best practices.</p></li><li><p>Track sprint progress, identify risks, and remove blockers.</p></li><li><p>Facilitate communication and coordination across cross-functional teams.</p></li><li><p>Drive continuous improvement in team processes and delivery efficiency.</p></li></ul><p></p><p></p><p></p><p><span class="emphasis-3"><b>WIN</b></span></p><p><span class="emphasis-3"><b>WHAT WE EXPECT OF YOU</b></span></p><p></p><p></p><p></p><p><b>Required Skills &amp; Qualifications:</b></p><p></p><ul><li><p>Strong experience in Agile/Scrum practices, including facilitating Scrum ceremonies.</p></li><li><p>Experience in requirements gathering and documentation.</p></li><li><p>Working knowledge of data platforms<br /><i>(e.g., Databricks or similar — monitoring and basic troubleshooting)</i> is a plus.</p></li><li><p>Willingness to learn new tools, technologies, and take on additional responsibilities</p></li></ul><p></p><p></p><p><b>Nice to Have:</b></p><p></p><ul><li><p>Bachelor’s or Master’s degree in Data Science, Computer Science, Analytics, Business Administration, or a related field. </p></li><li><p>7&#43; years of experience in  data analytics  or business intelligence, preferably within the pharmaceutical, life sciences, or healthcare industry. </p></li><li><p>Demonstrated experience in managing global data projects and collaborating with cross-functional teams in a matrixed organization. </p></li><li><p>Familiarity with cloud platforms such as AWS, Azure, or GCP, and experience in integrating data visualization solutions with cloud-based architectures. </p></li><li><p>Experience working in enterprise or large-scale environments.</p></li><li><p>Familiarity with test management or defect tracking tools.</p></li></ul><p></p><p></p><p><b>What This Role Requires:</b></p><p></p><ul><li><p>A strong Communicator who can lead business requirements effectively</p></li><li><p>Ability to bridge business, testing, and delivery teams</p></li><li><p>A proactive mindset with willingness to drive team coordination and continuous improvement</p></li><li><p>Ability to work collaboratively with cross-functional teams and manage multiple tasks simultaneously </p></li><li><p>Strong analytical and problem-solving skills to interpret complex data and provide actionable insights </p></li></ul><p></p><p></p><p></p><p><span class="emphasis-3"><b>THRIVE</b></span></p><p><span class="emphasis-3"><b>WHAT YOU CAN EXPECT OF US</b></span></p><p></p><ul><li><p>Vast opportunities to learn, develop, and move up and across our global organization.</p></li><li><p>Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</p></li><li><p>Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits.</p></li><li><p>Flexible work arrangements.</p></li></ul><p></p><p></p><p><span class="emphasis-3"><b>APPLY NOW</b></span></p><p></p><p>Objects in your future are closer than they appear. Join us.</p><p></p><p></p><p><span class="emphasis-3"><b>CAREERS.AMGEN.COM</b></span></p><p></p><p></p><p><span class="emphasis-3"><b>EQUAL OPPORTUNITY STATEMENT</b></span></p><p></p><p></p><p>AMGEN is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/lead-data-and-analytics-engineer-amgen/6a05f5fa2f1861929d2531b7</link><guid isPermaLink="true">http://biotechroles.com/lead-data-and-analytics-engineer-amgen/6a05f5fa2f1861929d2531b7</guid><pubDate>Thu, 14 May 2026 16:19:06 GMT</pubDate><company>Amgen</company><location>Portugal - Lisbon</location><salary>$75000-110000</salary><type>Full time</type></item><item><title><![CDATA[EU Regulatory Affairs Senior Manager (Biosimilars)]]></title><description><![CDATA[<h2><b>Career Category</b></h2>Regulatory<h2></h2><h2><b>Job Description</b></h2><div><b>HOW MIGHT YOU DEFY IMAGINATION?</b></div><div><div><div><div><div><div><div><div><div><p></p><p>If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.</p></div></div></div></div></div></div></div></div></div><p></p><p><b>EU REGULATORY AFFAIRS SENIOR MANAGER - BIOSIMILARS</b></p><p></p><p><b>LIVE</b></p><p><b>What you will do</b></p><p><span>In this vital role you will work to support the regulatory, safety and product development needs of the Amgen Biosimilars Operating Unit through detailed development and implementation of European regulatory strategies, submissions, and plans.</span></p><p>Representing the region, you will be responsible for advising the GRT on regional considerations in developing strategy, and ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders.</p><ul><li>Plan and manage regulatory submissions for products within Amgen&#39;s biosimilar portfolio in compliance with global filing plans and local regulatory requirements</li><li>Implement product related regulatory strategies, Regulatory Affairs processes and activity planning</li><li>Lead development of regional regulatory documents and meetings in accordance with GRT strategy</li><li>Provide regulatory direction on regional regulatory mechanisms to optimize product development</li><li>Participate in the development and execution of regional regulatory product strategies, including precedence, risk management and contingency planning</li><li>Consistent with GRT strategy, advise on regulatory implications and requirements related to regional development plans and objectives</li><li>Lead Health Authority and Agency Interactions and document and communicate outcomes appropriately</li><li>Ensure and lead regulatory compliance for biosimilar products (eg, agency commitments)</li><li>Ensure all filings are maintained per regulatory requirements and consistent with biosimilar strategy throughout product development and long-term planning</li></ul><p></p><p><b>Be part of our team</b></p><p>You would be joining the European Regulatory team, part of the Global Regulatory Affairs function in Europe. You would be working with colleagues who are responsible for leading the European regulatory strategies and submissions for development and marketed products from first in human clinical trials to marketing authorisation, and throughout the products lifecycle.</p><p></p><p><b>WIN</b></p><p><b>What we expect of you</b></p><p><span>We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:</span></p><ul><li>Degree educated in a scientific discipline</li><li>Extensive experience of the regional Biosimilars regulatory environment</li><li>Proven track record of developing and executing regional Biosimilars regulatory strategy</li><li>In-depth understanding of the drug life cycle and development process from a regulatory perspective</li><li>In-depth understanding of the registration procedures in region for MA, post approval changes, extensions and renewals.</li><li>Ability to lead teams and work collaboratively in a dynamic environment</li><li>Proactive approach to problem solving</li><li>Ability to understand and communicate scientific/clinical information</li><li>Ability to anticipate regulatory agency expectations</li><li>Strong awareness of the needs of internal and external stakeholders, and the role of Regulatory Affairs in driving successful drug development</li></ul><p></p><p><b>THRIVE</b></p><p><b>What you can expect of us</b></p><p>As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.</p><ul><li><p>Growth opportunities to learn and move up and across our global organization</p></li><li><p>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</p></li><li><p>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</p></li></ul><p></p><p><b>APPLY NOW</b></p><p><b>for a career that defies imagination</b></p><p>In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.</p><p></p><p><b>careers.amgen.com</b></p><p></p><p></p><p><b>Equal Opportunity Statement</b></p><p></p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p></p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>.]]></description><link>http://biotechroles.com/eu-regulatory-affairs-senior-manager-biosimilars-amgen/6a05f5fa2f1861929d2531b6</link><guid isPermaLink="true">http://biotechroles.com/eu-regulatory-affairs-senior-manager-biosimilars-amgen/6a05f5fa2f1861929d2531b6</guid><pubDate>Thu, 14 May 2026 16:19:06 GMT</pubDate><company>Amgen</company><location>United Kingdom - Uxbridge</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[ViiV Healthcare (Senior) Medical Science Liaison - Los Angeles, CA]]></title><description><![CDATA[<p><b>Region: Los Angeles, CA</b></p><p></p><p>ViiV Healthcare is a global specialty HIV company, the only one that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV Healthcare is highly mission-driven in our unrelenting commitment to being a trusted partner for all people living with and affected by HIV. Our aim is to think, act, and connect differently through a focus on education on for the prevention and treatment for HIV.  We go to extraordinary lengths to deliver the sorts of breakthroughs, both in prevention, treatments, care solutions and communities, that really count. We go beyond the boundaries of medicine by taking a holistic approach to HIV through developing and supporting sustainable community programs and improving access to care.  We are fully committed to push through every challenge until HIV/AIDS is eradicated. ViiV Healthcare has played a significant part in delivering breakthroughs that have turned HIV into a manageable health condition. We offer the largest portfolio of HIV medicines available anywhere, and we continue our work to cater for the widest possible range of needs in response to the HIV epidemic.</p><p></p><p>We are aware of how much is at stake for those at-risk or affected by HIV and we show up every day 100% committed to the patients. Our work culture is fast-paced, diverse, inclusive, competitive, and caring. But ViiV Healthcare isn’t just somewhere to work – it’s a place to belong, an invitation to bring your very best, and a team full of impact-driven team members who are hungry to make a difference.</p><p></p><p>The <b>(Senior) </b><b><b>Medical Sc</b>ience Liaison (MSL)</b> role is a field based, customer-facing, non-promotional medical and scientific position within the <b>Los Angeles, CA </b>area. The MSL’s key objective is to create impact through advancing clinical practice within the assigned territory that leads to improved patient outcomes. The MSL serves as a scientific expert in HIV treatment and prevention, understands territory and market influences, engages scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop their territory and execute all relevant activities in alignment with the medical strategic plan. The MSL will Inform and shape medical strategy through application of a curious mindset to collect impactful and actionable insights to drive the development and commercialization of our products.</p><p></p><p></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following</p><ul><li><p><b>Scientific Expertise:</b> Build strong scientific acumen and serve as a primary point of contact for medical and scientific inquiries in HIV treatment and prevention supporting scientific engagement for territory. Provide advanced scientific and clinical knowledge to internal teams and external stakeholders.</p></li><li><p><b>Stakeholder Engagement:</b> Identify, develop, and maintain relationships with external experts, researchers, and healthcare professionals. Maintain a strategic plan to provide support to external experts in order to facilitate scientific discussions and collaborations to support ViiV Medical’s scientific and clinical objectives. Engagements may include but not limited to emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within their territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle.</p></li><li><p><b>Clinical Insights:</b> Gather and relay insights from the field to inform product development, clinical trial design, and market strategies. Provide feedback on ViiV products and services.</p></li><li><p><b>Education and Training:</b> Develop and deliver scientific presentations and training sessions for healthcare professionals and internal teams. Support the creation of educational materials and provide scientific training to colleagues.</p></li><li><p><b>Compliance and Documentation:</b> Ensure all activities comply with regulatory guidelines and company policies. Maintain accurate records of interactions and outcomes.</p></li><li><p><b>Leadership and Mentorship:</b> Act as a role model of ViiV’s culture and values. Mentor and coach new or less experienced MSLs and lead scientific or strategic projects to elevate team acumen.</p></li><li><p><b>Safety Communication:</b> Disseminate important safety information to healthcare professionals as directed by Medical Affairs or Research and Development teams.</p></li><li><p><b>Agility and Adaptability:</b> Interface with a wide range of internal and external stakeholders, including external experts, healthcare professionals, investigators, professional societies, advocacy groups, and formulary decision-makers.</p></li><li><p><b>Clinical Development Support:</b> Assist in clinical development activities, including GSK and Investigator Sponsored Studies (ISS). Work with Clinical Teams to improve site performance and provide insights into GSK research interests.</p></li></ul><ul><li><p><b>National Meetings</b>: Attend both national and regional scientific/medical meetings to gain medical voice of the customer on recent data being presented on products and disease states of interest to ViiV.</p></li><li><p><b>Matrix Collaboration</b>: Conducts business with a One-ViiV mindset compliantly and regularly engaging across matrix stakeholders.</p></li><li><p><b>Administration</b>: Execute all responsibilities and training (i.e., Veeva CRM, email, expense report mylearnings) in a timely manner, including profiling of core customers and ensuring up-to-date information in the CRM</p></li></ul><p></p><h1><span class="emphasis"><i><b>Why you?</b></i></span></h1><p></p><p><b>Basic Qualifications: </b></p><p><i>We are looking for professionals with these required skills to achieve our goals:</i></p><ul><li><p>Advanced degree (MD or DO or PharmD or PhD or APP)</p></li><li><p>3&#43; years of clinical experience in HIV OR Infectious Disease</p></li><li><p>Stakeholder management experience</p></li><li><p>Valid Driver’s License</p></li><li><p>Ability to travel 40-60%</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><p><i>If you have the following characteristics, it would be a plus:</i></p><ul><li><p>HIV field medical experience in the US</p></li><li><p>Proven track record of consistent, high performance within Field-Based Medical Affairs</p></li><li><p>Solid grounding in clinical, medical, and pharmaceutical science with demonstrated ability to rapidly assimilate specific and detailed knowledge in these areas.</p></li><li><p>Experience evaluating and effectively communicating evidence-based medicine with strong scientific communication and presentation skills</p></li><li><p>Leadership skills and experience, including high business acumen, stakeholder management, as well as successful project participation and completion</p></li><li><p>Demonstrated excellence in mentoring fellow MSLs, leading complex field based medical team initiatives, participating in and representing field-based medical on internal cross-functional team, and contributing to strategic planning and development of team’s objectives.</p></li><li><p>Experience engaging effectively one on one and in group settings</p></li><li><p>Effective communication skills</p></li></ul><p></p><p>#LI-ViiV</p><p>#LI-GSK</p><p>#LI-Remote</p>The US annual base salary for new hires in this position ranges from $168,750 to $281,250.  The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.&amp;#xa;&amp;#xa;If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit <a target="_blank" href="https://us.gsk.com/media/7963/ustrataglance-jobpostings.pdf">GSK US Benefits Summary</a><a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"> </a>to learn more about the comprehensive benefits program ViiV offers US employees. All ViiV employees receive the same benefits options and plans as GSK employee.</p><p></p><p><b>Why Us?</b></p><p>At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. </p><p></p><p>We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>GSK</u></span></a> and <a target="_blank" href="http://www.Pfizer.com"><span style="color:#0000ff"><u>Pfizer</u></span></a> in 2009, with <a target="_blank" href="http://www.Shionogi.com"><span style="color:#0000ff"><u>Shionogi</u></span></a> joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.</p><p></p><p>Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. </p><p></p><p>Having a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a></p><p></p><p>ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/viiv-healthcare-senior-medical-science-liaison-los-angeles-ca-gsk/6a05f4ec2f1861929d2531b5</link><guid isPermaLink="true">http://biotechroles.com/viiv-healthcare-senior-medical-science-liaison-los-angeles-ca-gsk/6a05f4ec2f1861929d2531b5</guid><pubDate>Thu, 14 May 2026 16:14:36 GMT</pubDate><company>GSK</company><location>Field Worker - USA</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Territory Account Manager - Miami South]]></title><description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><span class="emphasis"><b>Position territory: Miami South</b></span></p><p></p><p>ViiV Healthcare is a global specialty HIV company, the only one that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV Healthcare is highly mission-driven in our unrelenting commitment to being a trusted partner for all people living with and affected by HIV. Our aim is to think, act, and connect differently through a focus on education on for the prevention and treatment for HIV.  We go to extraordinary lengths to deliver the sorts of breakthroughs, both in prevention, treatments, care solutions and communities, that really count. We go beyond the boundaries of medicine by taking a holistic approach to HIV through developing and supporting sustainable community programs and improving access to care.  We are fully committed to push through every challenge until HIV/AIDS is eradicated. ViiV Healthcare has played a significant part in delivering breakthroughs that have turned HIV into a manageable health condition. We offer the largest portfolio of HIV medicines available anywhere, and we continue our work to cater for the widest possible range of needs in response to the HIV epidemic.</p><p></p><p>We are aware of how much is at stake for those at-risk or affected by HIV and we show up every day 100% committed to the patients. Our work culture is fast-paced, diverse, inclusive, competitive, and caring. But ViiV Healthcare isn’t just somewhere to work – it’s a place to belong, an invitation to bring your very best, and a team full of impact-driven team members who are hungry to make a difference.</p><p></p><p>While we have been improving lives of HIV patients for 30 years, this is an especially exciting time to be at ViiV Healthcare, as we evaluate novel approaches to treatment and prevention that could further reduce the impact of HIV on individuals and communities.</p><p></p><p>ViiV Healthcare is seeking an experienced, results-driven professional in Specialty Sales for the position of <b>Territory Account Manager (TAM) </b>on the long-acting HIV Injectable Treatment Sales team. The ability to thrive in a fast-paced, complex environment and work with HCPs to adopt a new approach to HIV treatment will be essential to delivering success in this role. Additionally, the abilities to partner cross-functionally and to remain highly adaptable in a launch context will be critical. It is expected that the successful candidate will have demonstrated experience in developing strategic business plans with specific, measurable, action-oriented objectives in accordance with territory and account level goals. Successful outcomes will include selling to HCPs, servicing their accounts, and being aligned to ViiV Healthcare’s mission of leaving no person with HIV behind. This will be achieved through driving results against business objectives and working effectively within an integrated account management framework in the setup and delivery of a buy and bill treatment model.</p><p></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:</p><ul><li><p>Deliver Results Through Exceptional Sales and Service</p></li><li><p>Identify, target, and win new business by influencing working with HCPs to adopt a new approach to HIV treatment</p></li><li><p>Engage with HCPs, nurses, staff, and administrators to accurately understand the clinical, organizational, and financial challenges and opportunities within target accounts</p></li><li><p>Leverage data analytics, business acumen, and market expertise to identify high-priority prospects</p></li><li><p>Prepare and execute business plans that are tailored to the unique needs of each customer and that help HCPs scale their treatment model to reach more patients</p></li><li><p>Coordinate, engage, and partner with multiple cross-functional team members (i.e., Clinical Nurse Educators and Field Reimbursement Managers) to deliver an integrated product experience to customers</p></li><li><p>Maintain a portfolio-based selling mindset and close internal communication loops to ensure customers experience a cohesive, integrated ViiV</p></li><li><p>Provide exceptional customer service by proactively anticipating and addressing HCP problems, needs and requests</p></li><li><p>Deliver and adapt execution plans to achieve performance goals and objectives utilizing; KPIs, scaling of successes, business problem solving, etc.</p></li><li><p>Develop and foster external relationships with key influential customers and thought leaders</p></li><li><p>Compliance, Accountabilities, and Values Based Culture</p></li><li><p>Act in ways consistent with ViiV’s culture, expectations, and values</p></li><li><p>Be an agent of change by embracing the ambiguity in a launch environment and seeing setbacks as opportunities to learn and grow</p></li><li><p>Escalate issues and risks when needed; display courage by ‘speaking up’</p></li><li><p>Understand and follow key compliance and regulatory guidelines</p></li></ul><p></p><h1><span class="emphasis"><b>Why you?</b></span></h1><p><span class="emphasis"><b>Basic Qualifications:</b></span></p><p></p><p><i>We are looking for professionals with these required skills to achieve our goals:</i></p><ul><li><p>BA/BS degree</p></li><li><p>5&#43; years of pharmaceutical sales experience</p></li><li><p>3 plus years’ specialty experience</p></li><li><p>Ability to travel domestically as necessary, which may include overnight travel, majority of time will be spent in market</p></li><li><p>Valid Driver&#39;s License</p></li></ul><p>​</p><p><span class="emphasis"><b>Preferred Qualifications:</b></span></p><p><i>If you have the following characteristics, it would be a plus:</i></p><ul><li><p>Degree in Business, Marketing, or Life Sciences</p></li><li><p>Strong planning and organization skills, analytical ability, business acumen, decision making ability, and problem-solving skills</p></li><li><p>Experience to influence and collaborate cross-functionally in a matrixed environment</p></li><li><p>Excellent written and oral communication skills</p></li><li><p>Experience in sales success in complex market access coverage situations</p></li><li><p>Experience working with HCPs to procure, manage, and administer cold chain treatment products</p></li><li><p>Knowledge of the HIV treatment and/or prevention markets</p></li><li><p>Bilingual in Spanish, preferred but not required</p></li><li><p>Experience partnering cross functionally within an integrated account team model that includes multiple field-based team members</p></li></ul><p></p><p><b>#LI-Remote</b></p><p>#ViiV2026</p><p>#LI-GSK</p></div></div></div></div></div></div></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit <a target="_blank" href="https://us.gsk.com/media/7963/ustrataglance-jobpostings.pdf">GSK US Benefits Summary</a><a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"> </a>to learn more about the comprehensive benefits program ViiV offers US employees. All ViiV employees receive the same benefits options and plans as GSK employee.</p><p></p><p><b>Why Us?</b></p><p>At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. </p><p></p><p>We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>GSK</u></span></a> and <a target="_blank" href="http://www.Pfizer.com"><span style="color:#0000ff"><u>Pfizer</u></span></a> in 2009, with <a target="_blank" href="http://www.Shionogi.com"><span style="color:#0000ff"><u>Shionogi</u></span></a> joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.</p><p></p><p>Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. </p><p></p><p>Having a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a></p><p></p><p>ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/territory-account-manager-miami-south-gsk/6a05f4db2f1861929d2531b4</link><guid isPermaLink="true">http://biotechroles.com/territory-account-manager-miami-south-gsk/6a05f4db2f1861929d2531b4</guid><pubDate>Thu, 14 May 2026 16:14:19 GMT</pubDate><company>GSK</company><location>USA - Florida - Miami South</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Director DDS Business Enablement & Implementation]]></title><description><![CDATA[<p><b>Job Title: Director, DDS Business Enablement &amp; Implementation</b><br /> </p><p><b>Job Purpose:</b></p><p><br />Drive the design and delivery of multiple, complex, high-impact initiatives that enhance Drug Development and Supply (DDS) performance, strengthen ways of working, and support organizational readiness for strategic change. Act as an integrator across functions, ensuring programs, processes, and innovations are translated into tangible impact and sustained adoption.</p><p></p><p><b>Key Responsibilities:   </b></p><p><b> </b><br /><b>1.    Strategic Program Design &amp; Delivery:</b> Shape, scope, and design major improvement and transformation initiatives aligned to enterprise priorities, ensuring clear outcomes, governance, and success measures. The in/out scope of those programs will be prioritized by the head of the BPI.<br /><b>2.    Enterprise Change Leadership: </b>Lead structured change approaches (Prosci or equivalent) for Drug Development and Supply (DDS) -wide initiatives, ensuring adoption, behaviour change, and long-term embedding of new processes or capabilities. <br /><b>3.    Performance Enablement:</b> Identify performance gaps and define targeted interventions—process improvements, capability uplift, or new ways of working—to enable higher-quality delivery.<br /><b>4.    Innovation:</b> Provide portfolio overview of Drug Development and Supply (DDS) innovation and capability portfolio delivery (delivered via the functional lines and/or external partnerships) including progress against plans (time, budget &amp; resource), implementation readiness and change plan to implement. Proactively identify any interventions to ensure that capabilities deliver agreed benefits. Partner with others in Chemistry, Manufacturing &amp; Controls (CMC) performance, Chemistry, Manufacturing &amp; Controls (CMC) Digital and MTT leads to ensure a holistic view of all innovation investments and resource demand.<br /><b>5.    Cross-Functional Partnership:</b> Serve as a trusted partner to functional leads and Chemistry, Manufacturing &amp; Controls (CMC) Performance Leads, ensuring alignment, clarity, and informed decision-making.<br /><b>6.    Process Stewardship:</b> Drive the standardization, optimization, and embedding of business processes, ensuring consistency and high-quality execution across Drug Development and Supply (DDS).<br /><b>7.    Capability Building: </b>Support development of team and organizational capabilities through targeted learning and skill- building initiatives.<br /><b>8.    Risk &amp; Issue Anticipation: </b>Identify potential risks to delivery or adoption and propose proactive mitigation strategies.</p><p></p><p><b>Basic Qualification: </b>   </p><ul><li><p>Degree in Life Sciences, Business, or related field; or equivalent by experience</p></li><li><p>Experience in program management, business transformation, operational excellence, or organizational change within complex, matrixed environments.</p></li><li><p>Experience in design, scope, and delivery of major cross-functional initiatives with clear outcomes, governance, and performance measures.</p></li><li><p>Experience working with cross-functional leaders and serving as a thought partner for decision-making across R&amp;D, Chemistry, Manufacturing &amp; Controls (CMC), or Operations.</p></li></ul><p><br /><b>Preferred Qualification:</b> </p><ul><li><p>Advanced degree in Life Sciences, Business, or related field; or equivalent by experience</p></li><li><p>Experience leading enterprise-level transformation programs in biopharma R&amp;D, CMC, or supply chain settings.</p></li><li><p>Demonstrated ability to manage innovation and capability portfolios, including oversight of milestones, resources, risks, and implementation readiness.</p></li><li><p>Experience of Chemistry, Manufacturing &amp; Controls (CMC) processes, digital capabilities, or manufacturing technologies, enabling integrated decision-making with performance and digital partners.</p></li><li><p>Experience driving process standardization and optimization, especially in regulated or highly cross-functional environments.</p></li><li><p>Experience designing and facilitating capability-building or organizational development programs.</p></li></ul><p></p><p><b>Working Arrangements:</b><br />•    This role offers a hybrid working model, with a mix of on-site and remote work. Remote or fully home-working arrangements are not available for this role.</p><p></p>• If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $173,250 to $288,750. &amp;#xa;&amp;#xa;The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.&amp;#xa;&amp;#xa;If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;Italian Salary Range / Fascia retributiva in Italia: EUR 88,500 to EUR 147,500 &amp;#xa;Belgium Salary Range / Fourchette salariale – Belgique: EUR 117,000 to EUR 195,000 &amp;#xa;&amp;#xa;The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.&amp;#xa;&amp;#xa;In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process.&amp;#xa;&amp;#xa;This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/director-dds-business-enablement-and-implementation-gsk/6a05f4da2f1861929d2531b3</link><guid isPermaLink="true">http://biotechroles.com/director-dds-business-enablement-and-implementation-gsk/6a05f4da2f1861929d2531b3</guid><pubDate>Thu, 14 May 2026 16:14:18 GMT</pubDate><company>GSK</company><location>UK - Hertfordshire - Stevenage</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Senior Director, Specialty Care, Global Pricing and Market Access]]></title><description><![CDATA[<p><b>Senior Director, Global Pricing and Market Access (Specialty Medicines)</b></p><p><b>Location: Upper Providence (US – Collegeville, PA): GSK HQ (London, UK</b></p><p></p><p>Global Pricing and Market Access (GPMA) are key to maximizing the value of our products for patients, healthcare systems and for the company. In order to further strengthen our capability in this critical function, we are looking for a senior leader to join the GPMA team who will bring technical and organizational expertise in strategic pricing and global market access in Specialty Medicines, as well as lead his/her respective team as we build our skills and capabilities consistently across the product areas.</p><p>The Senior Director Specialty Medicines GPMA will partner closely with key stakeholders in R&amp;D, Commercial, Medical, RWE, Government Affairs, Policy, and other functions to secure the early input and evidence generation required to deliver competitive Target Medicine Profiles, clinical and real-world development plans, and the delivery of reimbursable dossiers for the markets. Strong collaboration with Regional and local access teams will also be essential to further strengthen our ability to reward innovation and make our products accessible to the patients who will benefit most.</p><p></p><p><b>Key Responsibilities will be:</b></p><p>Lead a team that will provide strategic advice and leadership to assigned Respiratory, Inflammation and Immunology Disease Area globally with respect to market access and pricing, to develop innovative and competitive Payer Value Propositions and Pricing Strategies for launch and pipeline assets.</p><p></p><p><b>Deliverables from the team at a cross-portfolio level will include:</b></p><ul><li>Development of GSK’s global strategy on pricing and access, embedded in the Integrated Asset Plan (IAP)</li><li>Customer insight into pricing and access trends</li><li>Innovation in approaches to pricing and access</li><li>Foresight into direction of travel for payers and development of GSK’s position on Payer approaches</li></ul><p></p><p><b>Deliverables to support individual assets within the assigned area will include, for example:</b></p><ul><li>Lead the cross-functional efforts (e.g., Global Market Access &amp; Pricing Team – GMAP / Value and Access Teams – VAT) to deliver close alignment between insights into payer evidence needs, and ensure execution of plans to generate evidence (Integrated Evidence Plan) to support payer value proposition and pricing strategy</li><li>Guidance to the Medicines Development Lead (MDL) and Medicines Commercial Lead (MCL) consolidating the payer questions/evidence needs for key markets to inform strategy and tactics</li><li>Input to the evidence generation plan to ensure it will address critical payer questions</li><li>A market access strategy within the brand plans, fit for purpose and aligned to the overall market access strategy</li><li>Assist country affiliates in their reimbursement negotiations by integrating country-specific needs into the pricing and market access strategy, value dossier, training on global materials and pricing/negotiation workshops</li><li>Effective team working with medical and outcomes staff to develop an integrated evidence plan and manage efficient interfaces with key countries</li><li>Represent the market access voice at the Medicines Commercial Team (MCT) and Medicines Development Team (MDT) and ensure that the market access strategy is reflected in key commercial and development decisions.</li></ul><p></p><p><span class="emphasis"><b>Why You?</b></span></p><p></p><p><span class="emphasis"><b>Basic Qualifications:</b></span></p><ul><li>Advanced Degree in Business, Medicine, Pharmacy, Health Economics, Health Policy or Science</li><li>15&#43; years of relevant experience acquired at pharmaceutical companies, Payer or Health Technology Assessment agencies, physician associations or relevant consultancy companies in a multi-national context</li><li>5&#43; years of experience working in an above-country role/Global team in the market access space</li><li>5&#43; years of experience working in the US payer or access environment</li><li>3&#43; years of People Management experience</li></ul><p></p><p><span class="emphasis"><b>Preferred Qualifications:</b></span></p><ul><li>Demonstrated ability to think strategically, manage uncertainty, and make sound global market access and pricing recommendations throughout the lifecycle</li><li>Agility and flexibility to support evolving team and business needs; recognized team player/coach</li><li>Exceptional oral and written communication skills, including the ability to develop and deliver effective presentations to senior leadership and tailor for different audiences</li><li>Demonstrated ability to effectively lead cross-functional matrix teams and build relationships across functions and geographies</li><li>Appreciation for External Relations and Public Health Issues in Specialty Medicine</li></ul><p></p><p></p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/senior-director-specialty-care-global-pricing-and-market-access-gsk/6a05f4d92f1861929d2531b2</link><guid isPermaLink="true">http://biotechroles.com/senior-director-specialty-care-global-pricing-and-market-access-gsk/6a05f4d92f1861929d2531b2</guid><pubDate>Thu, 14 May 2026 16:14:17 GMT</pubDate><company>GSK</company><location>USA - Pennsylvania - Upper Providence</location><salary>$220000-320000</salary><type>Full time</type></item><item><title><![CDATA[Senior MES Engineer]]></title><description><![CDATA[<p>The Sr. MES Engineer will p<span>rovide engineering and technical support for manufacturing execution systems in the Biopharmaceutical Operations facility.<span>  </span>Evaluate and develop technology, plan and implement modifications, troubleshoot and support manufacturing execution systems,</span><span> </span><span>and assist in night shift troubleshooting activities during processing operations</span><span>.<span>  </span><span> </span></span></p><p></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career.  These responsibilities include some of the following:</p><ul><li>Provide technical leadership in support of MES (Emerson Syncade and InfoLog) systems and network infrastructure, including electronic batch records, ensuring business continuity and compliance.</li><li>Collaborate with building stakeholders throughout the automation lifecycle: gather system/end user requirements; complete design, implementation, and testing/validation of changes; maintain documentation; maintain and monitor various systems.</li><li>Provide subject matter expertise and technical ownership of MES deployments and associated systems.</li><li>Plan, prioritize, and manage updates to the execution system designs due to process changes, audits, and CAPA actions through collaboration with organization stakeholders.</li><li>Work in a way that models respect for safety and EHS, quality compliance, data integrity, and engineering standards.</li><li>Troubleshoot and resolve real-time operational issues, supporting global Tech and automation staff.</li><li>Support visualization and accessibility of aggregate data using tools like PowerBI, InfoBatch, and SQL.</li><li>Build relationships across Production, Quality, and Global Tech teams to establish robust communication processes.</li><li>Represent MES systems in regulatory inspections and provide user support for technical issues.</li><li>Troubleshoot and diagnose problems with manufacturing execution systems; generate recommendations and then develop/execute solutions to correct and resolve.</li><li>Adhere to, develop, and continuously improve the operation and maintenance procedures for manufacturing execution systems.</li><li>Support the maintenance and upkeep of the operational technology environment through administration of  systems, networks, databases, and accounts.  This includes servers, hosts, and analytical equipment.</li><li>Support site technology related to systems integration and digital transformation initiatives. Stay current with developments in the field of controls and manufacturing execution systems.    </li><li>Lead and develop those around you through active engagement with stakeholders and by modeling professional behaviors.<p></p></li></ul><h1></h1><h1><span class="emphasis"><i><b>Why you?</b></i></span></h1><h2><span class="emphasis">Basic Qualifications:<b> </b></span></h2><p>We are looking for professionals with these required skills to achieve our goals:</p><ul><li>BS/BA in engineering, life sciences, biology or equivalent technical discipline</li><li>4&#43; years of experience in design, programming, start-up, and troubleshooting of manufacturing execution systems (Syncade)<p></p></li></ul><p></p><h2><span class="emphasis">Preferred Qualifications:</span></h2><p>If you have the following characteristics, it would be a plus:</p><ul><li>Ability to diagnose problems, generate options, prioritize issues, select optimal solutions, and implement decisions/resolve problems</li><li>A demonstrated ability to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines</li><li>Experience in systems/account administration, network design, and server troubleshooting</li><li>Experience coding Visual Basic and similar languages</li><li>Experience working in a GMP environment</li><li>Experience in the design, programming, start-up, and troubleshooting of PLC (Allen Bradley) or DCS (DeltaV) systems</li><li>Knowledge in current standards of control system platforms and computer system validation</li></ul><p></p><h1><b>#LI-GSK</b></h1>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/senior-mes-engineer-gsk/6a05f4d72f1861929d2531b1</link><guid isPermaLink="true">http://biotechroles.com/senior-mes-engineer-gsk/6a05f4d72f1861929d2531b1</guid><pubDate>Thu, 14 May 2026 16:14:15 GMT</pubDate><company>GSK</company><location>USA - Pennsylvania - King of Prussia</location><salary>$110000-145000</salary><type>Full time</type></item><item><title><![CDATA[Estágio em Operações de Qualidade, 2026]]></title><description><![CDATA[<p><span class="emphasis"><b>Ajude-nos a vencer doenças e melhorar a saúde da população através de nossa oportunidade de</b><b> Estágio em Operações de Qualidade.</b></span></p><p></p><p><b>Educação necessária:</b> Cursando ensino superior em Farmácia ou áreas correlatas, com previsão de formatura a partir de Dezembro 2028.</p><p></p><p><b>Previsão de Data de início:</b> Julho de 2026</p><p><b>Data limite para inscrição:</b> 25 de Maio de 2026</p><p><b>Previsão da data de entrevista: Junho de 2026</b></p><p></p><p><span class="emphasis"><b>Buscando por uma real experiência de trabalho e poder impactar positivamente a vida de bilhões de pessoas?</b></span></p><p></p><p><span class="emphasis">Uma vaga de Estágio na GSK oferece a você a oportunidade de iniciar sua carreira – De ter uma função com impacto genuíno! Você irá ter um trabalho sério e desafiador, trabalhando em projetos reais. Você também aprenderá conosco, desenvolverá suas habilidades e ganhar experiência para onde o futuro lhe levar!</span></p><p></p><p><span class="emphasis"><b>Quem somos?</b></span></p><p></p><p>GSK é uma empresa Biofarmacêutica global com um propósito especial – Unir ciência, tecnologia e talento para vencer as doenças juntos. Avançar significa prevenir doenças, além de tratá-las. Nós buscamos impactar a saúde de 2.5 bilhões de pessoas ao redor do mundo nos próximos 10 anos.</p><p>Nosso sucesso depende de nossas pessoas. Nós queremos que a GSK seja um lugar onde as pessoas se sintam inspiradas, encorajadas e desafiadas para serem a melhor versão de si! Um lugar onde as pessoas possam ser elas mesmas – se sentindo bem-vindas, valorizadas e inclusas. Onde elas possam continuar crescendo e se preocupar com seu bem-estar. Se você compartilha nossa ambição, junte-se a nós em nossa jornada de vencer as doenças juntos.</p><p></p><p>Dê o play e confira os relatos dos nossos estagiários e aprendizes!</p><p><br />Documentário completo no link abaixo:</p><p><a href="https://www.youtube.com/watch?v&#61;0xF7mG4Qa6A" target="_blank">We are the future | Documentário - Completo - YouTube</a></p><p></p><p> <br /><span class="emphasis"><b>O que você fará? </b> </span></p><p>Nossa área de Operações de Qualidade é responsável por estabelecer e manter padrões de qualidade dos produtos, sistemas e processos internos. Nós implementamos políticas corporativas, legislações sanitárias e desenvolvemos procedimentos visando a manutenção da qualidade dos produtos e a conformidade regulatória. Essa oportunidade lhe permitirá estar em contato direto com as padrões de qualidade da empresa, desenvolvendo uma visão estratégica sobre os produtos da GSK e como manter tal padrão de qualidade. Algumas de suas responsabilidades serão:</p><ul><li><p>Prestar suporte ao farmacêutico responsável</p></li><li><p>Elaborar documentações técnicas</p></li><li><p>Prestar suporte na avaliação de produtos devolvidos</p></li><li><p>Prestar suporte no acompanhamento de Auditorias e inspeções regulatórias</p></li><li><p>Participar do fluxo de revisão e aprovação dos acordos internos de qualidade e das avaliações de risco de distribuição</p></li><li><p>Prestar suporte no processo de gerenciamento de  produtos controlados (Portaria n° 344/98)</p></li><li><p>Prestar suporte no processo de emissão de Certificados de Liberação de Vacinas junto ao INCQS</p></li><li><p>Realizar atividades sistêmicas e documentais;</p></li></ul><p></p><p><span class="emphasis"><b>O que estamos buscando?</b>  </span></p><p>Estamos à procura de Estudantes com essas características para alcançar nossos objetivos:</p><ul><li><p>Pacote Office Intermediário.</p></li><li><p>Inglês Avançado.</p></li><li><p>Perfil pró-ativo e com habilidade para lidar bem com processos administrativos.</p></li><li><p>Resiliência e criatividade para propor melhorias.</p></li><li><p>Organização e atenção aos detalhes.</p></li><li><p>Bom relacionamento interpessoal, espírito de equipe e boa comunicação.</p></li><li><p>Disponibilidade para estagiar em modelo híbrido em Duque de Caxias/RJ, por 6 horas diárias, preferencialmente entre 8h e 17h.</p></li></ul><p></p><p><b>O que oferecemos? </b> </p><ul><li><p>Experiência de trabalho, treinamento formal e informal através de cursos, mentorias e programas de desenvolvimento.</p></li><li><p>Bolsa auxílio mensal e demais benefícios.</p></li></ul><p></p><p><span class="emphasis"><b>Inscreva-se agora! </b></span></p><p>Ao se inscrever na vaga, o site estará em inglês, assim como as perguntas dos questionários, porém você pode mudar a linguagem para Português no canto superior direito da tela. </p><p></p><p><b>Precisa de ajuda com sua inscrição? </b></p><p>Nos mande um e-mail em <a href="mailto:AM.Earlycareers&#64;gsk.com" target="_blank"><b>AM.Earlycareers&#64;gsk.com</b></a> e nos diga como podemos ajudá-lo. </p><p></p><p>Incentivamos todas as pessoas qualificadas a se candidatarem. Valorizamos a diversidade de origens e experiências de vida e temos um forte compromisso com a inclusão.</p><p></p><p><span class="emphasis"><b>Convidamos jovens talentos da GSK</b></span><br />para compartilhar suas vivências, desafios e perspectivas de futuro.</p><p></p><p><span class="emphasis"><b>Assista ao documentário completo no link abaixo:</b></span></p><p><a href="https://www.youtube.com/watch?v&#61;0xF7mG4Qa6A" target="_blank">We are the future | Documentário - Completo</a></p><p></p><p>#EarlyCareers</p><p>#Brazilinternships2026</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.        </p><p></p><p>If you require any adjustments or accommodation during the selection process to better showcase your abilities, please let our team know as soon as we contact you. We&#39;re here to support you.</p><p></p><p>When applying, you may also choose to provide personal information, which helps us ensure a more inclusive selection process. Rest assured, your information will be treated with the utmost confidentiality and will not be accessible to hiring managers. Let’s keep maintaining an inclusive and welcoming workplace.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Find more about life at GSK at <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>www.gsk.com</u></span></a></p>]]></description><link>http://biotechroles.com/estagio-em-operacoes-de-qualidade-2026-gsk/6a05f4d72f1861929d2531b0</link><guid isPermaLink="true">http://biotechroles.com/estagio-em-operacoes-de-qualidade-2026-gsk/6a05f4d72f1861929d2531b0</guid><pubDate>Thu, 14 May 2026 16:14:15 GMT</pubDate><company>GSK</company><location>Brazil - Rio de Janeiro</location><salary>$1000-2000</salary><type>Part time</type></item><item><title><![CDATA[Estagio em Garantia de Qualidade, 2026]]></title><description><![CDATA[<p><span class="emphasis"><b>Ajude-nos a vencer doenças e melhorar a saúde da população através de nossa oportunidade de</b><b> Estágio em Garantia de Qualidade.</b></span></p><p></p><p><b>Educação necessária:</b> Cursando ensino superior em Farmácia ou Química a partir do 3º período  com previsão de Graduação a partir de Dezembro 2028.</p><p></p><p><b>Previsão de Data de início:</b> Julho de 2026</p><p><b>Data limite para inscrição:</b> 25 de Maio de 2026</p><p><b>Previsão da data de entrevista: Junho de 2026</b></p><p></p><p><span class="emphasis"><b>Buscando por uma real experiência de trabalho e poder impactar positivamente a vida de bilhões de pessoas?</b></span></p><p></p><p><span class="emphasis">Uma vaga de Estágio na GSK oferece a você a oportunidade de iniciar sua carreira – De ter uma função com impacto genuíno! Você irá ter um trabalho sério e desafiador, trabalhando em projetos reais. Você também aprenderá conosco, desenvolverá suas habilidades e ganhar experiência para onde o futuro lhe levar!</span></p><p></p><p><span class="emphasis"><b>Quem somos?</b></span></p><p></p><p>GSK é uma empresa Biofarmacêutica global com um propósito especial – Unir ciência, tecnologia e talento para vencer as doenças juntos. Avançar significa prevenir doenças, além de tratá-las. Nós buscamos impactar a saúde de 2.5 bilhões de pessoas ao redor do mundo nos próximos 10 anos.</p><p>Nosso sucesso depende de nossas pessoas. Nós queremos que a GSK seja um lugar onde as pessoas se sintam inspiradas, encorajadas e desafiadas para serem a melhor versão de si! Um lugar onde as pessoas possam ser elas mesmas – se sentindo bem-vindas, valorizadas e inclusas. Onde elas possam continuar crescendo e se preocupar com seu bem-estar. Se você compartilha nossa ambição, junte-se a nós em nossa jornada de vencer as doenças juntos.</p><p></p><p>Dê o play e confira os relatos dos nossos estagiários e aprendizes!</p><p><br />Documentário completo no link abaixo:</p><p><a href="https://www.youtube.com/watch?v&#61;0xF7mG4Qa6A" target="_blank">We are the future | Documentário - Completo - YouTube</a></p><p></p><p> <br /><span class="emphasis"><b>O que você fará? </b></span> </p><p></p><p>A área de <b>Garantia da Qualidade</b> é responsável por garantir que os processos e produtos atendam aos padrões regulatórios e internos, seguindo rigorosamente as legislações da ANVISA e diretrizes da GSK.</p><p>Seu estágio consiste em atuar de forma administrativa, focado no suporte no processo de tratamento de reclamações relacionadas à qualidade de produtos.</p><p></p><ul><li><p>Receber e registrar reclamações de clientes, distribuidores e pacientes encaminhadas pelo SAC.</p></li><li><p>Realizar triagem, classificação e encaminhamento das demandas para o site fabricante para investigação.</p></li><li><p>Preparar amostras para envio ao fabricante, seguindo os procedimentos internos.</p></li><li><p>Efetuar cadastro e atualização de informações nos sistemas internos.</p></li><li><p>Apoiar no envio de amostras físicas para processos de exportação, garantindo conformidade com a legislação da ANVISA.</p></li><li><p>Elaborar comunicações que serão enviada aos clientes com o retorno das análises realizadas.</p></li><li><p>Apoiar no gerenciamento das etapas internas para pagamentos de fornecedores de qualidade.</p></li></ul><p></p><p><span class="emphasis"><b>O que estamos buscando? </b></span> </p><p></p><p>Estamos à procura de Estudantes com essas características para alcançar nossos objetivos:</p><ul><li><p>Inglês Intermediário/avançado.</p></li><li><p>Excel intermediário/avançado.</p></li><li><p>Boa comunicação e relacionamento interpessoal.</p></li><li><p>Perfil colaborativo e trabalho em equipe.</p></li><li><p>Organização e atenção aos detalhes.</p></li><li><p>Disponibilidade para estagiar presencialmente em Jacarepaguá por 6 horas diárias, entre 8h e 17h.</p></li></ul><p></p><p><span class="emphasis"><b>O que oferecemos? </b> </span></p><ul><li><p>Experiência de trabalho, treinamento formal e informal através de cursos, mentorias e programas de desenvolvimento.</p></li><li><p>Bolsa auxílio mensal e demais benefícios.</p></li></ul><p></p><p></p><p><span class="emphasis"><b>Inscreva-se agora! </b></span></p><p>Ao se inscrever na vaga, o site estará em inglês, assim como as perguntas dos questionários, porém você pode mudar a linguagem para Português no canto superior direito da tela. </p><p></p><p><b>Precisa de ajuda com sua inscrição? </b></p><p>Nos mande um e-mail em <a href="mailto:AM.Earlycareers&#64;gsk.com" target="_blank"><b>AM.Earlycareers&#64;gsk.com</b></a> e nos diga como podemos ajudá-lo. </p><p></p><p>Incentivamos todas as pessoas qualificadas a se candidatarem. Valorizamos a diversidade de origens e experiências de vida e temos um forte compromisso com a inclusão.</p><p></p><p><span class="emphasis"><b>Convidamos jovens talentos da GSK</b></span><br />para compartilhar suas vivências, desafios e perspectivas de futuro.</p><p></p><p><span class="emphasis"><b>Assista ao documentário completo no link abaixo:</b></span></p><p><a href="https://www.youtube.com/watch?v&#61;0xF7mG4Qa6A" target="_blank">We are the future | Documentário - Completo</a></p><p></p><p>#EarlyCareers</p><p>#Brazilinternships2026</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.        </p><p></p><p>If you require any adjustments or accommodation during the selection process to better showcase your abilities, please let our team know as soon as we contact you. We&#39;re here to support you.</p><p></p><p>When applying, you may also choose to provide personal information, which helps us ensure a more inclusive selection process. Rest assured, your information will be treated with the utmost confidentiality and will not be accessible to hiring managers. Let’s keep maintaining an inclusive and welcoming workplace.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Find more about life at GSK at <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>www.gsk.com</u></span></a></p>]]></description><link>http://biotechroles.com/estagio-em-garantia-de-qualidade-2026-gsk/6a05f4d62f1861929d2531af</link><guid isPermaLink="true">http://biotechroles.com/estagio-em-garantia-de-qualidade-2026-gsk/6a05f4d62f1861929d2531af</guid><pubDate>Thu, 14 May 2026 16:14:14 GMT</pubDate><company>GSK</company><location>Brazil - Rio de Janeiro</location><salary>$1000-2000</salary><type>Part time</type></item><item><title><![CDATA[Gerente de Marketing Vacunas Adultos CVMD (experiencia Cardiorrenometabólico)]]></title><description><![CDATA[<p><b>troducción del negocio</b></p><p><span><span>GSK</span></span> mantiene su compromiso de alcanzar ambiciosos objetivos comerciales para el futuro. Para 2031, aspiramos a alcanzar £40 mil millones en ventas anuales, aprovechando el sólido impulso de nuestro desempeño actual para incrementar significativamente nuestro impacto positivo en la salud de miles de millones de pacientes a nivel mundial. Nuestra estrategia <i>Ahead Together</i> se centra en la intervención temprana para prevenir y modificar el curso de las enfermedades, protegiendo a las personas y apoyando a los sistemas de salud.</p><p>Nuestro portafolio diverso está compuesto por vacunas, medicamentos especializados y medicamentos generales.</p><p>A través de la innovación continua y un enfoque dedicado en la excelencia científica y técnica, nos esforzamos por desarrollar y lanzar nuevos tratamientos innovadores que aborden desafíos críticos de salud.</p><p><b>Resumen del Puesto</b></p><p></p><p>Lideraras  y desarrollaras la estrategia de negocio de la vacuna contra el Herpes Zóster para GSK Colombia, incluyendo perspectivas a corto y largo plazo, y la estrategia de ruta al mercado.</p><p>Trabajarás de manera cercana con los equipos de ventas, médico, acceso al mercado y equipos globales para entregar planes integrados multicanal. Valoramos la curiosidad, la comunicación clara y la resolución práctica de problemas. Este rol ofrece oportunidades de crecimiento, la posibilidad de dar forma a planes locales y la oportunidad de generar un impacto significativo alineado con nuestra misión de unir ciencia, tecnología y talento para adelantarnos juntos  a la enfermedad</p><p></p><p><b>Responsabilidades</b><br />Este rol te brindará la oportunidad de liderar actividades clave para impulsar tu desarrollo profesional. Entre las responsabilidades se incluyen:</p><ul><li>Desarrollar e implementar planes locales de producto basados en las necesidades de los clientes y en insights de mercado.</li><li>Diseñar y ejecutar campañas promocionales omnicanal y actividades digitales.</li><li>Trabajar con los equipos locales de ventas para apoyar lanzamientos, despliegue táctico e implementación en campo.</li><li>Recopilar insights de clientes y stakeholders, y compartir los hallazgos con equipos globales y locales.</li><li>Gestionar insumos de pronóstico, presupuestos promocionales y seguimiento básico del desempeño comercial.</li><li>Coordinar actividades transversales con los equipos de Medical, Supply, Market Access y colegas globales.</li></ul><p></p><p><b>¿Por qué tú?</b></p><p><b>Requisitos básicos</b><br />Buscamos profesionales con las siguientes habilidades y calificaciones requeridas para alcanzar nuestros objetivos:</p><ul><li>Título universitario en Marketing, Administración de Empresas, Ciencias de la salud o disciplina relacionada.</li><li>Mínimo 5 años dentro de la industria farmacéutica y 3 años de experiencia en gestión de producto.</li><li>Experiencia en planificación o ejecución de campañas multicanal o de marketing digital.</li><li>Sólidas habilidades de relacionamiento y colaboración con stakeholders.</li><li>Solidez en toma de decisiones basadas en datos.</li><li>Español fluido e inglés a nivel profesional.</li><li>Experiencia en portafolios <b>Cardio metabólicos, endocrinología y Nefrología</b></li></ul><p></p><p><b>Requisitos deseables</b><br />Se valorará adicionalmente:</p><ul><li>Experiencia en marketing farmacéutico o de salud y conocimiento de las normativas promocionales locales.</li><li>Experiencia apoyando lanzamientos de producto o gestionando el ciclo de vida de marca.</li><li>Conocimientos básicos financieros y de proyección (forecasting).</li><li>Experiencia trabajando con equipos globales de marca o en proyectos internacionales.</li><li>Experiencia o certificación en gestión de proyectos.</li><li>Comodidad en el uso de analítica y datos de mercado para la toma de decisiones.</li></ul><p></p><p><b>Cómo postular</b><br />Si este rol se alinea con tu experiencia y aspiraciones, te invitamos a postularte. Cuéntanos por qué este rol es importante para ti y cómo generarías impacto. Damos la bienvenida a candidatos de todos los orígenes y experiencias que compartan nuestro compromiso con la inclusión y la mejora de la salud para las personas en todo el mundo.</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>If you require any adjustments or accommodation during the selection process to better showcase your abilities, please let our team know as soon as we contact you. We&#39;re here to support you.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Our inclusive workplace makes our employees feel engaged by the contribution they make, by affording them equal treatment regardless of actual or perceived characteristics. As so, when you apply for a job at GSK, it is not necessary to include on your resume information such as: race, color, ethnicity, age, gender, sexual orientation, marital status, religion, origin, photographs or any other personal characteristics.</p><p> </p><p>Find out what life at GSK is really like <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>www.gsk.com</u></span></a></p>]]></description><link>http://biotechroles.com/gerente-de-marketing-vacunas-adultos-cvmd-experiencia-cardiorrenometabolico-gsk/6a05f4d62f1861929d2531ae</link><guid isPermaLink="true">http://biotechroles.com/gerente-de-marketing-vacunas-adultos-cvmd-experiencia-cardiorrenometabolico-gsk/6a05f4d62f1861929d2531ae</guid><pubDate>Thu, 14 May 2026 16:14:14 GMT</pubDate><company>GSK</company><location>Bogota Torre Cusezar</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Sales Representative - Jacksonville, FL]]></title><description><![CDATA[<p><b><span>Territory: </span></b><span>Includes but is not limited to: <b>Jacksonville, FL</b></span></p><p><span> </span></p><div><div><p><span><span>At GSK we unite science,<span> </span></span><span>talent</span><span><span> </span>and technology to get ahead of disease together.<span> </span></span><span>We’ve</span><span><span> </span>transformed R&amp;D and commercial execution to deliver<span> </span></span><span>life</span></span><span>‑</span><span><span>changing</span><span><span> </span>vaccines and specialty medicines. If<span> </span></span><span>you’re</span><span><span> </span>ready to improve the lives of billions and grow your career in a<span> </span></span><span>purpose</span></span><span>‑</span><span><span>driven</span><span><span> </span>company, join us.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span class="emphasis"><b>About the Role</b></span><span> </span></p></div><div><p></p><p><span><span>The GSK<span> </span></span></span><i><span>US Respiratory<span> </span></span><span>&amp; Anti-Infectives<span> </span></span></i><b><span>Sales</span></b><span><span><span> </span>Professional<span> </span></span><span>is responsible for</span><span><span> </span></span><span>engaging physicians</span><span><span> </span>and allied health professionals across independent practices, physician groups, and hospital systems to drive<span> </span></span><span>appropriate prescribing</span><span><span> </span>of GSK products. This includes influencing prescribing decisions versus competitive therapies for relevant disease states through compliant, face-to-face interactions, in alignment with approved product<span> </span></span><span>indications</span><span><span> </span>and prescribing information.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>This role gives you the opportunity to build your skills and grow your career. Key responsibilities include</span><span>:</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span class="emphasis"><b>Key Responsibilities</b> </span></p></div><div><ul><li><p><span><span>Drive territory sales and market share growth across promoted COPD, asthma, and anti-infective products through targeted, compliant, evidence-based customer engagement.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Own territory business planning; analyze sales data and execute actions to meet goals.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Develop dynamic call plans and collaborate with local territory colleagues to maximize reach and frequency.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Build strong partnerships with Marketing, Payer Relations, Medical (MSLs), and other internal stakeholders to align strategy and resources.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Plan and deliver in-services, educational programs, and sample distribution<span> </span></span><span>in accordance with</span><span><span> </span>FDA regulations and company policy.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Complete administrative responsibilities accurately and on time (e.g., sample accountability, call reporting, eLearning, and expense reporting).</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Comply with</span><span><span> </span>GSK policies, ethical standards, and all applicable regulatory requirements.</span></span><span> </span></p></li></ul></div><div><div><div><p></p><p><span class="emphasis"><b>Why You? </b></span></p></div><div><p></p><p><span class="emphasis"><b>Basic Qualifications </b></span></p></div><div><ul><li><p><span><span>BA/BS from an accredited institution</span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Valid driver’s license;<span> </span></span><span>driving is an essential function of this role</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Willingness to travel within the territory, including occasional overnight and weekend travel, based on business needs</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>The selected candidate will be hired at the<span> </span></span><span>appropriate level</span><span><span> </span>based on experience</span><span>:</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><b><span>Grade 8</span></b><span>:<span> </span></span><span>Minimum of<span> </span></span><span>2<span> </span></span><span>years</span><span><span> </span>of</span><span><span> </span>pharma</span><span>ceutical<span> </span></span><span>or<span> </span></span><span>business</span><span>-</span><span>to</span><span>-</span><span>business<span> </span></span><span>sales experience</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><b><span>Grade 7</span></b><span>:</span><span><span> </span></span><span>Minimum of<span> </span></span><span>5 years<span> </span></span><span>of<span> </span></span><span>pharma</span><span>ceutical<span> </span></span><span>or<span> </span></span><span>business</span><span>-</span><span>to</span><span>-</span><span>business<span> </span></span><span>sales experience</span></span><span> </span></p></li></ul></div><div><p></p><p><span class="emphasis"><b>Preferred Qualifications</b></span><span> </span></p></div><div><ul><li><p><span><span>Bilingual<span> </span></span><span>preferred based on location</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>A</span><span>ccount management experience within local IDNs/large hospital systems</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience in respiratory/allergy or other healthcare sales</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Familiarity with managed care, formularies, retail pharmacy operations, prior authorization processes</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong presentation,<span> </span></span><span>influencing</span><span><span> </span>and business planning skills</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Self</span></span><span>‑</span><span><span>starter</span><span><span> </span>with attention to detail and ability to manage multiple priorities</span></span><span> </span></p></li></ul></div><div><p></p><p><span class="emphasis"><b>Core Capabilities</b> </span></p></div><div><ul><li><p><span><span>Winning mindset and results orientation</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ambitious goal setting and performance discipline</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Courage to challenge constructively and resilience to overcome setbacks</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Change leadership and continuous improvement mindset</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Accountability, team<span> </span></span><span>inspiration</span><span><span> </span>and influential communication</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div></div><div><p><span><span>We invest in development and transparent talent managemen</span><span>t. G</span><span>row your career with meaningful work that<span> </span></span><span>impacts</span><span><span> </span>patients and communities. Join our challenge to get Ahead Together.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>#LI-GSK</span></span><span> </span></p></div><div><p><span><span>#LI-Remote</span></span><span> </span></p></div><div><p><span><span>#GSKCommercial</span></span><span> </span></p></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pharmaceutical-sales-representative-jacksonville-fl-gsk/6a05f4d52f1861929d2531ad</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-sales-representative-jacksonville-fl-gsk/6a05f4d52f1861929d2531ad</guid><pubDate>Thu, 14 May 2026 16:14:13 GMT</pubDate><company>GSK</company><location>USA - Florida - Jacksonville</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Day Operations Technician]]></title><description><![CDATA[<p>You will join our Singapore manufacturing team as a Day Operations Technician. You will operate and support production activities during the day shift to deliver safe, compliant and reliable supply. You will work closely with operators, engineers and quality colleagues to follow procedures, keep clear records and help solve routine problems. We value team members who are curious, careful and ready to learn. This role gives you hands-on skill development, visible impact and clear pathways to grow while uniting science, technology and talent to get ahead of disease together.</p><p></p><p><span class="emphasis"><b>Responsibilities</b></span><br />This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><ul><li><p>Operate production and supporting equipment safely and efficiently, following standard operating procedures.</p></li><li><p>Perform routine inspections, basic maintenance, lubrication and simple repairs using hand tools.</p></li><li><p>Prepare production areas and support changeovers and set-up tasks during the day shift.</p></li><li><p>Collect in-process samples, perform basic checks and record results accurately.</p></li><li><p>Maintain clear production records, logbooks and follow good documentation practices.</p></li><li><p>Report equipment faults, suggest improvements and support basic root-cause activities.</p></li><li><p>Work with the day shift team to meet production plans while prioritising safety and quality.</p></li><li><p>Follow permit-to-work and site safety procedures at all times.</p></li><li><p>Keep production areas clean and maintain good housekeeping standards.</p></li><li><p>Participate in shift handovers, briefings and on-the-job training to stay current.</p></li><li><p>Support materials handling, inventory movements and correct storage practices.</p></li><li><p>Contribute practical ideas for efficiency and quality improvements and help implement agreed changes.</p></li></ul><p><br /><span class="emphasis"><b>Basic Qualification</b></span><br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li><p>Minimum NITEC, ITE or secondary school qualification. Technical certificates or a polytechnic diploma is a plus.</p></li><li><p>At least 1 year of hands-on experience in manufacturing, production, or a technical trade.</p></li><li><p>Practical experience operating or supporting production or utility equipment.</p></li><li><p>Comfortable working on-site in a production environment and able to follow safety guidance.</p></li><li><p>Clear written and spoken English and basic record-keeping skills.</p></li><li><p>Willingness to work on-site full time on the day shift and support handovers.</p></li></ul><p><br /><span class="emphasis"><b>Preferred Qualification</b></span><br />If you have the following characteristics, it would be a plus:</p><ul><li><p>Prior experience in pharmaceutical, biotech or regulated manufacturing.</p></li><li><p>Familiarity with good manufacturing practices and clear documentation standards.</p></li><li><p>Basic troubleshooting skills and experience with simple problem-solving tools.</p></li><li><p>Experience with materials handling equipment such as pallet trucks.</p></li><li><p>Basic computer literacy for recording data and using production systems.</p></li><li><p>Interest in developing toward specialist or supervisory roles.</p></li></ul><p></p><p><span>To learn more about Singapore GSK and our people, please click on this link:<span> </span><a href="https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore" target="_blank"><u>https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore</u></a> </span></p><p><span> #Li-GSK </span></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact <a target="_blank" href="mailto:APACRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>APACRecruitment.Adjustments&#64;gsk.com</u></span></a>. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/day-operations-technician-gsk/6a05f4d52f1861929d2531ac</link><guid isPermaLink="true">http://biotechroles.com/day-operations-technician-gsk/6a05f4d52f1861929d2531ac</guid><pubDate>Thu, 14 May 2026 16:14:13 GMT</pubDate><company>GSK</company><location>Singapore - Jurong</location><salary>$22000-35000</salary><type>Full time</type></item><item><title><![CDATA[Principal Data Scientist]]></title><description><![CDATA[<p>GSK is one of the world&#39;s pre-eminent pharmaceutical and healthcare companies. We take pride in leading a healthcare revolution. Through disruptive approaches in R&amp;D and commercial business processes, our Data &amp; Analytics team integrates, simplifies, and unlocks all our data. This drives innovation, decision-making, and allows us to better serve our patients, healthcare professionals, and consumers</p><p></p><p>This role will provide YOU the opportunity to lead key activities to progress YOUR career.  Responsibilities include some of the following:</p><ul><li><p>Develop and deliver high quality, analytics and insights using ML and statistical models to uncover business learnings at the patient, HCP/EE segment, and health system level aligned with analytical priorities for:</p><ul><li><p>Customer Segmentation</p></li><li><p>Impact Measurement</p></li><li><p>Omnichannel analytics</p></li><li><p>Resource Allocation and budget Optimization</p></li><li><p>Experimental design (test/control) analyses</p></li></ul></li><li><p>Understand data science opportunities, based on analytical knowledge and business acumen, needed to deliver innovative solutions;  uncover drivers of business performance, customer behaviors, and patient treatment gaps to improve strategic opportunities.</p></li><li><p>Act as a data science expert, by learning and contributing to GSKs’ data science community to grow their data skills, build best practices, and grow data science literacy within the organization.</p></li><li><p>Earn the trust of stakeholder partners and team members to drive data-driven decisions through active engagement, advanced analytics expertise, demonstrated learning, and business knowledge.</p></li><li><p>Apply expertise with feature engineering, model training, and validation;  work collaboratively on pipelines for data ingestion, productionized models, and ensure scalability, reproducibility, and effective monitoring.</p></li><li><p>Establish and define project plans with success metrics, proactively seek inputs and requirements needed to complete analyses, and deliver milestones according to plan.</p></li><li><p>Collaborate on cross-matrix teams and demonstrate subject matter expertise with other teams/functions to drive efficiency and seamless decision making.</p></li><li><p>Recommend solutions and propose options with pros and cons to drive better data driven decision making.  Translate analytical outputs into clear summaries for stakeholders demonstrating accountability for accuracy, quality, and timeliness of deliverables.</p></li><li><p>Use storytelling, powerful visualizations to demonstrate power of utilizing data science with business partners and analytics team members which enable fact-based recommendations that inspire usage for data driven decisions. </p></li></ul><p></p><p><b>Why you? </b></p><p><b>Basic Qualifications: </b></p><ul><li><p>Bachelor&#39;s degree with 10&#43; yrs of Industry experience, master&#39;s or PhD with 8&#43; yrs of Industry experience.</p></li><li><p><b><span>Proficiency in analytics tools/languages such as SQL, Python, PySpark, and visualization tools</span></b></p></li><li><p><b><span>Proficiency in statistical and ML models </span></b></p></li><li><p>Demonstrated skill in effective communication to technical and non-technical audiences; ability to present complex analyses simply.</p></li><li><p>Prior work experience, proactively identifying areas for analysis including the application for machine learning, demonstrating analytic curiosity to develop innovative solutions to solve complex problems.</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>Enthusiasm for leveraging Real World Data</p></li><li><p>Effective communicator w/ strong business acumen knowledge</p></li><li><p>Understanding of business needs and ability to develop appropriate solutions</p></li><li><p>Demonstrate teamwork and strong collaborative partnerships with experience mentoring junior data scientists</p></li><li><p>Familiarity with healthcare-related datasets, such as claims data (e.g., , IQVIA, Komodo, Optum), pharma retail data</p></li></ul><p></p><p><b>Top skills to prioritize (Top 3–4)</b></p><ul><li><p>Machine learning &amp; statistical modeling (incl. feature engineering, training, validation)</p></li><li><p>Programming &amp; data querying: Python, SQL (plus PySpark for large-scale data)</p></li><li><p>Applied analytics for commercial/omnichannel use cases (segmentation, impact measurement, experimentation, optimization)</p></li><li><p>Stakeholder communication &amp; storytelling (translate insights for technical/non-technical audiences)</p></li></ul>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/principal-data-scientist-gsk/6a05f4d32f1861929d2531ab</link><guid isPermaLink="true">http://biotechroles.com/principal-data-scientist-gsk/6a05f4d32f1861929d2531ab</guid><pubDate>Thu, 14 May 2026 16:14:11 GMT</pubDate><company>GSK</company><location>Bengaluru Luxor North Tower</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Production Lead Derms]]></title><description><![CDATA[<p><b>Role Summary</b></p><p>You will lead day-to-day production activities for a dermal manufacturing unit in a regulated environment. You will work closely with quality, engineering, maintenance, planning and supply teams. We value clear decision-making, practical problem solving and coaching people. This role offers growth, real impact on supply reliability, and a chance to help GSK unite science, technology and talent to get ahead of disease together.</p><p><br /><b>Key Responsibilities</b></p><p>- Lead and manage daily production operations to meet safety, quality, delivery and productivity targets.<br />- Supervise and develop production technicians to maintain competence and ensure right-first-time execution.<br />- Own the production schedule for the unit and adapt resources to meet weekly and monthly supply plans.<br />- Act as the unit subject matter expert during internal and external inspections and ensure inspection readiness.<br />- Lead investigations of critical deviations, support CAPA delivery and ensure timely closure of actions.<br />- Identify and lead continuous improvement projects to improve reliability, reduce waste and increase operational efficiency.<br />- Ensure all production activities follow current good manufacturing practices and site quality procedures.<br />- Approve and maintain production instructions and batch records for safe and compliant execution.<br />- Plan and allocate manpower based on forecast and operational requirements.<br />- Coordinate preventive maintenance, validations and equipment availability with engineering and maintenance.<br />- Support budgeting and capital expenditure planning for the unit.<br />- Maintain a safe working environment and promote open, honest feedback and learning.<br /><br /><b>Education, Experience &amp; Skills</b></p><p>- Bachelor’s Degree in Pharmacy (B-Pharm), Pharm-D or a master’s in a related field.<br />- Minimum 5 to 7 years of experience in a regulated manufacturing environment, preferably pharmaceutical.<br />- At least 3 years in a production leadership or supervisory role.<br />- Strong knowledge of good manufacturing practices, batch documentation and quality systems.<br />- Experience managing deviations, CAPA and audit or inspection readiness.<br />- Hands-on experience with dermal or topical finished dosage manufacturing.<br />- Experience with Lean, Six Sigma or other continuous improvement methods.<br />- Practical exposure to process validation, change control and computerized manufacturing systems.<br />- Strong planning, problem-solving and data-driven decision-making skills.<br />- Experience coaching and developing teams and supporting succession planning.<br /><br /><b>Work Arrangement</b><br />This role is on-site to support hands-on manufacturing and team leadership. Shift patterns will reflect site operational needs.</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?<br />Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Contact information:</b><br />You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/production-lead-derms-gsk/6a05f4d22f1861929d2531aa</link><guid isPermaLink="true">http://biotechroles.com/production-lead-derms-gsk/6a05f4d22f1861929d2531aa</guid><pubDate>Thu, 14 May 2026 16:14:10 GMT</pubDate><company>GSK</company><location>Pakistan - Sindh - Karachi</location><salary>$15000-25000</salary><type>Full time</type></item><item><title><![CDATA[Business Executive - Lucknow]]></title><description><![CDATA[<p>Business Introduction<br />GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.<br />Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.<br />Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.<br /><br /><br />Position Summary<br />You will lead commercial growth and customer engagement across an assigned territory in India. You will build trusted, professional relationships with healthcare teams and institutional partners. You will design and deliver territory plans that drive business results and support better patient outcomes. We value clear communicators who act with integrity, curiosity and practical commercial thinking. This role offers visible impact, strong learning and the chance to work with colleagues uniting science, technology and talent to get ahead of disease together.<br /><br />Responsibilities<br />This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<br />- Build and maintain trusted relationships with healthcare professionals, hospital teams and institutional stakeholders across your territory.<br />- Create and deliver territory business plans that meet commercial targets and support improved patient outcomes.<br />- Conduct professional visits and educational meetings to share evidence and practical insights clearly and responsibly.<br />- Collect market and customer feedback and use insights to shape local plans and improve performance.<br />- Work with colleagues across functions to address customer needs and ensure high-quality delivery.<br />- Ensure all activities follow company policies, quality standards and local regulations.<br /><br />Why You?<br /><br />Basic Qualification<br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:<br />- Bachelor’s degree in any discipline; a background in science, pharmacy or medicine is an advantage.<br />- 1–3 years of customer-facing experience in sales, field roles or account management.<br />- Strong spoken and written communication skills in English and relevant local languages.<br />- Comfortable using everyday computer tools such as Word, Excel and mobile apps.<br />- Valid driver’s license and willingness to travel regularly within the assigned territory.<br />- Customer-focused mindset with integrity and a commitment to ethical behaviour.<br /><br />Preferred Qualification<br />If you have the following characteristics, it would be a plus:<br />- Prior experience in healthcare or pharmaceutical field roles.<br />- Ability to interpret and communicate scientific or clinical information clearly.<br />- Planning and analytical skills to develop and monitor territory performance.<br />- Experience organising professional meetings or educational events.<br />- Comfortable working independently and as part of a team.<br />- Fluency in additional local languages.<br /><br />Work pattern and location<br />This role is on-site in India with regular travel across the assigned territory. Some flexible time for administrative tasks may be possible, but a regular presence in the field is required.<br /><br />Ready to apply?<br />If this role speaks to you, we would like to hear from you. Please submit your CV and a brief note explaining why this opportunity appeals to you. We welcome applicants from all backgrounds and encourage people who value inclusion to apply.</p><p></p><p><span><span><span><b>Job Location - Lucknow </b>#LI-Remote </span></span></span></p><p><span><span><span> </span></span></span></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/business-executive-lucknow-gsk/6a05f4d22f1861929d2531a9</link><guid isPermaLink="true">http://biotechroles.com/business-executive-lucknow-gsk/6a05f4d22f1861929d2531a9</guid><pubDate>Thu, 14 May 2026 16:14:10 GMT</pubDate><company>GSK</company><location>Field Worker - IND Rx</location><salary>$12000-25000</salary><type>Full time</type></item><item><title><![CDATA[Assistant Manager Manufacturing]]></title><description><![CDATA[<p><b>Job Purpose:</b></p><p>You will lead and support production and manufacturing operations to deliver safe, high-quality products on time. You will work closely with operations, quality, engineering and planning teams. We value clear communicators who coach teams, solve problems and drive continuous improvement. This role offers growth, hands-on learning and the chance to make a meaningful impact while uniting science, technology and talent to get ahead of disease together.</p><p><br /><b>Responsibilities:</b></p><p>- Plan, coordinate and supervise daily manufacturing and packaging activities to meet schedules, quality and safety standards.<br />- Coach and develop production teams; set clear expectations and provide regular feedback.<br />- Support compliance and quality systems through investigations, corrective and preventive actions (CAPAs), change controls and audit readiness.<br />- Maintain accurate production records, batch documentation and system postings.<br />- Work with engineering and planning to manage equipment availability, material flow and capacity.<br />- Lead continuous improvement projects to increase efficiency, reduce waste and improve key performance metrics.<br /><br /><b>Education, Experience &amp; Skills:</b><br />- Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Engineering, Chemistry or related field, or equivalent experience.</p><p>- 3 or more years’ experience in pharmaceutical manufacturing, filling or packaging operations.<br />- Experience with SAP, manufacturing execution systems or inventory management tools.<br />- Experience in production operations with supervisory or frontline leadership exposure.<br />- Problem-solving experience with root cause analysis and CAPA processes.<br />- Ability to use manufacturing systems or enterprise resource planning tools for data posting.<br />- Training or experience in Lean, Six Sigma or operational excellence methods.<br />- Experience conducting or supporting audits and audit readiness activities.<br />- Strong communication and coaching skills for cross-functional collaboration.</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?<br />Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Contact information:</b><br />You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p>]]></description><link>http://biotechroles.com/assistant-manager-manufacturing-gsk/6a05f4d12f1861929d2531a8</link><guid isPermaLink="true">http://biotechroles.com/assistant-manager-manufacturing-gsk/6a05f4d12f1861929d2531a8</guid><pubDate>Thu, 14 May 2026 16:14:09 GMT</pubDate><company>GSK</company><location>Pakistan - Sindh - Karachi</location><salary>$12000-22000</salary><type>Full time</type></item><item><title><![CDATA[Engagement Specialist & Executive Assistant]]></title><description><![CDATA[<p></p><p><b>Roles and Responsibilites:</b></p><p></p><p> <b>Employee Engagement</b></p><ul><li><p>Lead and oversee the GCC Finance group employee engagement plan</p></li><li><p>Organize &amp; execute GCC Finance group town halls and events</p></li><li><p>Lead and guide the employee resource groups in delivering culture-building activities to bring the Hub community together</p></li><li><p>Ensuring all communication and engagement plans follow industry standards, internal policies, and best practices</p></li><li><p>Track and record engagement expenditures</p></li><li><p>Create impactful storytelling video compilation and other digital content for Hub activities (pre- and post-event)</p></li></ul><p>Work in partnership with other GSK’s Subject matter experts, communication specialists, Global capability &amp; engagement lead locally &amp; in other countries.</p><p></p><p><b><i>Executive Support:</i></b></p><ul><li><p>Manage complex calendars, prioritize meetings, manage meeting logistics and resolve scheduling conflicts as needed to protect the Exec’s time.</p></li><li><p>Coordinate international travel, visas, travel expenses and produce complex travel itineraries when needed for senior staff within GFS.</p></li><li><p>Serve as key point of contact for general department questions. </p></li><li><p>Work collaboratively to escalate and resolve issues.</p></li><li><p>Coordinate and plan department meetings and gatherings</p></li><li><p>Mentor, coach, train others on use of internal systems and processes as required</p></li></ul><ul><li><p>Maintain a high degree of proficiency in a variety of database, software, and internal systems in order to provide high-quality administrative support</p></li><li><p>Manage multiple concurrent tasks and appropriately prioritise workload. </p></li><li><p>Communicate and interact with various senior leaders in GSK.</p></li></ul><p></p><p> <b><i>We are looking for professionals with these required skills to achieve our goals:</i></b></p><ul><li><p>Any graduate or post-graduate</p></li><li><p>Proven work experience as a project coordinator or similar role with 5 to 8years of relevant experience.</p></li><li><p>Excellent interpersonal and organizational skills (The most crucial skill for this role), ability to effectively communicate, influence and work well with others in a culturally diverse matrixed organization.</p></li><li><p>High proficiency in a broad range of computer skills including Outlook, Word, Excel, PowerPoint, Share Point/ Team Sites, and demonstrated ability to learn new software. Good knowledge of contemporary digital communications and social media best practices</p></li><li><p>Flexible to work in different time zones and can adapt to the program needs (no night shift or weekend work).</p></li><li><p>Experience in managing a portfolio of engagement activities across a broad range of areas</p></li><li><p>Experience in creating and executing communication and engagement plans that support business objectives and increase employee engagement</p></li><li><p>Able to grasp and champion GSK purpose, strategy, and culture.</p></li></ul><p> .</p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/engagement-specialist-and-executive-assistant-gsk/6a05f4d02f1861929d2531a7</link><guid isPermaLink="true">http://biotechroles.com/engagement-specialist-and-executive-assistant-gsk/6a05f4d02f1861929d2531a7</guid><pubDate>Thu, 14 May 2026 16:14:08 GMT</pubDate><company>GSK</company><location>Bengaluru Luxor North Tower</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Audit Senior Lead (EMEA GMP Audit)]]></title><description><![CDATA[<p></p><p>Are you an experienced Biopharm, Vaccines, or Pharmaceutical professional looking for an exciting opportunity to leverage your expertise to support GSK Senior Management in the identification, prioritisation, and monitoring of quality, compliance, and technical risks? If so, this role within our Quality organisation could be a great opportunity for you.</p><p></p><p><b>Position Details:</b></p><p>The purpose of the Audit Senior Lead role is to perform and manage GMP (Good Manufacturing Practice) and Compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities that supply highly regulated markets. You will be responsible for evaluating the compliance of GSK Global Supply Chain (internal and external) facilities with GMP, applicable policies and procedures, and regulatory and contractual commitments. Your remit will include audits of (Global Supply chain internal and external networks) manufacturing facilities and operations, Local Operating Companies (LOCs), R&amp;D and Logistics Service Providers (LSPs).<br /><br />In this role, you will also provide sterile manufacturing subject matter expertise for the GSK Global Supply Chain EMEA auditing team. Strong communication and influencing skills will be key to success.</p><p></p><p><b>Key Responsibilities include:</b></p><p><i>More experienced staff may undertake:</i></p><ul><li><p>Manage complex stakeholder engagement for audits across the network (which may include Supply Chain Directors, Site Directors, Site Quality Directors, VPs/Heads of support functions, and Research &amp; Development Quality).</p></li></ul><p></p><p><i>Typical work output will involve:</i></p><ul><li><p>Performing audits of Global Supply Chain (GSC) sites, LOCs, and external manufacturing sites (including R&amp;D), LSPs and facilities supplying EMEA and other highly regulated markets.</p></li><li><p>Preforming Unannounced audits.</p></li><li><p>Preforming for-cause audits based on regulatory actions or identified risk.</p></li><li><p>Preforming process, quality system-specific, and targeted audits.</p></li><li><p>Performing audits against risk mitigation plans or regulatory citation commitments.</p></li><li><p>As an output, it is critical to produce clear, concise, and objective audit reports to ensure senior management is appraised of identified risks and that appropriate corrective action plans are implemented.</p></li></ul><p></p><p><b>Location:  </b>This role can be based at any of the following manufacturing sites:  Ware, Worthing, Barnard Castle (UK), Siena, Parma (Italy), Wavre, Rixensart (Belgium) or Tres Cantos (Spain).</p><p></p><p><b>Travel: </b>Please note that the successful applicant will need to travel to sites across the network as part of the role. <b>We anticipate travel will be approximately up to 40% of your time.</b></p><p></p><p><br /><b>CLOSING DATE for applications: Friday 29th of May 2026 (COB).</b></p><p></p><p></p><p><b>Basic Qualifications: </b></p><p><i>We are looking for professionals with the following required skills:</i></p><ul><li><p>Degree in a relevant Scientific, Technical or Engineering discipline.</p></li><li><p>Relevant and specific experience obtained from working in Steriles/ Biopharm / Vaccines / Pharmaceutical industries.</p></li><li><p>Subject matter expertise / knowledge of world-wide cGMPs, regulatory requirements, standards and Quality Management Systems for Steriles/ Biopharm / Vaccines / Pharmaceutical Manufacturing and Packing.</p></li><li><p>Experience in identifying and/or managing complex Quality and Compliance risks and issues.</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><p><i>If you have the following skills and characteristics, it would be a benefit:</i></p><ul><li><p>Previous auditing experience preferred (e.g. Proficiency and experience in planning, performing and reporting Quality and Regulatory Compliance audits).</p></li><li><p>Working knowledge and ability in evaluation of Data Integrity and ALCOA&#43; principles within the Pharmaceutical industry.</p></li><li><p>Increasing knowledge of AI tools, applications and ways of working in the Pharmaceutical industry</p></li><li><p>Auditor formal accreditation/certification.</p></li><li><p>Experience managing the interface with stakeholders (Site Directors, Site Quality Directors, VPs and Heads of Support Functions).</p></li></ul><p></p><p>If you would like to learn more about our company wide benefits and life at GSK we would suggest looking at our webpage <a href="https://www.gsk.com/en-gb/careers/life-at-gsk/" target="_blank">Life at GSK | GSK</a>.</p><p></p>&amp;#xa;&amp;#xa;Italian Salary Range / Fascia retributiva in Italia: EUR 73,050 to EUR 121,750 &amp;#xa;Spanish Salary Range / Rango salarial en España: EUR 0 to EUR 0 &amp;#xa;Belgium Salary Range / Fourchette salariale – Belgique: EUR 78,750 to EUR 131,250 &amp;#xa;&amp;#xa;The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.&amp;#xa;&amp;#xa;In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process.&amp;#xa;&amp;#xa;This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/audit-senior-lead-emea-gmp-audit-gsk/6a05f4cf2f1861929d2531a6</link><guid isPermaLink="true">http://biotechroles.com/audit-senior-lead-emea-gmp-audit-gsk/6a05f4cf2f1861929d2531a6</guid><pubDate>Thu, 14 May 2026 16:14:07 GMT</pubDate><company>GSK</company><location>UK - Hertfordshire - Ware</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager- Implementation Committee-GCC]]></title><description><![CDATA[<p>Job Purpose:</p><p>The current approved GSK vaccine portfolio includes around fifty different products. The product portfolio needs continuous process and product maintenance to always keep the products in a compliant state and keep continuous improvements of the manufacturing process and analytical methods.</p><p>The product Implementation Committee’s (IC&#39;s) ensure supply continuity of Vaccines Product. The team is responsible, based on the level of the regulatory submission, for:</p><p>1. Tracking the monitoring of all the Change Controls, in the approved CMC envelope, with Tell &amp; Do impact and/or with supply impact until interim/final closure</p><p>2. Providing GO/NO GO Market implementation decision (before the implementation into manufacturing operations or QC laboratories and first supply to markets)</p><p>3. Monitoring the CMC ( Chemistry, Manufacturing and Controls )Envelope starting from its final endorsement by PSLT( Product Strategy Lead Team ) and all along its cycle.</p><ul><li><p>The Implementation Committee Manager is responsible to facilitate and lead the Implementation Committee for the vaccines under her/his responsibility, managing Global cross functional teams.</p></li><li><p>Ensures continuous exchange of knowledge and close collaboration with molecular stewards and master data team in global MSAT( Manufacturing, Science and Technology ) as well as Regulatory and Global Supply.</p></li></ul><p>Key Responsibilities:</p><ul><li><p>The Implementation Committee Manager has the following key responsibilities:</p></li><li><p>To facilitate and lead the Implementation Committee for the products under her/his responsibility managing global cross functional teams based in different geographic areas.</p></li><li><p>The IC manager must check the definition and follow up of the market implementation strategies of changes having a regulatory impact (i.e. Tell &amp; Do changes), to ensure geographic expansion, supply continuity in the market in all countries, keeping alignment with the Product Life Cycle Management plan priorities owned by PSLT ( Product Strategy Lead Team )and CMC( Chemistry, Manufacturing and Controls ) product envelopes.</p></li><li><p>Facilitate and record decision of product IC teams on GO/No GO decisions for market implementation, in alignment with supply needs and risks raised by IC stakeholders</p></li><li><p>Monitoring the CMC envelope starting from its final endorsement by PSLT and all along its cycle.</p></li><li><p>Ensuring appropriate communication of issues or risks to the ad hoc governance meetings/boards and look for or confirm mitigation plans</p></li></ul><p>Knowledge, Education &amp; Experience Required:</p><ul><li><p>Advanced degree in process engineering sciences, and/or academic level in life sciences in general (biology, biomedical science, pharmacist, chemistry, chemical engineering).</p></li><li><p>Minimum 10 years applicable experience in biopharmaceutical manufacturing and / or experience in QA, QC, R&amp;D within a biological environment</p></li><li><p>Proven experience in project management</p></li><li><p>Excellent understanding of the framework within which a pharmaceutical product has to be maintained in compliance: Authorities / Scientific / Business</p></li><li><p>Good understanding of change control process</p></li><li><p>Good understanding of production &amp; QC master data</p></li><li><p>Understanding of regulatory level in main regions (US/EU) and of supply chain mechanisms</p></li><li><p>Comfortable with IT tools needed for the job (e.g., Excel, VeeVa Suppliable Table, , SAP)</p></li></ul><p>Other Job-Related Skills:</p><ul><li><p>Proven Track record in problem solving and global project management.</p></li><li><p>Good skills in project management, change management and team/meeting facilitation.</p></li><li><p>Ability to plan, manage and lead cross-functional teams (matrix leadership) and projects to obtain desired business objectives.</p></li><li><p>Good interpersonal communication and negotiation skills</p></li><li><p>Cross cultural experience and proven ability to work in a complex and multi-cultural environment.</p></li><li><p>Proven ability to communicate and negotiate effectively with different levels of management across functional, national, and cultural boundaries.</p></li><li><p>Proven ability of understanding compliance requirements</p></li></ul><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/senior-manager-implementation-committee-gcc-gsk/6a05f4cf2f1861929d2531a5</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-implementation-committee-gcc-gsk/6a05f4cf2f1861929d2531a5</guid><pubDate>Thu, 14 May 2026 16:14:07 GMT</pubDate><company>GSK</company><location>Bengaluru Luxor North Tower</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Regional Medical Affairs Manager Center South -Lung Cancer (RMAM) (m/f/d)]]></title><description><![CDATA[<div></div><div><div><div><div><div><div><div><div><p>You will lead regional medical affairs in your area of Germany, building trusted relationships with healthcare professionals and research partners. As a Regional medical Affairs Manager you will gather and share clinical insights and collaborate with cross-functional teams to shape and deliver impactful medical plans. You grow your expertise while helping drive meaningful outcomes for patients through science, technology, and teamwork.</p><p></p><div><p><b>Responsibilities</b><br />This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><ul><li><p>Build and maintain scientific relationships with healthcare professionals and external clinical experts in the region</p></li><li><p>Deliver evidence-based medical education and scientific exchange in person and using digital channels for the area lung cancer</p></li><li><p>Respond to medical and scientific enquiries from healthcare professionals in a timely and compliant way.</p></li><li><p>Support clinical research collaborations, including identifying study centres and enabling investigator-initiated research.</p></li><li><p>Capture, synthesize and share local clinical insights to inform medical strategy and cross-functional planning.</p></li><li><p>Plan and run regional medical activities such as advisory boards, symposia and educational meetings.</p></li></ul><p></p><p></p><p><br /><b>Basic Qualification </b></p><p>We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li><p>Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent).</p></li><li><p>Minimum 3 years ideally experience in medical affairs, medical science liaison, clinical research in <b>lung cancer</b></p></li><li><p>Strong clinical and scientific knowledge relevant to the therapy area.</p></li><li><p>Excellent verbal and written communication skills in German and English.</p></li><li><p>Willingness and ability to travel regularly within the assigned region.</p></li><li><p>- Solid understanding of regulatory, ethical and compliance requirements in the pharmaceutical environment.</p></li></ul><p><br /><b>Preferred Qualification</b><br />If you have the following characteristics, it would be a plus:</p><ul><li><p>Prior experience in oncology, hematology or a related therapy area.</p></li><li><p>Experience supporting investigator-initiated trials or clinical partnerships.</p></li><li><p>Experience designing or delivering omnichannel engagement plans and digital medical communications.</p></li><li><p>Project management or budget management experience.</p></li><li><p>Experience presenting at national or regional scientific meetings.</p></li><li><p>A collaborative mindset and commitment to inclusive working with diverse stakeholders.</p></li></ul><p><br /> </p><p></p><p>Weitere Informationen:  </p><p><a href="https://www.gsk.com/en-gb/investors/financial-reports/annual-report-2023/" target="_blank">Annual Report </a> </p><p><a href="https://www.gsk.com/en-gb/research-and-development/our-pipeline/" target="_blank">Product Pipeline</a> </p><p>#EBDE </p><p>#LI-ViiV </p><p>#LI-Remote</p></div></div></div></div></div></div></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:DE.Contact-Recruitment&#64;gsk.com"><span style="color:#0000ff"><u>DE.Contact-Recruitment&#64;gsk.com</u></span></a> where you can also request a call.</p><p></p><p>Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to <span style="font-size:14px">ethnicity</span>, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/ </u></span></a></p>]]></description><link>http://biotechroles.com/senior-regional-medical-affairs-manager-center-south-lung-cancer-rmam-mfd-gsk/6a05f4ce2f1861929d2531a4</link><guid isPermaLink="true">http://biotechroles.com/senior-regional-medical-affairs-manager-center-south-lung-cancer-rmam-mfd-gsk/6a05f4ce2f1861929d2531a4</guid><pubDate>Thu, 14 May 2026 16:14:06 GMT</pubDate><company>GSK</company><location>Field Worker - DEU (Munich)</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Senior Director Translational Data Sciences]]></title><description><![CDATA[<p></p><p>We are a science-led, global pharmaceutical company committed to closing the gap between biological discovery and clinical impact. Our translational mission is to decode the molecular and cellular architecture of human disease, using multi-omics data as the connective tissue between causal mechanistic insight and patient outcome., we are building the analytical infrastructure that turns complex biological signals into actionable clinical hypotheses. </p><p>We believe that the next generation of translational leadership will be defined by the ability to move fluidly between deep genomic profiling, including at single-cell and spatial resolution, and AI-driven data integration to derive and apply insights to identify and develop transformative medicines for patients. This role has been created for a scientist who can operate at that interface with rigour, creativity, and strategic clarity. </p><p></p><h2>Position Overview </h2><p>We are seeking an exceptional and ambitious scientific leader to serve as Senior Director of Translational Data Sciences. This individual will define and drive our translational data strategy across the continuum from disease biology to clinical readout, integrating multi-omics platforms with AI-driven analytics to bridge the gap between mechanistic discovery and therapeutic decision-making. </p><p>The successful candidate will combine deep expertise in spatial, single-cell and/or other multi-omics with a demonstrated record of delivering insights from agentic AI systems. Critically, we are looking for someone who can move between scientific rigour and strategic execution: a leader who communicates directly with R&amp;D and clinical development executives, structures external alliances, and holds themselves and their team accountable to the clinical relevance of every analytical platform they deploy. </p><p></p><p>This is a rare opportunity for a senior data scientist with clinical and/or basic science training to shape how a leading pharmaceutical organisation connects omics data to patient outcomes, at a moment when the tools to do so are more powerful than ever before. </p><p></p><h2>Key Responsibilities </h2><p>Scientific Strategy. Develop and execute the Translational Data Sciences strategy, with accountability for portfolio-level outcomes across multiple therapeutic areas including respiratory, renal, hepatology, and immune-mediated disease. </p><p>Data Sciences and AI. Leverage the potential of data sciences for pipeline progress through team leadership, collaboration across Translational &amp; Developmental Sciences and application across therapy areas and the broader organisations across GSK including R&amp;D Technologies and AIML. </p><p>Partnership &amp; Alliance Leadership. Establish and maintain high-value partnerships with leading academic laboratories, companies, and international consortia; represent the organisation at international scientific forums and translate external innovation into internal competitive advantage. </p><p>Translational Integration. Work directly with R&amp;D leadership to align computational strategy with clinical development priorities, ensuring that AI-derived insights are translatable into actionable hypotheses spanning target identification and validation, biomarker discovery, and patient stratification to support pipeline delivery and clinical trial success. </p><p>Team Leadership. Build and mentor an interdisciplinary team of computational biologists, AI/ML engineers, and clinician-scientists and wet-lab scientists; foster a culture of scientific excellence, methodological rigour, and collaborative ambition.  </p><p>Scientific Visibility. Contribute to the organisation&#39;s external positioning through publications, conference presentations, and academic collaborations. </p><p></p><h2>Qualifications </h2><p>Basic qualifications: </p><p>Physical sciences (Maths, Computer Science, Physics, Chemistry, Engineering etc) or Biological sciences (Biology, Biochemistry, Bioengineering etc) undergraduate degree or Medical degree </p><p>PhD in data science, computer science, computational biology, bioinformatics, or a closely related discipline;  </p><p>Extensive experience spanning academic and industrial drug discovery environments, with a demonstrable record of leading high-impact computational biology programmes from conception through to application to drug discovery or development challenges. </p><p>Prior line management experience and experience building and leading interdisciplinary teams across computational, experimental, and translational disciplines in both academic and industrial settings. </p><p>Demonstrated experience structuring and managing strategic partnerships with academic institutions and companies, including contribution to alliance governance. </p><p>Familiarity with the translational interface between target biology and clinical development; experience with adaptive clinical trial design and biomarker-driven patient stratification is highly desirable. </p><p>Experience presenting to executive leadership, external partners, and international scientific audiences. </p><p></p><h2>Preferred qualifications: </h2><p>Expert command of spatial transcriptomics platforms and single-cell multi-omics analysis, with fluency in applying established analytical frameworks and the capability to develop novel methods where existing approaches are insufficient. Ideally, also with experience of integration of genomic insights with germline genetic evidence to derive causal mechanistic insight.  </p><p>Deep expertise across the full spectrum of modern ML for biology: graph neural networks, Bayesian causal inference, topological data analysis, deep generative models (VAEs, diffusion models, GANs), and reinforcement learning, applied to biological discovery problems. </p><p>Proven ability to design and deliver agentic AI systems integrating large language model APIs, generative AI frameworks, and analysis workflows for automated biological insight generation. </p><p></p><h2>What We Offer </h2><p>A leadership mandate at the frontier of genomic- and AI-enabled drug discovery, embedded within an organisation that is investing decisively in computational biology and translational data platforms. You will have direct influence on R&amp;D Translational strategy and leadership, operational autonomy to build and execute your vision, and the institutional resources to deliver at scale. We offer a competitive senior compensation package, flexible hybrid working, and a genuine commitment to scientific impact. </p><p></p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. </p><p></p><p>We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p></p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/locations/united-kingdom/"><span style="color:#0000ff"><u>Link</u></span></a> where you will find answers to multiple questions we receive</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/senior-director-translational-data-sciences-gsk/6a05f4cd2f1861929d2531a3</link><guid isPermaLink="true">http://biotechroles.com/senior-director-translational-data-sciences-gsk/6a05f4cd2f1861929d2531a3</guid><pubDate>Thu, 14 May 2026 16:14:05 GMT</pubDate><company>GSK</company><location>UK - Hertfordshire - Stevenage</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager - Finance Risk & Control]]></title><description><![CDATA[<p>Our Global Finance Risk Management and Controls (FRMC) team support the Global Finance Organisation to meet compliance reporting requirements. For Projects &amp; Change pillar of FRMC we are currently looking for agile, high-performing talent, Qualified Accountant with experience in risk management among other areas, to provide support to a diverse range of stakeholders across the organisation. As part of a modern, technology-led function delivering world-class service, you will be well-positioned to learn and develop your skills to progress in your career, laterally and vertically, working in a diverse and culturally rich environment with some of the best and brightest in the field. </p><p></p><p><b>This role will provide YOU the opportunity to lead key activities to progress YOUR career.  </b></p><p>This role provides support for global projects significantly impacting Global Finance such as global process changes, transformations, system implementation or migrations, digitalisation using RPA/AI/ML, target operating model (TOM) roll out, and risk mitigation across key processes. This role is a business ‘risk-mitigation’ partner to finance services global process owners (GPOs) or project managers in assessing risks and identifying mitigation controls for various projects (e.g. supporting transformation activities including control ownership changes, knowledge transfer, reviewing updates of key policies, introduction of new tools – Cash allocation, Vendor creation, Vendor portal). The role will also identify opportunities for process simplification, automation and efficiency. </p><p><b>Role Expectation</b></p><ul><li><p>Partner with relevant project managers or GPOs to ensure adequate risk mitigation robust plans are built by the organization. Involvement is needed both in regular weekly project calls and in identified opportunities to transform processes (implementation of new tools, process convergence, standardization and productivity improvement) to monitor risk, impact on controls and deliver tangible benefits to the business.</p></li><li><p>Understand inherent and emerging risks in proposed finance process changes and ensure that process risks are identified, mitigated, controlled and reported appropriately.</p></li><li><p>Being the ‘go to’ person in Finance Risk Management and Controls (FRMC) team for ongoing projects or process design issues for the operations teams and risk management teams</p></li><li><p>Understand and escalate requests for changes to control design at all service locations based on the identified gaps, changes in the processes or outputs from data analytics.</p></li><li><p>Support identification of rationalization opportunities and ERP application through risk assessment of the proposed tool or new process.</p></li><li><p>Interact with key process stakeholders to understand current and emerging business requirements – appreciate risks to implementation and ownership of proposed controls</p></li><li><p>Review relevant policies / SOPs for the newly designed processes to ensure process risks and controls are sufficiently documented.</p></li><li><p>Ensure process map documentation includes agreed variations for local legal, fiscal or system limitations, including RACI and key controls.</p></li><li><p>Participating in key business change initiatives as the voice of the risk &amp; compliance team</p></li><li><p>Provide risk &amp; compliance inputs as part of project team for large process design projects to support major business change and present to governance team the proposed changes in internal controls supporting business/GPO in getting the approval of designed changes</p></li></ul><p></p><p><b>We would like to speak to you if you have these experience and skills</b></p><ul><li><p>Qualified Auditor or Accountant (CA, ACCA, CPA, CIMA, CISA, DISA, ICAI or equivalent) with at least 10 years post qualifying experience</p></li><li><p>Strong finance background with commercial experience, preferably at a global level.</p></li><li><p>Significant experience in finance processes and operations, including a minimum 3-4 years in SOX Compliance; External or Internal Audit, Financial Control and/or Risk Management with a Big 4 audit firm or international corporates.</p></li><li><p>Significant experience with internal control design and risk identification.</p></li><li><p>Knowledge of Sarbanes Oxley legislation.</p></li><li><p>Understanding of ERP systems, preferably SAP environment and some experience with Data Analytics.</p></li><li><p>Experience of a global business process change project environment and ability to comfortably work in international environment</p></li><li><p>Prior experience in Artificial Intelligence (AI) and Robotic Process Automation (RPA) projects or programs, particularly in design, deployment, risk management, or audit.</p></li><li><p>Familiarity with digital tools such as Power BI, Celonis, Alteryx, etc. or similar platforms, with an emphasis on leveraging these tools for process improvements, analytics, and controls optimisation projects.</p></li></ul><p></p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/senior-manager-finance-risk-and-control-gsk/6a05f4cb2f1861929d2531a2</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-finance-risk-and-control-gsk/6a05f4cb2f1861929d2531a2</guid><pubDate>Thu, 14 May 2026 16:14:03 GMT</pubDate><company>GSK</company><location>Bengaluru Luxor North Tower</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Clinical Sciences Project Manager]]></title><description><![CDATA[<p></p><p>We are a specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV. Born out of a partnership between GSK and Pfizer in 2009, with Shionogi joining in 2012, our ambition is to end the HIV epidemic.</p><p><br />As the pioneers in HIV innovation, we constantly look to push the boundaries of science to develop medicines that can change lives and give people more choice. Beyond our medicines, we are proud of our deep connection with the HIV community and work with partners to advance research and development, address HIV-related stigma, increase access to our medicines and provide funding and support to local community organisations to support their efforts in the HIV response.</p><p><br />We are ViiV Healthcare. Here until HIV and AIDS are not.</p><div></div><div></div><p></p><p></p><p></p><p><span class="emphasis"><b>Role Overview</b></span></p><p>This unique role represents a great opportunity to join the ViiV Healthcare Global Collaborative Studies Group (CSG), which currently supports over 120 investigator sponsored research (ISR) studies, generating important evidence on our products, and for the field of HIV, across the world.</p><p></p><p>This role involves developing, refining, and executing processes, risk management strategies, and other activities essential to the ongoing success of the CSG team and our ISR program.  The role includes taking a leadership role in management and delivery of our Request for Proposal study process. It may also involve managing certain study related activities, a potential development opportunity for the right candidate.</p><p></p><p>The optimal candidate will be self-motivated, with an innovative mindset and strong problem solving, digital and project management capabilities, a desire to support evidence generation across the ViiV portfolio and a passion for contributing to the ViiV mission of leaving no person living with HIV behind.</p><p></p><p>The Primary Purpose of the role is to support the Global Collaborative Studies Group (CSG) in the review, execution and management of ViiV Healthcare (VH) supported studies such as investigator sponsored studies (ISS) and supported collaborative studies (SCS) by strengthening and implementing processes and ways of working to improve efficiency, communication of program outputs and study management activities.</p><p></p><p></p><p></p><p></p><p></p><p><span class="emphasis"><b>In this role you will</b></span></p><ul><li><p><span>Support the CSG team, including Regional Investigation Leads (RILs), with study related activities and process management, such as budget and milestone monitoring and updating, risk management and tracking, and optimisation of processes for ensuring timely and compliant study review, progression and start up and study close out</span></p></li><li><p><span>Support prioritised evidence generation aligned to Integrated Evidence plans by generating regular updates on ISR study progress and publication plans</span></p></li><li><p><span>Optimise process for and lead central project management of Request for Proposal (RFP) study programs, in conjunction with project teams, RILs, external facing teams and Global Medical Operations as applicable</span></p></li><li><p><span>Work cross functionally with key internal stakeholders groups to ensure timely, compliant and efficient delivery of ViiV support for and communication of ISS and SCS. K</span><span>ey collaborators will include (but are not limited to): Medical Affairs (global, regional and local); Clinical Operations and Clinical Supply team</span><span>s; Finance; </span><span>Scientific Communications and Legal </span></p></li><li><p><span>Co-ordinate and support the development and implementation of training materials and programs for Study Accountable Persons (SAPs) and medical team members  </span></p></li><li><p><span>Co-ordinate and support the execution of Global review and ISS update meetings, materials and minutes</span></p></li><li><p><span>To serve as SAP for specific studies including supporting life cycle and close out activities (mentored by senior CSG member) – potential development component to role, as applicable</span></p></li><li><p><span>Support use of and embed ViiV Enhance and appropriate project management and digital tools within CSG activities</span></p></li></ul><p></p><p></p><p></p><p></p><p></p><p><span class="emphasis"><b><i>Why You?</i></b></span></p><p><span class="emphasis"><b>Qualifications &amp; Skills:</b></span></p><p>We are looking for professionals with these required skills to achieve our goals:</p><ul><li><p>Life Science degree (MSc, PharmD, PhD, etc)</p></li><li><p>Pharmaceutical industry and/or clinical research experience</p></li><li><p>Understanding of clinical trial process from study concept to publication</p></li><li><p>Project management experience including the design, planning, governance, phasing and implementation of projects as well as tools and techniques for issues and risk management, decision making and reporting</p></li><li><p>Proficiency in multiple digital and software applications and ability to provide expertise and lead user capability</p></li></ul><p></p><p></p><p></p><p></p><p><span class="emphasis"><b>Preferred Qualifications &amp; Skills:</b></span></p><p>If you have the following characteristics, it would be a plus:</p><ul><li><p>Knowledge of and experience in the HIV therapy area </p></li><li><p>Experience in managing multiple projects, including complex projects, in a matrix environment </p></li><li><p>Strong teamworking and relationship building skills with external and internal partners across multiple functional areas</p></li><li><p>Excellent written and spoken communication and able to effectively influence within team and across partner groups</p></li></ul><p></p><p></p><p></p><p></p><p><span class="emphasis"><b><i>Why ViiV?</i></b></span></p><p>ViiV Healthcare is a global specialty HIV company, the only company that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV is highly mission-driven in our unrelenting commitment to leave no person living with HIV behind. We do this by being a trusted partner for all people living with and affected by HIV. Our aim is to think, act, and connect differently through a focus on education on and treatment. We go to extraordinary lengths to deliver the sorts of breakthroughs, both in treatments, care solutions and communities, that really count. We go beyond the boundaries of medicine by taking a holistic approach to HIV through developing and supporting sustainable community programs and improving access to care.  We will push through every challenge until HIV/AIDS is eradicated.</p><p></p><p>ViiV has played a significant part in delivering breakthroughs that have turned HIV into a manageable health condition. We offer the largest portfolio of HIV medicines available anywhere, and we continue our work to cater for the widest possible range of needs in response to the HIV pandemic.</p><p></p><p>We are aware of how much is at stake for those affected by HIV and we show up every day 100% committed to the patients. Our work culture is fast-paced, diverse, inclusive, competitive, and caring. But ViiV isn’t just somewhere to work – it’s a place to belong, an invitation to bring your very best, and a team full of impact-driven team members who are hungry to make a difference.</p><p></p><p>While we have been improving lives of HIV patients for 30 years, this is an especially exciting time to be at ViiV, as we evaluate novel approaches to treatment and prevention that could further reduce the impact of HIV on individuals and communities.</p><p></p><p>ViiV Healthcare is a company 100% focused on HIV that is majority owned by GSK, a global biopharma organization. As an employee of ViiV, you are part of a team united by a clear mission to leave no person living with HIV behind. Additionally, through our shareholder relationship with GSK, you have access to a range of shared benefits and career development opportunities.</p><p></p><p></p><p></p><p></p><p></p><p><span class="emphasis"><b>Closing Date for Applications: Wednesday 27th May 2026 (COB)</b></span></p><p></p><p>Please take a copy of the Job Description, as this will not be available post closure of the advert. <br /> </p><p>When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.</p><p><br /><i>During the course of your application, you will be requested to complete voluntary information which will be used in monitoring the effectiveness of our equality and diversity policies. Your information will be treated as confidential and will not be used in any part of the selection process.  If you require a reasonable adjustment to the application / selection process to enable you to demonstrate your ability to perform the job requirements, please contact 0808 234 4391. This will help us to understand any modifications we may need to make to support you throughout our selection process.</i></p><p></p><p>#LI-GSK</p><p>#LI-Hybrid</p><p></p><p></p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why Us?</b></p><p>At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. </p><p></p><p>We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>GSK</u></span></a> and <a target="_blank" href="http://www.Pfizer.com"><span style="color:#0000ff"><u>Pfizer</u></span></a> in 2009, with <a target="_blank" href="http://www.Shionogi.com"><span style="color:#0000ff"><u>Shionogi</u></span></a> joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.</p><p></p><p>Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. </p><p></p><p>Having a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.</p><p></p><p>ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law                                                                                                                                                                                                                                                                                                                                                       </p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:HR.AmericasSC-CS&#64;gsk.com"><span style="color:#0000ff"><u>HR.AmericasSC-CS&#64;gsk.com</u></span></a> where you can also request a call.                                                                                                                                                                               </p><p></p><p>Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the link <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/clinical-sciences-project-manager-gsk/6a05f4ca2f1861929d2531a1</link><guid isPermaLink="true">http://biotechroles.com/clinical-sciences-project-manager-gsk/6a05f4ca2f1861929d2531a1</guid><pubDate>Thu, 14 May 2026 16:14:02 GMT</pubDate><company>GSK</company><location>UK – London – New Oxford Street</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Senior - Regulatory Specialist, Variations]]></title><description><![CDATA[<p>Business Introduction<br />At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&amp;D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.<br />Find out more:<br /><a href="https://www.gsk.com/en-gb/innovation/" target="_blank">Our approach to R&amp;D</a><br /> </p><p><span><span><span><span><b>Position Summary</b></span></span></span></span></p><ul><li><p><span><span><span><span>Role requires a general understanding of submission requirements for multiple countries/ submission types and an ability to work in a matrix environment.<br />Responsible for timely delivery of regulatory activities of multiple<b> </b>Vx projects across dosage forms.</span></span></span></span></p></li><li><p><span><span><span><span>Represents<b> CMC Delivery team</b> on Regulatory Networks and Matrix Teams providing guidance to Pharma Supply Chain (PSC), Commercial, Quality Assurance, 3<i>rd</i> Party Contract Manufacturing Organizations and Office of the Chief Medical Officer (OCMO) to produce appropriate components for global regulatory dossiers.</span></span></span></span></p></li><li><p><span><span><span><span>Will serve as a mentor/trainer for new team members. </span></span></span></span></p></li></ul><p><span><span><span><span>     May act as a Subject Matter Expert for specific areas for consultation within    </span></span></span></span></p><p><span><span><span><span>the team/ department as well as externally outside the department.<br /><br /><b>Responsibilities</b><br />Independently and confidently executes agreed dossier strategy.</span></span></span></span></p><ul><li><p><span><span><span><span>Independently manages multiple Rx and/or Vx project assignments simultaneously; assignments will range in complexity, but more complex work is expected.</span></span></span></span></p></li><li><p><span><span><span><span>Independently completes data assessment to ensure dossier is fit for purpose.</span></span></span></span></p></li><li><p><span><span><span><span>Identifies risks associated with submission data and information packages.</span></span></span></span></p></li><li><p><span><span><span><span>Escalates issues with line manager that have business impact.</span></span></span></span></p></li><li><p><span><span><span><span>May act as reviewer/approver for dossiers prepared by peers and identifies improvement opportunities for Regulatory processes, policies and systems.</span></span></span></span></p></li><li><p><span><span><span><span>Understands regulations, guidelines, procedures and policies relating to registration and manufacturing of pharmaceutical products, to expedite submission, review and approval of global applications. May provide consultation and solutions being the subject matter expert in specific areas of expertise. Acts as mentor/trainer for new staff.</span></span></span></span></p></li><li><p><span><span><span><span>Understands internal/external Regulatory environment.</span></span></span></span></p></li><li><p><span><span><span><span>Actively builds an organisational network (PSC, LOC, PO and other relevant stakeholders), promotes and is engaged in knowledge and experience sharing.</span></span></span></span></p></li><li><p><span><span><span><span>Communicates across GSK, as necessary regarding project and policy issues ensuring optimum position for GSK.<br /><br /><br /><b>Preferred Qualification</b></span></span></span></span></p></li><li><p><span><span><span><span>Bachelor’s degree.( Chemistry, pharmacy or other related science or technical bachelor’s degree.</span></span></span></span></p></li><li><p><span><span><span><span>Working in complex environment within a scientific organization<br />Minimum 3-8 years of experience</span></span></span></span></p></li><li><p><span><span><span><span>Broad understanding of the pharmaceutical industry, drug development environment, and R&amp;D processes and objectives.</span></span></span></span></p></li><li><p><span><span><span><span>Global/ EMAP Regulatory submission experience - Knowledge of regulatory agency guidelines</span></span></span></span></p></li><li><p><span><span><span><span>Excellent organisational skills, attention to detail and commitment to deliver high quality output, even under pressures sometimes demanded by regulatory deadlines</span></span></span></span></p></li><li><p><span><span><span><span>Excellent written and verbal communication skills and ability to present information in a clear and concise manner</span></span></span></span></p></li><li><p><span><span><span><span>Ability to interpret and advise on guidelines and requirements on a global basis, reflecting recent GSK experience</span></span></span></span></p></li><li><p><span><span><span><span>Ability to build effective working relationships and work in a matrix environment effectively</span></span></span></span></p></li><li><p><span><span><span><span><span>Ability to think flexibly in order to meet constantly shifting priorities and timelines.</span></span></span></span></span></p></li></ul><p><br />Work Arrangement<br />This role is on-site in India. You will work closely with local and global colleagues and may join cross-site virtual meetings.<br /><br />What to expect next<br />If you are ready to grow your regulatory career and help deliver meaningful patient impact, we want to hear from you. Please apply and tell us how your skills and experience match this role. If you need any adjustments during the recruitment process, please let our recruitment team know so we can support you.</p>&amp;#xa;The annual base salary in Poland for new hires in this position ranges from PLN 144,750 to PLN 241,250 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.   Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion).   All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave &amp; care of family member leave.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/senior-regulatory-specialist-variations-gsk/6a05f4ca2f1861929d2531a0</link><guid isPermaLink="true">http://biotechroles.com/senior-regulatory-specialist-variations-gsk/6a05f4ca2f1861929d2531a0</guid><pubDate>Thu, 14 May 2026 16:14:02 GMT</pubDate><company>GSK</company><location>Bengaluru Luxor North Tower</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Computational Biologist]]></title><description><![CDATA[<p>We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.</p><p></p><p>We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.</p><p></p><p>Discover more about our company wide benefits and life at GSK on our webpage <a href="https://www.gsk.com/en-gb/careers/life-at-gsk/" target="_blank">Life at GSK | GSK</a></p><p></p><p><b>Computational Biologist</b></p><p></p><p><b>Job Purpose </b></p><p>We are seeking a talented and motivated individual to join our team as a Principal Scientist in Translational Omics (TO). The successful candidate will have demonstrated experience in diverse data-types e.g. genetics, transcriptomics, histopathology imaging, in state-of-the art computational biology methods and its application to biological, translational and/or clinical questions in drug discovery and development.</p><p></p><p>The Principal Scientist will be expected to inform genomics analysis, interpretation and project impact in Hepatology and relevant biology as well as using their knowledge of the internal and external data landscape to address scientific questions. They will be communicating their results and interpretation to peers and leaders. They will have experience working in multi-disciplinary teams to answer complex scientific questions.</p><p></p><p><b>Key Accountabilities / Responsibilities: </b></p><p></p><ul><li>Apply expertise in -omics and imaging and use of relevant state-of-the-art computational methods as well as pertinent knowledge of disease and biology to support the discovery and development of new medicines.</li><li>Generate and evaluate genomic/histopathology imaging evidence to support therapeutic target and/or biomarker hypotheses as well as mechanistic understanding</li><li>Identify and/or evaluate relevant internal and external data sets for analyses.</li><li>Provide clear and concise communication of results and interpretation to peers and leaders.</li><li>Collaborate effectively in multi-disciplinary teams to answer complex scientific questions.</li><li>Demonstrate initiative in identifying and implementing creative and state-of-the-art analytical solutions to address challenging scientific questions.</li><li>Work with agility to adapt rapidly to changing priorities and timelines.</li></ul><p></p><p><b>Qualifications, Knowledge, Skills and Experience </b></p><ul><li>Demonstrable translational expertise in Hepatology and MASH, including in vitro, in vivo and in silico work, complemented by a clear understanding of clinical data and disease</li><li>Strong analytical competence and ability to interpret results across multiple data types</li><li>Experience working across academia and industry collaborations</li><li>Effective collaboration with Pathologists and AI-based image analysis across platforms (PathAI, HistoIndex and PharmaNEST)</li><li>Demonstrated experience to write R or python code to impact analyses</li><li>Demonstrated understanding of internal and external data landscape to address and impact a range of scientific questions.</li><li>Excellent communication skills to effectively convey complex scientific concepts to peers and leaders.</li><li>Experience working in multi-disciplinary teams to answer scientific questions.</li><li>Proactive and innovative mindset with the ability to identify and implement creative solutions.</li><li>Strong problem-solving and analytical skills.</li><li>Ability to work with agility and adapt to changing priorities and timelines.</li><li>Passion for advancing the science of drug target identification and validation.</li></ul><p></p><p><b>How to apply</b></p><p>We welcome applications from people with different backgrounds and experiences. If this role speaks to you, please apply and tell us briefly how your skills and experience match the responsibilities and qualifications listed. We look forward to hearing from you.</p><p>Closing Date for Applications – 20/05/2026</p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p> </p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p> </p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p> </p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p> </p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p> </p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/computational-biologist-gsk/6a05f4c92f1861929d25319f</link><guid isPermaLink="true">http://biotechroles.com/computational-biologist-gsk/6a05f4c92f1861929d25319f</guid><pubDate>Thu, 14 May 2026 16:14:01 GMT</pubDate><company>GSK</company><location>UK - Hertfordshire - Stevenage</location><salary>$100000-150000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director- GSC Portfolio Optimization -GCC]]></title><description><![CDATA[<p><span>Job purpose:</span></p><p><span>The Supply Chain Strategy team designs the supply chains to bring world class GSK medicines and vaccines to patients. The Strategy team is responsible for product and network strategy, including the delivery of Strategic programmes.</span></p><p><span> </span></p><p><span>This role focuses on portfolio strategy and optimisation within General Medicines. The Portfolio Optimisation associate director is responsible for managing and enhancing the performance of the General Medicine portfolio. This role focuses on aligning supply chain capabilies with Commercial strategy to ensure product availability, profitability and compliance with medical and regulatory requirements.</span></p><p><span> </span></p><p><span>This role requires close collaboration with the cross functional Portfolio Optimisation team including Commercial to make recommendations on product discontinuation and divestments.</span></p><p><span> </span></p><p><span>Standard <span> </span>project management tools will be used to manage the portfolio Optimisation process, provides portfolio management expertise, coaching and support to members of the Portfolio Optimisation team. </span></p><p></p><p></p><p><span>Responsibilities:</span></p><p><span>Collaborate with Commercial, Medical, Regulatory, and Manufacturing sites to review General Medicine brands and recommend optimizations.</span></p><p><span>Facilitate the Quarterly Portfolio Optimisation board, the governance meeting where<span>  </span>the Senior VP Gen Med Commercial makes decisions on brand discontinuations.</span></p><p><span>Conduct data-driven portfolio reviews with Commercial, supply planning teams and Finance.</span></p><p><span>Develop dashboards and reports for cross-functional decision-making.</span></p><p><span>Serve as the primary contact for portfolio discussions between supply chain and commercial teams.</span></p><p><span>Engage with functional teams to secure resources and mobilize the project team.</span></p><p><span>Clarify roles and responsibilities within project teams and ensure compliance with GSK&#39;s decision-making structures.</span></p><p><span>Establish and maintain portfolio governance processes, including performance tracking and reporting.</span></p><p><span>Implement standard project management oversight, including planning, tracking, and reporting progress, risks, and issues.</span></p><p><span>Facilitate project budget development and manage spending within budget.</span></p><p><span>Identify and engage stakeholders, addressing their needs and concerns to support project updates and decisions.</span></p><p><span>Provide accurate information to stakeholders and contribute to governance papers for project status and risk recommendations.</span></p><p><span>Support and share best practices with the Strategy team.</span></p><p><span>Promote continuous improvement in portfolio management practices including digitalisation and use of AI.</span></p><p></p><p></p><p><span>Basic qualifications:</span></p><ul><li><p>Role requires understanding of end to end Pharma supply chain design and operations.</p></li><li><p>Minimum 15 yrs of experience  working with Pharma brands and understanding of pharmaceutical product lifecyles.</p></li><li><p>Strong commercial acumen with the ability to balance profitability, operational efficiency and market/medical needs.</p></li><li><p>Awareness of the supply chain or business area and key priorities to inform day to day activities in support of programme execution.</p></li><li><p>Demonstrated project leadership and management skills.</p></li><li><p>Demonstrated effective communications skills both written &amp; oral coupled with the ability to tailor to any one of a wide variety of audiences.</p></li><li><p>Attention to detail; a focus on output, content &amp; delivery to ensure that there is tangible progress.</p></li><li><p>Agile and willingness to learn.</p></li><li><p>Capacity to adapt priorities, organization and promote change management. Ability to work with tight deadlines.</p></li><li><p>Experience with continuous improvement</p></li><li><p>Ability to work cross-functionally and use networks throughout GSK</p></li></ul><p></p><p></p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>Inclusion at GSK:</b></p><p>As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.</p><p></p><p>Please contact our Recruitment Team at <a target="_blank" href="http://IN.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>IN.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.</p><p></p><p><b>GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.</b></p><p></p><p>If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing <a target="_blank" href="http://askus&#64;gsk.com"><span style="color:#0000ff"><u>askus&#64;gsk.com</u></span></a>, so that we can confirm to you if the job is genuine.</p><p> </p>]]></description><link>http://biotechroles.com/associate-director-gsc-portfolio-optimization-gcc-gsk/6a05f4c82f1861929d25319e</link><guid isPermaLink="true">http://biotechroles.com/associate-director-gsc-portfolio-optimization-gcc-gsk/6a05f4c82f1861929d25319e</guid><pubDate>Thu, 14 May 2026 16:14:00 GMT</pubDate><company>GSK</company><location>Bengaluru Luxor North Tower</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Marketing Manager, Flu Franchise]]></title><description><![CDATA[<p>Job Description</p><p>GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to leverage our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centered on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems. Our diverse portfolio consists of vaccines, specialty medicines, and general medicines. Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.<br /><br /><b>Position Summary </b></p><p><br />You will lead marketing activities for the Flu franchise in the U.S., working with colleagues across commercial, medical, market access, regulatory, digital, and external partners. You will create and deliver clear, customer-focused marketing plans that help increase immunization rates and improve public health. We value people who think strategically, act with integrity, and care about measurable impact. This role offers growth, visible impact, and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.<br /><br /><b>Key Responsibilities</b></p><p><br />This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:</p><ul><li>Lead annual demand planning and channel strategies across direct, public, retail, and institutional segments.</li><li>Co-create and drive the US marketing plan with internal and global stakeholders.</li><li>Develop marketing mix and content strategy for HCP and consumer channels, including digital and field enablement.</li><li>Lead cross-functional core team meetings and coordinate stakeholder engagement for initiative deployment.</li><li>Provide pricing and contracting recommendations and support budget planning and forecasting.</li><li>Measure campaign performance and recommend data-driven optimizations.</li></ul><p></p><p><b>Why You?</b></p><p></p><p><b>Basic Qualifications</b></p><p></p><p>We are seeking professionals with the following required skills and qualifications to help us achieve our goals:</p><ul><li>Bachelor’s degree in Marketing, Business, Life Sciences, or related field.</li><li>3&#43; years of pharmaceutical, vaccines, or healthcare marketing experience.</li><li>Experience developing and executing integrated HCP and consumer marketing plans.</li><li>Experience with pharmaceutical promotional review and compliance processes.</li></ul><p><br /><b>Preferred Qualifications</b></p><p><br />If you have the following characteristics, it would be a plus:</p><ul><li>Advanced degree or MBA in Marketing, Business, or related field.</li><li>Experience in vaccines or public health immunization programs.</li><li>Experience with demand planning, pricing, and contracting in healthcare.</li><li>Strong analytical skills and experience using data to optimize channel mix and content.</li><li>Experience managing external agencies and multiple vendor relationships.</li><li>Comfort using digital marketing tools, analytics platforms, and emerging technologies.</li><li>Ability to work effectively in a matrixed environment with cross-functional teams.</li><li>Demonstrated project management skills, including timeline, vendor and budget management.</li></ul><p><br />This role is hybrid. You will work both remotely and on-site as required by the team. Expect occasional domestic travel up to 10-20% for stakeholder meetings and field engagement.</p><p></p><p><b><span>#LI-GSK</span></b></p><p><b><span>#GSKCommercial</span></b></p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/marketing-manager-flu-franchise-gsk/6a05f4c82f1861929d25319d</link><guid isPermaLink="true">http://biotechroles.com/marketing-manager-flu-franchise-gsk/6a05f4c82f1861929d25319d</guid><pubDate>Thu, 14 May 2026 16:14:00 GMT</pubDate><company>GSK</company><location>USA - Pennsylvania - Philadelphia</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Director, Business Strategy and Operations]]></title><description><![CDATA[<p>Are you excited by the opportunity to operate at the heart of GSK’s UK Commercial organisation? Are you passionate about leading people, driving innovation, and embedding a high‑performance culture?</p><p></p><p>As Senior Director, Business Strategy &amp; Operations for UK Commercial you will play a critical, highly visible role in shaping the future of GSK UK. You will lead a diverse, high‑impact organisation across performance, strategy, insights, capabilities, and operations, with accountability for driving excellence and delivering against our ambitions for growth &amp; delivering our exciting new launches. You will be a driving digital transformation, including AI acceleration to unlock enhanced impact and efficiencies across the organisation in line with core operations and processes.</p><p></p><p>This role partners directly with the UK Commercial General Manager and UKLT. You will help steer the UK business through data‑driven insights, operational excellence, and strategic clarity—ensuring the organisation is aligned, performing, and accelerating delivery against our objectives.</p><p></p><p><b>Our Mission &amp; Vision</b></p><p>Mission:<br />- To unleash excellence and drive growth across the UK organisation—elevating performance, accelerating strategic progress, and enabling teams to operate at their very best</p><p>Vision:<br />- To be proactive performance enhancers—constantly hunting opportunities to <i>make the boat go faster</i>.<br />- We unlock insights, modernise operations, build capability, and create the conditions for high‑performance teams to win.</p><p></p><p><b>Core Areas of Leadership &amp; Focus</b></p><p>You will lead the UK Commercial organisation in the following areas of focus:</p><p></p><ul><li><p>Driving digital transformation, including AI acceleration to enhance effectiveness &amp; efficiencies across all core areas of focus</p></li><li><p>Enhancing our infield competitiveness through all aspects of Sales Force Effectiveness (SFE) and Sales Force Incentives (SFI) including maximising effectiveness in our high impact channels such as HCP Meetings</p></li><li><p>Supporting customer‑facing teams with core platforms and processes (Veeva, NBA, etc.) whilst innovating to ensure future fitness</p></li></ul><ul><li><p>Driving enterprise‑wide capability uplift across commercial, analytical and execution excellence</p></li></ul><ul><li><p>Embedding global data, analytics, and market research into UK strategic and operational needs</p></li><li><p>Driving a data‑driven mindset and enabling predictive, diagnostic, and AI‑enhanced insight generation</p></li><li><p>Leading the UK Performance Management Process, ensuring a strong, transparent performance culture</p></li></ul><ul><li><p>Ownership of the UK Commercial Governance Framework</p></li><li><p>Ensuring safe, compliant, and high‑quality commercial operations</p></li></ul><p></p><p>…………………………………………………………………….</p><p></p><p><b>Chief of Staff to the UK Leadership Team</b></p><p>You will act as a strategic integrator and orchestrator for the UKLT:</p><ul><li><p>Strategic thought partnering for the UK GM and UKLT to identify organisational wide opportunities to enhance UK performance </p></li><li><p>Coordinate monthly UKLT meetings, setting agendas and facilitating effective discussion</p></li><li><p>Lead Monthly Performance Review (MPR) preparations with Region</p></li><li><p>Partner across the UKLT to ensure decisions are followed through to impact</p></li><li><p>Lead preparation for senior leader country visits, working closely with global/regional Chiefs of Staff</p></li><li><p>Driving continuous improvement in operating rhythms, routines, and performance discussions</p></li></ul><p>This component requires exceptional organisational influence, strategic intuition, and an ability to create clarity and alignment across senior stakeholders.</p><p></p><p><b>…………………………………………………………………</b></p><p></p><p><b>Basic Qualifications</b></p><ul><li><p>Bachelor’s degree</p></li><li><p>Senior commercial experience within the pharmaceutical industry</p></li><li><p>Demonstrated success leading commercial or operational teams</p></li><li><p>Proven ability to build strong relationships with senior stakeholders</p></li><li><p>Experience working cross‑functionally</p></li><li><p>Experience in omnichannel and digital transformation</p></li><li><p>Strong communication and interpersonal skills</p></li><li><p>Demonstrated problem‑solving capability</p></li><li><p>Strong data acumen and proficiency with platforms (IQVIA, PowerBI, Azure)</p></li><li><p>Experience with transformation &amp; change management</p></li></ul><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>Experience across local, regional, and/or global pharmaceutical roles</p></li><li><p>Global/Regional exposure</p></li><li><p>MBA or equivalent strategic/leadership qualification</p></li></ul><p></p><p><b>Overall Impact</b></p><p>This role is a unique opportunity to shape the performance, strategy, and operating rhythm of one of GSK’s most important markets. You will build the conditions for organisational success—strengthening insights, capabilities, operations, governance, and strategic clarity—while empowering teams to deliver excellence and growth.</p><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. </p><p></p><p>We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p>We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.</p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:UKRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments&#64;gsk.com</u></span></a> where you can also request a call.</p><p></p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the <a target="_blank" href="https://www.gsk.com/en-gb/locations/united-kingdom/"><span style="color:#0000ff"><u>Link</u></span></a> where you will find answers to multiple questions we receive</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/senior-director-business-strategy-and-operations-gsk/6a05f4c72f1861929d25319c</link><guid isPermaLink="true">http://biotechroles.com/senior-director-business-strategy-and-operations-gsk/6a05f4c72f1861929d25319c</guid><pubDate>Thu, 14 May 2026 16:13:59 GMT</pubDate><company>GSK</company><location>UK – London – New Oxford Street</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Strategic Oncology Account Director (Field-based)]]></title><description><![CDATA[<p>The <b>Strategic Oncology Account Director</b> <b>(SOAD)</b> is responsible for cultivating mutually beneficial relationships with C and D-suite decision makers across assigned community oncology accounts. Serving as the primary GSK account lead and subject matter expert, you will advance GSK brand objectives by enhancing awareness and removing patient access barriers to our products.  You will pave a path for successful product launches and growth for new and existing portfolio products. You will deliver compelling value propositions, engage in fruitful virtual and live customer discussions and foster an aligned cross‑functional, collaborative approach with your medical, contracting strategy, brand and sales team colleagues within GSK. As subject matter expert, you will inform internal GSK colleagues with timely and accurate customer insights, captured and shared during regular live meetings and through strategic business planning documentation. You will represent GSK at educational and business conferences and ensure a credible, reliable and professional image.</p><p></p><p><b>Key Responsibilities:</b></p><ul><li>Strategic account management, business planning, profiling and documenting of insights to inform Market Access Contracting &amp; Brand Strategy and Medical Teams for assigned accounts</li><li>Develop lasting business relationships with C- &amp; D-Suite level stakeholders within assigned accounts</li><li>Secure GSK product adoption, integration and on-label access within EMRs, formularies, order sets, etc.</li><li>Be accountable to achieving results, including successful contractual agreements and access metrics</li><li>Provide timely, insightful and actionable oncology marketplace and market access knowledge and updates to internal and external stakeholders</li><li>Comply with all GSK policies and ways of working guidance</li></ul><p></p><p><b>Why You?</b></p><p><b>Basic Qualifications:</b></p><ul><li>Bachelor’s degree</li><li>Minimum 2 years of oncology sales, marketing and/or account management experience in the pharma industry</li><li>Demonstrated knowledge of the economic framework of the oncology practice environment, Medicare, Medicaid, commercial payers and coding and billing for IV therapies</li><li>Experience supporting oncology pharmaceutical product launches and lifecycle management</li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li>Prior experience managing sales teams or other first line leader experience</li><li>Experience supporting account-level contracting and pricing strategies</li></ul><p></p><p>#LI-GSK</p><p>#GSKCommercial</p><p>#LI-Remote</p>The US annual base salary for new hires in this position ranges from $186,750 to $311,250.  The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.&amp;#xa;&amp;#xa;If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/strategic-oncology-account-director-field-based-gsk/6a05f4c62f1861929d25319b</link><guid isPermaLink="true">http://biotechroles.com/strategic-oncology-account-director-field-based-gsk/6a05f4c62f1861929d25319b</guid><pubDate>Thu, 14 May 2026 16:13:58 GMT</pubDate><company>GSK</company><location>Field Worker - USA</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Director, Global Strategic Insights – Oncology]]></title><description><![CDATA[<p>At GSK, we unite science, technology and talent to get ahead of disease together. We prioritize research into vaccines and medicines across our four core therapeutic areas of infectious diseases, HIV, respiratory/immunology, and oncology. We also remain open to other opportunities where the science aligns with our strategic approach.</p><p></p><p>Do you have an entrepreneurial spirit, insatiable curiosity, broad pharma expertise, and a strong commitment to deploying insights to guide business strategy? If so, consider being a key partner in the growth of GSK Oncology as <b>Global Strategic Insights (GSI) Director.</b></p><p></p><p>In this role, you will drive strategic insight generation that will define and shape Global Product Strategy for one of our Oncology brands, one which is a critical launch asset from the Anti-drug Conjugate (ADC) portfolio and the EMBOLD clinical development program. Working closely with the Global Product Strategy Commercialization Leader and a wide, cross-functional group of partners, you will:</p><ul><li>Lead insight generation to shape and drive commercial forecasts for business governance milestones, in close partnership with cross-functional teams</li><li>Define, structure, plan, and commission global market research to proactively address key business questions and generate actionable and concise recommendations</li><li>Leverage technology and innovation to increase efficiency and/or effectiveness in insight generation, while maintaining rigor and quality</li><li>Develop robust forecast models ensuring seamless integration of market and customer insights into sound forecasts that contribute to investment planning decisions</li><li>Partner with the Global Competitive Intelligence team to closely monitor the latest external developments, and translate these into concise and impactful recommendations</li><li>Be a thought-partner for the cross-functional teams</li></ul><p></p><p><i>This role will provide YOU the opportunity to lead key activities to progress YOUR career.  These responsibilities include some of the following:</i></p><ul><li>Lead multiple workstreams, and exert influence within cross-functional matrices</li><li>Harness the latest research and analytical methodologies to drive a competitive edge for GSK</li><li>Develop deep subject matter expertise in lead indication, tracking trends, current and evolving competitive landscapes, and generating long-term strategic outlooks</li><li>Deliver well-integrated, actionable insights and ensure their strategic application to support global strategy, governance, and investment decisions</li><li>Manage vendor relationships to achieve a mutually rewarding partnership while ensuring excellence in insight generation execution</li><li>Leverage a wide range of tools and resources to identify opportunities, assess program potential, and provide guidance to optimize development plans</li><li>Continue to build your ability to influence the planning and activities of cross-functional teams to help create alignment, clarity, and a clear sense of shared responsibility for the brands you work on.</li></ul><p></p><p><b><i>Why you?</i></b></p><p><b><i>Basic Qualifications</i></b><br /><i>We are looking for professionals with these required skills to achieve our goals:</i></p><ul><li>Bachelor’s Degree</li><li>Strong track record of pharmaceutical industry experience, preferably encompassing both global and regional business analytics &amp; insights roles</li><li>Direct Oncology commercialization experience or relevant consulting experience</li><li>Significant experience conducting market research, combined with forecasting expertise</li></ul><p></p><p><b><i>Preferred Qualifications</i></b><br /><i>If you have the following characteristics, it would be a plus:</i></p><ul><li>MBA, MS, or MA in business, marketing science, or science</li><li>Demonstrated ability to apply data and analyses to drive high impact business decisions</li><li>Ability to leverage and synthesize a broad range of information sources to develop insight and generate clear, actionable recommendations that impact/drive decision-making at a business unit level</li><li>Demonstrated ability to influence senior commercial leadership and confidently defend informed recommendations, combined with strong communication and presentation skills</li><li>Prior experience supporting product launch and/or business development opportunity assessment</li><li>Agility, flexibility, and comfort with ambiguity</li></ul><p></p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/director-global-strategic-insights-oncology-gsk/6a05f4c62f1861929d25319a</link><guid isPermaLink="true">http://biotechroles.com/director-global-strategic-insights-oncology-gsk/6a05f4c62f1861929d25319a</guid><pubDate>Thu, 14 May 2026 16:13:58 GMT</pubDate><company>GSK</company><location>USA - Pennsylvania - Upper Providence</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Director, AI Analytics and Reporting Enablement]]></title><description><![CDATA[<p></p><p>The Director, AI Analytics &amp; Reporting Enablement provides strategic leadership for enterprise analytics transformation within U.S. Commercial. This role owns the vision, strategy, and execution for scalable BI, GenAI, and advanced analytics capabilities (e.g., GiGi for Analytics using ThoughtSpot) —enabling data-driven decision-making across marketing, sales, market access, patient services, and broader enterprise teams.<br /><br />The Director sets the long-term analytics enablement roadmap, leads analytics productization efforts, and ensures high-quality, governed, and compliant use of commercial data assets. This leader acts as a trusted advisor to senior executives, oversees platform adoption at scale, and leads a high-performing cross-functional team that drives innovation, operational excellence, and measurable business impact.</p><p>Importantly, this role is expected to execute on the analytics remit of the role while raising the skill level of the same across the I&amp;A team.  This means the incumbent will be balancing hands-on execution in BI/AI/analytics platforms, problem-solving, and data exploration, while simultaneously providing strategic direction, mentorship, and leadership. The Director models best practices, rolls up their sleeves when needed, and actively supports the team in overcoming technical and organizational challenges.</p><h2></h2><h2>Stakeholder Engagement</h2><p>This position will be closely partnered with:</p><ul><li><p>Commercial leadership teams (marketing, sales, market access)</p></li><li><p>Insights &amp; Analytics colleagues across U.S. Commercial</p></li><li><p>Technology partners for data integration and governance</p></li><li><p>Senior leaders across the enterprise for influence and adoption</p></li></ul><p>Interactions will go beyond transactional support—requiring influence, storytelling, and change management skills to ensure adoption of new analytics solutions.</p><h2></h2><h2>Key Deliverables &amp; Responsibilities:</h2><ul><li><p><b>Strategy &amp; Roadmap - </b>Define and execute the multi-year strategy for enterprise BI, AI, and analytics enablement to maximize commercial impact.</p></li><li><p><b>Commercial Use Case Prioritization - </b>Identify, evaluate, and prioritize high-value analytics and AI use cases that advance brand, access, field, and omnichannel objectives.</p></li><li><p><b>Platform Ownership - </b>Serve as product owner for the AI enterprise analytics ecosystem, ensuring solutions are scalable, integrated, and user-centric.</p></li><li><p><b>Governance &amp; Compliance - </b>Establish and maintain governance standards for data quality, semantic modeling, AI/ML lifecycle, and compliant analytics practices.</p></li><li><p><b>Player-Coach Leadership - </b>Lead, mentor, and develop the AI analytics enablement team while personally contributing hands-on to BI development and problem-solving.</p></li><li><p><b>Stakeholder Partnership -</b> Act as a strategic advisor to senior commercial leaders by translating analytics capabilities into clear business decisions and outcomes.</p></li><li><p><b>AI/ML &amp; GenAI Innovation - </b>Drive evaluation, piloting, and scaling of advanced analytics, AI/ML, and GenAI solutions that enhance commercial performance.</p></li><li><p><b>Operational Excellence - </b>Oversee delivery of high-quality dashboards, reporting tools, and insight workflows that improve speed-to-decision and data reliability.</p></li><li><p><b>Adoption &amp; Change Management - </b>Lead adoption efforts through training, storytelling, and change leadership to embed AI-first, data-driven ways of working.</p></li><li><p><b>Vendor &amp; Budget Oversight - </b>Manage vendors, contracts, and analytics investments to ensure cost-efficient delivery of high-value capabilities.</p></li></ul><h2></h2><p><b>Basic Qualifications:</b></p><ul><li><p>Bachelor’s degree in quantitative or business discipline</p></li><li><p>At least 10 years of experience in analytics, data science, or business intelligence</p></li><li><p>At least 5 years of experience leading functional or cross-functional teams and driving cross-functional analytics initiatives</p></li><li><p>Experience scaling analytics platforms and driving broad enterprise adoption</p></li><li><p>Hands on experience with ThoughtSpot and Liveboards</p></li><li><p>Fluent in SQL, semantic modeling concepts, cloud data environments, and key commercial data sources (such as patient-level claims)</p></li><li><p>Proven track record of translating analytics into clear business impact as well as influencing senior stakeholders</p></li><li><p>Experience in balancing strategic leadership with hands-on technical contribution</p></li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li><p>MBA or advanced degree in Data Science, Statistics, Computer Science, or related field</p></li><li><p>15&#43; years of experience in analytics, data science, or business intelligence</p></li><li><p>8&#43; years of experience leading functional or cross-functional teams and driving analytics initiatives</p></li><li><p>Hands-on experience with BI/analytics tools (ThoughtSpot, Tableau, Power BI) including semantic data modeling</p></li><li><p>Familiarity with cloud environments (AWS, Azure, GCP) and data technologies (Spark, Databricks)</p></li><li><p>Proven track record leading, building and scaling advanced analytics, AI/ML, and GenAI solutions</p></li><li><p>Ability to simplify complex analytics into compelling, actionable business narratives</p></li><li><p>Proven track record influencing VP-level stakeholders and navigating complex cross-functional environments.</p></li></ul><p></p><p>#LI-GSK</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>Please visit  <a target="_blank" href="http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf"><span style="color:#0000ff"><u>GSK US Benefits Summary</u></span></a>  to learn more about the comprehensive benefits program GSK offers US employees. </p><p></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><span style="color:#292a2e">If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><a target="_blank" href="mailto:usrecruitment.adjustments&#64;gsk.com"><span style="color:#1868db"><u>usrecruitment.adjustments&#64;gsk.com</u></span></a>                                                                                                                                                                                                                                                      </p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/director-ai-analytics-and-reporting-enablement-gsk/6a05f4c52f1861929d253199</link><guid isPermaLink="true">http://biotechroles.com/director-ai-analytics-and-reporting-enablement-gsk/6a05f4c52f1861929d253199</guid><pubDate>Thu, 14 May 2026 16:13:57 GMT</pubDate><company>GSK</company><location>USA - Pennsylvania - Philadelphia</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Pharmacovigilance Quality Assurance Director]]></title><description><![CDATA[<p></p><h1><b>Pharmacovigilance Quality Assurance Director</b></h1><p><br />We are a specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV.</p><p><br />As the pioneers in HIV innovation, we constantly look to push the boundaries of science to develop medicines that can change lives and give people more choice. Beyond our medicines, we are proud of our deep connection with the HIV community and work with partners to advance research and development, address HIV-related stigma, increase access to our medicines and provide funding and support to local community organisations to support their efforts in the HIV response.<br /><br />We are ViiV Healthcare. Here until HIV and AIDS are not.<br /><br /><br />Position Summary</p><p>We are looking for an experienced <b>Pharmacovigilance Quality Assurance Director</b> to lead and maintain a robust PV Quality Assurance programme, ensuring that pharmacovigilance activities supporting our products remain fully compliant with global regulations and internal quality standards.</p><p></p><p>In this senior role, you will act as a trusted quality and compliance partner, providing oversight, assurance and strategic guidance across the pharmacovigilance system. You will work closely with senior stakeholders, quality teams, and service providers to identify risk, drive continuous improvement and, most importantly, ensure patient safety.</p><p></p><p></p><p><b><i>Key Responsibilities</i></b></p><p>As Pharmacovigilance Quality Assurance Director, you will:</p><ul><li><p>Provide independent quality assurance and oversight of pharmacovigilance processes to ensure compliance with global PV legislation, company policies and regulatory expectations</p></li><li><p>Lead and manage the PV QA programme, including audit risk assessments, audit planning, execution oversight and follow-up</p></li><li><p>Oversee and track Corrective and Preventive Actions (CAPAs), verifying effectiveness and escalating risks or issues where required</p></li><li><p>Act as a key point of contact for PV inspection readiness and inspection management, ensuring teams are fully prepared and supported</p></li><li><p>Review and oversee audit outcomes that impact supported products, including those conducted by internal and external quality functions</p></li><li><p>Partner with senior leadership to identify quality, compliance and risk areas, agreeing and monitoring remediation plans</p></li><li><p>Maintain and develop Pharmacovigilance System Master File (PSMF) content related to audit and deviation management</p></li><li><p>Generate and present quality metrics, reports and insights to governance and oversight forums</p></li><li><p>Provide expert advice on PV compliance, quality improvement, risk assessment and regulatory interpretation</p></li><li><p>Support the ongoing development of the Quality Management System (QMS) underpinning pharmacovigilance activities</p></li><li><p>Build and maintain strong working relationships across internal quality and compliance teams and with external partners</p></li><li><p>Contribute to and deliver training programmes within your area of expertise</p></li></ul><p></p><p></p><p></p><p><b><i>About You</i></b></p><p>We are looking for a high energy individual who can bring their market preparation and launch excellence expertise to this pivotal role. Pioneering new approaches, creative thinking and helping us to differentiate ViiV.</p><p>To be successful in this role, you will bring:</p><ul><li><p>Extensive experience in Pharmacovigilance Quality Assurance, PV compliance or regulatory quality within the pharmaceutical or biotechnology industry</p></li><li><p>Strong knowledge of global PV and GCP legislation, regulatory guidelines and inspection expectations</p></li><li><p>Proven experience managing PV audits, inspections and CAPAs</p></li><li><p>Confidence engaging with and influencing senior stakeholders on quality, risk and compliance matters</p></li><li><p>Excellent analytical, communication and stakeholder management skills</p></li><li><p>A proactive, collaborative mindset with a strong focus on patient safety and continuous improvement</p></li></ul><p></p><p></p><p></p><p><b>Location and Working Pattern</b><br />This role is based at our UK HQ in Central London, and operates on a hybrid working model. You will be expected to work on-site 2/3 days per week to collaborate with cross-functional teams and support critical activities.</p><p></p><p></p><p></p><p><b>Closing Date for Applications – CoP 22nd May 2026</b></p><p>Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ for your online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you provide in your cover letter and CV will be used to assess your application.</p><p></p><p></p><p></p><p>#LI-ViiV</p><p>#LI-GSK</p><p>#Hybrid</p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why Us?</b></p><p>At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. </p><p></p><p>We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>GSK</u></span></a> and <a target="_blank" href="http://www.Pfizer.com"><span style="color:#0000ff"><u>Pfizer</u></span></a> in 2009, with <a target="_blank" href="http://www.Shionogi.com"><span style="color:#0000ff"><u>Shionogi</u></span></a> joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.</p><p></p><p>Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. </p><p></p><p>Having a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.</p><p></p><p>ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law                                                                                                                                                                                                                                                                                                                                                       </p><p></p><p>Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at <a target="_blank" href="mailto:HR.AmericasSC-CS&#64;gsk.com"><span style="color:#0000ff"><u>HR.AmericasSC-CS&#64;gsk.com</u></span></a> where you can also request a call.                                                                                                                                                                               </p><p></p><p>Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the link <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/pharmacovigilance-quality-assurance-director-gsk/6a05f4c32f1861929d253198</link><guid isPermaLink="true">http://biotechroles.com/pharmacovigilance-quality-assurance-director-gsk/6a05f4c32f1861929d253198</guid><pubDate>Thu, 14 May 2026 16:13:55 GMT</pubDate><company>GSK</company><location>UK – London – New Oxford Street</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Junior PS Operations Analyst]]></title><description><![CDATA[<p><br /><b>Junior PS Operations Analyst, Americas SC Actions Summary <u>with Spanish and English </u></b><br /><br /><span>Support day-to-day operational activities within the PS function to ensure timely, compliant delivery of products and services. Execute transactional tasks, maintain accurate records, coordinate with internal and external stakeholders, and escalate issues in accordance with SOPs and regulatory requirements.</span><br /> </p><p><span class="emphasis"><b>Key responsibilities:</b></span></p><ul><li><span>Execute operational transactions including order processing, shipment coordination, inventory updates, and sample management.</span></li><li><span>Maintain data integrity and traceability through accurate system entries (ERP/WMS/CRM) and documentation.</span></li><li><span>Monitor operational KPIs and produce regular status reports and dashboards for the Operations Lead.</span></li><li><span>Prepare and verify shipment documentation (BOLs, packing lists, certificates) to ensure compliance with internal procedures.</span></li><li><span>Log and coordinate responses for deviations, incidents and CAPAs with Quality and Compliance teams.</span></li><li><span>Serve as a primary contact for routine queries from internal stakeholders and third‑party logistics providers; escalate complex issues promptly.</span></li><li><span>Participate in continuous improvement initiatives (5S, Kaizen) and support process standardisation.</span></li><li><span>Provide backup support for basic planning activities such as replenishment requests and demand reconciliation.</span></li><li><span>When assigned to reporting activities, Tier 1 personnel must report to and liaise with the Global LTI Team upon commencement and throughout the reporting process.</span><br /> </li></ul><p><span class="emphasis"><b>Basic qualifications:</b></span></p><ul><li><span>Fluent in Spanish and English</span></li><li><span>0–3 years’ experience in operations, supply chain, logistics or customer service; experience in a regulated environment preferred.</span></li><li><span>Familiar with Microsoft Excel</span></li><li><span>Strong attention to detail and demonstrated ability to follow SOPs and work instructions.</span><br /> </li></ul><p><span class="emphasis"><b>Preferred qualifications:</b></span></p><ul><li><span>Prior exposure to pharmaceutical, biotech or healthcare operations.</span></li><li><span>Experience with data visualisation tools (Power BI, Tableau) is a plus.</span><br /> </li></ul><p><span><b>Skills &amp; competencies</b></span></p><ul><li><span>Clear, professional communication and stakeholder management.</span></li><li><span>Organized, reliable, and able to prioritize competing tasks under tight deadlines.</span></li><li><span>Problem‑solving mindset with appropriate escalation discipline.</span></li><li><span>Team player with a continuous improvement orientation.</span></li><li><span>Flexibility to support occasional after‑hours activities (shipping windows, vendor coordination).</span></li></ul><p><span> </span></p><p><span class="emphasis"><b>Benefits: </b></span></p><ul><li>Career at one of the leading global healthcare companies</li><li>Contract of employment</li><li>Attractive reward package (annual bonus &amp; awards for outstanding performance, recognition awards for additional achievements and engagement, holiday benefit)</li><li>Life insurance and pension plan</li><li>Private medical package with additional preventive healthcare services for employees and their eligible</li><li>Sports cards (Multisport)</li><li>Possibilities of development within the role and company’s structure</li><li>Personalized learning approach</li><li>Extensive support of work life balance</li><li>Supportive community and integration events</li><li>Modern office with creative rooms, fresh fruits everyday</li><li>Free car and bike parking, locker rooms and showers.</li></ul><p>#LI-GSK<br />G10</p>&amp;#xa;The annual base salary in Poland for new hires in this position ranges from PLN 72,975 to PLN 121,625 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.   Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion).   All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave &amp; care of family member leave.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p>As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at <a target="_blank" href="mailto:pl.recruitment-adjustments&#64;gsk.com"><span style="color:#0000ff"><u>pl.recruitment-adjustments&#64;gsk.com</u></span></a> to discuss your needs.    <b>                                                                                                                                                                                </b></p><p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a></p>]]></description><link>http://biotechroles.com/junior-ps-operations-analyst-gsk/6a05f4c32f1861929d253197</link><guid isPermaLink="true">http://biotechroles.com/junior-ps-operations-analyst-gsk/6a05f4c32f1861929d253197</guid><pubDate>Thu, 14 May 2026 16:13:55 GMT</pubDate><company>GSK</company><location>Poznan Pastelowa</location><salary>$35000-48000</salary><type>Full time</type></item><item><title><![CDATA[Representante de Ventas - Medellin]]></title><description><![CDATA[<div><div>Job Description</div></div><div><div><div><div><div><div><div><div><div><p><b>Introducción del Negocio</b></p><p>GSK mantiene su compromiso de alcanzar ambiciosos objetivos comerciales de cara al futuro. Para 2031, aspiramos a generar £40 mil millones en ventas anuales, aprovechando nuestro sólido impulso de desempeño actual para aumentar significativamente nuestro impacto positivo en la salud de miles de millones de pacientes a nivel global. Nuestra estrategia <i>Ahead Together</i> se centra en la intervención temprana para prevenir y modificar el curso de las enfermedades, protegiendo a las personas y apoyando a los sistemas de salud.</p><p>Nuestro portafolio diverso está compuesto por vacunas, medicamentos especializados y medicamentos generales.</p><p>A través de la innovación continua y un enfoque dedicado en la excelencia científica y técnica, buscamos desarrollar y lanzar nuevos tratamientos innovadores que aborden desafíos críticos de salud.</p><p><b>Resumen del Cargo</b></p><p>Somos GSK y buscamos una persona que conecte con profesionales de la salud para mejorar el acceso a soluciones médicas en Colombia. En este rol trabajarás de manera cercana con equipos de acceso, medical y marketing. Valoramos personas con orientación comercial, sólidas habilidades relacionales y ética profesional. Aquí podrás crecer profesionalmente, influir en la experiencia de los pacientes y contribuir a nuestro propósito de unir ciencia, tecnología y talento para adelantarnos a la enfermedad juntos.</p><p>Este cargo te brindará la oportunidad de liderar actividades clave para impulsar tu carrera profesional. Entre las responsabilidades se incluyen:</p><ul><li><p>Desarrollar y ejecutar planes de cuenta y rutas comerciales para alcanzar objetivos de ventas y cobertura.</p></li><li><p>Mantener y ampliar relaciones con profesionales de la salud, instituciones y puntos de dispensación.</p></li><li><p>Implementar estrategias comerciales y de acceso en el territorio, dando seguimiento desde la generación de demanda hasta la entrega.</p></li><li><p>Gestionar los recursos del territorio, incluyendo material promocional y muestras, cumpliendo políticas y estándares.</p></li><li><p>Trabajar activamente con equipos multifuncionales para maximizar el valor para pacientes y stakeholders.</p></li><li><p>Mantener conocimientos actualizados sobre la enfermedad, normativa sanitaria y competencia.</p></li></ul><p><b>Responsabilidades</b></p><ul><li><p>Preparar y ejecutar visitas estratégicas a clientes para transmitir información clara, relevante y basada en evidencia.</p></li><li><p>Monitorear indicadores de productividad y reportar el progreso de manera oportuna y precisa.</p></li><li><p>Identificar oportunidades de inclusión en listados y mejorar condiciones de acceso en cuentas clave.</p></li><li><p>Utilizar herramientas digitales y CRM para gestionar y asegurar la calidad de la información del territorio.</p></li><li><p>Participar en programas de formación y certificación de visitas.</p></li><li><p>Actuar con integridad, respetando las políticas internas y la normativa del sector salud.</p></li></ul><p><b>¿Por qué tú?</b></p><p><b>Requisitos Básicos</b></p><p>Buscamos profesionales con las siguientes habilidades y calificaciones requeridas para ayudarnos a alcanzar nuestros objetivos:</p><ul><li><p>Título universitario en áreas comerciales, administrativas, salud, economía, ingeniería o afines.</p></li><li><p>Mínimo 3 años de como representante médico manejando la <b>línea cardio metabólica, endocrinología y/o nefrología.</b></p></li><li><p>Licencia de conducción vigente y disponibilidad para desplazamientos dentro del territorio asignado.</p></li><li><p>Experiencia en manejo de herramientas CRM (Veeva)</p></li><li><p>Excelentes habilidades de comunicación y capacidad para construir relaciones de confianza con clientes.</p></li><li><p>Compromiso con el cumplimiento normativo, la ética profesional y el trabajo en equipo.</p></li></ul><p><b>Calificaciones Deseables</b></p><p>Si cuentas con las siguientes características, será un valor agregado:</p><ul><li><p>Experiencia específica en productos de especialidad o alto costo.</p></li><li><p>Conocimiento del sistema de salud colombiano y procesos de acceso a medicamentos.</p></li><li><p>Bilingüismo en español e inglés en nivel básico o intermedio.</p></li><li><p>Capacidad para liderar presentaciones a grupos y jornadas formativas.</p></li><li><p>Alto nivel de iniciativa, orientación a resultados y agilidad de aprendizaje.</p></li></ul><p><b>Ubicación y Modalidad</b></p><ul><li><p>Posición basada en Medellin.</p></li><li><p>Modalidad: 100% presencial / trabajo de campo con desplazamientos regulares dentro del territorio.</p></li><li><p>Reporta al equipo comercial local y colabora con equipos multifuncionales.</p></li></ul><p><b>Cómo Postular</b></p><p>Si te motiva contribuir a mejorar la salud de las personas y deseas crecer profesionalmente en un entorno de aprendizaje, te invitamos a postular. Presenta tu CV y una breve carta explicando por qué te interesa este rol y cómo puedes aportar. Esperamos conocerte y explorar juntos cómo puedes crecer con nosotros.</p></div></div></div></div></div></div></div></div></div><p></p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p> </p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>If you require any adjustments or accommodation during the selection process to better showcase your abilities, please let our team know as soon as we contact you. We&#39;re here to support you.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p> </p><p>Our inclusive workplace makes our employees feel engaged by the contribution they make, by affording them equal treatment regardless of actual or perceived characteristics. As so, when you apply for a job at GSK, it is not necessary to include on your resume information such as: race, color, ethnicity, age, gender, sexual orientation, marital status, religion, origin, photographs or any other personal characteristics.</p><p> </p><p>Find out what life at GSK is really like <a target="_blank" href="http://www.gsk.com"><span style="color:#0000ff"><u>www.gsk.com</u></span></a></p>]]></description><link>http://biotechroles.com/representante-de-ventas-medellin-gsk/6a05f4c22f1861929d253196</link><guid isPermaLink="true">http://biotechroles.com/representante-de-ventas-medellin-gsk/6a05f4c22f1861929d253196</guid><pubDate>Thu, 14 May 2026 16:13:54 GMT</pubDate><company>GSK</company><location>COL - Antioquia - Medellín</location><salary>$18000-35000</salary><type>Full time</type></item><item><title><![CDATA[Veterinary Services Specialist - 3Rs]]></title><description><![CDATA[<p></p><p><b>Job title: </b>Veterinary Services Specialist - 3Rs </p><p><b>Location</b>: Siena</p><p><b>Employment type:</b> Indeterminato, Full time</p><p><b>Working schedule</b>: A giornata, con reperibilità nel fine settimana a rotazione</p><p><b>Closing date for applications: </b>28 maggio 2026 COB</p><p></p><p></p><p><span class="emphasis"><b>Scopo:</b></span></p><p><span>Eseguire in autonomia e supportare la programmazione di tutte le attività veterinarie di ARC in accordo alle procedure operative interne, alle disposizioni di legge, alle GLP/GMP e alle norme di sicurezza .</span></p><p><span>La persona incaricata ricopre il ruolo in accordo ai requisiti:</span></p><p><span><span>·<span>       </span></span></span><span>Decreto Legislativo 04 Marzo 2014 n. 26, in materia di protezione degli animali utilizzati a fini scientifici e altra legislazione vigente relativa, </span></p><p><span><span>·<span>       </span></span></span><span>Decreto Ministeriale 05 Agosto 2021<span>  </span>“Disciplina sulla formazione degli addetti ai compiti e alle funzioni di cui all&#39;articolo 23, comma 2, del decreto legislativo n. 26/2014, </span></p><p><span><span>·<span>       </span></span></span><span>Decreto Direttoriale 18 Marzo 2022 “Formazione degli addetti ai compiti e alle funzioni di cui all&#39;articolo 23, comma 2, del decreto legislativo n. 26/2014”.</span></p><p></p><p></p><p></p><p><span class="emphasis"><b>Principali responsabilità:</b></span></p><p><span><span>•<span>       </span></span></span><span>Valutare e assicurare lo stato di salute e di benessere degli animali in acclimatamento, in stabulazione, in sperimentazione nonché gli animali sentinella in base ai programmi sperimentali e sanitari pianificati, attraverso l&#39;esecuzione di interventi mirati alla salvaguardia della salute e del benessere degli animali.</span></p><p><span><span>•<span>       </span></span></span><span>Supportare il Veterinario designato per le attività inerenti il monitoraggio microbiologico dello stabilimento utilizzatore e i programmi di medicina preventiva.</span></p><p><span><span>•<span>       </span></span></span><span>Partecipare ai turni di reperibilità veterinaria.</span></p><p><span><span>•<span>       </span></span></span><span>Supportare l&#39;esecuzione delle ispezioni veterinarie da parte delle autorità preposte.</span></p><p><span><span>•<span>       </span></span></span><span>Espletare e supervisionare ed eseguire in maniera adeguata ed in linea con i requisiti di legge e le linee guida internazionali le procedure di eutanasia, i trattamenti terapeutici, anestesiologici ed analgesici degli animali stabulati ed utilizzati presso lo stabilimento utilizzatore.</span></p><p><span><span>•<span>       </span></span></span><span>Supportare il Veterinario Designato nella gestione del programma di reinserimento degli animali laboratorio in accordo al programma di reinserimento aziendale, alle raccomandazioni FELASA, al Decreto Legislativo n. 26 del 04 Marzo 2014 ed al Decreto Ministeriale 31 Dicembre 2021 “</span><span>Individuazione dei requisiti strutturali e gestionali per lo svolgimento delle attività di reinserimento e reintroduzione degli animali utilizzati o destinati a essere utilizzati per fini scientifici</span><span>“.</span></p><p><span><span>•<span>     </span></span>Supportare iI veterinario designato nella gestione delle attività veterinarie di reparto, in particolare delle registrazioni di legge, all’esecuzione delle attività correlate al monitoraggio ed alla supervisione dei progetti di ricerca, alla gestione delle scorte farmaci e medicinali stupefacenti (in qualità di sostituto del responsabile delle scorte), alla stesura di report e procedure richieste, alla revisione dei protocolli sperimentali nonché allo sviluppo, l’implementazione e il mantenimento dei programmi relativi a progetti di 3Rs.</span></p><p><span><span>•<span>       </span></span></span><span>Partecipare all&#39;elaborazione e alla revisione <span> </span>delle procedure aziendali necessarie alla corretta esecuzione delle attività di reparto ed eseguirne l&#39;addestramento.</span></p><p><span><span>•<span>        </span></span></span><span>Supportare il veterinario designato nell&#39;esecuzione di training interni specifici per la manipolazione ed il contenimento degli animali, la somministrazione di farmaci o composti oggetto di studio nei progetti di ricerca R&amp;D e QC, il riconoscimento dei segni clinici di dolore, sofferenza, malattia e distress, l’applicazione di adeguate metodiche di eutanasia, l’applicazione e la revisione del programma di enrichment, l’implementazione delle normative vigenti in materia di salute e benessere degli animali da laboratorio e l’applicazione del principio delle 3Rs.</span></p><p><span><span>•<span>        </span></span></span><span>Assicurare il rispetto delle misure di sicurezza nella propria area di competenza, mettendo a disposizione i DPI stabiliti, nonché rendere edotti i collaboratori dei rischi cui sono soggetti e delle corrette procedure di lavoro.</span></p><p><span><span>•<span>        </span></span></span><span>Fornire supporto veterinario nel contesto dei progetti di ricerca autorizzati dall’Autorità competente ricoprendo le funzioni A, D in accordo all’Art. 23 comma 2 del D. Lgs. 26/2014.</span></p><p><span><span>•<span>        </span></span></span><span>Attuare ed osservare le disposizioni impartite dal datore di lavoro in materia di salute, sicurezza sui luoghi di lavoro ed ambiente nella propria area di competenza, rispettando le norme previste da </span><span>DIgs 81/2008, 152/06 ed EHS&amp;S Standards Corporate.</span></p><p><span><span>•<span>        </span></span></span><span>Indossare correttamente i dispositivi di protezione individuali, le attrezzature di lavoro e segnalare al proprio superiore ogni rischio imprevisto per assumere le azioni opportune.</span></p><p></p><p></p><p></p><p><span class="emphasis"><i><b>Why You?</b></i></span></p><p><span class="emphasis"><b>Basic Qualifications &amp; Skills</b></span></p><p><b>Siamo alla ricerca di persone con le seguenti competenze per raggiungere i nostri obiettivi: </b></p><ul><li><p><span>Laurea Magistrale in Medicina Veterinaria</span></p></li><li><p>Abilitazione all’esercizio della professione di Medico Veterinario</p></li><li><p>Buona conoscenza dei sistemi informatici (pacchetto Office)</p></li><li><p>Buona conoscenza dell&#39;inglese parlato e scritto</p></li></ul><p></p><p></p><p><span class="emphasis"><b>Preferred Qualifications &amp; Skills</b></span></p><p><b>Le seguenti caratteristiche saranno considerate un plus:</b></p><p></p><p>Essere in possesso dell’attestato di formazione per le seguenti funzioni:</p><ul><li>Funzione “A”, personale che esegue procedure su animali da laboratorio in accordo all’Art. 23 comma 2 del D.Lgs. 26/2014: Ruolo e mansione aziendale identificabile con il ruolo di tecnico Animal Experiment (AE) o medico veterinario clinico incluso nel team “3Rs and Veterinary Services”, coinvolto nell’esecuzione di procedure sperimentali su animali da laboratorio nel contesto di progetti di ricerca autorizzati dall’autorità competente.</li><li>Funzione “D”, personale che effettua la soppressione degli animali da laboratorio in accordo all’Art. 23 comma 2 del D.Lgs. 26/2014: mansione aziendale identificabile con il ruolo di tecnico Animal Experiment o medico veterinario membro del team “3Rs and Veterinary Services” che svolge la soppressione degli animali da laboratorio.</li><li>Essere conforme ai requisti di sviluppo professionale continuo inerenti i crediti ECM per la professione di medico veterinario ed i crediti CFP previsti per assolvere le funzioni A, D in accordo all’Art. 23 comma 2 D. Lgs. 26/2014.</li></ul><p></p><p></p><p></p><p></p><p></p><p><span class="emphasis"><i><b>What we offer:</b></i></span></p><ul><li><p>Permanent contract in a very Inclusive environment</p></li><li><p>Flexible Benefits</p></li><li><p>Company Healthcare Plan</p></li><li><p>Integrative pension fund</p></li><li><p>Employee Assistance Programme</p></li><li><p>Prevention services and vaccination clinic</p></li><li><p>Tax assistance</p></li><li><p>Local nursery agreement</p></li><li><p>Postal service, laundry, shoe repair and tailoring</p></li><li><p>On Site Gym</p></li><li><p>On Site canteens and coffee corners</p></li><li><p>Free company bikes and shuttle</p></li></ul><p></p><p></p><p></p><p></p><p><i>Please take a copy of the Job Description, as this will not be available post closure of the advert. </i></p><p><i>When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.</i></p><p></p>&amp;#xa;&amp;#xa;Italian Salary Range / Fascia retributiva in Italia: EUR 34,725 to EUR 57,875 &amp;#xa;&amp;#xa;The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role.&amp;#xa;&amp;#xa;In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process.&amp;#xa;&amp;#xa;This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.&amp;#xa;&amp;#xa;La fascia salariale della Retribuzione Annua Lorda (RAL) per i nuovi assunti in questa posizione è indicata sopra per ciascuna sede applicabile. Queste fasce tengono conto di diversi fattori, tra cui le competenze, l'esperienza, il livello di istruzione del candidato e le condizioni di mercato per il ruolo.&amp;#xa;&amp;#xa;Inoltre, questa posizione potrebbe prevedere un bonus annuale e la partecipazione al nostro programma di incentivazione a lungo termine basato sull’assegnazione azioni, in funzione del livello del ruolo. Informazioni più dettagliate sull’intero pacchetto retributivo e sui benefit saranno fornite durante il processo di selezione.&amp;#xa;&amp;#xa;Questo ruolo è aperto a candidati basati in diversi paesi; per tale motivo sono indicate le fasce retributive relative a ciascun paese. La pubblicazione di tali fasce, per altri paesi, che sono possibili sedi lavorative per questa posizione, risponde a normative locali in materia di trasparenza retributiva, che richiedono l’indicazione delle retribuzioni negli annunci di lavoro. Qualora per una specifica sede o paese non sia indicata una fascia retributiva, le relative condizioni economiche saranno discusse nel corso del processo di selezione.  E’ importante considerare che le retribuzioni variano da paese a paese in base alle competenze, all’esperienza, al livello di istruzione del candidato e alle condizioni di mercato per il ruolo. Le offerte vengono generalmente formulate all’interno della fascia indicata, tenendo conto delle competenze, dell’esperienza e delle qualifiche del candidato; il limite superiore è di norma riservato a candidati con un’esperienza particolarmente consolidata o a circostanze eccezionali coerenti con tali criteri.<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p>Should you require any specific adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on <a target="_blank" href="mailto:ita-inclusion.recruitment&#64;gsk.com"><span style="color:#0000ff"><u>ita-inclusion.recruitment&#64;gsk.com</u></span></a>.</p><p></p><p>Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.</p><p></p><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK&#39;s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><p></p><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/ </u></span></a></p>]]></description><link>http://biotechroles.com/veterinary-services-specialist-3rs-gsk/6a05f4c22f1861929d253195</link><guid isPermaLink="true">http://biotechroles.com/veterinary-services-specialist-3rs-gsk/6a05f4c22f1861929d253195</guid><pubDate>Thu, 14 May 2026 16:13:53 GMT</pubDate><company>GSK</company><location>Italy - Siena</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Global Study Lead]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><span>The Global Study Lead is responsible for ensuring that all studies are designed, planned, executed, monitored, closed out and documented in an appropriate manner within the planned timeframe and cost; ensuring that the sponsor responsibilities are fulfilled, while assuring compliance to all applicable regulatory requirements. Responsible for the timeline and budget planning and execution of studies. Assigns and ensures delivery of specific tasks to/from other members of the study team. Provides oversight to outside support including CROs, consultants and/or medical advisors</span></p><p></p><p><b><b>The Opportunity: </b></b></p><p></p><p><span>The key accountabilities for this position include, but are not limited to:</span></p><ul><li><p><span>Leads the global study team with full accountability for the study deliverables with respect to quality, budget and timelines, in collaboration with the Study Team and ensures the development of high quality study designs for sponsored studies in collaboration with internal and external experts </span></p></li><li><p><span>In collaboration with Program Leadership, prepares different scenarios for evidence generation (e.g. study, real-world evidence) in cross-functional collaboration (e.g. with Regulatory Affairs, R&amp;D, CDMA Project Teams) to support global strategies and planning of timeline and costs</span></p></li><li><p><span>Develops key study documents (i.e., Design Validation Plan, protocol, study training materials, study forms and templates, study report)</span></p></li><li><p><span>Oversees planning and operational aspects of companion diagnostics studies sponsored by Pharma partners</span></p></li><li><p><span>Accountable for study-level budget of assigned studies.</span></p></li><li><p><span>Adherence to regulations, guidelines and standard operating procedures, and ensures audit/inspection readiness.</span></p></li><li><p><span>Execution of sponsored studies for assigned areas of focus for registrational and/or non-registrational purposes through all study phases (planning, start-up. conduct and close-out). Oversees study activities outsourced to a service provider (i.e., CRO). </span></p></li><li><p><span>Ensure that study results are published in collaboration with the Publication Team.</span></p></li><li><p><span>Oversees projects to ensure completion on-time, within scope and budget; and tracks project performance to analyze the completion of short and long term goals. </span></p></li><li><p><span>Build and maintain strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, including CROs, in meeting business goals and ensuring operational excellence. </span></p></li></ul><p></p><p><b><b>Who you are:</b></b></p><p></p><ul><li><p><span>You have a  bachelor&#39;s degree in Life Sciences or related field </span></p></li><li><p><span>You have 5&#43; years of experience managing the full lifecycle of sponsored studies, ensuring projects meet performance goals within scope, quality, budget, and timeline. </span></p></li><li><p><span>You have extensive experience in ensuring that study results are published in collaboration with the Publication Team.</span></p></li><li><p><span>You have in-depth knowledge and experience in the role of Clinical Operations in product development; are aware of Roche’s place in the market and our value proposition to patients and customers.</span></p></li><li><p><span>You have e</span><span>xperience with PHCS and Companion Diagnostic trials, specifically within pathology and core lab indications</span></p></li><li><p><span>You have experience managing complex projects by using analytical judgment and innovative thinking to assess risks and solve difficult problems. </span></p></li><li><p><span>You have prior experience building and  maintaining strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, including Pharma partners or CROs, in meeting business goals and ensuring operational excellence. </span></p></li></ul><p></p><p><b><b>Preferred Qualifications:</b></b></p><ul><li><p><span>You have an advanced degree in Life Sciences or a related field</span></p></li></ul><p><b><span> </span></b></p><p><span>Relocation benefits are not available for this posting  </span></p><p></p><p><span>The expected salary range for this position based on the primary location of Tucson Off Campus is $100,400--186,400.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  </span></p><p></p><p><span>This position also qualifies for the benefits detailed at the link provided below.</span></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p><b> </b></p><p><b> </b></p>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Tucson. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/global-study-lead-roche/6a05f3f42f1861929d253194</link><guid isPermaLink="true">http://biotechroles.com/global-study-lead-roche/6a05f3f42f1861929d253194</guid><pubDate>Thu, 14 May 2026 16:10:28 GMT</pubDate><company>Roche</company><location>Tucson</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Clinical Site Manager]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><span>The Clinical Site Manager is responsible for designing, planning, coordinating and conducting all activities involved in initiating, monitoring, and completing clinical research studies in the clinical study sites and delivering as appropriate other data generation methodologies. Work independently to ensure studies are delivered, recorded and reported in accordance with protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements.</span></p><p></p><p><b><b> The Opportunity:   </b></b></p><p></p><ul><li><p><span>Act as primary contact and clinical trial expert for assigned study site personnel for execution of the study - including training and coordinating certification of study site personnel and providing technical assistance, as necessary.</span></p></li><li><p><span>Perform site assessments/site qualification visits in the site selection decision process.</span></p></li><li><p><span>May participate in and ensure site activation (contracting, IRB/EC/Health Authority approvals are, etc.) are properly obtained, maintained and meet regulatory requirements in collaboration with relevant RDS Functions prior to initiation of the investigational site.</span></p></li><li><p><span>Develop key study site documents (e.g. Study Monitoring Plan, informed consent documents, source documents, patient instruction guides and case report forms, etc.) and contribute technical expertise in the review of study protocols, data management plans, reports and manuscript, etc.</span></p></li><li><p><span>Collaborate cross-functionally with R&amp;D, Field Service, Study Management, Biometrics, etc. to deliver best solutions.</span></p></li><li><p><span>Deliver all data generation/validation and site monitoring activities including end-to-end site visits per relevant regulations and processes.</span></p></li><li><p><span>May participate in the oversight of CRO delivery of Site Management activities, including training of CRO CRAs.  This includes escalation of any issues.</span></p></li><li><p><span>May work with international investigators and key customers as well.</span></p></li><li><p><span>May coach colleagues and help others develop expertise/skills</span></p></li><li><p><span>Accountable for site-level budget of assigned sites</span></p></li><li><p><span>Work independently and is autonomous</span></p></li></ul><p><span> </span></p><p><b><b>Who You Are:  </b></b></p><ul><li><p><span>You have a Bachelor’s degree in a scientific discipline</span></p></li><li><p><span>You have 3 years of experience in a regulated, CRO, diagnostic and or pharmaceutical industry       </span></p></li><li><p><span>You adhere to regulations, guidelines and standard operating procedures, and ensure ongoing audit/inspection readiness.</span></p></li><li><p><span>You have prior experience with clinical trial management and bio-sample (clinical testing) management and quality assurance</span></p></li><li><p><span>You have prior experience validating  product performance claims, supplying data for critical Regulatory submissions, defining the functional and clinical utility of our products, and obtaining the opinions and input regarding our products from laboratories or customers.</span></p></li><li><p><span>You have executed Site Management activities for sponsored studies for assigned areas of focus for registrational and/or non-registrational purposes through all study phases (start-up, conduct and close-out).</span></p></li><li><p><span>You have worked  in local and global study teams, including virtual teams and exhibit diversity and cultural awareness.</span></p></li><li><p><span>You have built and maintained strong, collaborative relationships with cross-functional team members, relevant internal and external stakeholders ,  in meeting business goals and ensuring operational excellence.</span></p></li></ul><p></p><p><b><b>Preferred Experience: </b></b></p><ul><li><p><span>You have experience working in a clinical laboratory environment or clinical lab study</span></p></li><li><p><span>You have experience in In Vitro Diagnostics (IVD) and Clinical Research Associate (CRA) operations.</span></p></li><li><p><span>You have experience with Ultra/Ultra Plus instrumentation and complex data transfer protocols.</span></p></li><li><p><span>You have prior experience within Companion Diagnostics</span></p></li></ul><p></p><p><span>Relocation benefits are not available for this posting  </span></p><p></p><p><span>The expected salary range for this position based on the primary location of Tucson-Off Campus is $79,000-146,800  . Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  </span></p><p></p><p><span>This position also qualifies for the benefits detailed at the link provided below.</span></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/clinical-site-manager-roche/6a05f3f32f1861929d253193</link><guid isPermaLink="true">http://biotechroles.com/clinical-site-manager-roche/6a05f3f32f1861929d253193</guid><pubDate>Thu, 14 May 2026 16:10:27 GMT</pubDate><company>Roche</company><location>Tucson</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Intern – RSS Business Analytics Team]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>The Position</p><p>Intern – RSS Business Analytics Team</p><p></p><p>The Opportunity</p><p>We are looking for a motivated and analytically-minded individual who is passionate about Data Science, Advanced analytics and Data management operations. As an Intern at our Costa Rica hub, you will be responsible for supporting our RSS Business Analytics team in delivering high-impact analytics solutions for Roche affiliates globally</p><p>In this position, you will be focusing on:</p><ul><li><p>Assisting in project execution: Working closely with RSS Business Analytics teams to deliver analytics solutions to real-world business problems.</p></li><li><p>Building Expertise: Gaining hands-on experience with programming languages , querying tools and data management platforms.</p></li><li><p>Data, Analytics, Data Science and AI / ML Exposure: Gaining knowledge of statistical methodologies and supporting various Data Science initiatives across the global network.</p></li><li><p>Stakeholder Communication: Preparing and presenting analytical findings to stakeholders in a structured and effective manner.</p></li></ul><h3>Who you are</h3><ul><li><p>Academic Profile: <b>You are a student currently pursuing a degree in Computer Science, IT, Industrial Engineering, Statistics, Biotechnology, or a related quantitative field</b></p></li><li><p>Analytical Thinker: You have a strong quantitative aptitude and the logical thinking ability required to derive insights from complex data.</p></li><li><p>Basic Tech-Foundation: You have a fundamental working knowledge of Python, SQL, and Excel (this is a significant advantage).</p></li><li><p><b>Effective Communicator: You possess strong verbal and written communication skills in English</b>.</p></li><li><p>Proactive Learner: You are a quick learner, self-motivated, and quality-focused, with an innovative mind and the ability to transition between multiple tasks.</p></li><li><p>Team Player: You enjoy working in a virtual, diverse, and collaborative team environment.</p></li></ul><h3>In exchange, we provide you with:</h3><ul><li><p>Continuous Growth: Unlock your potential through an extensive ecosystem of learning resources. We offer hands-on training with cutting-edge industry tools, empowering you to architect your own unique career path within the health-tech landscape.</p></li><li><p>An Inclusive Global Ecosystem: Join a vibrant, multicultural workplace where diverse perspectives are our greatest strength. Here, we prioritize cross-border collaboration, celebrate our collective wins, and genuinely enjoy the journey as one team.</p></li><li><p>Work with Purpose: Your contributions go far beyond the screen. You will engage in high-stakes projects that translate into tangible, life-saving healthcare advancements for patients and communities across the globe</p></li></ul><p>Who we are</p><p>A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p>Let’s build a healthier future, together.</p><p>Roche is an Equal Opportunity Employer</p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/intern-rss-business-analytics-team-roche/6a05f3f22f1861929d253192</link><guid isPermaLink="true">http://biotechroles.com/intern-rss-business-analytics-team-roche/6a05f3f22f1861929d253192</guid><pubDate>Thu, 14 May 2026 16:10:26 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Technical Support Specialist ( Slovak & Czech language)]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h2></h2><p style="text-align:inherit"></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><span>This role is based in the Regional Customer Support Center which is dedicated to providing excellence while helping laboratory personnel using our products. We operate with a holistic approach, which means that we take care of our product portfolio from the idea through development and market launch to phase-out. The outstanding variety of technologies applied in this area offers you great learning opportunities.</span></p><p></p><p></p><p><span><b>Technical Support Specialist ( Slovak &amp; Czech language)</b></span></p><p></p><p><span><b>Locations:</b> Warsaw, Prague or Bratislava (Your choice!)</span></p><p></p><p><span><b>Are you ready to transition from technical expertise to life-changing impact?</b> Our Regional Customer Support Center (RCSC) is the intellectual engine behind laboratory excellence in Central Europe. We are looking for a <b>Czech and/or Slovak-speaking talent</b> who is hungry for knowledge, enjoys problem-solving, and is ready to master the world’s most advanced diagnostic technologies.</span></p><p></p><p>At Roche, we offer a <b>hybrid work model</b> that combines flexibility with in-person collaboration. For now, we require our employees to be in our offices on average two days per week. The specific office days may vary depending on business needs, such as workshops, conferences, town halls, team meetings, and other collaborative events.</p><p></p><p></p><p><span><b>The Opportunity: </b></span></p><p></p><p><span><b>More Than Just Support</b> This isn&#39;t a typical helpdesk role. This is an engineering and application consultancy position where you become the &#34;guardian&#34; of diagnostic accuracy.</span></p><ul><li><p><span><b>Master the Complexity:</b> You will work with high-end IVD (In-Vitro Diagnostics) systems that combine robotics, complex biochemistry, and advanced IT.</span></p></li><li><p><span><b>Continuous Growth:</b> We provide an intensive, world-class training program. We don’t expect you to know everything on day one, but we expect you to be the one who never stops asking &#34;why?&#34;.</span></p></li><li><p><span><b>Agile Impact:</b> Join a team where your proactivity isn&#39;t just welcomed – it&#39;s required. You will prevent issues before they happen, using digital twins and remote diagnostic tools.</span></p></li></ul><p></p><p></p><p><span><b>Who You Are:</b></span></p><ul><li><p><span><b>Education: </b>You have a degree in Engineering, IT, Biochemistry, Lab Diagnostics or equivalent. More importantly, you have a &#34;detective’s mind&#34; for troubleshooting.</span></p></li><li><p><span><b>Language Power:</b> You are a native or C1/C2 speaker of <b>Czech and/or Slovak</b>. Your <b>English</b> is strong enough to lead you through international trainings and global technical forums.</span></p></li><li><p><span><b>The &#34;Lab-to-Office&#34; Bridge:</b> If you’ve worked in a clinical lab and feel you’ve outgrown your current walls, we want your diagnostic logic. We will teach you the engineering; you bring the passion for science.</span></p></li><li><p><span><b>Resilience &amp; Ambition:</b> You are someone who sees a complex technical error not as a problem, but as a challenge to be conquered.</span></p></li></ul><p></p><p></p><p><span><b>What Roche Offers You:</b></span></p><ul><li><p><span><b>Autonomy:</b> A hybrid work model in Warsaw, Prague, or Bratislava.</span></p></li><li><p><span><b>Unmatched Portfolio:</b> Access to technologies that are setting the standard for the next decade of healthcare.</span></p></li></ul><p></p><p><u>The role is an 18 - month contract via an external agency. </u></p><p></p><p>For the Bratislava location the salary starts from 1 600 EUR gross / month. For the Prague location, the salary starts from 48 300 CZK / month. Final salary depends on the successful candidate&#39;s level of experience, skills and qualifications.</p><p></p><p><b>INTERESED? APPLY! </b></p><p></p><p>If you feel this offer suits a friend of yours, feel free to share it. </p><p></p><p>Want to know what it’s like to be a part of Roche?  Check out our blog!  </p><p><a href="https://diagnostics.roche.com/global/en/careers/roche-careers.html" target="_blank"><u>https://diagnostics.roche.com/global/en/careers/roche-careers.html</u></a></p><p></p><p><i>The controller of your personal data is Roche Diagnostics Polska sp. z o.o., ul. Domaniewska 28, 02-672 Warsaw. The data is processed for the purpose of recruitment. You have the right to access data, rectify it, delete it, limit processing, transfer it and - if processing is based on your consent - withdraw this consent at any time. Contact the Data Protection Officer at: dia.daneosobowe&#64;roche.com. More information on the principles of processing your personal data by Roche at the link: </i><a href="https://www.roche.pl/privacy-policy-recruitment-dia-en" target="_blank"><u>https://www.roche.pl/privacy-policy-recruitment-dia-en</u></a><i>.</i></p><p></p><p><i>Roche Diagnostics sp. z o.o.  operates in full compliance with the law and does not tolerate any violations. Roche Diagnostics sp. z o.o.  has implemented a Procedure for Reporting Violations of Law. If you wish to report any irregularities related to our activities, all necessary information regarding the reporting process can be found on our website: </i><a href="https://www.roche.pl/kontakt/ochrona-sygnalistow-zglaszanie-naruszen" target="_blank"><u>https://www.roche.pl/kontakt/ochrona-sygnalistow-zglaszanie-naruszen</u></a><i>.</i></p><p></p><h3><b>Compensation &amp; Benefits</b></h3>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Warsaw. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><p>Information about the compensation package for this position will be provided ahead of any interview</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/technical-support-specialist-slovak-and-czech-language-roche/6a05f3f12f1861929d253191</link><guid isPermaLink="true">http://biotechroles.com/technical-support-specialist-slovak-and-czech-language-roche/6a05f3f12f1861929d253191</guid><pubDate>Thu, 14 May 2026 16:10:25 GMT</pubDate><company>Roche</company><location>Warsaw</location><salary>$28000-42000</salary><type>Full time</type></item><item><title><![CDATA[Director, Head of Facilities & Engineering]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p>Are you a visionary leader with a passion for transforming facilities operations to support cutting-edge science and patient care? Join Roche Diagnostics as the <b>Director of Facilities &amp; Engineering </b>for our Bay Area sites, where you&#39;ll take charge of shaping the strategic direction and operational excellence of our Pleasanton and Santa Clara campuses. This pivotal role offers the opportunity to oversee large-scale capital projects, optimize site master plans, and drive continuous improvements in reliability, safety, and efficiency. As a key member of the Site Leadership Team, you will inspire and develop a high-performing team, foster a culture of innovation, and ensure our facilities meet the highest standards of compliance and performance—empowering Roche’s mission to deliver extraordinary outcomes for patients around the world.</p><p></p><p>This role is responsible for the strategic leadership of all Facilities &amp; Engineering initiatives across the Bay Area sites (<b>Pleasanton and Santa Clara</b>). This includes directing operations and maintenance, campus master planning, capital investment strategies and execution, asset lifecycle management, and reliability engineering. The Director is ultimately accountable for ensuring facilities operations are compliant, reliable, fiscally responsible and directly support the organization&#39;s overarching business objectives.  This leader inspires and empowers a culture of operational excellence where every employee can achieve extraordinary outcomes for customers and patients every day.</p><p></p><p>The Opportunity</p><p>Responsibilities</p><ul><li><p><span>Oversees the curation and management of the Facilities CAPEX portfolio for Roche Diagnostics Sites in the Bay Area. Directs all facility related capital projects in support of the Facility Master Plan. Capital projects range from 100,000 USD to 100,000,000 USD with the following responsibilities: project scope, cost and schedule development, funding documentation development and presentation to senior management, construction, move coordination and project close-out. May direct capital project planning and execution for sites outside the Bay Area based on need and available resources. </span></p></li><li><p><span>Develops and executes annual and long range strategic Facility Master Plans based on Site Business Plans. Plan development and execution requires interaction across all functional areas of the business and senior management, with strong negotiation skills to solve complex problems affecting nearly all employees at Roche sites. </span></p></li><li><p><span>Direct facility operations and maintenance programs performance measurement, service provider management, and resource planning as well as developing, sharing and adopting technical innovations, life cycle costing models, best practices, KPIs and benchmarking information with the global Facilities community.</span></p></li><li><p><span>Direct engineering services which include life cycle costing, energy conservation, asset management, reliability engineering, performance measurement and resource planning.</span></p></li><li><p><span>Directs and leads efforts to ensure engineering-related policies, procedures, and practices are effective, efficient and consistent. Provides regular, consistent updates on facilities and engineering matters to support ongoing awareness and continuity of business operations.</span></p></li><li><p><span>Interacts at a high level with internal and external resources to ensure the Company is in compliance with local, state, federal, and corporate regulations as well as internal Quality System and regulatory compliance programs.</span></p></li><li><p><span>Develops and is accountable for department and capital budgets, and manages budgets by identifying cost reduction or savings opportunities. Directs budget formulation and adjustment to ensure transparency. Partners closely with other groups and functions to ensure user requests are met in a timely and cost effective manner, maximizing business value of each project and the entire portfolio.</span></p></li><li><p><span>As a member of the Bay Area Site Operations Leadership Team, translates and directs organizational strategy into business goals to lead a customer focused, high performing Facilities &amp; Engineering function. Acts as a leader in the broader Roche Diagnostics Global Sites network, sharing Engineering expertise and guidance with other teams and sites.</span></p></li><li><p><span> Develops leaders throughout the organization and assures the development of all individuals within the organization. This leader serves through transformational leadership roles of Visionary, Architect, Coach and Catalyst (VACC).</span></p></li><li><p><span>Uses analytical tools, strong business relationships, and industry data to anticipate and plan for engineering services and capital investments for the sites.</span></p></li><li><p><span>Other duties as assigned by management.</span></p></li></ul><p><span>​</span></p><p>Who You Are</p><p><span>Requirements:</span></p><ul><li><p><span>12&#43; years facilities/plant management experience,  preferably in a diagnostic, pharmaceutical or  biotechnology industry with 7 years of progressive  management/leadership experience.</span></p></li><li><p><span>Bachelor&#39;s Degree in engineering, architecture, science, technology or related field, or equivalent combination of education and work related experience (&gt;12 years).</span></p></li><li><p><span>Capital Project management experience and/or Plant Engineering, preferably in a diagnostic, pharmaceutical or biotechnology industry </span></p></li><li><p><span>Preferred Skills:</span></p><ul><li><p><span>Master&#39;s Degree in engineering, architecture, or Facilities Mgt.</span></p></li><li><p><span>International Facility Management Association (IFMA) Certified Facility Manager (CFM).</span></p></li></ul></li></ul><p></p><p>This position is not eligible for relocation.</p><p>The expected salary range for this position based on the primary location of California is $180,000 - $334,200 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="http://yourlifeyourrewards.com/" target="_blank"><u>Benefits</u></a> </p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/director-head-of-facilities-and-engineering-roche/6a05f3f12f1861929d253190</link><guid isPermaLink="true">http://biotechroles.com/director-head-of-facilities-and-engineering-roche/6a05f3f12f1861929d253190</guid><pubDate>Thu, 14 May 2026 16:10:25 GMT</pubDate><company>Roche</company><location>Santa Clara</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Production Test Technician (2nd shift)]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</p><p></p><p>A Production Test Technician&#39;s responsibilities include testing of Company products following documented procedures to assure conformance to specifications and standards, completing written records of work done, and identifying and documenting non-conformances in piece parts, assemblies and test results. In addition, a Production Test Technician must be able to effectively troubleshoot routine and unusual test failures to the subassembly level, occasionally consulting with more experienced technicians.</p><p></p><p>A Production Test Technician is expected to assist other technicians in troubleshooting as needed. Responsibilities may also include assembly of Company products, as well as solving problems at test while maintaining take time and production goals. Production Test Technicians may also assist with on-the-job training of other Production Test Technicians.</p><p></p><p><b>The Opportunity</b></p><ul><li><p>Reads and follows assembly drawings, test procedures and other written instructions. Tests assembled instruments for circuit continuity and operational reliability.</p></li><li><p>Strips and crimps wire and assembles into electrical connectors.</p></li><li><p>Identifies defects and non-conforming parts and performs in-process inspections. Recognizes and acts on non-conforming test results.</p></li><li><p>Completes appropriate manufacturing forms accurately, to include fan charts, hour/hour charts.</p></li><li><p>Troubleshoots routine test failures to the sub-assembly level, and component level. Calibrates instruments according to specifications.</p></li><li><p>Analyzes test results and repairs or adjusts instruments according to analysis.</p></li><li><p>Records test results and writes report on fabrication techniques used. Monitors work to ensure quality, and continuously promote Quality First Time.</p></li><li><p>Other duties as assigned by management.</p></li></ul><p></p><p><b>Who You Are</b></p><ul><li><p>You hold an Associate&#39;s Degree in Electronics, Electrical Engineering, or another technical field.</p></li><li><p>You have 3-5 years related experience and/or training; or equivalent combination of education and experience.</p></li></ul><p></p><p><b>Behaviors, competencies, and qualities of the ideal Production Test Technician</b></p><ul><li><p>Read and understand electrical, mechanical, and pneumatic schematics, assembly drawing and work procedures.</p></li><li><p>Use of test equipment; for example, digital voltmeter and precision weight scale.</p></li><li><p>Use of hand tools; for example, screwdrivers, wrenches, nut-drivers and ruler. Accurately recognize non-conforming test results.</p></li><li><p>Communicate the theory of operation for systems under test.</p></li><li><p>Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.</p></li><li><p>Effectively present information and respond to questions from groups of peers, managers, clients and customers.</p></li><li><p>Ability to work with mathematical concepts such as probability and statistical inference. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Ability to compute rate, ratio and percent and to draw and interpret graphs.</p></li></ul><p></p><p>The expected salary range for this position based on the primary location of Marana, AZ is 42,700.00 -<span>  </span>79,300.00 USD Annual . Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p></p><p><b>Are you ready to apply?</b></p><p></p><p><b>Relocation benefits are not available for this position.</b></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/production-test-technician-2nd-shift-roche/6a05f3f02f1861929d25318f</link><guid isPermaLink="true">http://biotechroles.com/production-test-technician-2nd-shift-roche/6a05f3f02f1861929d25318f</guid><pubDate>Thu, 14 May 2026 16:10:24 GMT</pubDate><company>Roche</company><location>Marana</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Invoicing Analyst]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p></p><p>The Invoicing Analyst performs a critical role in completing the final steps in creating manual invoicing. The Invoicing Analyst is responsible for creating and delivering accurate and timely invoices to the customer. The Invoicing Analyst will also issue credit memos and corrected invoices for Roche products and services.</p><p></p><p><u><b>Invoicing Analyst - Position Competencies:</b></u></p><p></p><p><b>Organized and Detail Oriented </b></p><p>- Ability to stay organized, prioritize workflow, be cognizant of deadlines, and attention to the finer details.</p><p><b>Technology Astute </b></p><p>- Ability to utilize technology to efficiently perform all job functions. Proficient in Enterprise Applications, SAP or Oracle preferred Internet savvy and working knowledge of web-based applications.</p><p><b>Communication </b></p><p>- Use clear language to communicate information. Proficient written and verbal communication skills are required.</p><p><b>Mathematical </b></p><p>- Ability to utilize mathematical skills. Perform basic formulas and calculations in MS Excel or Google Sheets.</p><p><b>Order to Cash Process </b></p><p>– Understanding of the Customer Order to Cash Process. Invoicing Analyst.</p><p></p><p></p><p><u><b>Duties and Responsibilities:</b></u></p><p></p><p>- Responsible for creating customer invoices in a timely and accurate manner.</p><p>- Follow up on system-related issues preventing the creation and delivery of customer invoices.</p><p>- Issue corrected invoices and credit memos for customer claims and disputes.</p><p>- When required contact customers and internal stakeholders for missing documentation.</p><p>- Identify third-party system issues, document them, and bring them to the next step for resolution.</p><p>- Invoicing Analysts prioritize workload by analyzing urgency and adhering to invoicing deadlines.</p><p>- Special projects and other duties as assigned.</p><p>- Recommend process improvement to increase dispute and invoicing efficiency.</p><p></p><p><u><b>Invoicing Analyst - Qualifications:</b></u></p><p></p><p>- Three (3) years of experience in invoicing or related function</p><p>- Excellent written and verbal communication skills.</p><p>- SAP experience.</p><p>- Proficient in using Google Office or Microsoft applications.</p><p></p><p><b><u>Pay transparency</u></b></p><p>The expected salary range for this position based on the primary location of Indianapolis is 52,900.00 - 98,200.00 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><i>Benefits</i></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/invoicing-analyst-roche/6a05f3f02f1861929d25318e</link><guid isPermaLink="true">http://biotechroles.com/invoicing-analyst-roche/6a05f3f02f1861929d25318e</guid><pubDate>Thu, 14 May 2026 16:10:24 GMT</pubDate><company>Roche</company><location>Indianapolis</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Technical Expert - eDiscovery]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p>We are seeking a highly skilled Technical Expert, particularly with eDiscovery expertise, to join our Roche Digital Technology (RDT) Group Functions eDiscovery and Forensics team.  In this critical role, you will act as the primary technical bridge between the RDT infrastructure team and the Business Product Owners in Legal and Compliance. </p><p><br />Your primary focus will support the technical aspects of eDiscovery and privacy processes, specializing in Microsoft Purview eDiscovery (Premium) and ensuring the defensible identification, collection, and preservation of electronically stored information (ESI) across a wide range of corporate systems and hardware, with a strong emphasis on Apple mobile ecosystems and mixed-OS laptop environments (macOS and Windows). </p><p></p><p><b>The Opportunity:</b><br />You will act as a subject matter expert, ensuring that all data is acquired in a legally defensible and forensically sound manner and maintaining a strict chain of custody to support litigation, internal investigations, and regulatory requests.  You will also proactively drive and implement prioritized projects that align with business needs. </p><p><br />Description of the area:</p><p>About RDT Group Functions Legal, Compliance &amp; Group Communication sub-Function</p><p></p><p>As a trusted and agile partner, we, as the Legal, Compliance &amp; Group Communication sub-Functions, are empowered to boost global innovative solutions with our business stakeholders in the Legal and Compliance digital prioritization journey.</p><p><br />Job Responsibilities:</p><ul><li>Defensible Data Preservation and Collection: Plan defensible procedures for and execute forensic imaging, end-to-end eDiscovery workflows in Microsoft Purview, and electronic data preservation and collection from company systems and corporate devices, helping to identify, preserve, and retrieve case-critical data globally, specifically focusing on Apple iPhones, iPads, MacBooks, and Windows-based laptops.</li><li>Data Processing: recommend and execute data processing in Relativity and Purview Premium, preparing the data for Legal review by utilizing Boolean searching, culling, and TAR (Technology-Assisted Review) / AI (Artificial Intelligence), preparing productions, and making process and technology recommendations to efficiently and effectively achieve set outcomes. </li><li>Legal Department Support: Act as a trusted IT liaison to internal and external counsel, translating complex technical concepts into clear legal realities and assisting the Legal and Compliance team in scoping preservation and collection efforts based on litigation holds. Develop and maintain trusting relationships with legal stakeholders, IT, and external parties.</li><li>Day-to-Day Operations &amp; Device Management: Handle day-to-day operations by accurately responding to time-sensitive requests. Develop and maintain Standard Operating Procedures (SOPs) for electronic data collections from a wide range of company systems, as well as remote and physical device acquisitions, including the secure storage and retirement of physical evidence.</li><li>Device &amp; Hardware Management: Coordinate the logistics of remote and physical device acquisitions. Manage the intake, secure storage, and return/retirement of physical evidence.</li><li>Chain of Custody &amp; Documentation: Generate and maintain meticulous documentation for all preservation, collection, processing, and production activities, ensuring a verifiable chain of custody and adherence to the Electronic Discovery Reference Model (EDRM). Organize, log, and maintain accurate internal metrics and process flows so they can be repeated with consistency.</li><li>Tool Management: Utilize, update, troubleshoot, and manage the lifecycle of industry-standard forensic and eDiscovery collection tools (e.g., Cellebrite, Druva, EnCase, FTK). Manage the lifecycle of these solutions.</li><li>Process Improvement &amp; Automation Deployment: Continuously evaluate and refine collection workflows to account for new OS updates (iOS, macOS, Windows 11) and emerging security features (e.g., FileVault, BitLocker, MDM profiles). Proactively deploying workflow automation/AI improvements. Contribute to the continuous improvement of legal and compliance data services.</li><li>Stakeholder Trust &amp; Communication: Proactively develop and maintain strong, trusting business relationships with key legal and compliance stakeholders, RDT, and other internal or external partners. Act as a trusted liaison to legal and compliance teams (e.g. eDiscovery and Internal Investigations) by exhibiting exceptional communication skills to translate complex technical concepts into clear legal realities for legal and compliance teams and non-technical stakeholders.</li></ul><p></p><p><b>Who you are:</b><br />(Education &amp; Experiences)</p><ul><li>Education: Bachelor&#39;s degree in Information Technology, Computer Science, or a related field.</li><li>Professional Experience: 5&#43; years of experience in eDiscovery, digital forensics, or specialized IT incident response, preferably within highly regulated industries such as Pharmaceuticals, Healthcare, or Finance.</li><li>Apple Ecosystem Mastery: Proven expertise in collecting ESI from iOS devices (iPhones/iPads) and macOS environments. Deep understanding of Apple’s file systems (APFS), encryption (FileVault), and Mobile Device Management (MDM) interactions.</li><li>Windows Proficiency: Strong working knowledge of Windows 10/11 environments, NTFS, BitLocker encryption, and remote collection methodologies.</li><li>Forensic Tool Competency: Hands-on experience with mobile and computer forensic data collection software (e.g., Cellebrite UFED/Physical Analyzer, Druva, Cellebrite Digital Collector/MacQuisition, EnCase, etc.).</li><li>Regulatory &amp; Legal Acumen: Prior discovery and/or privacy experience with a deep understanding of relevant national and international regulations, including EDRM lifecycle, legal holds, data privacy regulations (e.g., GDPR, CCPA), and the principles of forensic soundness.</li><li>Project &amp; Stakeholder Management: Experience effectively and proactively coordinating multiple functional areas and stakeholders, with the ability to handle multiple priorities and projects simultaneously with a high degree of accuracy and professionalism.</li><li>Soft Skills: Exceptional ability to maintain a positive, constructive attitude in ambiguous situations, manage complexity and high pressure productively, and utilize interpersonal skills to inspire trust with business stakeholders, and communicate highly technical concepts to non-technical stakeholders, particularly legal counsels, forensic experts and HR partners.</li></ul><p><br />Preferred Qualifications:</p><ul><li>Relevant industry certifications: CFCE, CCE, EnCE, CCME, or GIAC Certified Forensic Examiner (GCFE/GCFA). RCA certification (RelativityOne).</li><li>Experience with enterprise eDiscovery platforms (e.g., Purview, Relativity, Exterro).</li><li>Familiarity with cloud data collections (Google Workspace, Microsoft 365, Slack).</li></ul><p><br />Technical Expertise</p><ul><li>Enterprise Platforms &amp; Cloud Data: Deep experience designing, building, and utilizing legally-defensible workflows in enterprise eDiscovery platforms, including  Microsoft Purview (Premium/Advanced) as a primary SME,  and Relativity, alongside familiarity with cloud data preservation collections across Google Workspace and Slack.</li><li>Automation &amp; Scripting: Proficiency in PowerShell for advanced search and reporting, experience with GenAI prompt writing for eDiscovery, Agentic AI, and data modeling.</li><li>Apple Ecosystem Mastery: Proven expertise in collecting ESI from iOS devices (iPhones/iPads) and macOS environments, featuring a deep understanding of Apple’s file systems (APFS), FileVault encryption, and Mobile Device Management (MDM) interactions.</li><li>Windows Proficiency: Strong working knowledge of Windows 10/11 environments, NTFS, BitLocker encryption, and remote collection methodologies.</li><li>Forensic Tool Competency: Hands-on experience with mobile and computer forensic data collection software such as Cellebrite (UFED/Physical Analyzer, Digital Collector/MacQuisition), Druva, EnCase, and FTK.</li><li>Analytical &amp; Agile Mindset: Strong problem-solving skills required to resolve complex technical issues, coupled with an Agile mindset that focuses on &#34;Reuse before Buy before Make&#34; and enabling a diverse group of partners to speak with a single voice.</li></ul><p></p><p>Are you ready to be the driving accelerator behind Roche’s vision for cutting-edge compliance digital solutions to realize desired outcomes for patients ultimately? Join us as we architect the future of Legal and Compliance digital and technology innovation in RDT Group Functions.</p><p></p><p>The expected salary range for this position based on the primary location of Indianapolis, is $107,800 - $200,200. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><b><u>Benefits</u></b></a></p><p></p><p><b>Relocation benefits are not available for this job posting.</b></p><p></p><p>#RDT2026</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/technical-expert-ediscovery-roche/6a05f3ef2f1861929d25318d</link><guid isPermaLink="true">http://biotechroles.com/technical-expert-ediscovery-roche/6a05f3ef2f1861929d25318d</guid><pubDate>Thu, 14 May 2026 16:10:23 GMT</pubDate><company>Roche</company><location>Indianapolis</location><salary>$110000-150000</salary><type>Full time</type></item></channel></rss>