{"data":[{"id":"6a7c1a6dafca8341b2272410","slug":"junior-web-qa-tester-axolabs","position":"Junior Web QA Tester","company":"Axolabs","location":"London","description":"<p>we’re seeking an ambitious Web QA Tester to join our team. This outstanding opportunity allows you to work closely with our outstanding web product management, engineering, and QA teams to ensure a flawless digital experience for our customers. By carefully performing tests and collaborating with various departments, you will help us maintain our competitive edge in the industry and provide outstanding quality to our clients.</p><p><strong>Key Responsibilities</strong></p><ul><li>Complete manual testing of website features and journeys, including functional, UAT, regression, and end-to-end testing, to ensure changes meet business, functional, and quality requirements.</li><li>Identify, document, and track defects using test management tools (e.g., Jira), providing complete and accurate evidence including steps, encouraged vs. actual results, and severity.</li><li>Develop and maintain test cases, test plans, and regression packs to ensure comprehensive and consistent pre-release validation across sprint cycles.</li><li>Work closely with web product management, engineering, QA, and business analysts to clarify requirements, validate fixes, support UAT, and contribute to release readiness.</li><li>Conduct cross-browser and mobile testing, investigate behavioral or functional issues, and provide input on opportunities for future automation.</li><li>Provide structured support to the L1/L2 web support teams. Validate issues, clarify defects, and supply clear test evidence. This enables rapid and accurate resolution of customer-reported problems.</li><li>Support knowledge transfer activities by identifying recurring support gaps and helping train teams or departments to strengthen platform understanding and reduce repeat issues.</li></ul><p><strong>Skills You'll Use Every Day</strong></p><ul><li>Strong attention to detail with a methodical, analytical approach to problem-solving and clear written and verbal communication.</li><li>Ability to complete structured manual testing, including functional, UAT, regression, and end-to-end testing, with an understanding of Software Development Life Cycle (SDLC) and Software Testing Life Cycle (STLC) principles.</li><li>Proficiency in identifying and reporting defects through tools like Jira, TestRail, or similar platforms.</li><li>Ability to coordinate closely with web product management, engineering, QA, and BA teams to aid in addressing problems and boost the clarity and quality of testing.</li><li>Comfortable performing cross-browser and cross-device validation to identify functional or usability issues.</li><li>Strong organizational abilities with the capacity to adhere to structured procedures, handle competing priorities, and meet sprint-based deadlines.</li><li>Curious, proactive approach with a willingness to learn new tools, techniques, and QA practices.</li></ul>","skills":["Python","R","MATLAB","Data Analysis","Statistical Software","Clinical Research","Molecular Biology","Regulatory Knowledge (FDA, EMA)","Biotech-Specific Software","Laboratory Techniques"],"labels":["Quality Assurance","Junior"],"experience_level":null,"employment_type":null,"salary":"$35000-45000","salaryEstimation":{"min":35000,"max":45000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/LGCGroup/744000142670258-junior-web-qa-tester?oga=true","companyUrl":"https://www.axolabs.com/","url":"https://biotechroles.com/junior-web-qa-tester-axolabs/6a7c1a6dafca8341b2272410","date":"2026-08-12T07:02:05.487Z","createdAt":"2026-08-12T07:02:05.486Z","updatedAt":"2026-08-12T11:12:43.049Z"},{"id":"6a7c1a6cafca8341b227240f","slug":"alliance-and-market-expansion-manager-axolabs","position":"Alliance & Market Expansion Manager","company":"Axolabs","location":"Ballina","description":"<p><strong>Position Summary</strong></p><p>As the Alliance &amp; Market Expansion Manager at LGC, you will be responsible for important strategic partnerships and growing our market presence. This role is highly important and offers the chance to work closely with our largest and most strategic customers. You will concentrate on two areas: strategic sales and engaging with partners' commercial leadership teams, along with managing key accounts at manufacturing and R&amp;D sites across APAC. Your contributions will be critical in converting end-user clinical diagnostics laboratories, network laboratories, and academic institutions, while also selling vital tools. If you bring strong IVD account management experience and knowledge of clinical biochemistry and immunoassay markets, this role suits you well!</p><p><strong>Key responsibilities:</strong></p><ul><li>Manage and achieve sales targets by leading a strategic sales process, accountable for revenue &amp; business unit goals</li><li>Serve as an internal champion for the strategic partner, striving for a great outcome for everyone and building long-term trust</li><li>Network at various levels within targeted client organizations, from C-level executives to laboratory scientists</li><li>Perform sales analysis and build near, mid &amp; long term forecast models</li><li>Define overall strategy with the strategic partner, formulate a road map to capture key new products and opportunities, present proposals, and conduct senior-level negotiations and contract agreements</li><li>Drive business reviews with our strategic customer, present current business performance, growth areas, and key projects, enabling future partnership growth</li><li>Act as the key sales contact for our corporate account, owning key commercial communications and supporting the sales organization as a primary sales resource</li><li>Lead a sales process aimed at delivering effective outcomes, involving cross-functional teams and requiring strong project management</li><li>Communicate customer demand and liaise with internal production on priorities &amp; delivery expectations</li><li>Coordinate product delivery requirements between the customer and production</li><li>Provide input to long-term planning and new product development pipeline and reviews</li><li>Drive international brand awareness, including global roadshows and tradeshows</li><li>Perform other duties as assigned</li></ul><p><strong>Work Conditions</strong></p><ul><li>Travel &amp; Time Expectations: Willing to travel up to 60%, including overnight (both domestically and internationally). This position may require evening or weekend hours in support of business and customer needs.</li><li>Work Setting: Primarily a home-based work environment, dependent on business needs</li></ul>","skills":["Python","R","MATLAB","Statistical analysis","Data analysis","Clinical research","IVD (In Vitro Diagnostics) knowledge","Regulatory knowledge (FDA/EMA)","Sales forecasting","Project management"],"labels":["Manager"],"experience_level":null,"employment_type":null,"salary":"$85000-120000","salaryEstimation":{"min":85000,"max":120000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/LGCGroup/744000142691689-alliance-market-expansion-manager?oga=true","companyUrl":"https://www.axolabs.com/","url":"https://biotechroles.com/alliance-and-market-expansion-manager-axolabs/6a7c1a6cafca8341b227240f","date":"2026-08-12T07:02:04.320Z","createdAt":"2026-08-12T07:02:04.319Z","updatedAt":"2026-08-12T11:12:34.355Z"},{"id":"6a7c1a6bafca8341b227240e","slug":"commercial-application-scientist-axolabs","position":"Commercial Application Scientist","company":"Axolabs","location":"Guildford","description":"<p>The Commercial Application Scientist role at LGC or equivalent experience is exceptionally outstanding, offering the opportunity to blend scientific expertise with strategic sales initiatives in a collaborative and ambitious environment. This position is built to support our revenue and margin goals while improving market development. As a pivotal member of our team, you will collaborate closely with Account Managers, Scientists, Marketing, and other sales professionals to drive our success.</p><p>To perform this job successfully, an individual must be able to perform each of the following essential functions satisfactorily:</p><ul><li>Sales Support: Provides technical sales assistance aimed at achieving the company’s revenue and margin targets. This role engages clients from executive leadership to laboratory teams, identifies appropriate solutions, quantifies their value, assists in proposal development, and plans implementation to drive sales success. The discovery phase and its findings are encouraged to result in specific products and features in the proposed solution. Metrics from this phase should be used to prepare detailed value propositions and demonstrate returns on investments within the proposal. Implementation and project plans are developed in accordance with the client’s operations, facilities, and timelines. You will work alongside Account Managers to coordinate technical methods, resources, and projects throughout the sales cycle.</li><li>Solution Engineering: Identifies, clarifies, and communicates outstanding client requirements to the LGC team. Determines relevant solution options to satisfy client needs. This often involves the identification and testing of a laboratory client’s assays within the framework of the LGC solution. The Application Scientist will lead and manage this process with support from the broader LGC team. When external third-party products or services are necessary, this role conducts evaluations to validate and recommend options. Prepares relevant implementation plans for assigned accounts and briefs service and science personnel on customer requirements before shipment and installations. This effort involves coordination with the Account Manager, Science, Service, and Engineering to ensure solutions align with product plans, schedules, and budgets.</li><li>Maintains a strong understanding of industry trends, laboratory technologies, and scientific applications. Also knows client operations, processes, and competitive offerings. This knowledge helps position LGC products to prospects. Represents LGC effectively at briefings, meetings, and trade events.</li><li>Other Duties as Assigned: Respond flexibly and collaboratively to business needs, both internal and external. Address important corporate initiatives when management requests it.</li><li>Geography: This role focuses primarily on support of customers and sales opportunities throughout Europe, Middle East, and Africa, and other geographies, as needed. To best support LGC’s primary targets for business growth, the ideal candidate must reside in The United Kingdom, Germany, or Denmark.</li></ul>","skills":["Python","R","MATLAB","Molecular Biology","Assay Development","Data Analysis","Statistical Software","Laboratory Techniques","Clinical Research","Regulatory Knowledge (FDA, EMA)"],"labels":["Sales & Commercial"],"experience_level":null,"employment_type":null,"salary":"$75000-110000","salaryEstimation":{"min":75000,"max":110000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/LGCGroup/744000142692565-commercial-application-scientist?oga=true","companyUrl":"https://www.axolabs.com/","url":"https://biotechroles.com/commercial-application-scientist-axolabs/6a7c1a6bafca8341b227240e","date":"2026-08-12T07:02:03.040Z","createdAt":"2026-08-12T07:02:03.039Z","updatedAt":"2026-08-12T11:13:40.985Z"},{"id":"6a7c1a69afca8341b227240b","slug":"manager-quality-assurance-axolabs","position":"Manager, Quality Assurance","company":"Axolabs","location":"Bellshill","description":"<p>The Manager, Quality Assurance, is crucial in leading our dedicated QA team and ensuring every product achieves high standards, customer satisfaction, and regulatory standards. This role is unique by providing an opportunity to operate in a dynamic environment where your contributions have a direct impact on our success and reputation.</p><p>To perform this job successfully, an individual must be able to capably perform each of the following essential duties:</p><ul><li>Oversee, manage, coordinate, lead, and prioritize quality assurance (QA) activities to guarantee adherence to ISO 9001, customer, regulatory, and quality management system (QMS) standards.</li><li>Lead and develop the QA team by defining priorities and arranging daily tasks. Deliver mentoring, training, and performance evaluation. Promote a culture of quality, ownership, conformity, and ongoing progress.</li><li>Coordinate product inspection, batch release, and disposition activities to guarantee products meet established quality, customer, and regulatory standards.</li><li>Coordinate quality system processes such as document control, record management, CAPA’s, deviations, non-conformances, change control, supplier quality, management review, and audits, acting as the site’s Management Representative.</li><li>Direct the establishment, execution, and continual advancement of the QMS by following quality performance statistics and reviewing quality data trends. Coordinate CAPA effectiveness and support quality aims. Explore ways to improve conformity and operational results.</li><li>Direct internal, customer, supplier, and regulatory audit processes, acting as the chief contact for auditors, regulatory authorities, customers, and suppliers; manage audit responses, regulatory inspections, and ensure the swift closure of audit findings, CAPA’s, deviations, and non-conformances.</li><li>Review and approve quality documentation, specifications, protocols, validation packages, technical reports, and quality records to guarantee alignment with internal and external requirements.</li><li>Monitor, examine, and share quality performance metrics and crucial compliance indicators, providing regular updates and recommendations via management review processes.</li><li>Lead continuous advancement projects by reviewing quality metrics, risk analyses, audit findings, customer insights, and operational performance patterns.</li><li>Work closely with Operations, Quality Control, Supply Chain, customers, suppliers, and regulatory bodies to advance business goals, ensure quality standards, and maintain regulatory adherence.</li><li>Provide leadership and subject matter expertise on quality systems, regulatory requirements, auditing, and industry guidelines, maintaining knowledge of ISO 9001, ISO 13485, and applicable FDA regulations.</li><li>Perform other duties as required to support quality, compliance, operational, and business objectives.</li></ul>","skills":["ISO 9001","ISO 13485","FDA regulations","Quality Management System (QMS)","CAPA (Corrective and Preventive Actions)","Auditing","Validation","Document Control","Data Analysis","Regulatory Compliance"],"labels":["Quality Assurance","Quality Assurance","Information Technology","Manager"],"experience_level":null,"employment_type":null,"salary":"$75000-110000","salaryEstimation":{"min":75000,"max":110000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/LGCGroup/744000142800309-manager-quality-assurance?oga=true","companyUrl":"https://www.axolabs.com/","url":"https://biotechroles.com/manager-quality-assurance-axolabs/6a7c1a69afca8341b227240b","date":"2026-08-12T07:02:01.729Z","createdAt":"2026-08-12T07:02:01.729Z","updatedAt":"2026-08-12T11:12:54.667Z"},{"id":"6a7c1a68afca8341b2272409","slug":"key-account-manager-informed-axolabs","position":"Key Account Manager - Informed","company":"Axolabs","location":"London","description":"<p>The Key Account Manager is responsible for the retention, growth, and development of all assigned Informed Supplements accounts including customer on-boarding, relationship development, strategic planning, and overall account ownership.</p>","skills":["Python","R","MATLAB","Data Analysis","Statistical Software","Clinical Research","Regulatory Knowledge (FDA)","Regulatory Knowledge (EMA)","Research Methodologies","Biotech-Specific Software"],"labels":["Sales & Commercial","Sales & Commercial","Manager"],"experience_level":null,"employment_type":null,"salary":"$75000-110000","salaryEstimation":{"min":75000,"max":110000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/LGCGroup/744000142886962-key-account-manager-informed?oga=true","companyUrl":"https://www.axolabs.com/","url":"https://biotechroles.com/key-account-manager-informed-axolabs/6a7c1a68afca8341b2272409","date":"2026-08-12T07:02:00.402Z","createdAt":"2026-08-12T07:02:00.401Z","updatedAt":"2026-08-12T10:34:47.380Z"},{"id":"6a7c1a64afca8341b2272407","slug":"fpanda-manager-facial-allergan-aesthetics-abbvie","position":"FP&A Manager, Facial, Allergan Aesthetics","company":"AbbVie","companySlug":"abbvie","location":"Markham, Markham","description":"<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>The Finance Manager for Facial and S&amp;OP plays a crucial role in providing business support to drive informed decision-making regarding our Facial portfolio and S&amp;OP process. This includes leading each Planning cycle (Plan, LBE, LRP) for full Facial with $21MM annual revenue. Additionally, the position involves managing the S&amp;OP role which is responsible for aligning demand, supply, inventory, and financial plans to support business objectives. This role facilitates cross-functional planning to improve forecast accuracy, service levels, capacity utilization, and decision-making across the organization. Key stakeholders for this role encompass the General Manager, Head of Sales, Head of Marketing, Finance Director, Controller, and Finance Shared Services (FSS).<em> </em></p><p><strong>Responsabilities</strong>:&#xa0;</p><ul><li>Lead the Annual Plan, Periodic Forecast and Long-Range Plan processes for Facial and S&amp;OP portfolio, ensuring that deliverables are reasonably predictive of future results.</li><li>Lead the monthly S&amp;OP process across Sales, Marketing, Supply Chain, Finance, and Operations</li><li>Consolidate demand, supply, inventory, and capacity inputs into an integrated plan</li><li>Analyze forecast trends, gaps, constraints, and risks; recommend corrective actions</li><li>Prepare and present S&amp;OP dashboards, scenarios, and executive summaries</li><li>Facilitate cross-functional meetings and drive consensus on planning decisions</li><li>Monitor key performance indicators such as forecast accuracy, service level, inventory health, and supply performance</li><li>Maintain planning data integrity and ensure timely updates in planning systems</li><li>Identify process improvements to enhance planning cadence, transparency, and alignment</li><li>Operate independently to prepare and communicate Facial and S&amp;OP financial and operational performance trends</li><li>Collaborate with Sales and Marketing teams to align strategic initiatives such as consumer activation (BD), marketing campaign with financial planning and optimizing decision-making processes.</li><li>Lead Sales and full P&amp;L modelling for new products launches and/or initiatives, set up internal control processes in accordance with Corporate financial policies and procedures. (e.g. Elite consumable revenue recognition and fraud monitoring, support Harmonica launch).</li><li>Partner with key stakeholders to develop and execute continual process improvements to allow for routine analytical reviews of financial and operational performance on supported areas, leveraging business analytical resources and tools.</li><li>Work directly with the commercial team, RTR team and Accounting Shared Service on monthly close process and financial reporting to ensure complete, accurate and timely monthly actual results, including variance analysis and provide monthly commentary to WEC Region.</li></ul>","skills":["Data Analysis","Statistical Software","Forecasting","Financial Modeling","S&OP (Sales and Operations Planning)","Cross-Functional Collaboration","Regulatory Knowledge (FDA)","Clinical Research","Inventory Management","Supply Chain Management"],"labels":["Manager"],"experience_level":null,"employment_type":null,"salary":"$120000-160000","salaryEstimation":{"min":120000,"max":160000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014526746-fp-a-manager-facial-allergan-aesthetics-?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/fpanda-manager-facial-allergan-aesthetics-abbvie/6a7c1a64afca8341b2272407","date":"2026-08-12T07:01:56.252Z","createdAt":"2026-08-12T07:01:56.251Z","updatedAt":"2026-08-12T11:12:29.729Z"},{"id":"6a7c1a63afca8341b2272406","slug":"senior-manager-market-research-rheumatology-abbvie","position":"Senior Manager, Market Research - Rheumatology","company":"AbbVie","companySlug":"abbvie","location":"Mettawa, Mettawa","description":"<p>The Senior Manager, Market Research -&#xa0;Rheumatology&#xa0;will design, implement, manage, analyze, and effectively communicate market research initiatives across the Rheumatology Portfolio supporting the Rheumatology HCP and Consumer Teams. The individual will derive high-impact learnings from qualitative and quantitative primary and secondary research and partner with Brand partners and external agencies to inform strategic and tactical decision-making. The ability to influence decisions based upon careful and strategic thinking and understanding of the business is critical to success.</p><p><strong>KEY RESPONSIBILITIES:</strong></p><ul><li>Act as a market research lead for the Rheumatology Marketing team, focused on providing strategic insights, forming a trusted relationship, and staying abreast of market dynamics and burgeoning trends within the space.</li><li>Be conversant with custom research methods, adept at supplier and stakeholder management, and able to independently lead custom research projects that deliver compelling and actionable learnings.</li><li>Perform thought-provoking and sophisticated syntheses of learnings across Insights, Analytics, and Competitive Intelligence to develop actionable recommendations that shape strategies and tactics.</li><li>Maintain organizational knowledge of the market, competitive trends, and industry developments and effectively communicate this knowledge to internal stakeholders.</li><li>Build relationships as a team player, while maintaining objectivity and lack of bias to represent the voice of the patient.&#xa0;</li><li>Demonstrate thoughtful confidence in presentation of learnings across different levels of the organization.</li><li>Appropriately manage and collaborate with research suppliers.</li><li>Monitor and manage research programs within budget and identify opportunities for cost savings where appropriate.</li><li>Ensure all activities are conducted in accordance with financial and ethical compliance guidelines.</li></ul>","skills":["Market Research","Qualitative Research","Quantitative Research","Data Analysis","Statistical Analysis","Competitive Intelligence","Stakeholder Management","Supplier Management","Clinical Research","Regulatory Compliance (FDA/EMA)"],"labels":["Research & Development","Marketing","Senior","Manager"],"experience_level":null,"employment_type":null,"salary":"$150000-200000","salaryEstimation":{"min":150000,"max":200000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014528732-senior-manager-market-research-rheumatology?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/senior-manager-market-research-rheumatology-abbvie/6a7c1a63afca8341b2272406","date":"2026-08-12T07:01:55.271Z","createdAt":"2026-08-12T07:01:55.270Z","updatedAt":"2026-08-12T11:53:25.857Z"},{"id":"6a7c1a62afca8341b2272405","slug":"associate-director-field-training-multiple-myeloma-abbvie","position":"Associate Director, Field Training - Multiple Myeloma","company":"AbbVie","companySlug":"abbvie","location":"Mettawa, Mettawa","description":"<p>The Associate Director of Oncology Training is responsible for the team developing and delivering the sales franchise curriculum for AbbVie&#xa0;US customer facing teams. This person will lead the development and delivery of the annual training strategy that aligns to our brand marketing strategic imperatives. This person will lead and work within cross functional teams&#xa0;made of participants from Training, Medical/ Clinical experts, Marketing, Sales Management, Medical, Regulatory, Legal,&#xa0;Market Access, other AbbVie Groups, and external vendor partners. They must be confident in and comfortable with cross functional&#xa0;team structure and adept at collaboration /influence management. This person will have fiscal responsibility for multiple budgets. This leader will be responsible for the development of their direct reports, by ensuring a customized onboarding plan is developed and followed. This person will work closely with cross functional partners and training leadership to create an engaging, high performing culture. Position will also require person to provide training&#xa0;design / development support. Leads and manages initiative and program design efforts involving external and internal&#xa0;organizations.</p><p>This person must also:</p><ul><li>Effectively represent the Field Training leadership team</li><li>Build and lead a team of highly effective trainers that build curriculum that fosters development of AbbVie Leadership Attributes and advances selling capabilities to drive performance within assigned sales franchises.</li><li>Be adept at using and applying artificial intelligence, adaptive learning and experiential training approaches</li><li>Develop and implement a proactive approach to measuring the impact of learning. Utilize data to inform updates in curriculum and to design future learning approaches</li><li>Interact with and influence all levels of line management to plan, design and develop learning strategies that will contribute to the achievement of related business objectives for assigned sales franchises.</li><li>Demonstrates a passion for driving excellence, with a focus on performance results that fosters accountability within self, direct reports, the Field Training department, commercial stakeholders, nurse ambassadors and training participants.</li><li>Leading / Driving the training strategy process, including analysis, design, development, implementation, and evaluation of performance focused training curricula to continuously improve the capabilities of the US Sales Organization.</li><li>Developing the franchise training team through effective coaching and leadership for success in current trainer role and for future commercial leadership opportunities.</li><li>Building effective relationships to work collaboratively with Senior Commercial Management, Cross-functional partners, Marketing, T&amp;D and other groups leading AbbVie learning initiatives, to drive performance through consistent development and delivery of effective commercial training.</li></ul>","skills":["FDA Regulatory Knowledge","EMA Regulatory Knowledge","Clinical Research","Molecular Biology","Data Analysis","Statistical Software","Python","R","MATLAB","Bioinformatics Tools"],"labels":["Legal & IP","Director","Artificial Intelligence","Associate"],"experience_level":null,"employment_type":null,"salary":"$160000-220000","salaryEstimation":{"min":160000,"max":220000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014529066-associate-director-field-training-multiple-myeloma?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/associate-director-field-training-multiple-myeloma-abbvie/6a7c1a62afca8341b2272405","date":"2026-08-12T07:01:54.118Z","createdAt":"2026-08-12T07:01:54.117Z","updatedAt":"2026-08-12T11:12:33.893Z"},{"id":"6a7c1a60afca8341b2272403","slug":"sr.-business-intelligence-specialist-abbvie","position":"Sr. Business Intelligence Specialist","company":"AbbVie","companySlug":"abbvie","location":"Seoul, Seoul","description":"<p><strong>Position: </strong>Sr. Business Intelligence Specialist<br>\n<strong>Reports to:</strong> Customer Excellence Director, Korea<br>\n<strong>Location:</strong> Seoul, South Korea<br>\n&#xa0;</p><p><strong>PRIMARY FUNCTION/OBJECTIVE</strong><br>\nResult oriented Business Analyst with a solid background in data analysis, including experience extracting&#xa0;<br>\nand manipulating data for data analysis, producing digestible business intelligence and actionable&#xa0;<br>\ninformation. Works with key business stakeholders to understand requirements and shape analytical&#xa0;<br>\ndeliverables.</p><p><br>\n<strong>CORE JOB RESPONSIBILITIES</strong></p><p>Followings with direct responsibilities and/or by collaborating SFE/MCM specialists.</p><ul><li>Works on data sets and complex data warehouse environments being able to integrate them&#xa0;effectively.</li><li>Designs, develops, and maintenance of scalable/automated/user-friendly systems to support&#xa0;ongoing metrics, reports, analyses, dashboards, etc. which drive key business decisions.</li><li>Uses problem solving skills and rapid development approach to deliver actionable output.</li><li>Builds stable, scalable, cost-effective solutions to extract data from diverse systems and&#xa0;transform extremely large datasets into actionable business information, including visualization&#xa0;tools to present the business information in an intuitive way, diagnosing and fixing complex data&#xa0;integrity problems and reducing or eliminating operational overhead.</li><li>Collaborates across the business and finance organizations to develop best practices for the&#xa0;function and advocate for improvements.</li><li>Prepare and implement analytics of ACE model in collaboration with SFE/MCM, in-field&#xa0;commercial and medical functions.</li><li>Enhance WWD capability by integrating external data and in-house data to provide business&#xa0;decision based on customer segmentations.</li><li>Establish daily WWD operation and culture with cost-effective, customer-centric, value&#xa0;propositioning way.</li><li>Lead the direction towards harmonized way of working and operation model across business&#xa0;intelligence and sales force effectiveness.</li></ul>","skills":["Python","R","MATLAB","Data Analysis","Statistical Software","Data Visualization","Data Warehousing","Business Intelligence","Sales Force Effectiveness (SFE)","Customer Segmentation Analytics"],"labels":["Senior","Specialist"],"experience_level":null,"employment_type":null,"salary":"$75000-110000","salaryEstimation":{"min":75000,"max":110000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014529776-sr-business-intelligence-specialist?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/sr.-business-intelligence-specialist-abbvie/6a7c1a60afca8341b2272403","date":"2026-08-12T07:01:52.897Z","createdAt":"2026-08-12T07:01:52.896Z","updatedAt":"2026-08-12T11:12:32.205Z"},{"id":"6a7c1a5fafca8341b2272400","slug":"sr.-ra-specialist-abbvie","position":"Sr. RA Specialist","company":"AbbVie","companySlug":"abbvie","location":"Seoul, Seoul","description":"<p><strong>Position: </strong>Sr. RA Specialist<br>\n<strong>Reports to:</strong> Regulatory Affairs Manager<br>\n<strong>Location:</strong> Seoul, South Korea</p><p><strong>PRIMARY FUNCTION/OBJECTIVE</strong></p><p>To manage the preparation of regulatory submissions of company products in order to obtain the necessary regulatory approvals and to provide regulatory input on regulatory matters to company personnel.</p><p><strong>CORE JOB RESPONSIBILITIES</strong></p><ul><li>Developing RA strategies - assess timeline and lead development of regulatory strategy for new assets and line extensions based on the regulatory requirements as well as reflecting cross-functional team considerations. Support RA manager in developing regulatory strategies.</li><li>Identifying and resolving regulatory issues and challenges that may arise during the product development, registration, or post-market phases</li><li>Collaborating with cross-functional teams, such as R&amp;D, Quality Assurance, and Marketing, to gather necessary information and support regulatory affairs activities.</li><li>Participating in problem-solving discussions and providing input on regulatory matters to support decision-making processes.</li><li>Set up timelines on managing variations in accordance with strategy</li><li>Reviewing and evaluating product labeling, packaging, and promotional materials to ensure compliance with regulatory requirements.</li><li>Conducting research on regulatory requirements and staying updated on changes in regulations and guidelines as Subject Matter Experts</li><li>Evaluation of impact, implementation plan on the marketed products (hurdle, current situation) risk management, problem solving</li><li>Product discontinuation/withdrawal/Marketing Authorization Transfer /co-promotion/co-marketing strategy reflecting feedback from internal stakeholders and global strategy</li><li>Conducting thorough reviews of contract terms and conditions to identify any regulatory implications or requirements that need to be addressed.</li></ul>","skills":["Regulatory Affairs","FDA Regulations","EMA Regulations","Clinical Research","Regulatory Submissions","Risk Management","Data Analysis","Python","R","MATLAB"],"labels":["Senior","Specialist"],"experience_level":null,"employment_type":null,"salary":"$65000-95000","salaryEstimation":{"min":65000,"max":95000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014529916-sr-ra-specialist?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/sr.-ra-specialist-abbvie/6a7c1a5fafca8341b2272400","date":"2026-08-12T07:01:51.718Z","createdAt":"2026-08-12T07:01:51.717Z","updatedAt":"2026-08-12T11:15:15.268Z"},{"id":"6a7c1a5eafca8341b22723fe","slug":"praktikum-im-bereich-technical-operations-operational-excellence-abbvie","position":"Praktikum im Bereich Technical Operations/ Operational Excellence","company":"AbbVie","companySlug":"abbvie","location":"Ludwigshafen, Ludwigshafen","description":"<p>Du möchtest während deines Praktikums die Abläufe in einer pharmazeutischen Produktion kennenlernen und dabei aktiv an der Optimierung von Prozessen mitwirken? Dann werde Teil unseres <strong>TechCenter- und Operational-Excellence-Teams</strong> am Standort Ludwigshafen.</p><p>Gemeinsam unterstützen wir die Herstellprozesse bestehender und neuer Produkte – mit besonderem Fokus auf <strong>feste Arzneiformen, Schmelzextrusion sowie das Packaging von Medizin- und Kombinationsprodukten</strong>. Dabei erhältst du spannende Einblicke in die pharmazeutische Produktion und kannst dein theoretisches Wissen direkt in der Praxis anwenden.</p><p><strong>Das lernst du bei uns</strong></p><ul><li><p>Du erhältst Einblicke in die Abläufe einer modernen pharmazeutischen Produktion und lernst verschiedene Produktions- und Geschäftsprozesse kennen.</p></li><li><p>Du unterstützt unsere Teams bei der <strong>Optimierung und Weiterentwicklung von Prozessen</strong> im Bereich Technical Operations und Operational Excellence.</p></li><li><p>Du sammelst praktische Erfahrungen in der <strong>Erfassung, Aufbereitung und Auswertung von Produktionsdaten</strong>.</p></li><li><p>Du lernst, wie <strong>Technikums- und Produktionsversuche</strong> vorbereitet, dokumentiert und ausgewertet werden.</p></li><li><p>Du bekommst Einblicke in die <strong>statistische Auswertung von Versuchs- und Prozessdaten</strong> und kannst diese selbstständig anwenden.</p></li><li><p>Du unterstützt bei der Erstellung und Weiterentwicklung von <strong>Schulungsunterlagen und digitalen Trainingsformaten</strong>.</p></li><li><p>Du erstellst Protokolle und unterstützt bei der Dokumentation von Versuchen, Projekten und Business-Prozessen.</p></li><li><p>Du arbeitest mit modernen digitalen Tools und erhältst die Möglichkeit, deine Kenntnisse in <strong>PowerPoint, SharePoint und Power BI</strong> weiterzuentwickeln.</p></li><li><p>Du unterstützt das Team im Tagesgeschäft und erhältst dabei einen umfassenden Einblick in die Zusammenarbeit verschiedener Funktionen innerhalb der pharmazeutischen Produktion.</p></li></ul><p>&#xa0;</p>","skills":["Python","R","MATLAB","Statistical Data Analysis","Data Analysis","Power BI","SharePoint","Process Optimization","Pharmaceutical Manufacturing","Documentation"],"labels":["Operations"],"experience_level":null,"employment_type":null,"salary":"$2000-3000","salaryEstimation":{"min":1800,"max":2500,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014530466-praktikum-im-bereich-technical-operations-operational-excellence?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/praktikum-im-bereich-technical-operations-operational-excellence-abbvie/6a7c1a5eafca8341b22723fe","date":"2026-08-12T07:01:50.400Z","createdAt":"2026-08-12T07:01:50.399Z","updatedAt":"2026-08-12T10:35:32.186Z"},{"id":"6a7c1a5cafca8341b22723f7","slug":"head-of-search-and-evaluation-external-innovation-china-abbvie","position":"Head of Search & Evaluation, External Innovation, China","company":"AbbVie","companySlug":"abbvie","location":"Shanghai, Shanghai","description":"<p>AbbVie’s Search &amp; Evaluation group is responsible for sourcing external innovation from the global innovation ecosystem, to supplement the on-market portfolio and innovative R&amp;D pipeline with strategically-aligned assets. The main focus for the Head of Search &amp; Evaluation, External Innovation, China, will be the sourcing of innovative assets and platforms supporting AbbVie’s ambitions on the global stage across key therapeutic areas including immunology, neuroscience, oncology, obesity, and other growth TAs. The S&amp;E group leads the scientific/technical assessment of partnering opportunities and coordinates all scientific/technical due diligence. The S&amp;E group works in close collaboration with AbbVie’s Business Development &amp; Acquisitions team and Transactions Legal. The scope of activities encompasses all types of assets (platforms, individual drug candidates, pipelines, and acquisition targets), all types of transactions (licenses, option agreements, R&amp;D collaborations, acquisitions), and all stages in development (discovery- to commercial-stage).</p><p>Responsibilities:<em>&#xa0;</em></p><p><em>The </em>Head of Search &amp; Evaluation, External Innovation, China<em> will </em></p><p>•Lead an S&amp;E team and proactively search for, identify, and evaluate potential partnering opportunities from biopharma companies, academic institutions, other non-profit research institutes, and life science venture capital investors in China.</p><p>•Lead the scientific/technical assessment of partnering opportunities, in close dialogue with the S&amp;E Therapeutic Area leads from the Global team, BD&amp;A colleagues, as well as subject matter experts from R&amp;D and other functional areas. This includes (1) managing interactions with external parties, (2) project management in the context of the assessment and deal process, (3) overseeing and actively contributing to the scientific/technical as well as overall evaluation process, (4) developing recommendations and proposals for senior management and governance committees.</p><p>•Coordinate or contribute to the conduct and completion of all scientific/technical due diligence activities, including the preparation and presentation of due diligence reports and management presentations.</p><p>•Track and communicate the status of active assessments and deal processes, including (1) information of key internal stakeholders on a timely basis (2) delivery of oral and written progress updates for executive-level audiences, and (3) timely capturing of interactions, events, correspondence and information materials in AbbVie’s information management systems.</p><p>•Network with existing and potential future partners from the innovation ecosystem in China, to ensure awareness of AbbVie’s strategic priorities for partnering and key capabilities as a partner to entities from China, BD objectives.</p><p>•Support to affiliate-level or global initiatives that foster the dialogue with potential partners from China, such as AbbVie-branded partnering days, local and regional partnering events.</p><p>•Collaborate as needed with AbbVie Ventures, for the sourcing and scientific/technical assessment of equity investment opportunities.&#xa0;</p><p>•Contribute towards the negotiation of non-binding term sheets and definitive agreements, including coordination and integration of all scientific/technical inputs (e.g., R&amp;D work plans, Clinical Development Plans, technical success criteria) into legal documents, and development of appropriate deal structures, risk mitigation and negotiating strategies to help ensure alignment with AbbVie’s TA objectives and functional management.</p><p>•Facilitate creation of institutional memory for opportunities by providing clear, concise assessments and recommendations for future reference. Fully leverage new and existing external and internal opportunity management tools to support the operations of the growing S&amp;E group as it relates to tracking incoming opportunities.</p><p>•This role will manage and mentor an S&amp;E team to fulfill the above responsibilities across therapeutic areas.</p>","skills":["Python","R","MATLAB","Clinical Research","Molecular Biology","Data Analysis","Statistical Software","FDA Regulations","EMA Regulations","Due Diligence"],"labels":["Head of"],"experience_level":null,"employment_type":null,"salary":"$180000-280000","salaryEstimation":{"min":180000,"max":280000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014531041-head-of-search-evaluation-external-innovation-china?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/head-of-search-and-evaluation-external-innovation-china-abbvie/6a7c1a5cafca8341b22723f7","date":"2026-08-12T07:01:48.825Z","createdAt":"2026-08-12T07:01:48.824Z","updatedAt":"2026-08-12T10:37:03.720Z"},{"id":"6a7c1a5bafca8341b22723f5","slug":"engineer-technology-ii-platform-and-full-stack-engineering-(all-genders)-(vollzeit-unbefristet)-abbvie","position":"Engineer Technology II – Platform & Full Stack Engineering (all genders) (Vollzeit, unbefristet)","company":"AbbVie","companySlug":"abbvie","location":"Ludwigshafen, Ludwigshafen","description":"<p>Herzlich willkommen bei AbbVie! Als Teil eines internationalen Unternehmens mit ca. 57.000 Mitarbeitern weltweit und rund 3.500 Mitarbeitern in Deutschland hast Du die Möglichkeit, eng mit uns zusammenzuarbeiten, um die gesundheitlichen Herausforderungen von morgen zu meistern. Du hast eine Leidenschaft für die Verbesserung der Gesundheitsversorgung auf der ganzen Welt? Du möchtest Dein Fachwissen einsetzen, um die Lebensqualität von Patienten zu verbessern? In einem herausfordernden Arbeitsumfeld, das Dir die Möglichkeit bietet, Deine eigenen Fähigkeiten zu erweitern und zu entwickeln? Dann bist Du bei uns richtig!</p><p>Stell dein Know-how unter Beweis und werde Teil unseres Teams am Standort Ludwigshafen als<strong> Engineer Technology II – Platform &amp; Full Stack Engineering (all genders)</strong></p><p><strong>Konkret bedeutet das:</strong></p><ul><li>Entwicklung, Implementierung und Betrieb robuster CI/CD-Pipelines und automatisierter Workflows unter Sicherstellung zuverlässiger und reproduzierbarer Prozesse für Software-Build, Integration, Testing und Deployment</li><li>Entwicklung und Pflege skalierbarer, modularer und testbarer Full-Stack-Lösungen, einschließlich Backend-Services und Frontend-Komponenten, unter Anwendung geeigneter Testverfahren</li><li>Integration und Standardisierung von Toolchains über den gesamten Software Development Lifecycle (SDLC) hinweg, einschließlich Versionsverwaltung, Build-Automatisierung, Artefaktmanagement und Security Scanning</li><li>Überwachung, Analyse und Optimierung der Performance von Pipelines und Anwendungen mithilfe von Observability-Funktionen</li><li>Verankerung und Durchsetzung von Sicherheits-, Compliance- und Qualitätskontrollen im Einklang mit unternehmensweiten und regulatorischen Anforderungen</li><li>Mitwirkung an Architektur- und technischen Designentscheidungen unter Anwendung bewährter DevOps-, Containerisierungs- und Infrastructure-as-Code-(IaC)-Praktiken</li><li>Unterstützung bei der Einführung von Governance-, Nachverfolgbarkeits- und Validierungspraktiken für KI-gestützte Softwareentwicklung in einem regulierten Umfeld</li></ul>","skills":["Python","R","MATLAB","CI/CD Pipelines","DevOps","Containerization","Infrastructure as Code","Full Stack Development","Data Analysis","Regulatory Compliance (FDA/EMA)"],"labels":["Information Technology"],"experience_level":null,"employment_type":null,"salary":"$85000-115000","salaryEstimation":{"min":85000,"max":115000,"currency":"USD","confidence":0.51},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014531215-engineer-technology-ii-platform-full-stack-engineering-all-genders-vollzeit-unbefristet-?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/engineer-technology-ii-platform-and-full-stack-engineering-(all-genders)-(vollzeit-unbefristet)-abbvie/6a7c1a5bafca8341b22723f5","date":"2026-08-12T07:01:47.573Z","createdAt":"2026-08-12T07:01:47.572Z","updatedAt":"2026-08-12T11:18:11.584Z"},{"id":"6a7c1a5aafca8341b22723f4","slug":"engineer-technology-ii-platform-and-full-stack-engineering-(all-genders)-(fulltime-regular)-abbvie","position":"Engineer Technology II – Platform & Full Stack Engineering (all genders) (fulltime, regular)","company":"AbbVie","companySlug":"abbvie","location":"Ludwigshafen, Ludwigshafen","description":"<p>Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place!</p><p><strong>Together, we break through</strong> – as <strong>Engineer Technology II – Platform &amp; Full Stack Engineering (all genders)</strong></p><p><strong>Make your mark:</strong></p><ul><li>Design, implement, and operate robust CI/CD pipelines and automated workflows, ensuring reliable and repeatable software build, integration, testing, and deployment processes</li><li>Develop and maintain scalable, modular, and testable full-stack solutions, including backend services and frontend components, using appropriate testing practices</li><li>Integrate and standardize toolchains across the SDLC including version control, build automation, artifact management, and security scanning</li><li>Monitor, analyze, and optimize pipeline and application performance with observability capabilities</li><li>Embed and enforce security, compliance, and quality controls aligned with enterprise and regulatory requirements</li><li>Contribute to architecture and technical design decisions, while applying DevOps, containerization, and infrastructure as code (IaC) best practices</li><li>Support implementation of governance, traceability, and validation practices for AI-assisted software development in a regulated environment</li><li>Produce and maintain technical documentation</li></ul>","skills":["Python","R","MATLAB","FDA regulations","EMA regulations","Clinical research","Molecular biology","Data analysis","Statistical software","DevOps"],"labels":[],"experience_level":null,"employment_type":null,"salary":"$75000-110000","salaryEstimation":{"min":75000,"max":110000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014531255-engineer-technology-ii-platform-full-stack-engineering-all-genders-fulltime-regular-?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/engineer-technology-ii-platform-and-full-stack-engineering-(all-genders)-(fulltime-regular)-abbvie/6a7c1a5aafca8341b22723f4","date":"2026-08-12T07:01:46.490Z","createdAt":"2026-08-12T07:01:46.488Z","updatedAt":"2026-08-12T11:12:34.882Z"},{"id":"6a7c1a59afca8341b22723f2","slug":"brand-manager-(oncology)-abbvie","position":"Brand Manager (Oncology)","company":"AbbVie","companySlug":"abbvie","location":"Maidenhead, Maidenhead","description":"<p>We are excited to recruit for a brand manager to join the Oncology team in order to support delivery of our Limitless ambitions.</p><p>The successful candidate will join an energetic, ambitious and agile team and work within a supportive environment which also offers opportunity for personal skills and career development.</p><p>The Brand Manager role will be based in our offices in Maidenhead and will own end-to-end marketing deliverables/projects to support the delivery of our ambition through focussed execution of our business priorities.</p><p><strong>Strategic planning &amp; execution</strong></p><ul><li>Campaign design and execution aligned to strategic priorities</li><li>Ensure clear measurement frameworks are in place to assess campaign execution and optimise accordingly</li><li>Key contributions to strategic and tactical plan development</li></ul><p><strong>Excellence in Execution</strong></p><ul><li>Ensure high quality content is co-created with key stakeholders to ensure high impact</li><li>Prioritise being ‘brilliant at the basics’ – embracing our systems and processes to ensure efficient ways of working and maximum impact</li><li>Identify opportunities to enhance our ways of working as a Oncology team and take accountability for making aligned changes</li></ul><p><strong>Stakeholder management</strong></p><ul><li>As part of a highly cross functional organisation, ensure relationships are fostered both internally and externally to deliver alignment and support for key initiatives.</li><li>This includes local, regional, global and external stakeholders (healthcare professionals, pharma service providers etc).</li></ul><p><strong>OmniChannel Transformation</strong></p><ul><li>Accelerate AbbVie’s journey towards omnichannel excellence to deliver the highest quality customer engagement within the industry</li><li>This includes support evolving ways of working across the UK affiliate</li><li>Support on the planning and execution of customer journeys, ensuring optimal impact and agility in optimising performance of campaigns</li></ul><p><strong>Maximising impact whilst ensuring the highest standards</strong></p><ul><li>Support the ongoing culture of compliance to the ABPI code and internal ways of working, whilst leveraging knowledge and experience of working with such frameworks to maximise the customer experience and impact of campaigns.</li></ul>","skills":["Python","R","MATLAB","Statistical Software","Data Analysis","Clinical Research","Regulatory Knowledge (FDA, EMA)","Molecular Biology","Biotech-specific Software","Research Methodologies"],"labels":["Marketing","Manager"],"experience_level":null,"employment_type":null,"salary":"$110000-150000","salaryEstimation":{"min":110000,"max":150000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014531453-brand-manager-oncology-?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/brand-manager-(oncology)-abbvie/6a7c1a59afca8341b22723f2","date":"2026-08-12T07:01:45.404Z","createdAt":"2026-08-12T07:01:45.403Z","updatedAt":"2026-08-12T11:59:36.497Z"},{"id":"6a7c1a58afca8341b22723f0","slug":"scientist-i-labormitarbeiter-analytical-development-(all-genders)-vollzeit-24m-befristet-abbvie","position":"Scientist I - Labormitarbeiter - Analytical Development (all genders) – Vollzeit 24M befristet","company":"AbbVie","companySlug":"abbvie","location":"Ludwigshafen, Ludwigshafen","description":"<p>Entfalte dein Potenzial – werde Teil unseres Laborteams bei PDS&amp;T DPA!<br>\n<br>\nFür den Bereich Product Development Science and Technology, Drug Product Analytical (PDS&amp;T DPA) suchen wir eine engagierte und analytisch versierte Persönlichkeit als Labormitarbeiter (all genders). Du wirkst als Teil der Laborteams aktiv mit bei der Entwicklung, Validierung, dem Transfer und der Etablierung verschiedenster physikalisch-chemischer Analysemethoden zur Prozessentwicklung und bewertest eigenständig die erhobenen Analysedaten.Dich erwartet eine zunächst auf 24 Monate befristete Anstellung in einem dynamischen Umfeld, das exzellente Forschung und praktische Anwendung vereint.<br>\n<br>\n<strong>Was Du bei uns bewegen könntest</strong></p><ul><li>Tauche ein in die spannende Welt der Analytik biologischer Arzneimittel und plane und führe eigenverantwortlich Tests durch für die Entwicklung, Etablierung, Validierung und den Transfer physikalisch-chemischer Methoden zur Qualitätskontrolleinheit.</li><li>Beurteile die Eignung bestehender Methoden, optimiere innovative elektrophoretische und chromatographische Methoden unter Einsatz der CDS Empower-Software.</li><li>Wende analytische Methoden, wie HPLC und CE sowie gängige Arzneibuchmethoden (pH, Farbbestimmung, Proteingehalt sowie nicht-sichtbare Partikel) im Rahmen der Prozessentwicklung an.</li><li>Bereite aussagekräftige Laborberichte in englischer Sprache vor, die u.a. als essenzielle Quelldokumente für Behördeneinreichungen dienen.</li><li>Engagiere dich aktiv in wissenschaftlichen und Digitalisierungs-Initiativen im engen Austausch mit internationalen Teams, insbesondere aus Europa und den USA, voran.</li></ul>","skills":["HPLC","Capillary Electrophoresis (CE)","Empower CDS Software","Physicochemical Analysis","Method Validation","Method Transfer","Quality Control","Data Analysis","Laboratory Reporting","Regulatory Submissions"],"labels":["Information Technology"],"experience_level":null,"employment_type":null,"salary":"$55000-75000","salaryEstimation":{"min":55000,"max":75000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014531581-scientist-i-labormitarbeiter-analytical-development-all-genders-vollzeit-24m-befristet?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/scientist-i-labormitarbeiter-analytical-development-(all-genders)-vollzeit-24m-befristet-abbvie/6a7c1a58afca8341b22723f0","date":"2026-08-12T07:01:44.149Z","createdAt":"2026-08-12T07:01:44.148Z","updatedAt":"2026-08-12T07:40:07.235Z"},{"id":"6a7c1a56afca8341b22723ef","slug":"scientist-i-laboratory-staff-analytical-development-(all-genders)-full-time-24-month-fixed-term-contract-abbvie","position":"Scientist I - Laboratory Staff - Analytical Development (all genders) – Full-time, 24-month fixed-term contract","company":"AbbVie","companySlug":"abbvie","location":"Ludwigshafen, Ludwigshafen","description":"<p>Unleash your potential — become part of our laboratory team at PDS&amp;T DPA!</p><p>For the Product Development Science and Technology, Drug Product Analytical (PDS&amp;T DPA) department, we are looking for a committed and analytically minded individual as a <strong>Laboratory Employee (all genders)</strong>. As part of the laboratory team, you will actively contribute to the development, validation, transfer, and establishment of a wide range of physicochemical analytical methods for process development and independently evaluate the analytical data collected. You can expect an initial 24-month fixed-term position in a dynamic environment that combines excellent research with practical application.</p><p><strong>What you could contribute here</strong></p><ul><li>Immerse yourself in the exciting world of biologics analytics and independently plan and carry out tests for the development, establishment, validation, and transfer of physicochemical methods for the quality control unit.</li><li>Assess the suitability of existing methods and optimize innovative electrophoretic and chromatographic methods using CDS Empower software.</li><li>Apply analytical methods such as HPLC and CE, as well as common pharmacopoeial methods (pH, color determination, protein content, and subvisible particles) as part of process development.</li><li>Prepare meaningful laboratory reports in English, which also serve as essential source documents for regulatory submissions.</li><li>Actively contribute to scientific and digitalization initiatives in close exchange with international teams, especially from Europe and the USA.</li></ul>","skills":["HPLC","Capillary Electrophoresis (CE)","CDS Empower Software","Physicochemical Analytical Methods","Method Validation","Method Transfer","Pharmacopoeial Methods (USP/EP)","Data Analysis","Regulatory Submissions (FDA/EMA)","Laboratory Reporting (English)"],"labels":["Legal & IP","Full-Time","Contract"],"experience_level":null,"employment_type":null,"salary":"$65000-90000","salaryEstimation":{"min":65000,"max":90000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014531715-scientist-i-laboratory-staff-analytical-development-all-genders-full-time-24-month-fixed-term-contract?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/scientist-i-laboratory-staff-analytical-development-(all-genders)-full-time-24-month-fixed-term-contract-abbvie/6a7c1a56afca8341b22723ef","date":"2026-08-12T07:01:42.807Z","createdAt":"2026-08-12T07:01:42.806Z","updatedAt":"2026-08-12T11:59:45.901Z"},{"id":"6a7c1a55afca8341b22723ed","slug":"account-specialist-anti-infectives-orlando-fl-abbvie","position":"Account Specialist, Anti Infectives - Orlando, FL","company":"AbbVie","companySlug":"abbvie","location":"Orlando, US-Virtual Office","description":"<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><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><strong>Responsibilities:</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.</li><li>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>","skills":["Python","R","MATLAB","Data Analysis","Statistical Software","Clinical Research","Regulatory Knowledge (FDA, EMA)","Molecular Biology","Research Methodologies","Biotech-Specific Software"],"labels":["Specialist"],"experience_level":null,"employment_type":null,"salary":"$75000-110000","salaryEstimation":{"min":75000,"max":110000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014533726-account-specialist-anti-infectives-orlando-fl?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/account-specialist-anti-infectives-orlando-fl-abbvie/6a7c1a55afca8341b22723ed","date":"2026-08-12T07:01:41.712Z","createdAt":"2026-08-12T07:01:41.710Z","updatedAt":"2026-08-12T08:00:17.882Z"},{"id":"6a7c1a54afca8341b22723ec","slug":"senior-manager-eqms-technologies-abbvie","position":"Senior Manager, eQMS Technologies","company":"AbbVie","companySlug":"abbvie","location":"North Chicago, North Chicago","description":"<p><strong>Purpose&#xa0;</strong></p><p>The Senior Manager –&#xa0;eQMS&#xa0;(electronic Quality Management System) Technologies&#xa0;is responsible for&#xa0;enabling data-driven quality and compliance decisions across&#xa0;the&#xa0;enterprise&#xa0;by developing&#xa0;and&#xa0;deploying&#xa0;advanced&#xa0;analytics,&#xa0;AI-enabled insights, and measurement solutions. This role&#xa0;partners&#xa0;with&#xa0;Quality, Business Technology Services (BTS), and process owners to define and execute&#xa0;the&#xa0;quality data strategy, improve data quality and accessibility, and deliver dashboards, metrics, and advanced analytics/AI&#xa0;that support continuous improvement,&#xa0;and global regulatory compliance. The position helps ensure effective quality insights and services are in place across R&amp;D to support&#xa0;more informed decision&#xa0;making, and&#xa0;proactive risk management&#xa0;in accordance with&#xa0;applicable policies, processes, procedures, and global regulatory requirements.&#xa0;</p><p><strong>Responsibilities&#xa0;</strong></p><ul><li>Support the development&#xa0;and execution&#xa0;of&#xa0;quality analytics and AI roadmaps&#xa0;aligned with RDQA, R&amp;D, and Enterprise Quality priorities.&#xa0;</li><li>Build and&#xa0;maintain&#xa0;automated reporting, dashboards, and KPI frameworks to&#xa0;monitor&#xa0;quality&#xa0;processes&#xa0;and&#xa0;eQMS&#xa0;health, performance, and compliance.&#xa0;</li><li>Develop advanced analytics and AI capabilities (e.g., trend, anomaly, and predictive risk signals) to&#xa0;identify&#xa0;quality and compliance risks earlier.&#xa0;</li><li>Partner with process owners and BTS to translate business needs into analytics requirements, data products, and insight-driven actions.&#xa0;</li><li>Establish data definitions, quality controls, and governance for key quality datasets and metrics.&#xa0;</li><li>Enable self-service use of dashboards and insights through training, playbooks, and documentation.&#xa0;</li><li>Review and approve&#xa0;SLC&#xa0;documentation to support compliant use of data and models in regulated environments.&#xa0;</li><li>Assess&#xa0;the&#xa0;adoption, impact, and performance of analytics solutions; apply feedback, statistical methods, root cause analysis, and data storytelling to drive continuous improvement.&#xa0;</li></ul>","skills":["Python","R","MATLAB","Statistical analysis","Data analysis","Predictive analytics","Machine learning","Data visualization","eQMS (electronic Quality Management System)","FDA regulations"],"labels":["Senior","Manager"],"experience_level":null,"employment_type":null,"salary":"$130000-170000","salaryEstimation":{"min":130000,"max":170000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014534236-senior-manager-eqms-technologies?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/senior-manager-eqms-technologies-abbvie/6a7c1a54afca8341b22723ec","date":"2026-08-12T07:01:40.503Z","createdAt":"2026-08-12T07:01:40.501Z","updatedAt":"2026-08-12T11:59:32.642Z"},{"id":"6a7c1a53afca8341b22723ea","slug":"medical-manager-nz-abbvie","position":"Medical Manager, NZ","company":"AbbVie","companySlug":"abbvie","location":"Wellington, Wellington","description":"<p>Are you a scientifically driven medical professional ready to help shape the future of healthcare in New Zealand? AbbVie is seeking an experienced, dynamic Medical Manager&#xa0;to lead specific therapeutic area strategy, drive evidence generation, and champion meaningful patient outcomes; all at the intersection of science, innovation, and real-world impact. If you're passionate about translating cutting-edge clinical insights into action while building influential relationships with New Zealand's leading clinicians and researchers, this is your opportunity to make a difference that matters.</p><p><strong>KEY DUTIES AND RESPONSIBILITIES</strong></p><ul><li>Maintain current knowledge of disease state, treatment paradigms,&#xa0;therapy aligned products,&#xa0;patient&#xa0;experience, and healthcare system factors.&#xa0;&#xa0;</li><li>Interpret emerging evidence and clinical data to inform decisions and scientific exchange.&#xa0;</li><li>Provide scientific input to cross-functional teams.&#xa0;</li><li>Develop medical plans informed by evidence, insights, priorities, and external trends.&#xa0;</li><li>Partner with key stakeholders to ensure aligned execution.&#xa0;</li><li>Anticipate scientific and system shifts and incorporate them into planning.&#xa0;</li><li>Represent Medical in brand, launch, and lifecycle forums&#xa0;</li><li>Plan&#xa0;and execute therapy area medical&#xa0;budget&#xa0;in line with AbbVie&#xa0;financial planning processes ensuring alignment with&#xa0;medical strategy.&#xa0;</li><li>Lead&#xa0;insight&#xa0;generation including those from&#xa0;field teams, external stakeholders&#xa0;and&#xa0;clinical trends&#xa0;using digital tools where&#xa0;appropriate.&#xa0;Translating&#xa0;insights into actionable recommendations&#xa0;and for the business.&#xa0;</li><li>Identify&#xa0;evidence&#xa0;gaps affecting care, access, and adoption.&#xa0;</li><li>Support&#xa0;and/or lead&#xa0;local evidence initiatives, including RWE, IIS, registries, and Phase IV studies&#xa0;aimed at closing evidence and access gaps.&#xa0;</li><li>Interpret evidence and communicate implications clearly.&#xa0;</li><li>Incorporate patient insights and lived experience into planning.&#xa0;</li><li>Engage with patient organisations to understand unmet needs and barriers to care.&#xa0;</li><li>Support initiatives that improve patient understanding, treatment pathways, and quality of care.&#xa0;</li><li>Help teams understand the patient journey and factors influencing treatment decisions&#xa0;</li><li>Build&#xa0;professional&#xa0;relationships with clinicians, researchers, investigators, societies, and professional organisations.&#xa0;</li><li>Plan and&#xa0;execute&#xa0;medical&#xa0;advisory boards&#xa0;and&#xa0;round&#xa0;tables.&#xa0;</li><li>Deliver scientific presentations and medical education programs to healthcare professionals individually or in&#xa0;groups (meetings, clinical sessions, etc.), where&#xa0;appropriate.&#xa0;</li><li>Ensure scientific exchange is balanced, transparent, and compliant with internal and external standards.&#xa0;</li><li>Support scientific elements of access, reimbursement, and policy initiatives.&#xa0;</li><li>Review promotional and non-promotional materials for accuracy, balance, fairness, and compliance.&#xa0;</li><li>Partner with Therapy Area Specialists to ensure consistent scientific communication.&#xa0;</li><li>Support approval processes, documentation, and medical accuracy across channels.&#xa0;</li><li>Demonstrate integrity and sound scientific judgement in all outputs.&#xa0;</li><li>Develop and drive&#xa0;the medical&#xa0;omnichannel&#xa0;strategy&#xa0;&#xa0;</li><li>Use&#xa0;the Content Authoring Tool (eWizard) to support omnichannel activities, including Customer Experience Flows or Journeys in the execution of medical strategy.&#xa0;</li><li>Use dashboards, analytics tools, and medical systems to support&#xa0;and improve&#xa0;strategy and insights&#xa0;generation.&#xa0;</li><li>Stay current on digital health trends, AI, and relevant technologies.&#xa0;</li><li>Develop&#xa0;eWizard&#xa0;materials and digital content to support scientific exchange.&#xa0;&#xa0;</li><li>Report any adverse event within 24 hours as per AbbVie’s policies and procedures.&#xa0;</li><li>Proactively participate in&#xa0;AbbVie’s&#xa0;WHS programs, adhere to policies and&#xa0;promote a safe work environment at all times.&#xa0;</li><li>Adhere to&#xa0;AbbVie’s&#xa0;internal codes of conduct and compliance processes.&#xa0;</li><li>Other ad hoc duties&#xa0;such as administrative duties, as requested.</li></ul>","skills":["Clinical Research","Data Analysis","Regulatory Knowledge (FDA/EMA)","Molecular Biology","Python","R","Real-World Evidence (RWE)","Statistical Software","Biostatistics","Omnichannel Digital Tools (eWizard)"],"labels":["Manager"],"experience_level":null,"employment_type":null,"salary":"$120000-160000","salaryEstimation":{"min":120000,"max":160000,"currency":"USD","confidence":1},"applyUrl":"https://jobs.smartrecruiters.com/AbbVie/3743990014534406-medical-manager-nz?oga=true","companyUrl":"https://abbvie.com/","url":"https://biotechroles.com/medical-manager-nz-abbvie/6a7c1a53afca8341b22723ea","date":"2026-08-12T07:01:39.243Z","createdAt":"2026-08-12T07:01:39.242Z","updatedAt":"2026-08-12T07:16:46.926Z"}],"pagination":{"page":1,"limit":20,"total":26312,"pages":1316}}