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Job Function:
QualityJob Sub Function:
Customer/Commercial QualityJob Category:
People LeaderAll Job Posting Locations:
Ciudad Juarez, Chihuahua, MexicoJob Description:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
About Electrophysiology
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
As Johnson & Johnson MedTech Electrophysiology, we have one goal – to ensure those with atrial fibrillation can live the lives they want. For more than 30 years, we’ve been the global market leader in the science and technology of cardiac arrythmia treatment. Our suite of tools means electrophysiologists are empowered to personalize their approaches for patients with effective and reproducible workflows. Together, we’re changing what it means to be diagnosed with atrial fibrillation or other cardiac arrhythmias.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
We are searching for the best talent for COSTUMER QUALITY DIRECTOR for Salvarcar Site, Ciudad Juarez
Purpose:
The Director, Worldwide Customer Quality, will take a leadership role in the administration of all facets of the customer complaint handling process to assure that the Company is providing effective customer service and fulfilling regulatory requirements.
You will be responsible for:
Under limited supervision and in accordance with all applicable federal, state, and local laws/regulations and Johnson & Johnson procedures and guidelines, this position:
Serves as the single point of contact for complaint handling for either the EP/NV.
Manages the daily process and teams responsible for: Opening domestic and international complaint files Assigning complaints Updating complaint databases Tracking investigation status Assisting failure investigations Quality release of serviced and repaired devices (Ethicon only) Customer responses and complaint filing
Provides support to associates preparing and submitting MedWatch and other international reports.
Oversees research and data analysis to respond to information requests related to reportable complaints and submits follow-up reports as required to regulatory agencies.
Implements procedures, training, and systems to support complaint handling for new product launches and lifecycle management.
Owns and leads worldwide complaint intake and investigation processes.
Coordinates all Health Authority interactions related to complaint handling.
Acts as the point of contact during audits and inspections involving complaint handling.
Manages projects related to: New product introductions Business acquisitions Complaint handling integration and representation
Provides analysis of complaint trends to Quality, Operations, and Technical Management.
Provides complaint information to Marketing and R&D to support continuous improvement initiatives.
Utilizes statistical tools to communicate field product quality information.
Trains Sales, Marketing, and Operations personnel on complaint handling requirements.
Executes departmental financial planning and budget tracking.
Develops team members and promotes a Credo-based culture.
Establishes strong partnerships with: Medical Affairs Customer Call Center Quality Operations R&D Professional Education Service Sales Marketing
Participates in strategic planning to improve customer response quality and timeliness.
Communicates business issues and opportunities to senior management.
Ensures team compliance with Health, Safety, and Environmental requirements.
Ensures compliance with all applicable federal, state, local, and company regulations, policies, and procedures.
Performs additional duties as assigned.
Qualifications / Requirements:
Required
BA/BS/BSN in a Scientific, Technical, Engineering, or Nursing field.
Demonstrated leadership capabilities.
Medical Device, Diagnostics, or other regulated healthcare industry experience.
Experience working in multi-site and matrix organizations.
Minimum 7 years of relevant experience.
Prior people leadership/supervisory experience.
Knowledge of statistical applications.
Knowledge of auditing practices.
QSR / ISO knowledge
Product and process knowledge
Quality Systems knowledge
Ability to manage multiple priorities
Confidentiality and discretion
Project management skills
Customer service orientation
Presentation skills
Conflict management
Analytical skills
Basic knowledge of liability law
Basic product-use knowledge
Process Excellence/statistical methodologies
MDR and Vigilance regulations
Regulatory submission practices
Product complaint systems
Auditing and compliance practices
General QA technical knowledge
Customer relations skills
Required Skills:
Preferred Skills:
Compliance Management, Continuous Improvement, Corrective and Preventive Action (CAPA), Developing Others, Fact-Based Decision Making, Give Feedback, Inclusive Leadership, ISO 9001, Leadership, Performance Measurement, Quality Control (QC), Quality Management Systems (QMS), Quality Processes, Quality Standards, Standard Operating Procedure (SOP), Succession PlanningDiscover exciting opportunities in sports technology. Join innovative companies transforming the sports industry through data, media, and cutting-edge tech.
Salary: $65000-110000
🤖 This salary estimate is calculated by AI based on the job title, location, company, and market data. Use this as a guide for salary expectations or negotiations. The actual salary may vary based on your experience, qualifications, and company policies.
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