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Featured Employers
Senior Supervisor, Quality Control
Company: Johnson & Johnson
Location: Raritan, NJ
Employment Type: Full Time
Date Posted: 09/04/2021
Expire Date: 11/03/2021
Job Categories: Accounting/Auditing, Biotechnology and Pharmaceutical, Healthcare, Practitioner and Technician, Human Resources, Information Technology, Quality Control, Research & Development, Medical, Environmental, Writing/Authoring
Job Description
Senior Supervisor, Quality Control

Janssen Supply Group, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Supervisor, Quality Control!


At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Janssen Supply Group, LLC is part of the Janssen Pharmaceutical Companies.


Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting opportunity!


The Quality Control Senior Supervisor is responsible for day-to-day Quality Control activities for the New Jersey Stability laboratory, ensuring GMP compliance, accuracy and timeliness of specified testing processes. The QC Senior Supervisor carries out duties in compliance with all local, state, federal, and international regulations and guidelines (including FDA, EPA, DEA, OSHA, etc.) as well as all company and site policies and procedures. They are responsible for carrying out supervisory responsibilities in accordance with the organization’s policies and applicable laws. They will be responsible for interviewing, hiring, training employees, appraising performance, rewarding and disciplining employees, addressing complaints, resolving conflict, and supporting internal and external audits. They will maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations.


Key Responsibilities:

  • Review/approve QC laboratory data for validity and accuracy according to cGMP/cGLP standards as needed
  • Make QC data decisions regarding the compliance of stability test results with established specifications
  • Review data trending, and reporting
  • Reviews/approves laboratory investigations
  • Ensure accuracy and completeness of executed analytical method qualification, validation, and transfer activities
  • Set testing priorities and manage work assignments
  • Train, develop, coach and mentor employees from a technical perspective as well as career development perspective
  • Lead recruitment and make hiring decisions for open QC positions
  • Manage performance of the laboratory staff and take disciplinary action, where required
  • Coordinate the schedules of resources and shift schedules, where required, to ensure efficient coverage for all operational needs
  • Establish performance objectives and development goals for employees



  • Minimum of a Bachelor’s Degree in Biology, Biochemistry, Microbiology, Chemistry or related scientific field is required

Skills & Experience:


  • Minimum six (6) years of relevant work experience
  • Experience in Medical Device, Biopharmaceutical, or Pharmaceutical industry
  • Work experience within a cGMP compliant Quality Control laboratory or equivalent environment
  • Proficiency with Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
  • Excellent written and verbal communication skills


  • Experience leading, coaching, or supervising direct or indirect personnel or teams
  • Knowledge of analytical techniques such as HPLC, GC, UV-Visible spectrophotometer, TOC, FTIR, or pH meters
  • Work experience with electronic Laboratory Inventory Management Systems (eLIMS)
  • Technical writing experience (e.g., SOPs, Work instructions, TMD, Protocol/Validation reports) and the ability to read/interpret technical documents
  • Experience, training or certification with Process Excellence tools and methodologies


  • Requires the physical ability to lift up to 20 lbs, stand or sit for extended periods of time in a laboratory setting, and ability to perform visual inspections of materials (color, appearance, particles, etc.) and to document observations during laboratory testing
  • Requires up to 10% domestic travel


Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location
United States-New Jersey-Raritan-1000 US HIghway 202
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