Director Quality Control

Johnson & Johnson MedTech

Raritan, New Jersey, United States
Base: $150,000.00 - $258,750.00; bonus/equity: eli...
Not specified
Cgmp compliance strategy
Quality control laboratory operations
Analytical and microbiological testing
Johnson & Johnson MedTech is seeking a Director of Quality Control for its CAR-T Manufacturing facility in Raritan, New Jersey. The ideal candidate will have extensive experience in biologics and cell therapy quality control, with a strong focus on leadership and compliance in a laboratory environment

Job Summary

  • The Quality Control Director leads laboratories to deliver testing and release while fostering continuous improvement and customer focus.
  • This role develops and implements cGMP compliance strategies and provides leadership to meet business, quality, and compliance goals.
  • Employees are eligible for comprehensive benefits including retirement plans, long-term incentives, and various paid time off programs.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Director of Quality Control for its CAR-T Manufacturing facility in Raritan, New Jersey. The ideal candidate will have extensive experience in biologics and cell therapy quality control, with a strong focus on leadership and compliance in a laboratory environment.

Salary

Base: $150,000.00 - $258,750.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: Retirement plans, vacation, sick time, parental leave, and other paid time off

Skills & Requirements

Must-have

  • cGMP compliance strategy
  • Quality Control laboratory operations
  • Analytical and microbiological testing
  • Regulatory agency inspection experience
  • Leadership of large QC labs
  • Trackwise and eLIMS experience

Nice-to-have

  • Cross-functional team collaboration
  • Continuous improvement culture
  • Strategic leadership and mentoring
  • Business and budget management
  • Customer focus and organizational excellence

Key Requirements

  • Bachelor’s degree in Science or related field
  • 10 years biologics/cell therapy QC experience
  • 5 years senior management experience
  • Experience hosting global regulatory inspections
  • Up to 10% domestic travel required

Work Rights

Not specified

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