Specialist Qa

Johnson & Johnson MedTech

Sassenheim, Netherlands
Base: 44,700.00 - 70,840.00; bonus/equity: annual ...
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Quality oversight of manufacturing operations
Gmp documentation and reporting
Aql execution and visual inspection
** Johnson & Johnson MedTech is seeking a Quality Assurance Specialist for their Sassenheim location, responsible for ensuring compliance with quality standards in manufacturing processes related to Lentivirus for CAR-T therapy. The role demands expertise in GMP environments and requires collaboration across various departments. **

Job Summary

  • The QA Specialist acts as a quality expert and ensures quality oversight of our AT products and processes.
  • The Specialist QA works in close collaboration with other local or global departments (Operations, Warehouse, QC, GET, MSAT and other site Quality teams).
  • In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions.

Matching Summary

Match Score: 75

** Johnson & Johnson MedTech is seeking a Quality Assurance Specialist for their Sassenheim location, responsible for ensuring compliance with quality standards in manufacturing processes related to Lentivirus for CAR-T therapy. The role demands expertise in GMP environments and requires collaboration across various departments. **

Salary

Base: 44,700.00 - 70,840.00; Bonus/Equity: annual bonus; Benefits: vacation days, parental leave, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, financial, physical and mental health programs, insurance plans

Skills & Requirements

Must-have

  • Quality oversight of manufacturing operations
  • GMP documentation and reporting
  • AQL execution and visual inspection
  • Review and approval of GMP documentation
  • Support for local or global projects

Nice-to-have

  • Knowledge of aseptic processing techniques
  • Experience in sterile manufacturing
  • Proficiency in English and Dutch

Key Requirements

  • 2-4 years of experience in a GMP regulated environment
  • QA experience is required
  • Experience in AQL / visual inspection
  • Degree in science related subject and /or business-related area

Work Rights

Not specified

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