Exp Anlst Quality Assurance

Johnson & Johnson Johnson & Johnson · Pharma · Gent, East Flanders, Belgium

Johnson & Johnson is seeking a QA Investigations Associate for their CAR-T hub in Ghent, Belgium. The role involves managing deviations, non-conformances, and implementing corrective and preventive actions (CAPAs) to ensure product and process quality in CAR-T manufacturing, adhering to ATMP/GMP requirements.

What you'd actually do

  1. Deviation & CAPA Management: Investigate deviations, non-conformances, and implement corrective and preventive actions (CAPAs) to ensure process integrity and product quality
  2. CAPA Implementation: Identify and implement corrective and preventive actions (CAPAs) to address quality issues from investigations, particularly those affecting product quality and patient safety
  3. Ensure that deviations with potential impact on patients and/or product supply are properly escalated.
  4. Ensure timely QA approval of GMP documentation and provide support in quality review meetings.
  5. Actively support continuous improvement initiatives and lean exercises.

Skills

Required

  • Master’s Degree in a scientific or technical field
  • at least 3 years cross functional experience in the pharmaceutical industry
  • Experience working in Quality Assurance
  • independently and successfully, prioritizing and managing multiple tasks simultaneously
  • proficiently negotiate and communicate with external and internal partners
  • Highly organized and capable of working in a team environment with a positive attitude

Nice to have

  • Experience with aseptic processing and technics
  • Up-to-date knowledge and in-depth understanding of relevant pharmaceutical legislation related to clinical trials and cGMP regulations related to manufacturing of cell therapy products