Johnson & Johnson

QA release associate

Ghent

October 11, 2024

QA Release Associate at Johnson & Johnson (Ghent, Belgium)
Are you ready to make a meaningful impact in the fight against cancer? Join our team at Johnson & Johnson to support the innovative CAR-T program in Europe!
About Us: At Johnson & Johnson, we are dedicated to harnessing the power of the human immune system to create groundbreaking therapies that aim to eliminate cancer cells. As part of our commitment to excellence in healthcare, we have established two state-of-the-art CAR-T manufacturing facilities in Ghent, Belgium.
The Role: We are currently seeking a QA Release Associate to join our Quality Assurance (QA) team. In this pivotal role, you will ensure that product and process-related investigations, complaints, and batch record reviews are executed accurately and in compliance with ATMP/GMP requirements.
Key Responsibilities:
  • Review batch documentation and analytical results.
  • Conduct in-depth investigations with a focus on technical, quality, and compliance expertise.
  • Timely investigation and escalation of deviations/complaints that may impact patients or product supply.
  • Define adequate CAPAs for quality-impacting investigations.
  • Support the preparation and follow-up of inspections and audits.
  • Participate in quality oversight programs and document GMP approvals.
  • Foster effective working relationships with business partners and Legend Biotech.
  • Manage and implement various quality system processes.
  • Provide coaching and training to operational and QA departments.


Qualifications
- What We’re Looking For:
  • Certified Industrial Pharmacist with a minimum of 2 years of experience in the pharmaceutical industry, preferably in a Quality department.
  • Strong knowledge of pharmaceutical legislation, c GMP regulations, and Good Tissue Practices.
  • Exceptional analytical thinking and decision-making skills.
  • Excellent verbal and written communication abilities.
  • Experience with quality systems and aseptic processing techniques is preferred.
  • Highly organized, motivated, and adaptable, with a team-oriented mindset.
Flexibility Matters: We value flexibility in our work environment. While there may be occasions where weekend shifts (6 AM - 6 PM) are required, we appreciate your adaptability as schedules may shift to day shifts based on operational needs.
Join Us! If you are passionate about quality assurance and eager to contribute to innovative cancer therapies, we want to hear from you! Apply now to be part of our mission at Johnson & Johnson.
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