Johnson & Johnson

QA Lab associate

Ghent

October 11, 2024

QA Lab Associate for CAR-T Hub at Johnson & Johnson
Are you ready to make a difference in the fight against cancer? The Advanced Therapy Quality team at Johnson & Johnson Innovative Medicine is searching for a passionate QA Lab Associate to join our CAR-T hub in Europe. This role can be based in either Beerse or Ghent, Belgium, and will involve a weekend shift (6 AM - 6 PM) .
About Us: At Johnson & Johnson, we are pioneering cutting-edge therapies that leverage the power of the human immune system to combat cancer. CAR-T (Chimeric Antigen Receptor T-cell Therapy) represents a groundbreaking approach, utilizing patients’ own T cells to specifically target and eliminate cancer cells.
Why Join Us? By joining our QA Lab organization, you will play a crucial role in delivering life-saving therapies to patients. Your work will directly impact the quality and safety of CAR-T products.
Key Responsibilities:
  • Provide compliance oversight for QC laboratories including microbiology and biotechnology, ensuring accurate review of laboratory investigations and trends in quality data.
  • Oversee Lab instrument qualification and support the drafting and approval of standard operating procedures.
  • Conduct spot-checks in QC Labs to ensure adherence to regulations, policies, and global procedures.
  • Thoroughly investigate non-conformances and ensure timely implementation of corrective and preventive actions.
  • Proactively drive compliance to reduce non-conformances in supported areas.
  • Support investigations and reports, interpreting results and making technical conclusions to manage risk effectively.
  • Recognize patterns and trends in reported data, and communicate insights to management.
  • Offer guidance on quality issues and participate in developing technical initiatives.
  • Independently interpret complex results and articulate recommendations for solutions, identifying risks and developing contingency plans.
  • Champion continuous improvement in quality processes.


Qualifications
Education:
  • Qualifications:
  • Education: Minimum of a Master’s Degree in Engineering, Science, or a related technical field.
  • Experience: At least 2 years of experience in Quality Assurance within a GMP environment.
  • Preferred experience in microbiological testing methods, biotechnology methods (such as flow cytometry, q PCR, ELISA), and cell culture.
Flexibility is Key: The training period will take place during day shifts on weekdays, transitioning to weekend shifts (6 AM - 6 PM) to support our operational needs.
What We Offer: At Johnson & Johnson, we are committed to the health and well-being of our employees. We offer robust programs and policies that promote the physical, mental, emotional, and financial health of our workforce.
Join Us! Don’t miss the chance to be part of a mission that changes lives. If you are excited about contributing to innovative cancer therapies and meet the qualifications, we encourage you to apply!
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