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Position summary
Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Analyst, Quality Control - CAR-T in Raritan, NJ !
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies.
Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR-T platform and investigational treatment.
Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting opportunity!
The Senior QC Analyst is responsible for conducting biochemical, microbiological, and/or general testing of raw materials/final product samples submitted to the QC laboratories. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
They typically work with a team of 5 – 15 other Analysts within the functional laboratory of the Quality Control department.
Key Responsibilities:
- Perform analytical testing and maintain a safe work environment in compliance with all applicable procedures, EHS, and GMP regulations
- Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories
- Work with Process Development team, Quality, and Operations organization to successfully transfer process/analytical testing to cGMP facility to manufacture products.
- Perform peer review of laboratory data and logbooks.
- Utilize electronic systems (LIMS, iLAB) for execution and documentation of testing
- Build, review, and approve relevant QC documents, SOP’s, and WI’s
- Train new laboratory personnel
- Complete invalid assay and general laboratory investigation records, CAPAs, change controls
- Support Health Authority inspections
- Provide input to functional laboratory meetings
What are Johnson & Johnson perks and benefits
Child care benefits
Paid maternity
Unpaid maternity
Paid paternity
Unpaid paternity
Paid adoptive
Short term disability
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