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Analyst, Laboratory Quality Control (1 of 2)

Company: Disability Solutions
Location: Raritan
Posted on: June 1, 2024

Job Description:

Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Analyst, Laboratory 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 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 QC Analyst is responsible for conducting biochemical and/or general testing of raw materials/final product samples submitted to the QC laboratories. Key Responsibilities:

  • Perform testing and maintain a safe work environment in compliance with all applicable procedures, EHS, and GMP regulations
  • Conduct 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 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
  • Complete invalid assay and general laboratory investigation records
  • Support Health Authority inspections
  • Provide input to functional laboratory meetings
  • Other duties will be assigned, as necessary.

Keywords: Disability Solutions, New Brunswick , Analyst, Laboratory Quality Control (1 of 2), Professions , Raritan, New Jersey

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