17 Pharmaceutical Validation Jobs in Bridgewater, NJ
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Associate Director Translational Bioanalytical Sciences (TBS) Insmed Incorporated - Bridgewater, New Jersey , Biochemistry, or another relevant field. Minimum of 8+ years’ post-doctoral experience or equivalent in the pharmaceutical, CRO or related industry within bioanalytical area across various modalities 7 days ago
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Principal Statistical Programmer Katalyst Healthcares & Life Sciences - Bridgewater, New Jersey Responsibilities: Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical 26 days ago
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Validation Specialist - (MES) Manufacturing Execution System TSR Consulting Services, Inc. - Summit, NJ, United States TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading Pharmaceutical company is hiring a MES Validation Specialist. Rate type: W2 only 20 days ago
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Quality Assurance Batch Reviewer the ASSURANCE group - Wharton, NJ, United States relevant experience in validation / batch processing role (regulated Cosmetic or Pharmaceutical industry) Familiar with validation discipline and processes. Familiar with CAPAs, Change Controls, OTC, FDA 19 days ago
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Quality Assurance Equipment/Computer System Validation Specialist II Johnson and Johnson - Raritan, NJ Janssen Pharmaceutical, a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance Equipment/Computer System Validation Specialist II-CAR-T Manufacturing 4 days ago
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Validation Engineer IV - Contractor Katalyst Healthcares & Life Sciences - Hopewell, New Jersey (CSV). Biopharma Process Experience Minimum of 10-15 years' experience in validation (with degree 10+: without 15+), biological quality assurance and/or quality control in an FDA-regulated biotechnology 5 days ago
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Senior Validation Engineer Katalyst Healthcares & Life Sciences - Parsippany, New Jersey in validation (PV, RESUME), specifically within the pharmaceutical sector. Subject matter expert in at least two (2) of the Qualification / Validation subjects specified below Sterile Process Equipment 2 days ago
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Manager, Validation Lead Daiichi Sankyo, Inc. - Bernards, NJ -hand knowledge of GAMP5, GxP and Non-GxP computer system validation and qualification and Computer Software Assurance (CSA), SDLC related to pharmaceutical operations. required - 1 or More Years Direct 17 days ago
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Contract Analytical Research and Development Chemist Lupin Pharmaceuticals Inc. - Somerset, New Jersey , etc. Experience in pharmaceutical Method Development, Method Validation and stability testing. Capable of writing reports suitable for regulatory submission with minimum supervision. Physical 14 days ago
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Scientific - Assistant Scientist TechDigital Corporation - New Brunswick, New Jersey and experience with HCP Elisa, Residual DNA testing, Protein A testing, method development for biologics, and method validation and transfer. Experience working in a quality laboratory for clinical or commercial 18 days ago
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