• Manufacturing Team Lead, CAR-T

    Bristol Myers Squibb (Summit, NJ)
    …in a manner consistent with site safety policies, quality systems, and GMP requirements. + Works in a team-based, cross-functional environment to complete production ... purification, and aseptic processing or lab technique + Knowledge of cGMP/ FDA regulated industry + Basic mathematical skills + General understanding of… more
    Bristol Myers Squibb (08/25/25)
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  • Clinical Manufacturing Associate

    Bristol Myers Squibb (Warren, NJ)
    …purification, and aseptic processing or lab technique + General knowledge of cGMP/ FDA regulated industry + Basic mathematical skills + General understanding of cGMPs ... education and experience is required + 2 - 5 years of relevant GMP manufacturing experience. On the floor experience which demonstrates proficiency and compliant… more
    Bristol Myers Squibb (08/24/25)
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  • Quality Associate

    Actalent (Basking Ridge, NJ)
    …regulations and process requirements. The Quality Associate must understand GMP and come from generic pharmaceutical, following SOPs diligently. Responsibilities ... and management. + Ability to take and follow directions. + Familiarity with FDA Labeling guidelines (21 CFR). + Excellent communication and organizational skills. +… more
    Actalent (08/19/25)
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  • Scientist, Analytical R&D

    Amneal Pharmaceuticals (Piscataway, NJ)
    …support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. + Develops and optimizes new ... + Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance. more
    Amneal Pharmaceuticals (08/19/25)
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  • Manager, CQV Portfolio Delivery

    Bristol Myers Squibb (Warren, NJ)
    …or Science related discipline. + Minimum of 5 years of experience in FDA -regulated industry (validation preferred), or 3 years and an advanced degree. A combination ... and pulling. + Primarily office environment but will be required to enter laboratory or GMP process areas donning proper gowning / lab coats or PPE such as safety… more
    Bristol Myers Squibb (08/17/25)
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  • Production Team Member

    Papa John's International (Cranbury, NJ)
    …at proper cooling temperature(s). + Maintain and document Good Manufacturing Practice ( GMP ) standards on cleanliness and sanitation to insure product is free of ... Sanitation and HACCP policies & procedures, federal, state and local regulations (OSHA, FDA , DOL) and all Papa John's International, Inc., policies & procedures. +… more
    Papa John's International (08/12/25)
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  • Specialist, QA Shop Floor

    Bristol Myers Squibb (Summit, NJ)
    …meetings with Subject Matter Experts (SMEs). + Conduct routine walkthroughs of GMP areas and communicate findings to area owners and Quality Management. + ... to support manufacturing. + Must have sound knowledge and experience in FDA -regulated cGMP manufacturing operations and processes. + Must be action-oriented and… more
    Bristol Myers Squibb (08/10/25)
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  • Associate Director, Technical Solutions

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …Expert-level proficiency in ISO 13485, Medical Device Regulation (MDR), and FDA requirements with demonstrated ability to convert complex regulatory guidelines into ... maintenance, with comprehensive understanding of international standards including ISO frameworks, GMP /GDP protocols, and USP-EP guidelines as they apply to medical… more
    BD (Becton, Dickinson and Company) (08/08/25)
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  • Associate Director Quality Assurance Compliance,…

    BeOne Medicines (Pennington, NJ)
    …commercial operations. + Ensuring that all activities are performed in accordance with GMP , SOPs and Health and Safety policies. + Ensuring the availability of ... of experience in quality assurance and/or quality control in an FDA -regulated biotechnology or pharmaceutical company with progressive levels of responsibility are… more
    BeOne Medicines (08/08/25)
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  • QA Lead Technical Operations - CAPA

    Sokol Materials & Services (Skillman, NJ)
    …its equivalent is preferred. QUALIFICATIONS: + Advanced Level of relevant experience in a GMP , GCP, or GXP with at least 8 years focused on product quality. ... integrity principles + Proven attention to details + Comfortable working in an FDA regulated environment. About the Role DUTIES AND RESPONSIBILITIES: * Provide QA… more
    Sokol Materials & Services (07/31/25)
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