• Quality Assurance Manager New Product Introduction

    Stryker (Mahwah, NJ)
    …Drive robust process risk management, including pFMEA, CQAs, and process validation . + Optimize inspection strategies through automation, lean principles, and ... years of experience in a regulated manufacturing environment (Medical Device, Pharmaceutical , Biomedical, or Automotive). + Experience leading and developing teams.… more
    Stryker (07/04/25)
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  • Safety Expert Statistician

    Sanofi Group (Bridgewater, NJ)
    …level. **Major Duties and Responsibilities** + Lead safety signal detection, validation , charaterisation and reporting for several projects with minimal direction ... you:** + PhD/MS in statistics or related discipline with 6 years of pharmaceutical experience Knowledge of epidemiology methods and concepts in safety context +… more
    Sanofi Group (07/02/25)
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  • Environmental, Health and Safety Senior Specialist

    Sokol Materials & Services (Skillman, NJ)
    …Integrity! Join Sokol GxP Services, where we partner with leading pharmaceutical and biotech companies to provide exceptional Commissioning, Qualification, and ... Validation (CQV) services. We are committed to fostering diversity, empowering local talent, and building strong community connections to bring the best-qualified… more
    Sokol Materials & Services (06/19/25)
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  • Clean Room Inspector/Packaging Operator - 1st…

    Integra LifeSciences (Plainsboro, NJ)
    …independently with minimal supervision. + Supports equipment evaluations and validation activities associated with the developed manufacturing processes + ... diploma or equivalent. + 0-2 years working in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly desirable. + Basic computer… more
    Integra LifeSciences (06/17/25)
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  • Automated Production Operator 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …events/non-conformances or customer complaints. + Supports equipment evaluations and validation activities associated with the developed manufacturing processes + ... equivalent with 2+ years of experience in the Medical Device industry or Pharmaceutical industry within a clean room environment preferred. + Must work and… more
    Integra LifeSciences (06/17/25)
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  • Scientist, Statistical Programming

    Merck (Rahway, NJ)
    …deliverables under the guidance of a senior level programmer. + Perform validation tasks according to departmental SOPs and collaborate effectively with outsource ... for R&D projects (data, analyses, tables, graphics, listings); knowledge of pharmaceutical development processes; and knowledge in CDISC SDTM and ADaM standards… more
    Merck (06/17/25)
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  • Quality Assurance Associate Director (M2)

    Lilly (Branchburg, NJ)
    …responsible experience with quality assurance or quality control in the pharmaceutical or biopharmaceutical industry. Experience must include a minimum of: 5 ... compliance; 5 years of experience with applying knowledge of computer systems validation per cGMPs and System/Software Development Lifecycle concepts; 5 years of… more
    Lilly (06/12/25)
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  • Automation Engineer (R2-R4)

    Lilly (Branchburg, NJ)
    …to support utility and manufacturing process automation efforts for pharmaceutical manufacturing facilities. Develop and configure data collection and reporting ... biologics manufacturing operations and for specification, installation, startup, and validation of process equipment. Liaise with information technology, engineering,… more
    Lilly (06/12/25)
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  • Director - Market Intel & Portfolio Insights

    Novo Nordisk (Plainsboro, NJ)
    …diverse internal and external network for primary intelligence gathering and cross- validation . + Oversee development of presentations with clear storylines to ... in, Competitive Intelligence, Commercial Insights, marketing, sales, business analytics, or pharmaceutical consulting required, or an MBA with at least ten years… more
    Novo Nordisk (06/04/25)
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  • Director, Neurology and Immunology HEVA Business…

    Sanofi Group (Morristown, NJ)
    …observational research, Clinical Outcomes Assessment (COA) development and validation , systematic literature review, evidence synthesis, value dossier development ... + Understanding of the legal and regulatory environment of the pharmaceutical industry, demonstrated integrity on work-related compliance considerations and solid… more
    Sanofi Group (05/26/25)
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