• Technical writer

    Capgemini (Raritan, NJ)
    …English, science writing, or other related discipline. + Writing experience in the medical device industry or any relevant industry + Experience in writing ... cases, scripts, and validation protocols in alignment with company, GxP, and regulatory policies. + Collaborate with cross-functional teams to gather and analyse… more
    Capgemini (07/11/25)
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  • Supervisor, Production - Weekend (Friday - Sunday)

    Integra LifeSciences (Plainsboro, NJ)
    …all established costs, quality, and delivery commitments are met, working within FDA medical device regulations, and applicable ISO standards. + Responsible for ... Manufacturing Center) to ensure the safety, efficacy, and quality of our medical devices. This includes assigning and monitoring weekend (Friday through Sunday)… more
    Integra LifeSciences (07/08/25)
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  • Therapeutic Specialist Tzield, Hackensack

    Sanofi Group (Ridgefield, NJ)
    …**Qualifications** + BA / BS degree required + 3+ years of pharmaceutical, biotech or medical device sales experience + Account Management sales and / or rare ... meetings as directed + Maintaining strict adherence to all legal, regulatory , ethical, administrative, and financial duties + Achieving and exceeding assigned… more
    Sanofi Group (08/29/25)
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  • Engineer, Biosurgery R&D LCM

    J&J Family of Companies (Raritan, NJ)
    …who will participate in the design, development, and commercialization of medical devices including those of formulated, biologic and mechanical design in ... technical and design reviews, documentation and Design History Files including regulatory filings + Support Design Verification and Design Validation activities such… more
    J&J Family of Companies (08/20/25)
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  • Associate IT Director - Business Partner Analyst

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …complementary technology experience + Experience delivering technology solutions in a Medical Device or Pharmaceutical regulated environment + Solid knowledge ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...of relevant Quality/ Regulatory standards (cGxP, CFR Part 11, etc.) + Proficiency… more
    BD (Becton, Dickinson and Company) (08/03/25)
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  • Sr. Program Manager

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …+ Master's degree + Experience working in a regulated industry, specifically medical device industry as particularly valuable **Primary Work Location and ... Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our… more
    BD (Becton, Dickinson and Company) (08/02/25)
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  • Corporate Account Manager - Post Acute…

    ConvaTec (NJ)
    Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the ... Bachelor's degree (BS/B. A.) required. + 5+ years of experience in device and/or healthcare sales, account management, or business development preferably within the… more
    ConvaTec (07/22/25)
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  • Director National Accounts - East

    Zimmer Biomet (Farmingdale, NJ)
    …years of experience in National Accounts Manager or a similar role within the medical device or orthopedic industry. * Strong experience in managing strategic ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...all contract terms are mutually beneficial and compliant with regulatory requirements. * Sales Enablement: Work closely with the… more
    Zimmer Biomet (07/18/25)
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  • Quality Engineer II

    Zimmer Biomet (Parsippany, NJ)
    …3-5 years of experience preferred. + Certified Quality Engineer (CQE) and Medical Device , particularly Orthopedic Industry experience preferred. + Combination of ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...the department as well as outside the company (suppliers, regulatory agencies, etc.). + Ability to deliver, meet deadlines… more
    Zimmer Biomet (07/11/25)
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  • Clean Room Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …+ 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience in a clean room ... records, required logs, books, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard… more
    Integra LifeSciences (08/30/25)
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