• Innovation Lead (Director)

    ThermoFisher Scientific (Grand Island, NY)
    …development, laboratory and lifecycle services to customers across pharmaceutical, biotechnology, medical device , academic and government entities. By harnessing ... The IL utilizes identified business priorities to shape the overarching product roadmap strategy and/or process workflow transformations. We currently have 2… more
    ThermoFisher Scientific (09/19/25)
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  • Associate Director, R&D

    BD (Becton, Dickinson and Company) (Covington, GA)
    …Engineering, or related field (Master's or Ph.D. preferred). + 10+ years of experience in medical device R&D, with at least 5 years in a people leadership or ... to lead an engineering team focused on design verification, product lifecycle management, and sustaining engineering for a diverse...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
    BD (Becton, Dickinson and Company) (09/04/25)
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  • UL - Sr. Test & Compliance Engineer

    Ultralife Corporation (Newark, NY)
    …throughout the product lifecycle. This role requires expertise in UL, CE, medical device testing standards as well as prior experience working with products ... + Analyze product risks and collaborate with engineering teams to develop test strategies to mitigate identified risks. + Prepare and maintain risk management… more
    Ultralife Corporation (07/28/25)
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  • Senior Quality Engineer I

    Zimmer Biomet (Warsaw, IN)
    …quality products to Zimmer. + Evaluate and disposition nonconformances conditions per medical device industry regulations and quality control procedures. + ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer… more
    Zimmer Biomet (07/02/25)
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  • Project Manager II

    ManpowerGroup (Milpitas, CA)
    …+ Strong knowledge of **FDA regulations (21 CFR Part 820), ISO 13485, medical device reporting (MDR), and complaint handling** . **Key Responsibilities** ... ISO 13485** , and other applicable regulations. + Support preparation and submission of ** Medical Device Reports (MDRs)** . + Assist with regulatory audits and… more
    ManpowerGroup (09/18/25)
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  • Principal Embedded Software Engineer

    J&J Family of Companies (Danvers, MA)
    …inputs into software specifications. + Design, development, and test software per medical device software development life cycle (IEC-62304) + Participate in ... with cross functional teams including post market quality engineering, product security and medical office in assessment...would be a big plus. + Experience in the medical device industry is strongly preferred. +… more
    J&J Family of Companies (09/18/25)
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  • Quality Control Technician

    ManpowerGroup (Pomona, CA)
    Our client, a leader in the medical device industry, is seeking a **Quality Control Technician** to join their team. As a **Quality Control Technician** , you ... will be part of the Quality Assurance department supporting product testing, inspection, and compliance activities. The ideal candidate...of experience in a quality assurance role within the medical device industry (preferred) + Ability to… more
    ManpowerGroup (09/12/25)
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  • R&D Fellow, Systems Engineering, Interventional…

    Philips (San Diego, CA)
    …solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. + You will ... and thorough manner. + You have experience working in the regulated medical device environment: demonstrating practical knowledge and experience with global… more
    Philips (08/21/25)
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  • Sr. Manufacturing Engineer

    Medtronic (Milwaukee, WI)
    …at least two (2) years' experience with each of the following: Manufacturing in medical device industry including Class I, Class II and Class III devices; ... studies for cost control, waste reduction and inventory control; NC & CAPA Investigations; Medical Device Quality & Regulatory Compliance (FDA 21 CFR Part 820,… more
    Medtronic (08/19/25)
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  • Senior Microbiologist

    Stryker (Flower Mound, TX)
    …do:** + Provide guidance on cleaning, disinfection, sterilization, and biocompatibility for reusable medical device design. + Develop , review, and approve ... microbiological or biological testing, R&D, or sterility assurance within the medical device , pharmaceutical or regulated industry. Preferred Qualifications: +… more
    Stryker (08/16/25)
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