• Associate Manager, Medical Device

    Regeneron Pharmaceuticals (East Greenbush, NY)
    …product + Responsible for the management and development of quality engineering team members + Represent Regeneron's medical device QMS during regulatory ... We are currently looking to fill a Manager, Medical Device Quality Assurance position on our Medical... Quality Assurance position on our Medical Device Sustaining Engineering QA team. This position… more
    Regeneron Pharmaceuticals (10/17/25)
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  • Quality Engineer 2, Device

    GRAIL (Durham, NC)
    …regular on-site presence (5 days a week) **Responsibilities:** + Support medical device Quality Engineering operations through expert interpretation, ... establishment, and execution of quality engineering concepts and principles in accordance...of 5 years of experience working within a medical device , pharmaceutical, or biotech quality management system.… more
    GRAIL (09/19/25)
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  • Medical Device Quality Engineer…

    Regeneron Pharmaceuticals (East Greenbush, NY)
    …are currently looking to fill a Quality Engineer position on the Medical Device Sustaining Engineering QA team. This position will provide Quality ... device risk management activities + You have a quality mind-set To be considered for this role you...role you must hold a Bachelor's degree in an Engineering subject area and the following amount of work… more
    Regeneron Pharmaceuticals (10/17/25)
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  • Design Quality Engineer

    Actalent (Minneapolis, MN)
    …specifications and qualification. Essential Skills + 5+ years of experience in medical device quality engineering . + Proficiency in design control and ... Job Title: Design Quality EngineerJob Description As a Design Quality...Additionally, you will oversee risk management activities throughout the device lifecycle, from concept to post-launch. Responsibilities + Lead… more
    Actalent (12/09/25)
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  • Quality Engineer

    Actalent (San Clemente, CA)
    …chemistry, or a related field. + Advanced-level experience in pharmaceutical or medical device quality engineering . + Hands-on experience with equipment ... in accordance with ICH and other relevant standards. Responsibilities + Lead quality engineering activities for the development and manufacturing of drug-eluting… more
    Actalent (12/02/25)
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  • Customer Quality Engineer

    onsemi (San Jose, CA)
    …up a clear strategy to improve them towards customer satisfaction Solid Medical Device Quality /Semiconductor Quality / Engineering background Review of ... engineering , failure analysis, product & test engineering , or production quality control in the semiconductor industry. Medical device exp. is a plus.… more
    onsemi (11/22/25)
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  • Associate Director, Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …+ Coordinate risk mitigation activities across clinical, regulatory, quality , and engineering functions + Perform safety reviews on device and combination ... Serve as clinical liaison to Global Device Team, including engineering , regulatory affairs, quality , and commercial functions + Coordinate interdepartmental… more
    Takeda Pharmaceuticals (12/04/25)
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  • Sr Quality Engineer

    Imperative Care (Campbell, CA)
    …and contribute to the development, manufacture, and distribution of Imperative Care's medical device products by applying Quality Engineering principles to ... Job Title: Sr Quality Engineer Location : This position is based...the organization. What You'll Bring + Bachelor's degree in engineering , or related discipline and a minimum of 5… more
    Imperative Care (10/16/25)
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  • Associate Principal Scientist - Device

    Merck (West Point, PA)
    …, Injection Moldings, Machine Learning (ML), Manufacturing Processes, Mechanical Testing, Medical Device Quality Systems, Medical Device Regulations, Medical ... **Job Description** **Associate Principal Scientist - Device Technical and Engineering Lead (Associate...strategic direction on programs they lead to ensure high quality products and robust manufacturing processes. This position interacts… more
    Merck (11/18/25)
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  • Head of Medical Device & SaMD…

    Takeda Pharmaceuticals (Lexington, MA)
    …ISO 13485, ISO 14971, MDR/IVDR, MDSAP). + Act as or designate the Device Quality Management Representative (QMR) and Person Responsible for Regulatory Compliance ... + Drive the design, implementation, and continuous improvement of operations and quality systems for medical device and digital health technologies, ensuring… more
    Takeda Pharmaceuticals (10/10/25)
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