• Principal MDR - Vigilance Specialist

    Medtronic (Los Angeles, CA)
    …our technology transforms lives Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or ... of resolutions to meet goals and objectives. Understand current and upcoming Medical Device Reporting (MDRs) and EU Vigilance Reporting requirements by… more
    Medtronic (12/12/25)
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  • Senior Polymers Scientist

    J&J Family of Companies (Warsaw, IN)
    …of statistical validation methodologies **Preferred:** + Prior experience with polymers used in the medical device industry is desirable. + Medical device ... Provide technical support materials to Orthopaedics business partners to improve device function, quality, and cost. Apply problem-solving and failure analysis… more
    J&J Family of Companies (12/06/25)
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  • Integration Project Manager - AI Ultrasound

    GE HealthCare (Boston, MA)
    …field. + Minimum 5-8 years of technical project management experience in healthcare software or medical device R&D, with a focus on AI or software integration. + ... a fast-growing business in GE HealthCare, is the global leader in ultrasound medical devices and solutions. The portfolio spans the continuum of care to enable… more
    GE HealthCare (12/05/25)
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  • Product Complaints Specialist

    DEKA Research & Development (Manchester, NH)
    …an immediate opening for a Product Complaints Specialist to work in a dynamic Medical Device Research and Development environment. The position reports to the ... + Responsible for reviewing and entering complaint information related to potential medical device issues. + Generate requests for additional information to… more
    DEKA Research & Development (12/05/25)
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  • Quality Analyst (Quality Control) (Evening 2:30pm…

    LSI Solutions (Victor, NY)
    …in 1986, located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive ... passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R)...preferred. + Familiarity with GMPs, Quality Standards, and Regulatory Compliance is highly desired. + Quality Control Inspection, Line… more
    LSI Solutions (12/01/25)
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  • Quality Engineer- Products and Systems

    Philips (Cambridge, MA)
    …of 3+ years' experience of Quality Engineering experience within FDA regulated, medical device product environments, with a focus in Design Quality/Control, ... working knowledge of Risk Management (ISO 14971) and global medical device product regulations, requirements and standards. + You have experience independently… more
    Philips (11/27/25)
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  • Repair Technician - Bilingual

    Adecco US, Inc. (Union City, CA)
    …technical and non-technical backgrounds. 6. Inspection and technical repair experience in the ** medical device field is highly desired.** 7. Some travel may be ... to determine the **root cause** of the complaint. 6. Perform routine testing of medical devices to replicate reported device complaints and assist in determining… more
    Adecco US, Inc. (11/18/25)
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  • Process Engineer

    Mentor Technical Group (Ponce, PR)
    …knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... and have at least two years of experience in validation within a medical device company. + Validation lifecycle knowledge / Hands on experience (Writing and… more
    Mentor Technical Group (11/15/25)
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  • Quality Technician II

    Kelly Services (O'Fallon, MO)
    …& Clinical is seeking a **Quality** **Technician II** for our client a top medical device manufacturer in O'Fallon, MO. If you're passionate about bringing the ... preferred) + Minimum 3 years' experience in manufacturing or quality control ( medical device experience preferred) + **Proficient with optical comparators,… more
    Kelly Services (11/12/25)
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  • Senior Design Assurance Engineer

    Philips (Plymouth, MN)
    …if:** + You have a minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of ... the QMS related to Design/Process Controls. + You have strong understanding of Medical Device QSR regulations/standards including ISO 13485, ISO 14971, 21CFR… more
    Philips (10/30/25)
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