• Medical Education Manager - West

    Hologic (Denver, CO)
    …particularly within the surgical and healthcare environment. + Comprehensive knowledge of medical device products relevant to the GYN Surgical division. + ... Medical Education Manager - West Denver, CO, United...Familiarity with healthcare compliance guidelines, regulations, and ethical standards. + Proficiency in… more
    Hologic (10/14/25)
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  • Senior Specialist Quality

    dsm-firmenich (Exton, PA)
    …experience with SAP, Arena and LIMS, have a Quality mindset, and possibly medical device experience please apply now! dsm-firmenich Biomedical is the world's ... biomaterial science and process innovation, and the leading resource for global medical device and pharmaceutical companies. **Responsibilities:** + The Senior… more
    dsm-firmenich (10/14/25)
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  • Principal AI/ML Engineer

    Abbott (Chicago, IL)
    …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...for ML models, including testing, rollout, rollback strategies, and compliance governance. + Ensure strict compliance with… more
    Abbott (08/26/25)
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  • Vice President, Digital Field Services

    GE HealthCare (Chicago, IL)
    …connected device tools. The ideal candidate will bring deep experience in the medical device or healthcare technology industry, have a proven track record in ... + Demonstrated experience leading IT in a **Services organization within the medical device or healthcare technology industry.** + Proven success deploying… more
    GE HealthCare (10/09/25)
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  • Senior Specialist, Quality Systems

    AbbVie (Worcester, MA)
    device related products. + Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device , biologics, and ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position… more
    AbbVie (10/09/25)
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  • Director, Quality

    Bausch + Lomb (Greenville, SC)
    …US Class II/Class III medical devices, as well as non-US medical device regulations, applicable sterile drug/aseptic processing regulations experience in the ... In-depth knowledge of applicable regulations and standards, both domestic and international ( medical device or drug). Proven technical and problem-solving skills… more
    Bausch + Lomb (09/24/25)
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  • Quality Systems Specialist

    AbbVie (Mettawa, IL)
    … related products preferred. + Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device , biologics, and ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position… more
    AbbVie (09/03/25)
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  • Clinical Study Manager

    ARTIDIS (Houston, TX)
    …to individual patients' needs and desired outcomes. Job Purpose ARTIDIS is a medical device start-up company that conducts clinical studies to validate and ... he/she is responsible that the study conduct is in compliance with the approved study protocol and Good Clinical...Investigator meetings).Being comfortable with measurement procedures of the ARTIDIS Medical Device . Qualifications + Degree in a… more
    ARTIDIS (10/15/25)
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  • Staff Regulatory Affairs Specialist

    embecta (Parsippany, NJ)
    …(eg engineering, bioengineering, biology, chemistry). + 5+ years Regulatory Affairs experience in medical device companies. + Must have current knowledge of the ... and Europe, and related regulatory affairs activities to ensure compliance with regulations and alignment with the objectives of...US and European Medical Device regulations. + Demonstrated success in… more
    embecta (10/07/25)
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  • Sr QA Manager

    Dentsply Sirona (Johnson City, TN)
    compliance with FDA, ISO 13485, MDSAP, EU MDR and other applicable global medical device standards and regulations. * Provide oversight of sterile medical ... We're Looking For:** ✔️ 5+ years of proven experience in Quality Management within the medical device industry ✔️ Strong knowledge of **sterile medical more
    Dentsply Sirona (10/04/25)
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