• Post Market Surveillance Analyst III

    Abbott (Burlington, MA)
    …types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory ... + 5 years related work experience **Preferred Qualifications** + 3+ years in MDR ( Medical Device Reporting) + Knowledge of the use, development, and regulatory… more
    Abbott (07/11/25)
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  • Senior CoreValve Therapy Consultant

    Medtronic (Cincinnati, OH)
    …surgery, Surgical Aortic Valve Replacement (SAVR) experience preferred + Strong, proven medical device sales track record with documented growth and achievements ... **A Day in the Life** **Bring your sales talents to a leader in medical technology and healthcare solutions. Rooted in our long history of mission-driven innovation,… more
    Medtronic (07/25/25)
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  • Registered Nurse (RN), Vascular Access

    LifePoint Health (Hickory, NC)
    …Access* Job Type: Fulltime Days * * *Your experience matters* At Frye Regional Medical Center, we are driven by a profound commitment to prioritize your well-being ... to your base compensation, this position also offers: ** . Comprehensive medical , dental, and vision plans, plus flexible-spending and health- savings accounts .… more
    LifePoint Health (07/23/25)
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  • Supervisor, Medical Events Group

    Abbott (Alameda, CA)
    …role will ensure the Medical Events Group (MEG) is compliant with global medical device reporting regulations. This position will be based out of our Abbott ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (07/26/25)
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  • Manager Global Medical Information

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …product complaint or adverse event of which made aware during the handling of medical information and medical device inquiries. + Contributes to ... of scientific response documents. + Limits corporate liability by meeting the medical ethical and legal responsibilities of providing product/ device related… more
    Otsuka America Pharmaceutical Inc. (06/21/25)
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  • Senior Embedded Software Engineer

    Abbott (Alameda, CA)
    …development is required. **Preferred Qualifications** + Solid knowledge of regulations for medical device development, (EN460001, ISO13485, FDA) is desirable. + ... preferred + Embedded UI design experience preferred + Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement… more
    Abbott (06/07/25)
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  • Sr. Engineering Tech-Mfg. Eng.

    Terumo Medical Corporation (Elkton, MD)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... to delicate equipment/molds. **Qualifications/ Background Experiences** + Experience in medical device industry and manufacturing environment a plus.… more
    Terumo Medical Corporation (07/09/25)
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  • LimFlow Account Manager - Missouri/ Kansas City…

    Stryker (KS)
    …or 6 years demonstrated successful sales experience. + Minimum 5 years of medical device industry experience selling physician preference therapies in the ... setting for the PAD/CLTI Patient. + Demonstrated ability to effectively establish new medical device therapies . + Experience in peripheral arterial and/or… more
    Stryker (08/02/25)
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  • Senior Staff R&D Engineer - Technical Lead

    Abbott (Santa Clara, CA)
    …providing engineering expertise in its creation and the development of this class 3 medical device product in this desirable technology space. Hiring Manager - ... equivalent combination of education and work experience. + Minimum 10 years in medical device development and/or other highly regulated industry. + Expertise… more
    Abbott (06/26/25)
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  • Regulatory Affairs Specialist II - Ventures…

    Abbott (Santa Clara, CA)
    …to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are ... PMA supplements and US device regulations or with EU and other international medical device regulations and submissions. + Ability to work within a team and… more
    Abbott (05/17/25)
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