• Regulatory Affairs Specialist II

    Abbott (Sylmar, CA)
    …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives… more
    Abbott (09/05/25)
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  • Principal Research Scientist I, Tissue Material…

    AbbVie (Irvine, CA)
    …in conducting R&D projects + Experience and working knowledge of medical device , drug and/or biologics, and combination product regulations (21 CFR 820, 21 ... in vivo and tissue processing methods to support development of novel medical device /tissue products. + Critically evaluate scientific or regulatory advances,… more
    AbbVie (09/23/25)
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  • Distinguished Scientist, Autoinjector Platform

    Merck (Rahway, NJ)
    …support of Autoinjectors. The ideal candidate will possess extensive knowledge in medical device engineering, particularly in the design, manufacturing, and ... & Technology (DD&T) organization to serve as a senior technical subject matter-expert and advisor for our Autoinjector platform....a minimum of 20 years of hands-on experience in medical device engineering, with a focus on… more
    Merck (08/28/25)
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  • Staff Engineer

    BD (Becton, Dickinson and Company) (Covington, GA)
    …5+ years of experience in advanced manufacturing engineering, product design, and/or technical leadership level in Medical Device or other highly ... & Process Design role in planning and execution of medical device projects for the Urology and...assume technical leadership of projects and champion technical excellence in product assembly. This role… more
    BD (Becton, Dickinson and Company) (08/27/25)
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  • Sr Regulatory Affairs Specialist (Remote)…

    J&J Family of Companies (New Brighton, MN)
    …math, engineering, medical , or other technical fields and Class III medical device experience are preferred. + Ability to work collaboratively in a ... aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease...based upon regulatory changes. + Provide regulatory input and technical guidance to product development and operations… more
    J&J Family of Companies (09/23/25)
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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 (09/06/25)
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  • Senior Aortic Clinical Specialist

    Medtronic (Des Moines, IA)
    …and effective use of devices. + Develop and maintain comprehensive clinical and technical product knowledge. + Understand current published Aortic and relevant ... implant procedures in accordance with Medtronic guidance. + Provide technical leadership for Aortic device procedures. Educate...+ Thorough working knowledge of medical terminology, medical proceduresand the medical device more
    Medtronic (09/25/25)
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  • Regulatory Affairs Associate II

    Terumo Aortic (Sunrise, FL)
    …Exportability and Certificates to Foreign Government from US FDA + Prepare and submit medical device reports or vigilance reports. + Perform various other duties ... field) from an accredited college or university and 3 years direct experience in medical device regulatory affairs + Minimum 5 years direct experience in … more
    Terumo Aortic (08/22/25)
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  • Senior Research Engineer

    Cook Medical (West Lafayette, IN)
    …Research Engineer, at Med Institute, will be responsible for various aspects of the medical device product development process, including but not limited to ... design controls, and design verification and validation testing. Previous medical device development experience is highly desirable. Responsibilities… more
    Cook Medical (09/11/25)
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  • Senior R&D Project Manager

    ZOLL Medical Corporation (Parsippany, NJ)
    …+ 5+ years managing technical product development. + Experience with medical device capital equipment development. + 10+ years of experience as an ... Lead design review and risk management activities. + Manage technical partners/ vendors supporting product development activities....engineer developing products, preferably in the medical device industry. + PMP certification desired.… more
    ZOLL Medical Corporation (09/11/25)
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