• District Manager - PVI Therapies

    Cook Medical (Syracuse, NY)
    …performing job functions and duties. The Peripheral Intervention division of Cook Medical focuses on device technology that addresses broad cardiovascular ... peripheral stents, and vena cava filters. For more information about Cook Medical , visit www.cookmedical.com Responsibilities * Develop new business and expands… more
    Cook Medical (09/12/25)
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  • Specialist, Medical Writing

    Edwards Lifesciences (Irvine, CA)
    Patients are at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate ... curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting cardiovascular disease. Patients with mitral and… more
    Edwards Lifesciences (09/06/25)
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  • EMC Test Technician

    DEKA Research & Development (Manchester, NH)
    …Technician to work closely with senior EMC and design engineers in a dynamic Medical Device Research and Development environment. This role will have a direct ... and accurately record findings + Gain in-depth knowledge of medical device functionality and intended clinical use...development stages + Collaborate with the EMC team to develop and refine work instructions, ensuring the accurate assessment… more
    DEKA Research & Development (07/18/25)
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  • Project Engineer

    Globus Medical, Inc. (Audubon, PA)
    …following:** + Three to seven years' experience in mechanical design engineering; Medical device experience strongly preferred + Bachelor's Degree in Mechanical ... At Globus Medical , we move with a sense of urgency...ensure designs meet specifications + Collaborating with marketing and product managers to develop forecasts and market… more
    Globus Medical, Inc. (08/14/25)
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  • Regulatory Affairs Manager

    Dentsply Sirona (Sarasota, FL)
    …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... who serve them. If you want to grow and develop as a part of a team that is...13485, EU MDR). + Experience with software as a medical device , AI and/or medical more
    Dentsply Sirona (09/18/25)
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  • Sr Business Development Mgr, ESD (East Coast)

    Fujifilm (Sacramento, CA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... marketing organization. The incumbent is responsible for supporting the product management group including, but not limited to market...with a Master's degree. + Minimum 10 years of medical device industry experience in a clinical… more
    Fujifilm (09/20/25)
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  • Reprocessing Engineer I

    Fujifilm (Bothell, WA)
    …**Essential Job Functions:** + Apply understanding of the fundamentals of medical device reprocessing to establish cleaning and disinfection procedures ... and processes comply with applicable industry guidance, standards, and regulations on medical device reprocessing. + Provide guidance to design teams when… more
    Fujifilm (09/09/25)
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  • Quality Assurance Engineer 2

    Teleflex (Coventry, CT)
    …leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades ... is preferred or 3+ years of Quality Assurance experience working in the medical device manufacturing environment (a combination of education and experience will… more
    Teleflex (09/05/25)
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  • Senior Manager, R&D Portfolio Program Management

    Bausch + Lomb (Kirkwood, MO)
    …future. Objective: Plan and manage/coordinate resources and activities related to ophthalmic medical device product development projects throughout Surgical ... Champion and lead projects as a project manager for ophthalmic medical device products (Electrical/Mechanical/Software-driven Capital Equipment and associated… more
    Bausch + Lomb (08/14/25)
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  • Sr. Prin. Development Engineer

    Medtronic (Boston, MA)
    …Have** + A minimum of 8 years of experience with direct medical device development + Experience with developing a product according to System Engineering ... impact by exploring a career with the world's leading Medical Device company, striving " _to alleviate...investigations and analysis + Partner with System Engineering to develop , review and decompose product requirements +… more
    Medtronic (09/20/25)
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