• Medical Device Regulatory Affairs…

    Abbott (Santa Clara, CA)
    …and scientists. **The Opportunity** We currently have several opportunities for the ** Medical Device Regulatory Affairs Development (RAD) Program** to be located ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
    Abbott (09/06/25)
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  • Technology Development Device Leader

    Global Foundries (Essex Junction, VT)
    …should be the foundation of a valuable, differentiated, and competitive customer solution. The Device Leader can expect to have the support and cooperation of ... a global manufacturing footprint spanning three continents. GlobalFoundries' Power Product Line Research and Development Organization is seeking qualified candidates… more
    Global Foundries (07/08/25)
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  • Senior Cyber Security Engineer, Mobile…

    Community Health Systems (Franklin, TN)
    …Manager of Endpoint Security. This role develops, engineers, and maintains the Mobile Device product within the Endpoint Security Program for the Cybersecurity ... of mobile device security + Scripting and Automation + IoT and medical device security principles **Licenses and Certifications** + CISSP, GIAC, OSCP, and… more
    Community Health Systems (09/13/25)
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  • Device Engineering Intern, Ulp CMOS (Summer…

    Global Foundries (Malta, NY)
    …transistor performance. You will collaborate across technology teams and engage with product line management to align device parameters with GLOBALFOUNDRIES' ... and Smart Mobile Devices. + Collaborate with cross-functional technology teams and product line management to define device performance targets, ensure… more
    Global Foundries (08/14/25)
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  • Sr Staff Scientist - Medical Device

    Astrix Technology (Essex County, NJ)
    **Sr Staff Scientist - Medical Device ** Science & Research Essex County, NJ, US Pay Rate Low: 128000 | Pay Rate High: 184000 + Added - 27/05/2025 Apply for Job ... _Our client, a world-leading medical device company focused on improving lives...This high-impact, visible role is key to driving innovation, product improvements, and global expansion within the Life Sciences… more
    Astrix Technology (08/11/25)
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  • Senior Software Engineer, Medical

    Hologic (Newark, DE)
    Senior Software Engineer, Medical Device Newark, DE, United States Located in Newark, DE, **Hologic** 's Innovation Center is continuing to offer job ... and ability to implement and test. + Ability to support & drive departmental best practices and product...secure coding principles or cybersecurity is a plus. + Medical device experience is a plus. +… more
    Hologic (07/30/25)
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  • Staff Engineer, Software Design Assurance…

    Abbott (Burlington, MA)
    …mobile applications and embedded software), non- medical software, and non- product software + Support software verification and validation activities ... oversight of R&D design control deliverables for development of medical product software (Cloud Patient Care Networks,...ISO 13485, ISO 14971, Software Standards (eg, 62304), EU Medical Device Regulations and MDSAP + Experience… more
    Abbott (09/12/25)
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  • Field Service Technician ( Medical

    IQVIA (Cincinnati, OH)
    **_IQVIA has an opportunity with one of the largest medical device manufacturers in the US. We welcome you to apply if interested! You will be asked to create an ... with healthcare professionals and participating in technical initiatives in medical device technology. You will be responsible...medical devices in a hospital setting with the support of an on-site team. This is a great… more
    IQVIA (09/24/25)
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  • Sr. Principal Scientist - TS/MS Device

    Lilly (Indianapolis, IN)
    …Expert (SME) Oversight** : + Demonstrate a strong ownership and stewardship for medical device design, manufacturing, labelling, and/or packaging processes you ... technical change agendas. Understand key regulations and their impact to the medical device design transfer and post-launch surveillance process. + Engage… more
    Lilly (09/12/25)
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  • Manager, Regulatory Affairs- Medical

    Bausch Health (Bothell, WA)
    …required + Must have a solid understanding of Change Management/Life Cycle Management of medical device products along with the impact of changes on US Canada ... written and communication skills. + Should have experience authoring complete 510(k) submissions, Medical Device license applications (Class II or above), EU MDR… more
    Bausch Health (07/10/25)
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