• Senior Specialist, Medical Writing

    Edwards Lifesciences (Irvine, CA)
    …Bachelor's Degree in a related field with 5 years of related experience working in medical affairs , clinical affairs and/or clinical science **What else we ... internal/external working relationships + The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment… more
    Edwards Lifesciences (09/27/25)
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  • Senior Clinical Engineer

    Abbott (Sylmar, CA)
    …of cardiac rhythm management (CRM) devices strongly preferred + 6+ clinical medical device experience or equivalent, ideally with CRM products + Demonstrated ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
    Abbott (09/12/25)
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  • Senior Specialist, Clinical Research Monitoring…

    Edwards Lifesciences (Los Angeles, CA)
    …+ Knowledge of cardiovascular physiology and structural heart anatomy + Previous medical device Clinical Research experience in cardiology + Clinical research ... Clinical Coordinator/CRA certification) + Prior clinical research experience with Class III Medical Devices including PMA, IDE and 510(k) + Excellent written… more
    Edwards Lifesciences (11/14/25)
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  • Senior Counsel Specialist, Assistant General…

    Genentech (South San Francisco, CA)
    …early and late stage research and development of pharmaceutical products, digital health, and medical devices . As a member of the R&D Law Group, this **"Senior ... support Research and Early Development, Clinical Operations, Global Product Development, and Medical Affairs functions by providing strategic legal advice to… more
    Genentech (10/28/25)
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  • Firmware Trace Engineer

    US Tech Solutions (Irvine, CA)
    …Experience at medical device manufacturer + Experience in active implantable medical devices + Working knowledge of IEC 60601 and/or 62304 + Experience ... you will be part of the evaluation and integration of firmware on Urology medical device technologies. As a technical hands-on contributor, you will focus… more
    US Tech Solutions (11/19/25)
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  • Compliance Quality Software Lead

    Abbott (Alameda, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... R&D, System Engineering, Product Quality, Technical Quality, CAPA, and Regulatory Affairs . **What You'll Work On** +...Quality responsibilities as they apply to the develop of medical device software, as well as the… more
    Abbott (11/08/25)
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  • Project Manager III

    Actalent (Irvine, CA)
    …to lead Quality Assurance (QA) activities for a strategic M&A initiative in the medical device industry. This role demands a strong leader capable of navigating ... complex situations and collaborating effectively with cross-functional teams, including Regulatory Affairs (RA) and Clinical Affairs (CA). . Responsibilities… more
    Actalent (11/19/25)
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  • Senior Research Scientist

    Abbott (Santa Clara, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... can grow the career you dream of. + Free medical coverage for employees* via the Health Investment Plan...other departments including Global Clinical Operations, Research & Development, Regulatory Affairs , and Biostatistics. + Writes, study… more
    Abbott (09/24/25)
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  • Senior Clinical Research Scientist - JJMT…

    J&J Family of Companies (Irvine, CA)
    …Organizations (CRO), and vendors, and with internal teams: medical affairs , data management, biostatistics, data programmers, and regulatory affairs ... content that communicates clinical and real-world data on the Company's Electrophysiology medical devices . This role is responsible for contributing scientific… more
    J&J Family of Companies (10/18/25)
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  • Sr. Specialist, Scientific Operations (Irvine, CA…

    J&J Family of Companies (Irvine, CA)
    …in quality regulatory compliance, complaint handling, adverse event reporting, medical device risk management processes, and experience with common bio ... Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory Affairs relating to the Scientific Operations...regulated environment including 3 years of direct experience with medical devices in the fields of technical… more
    J&J Family of Companies (11/22/25)
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