• Regulatory Affairs Manager, Diagnostics/IVD

    Kelly Services (Oakland, CA)
    …years of related experience . 6-8 years of regulatory experience in a medical device and/or diagnostics company involved with development, manufacturing, testing ... is responsible for supporting the development and operations team's compliance with FDA , CLIA, CAP, IVDR, and other global regulatory requirements. This position… more
    Kelly Services (08/08/25)
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  • Senior Principal Vascular Therapy Development Rep…

    Medtronic (Orange, CA)
    …+ **SR4:** 10 years B2B or Healthcare Sales with 5 years experience selling Medical device or medical capital equipment **NICE TO HAVE- DESIRED/PREFERRED ... timely and sound decisions. + Thorough working knowledge of medical terminology, medical procedures and the medical device industry. + Excellent customer… more
    Medtronic (08/15/25)
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  • Specialist, Clinical Safety

    Terumo Neuro (Aliso Viejo, CA)
    …review, investigation, and assessment of adverse events. 5. Class III medical device safety experience. **External-Facing Title:** Specialist, Clinical Safety ... results. + Partner with clinical research project managers and Medical Affairs and Safety Manager to ensure safety startup...+ Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as… more
    Terumo Neuro (07/12/25)
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  • CQV Engineers/Specialists - Open Applications

    VTI Life Sciences (Los Angeles, CA)
    …engineers looking to accelerate their careers in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support ... Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training,… more
    VTI Life Sciences (06/24/25)
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  • Cloud DevOps Engineer II

    Abbott (Sylmar, CA)
    …ensure the reliability and scalability of our applications that support our life-changing medical device software. You'll work closely with developers, QA, and ... ensure our systems are fast, reliable, and compliant with FDA and ISO standards. **What You'll Work On** As...+ Experience working in regulated environments, ideally in the medical device or healthcare space. + Knowledge… more
    Abbott (07/18/25)
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  • Area Sales Manager - Northern California - IHFM

    Edwards Lifesciences (San Francisco, CA)
    …We are rewriting the playbook on heart failure treatment. We're not just a medical device company; we're trailblazers on a mission to redefine healthcare. Our ... Sensor is revolutionizing how heart failure is managed, improving quality of life while slashing hospital admissions and health...5 years experience of progressive sales experience in the medical device industry + Experience in cardiac… more
    Edwards Lifesciences (07/02/25)
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  • Staff R&D Engineer

    Imperative Care (Campbell, CA)
    …discipline and a minimum of 8 years of related experience developing flexible medical device instruments; or equivalent combination of education and work ... experience in related regulated industry. + MS in Engineering and experience in medical device development in a start-up environment preferred. + Statistical… more
    Imperative Care (08/01/25)
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  • R&D Fellow, Systems Engineering, Interventional…

    Philips (San Diego, CA)
    …solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. + You ... manner. + You have experience working in the regulated medical device environment: demonstrating practical knowledge and...60601, IEC 62304, IEC 62366, UL, ANSI, ASTM, ISO, FDA ). + You must be able to successfully perform… more
    Philips (08/21/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Sacramento, CA)
    …United States. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in… more
    Fujifilm (07/24/25)
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  • Utilities/Facilities Site Leader (Regulated…

    Mentor Technical Group (Millbrae, CA)
    …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... of dealing in a challenging environment. + Knowledge and experience on pharmaceutical, medical device or biotechnology manufacturing is required. + Willing to… more
    Mentor Technical Group (08/27/25)
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