• Senior Quality Systems Specialist

    Danaher Corporation (Sunnyvale, CA)
    …Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) ... participating regulatory authorities + Provide cross-functional compliance support for global QMS and Intracompany Quality Agreement requirements. Function as… more
    Danaher Corporation (08/16/25)
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  • Director, Design Assurance

    Imperative Care (Campbell, CA)
    …audits by external bodies (Notified Body, FDA, etc.) and internal audits to maintain regulatory compliance . + Oversee quality and compliance issues, actively ... objectives. + Lead the design assurance team and ensure compliance with domestic and international regulatory standards...+ Ability to comprehend principles of engineering, physiology, and medical device use Employee Benefits include a… more
    Imperative Care (07/01/25)
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  • Digitiva Marketing Lead

    Astellas Pharma (South San Francisco, CA)
    …marketing projects from concept to delivery. + Experience working cross-functionally with compliance , regulatory , sales, and medical affairs teams. + ... The DIGITIVA solution is a combination of a hardware medical device , a patient-facing mobile app, and...Process (MAP) team to ensure all marketing materials meet compliance , regulatory , and legal requirements. + Maintain… more
    Astellas Pharma (08/23/25)
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  • Senior Engineer Supplier

    Abbott (Pleasanton, CA)
    …Qualifications** + Master's Degree. + Minimum 5 years working with in a medical device manufacturing company or similarly regulated industry. Apply Now ... of various financial scenarios and makes recommendations to management. + Knowledge of regulatory and compliance requirements linked to manufacturing. + Teach &… more
    Abbott (08/29/25)
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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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  • Quality Administrative Assistant

    Aerotek (Santa Rosa, CA)
    …data analysis. + Experience with auditing tools and software. + Background in the medical device industry is beneficial. **Why Work Here?** Relucent offers a ... + Implement and oversee document control processes to ensure compliance with quality standards. + Assist in planning and...role is based in an office environment within a medical device company, offering a structured and… more
    Aerotek (08/22/25)
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  • Senior Manager Contributions

    CalSTRS (Sacramento, CA)
    …1,750 school employers and the State to meet financial reporting requirements and regulatory compliance . The incumbent is also responsible for billing and ... system like pension system. + Knowledge and experience with compliance of pension laws, rules and regulations. + Strong...+ Flexible work hours + Remote work options + Medical benefits, including health, dental and vision insurance +… more
    CalSTRS (08/22/25)
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  • Sr. Manager- Software Design Assurance

    Philips (San Diego, CA)
    …tools, and innovative methodologies to continuously enhance software quality and regulatory compliance . + Will oversee the development, maintenance, and ... You have a minimum of 8+ years' experience in FDA regulated, IEC 62304 medical device software environments (SiMD/SaMD), with a focus on Software Design… more
    Philips (08/09/25)
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  • Clinical Research Associate I - Butte Lab…

    Cedars-Sinai (Los Angeles, CA)
    …will be involved in the development and possible commercialization of a novel medical device technology. Interest or experience in a start-up environment with ... will assist in the effort in validating the clinical trial of groundbreaking medical imaging systems. The job will provide an outstanding opportunity to work with… more
    Cedars-Sinai (08/23/25)
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  • Supplier Quality Auditing Manager

    Hologic (San Diego, CA)
    …Supplier Quality Sr. Director/Director that may affect product quality or regulatory compliance . + **Interdepartmental Collaboration:** Work with other Global ... auditing program, ensuring that our suppliers adhere to rigorous regulatory and quality standards. You will lead and guide...roles + Clean driver's license + Proficient knowledge of Medical Device Regulations, In Vitro Diagnostic Regulation,… more
    Hologic (06/24/25)
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