• Software Quality Engineer II

    Abbott (Sylmar, CA)
    …Ensures software systems are developed, validated and maintained in compliance with regulatory and business procedures. As a global leader in Cardiac Rhythm ... Abbott is a global healthcare leader that helps people...other relevant regulations for medical devices. Previous experience with regulatory body. Knowledge of software regulations and compliance more
    Abbott (08/20/25)
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  • Sr. Clinical Research Specialist - JJMT…

    J&J Family of Companies (Irvine, CA)
    At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, ... we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact… more
    J&J Family of Companies (09/11/25)
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  • Cardiac Surgery Field Inventory Analyst

    Medtronic (Los Angeles, CA)
    …**About Medtronic** We lead global healthcare technology ... record and subject to regular driver's license review for compliance purposes. Must Have: Minimum Requirements + Bachelor's degree...Employers and the California Fair Chance Act. We lead global healthcare technology and boldly attack the… more
    Medtronic (09/11/25)
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  • Senior Manager, Clinical Programs

    Danaher Corporation (Vista, CA)
    …a team of clinical study managers, driving strategic operational execution, ensuring regulatory compliance , and achieving key milestones for critical clinical ... (IHC) & In Situ Hybridization (ISH). + Advanced degree in Science, Healthcare , or Regulatory /Clinical Affairs + Professional certification in Clinical Research… more
    Danaher Corporation (09/09/25)
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  • Sr Manager - Product Security

    BD (Becton, Dickinson and Company) (Irvine, CA)
    …PSO provide guidance to successfully deliver best-in-class secure products, consistent with global regulatory requirements over the lifecycle. This role works in ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...partnership with R&D, Enterprise Security, Quality, Regulatory Affairs, and leaders at corporate, regional, and business-unit… more
    BD (Becton, Dickinson and Company) (08/09/25)
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  • Executive Director, Medical Affairs, Ophthalmology

    Merck (Sacramento, CA)
    …growth opportunities and drive innovation. + In-depth expertise in local regulatory frameworks, ethical standards, and pharmaceutical compliance requirements. + ... understands Our Company's enterprise level strategies and leads cross-functionally with the Global Medical and Scientific Affairs Therapeutic Area (GMSA TA) teams to… more
    Merck (09/09/25)
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  • Symplicity Spyral Territory Manager…

    Medtronic (Fresno, CA)
    …**About Medtronic** We lead global healthcare technology ... in a dynamic, evolving environment with a "project mentality." ** Compliance & Reporting** - Maintain accurate records of account...Employers and the California Fair Chance Act. We lead global healthcare technology and boldly attack the… more
    Medtronic (08/29/25)
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  • Director, Income Tax Accounting

    Humana (Sacramento, CA)
    …both ASC 740 and SSAP 101, supporting our financial integrity and regulatory obligations. The ideal candidate will bring deep technical expertise, strong leadership, ... tax provisions under ASC 740 and SSAP 101, ensuring accuracy and compliance with US GAAP and statutory accounting principles. + Oversee tax-related disclosures… more
    Humana (09/12/25)
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  • Medical Science Liaison - West

    IQVIA (Los Angeles, CA)
    …to propel their careers forward and contribute to driving performance. As a global leader in commercial solutions, IQVIA is dedicated to delivering impact both ... done in a strictly scientific, non-promotional manner, and in full compliance with applicable laws and regulations, guidelines, codes of conduct.… more
    IQVIA (08/08/25)
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  • CRA 2/Sr. CRA 1, Early Clinical Development, US,…

    IQVIA (Carlsbad, CA)
    …you will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, regulatory guidelines, and sponsor requirements. Your ... to address expectations and resolve issues. + Assess site performance and compliance with regulatory standards, escalating quality concerns when necessary. +… more
    IQVIA (09/04/25)
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