• Medical Device Regulatory

    Oracle (Washington, DC)
    …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
    Oracle (12/22/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Washington, DC)
    …in related field or equivalent work experience, preferred + 2+ years' experience in Medical Device Regulatory Affairs /Quality experience preferred + ... **_What Regulatory Affairs contributes to Cardinal Health_**... and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory more
    Cardinal Health (12/13/25)
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  • Regulatory Affairs Associate…

    GRAIL (Washington, DC)
    …, development, clinical affairs , quality, or program management within the IVD, medical device , or pharmaceutical industries is required. + Regulatory ... FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such...and international regulatory frameworks and processes for medical device development and approvals is required.… more
    GRAIL (12/03/25)
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  • Exec Director, Regulatory Affairs

    Gilead Sciences, Inc. (Washington, DC)
    …directly relevant professional experience in small molecule and biologics development, global CMC regulatory affairs and CMC technical areas of at least 16 years ... and approval timelines. Provide guidance to PDM Teams and Device Teams to align development and regulatory ...or MD. + Demonstrated track record in leading CMC regulatory affairs initiatives, innovative CMC regulatory more
    Gilead Sciences, Inc. (12/03/25)
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  • Senior Manager, CMC Global Regulatory

    Otsuka America Pharmaceutical Inc. (Washington, DC)
    **Job Summary** The Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global ... relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs , Global Regulatory Strategy, Manufacturing facilities,… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Washington, DC)
    …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to healthcare… more
    Fujifilm (12/16/25)
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  • GRA Device Associate

    Sanofi Group (Washington, DC)
    …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...teams. + Contribute to and execute innovative and sustainable medical device regulatory strategies covering… more
    Sanofi Group (12/19/25)
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  • Senior Vice President, Healthcare Public…

    FleishmanHillard (Washington, DC)
    …intersection of healthcare and public affairs in service to pharmaceutical and medical device companies, as well as third party organizations to include ... Additional desired areas of expertise include issues advocacy and public affairs campaigns, strong writing skills, and stakeholder engagement with policy and… more
    FleishmanHillard (11/25/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Washington, DC)
    …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Regulatory Science & Policy Director

    Philips (Washington, DC)
    …a minimum of 10+ years' experience in FDA Regulations, Global Regulatory Affairs , Policies and Standards within the Medical Device /Technology industry or ... The Regulatory Science & Policy Director is responsible for...Director is responsible for guiding the analysis of global regulatory requirements, policies and industry standards to identify their… more
    Philips (10/03/25)
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