• Sr Manager, Clinical Logistics

    Gilead Sciences, Inc. (Foster City, CA)
    …the opportunity to lead complex, high-impact initiatives, ensure compliance with international regulatory standards, and drive operational excellence across a ... investigational medicinal products (IMPs), ensuring strict compliance with GDP and international regulations. + Drive innovation by introducing best practices and… more
    Gilead Sciences, Inc. (11/27/25)
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  • Associate Medical Director/Principal Investigator…

    ThermoFisher Scientific (Las Vegas, NV)
    …Knowledge of important regulatory considerations and experience with national and/or international regulatory authorities + Ability to assess the safety and ... and business development staff. Supports local team in all quality initiatives and regulatory requirements at a busy Phase 1 32 bed facility understanding that… more
    ThermoFisher Scientific (11/20/25)
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  • Senior Civil Structural Engineer New Nuclear Plant…

    GE Vernova (Wilmington, NC)
    …Interface with internal and external customers, suppliers, partners, the NRC and international regulatory authorities on technical issues. + Incorporate design ... disposition + Perform work tasks in accordance with current regulatory guides and industry standards applicable to the Systems...+ Willing to travel up to 25% domestic and international + This role requires access to US export-controlled… more
    GE Vernova (11/20/25)
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  • Quality Compliance, Senior Manager

    Amgen (Washington, DC)
    …inspectional commitments, as applicable. + Provides support for domestic and international Regulatory Authority Inspections when necessary. + Provides technical ... support the audit process (eg, read and understand how to apply regulatory requirements including changes to regulations, guidelines and standards, trends and… more
    Amgen (11/15/25)
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  • Vice President Quality Assurance

    Cytel (Hagatna, GU)
    …or CRO environments. + Deep knowledge of GCP, ICH guidelines, and international regulatory inspection practices. + Proven success building and leading ... highest standards of compliance with Good Clinical Practice (GCP) and international regulations, while driving innovation in quality oversight. The Vice President… more
    Cytel (10/07/25)
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  • Product Safety Engineer - Ditch Witch

    The Toro Company (Perry, OK)
    …Toro Company, you will be responsible for: + Evaluate and interpret US and International product safety and regulatory standards as they apply to divisional ... relevant experience in product safety or product testing. + Experience in international standards and regulatory requirements for earthmoving, construction, or… more
    The Toro Company (10/12/25)
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  • Clinical Affairs Manager, Interventional Access…

    Teleflex (Minneapolis, MN)
    …(QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which Teleflex complies. **TRAVEL REQUIRED: ... in patients' lives. **Position Summary** **TRAVEL REQUIRED: 50% (Domestic and International ; overnight required)** The Clinical Affairs Manager will provide clinical… more
    Teleflex (09/13/25)
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  • Associate Director, Clinical Research (US Remote)

    Terumo Neuro (Aliso Viejo, CA)
    …3. Strong knowledge of clinical trial processes and both US and international (OUS) regulatory requirements. 4. Excellent organizational, analytical, and ... team leadership, and strong cross-functional collaboration with Medical Affairs, PACE, Regulatory , Clinical Safety, and Data Management. Ensure high standards of… more
    Terumo Neuro (11/21/25)
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  • FSP Document Review Specialist II (North America)

    ThermoFisher Scientific (Waltham, MA)
    …concepts, GCP, guidelines (eg, ICH), and requirements of the FDA and other international regulatory agencies. + Attentive to detail and quality of documents, ... Document Review Specialist within the FSP Team, you will effectively review regulatory documents, including but not limited to submissions documents, protocols and… more
    ThermoFisher Scientific (11/26/25)
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  • Principal Scientific Advisor (Remote)

    Charles River Laboratories (Wilmington, MA)
    …of therapeutic products. Successful individuals have knowledge of domestic and international regulatory expectations and requirements; and can provide ... an experienced professional with expertise in establishing effective scientific and regulatory strategies to advance new medicines through the various stages of… more
    Charles River Laboratories (11/24/25)
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