• Senior Director, Expert Volunteer Operations

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …scientific organization that collaborates with the world's leading health and science experts to develop rigorous quality standards for medicines, dietary ... and levels of the organization to fulfill their responsibilities including the Chief Science Office/Chair to the Counsel of Experts, DSCP Leadership Team, GSSD, GEA,… more
    The US Pharmacopeial Convention (USP) (12/17/25)
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  • Director/Senior Director, Global Process Owner…

    Lilly (Raleigh, NC)
    …and implementation tools and ensure they are designed according to regulatory , industry and company expectations. + Provide governance, lead the implementations ... external organizations and industry organizations to monitor policy changes for regulatory / external environments and advocate / influence quality related policies… more
    Lilly (10/24/25)
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  • Plastics Issues and Advocacy Advisor

    ExxonMobil (Washington, DC)
    …where you work, as well as longer-term programs such as leaves of absence and part - time work. + Comprehensive medical, dental, and vision plans. + Culture of ... Policy Engagement and Advocacy: Drive proactive engagement with policymakers, regulatory agencies, and industry associations to influence legislation and regulations… more
    ExxonMobil (01/07/26)
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  • Wildfire Risk Engineer / Senior Wildfire Risk…

    Hawaiian Electric (Honolulu, HI)
    …and application of wildfire risk models for strategic planning and regulatory reporting. Incorporates system asset characteristics and performance, geospatial and ... analysis workflows and tools for efficiency and accuracy. + Assists with regulatory filings and reporting that include wildfire risk methodologies. + Integrates… more
    Hawaiian Electric (10/28/25)
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  • Automation Maintenance Technician (6PM to 6AM)

    Amgen (New Albany, OH)
    **Join Amgen's Mission of Serving Patients** At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients ... happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges...the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform… more
    Amgen (11/27/25)
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  • Medical Director - Physician -Early Clinical…

    Lilly (San Diego, CA)
    …translational leader who can bridge the critical gap between discovery science and clinical application, driving the development of transformational medicines for ... test therapeutic hypotheses + Collaborate with clinical pharmacology, biostatistics, regulatory affairs, operations, and other stakeholders to optimize study design… more
    Lilly (01/15/26)
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  • Quality Systems Manager

    West Pharmaceutical Services (Scottsdale, AZ)
    …and cross-functional collaboration. + Monitor and maintain compliance with global quality and regulatory standards, including 21 CFR Part 820, ISO 13485, and EU ... knowledge of regulatory and governmental guidelines and requirements (21 CFR Part 820, ISO 13485, EU-MDR, cGMP, GLP). + Experience in regulated industry such… more
    West Pharmaceutical Services (12/17/25)
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  • Supervisor - IHC

    Caris Life Sciences (Phoenix, AZ)
    …that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: _"What would I do if this ... multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.** **Position… more
    Caris Life Sciences (01/14/26)
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  • Senior Environmental Specialist

    Dow (Deer Park, TX)
    …Park (TX, USA), Texas, United States of America Schedule:Full time Date Posted:01/12/2026 Job Number:R2064669 Position Type:Regular Workplace Type:Onsite At ... to deliver a sustainable future for the world through science and collaboration. If you're looking for a challenge...of assigned plant(s), site, hub and business. + Leads regulatory testing as required by permit and regulations or… more
    Dow (01/13/26)
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  • Associate Director, Quality Risk Specialist

    Bristol Myers Squibb (Madison, NJ)
    …years QA experience or relevant experience in quality management, biomedical science , clinical development, or regulatory compliance. **Required Competencies:** ... to clinical trials teams throughout study lifecycle. + Provide regulatory intelligence on current and upcoming regulations to ensure...and New Years Day. All global employees full and part - time who are actively employed at and… more
    Bristol Myers Squibb (01/13/26)
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