• Validation Manager

    Astellas Pharma (Westborough, MA)
    **Validation Manager** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and ... to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!...around the world. We are committed to turning innovative science into medical solutions that bring value and hope… more
    Astellas Pharma (11/21/25)
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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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  • Project Manager - Performance Improvement - Full…

    Emanate Health (West Covina, CA)
    …you do at Emanate Health affects lives. When you join Emanate Health, you become part of a team that works together to strengthen our communities and grow as ... improvement projects that directly support hospital strategic priorities and regulatory compliance goals. The Project Manager collaborates with stakeholders on… more
    Emanate Health (12/10/25)
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  • Business Unit Risk Advisor Leader - Chief…

    Truist (Dallas, TX)
    …no less than 10 days of vacation (prorated based on date of hire and by full- time or part - time status) during their first year of employment, along with ... support and oversight for change activities (both business and regulatory change). 6. Provide oversight and support for open...any non-temporary position for which you apply, based on full- time or part - time status, position,… more
    Truist (01/09/26)
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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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  • Clinical Research Coordinator

    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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  • Clinical Research Medical Director,…

    Amgen (Washington, DC)
    **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 (11/14/25)
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  • Manager, Parenteral Manufacturing - Isolation…

    Bristol Myers Squibb (Manati, PR)
    …annual Global Shutdown between Christmas and New Years Day.** **All global employees full and part - time who are actively employed at and paid directly by BMS at ... procedures, lyophilization, and sanitization, to maintain operational readiness and regulatory compliance. 2. Production Scheduling & Coordination Aligns manufacturing… more
    Bristol Myers Squibb (01/09/26)
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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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