• Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Augusta, ME)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... cross-functional ad-hoc projects or assignments that require safety input, ensures compliance with regulations/internal SOPs, and fosters a culture of "Safety First"… more
    Sumitomo Pharma (08/15/25)
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  • Supervisor, Production Operations

    Curia (Albuquerque, NM)
    …processes, and overseeing formulation tasks. Additionally, the supervisor ensures compliance with all relevant regulations and procedures, maintains current good ... organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At… more
    Curia (08/12/25)
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  • Associate Director, Clinical Research, Value…

    Takeda Pharmaceuticals (Lexington, MA)
    …within assigned TA in accordance with all applicable internal legal and compliance policies as well as external US-specific regulatory guidelines. + Partners with ... project plan execution and holds to the highest standards for operational excellence and compliance in all US Medical activities. + Drive and deliver all aspects of… more
    Takeda Pharmaceuticals (08/02/25)
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  • Associate Director, Viral Vector Downstream…

    Gilead Sciences, Inc. (Oceanside, CA)
    …operational efficiency, reduce costs, and ensure safety while maintaining regulatory compliance + Determine metrics for success and evaluate performance against ... prevent issues + Leads supervisors to ensure safety and compliance are adhered to by team and drives culture...and 2+ years of experience in manufacturing in the pharmaceutical industry OR + A MS/MA and 8+ years… more
    Gilead Sciences, Inc. (07/31/25)
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  • Manager, Microbiology

    Curia (Albuquerque, NM)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... by Site Leadership + Oversees the review and implementation of compliance guidelines, industry trends, customers projects (Method Transfer, Development, etc.),… more
    Curia (07/25/25)
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  • Senior Director, Site Quality Head, Goa

    Teva Pharmaceuticals (Parsippany, NJ)
    …Packaging and Laboratory Operations to ensure a mature culture of quality, compliance with regulatory requirements and quality of products. This oversight includes ... complaint investigations; CAPA Creation and implementation; trending and metrics, compliance with validation requirements; verification that equipment, facility and… more
    Teva Pharmaceuticals (09/06/25)
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  • Quality Operations Specialist III

    Curia (Albuquerque, NM)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... helps establish and maintain cross-departmental relationships to enhance overall compliance and efficiency. The Specialist III supports facilities, validation,… more
    Curia (07/12/25)
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  • Pharmacy Services Director

    Houston Methodist (Houston, TX)
    …Pharmacy Services position is responsible for the provision of quality pharmaceutical care in accordance with accepted ethical and professional practices and ... for employee engagement, adequate staffing levels, budget development and compliance , staffing decisions such as hiring and terminating employment, coaching… more
    Houston Methodist (06/23/25)
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  • Director, Global External Manufacturing, OSD

    Gilead Sciences, Inc. (Foster City, CA)
    …within our global external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements, and environmental, health, and safety ... is part of the Manufacturing Operations group within the larger Pharmaceutical Development and Manufacturing organization (PDM). The preferred candidate will have… more
    Gilead Sciences, Inc. (09/14/25)
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  • Director, Labeling Council and Regional Labeling

    Takeda Pharmaceuticals (Boston, MA)
    …execute on strategic actions for continuous improvement and compliance . + Demonstrates Takeda leadership behaviors. **Minimum** **Requirements/Qualifications:** + ... degree (or equivalent) required, masters preferred. + 7+ years experience in pharmaceutical industry, with 4 years in Regulatory Affairs, labeling or quality… more
    Takeda Pharmaceuticals (09/13/25)
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