• Director Pharmacy

    Dignity Health (Bakersfield, CA)
    …pharmacy care to patients and improve outcomes. Assures departmental competency and compliance to all regulatory accreditation and hospital standards of care. + ... strategies for pharmacy care + Partners with colleagues and communicates that pharmaceutical care is an integral component of the integrated health care delivery… more
    Dignity Health (08/24/25)
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  • Sr. Director - Profiling and Design

    Lilly (Indianapolis, IN)
    …compensation reviews. * Oversee departmental expenses and cost center management. ** Compliance ** * Ensure project execution aligns with corporate policies and ... hold a valid passport. **Preferred Qualifications** * Experience in active pharmaceutical ingredients (API) or drug product platforms. * Familiarity with capital… more
    Lilly (08/23/25)
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  • Pharmacy Director

    Arkansas Children's (Little Rock, AR)
    …management, human resource management, and quality improvement. Responsible for ensuring compliance with all applicable laws and regulatory agencies. Coordinates the ... provision of optimal pharmaceutical care with available resources. **Additional Information:** **Required Education:** Doctorate **Recommended Education:**… more
    Arkansas Children's (08/16/25)
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  • Associate Director , Scientific…

    Gilead Sciences, Inc. (Foster City, CA)
    …gather relevant data to support scientific arguments and conclusions. + Ensure compliance with publication guidelines and ethical standards (eg, ICMJE, GPP, CONSORT) ... Viral Hepatitis, Chronic Liver Diseases, and Inflammation preferably within the pharmaceutical industry. + Therapeutic area experience + CMPP certification preferred… more
    Gilead Sciences, Inc. (08/13/25)
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  • Medical Director , Diagnostic Cardiology

    GE HealthCare (Waukesha, WI)
    …+ Lead medical reviews of promotional and scientific materials to ensure compliance with applicable regulations and clinical accuracy + Provide Medical inputs ... + 8+ years' experience working in the medical technology, medical device, or pharmaceutical industry in Medical or Clinical Affairs roles + MBA or Masters degree… more
    GE HealthCare (07/29/25)
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  • Associate Director - Global Robotics…

    Lilly (Indianapolis, IN)
    …champion for safety activities and a role model for diversity, ethics, and compliance . + Complete all HR related tasks such as performance management plans, ... within manufacturing sites. + 2+ years of experience within Pharmaceutical Manufacturing, preferably within an operational manufacturing site. + Proficiency… more
    Lilly (07/23/25)
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  • Associate Director - Critical Utilities

    Takeda Pharmaceuticals (Thousand Oaks, CA)
    …work environment by adhering to safety guidelines and policies and enforcing compliance with California state, regulatory, and federal EPA regulations + Oversee the ... required + Minimum 10 years of related experience. Experience in the pharmaceutical , biotechnology or other FDA-regulated industry strongly preferred + Minimum 5… more
    Takeda Pharmaceuticals (07/23/25)
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  • Director - Experienced Discovery Toxicology…

    Lilly (Indianapolis, IN)
    …leading toxicology projects to support the discovery and development of new pharmaceutical products while working closely with cross-functional teams to ensure the ... + Collect, analyze, and interpret toxicological data, ensuring accuracy and compliance with regulatory standards. + Prepare and present project findings, updates,… more
    Lilly (07/16/25)
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  • Associate Director - API SAP EWM

    Lilly (Indianapolis, IN)
    …SAP EWM design and MES Integration. + Ensure adherence to all quality, compliance and data integrity requirements. + Establish key relationships with business users ... and use of SAP, WM and MES integration. + Experience supporting pharmaceutical manufacturing and distribution warehouses with a solid understanding of processes… more
    Lilly (07/09/25)
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  • Future Opportunities- Join Our Talent Pipeline…

    AbbVie (North Chicago, IL)
    …and acts as a therapeutic area resource. + Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities. + Responsible for ... Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred. +… more
    AbbVie (07/04/25)
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