• Director , Drug Metabolism

    Gilead Sciences, Inc. (Foster City, CA)
    …**Job Description** **Specific Responsibilities:** The primary responsibility of this Biologics DMPK Director position is to serve as an expert in the PK and ... + Lead the DMPK strategy for programs at various stages of drug discovery/development in collaboration with inter-disciplinary team; champion activities to deliver… more
    Gilead Sciences, Inc. (07/24/25)
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  • Executive Director , Prescription…

    JPMorgan Chase (Jersey City, NJ)
    …they have access to the best possible care and resources. As the Executive Director , Prescription Drug lead within the Benefits Department at JPMorgan Chase, you ... will manage and enhance our Prescription Drug offerings and other benefits programs. Your role will...prescription drugs, dental and vision + Monitor legislative and regulatory changes to ensure compliance with new and existing… more
    JPMorgan Chase (07/01/25)
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  • Senior Director Antibody- Drug

    Lilly (Indianapolis, IN)
    …has an expanding and diverse portfolio of ADCs that require thorough drug -linker process development and regulatory submission strategies, often with compressed ... accelerate the development of lifesaving new medicines for our patients. Our antibody- drug conjugate (ADC) team seeks to perform innovative and cutting-edge research… more
    Lilly (07/09/25)
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  • Director , Drug Metabolism…

    Gilead Sciences, Inc. (Foster City, CA)
    …responsibility of this position is to lead biotransformation activities in the Drug Metabolism Department and in collaboration with the Clinical group. The scientist ... compounds in vitro and in vivo to understand metabolic pathways to support drug discovery and development. More broadly, the scientist is expected to integrate this… more
    Gilead Sciences, Inc. (08/01/25)
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  • Associate Director , MSAT, Downstream…

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    **Job Summary** **​** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes ... review technical reports, protocols, risk assessments, and relevant sections of regulatory submissions (IND, BLA, MAA, etc.) related to downstream processing. +… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Associate Director , Engineering (API…

    Merck (Rahway, NJ)
    **Job Description** As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a pivotal role ... + Review process change requests and deviation reports while ensuring regulatory compliance. **Education and Minimum Requirements:** + Bachelor's degree in… more
    Merck (07/24/25)
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  • Sr Director , Drug Metabolism

    Gilead Sciences, Inc. (Foster City, CA)
    …presentation/publication. Comfortable working with and educating colleagues in drug metabolism, toxicology and clinical pharmacology departments, on strategies ... to understand drug metabolism and disposition. Demonstrates excellent scientific verbal and...written to communicate clear messages and are ready for regulatory submissions. State of the art bioanalysis by LC/MS,… more
    Gilead Sciences, Inc. (07/30/25)
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  • Director , Sterile Product Development

    Merck (Rahway, NJ)
    …and inclusive work environment. **Essential Knowledge, Duties & Responsibilities for the Director Include:** + Sterile drug product development concepts, tools, ... team is responsible for the research and development of sterile & parenteral drug products for biologics, Antibody Drug Conjugates and Small Molecules, including… more
    Merck (07/24/25)
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  • Sr. Director - Medical Development-Obesity

    Lilly (Indianapolis, IN)
    …life better for people around the world. **Responsibilities:** The Senior Medical Director is delegated various responsibilities by the Medical Development AVP or ... management team in fulfilling corporate goals and initiatives. The Senior Medical Director will provide strong leadership and ability to influence, both within and… more
    Lilly (07/10/25)
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  • Sr AD / Director , Clinical Pharmacology…

    Boehringer Ingelheim (Ridgefield, CT)
    …impact of renal/hepatic impairment, food effect on PK, QT prolongation and pediatric drug development). The Director , Clinical Pharmacology Lead (D-CPhL) acts as ... management and matrix leadership. + Expert knowledge in CP, BioPharma, clinical drug development and relevant regulatory guidelines. + Recognized and respected… more
    Boehringer Ingelheim (06/14/25)
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