• Sr. Director - TS/MS (Not Remote - New…

    Lilly (Indianapolis, IN)
    …startup into GMP manufacturing operations._ **Position Overview** The Senior Director of Technical Services/Manufacturing Science (TS/MS) oversees the site's TS/MS ... + Oversee all aspects of TS/MS, including new product introduction, process development , and optimization. + Ensure validated processes and compliance with cGMP and… more
    Lilly (09/04/25)
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  • Medicare-Medicaid Pharmacy Director

    Humana (Lansing, MI)
    …and help us put health first** The Clinical Pharmacist Lead monitors drug development pipeline, and medical literature, while providing clinical support ... diverse scope and complexity ranging from moderate to substantial. The Pharmacy Director , internally known as a Clinical Pharmacy Lead, plans, directs, and monitors… more
    Humana (09/09/25)
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  • Director , Quantitative Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …fields critical for drug development , such as statistics, drug metabolism, pharmacology, toxicology, bioanalysis, and pharmaceutical science. + Ability ... Objectives: + Leads strategic, scientific, and operational aspects of multiple drug development projects with a high level of technical and strategic… more
    Takeda Pharmaceuticals (09/09/25)
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  • Associate Director , Commercial Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …to meet the Company's objectives and goals + Provide strategic advice for the development of Office Of Prescription Drug Promotion advisory submissions and sub ... lives. Read more: careers.bms.com/working-with-us . **Description:** The role of Associate Director of US Commercial Regulatory Affairs requires the ability to apply… more
    Bristol Myers Squibb (08/25/25)
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  • Director , Business Excellence Portfolio…

    AbbVie (Irvine, CA)
    …impact projects and professional development experiences spanning the entire drug development value chain. The position requires strong analytical skills, ... will have a direct impact on the future success of AbbVie. As a Director of Business Excellence Strategy, you will partner with leaders across AbbVie to optimize… more
    AbbVie (08/08/25)
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  • Associate Director - CTF Delivery…

    Lilly (Indianapolis, IN)
    …ultimately enabling organizational and corporate initiatives (eg ICRO). + Lead the development of a comprehensive strategy and data standards for Data Reporting and ... a high school diploma and 7 years of clinical experience in a pharmaceutical , biotech, CRO, or Regulatory agency and established analytics background, preferably in… more
    Lilly (09/05/25)
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  • Global Safety Medical Director

    Amgen (Washington, DC)
    …and transform the lives of patients while transforming your career. **Global Safety Medical Director ** **What you will do** Let's do this. Let's change the world. In ... analysis plans, and clinical study reports + Prepare/review safety sections of new drug applications and other regulatory filings + Serve as safety expert on… more
    Amgen (08/21/25)
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  • Senior Director , Quality Control (Cvrm)

    Genentech (Holly Springs, NC)
    …Pharma Technical Operations (PT) is responsible for managing all aspects of end-to-end drug substance and drug product manufacturing and supply. From the raw ... new site will focus on large volume low cost Drug Product manufacturing. **The Opportunity** As the Head of...evaluate the achievement of goals. You will support the development of employees. **Who you are:** + You hold… more
    Genentech (09/06/25)
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  • Field Medical Director , Oncology,…

    Pfizer (Annapolis, MD)
    **Why Patients Need You** The Oncology Field Medical, Director is responsible for providing therapeutic area/product expertise for the malignant hematology ... Pfizer Medical Affairs in order to contribute to Medical content strategy development and execute aligned Field Medical tactics. + Maintain effective and appropriate… more
    Pfizer (09/11/25)
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  • Principal Medical (Science) Director , CVRM

    Genentech (South San Francisco, CA)
    … and reimbursement landscapes + Experience or relevant knowledge of pre-approval drug development trials and post marketing medical evidence generation, ... (eg PharmD, PhD, MD etc.) + Minimum 8-10 years of relevant clinical / medical pharmaceutical /biotechnology industry experience with knowledge of CVRM development more
    Genentech (09/06/25)
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