• Associate Director, Global Labeling

    Takeda Pharmaceuticals (Boston, MA)
    …In alignment with TAU/MPD Labeling Lead, coordinates the process to obtain labeling approval by Labeling Senior Management Cross-functional team (Global ... bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you...and alignment of the labeling strategy and labeling content. Interface with Senior Management Cross-Functional… more
    Takeda Pharmaceuticals (07/25/25)
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  • AD Promo Lead/ Associate Director, Americas…

    Chiesi (Cary, NC)
    …new labeling and changes to existing labeling , and submission of labeling information to regulatory authorities in the United States and Canada. Main ... duties in Canada. + Manage and oversee the submission of promotional labeling materials and supporting documentation to regulatory agencies in accordance… more
    Chiesi (07/24/25)
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  • Senior Director, Corporate…

    Edwards Lifesciences (Irvine, CA)
    …that we are supporting the needs and interests of the patients we serve. The Senior Director, Corporate & Regulatory Counsel role is a blend of subject matter ... legal expert and strong business acumen. The Senior Director, Corporate & Regulatory Counsel will...the Edwards Headquarters, in Irvine CA and reporting to Senior Vice President, Associate General Counsel, TAVR… more
    Edwards Lifesciences (06/12/25)
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  • AD / Sr AD, US Product CMC Regulatory

    Boehringer Ingelheim (Ridgefield, CT)
    …can support projects of increasing regulatory complexity and/or business impact. The Senior Associate Director, US Product CMC Regulatory Affairs is ... to FDA concerning assigned US investigational and marketed product interactions. The Senior Associate Director position is expected to support projects of… more
    Boehringer Ingelheim (07/25/25)
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  • Senior Director - Medical Global…

    Lilly (Indianapolis, IN)
    Senior Director-Medical is delegated various responsibilities by the Associate Vice-president or equivalent role to provide leadership, supervision, coordination, ... all necessary regulatory standards. + Provide support for global registrations, labeling and label modifications, and resolution of regulatory issues. +… more
    Lilly (07/08/25)
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  • Global Safety Senior Scientist

    Amgen (Washington, DC)
    …us and transform the lives of patients while transforming your career. **Global Safety Senior Scientist** **What you will do** Let's do this. Let's change the world. ... management system + Author Safety Assessment Reports and other safety documents and regulatory responses in collaboration with the GSO + Search and review adverse… more
    Amgen (07/19/25)
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  • Wastewater Treatment Operator/ Senior

    Allegion (Indianapolis, IN)
    regulatory submittal. + Perform weekly hazardous waste inspections as per regulatory requirements. + Ensure proper labeling and management of hazardous ... individual to join our team as a Wastewater Treatment Operator or Senior Wastewater Treatment Operator, depending on experience and qualifications. This role is… more
    Allegion (06/22/25)
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  • Oncology Infusion Senior Acute Pharmacy…

    Banner Health (Phoenix, AZ)
    …you are looking to leverage your abilities - apply today. As an **Oncology Senior Acute Pharmacy Technician** , you will be responsible for cleanroom procedures, IV ... better as we aim to prevent and cure cancer. As an **Oncology Infusion Senior Acute Pharmacy Technician** , you will be supported by chemotherapy trained Pharmacy… more
    Banner Health (07/21/25)
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  • Associate Director - Supply Chain

    Lilly (Philadelphia, PA)
    …to make life better for people around the world. **Position Overview:** The Associate Director, Supply Chain will lead and grow a supply chain team responsible ... maintaining approved suppliers/products for global operations, demand/supply/capacity planning, sourcing, labeling , dispensing, inventory management, shipping, distribution, and selection of… more
    Lilly (07/22/25)
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  • Associate Director, Clinical Supply Project…

    Merck (West Point, PA)
    …portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites globally. The ... a lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines, strategies… more
    Merck (07/24/25)
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