• Global Senior Director Medical Affairs…

    Merck (Rahway, NJ)
    **Job Description** The Global Senior Director of Medical Affairs (GDMA) for Melanoma coordinates the development of the Global Scientific and Medical Affairs Plans ... coordination in alliances that our company may have with other pharmaceutical companies **Scientific & Technical Leadership** + Communicates both scientific and… more
    Merck (09/12/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Salem, OR)
    **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... validation and implementation activities for drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Director , Biologics Process Development…

    Merck (Rahway, NJ)
    …pipeline programs using fed-batch and continuous manufacturing platforms. The Director , Biologics Process Development (BPD) within the Biologics Process Research ... and will advance a culture of scientific excellence and compliance with our company's procedures for recording time, data...field with 10+ years of relevant experience in the pharmaceutical industry; MS with 13+ years of relevant experience;… more
    Merck (08/20/25)
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  • Director , Commercial Analytics - New…

    Sumitomo Pharma (Providence, RI)
    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 ... LinkedIn (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=2504638834&u=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsumitomo-pharma-america%2F&a=LinkedIn) . **Job Overview** The ** Director , Advanced Analytics-New Products/Innovation** will be… more
    Sumitomo Pharma (07/30/25)
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  • Sr. Director , Global Scientific Engagement…

    Chiesi (Boston, MA)
    …care and consumer-facing self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social ... many other enriching diversities. Chiesi USA Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent… more
    Chiesi (07/24/25)
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  • Associate Director - Automation Engineering…

    Lilly (Lebanon, IN)
    …medicines, while also reducing costs and environmental impact. The Associate Director -Automation Engineering - Control System Validation and Data Analytics, is ... data engineers that support the daily operations of the facility. The Associate Director is also responsible for the productivity and development of the employees… more
    Lilly (08/29/25)
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  • Director , Contract Strategy…

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    …and balancing the needs of the business against Regeneron capabilities and compliance requirements. The Director , Contract Strategy will own specific accounts ... (either IDNs, GPOs, Payer) for the purpose of strategy development. The Director , Contract Strategy is a proven leader supporting the development, refinement of… more
    Regeneron Pharmaceuticals (09/13/25)
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  • Director of Quality

    Kelly Services (Coppell, TX)
    **Title:** Director of Quality **Location:** Fort Worth, TX **Salary:** Commensurate w/ experience + Benefits The ** Director of Quality** will be responsible for ... that inspect and improve the quality of products. The Director ensures that the products meet and exceed standards...the company goals and strategic initiatives while ensuring regulatory compliance . As head of the Quality department, the position… more
    Kelly Services (07/29/25)
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  • Associate Director , Clinical Program…

    Takeda Pharmaceuticals (Boston, MA)
    …Management and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and ... the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the … more
    Takeda Pharmaceuticals (07/16/25)
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  • Associate Director , GVP Audits

    Gilead Sciences, Inc. (Foster City, CA)
    …Join Gilead and help create possible, together. **Job Description** The Associate Director , Good Pharmacovigilance Practice (GVP) Audits, serves as a key role within ... Annual Audit Program. Reporting to the Head of GVP Audits, the Associate Director contributes to the strategic development and operational execution of the GVP audit… more
    Gilead Sciences, Inc. (08/08/25)
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