• Associate Principal Scientist

    Merck (West Point, PA)
    …the growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist who is an experienced drug product ... transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group… more
    Merck (03/20/25)
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  • Associate Principal Scientist

    Merck (Lower Gwynedd, PA)
    …and expanding your career. We are seeking a highly motivated Senior Scientist to join the Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalysis ... as well as selecting and designing applicable assays capable to meet regulatory expectations for vaccine or biologics development. The candidate should be current… more
    Merck (03/12/25)
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  • Associate Principal Scientist

    Merck (West Point, PA)
    …process enhancements, next generation process development, and authoring of regulatory submissions. Under the general scientific and administrative direction of ... functional area on cross-functional and cross-divisional teams. + Authors required regulatory and technical documentation. Ensures that processes are developed and… more
    Merck (03/19/25)
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