• Merck & Co. (North Wales, PA)
    …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
    HireLifeScience (09/30/25)
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  • Merck & Co. (North Wales, PA)
    …span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-Design and maintain statistical ... and systems and database expertise;US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
    HireLifeScience (09/03/25)
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  • Associate Principal Scientist

    Organon & Co. (Plymouth Meeting, PA)
    …to the Director or Executive Director in Organon Regulatory CMC, the Associate Principal Scientist is responsible for developing and implementing ... with global regulations and guidances and Organon procedures. The Associate Principal Scientist will lead...products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
    Organon & Co. (10/09/25)
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  • Associate Principal Scientist

    Merck (West Point, PA)
    …within Analytical Chemistry in Development and Supply (ACDS) is seeking applicants for an Associate Principal Scientist position available at the Rahway, NJ ... to drive late-stage pharmaceutical drug product development and commercialization. The Associate Principal Scientist responsibilities include, but not… more
    Merck (10/11/25)
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  • Associate Principal Scientist

    Merck (West Point, PA)
    …investigations, process validation, second generation process development and authoring of regulatory submissions. We are seeking a strategic and technical leader ... Provide technical oversight of cell culture process development, process characterization and regulatory filing activities to ensure a smooth and clear path to… more
    Merck (10/09/25)
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  • Associate Principal Scientist

    Merck (North Wales, PA)
    …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
    Merck (09/30/25)
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  • Associate Principal Scientist

    Merck (North Wales, PA)
    …the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. + Design and maintain ... systems and database expertise; + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
    Merck (09/03/25)
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  • Sediment Remediation Practice Lead - Environmental…

    Burns & McDonnell (Conshohocken, PA)
    **Description** Burns & McDonnell is seeking an Associate / Principal Engineer, Hydrogeologist, Scientist in a related field to join our successful team of ... capping, and other industry standard methods. + Strong working knowledge of regulatory frameworks, including CERCLA, RCRA, Section 401 and Section 404 permitting. +… more
    Burns & McDonnell (07/23/25)
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