• Merck & Co. (Rahway, NJ)
    Job DescriptionGRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/ Principal Scientist /Sr ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
    HireLifeScience (07/19/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls( Associate Director Equivalent) Our company's ... to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements.- - Principal ResponsibilitiesLead/contribute to… more
    HireLifeScience (07/30/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionJoin Our Team as an Associate Principal Scientist / Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... cross-functional teams to foster collaboration and innovation.Document Excellence: Author regulatory and technical documentation, ensuring all processes align with… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist / Associate Director, has primary responsibility for ... reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programsIn collaboration… more
    HireLifeScience (07/23/25)
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  • Merck & Co. (Rahway, NJ)
    …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 (07/26/25)
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  • Associate Principal Scientist

    Organon & Co. (Jersey City, NJ)
    **Job Description** **The Position** The Associate Principal Scientist ( Associate Director) is responsible for developing and implementing Regulatory ... with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead...projects and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
    Organon & Co. (07/22/25)
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  • Associate Principal Scientist

    Organon & Co. (Jersey City, NJ)
    …project teams and alliance partners to develop and implement world-wide regulatory strategies for assigned biosimilar projects, with a specific focus on ... Regulatory CMC (Chemistry, Manufacturing, and Controls) requirements. This role...development due diligence activities. **Responsibilities** + Provide global strategic regulatory CMC overview for respective products and portfolio. +… more
    Organon & Co. (07/30/25)
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  • Associate Principal Scientist

    Merck (Rahway, NJ)
    **Job Description** GRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/ Principal Scientist ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
    Merck (07/19/25)
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  • Associate Principal Scientist

    Merck (Rahway, NJ)
    **Job Description** Join Our Team as an Associate Principal Scientist / Associate Director in Biologics Drug Substance Commercialization! Are you ready to ... teams to foster collaboration and innovation. + Document Excellence: Author regulatory and technical documentation, ensuring all processes align with our company's… more
    Merck (07/24/25)
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  • Associate Principal Scientist

    Merck (Rahway, NJ)
    …Description** **Role Summary** + Under the guidance of a senior leader, an Associate Principal Scientist / Associate Director, has primary responsibility ... barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs + In… more
    Merck (07/23/25)
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  • Associate Principal Scientist

    Merck (Rahway, NJ)
    …process validation, second generation process development and authoring of regulatory submissions. Under the general scientific and administrative direction of ... next generation process development and characterization, process validation, and regulatory submission authoring **In this role, the successful candidate will… more
    Merck (07/17/25)
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  • Associate Principal Scientist

    Merck (Rahway, NJ)
    …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 (07/26/25)
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  • Sediment Remediation Practice Lead - Environmental…

    Burns & McDonnell (Morristown, NJ)
    **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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