• Senior Microbiology Analyst

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …and/or preventive actions and implements these actions within the laboratory. + Performs GMP review of test data to ensure that test results meet all ... is in a fast-paced, FDA regulated environment in the Pharmaceutical Industry. This role is mainly responsible for completing...test procedures + Perform data analysis, compile data and generate reports for management review .… more
    Glenmark Pharmaceuticals Inc., USA (07/24/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Topeka, KS)
    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 ... (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contributes to content as needed + Advises team… more
    Sumitomo Pharma (09/09/25)
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  • Strategic Account Manager - Remote ( digital…

    AssistRx (Orlando, FL)
    The Senior Account Manager cultivates and maintains AssistRx's relationship with our Pharmaceutical manufacturing partners. In this role, you'll be working with ... pharmaceutical executives (Associate Director and above) on a daily...* Experience with reviewing and providing insights on healthcare data analysis and reporting Responsibilities + Forms strategic partnership… more
    AssistRx (09/10/25)
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  • NA Sr Manager QS and Perf Monitoring

    J&J Family of Companies (Titusville, NJ)
    …LOCs, providing in-depth data analysis of product information including complaint data . Prepare annual Quality Review for Puerto Rico. Ensure compliance ... Canadian Janssen commercial companies. This includes: + Quality System Management Review (QSMR) Lead for the North American Region including commercial businesses… more
    J&J Family of Companies (09/05/25)
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  • Manager, Microbiology

    Curia (Albuquerque, NM)
    …interactions, site metrics meetings, site-wide improvement projects, budgeting, and data review and interpretation, including protocols, investigations, and ... (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to...monitoring systems and equipment + Ensures proper recording and review of data + Test the integrity… more
    Curia (07/25/25)
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  • Research Assistant/Associate Professor (Proteomics…

    University of Maryland, Baltimore (Baltimore, MD)
    …or Research Associate Professor, non-tenure track, in the Department of Pharmaceutical Sciences.Theprimary scope of the position is to perform experimental research ... CONTROLS_* This position is responsible to the Chair of the Department of Pharmaceutical Sciences with research reporting responsibility to the Director of the Mass… more
    University of Maryland, Baltimore (07/16/25)
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  • Post-Doctoral Regulatory Affairs Fellow - Policy…

    Boehringer Ingelheim (Ridgefield, CT)
    …competencies necessary to contribute to their respective functional area within a pharmaceutical company. The Fellow will be based at Boehringer Ingelheim's US ... of the broad range of opportunities available to a pharmacist in the pharmaceutical industry. As an employee of Boehringer Ingelheim, you will actively contribute to… more
    Boehringer Ingelheim (08/30/25)
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  • Director Regulatory Compliance

    Charles River Laboratories (Wayne, PA)
    …regulatory auditors prepare appropriate summaries and reports of such audits. ⦁ Review and endorse regulatory and client audit responses and corrective action ... applications, supplements, annual reports, and master files. ⦁ Participate in the review and development of quality agreements with clients and contract service… more
    Charles River Laboratories (06/19/25)
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  • Quality Control Analyst III

    Curia (Rensselaer, NY)
    …needed, troubleshoot issues + Participate in or assist with test method validations + Evaluate data for trends and review data + Support supervisors in OOS ... author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools +… more
    Curia (08/08/25)
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  • Executive Director of R&D Global Quality (Remote)

    Otsuka America Pharmaceutical Inc. (Albany, NY)
    …the R&D audit program, engage with regulatory authorities, and maintain clinical data integrity. The leader will be responsible for providing a compelling vision ... and Risks will be reported periodically to Senior Management through the Management Review process to ensure alignment with Company policy and strategy and gain a… more
    Otsuka America Pharmaceutical Inc. (09/12/25)
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