• Sr . Specialist , RA

    West Pharmaceutical Services (Exton, PA)
    Sr . Specialist , RA Project Management Requisition ID: 66487 Date: Dec 8, 2024 Location: Exton, Pennsylvania, US Department: Regulatory Affairs ... and planet through our sustainability efforts. **Job Summary:** This Senior Specialist , Regulatory Project...execution of project objectives in line with regulatory affairs ( RA ) team's priorities.… more
    West Pharmaceutical Services (12/21/24)
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  • Sr Regulatory Affairs

    Globus Medical, Inc. (Audubon, PA)
    …possible. **Position Summary** **:** Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with ... Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking and control systems. Keeps… more
    Globus Medical, Inc. (12/21/24)
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  • Senior Quality Assurance Supplier…

    Catalent Pharma Solutions (Philadelphia, PA)
    …at least four years of experience + Strongly preferred degree in Regulatory Affairs , Biotechnology, Manufacturing, Operations, Supply Chain, Engineering or ... ** Senior Quality Assurance Supplier Specialist ** **Position...and stock materials and customer-requested specifications where applicable. The Sr . QA Supplier Specialist will also initiate… more
    Catalent Pharma Solutions (12/13/24)
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  • Clinical Research Monitoring Specialist

    University of Pennsylvania (Philadelphia, PA)
    …and resources, and much more. Posted Job Title Clinical Research Monitoring Specialist Senior (Cancer Center) Job Profile Title Clinical Research Monitoring ... Specialist Senior Job Description Summary The Abramson...IND/IDE in both adult and pediatric research. Must understand regulatory affairs and their applications to Quality… more
    University of Pennsylvania (10/03/24)
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  • Clinical Research Monitoring and Auditing…

    University of Pennsylvania (Philadelphia, PA)
    …regulations, GCP and IND/IDE in both adult and pediatric research. Must understand regulatory affairs and their applications to Quality Control and Quality ... Monitoring (DOCM) is seeking a The Clinical Research Quality Specialist , Sr . to support our clinical research...centers. Additional experience in clinical research ie Data Management, Project Management, Drug Safety are a strong plus. The… more
    University of Pennsylvania (12/08/24)
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  • OncoImmuno Cross Functional Area Intern

    J&J Family of Companies (Spring House, PA)
    …practices in data management to enable system level software designs Regulatory Affairs Associate: + Conducting a research project on a topic impacting the ... Delivery Unit and Trial Management, Portfolio Asset management, and Regulatory Affairs . As as ummer i ntern...will be expected to present their work to their project teams, the oncology or immunology Senior more
    J&J Family of Companies (11/23/24)
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