• Practice Manager

    Penn Medicine (Philadelphia, PA)
    …supervision and direction in regards to all administrative, financial, regulatory , quality , human resources, patient/employee satisfaction, and clinical ... all areas of accountability are compliant with all federal, state and local regulatory standards and requirements, including DOH, TJC, FDA , HIPAA, HCFA, DPW,… more
    Penn Medicine (11/04/25)
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  • Manager, Maintenance Mechanics - DPI

    United Therapeutics (Research Triangle Park, NC)
    …across multiple control systems. This role will ensure strict adherence to safety, quality and regulatory standards, and drive continuous improvement. + Manage ... pulmonary arterial hypertension ( **PAH** ). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung… more
    United Therapeutics (12/19/25)
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  • Manager, Clinical Affairs APM

    BD (Becton, Dickinson and Company) (Irvine, CA)
    …and managing clinical research activities that support product development, regulatory submissions, and commercialization. The position oversees the planning and ... cross-functional collaboration, and implementation of standardized processes to ensure high- quality clinical outcomes. This position requires strong leadership, organizational… more
    BD (Becton, Dickinson and Company) (12/19/25)
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  • Clinical Research Coordinator II, Thoracic…

    Cedars-Sinai (Beverly Hills, CA)
    …regarding data quality and study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse ... all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). Primary Duties and Responsibilities +… more
    Cedars-Sinai (12/17/25)
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  • Packaging Development Scientist IV

    Bayer (Myerstown, PA)
    …cGMPs) requirements. + Ensure processes are appropriately validated to conform to regulatory compliance ( FDA ) guidelines. Provides technical advice in the ... packaging operations; troubleshooting commercial packaging operations; and implementation of quality and cost improvement programs. Also, responsible to support the… more
    Bayer (12/16/25)
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  • Environmental Monitoring and Sampling Technician

    Mentor Technical Group (PR)
    …timely, efficient and compliant with corporate policies, SOPs, cGMP regulations, and regulatory agencies regulations ( FDA , EMEA). + Assures a streamlined and ... provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical… more
    Mentor Technical Group (12/13/25)
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  • Packaging Technician (GMP)

    Mentor Technical Group (Monroe, NC)
    …Practices). + Follow SOPs (Standard Operating Procedures), safety guidelines, and regulatory requirements. + Perform in-process quality checks to ensure ... biotech, or medical device industry). + Knowledge: + Familiarity with GMP, FDA , and regulatory requirements for packaging operations. + Understanding of… more
    Mentor Technical Group (12/10/25)
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  • Medical Device Packager

    Kelly Services (Kennesaw, GA)
    …Engineering, Quality Engineering, Operations Management, OEM, Customers, Physicians, Patients, FDA Inspectors, Regulatory Bodies, Auditors As part of our ... involves machinery operation, process monitoring, and teamwork to maintain high- quality production standards. **Key Responsibilities** + Perform and/or lead filling,… more
    Kelly Services (12/09/25)
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  • Regional RCM Manager

    ADM (Decatur, IL)
    …to build reliability competencies across the region. + Ensure compliance with food safety, quality , and regulatory standards (GMP, FDA , OSHA). + Collaborate ... fans, blowers, and material handling systems. + Knowledge of regulatory standards including GMP, FDA , and OSHA....to the outcome of the solution, we enrich the quality of life the world over. Learn more at… more
    ADM (12/05/25)
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  • Senior Scientist: IVD Assay Developer

    Nanobiosym, Inc. (Cambridge, MA)
    …+ Lead molecular diagnostic assay development in a hands-on manner through successful FDA submission + Manage and contribute to regulatory documents + Project ... managerial and leadership expertise in assay development + Strong understanding of FDA and global regulatory requirements + Prefer commercial assay experience… more
    Nanobiosym, Inc. (12/04/25)
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