• Diagnostic XRay Supervisor

    Penn Medicine (Plainsboro, NJ)
    …responsible for the daily workflow for his/her assigned area to support quality patient care. Assists Radiology leadership in the day-to-day technical operation of ... associate director, radiology director, medical staff, and administration to ensure that quality patient care is delivered. Actively supervises the quality of… more
    Penn Medicine (09/03/25)
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  • Facilities Maintenance Associate II

    University of Colorado (Aurora, CO)
    …scheduling as per Gates Biomanufacturing facilities' standard operating procedure to meet FDA good manufacturing practice (GMP) compliance . + Participate in new ... **Job Summary:** Key Responsibilities: **Project Management, Process Improvement & Regulatory Compliance - 10%** + Evaluate and ensure traceability and status… more
    University of Colorado (08/20/25)
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  • Scientist / Sr. Scientist, Analytical Development

    Cambrex High Point (Waltham, MA)
    …Strong working knowledge of GMP requirements, ICH guidelines, and regulatory expectations ( FDA , EMA). + Experience in quality control testing, stability ... manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career...tests as required to support product release, stability, and compliance . + Author and review analytical protocols, reports, and… more
    Cambrex High Point (08/14/25)
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  • Lead Clinical Laboratory Scientist

    Veterans Affairs, Veterans Health Administration (Phoenix, AZ)
    compliance with rules and regulations of assorted regulatory agencies such as CAP, FDA , JC, AABB, and OSHA. Coordinates quality control activities with the ... Quality Manager, Laboratory Manager, Regional Technical Specialist, National Quality and Compliance Agent, Regional Program Manager, Regional Director,… more
    Veterans Affairs, Veterans Health Administration (07/31/25)
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  • Distribution Associate, Inbound

    Glenmark Pharmaceuticals Inc., USA (Allentown, PA)
    …returns adhering to company policies, procedures, and documentation requirements + Maintain FDA and DEA regulatory compliance by ensuring cleanroom integrity and ... Management System (WMS) for real-time inventory control and traceability. support the Quality and Customer Service teams in resolving Inventory issues using SAP, WMS… more
    Glenmark Pharmaceuticals Inc., USA (07/18/25)
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  • Manager, CSV & Data Integrity

    Charles River Laboratories (Memphis, TN)
    …Administrators of computerized systems/laboratory instrumentation. Coordinate with operations, quality assurance, information technology, and vendor staff, to assure ... structure, staffing requirements and succession plans. * Work closely with Operational, Quality Assurance and IT staff to promote the understanding of * computerized… more
    Charles River Laboratories (09/13/25)
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  • Milk Receiver

    Actalent (East Syracuse, NY)
    …Description The Raw Lab Milk Receiver plays a crucial role in ensuring the quality and compliance of dairy products. This position involves receiving trailers of ... bulk products and testing raw and heat-treated dairy ingredients to meet FDA and NYS regulations. The role supports the manufacturing of dairy-related products by… more
    Actalent (09/09/25)
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  • Environmental Health and Safety Specialist

    Charles River Laboratories (Cambridge, MA)
    …RESPONSIBILITIES: + Establish, administer, and update specific EH&S programs for compliance with state and federal Occupational Safety and Health Administration ... on safety and environmental issues. Review new regulatory standards and make compliance recommendations. + Inspect the facilities for compliance with OSHA… more
    Charles River Laboratories (09/04/25)
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  • Director of Monitoring, Ethics and Business…

    Sanofi Group (Morristown, NJ)
    …including email monitoring, live monitoring activities, and other projects in compliance with pharmaceutical industry regulations and company policies. As a Monitor ... the Ethics & Business Integrity department at Sanofi, you will lead compliance monitoring activities within the US Monitoring Team. This pivotal role collaborates… more
    Sanofi Group (08/01/25)
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  • Associate Director, Inspection Readiness

    Bristol Myers Squibb (New Brunswick, NJ)
    …* Monitor and assess global regulatory inspection outcomes, enforcement actions, quality and compliance metrics, and external signals, leveraging these ... advance benchmark inspection readiness and support a culture of quality and compliance . * Perform comprehensive on-site...have worked for the US Food & Drug Administration ( FDA ), within the past 10 years (2015-2025) in a… more
    Bristol Myers Squibb (09/12/25)
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