• GMP Document Control

    ManpowerGroup (Rockville, MD)
    Our client, a leader in the pharmaceutical industry, is seeking a Pharma Document Control Associate to join their team. The ideal candidate will have strong ... will align successfully in the organization. **Job Title:** Pharma Document Control Associate **Location:** Rockville, MD **Pay...per respective SOP. + Archive and maintain GLP and GMP documents with an accurate inventory, both on and… more
    ManpowerGroup (06/03/25)
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  • QA Specialist I - Quality Systems

    Charles River Laboratories (Rockville, MD)
    …investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as ... industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Key Responsibilities and Duties: Establishes… more
    Charles River Laboratories (05/22/25)
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  • QA Specialist II - Shift is 12pm - 10:30pm, Wed…

    Charles River Laboratories (Rockville, MD)
    …and labels to manufacturing departments by verifying the accuracy and completeness from QA Document Control * Ensure SOPs are current and effective, and staff ... compile the batch record review records and batch disposition documents required for GMP operation on timely basis. Key Responsibilities and Duties: * Provide QA… more
    Charles River Laboratories (07/11/25)
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  • Verification Scientist IV

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …related to current Good Manufacturing Practice (cGMP) site audits, quality control and manufacturing (QCM) product documentation reviews, and test design for ... + Conducts thorough review and evaluation of QCM [i.e., quality control and manufacturing] documents and other data received from pharmaceutical, ingredient… more
    The US Pharmacopeial Convention (USP) (05/07/25)
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  • Senior Manager, Verification Programs

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …related to current Good Manufacturing Practice (cGMP) site audits, quality control and manufacturing (QCM) product documentation reviews, and test design. In ... Manufacturing Practice (cGMP) facilities engaged in the manufacturer and/or quality control of dietary supplements and/or pharmaceuticals. * Knowledge of and… more
    The US Pharmacopeial Convention (USP) (04/30/25)
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  • Quality Operations Supervisor

    Charles River Laboratories (Rockville, MD)
    …Records (BPRs) and associated supporting documentation including logbooks, Quality Control (QC) testing reports, environmental monitoring reports, etc. * Support ... to drive completion * Create, review and approve documents in electronic document management systems * Serve as QOps representative for client project teams… more
    Charles River Laboratories (05/22/25)
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  • Technical Trainer I

    Charles River Laboratories (Poolesville, MD)
    …Maryland. As the **Technical Trainer I** , you will develop, deliver, document , and report technical skills training programs involving both small and large ... regulations. Additional responsibilities include: + Direct, schedule, perform and document all relevant Task-specific technical, husbandry and administrative training… more
    Charles River Laboratories (07/19/25)
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  • Sr. Supply Chain Coordinator

    Charles River Laboratories (Hanover, MD)
    …meet specifications, standards, cost-efficient, with adequate supply for testing. + Document inventory properly and communicate any issues with upper management ... + Manage, log, assign lot numbers (as applicable) and appropriately document all Receipt (incoming) and Shipment (outgoing) of materials, documents, testing… more
    Charles River Laboratories (05/17/25)
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  • Technical Trainer

    Charles River Laboratories (Bethesda, MD)
    …site in Bethesda, MD. As the Technical Trainer you will develop, deliver, document , and report technical skills training programs involving both small and large ... by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment.… more
    Charles River Laboratories (07/16/25)
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  • Project Manager I (Cagewash Manager)

    Charles River Laboratories (Bethesda, MD)
    …visits would also be a responsibility of this position. + Identify, document , and/or report environmental or cagewash abnormalities. + Use of computer programs ... by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment.… more
    Charles River Laboratories (06/11/25)
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