• 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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  • Manager, QA Document Control

    Catalent Pharma Solutions (Harmans, MD)
    …are met and leading continuous improvement initiatives. The Document Control function supports both the GMP and development operations. Catalent, ... support Phase I/II/III/commercial operations. + Manages document control processes and systems for GMP activities...document control processes and systems for GMP activities in compliance with internal procedures and policies,… more
    Catalent Pharma Solutions (06/24/25)
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  • Quality Control Technician

    Adecco US, Inc. (Sterling, VA)
    Control Technician include but are not limited to:** + Conduct and document food quality control inspections + Monitor employee hygiene and Good ... Adecco is assisting a local client recruiting for **Quality Control Technician** opportunities in **Sterling, VA** . This is...Manufacturing Practices ( GMP ) + Collect samples for testing and assist with… more
    Adecco US, Inc. (06/17/25)
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  • QA Specialist II - Shift is 12pm - 10:30pm, Sun…

    Charles River Laboratories (Rockville, MD)
    …including investigation/deviation management, CAPA tracking, Effectiveness Verification, change control , internal and external audits. This position will facilitate ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. **Key Responsibilities and Duties:** *… more
    Charles River Laboratories (06/14/25)
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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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  • Manager, Sterility Assurance

    Catalent Pharma Solutions (Harmans, MD)
    …development and implementation of the site Sterility Assurance Program. + Develop, document and manage microbial control strategy for production processes from ... audit observations, aseptic trainings, DE study and sterility assurance/contamination control related GMP documentations. + Drive continuous improvement… more
    Catalent Pharma Solutions (06/24/25)
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  • Senior Computer Systems Validation Engineer

    Catalent Pharma Solutions (Harmans, MD)
    …recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders ... critical computer systems and laboratory documentation to support the commercial GMP manufacturing of biological drug substance and drug product. Responsibilities… more
    Catalent Pharma Solutions (06/25/25)
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  • Manager, QA Systems

    Catalent Pharma Solutions (Harmans, MD)
    …: + Serve as the QA-CSV liaison with the Engineering, Quality Control , IT and Validation organizations to support SaaS enterprise computer systems validation ... and LES modules, Electronic Laboratory Notebook (ELN), OpenText Documentum Electronic Document Management System (EDMS), MODA Software, JDE Edwards etc. + Design… more
    Catalent Pharma Solutions (04/16/25)
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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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  • Principal Engineer, Equipment Process

    Catalent Pharma Solutions (Harmans, MD)
    …Quality Systems to implement equipment, facility, and automation change control , document revisions, and conduct equipment/system/instrumentation failure ... recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders… more
    Catalent Pharma Solutions (06/26/25)
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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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  • Building Management Technician

    TAI (Frederick, MD)
    …maintenance program. + Identify and recommend initiatives for continuous improvement. + Document and review GMP maintenance activities in SAP. + Assisting ... What You'll Be Doing:** + Painting, drywall, cleaning, pest control , light plumbing work, light door repairs and adjustments,...cGMP regulations, FDA, USP and ISPE guidelines + Champion GMP compliance and maintenance best practices to support a… more
    TAI (06/17/25)
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  • Sr Packaging Controls Engineer

    Florida Crystals Corporation (Baltimore, MD)
    …instrumentation and control systems in support of plant production, quality, GMP and safety goals. Design and implement changes to the instrumentation and ... control systems in the plant. This person will also...information systems through security and redundant system backups. + Document and develop systems for consistency. + Provide operation,… more
    Florida Crystals Corporation (06/27/25)
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  • Senior IT Engineering Specialist

    Gilead Sciences, Inc. (Frederick, MD)
    …and administration of computer systems and lab instruments in a regulated GMP environment. + Provide maintenance and support requests to address IT operational ... IT teams to deliver innovative, scalable, and compliant IT solutions. + Document user and functional requirements. + Support IT architecture by working closely… more
    Gilead Sciences, Inc. (06/08/25)
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  • Associate Scientist, QC Microbiology

    Catalent Pharma Solutions (Harmans, MD)
    …of ISO, USP, EU, CFR, cGMP, and GLP in the Microbiology laboratory and GMP Cleanrooms at all times. + Document Environmental Monitoring results utilizing Good ... The **Associate Scientist** will assist with the end-to-end contamination control and sterility assurance practices for Catalent's aseptic production process. This… more
    Catalent Pharma Solutions (07/03/25)
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  • Quality Assurance Supervisor

    TreeHouse Foods, Inc. (Cambridge, MD)
    …Allergen Control , Non-Conforming Products, Recalls, Food Safety Plans, and pest control systems. + Conduct GMP and sanitation audits and summarize technical ... attempt to impersonate our company by sending fake job offers, interview, and sensitive document requests. If you receive an email claiming to be from us, always… more
    TreeHouse Foods, Inc. (04/23/25)
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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 (04/19/25)
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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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  • 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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