• 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 (03/04/25)
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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 (04/29/25)
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  • Document Control Administrator II…

    ThermoFisher Scientific (Frederick, MD)
    …coat, ear plugs etc.) **Job Description** Join Thermo Fisher Scientific as a Document Control Administrator II for a meaningful career where your contributions ... 40 lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree… more
    ThermoFisher Scientific (04/12/25)
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  • Associate III, Manufacturing

    Catalent Pharma Solutions (Baltimore, MD)
    …Associate III Fill/Finish is responsible for supporting the overall GMP Fill/Finish manufacturing processes in accordance with Good Manufacturing Practices ... GMP ). Accountable for final formulation and filling for the...equipment for processing. + Ensure compliance with established internal control procedures. + Operate automated and semi-automated fill/finish equipment,… more
    Catalent Pharma Solutions (04/10/25)
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  • QA Specialist II - Quality Systems and Compliance

    Charles River Laboratories (Rockville, MD)
    …investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. This includes but is not limited… more
    Charles River Laboratories (05/11/25)
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  • QA Specialist II - Shift is 12pm - 10:30pm, Wed…

    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 (04/11/25)
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  • Director, Quality Systems

    Gilead Sciences, Inc. (Frederick, MD)
    control , deviations, corrective and preventative actions (CAPA), training, and document control . The Director will provide technical expertise and strategic ... change control , deviation management, CAPA, training, and document control . + Serves as the primary...regulatory submissions and on-site inspections related to quality systems. ** GMP Compliance and Quality Control :** + Ensure… more
    Gilead Sciences, Inc. (05/10/25)
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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 (04/29/25)
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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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  • Process Engineer - Equipment

    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 (04/30/25)
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  • Associate Process Engineer

    Perdue Farms, Inc. (Salisbury, MD)
    Document test results & conclusions, process parameters, critical control points and specifications. + Review engineering drawings, process sequence descriptions ... problems and implement effective solutions. Perform a robust situation assessment, document manufacturing methods, and procedures. + Analyze and trend data to… more
    Perdue Farms, Inc. (04/03/25)
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  • Process Engineer

    Perdue Farms, Inc. (Salisbury, MD)
    Document test results & conclusions, process parameters, critical control points and specifications. + Review engineering drawings, process sequence descriptions ... problems and implement effective solutions. Perform a robust situation assessment, document manufacturing methods, and procedures. + Analyze and trend data to… more
    Perdue Farms, Inc. (04/03/25)
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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 - Aseptic Filling

    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 (03/27/25)
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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 (04/02/25)
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  • Senior Controls Engineer

    TAI (Owings Mills, MD)
    …for a Senior Controls Engineer with a background in specifying, designing and programming control systems. **Here's a Taste of What You'll Be Doing:** + Research and ... of scope and additional services. + Coordinate all aspects of project document completion. + Direct contributing engineers and CAD designers for the preparation… more
    TAI (02/15/25)
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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. (04/15/25)
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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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  • Sr. Manufacturing Operator, 6p-6:30a, 12 Hours, TR…

    Terumo Medical Corporation (Elkton, MD)
    …Quality System; including but not limited to: process controls, inspection procedures, document /data control , and change control practices. 14. Participates ... technology by providing improvements and stabilization to the process. 7. Set, control , and confirm process parameters. 8. Properly package plastic component within … more
    Terumo Medical Corporation (03/13/25)
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