• 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 (07/23/25)
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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 (07/25/25)
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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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  • 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 (07/16/25)
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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. (07/03/25)
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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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  • 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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