***Drug screen & criminal background check will be required POSITION SUMMARYThe QA Documentation Assistant supports quality assurance documentation and release activities within a GMP-regulated manufacturing environment. This role is responsible for auditing manufacturing and packaging records, ensuring compliance with cGMPs, SOPs, and plant quality standards, and supporting timely production release.REQUIRED QUALIFICATIONS•   High School diploma or GED with at least 5 years of document review or auditing experience in a cGMP environment•   Strong PC skills; proficiency with Microsoft Office•   Experience using SAP, MES, or similar automated inventory systems•   Demonstrated ability to interpret records, perform accurate calculations, and maintain organized documentation•   Strong communication and interpersonal skills•   Ability to lift 50 lbsRESPONSIBILITIES•   Audit manufacturing and packaging documentation for GMP and quality compliance•   Review batch manufacturing and packaging records for accuracy, completeness, and calculations•   Assign material disposition and support release of intermediates and packaging components•   Issue and reconcile manufacturing, packaging, and QC laboratory documentation•   Write, revise, and maintain SOPs within area of responsibility•   Support document control, filing, and maintenance of batch record archives•   Coordinate priorities with documentation auditors, production, QA, and supply chain teams•   Maintain quality databases, reports, and release tracking tools**Only those lawfully authorized to work in the designated country associated with the position will be considered.** **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.** Employment Type: TEMPORARY