QA Associate Location: Slough (Fully Onsite) Contract Length: 9 months (with potential to extend) Pay Rate: £21.92 per hour Role Purpose & Scope As a member of the QA Operations Documentation Control Team, your primary responsibility will be to perform Batch Consolidation (auditing) for QC Biochemistry and Microbiology testing activities related to Drug Product (DP) and Drug Substance (DS). You will ensure all QC testing activities are complete and meet release specifications. You will also proactively issue GMP documents and labels to Manufacturing in line with schedules and timelines. Key Responsibilities Coordinate and perform batch consolidation for QC Biochemistry and Microbiology testing. Ensure all testing activities are complete and meet release specifications. Issue GMP documents and labels to Manufacturing, ensuring accuracy and timeliness. Liaise with internal departments to gather required information and maintain effective communication. Support QA Operations in continuous improvement of quality systems and processes. Assist in audit preparation and provide documentation during audits. Lead and manage quality records (Deviations, CAPAs, Change Controls, Investigations). Author, review, and approve GMP documentation. Maintain the archiving system and coordinate document retrieval. Ensure training compliance and maintain an up-to-date training profile. Prioritise workload to meet strict deadlines and supp...