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Quanta part of QCS Staffing | Central London, United Kingdom | Posted June 21, 2026
Position Overview
Key responsibilities
:
The final review of clinical batch records to ensure compliance with GMP and conformance with regulatory filings. Compilation and approval data packs and presentation to the QP for final release. Work closely with global functions supporting the clinical supply chain, as well as clinical manufacturing sites internally and externally. Experience required: Excellent communication skills An ability to manage issue resolution Confidence to work with minimal supervision Existing experience in a QA role in a GMP environment If this role is of interest to you, please apply now!
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