Description
Thermo Fisher Scientific is hiring a QA Validation & Qualification Documentation Reviewer in Swindon to review qualification and validation documentation across GMP activities. The role assesses completeness, accuracy, traceability, data integrity, deviations, change controls, and alignment with approved procedures and GMP requirements; supports QA review and approval workflows; collaborates with cross-functional teams; and escalates complex technical, regulatory, scientific, or data integrity concerns. The position requires a science-based degree, pharmaceutical validation document-review experience, knowledge of process and cleaning validation, statistical software, EU/US GMP regulations, and technical writing skills.
