Contract QA Validation Engineer - Sterile Pharma (Swindon) £55-£65 per hour | 3-6 Month Contract (Potential Extension) Are you a meticulous QA Validation Engineer with a strong background in sterile pharmaceutical manufacturing? We're seeking an experienced contractor to join our team in Swindon as a Document Reviewer for Commissioning, Qualification, and Validation (CQV) activities. This is an excellent opportunity to apply your expertise in a critical role, ensuring compliance and quality in a dynamic environment. About the Role: As a key member of our team, you'll be responsible for the comprehensive review and assessment of CQV documents for a range of equipment used in sterile pharmaceutical manufacturing. Your sharp eye for detail will be crucial in identifying discrepancies and ensuring all documentation adheres to the highest industry standards. What You'll Be Doing: Thoroughly review and assess commissioning, qualification, and validation documents for various sterile pharmaceutical manufacturing equipment. Ensure all documentation strictly complies with cGMP, FDA regulations, and other relevant industry standards. Proactively identify and document any discrepancies, gaps, or non-conformities within CQV documents. Provide clear, actionable recommendations for corrective actions and improvements to maintain compliance and quality. Collaborate effectively with cross-functional teams, including eng...