Job Opportunity: QA Validation Engineer Location: SwindonContract Type: Temporary (Inside IR35)Duration: 3 to 6 months (with potential for extension)Working Pattern: Full Time, 40 hours per week, 8:30am - 5:00pm (30-minute unpaid lunch break)Hourly Rate: 26.44 - 31.23 per hour (equivalent to 55,000 - 65,000 per annum)Start Date: ASAPAre you ready to take your career to the next level in the dynamic world of pharmaceuticals? Our client is urgently seeking a QA Validation Engineer with a passion for ensuring top-notch quality in sterile pharmaceutical manufacturing! Join a vibrant team in Swindon and make a significant impact on a high-profile project.What You''ll Do:As a QA Validation Engineer, you will be at the forefront of quality assurance within a sterile manufacturing environment. Your responsibilities will include:Reviewing and Assessing: Evaluate CQV documentation for equipment used in sterile manufacturing.Compliance Checks: Ensure all documentation meets cGMP, FDA, and other relevant regulatory standards.Identifying Issues: Spot gaps, discrepancies, and non-conformities in validation documents.Recommending Solutions: Propose corrective actions and quality enhancements.Collaborating: Work closely with Engineering, QA, and Operations teams to resolve documentation challenges.Maintaining Records: Keep accurate, timely records of document reviews.Staying Updated: Keep abreast of evolving regulatory and industry best practises related to sterile manufacturing.What You Bri