Were seeking aValidation Engineer to support a high-impact project with our Global Biologics client, ensuring compliance and validation of cutting-edge equipment, systems, and processes in a cGMP environment. This is a fantastic opportunity to work with a global leader in pharmaceuticals and contribute to critical validation lifecycle activities. Key Responsibilities: ? Execute and document FAT/SAT/IOQ protocols. ? Design and manage validation studies for equipment/processes (aseptic processing, lyophilisation, sterilisation, etc.). ? Ensure adherence to FDA/EU regulations, GAMP, ISPE, and AAMI/ANSI standards. ? Maintain validation documentation and support Site Change Control. ? Troubleshoot validation issues and collaborate cross-functionally. Ideal Candidate: ?Education: Degree in Science (Chemistry, Microbiology, Pharmacy) or Engineering (Chemical/Mechanical/Electrical). ?Experience: 3-5 years in healthcare/pharma manufacturing, with validation/product development expertise. ?Technical Skills: Knowledge of steam/dry heat validation, GMP, and quality management systems. Familiarity with pack lines, autoclaves, or fill lines is a plus. ?Soft Skills: Adaptable, pragmatic problem-solver with strong communication and project management skills. Skills: Document Execution Validation Studies Steam/Dry Heat Validation GMP Autoclaves Filling Lines