Validation Engineer Permanent or SubContractor Opportunity We are seeking a talented Validation Engineer to join our team, where youll have the opportunity to support cutting-edge projects and make a real impact on product quality and compliance for our client based in the Midlands. This position is available on either a permanent basis or through a subcontract arrangement, offering flexibility for the right candidate. Responsibilities: As a Validation Engineer, you will: Write and execute process validation protocols and reports for new product introductions and revalidations. Support continuous improvement through Lean Six Sigma methodologies. Drive compliance with ISO 13485 and ISO 14001 standards. Lead and participate in cross-functional teams, including vendor liaison on key projects. Conduct risk assessments and root cause analyses, implementing corrective actions via change management. Review and execute FAT and SAT protocols. Directly support GMP and regulatory audits. Deliver training and mentor colleagues to strengthen validation knowledge across the business. Perform data analysis to guide informed decision-making and improvements. Requirements: Third-level qualification in Engineering, Polymer Science, or equivalent manufacturing experience. Minimum 2 years experience as a Validation Engineer in injection moulding or medical device manufacturing. Strong background in statistical analysis (Minitab), SPC, and validation methodologies. Excellent communication, interpersonal, and influencing skills. Hands-on experience in problem solving (FMEA, Fishbone diagrams, 5 Whys, etc.). Why Join? Be part of an innovative, dynamic team driving new product introduction and process excellence. Work in a regulated, high-quality environment with opportunities to expand your expertise. Flexible engagement options: join on a permanent basis or as a subcontractor to suit your career path. For more details on the position reach out to Gillian Nicholson Skills: validation validation engineer polymer