Validation Engineer – Permanent or SubContractor Opportunity
We are seeking a talented Validation Engineer to join our team, where you’ll 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
