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
* 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 gillian.nicholson@collinsmcnicholas.ie
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