Process Development Engineer

We are recruiting a Process Development Engineer to support the successful transfer of new medical device products from R&D into full-scale manufacturing. This role plays a key part in ensuring design intent, quality, regulatory compliance and operational efficiency are maintained through validation and into commercial production.

Working cross-functionally with R&D, Quality, Operations, Supply Chain and Regulatory teams, you will help deliver robust, repeatable and scalable manufacturing processes within a highly regulated medical device environment.

Key responsibilities

• Support product transfer from development into manufacturing, ensuring process, documentation and resource readiness


• Develop, optimise and validate manufacturing processes, work instructions and processing methods


• Support Design for Manufacturability (DfM) activities early in the product lifecycle


• Develop and execute process validation strategies in line with regulatory standards (e.g. FDA 21 CFR 820, ISO 13485)


• Define and execute equipment qualification activities


• Conduct risk management activities, including PFMEA, and drive mitigation actions


• Lead root cause analysis and corrective/preventive actions during pilot builds and early production


• Generate technical and regulatory documentation including validation protocols, reports and process specifications


• Maintain audit readiness and ensure alignment with Quality Management System requirements


• Support pilot builds, manufacturing scale-up and external supplier process development


• Carry out additional duties in support of departmental and site objectives

What we’re looking for

• Minimum of HND (or equivalent) in a relevant engineering discipline


• Experience working in a regulated manufacturing environment, ideally medical devices


• Strong understanding of process design and industrialisation


• Experience with process validation, statistical methods and Six Sigma tools


• Exposure to New Product Introduction (NPI) or design transfer activities


• Working knowledge of ISO 13485 and FDA Quality System Regulations


• Ability to develop process solutions including jigs, fixtures, tooling and equipment


• Strong problem-solving capability with a structured, data-driven approach


• Excellent communication skills and ability to work effectively in cross-functional teams


• High attention to detail with disciplined documentation practices


• Proactive, results-driven mindset with clear ownership of deliverables