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Process Development Engineer

Job in Renfrew, Renfrewshire, PA4, Scotland, UK
Listing for: Terumo Aortic
Full Time position
Listed on 2026-09-14
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Process Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 40000 - 65000 GBP Yearly GBP 40000.00 65000.00 YEAR
Job Description & How to Apply Below

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
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