Project Engineer Medical Devices jobs

Validation Engineers in medical device environments play a critical role in ensuring that complex systems and processes meet rigorous regulatory standards and perform reliably in the field. This is an opportunity to register your interest in future Validation Engineer positions where you could contribute to the delivery of Class III medical devices under ISO 13485 and IEC 62304, supporting products that reach patients who depend on them.

Please note the content of this advert does not represent a live vacancy.

About the opportunity

Roles of this type may sit within regulated, quality-focused engineering teams responsible for validating system design, manufacturing processes and real-world performance across Class III medical device programmes. You could work on late-stage validation activities, supporting the transition from design verification through to commercial release, with scope to coordinate across engineering, quality and regulatory functions to ensure compliance and product safety.

Typical role overview

• Location: Birmingham, West Midlands, England — on-site
• Type: Contract · Full-time
• Rate: £300–400 per day
• Domain: Class III medical device · ISO 13485 · IEC 62304

What you would do

Typical responsibilities could include:

• Planning and executing validation protocols aligned to ISO 13485 and IEC 62304 requirements
• Designing test strategies and validation studies to demonstrate system performance and safety
• Coordinating validation activities across engineering, manufacturing and quality teams
• Documenting validation results, analysis and traceability to regulatory requirements
• Supporting regulatory submissions and responses with validation data and evidence
• Contributing to design reviews, risk assessments and process improvements
• Maintaining validation records and supporting external audits and inspections

What you could bring

Most roles of this type require the following:

• Bachelor's degree in Computer Science, Engineering or a related scientific discipline
• 2–4 years' validation, quality assurance or test engineering experience in a regulated environment
• Working knowledge of ISO 13485, IEC 62304 and Class III medical device validation
• Familiarity with design controls, design verification, design validation and design transfer
• Experience with validation planning, protocol design and statistical analysis
• Strong attention to detail, documentation discipline and regulatory compliance mindset
• Ability to work independently and coordinate across multiple functional teams

What roles of this type could offer

Most roles of this type offer the following, dependent on the industry and seniority of the role:

• Exposure to end-to-end validation of life-critical medical devices
• Opportunity to build deep expertise in regulated validation methodologies and standards
• Involvement in bringing Class III devices through to commercial release
• Potential to progress toward senior validation or quality leadership roles
• Professional development in a structured, compliance-focused environment
• Contract flexibility and the opportunity to work on diverse programmes across the medical device sector

About SThree

SThree is the global STEM workforce consultancy.
We advise businesses, build expert teams and deliver project solutions to outpace tomorrow, together.

Across the UK, we connect talented specialists with cutting-edge opportunities across technology, engineering, life sciences and financial services supported by our offices in London, Birmingham, Manchester, Glasgow and Leeds

How to register interest

If you are interested in being added to our database to be considered for future opportunities, registering is quick and easy. No cover letter required. We will be in touch when we are instructed on these roles to discuss the next step in your career.