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    • This opportunity invites professionals to register their interest in future System Validation Engineer roles focused on Class III medical device validation and…
    • Ensure service provided is invoiced if not under warranty.
    • Experience in the Field service and/or hospital environment.
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    • System Validation Engineers in medical device settings could play a critical role in ensuring that Class III devices meet rigorous regulatory standards before…
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Job Post Details

System Validation Engineer - job post

SThree
3.3 out of 5 stars
Birmingham
£300 - £400 a day - Fixed term contract
You must create an Indeed account before continuing to the company website to apply

Job details

Pay

  • £300 - £400 a day

Job type

  • Fixed term contract

Location

Birmingham

Full job description

This opportunity invites professionals to register their interest in future System Validation Engineer roles focused on Class III medical device validation and compliance. These positions centre on ensuring that sophisticated medical devices meet rigorous regulatory standards through comprehensive testing and validation protocols across development and manufacturing lifecycles.

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

About the opportunity

This is an opportunity to register your interest in future System Validation Engineer positions within Class III medical device development and manufacturing environments. Roles of this type would support the delivery of life-changing technology by ensuring that devices meet stringent regulatory requirements under ISO 13485 and IEC 62304, with potential involvement across design verification, design validation and ongoing quality assurance activities.

Typical role overview

  • Location: Birmingham, West Midlands, England
  • Type: Contract · Full-time
  • Rate: £300–400 per day
  • Domain: Class III Medical Device · Validation & Compliance · ISO 13485 & IEC 62304

What you would do

Typical responsibilities could include:

  • Developing and executing test protocols and validation plans aligned with IEC 62304 and ISO 13485 requirements
  • Conducting functional, performance and safety testing across hardware, software and integrated systems
  • Documenting test results, traceability matrices and validation reports for regulatory submission
  • Supporting design verification and design validation activities throughout the product development lifecycle
  • Collaborating with engineering, quality and regulatory teams to ensure compliance with Class III medical device standards
  • Contributing to continuous improvement of validation processes and procedures
  • Identifying and reporting deviations, non-conformances and potential risks during testing and validation activities

What you could bring

Most roles of this type require the following:

  • Bachelor's degree in Computer Science, Engineering or a related technical discipline
  • Working knowledge of ISO 13485 (Medical Device Quality Management) and IEC 62304 (Medical Device Software Lifecycle)
  • Experience with Class III medical device validation, testing or quality assurance
  • Proficiency in test planning, test execution and technical documentation
  • Familiarity with design controls, traceability and regulatory compliance frameworks
  • Strong analytical and problem-solving capabilities
  • Authorization to work in the United Kingdom

Nice-to-have qualifications could include:

  • Additional certifications in quality management or medical device compliance
  • Experience with specific validation tools or test automation platforms
  • Exposure to FDA or international regulatory submission processes
  • Understanding of risk management frameworks such as ISO 14971

What roles of this type could offer

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

  • Engagement in mission-critical validation work that directly supports patient safety and regulatory compliance
  • Exposure to sophisticated Class III medical device technologies and regulated development environments
  • Potential to develop deep expertise in medical device validation standards and best practices
  • Collaboration with experienced engineering and quality teams
  • Clear technical progression and skill development in a specialized, high-impact domain
  • The flexibility and variety that contract-based engagement can provide

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.

Disclaimer:
Please note that the content of this advert does not represent a live vacancy or any guarantee of future vacancies, and by responding to this advert you agree to us adding your details to our database for future opportunities.

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