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# Test Technician / Test Specialist - Leeds, UK

- **Company:** Vita Global Sciences
- **Location:** Leeds, United Kingdom
- **Experience:** Starter
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Computational Fluid Dynamics, Document Management Systems, Laboratory Information Management Systems, Verification and Validation (Software), Test Data, 21 CFR Part 820 Quality System Regulation, Modeling and Simulation
- **Published:** October 15, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=bac9b0e0066aa0c7

## About the Role

Test Technician / Test Specialist - Medical Devices Location: Leeds, United Kingdom Employment Type: Full-time, On-site (with some flexibility) Our client, a global leader in the medical device industry, is seeking a motivated Test Technician / Test Specialist to join their product testing and verification team in Leeds. This is an exciting opportunity to work hands-on with cutting-edge medical technologies, collaborating closely with experienced engineers and scientists in a highly regulated, innovative environment. This position is ideal for professionals aiming to advance toward roles such as Product Test Engineer, Verification & Validation (V&V) Engineer, or Mechanical Test Engineer. It offers valuable exposure to product lifecycle development, ISO/FDA compliance, and computational modelling as part of the verification process. Key Responsibilities * Plan, coordinate, prepare, and execute mechanical product tests in collaboration with Senior Test Engineers. * Conduct routine
and complex mechanical and functional testing activities independently, ensuring adherence to SOPs, ISO standards, and FDA/UK regulatory requirements. * Evaluate and interpret test data, prepare test protocols and reports, and maintain records within laboratory information management systems (LIMS). * Support the development and validation of new test methods, and contribute to the creation and revision of standard operating procedures (SOPs). * Utilise computational modelling and simulation tools to support test planning, data interpretation, and product performance prediction. * Maintain and update test documentation within the document management system. * Collaborate with R&D, Quality, and Manufacturing teams to ensure all testing deliverables meet project timelines and regulatory standards. * Participate in continuous improvement initiatives, driving efficiency, accuracy, and innovation in the test environment. Profile & Qualifications * Completed apprenticeship (e.g.
Mechanical / Laboratory Technician) or Bachelor's/Master's degree in Biomedical Engineering, Mechanical Engineering, Materials Science, or a related discipline. * 1-2 years of relevant experience in product testing, verification & validation (V&V), or medical device testing. * Hands-on experience with mechanical testing equipment, measurement tools, and data acquisition systems. * Exposure to or interest in computational modelling (e.g., FEA, CFD, or other simulation tools) is strongly preferred. * Working knowledge of ISO 13485, ISO 14155, or FDA 21 CFR Part 820 standards is an advantage. * Strong attention to detail, analytical thinking, and problem-solving skills. * Excellent written and verbal communication skills in English. * Proactive, team-oriented mindset with the ability to work effectively in a fast-paced and regulated environment. What's Offered * Opportunity to work for a world-class medical technology company developing life-changing products. *
Competitive salary and comprehensive benefits package. Must haves/ Nice haves: From discission but still pending formal JD Must-Haves Hands-on functional and mechanical testing experience - proven ability to plan, execute, and interpret physical tests. Understanding of verification and validation processes - especially in regulated or high-quality environments. Applied experience in computational modeling/simulation - able to bridge physical testing with virtual modeling. Strong communication skills - able to clearly explain test methods, results, and insights to cross-functional teams. Nice-to-Haves Experience in regulated industries - ideally medical devices, but other regulated environments are also valuable. Exposure to electromechanical components - testing or design experience with complex systems. Combination of systems experience - understanding how mechanical, electrical, and software elements interact. Flexibility for on-site work - full on-site (5
days) preferred, though hybrid possible if simulation-heavy. * Professional development opportunities and hands-on training in verification, validation, and computational modelling. * Collaborative, inclusive, and innovation-driven culture with a focus on quality and continuous improvement.