Test Technician / Test Specialist - Leeds, UK

Vita Global Sciences
Leeds, United Kingdom
about 1 month ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Starter
Experience required
1 year minimum
Working hours
Regular working hours
Languages
English
Job source

Tech stack

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

Requirements

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.

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