7 of 7 Contract ISO 13485 Jobs in the UK

tests Experience converting requirements into structured test cases and procedures Experience working with medical devices running embedded software Working knowledge of IEC 62304 and ISO 13485 Good understanding of the full software engineering lifecycle Able to work independently and self-manage a standalone testing function Desirable Knowledge …/or ISO 14971 Contract Details 6 month initial contract, with potential to extend 3 days per week onsite in Manchester Up to £425 per day, Outside IR35 How to Apply If you have embedded software V&V experience within a regulated medical device environment and IEC 62304/ ...

help monitor budget spend against timelines. Risk & Compliance Awareness: Support the team in ensuring project documentation strictly adheres to global regulatory standards (e.g., FDA, ISO 13485, GMP). Flag early risks or bottlenecks to senior leads. Stakeholder Communication: Maintain action logs, prepare progress updates, and assist with draft ...

internal and external engineers and scientists. Required Qualifications & Experience Regulated Industry Experience: 5+ years of experience in a regulated industry where Quality Systems (e.g., ISO 13485) are essential. Electromechanical Ownership: Proven experience owning complex electromechanical systems or subsystems through design, verification, and transfer to production. Verification & Validation: Strong ...

internal and external engineers and scientists. Required Qualifications & Experience Regulated Industry Experience: 5+ years of experience in a regulated industry where Quality Systems (e.g., ISO 13485) are essential. Electromechanical Ownership: Proven experience owning complex electromechanical systems or subsystems through design, verification, and transfer to production. Verification & Validation: Strong ...

detail and communication skills Desirable Experience Medical device, diagnostics, IVD or MedTech experience Experience working in a regulated environment Knowledge of IEC 62304, ISO 13485 or similar standards Embedded software, system testing or hardware/software integration experience Experience mentoring junior engineers Why Apply? This is a chance ...

continuous improvement initiatives. What We Are Looking For Regulated Industry Experience: Experience working within a strictly regulated environment (highly prefer medical devices under ISO 13485/FDA 21 CFR Part 820, though Pharmaceuticals or Aerospace will be considered). Validation Background: Proven track record as a Validation Engineer ...

coaching-led, collaborative style - you assess how a team works before suggesting improvements, and you bring the team with you Experience in medical devices (ISO 13485, IEC 62304) or another heavily regulated, compliance-driven industry is a strong plus Exposure to embedded software development environments is beneficial ...