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# System Validation Engineer

- **Company:** SThree Plc
- **Location:** London, UK
- **Salary:** £78,000.0 - £104,000.0
- **Contract:** Temporary contract
- **Skills:** Document Management Systems, Software Engineering, System Testing, Information Technology
- **Published:** August 26, 2026
- **Apply:** https://uk.indeed.com/viewjob?jk=7510fb50a75d6a59

## About the Role

* Bachelor's degree in Computer Science, Software Engineering or a related discipline
 * Experience in system validation, testing or quality assurance within a medical device or regulated environment
 * Working knowledge of ISO 13485, IEC 62304 and Class III medical device requirements
 * Proficiency with test management tools and documentation systems
 * Strong analytical and problem-solving skills
 * Authorization to work in the United Kingdom

## Description

System Validation Engineers in medical device settings could play a critical role in ensuring that Class III devices meet rigorous regulatory standards before reaching patients. This is an opportunity to register your interest in future System Validation Engineer positions within a regulated medical device environment, where roles could contribute directly to product quality and patient safety., Roles of this type may sit within a collaborative engineering environment focused on Class III medical device validation and compliance. The work could involve partnering with cross-functional teams to design, execute and document validation activities under ISO 13485 and IEC 62304, with scope to contribute to delivering devices that meet the highest regulatory standards., * Supporting the design and execution of system validation protocols and test cases

 * Conducting validation testing and documenting results in compliance with IEC 62304 and ISO 13485
 * Coordinating with engineering, quality and regulatory teams to ensure validation completeness
 * Preparing validation reports and supporting regulatory submissions
 * Contributing to traceability matrices linking requirements to validation activities
 * Escalating validation findings and supporting corrective action processes, Most roles of this type offer the following, dependent on the industry and seniority of the role:
 * Exposure to end-to-end system validation within a heavily regulated environment
 * Opportunity to contribute to devices that support patient safety and clinical outcomes
 * Potential for extension or permanent placement, subject to business requirements
 * Collaborative working within a quality-focused engineering culture
 * Professional development in medical device compliance and validation methodologies