An established medical technology manufacturer is seeking a Quality Engineer to provide hands-on quality support across UK-based manufacturing and external supply partners. This role plays a key part in ensuring products are manufactured and supplied in line with regulatory expectations, internal quality standards, and customer requirements.
Working closely with manufacturing, engineering, and wider quality teams, you will help maintain strong quality systems, support validation and investigation activities, and drive continuous improvement across both internal operations and manufacturing partners.
This is an opportunity to join a growing organisation where quality plays a central role in product integrity and patient safety. You’ll be trusted with real responsibility, given exposure to both manufacturing and supplier quality activities, and supported to develop your technical and regulatory expertise.
Key Responsibilities
Provide quality oversight for UK manufacturing and outsourced production activities, ensuring compliance with regulatory standards and internal procedures
Act as a quality interface with external manufacturing partners, supporting effective supplier quality controls and performance management
Support process and equipment validation activities, ensuring documentation is accurate, complete, and audit-ready
Maintain and update quality system documentation, including procedures, records, and reports
Lead and support non-conformance investigations, applying structured root cause analysis and driving effective corrective and preventive actions (CAPAs)
Contribute to continuous improvement initiatives while safeguarding product quality and compliance
Support supplier and component quality activities, including change control, supplier corrective actions (SCARs), and quality issue resolution
Participate in and support supplier audits (remote and on-site), as well as internal audits
Collaborate cross-functionally with manufacturing, engineering, supply chain, and regulatory teams to ensure consistent quality outcomes
What We’re Looking For
Experience working in a Quality Engineering role within a regulated manufacturing environment (medical devices preferred)
Strong working knowledge of quality management systems and regulatory requirements
Practical experience with root cause analysis tools and CAPA management
Exposure to supplier quality management and contract manufacturing oversight
Comfortable working cross-functionally and influencing stakeholders without direct authority
Methodical, detail-focused approach with the confidence to challenge when needed
If it sounds like an ideal opportunity, please apply for immediate consideration.
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