Quality Inspector – ISO 13485

Quality Inspector – ISO 13485

Harwell, Oxfordshire

Join a dynamic team at a leading medical device company currently based in Harwell, Oxfordshire.

They are looking for a detail-oriented Quality Inspector to support their medical device manufacturing, ensuring all products meet strict ISO 13485 standards and regulatory compliance requirements.

Key Responsibilities for this Quality Inspector – ISO 13485 role:
• Inspect and verify medical devices at various stages of production, ensuring compliance with ISO 13485 and internal quality standards.
• Maintain accurate inspection records and complete quality documentation.
• Report and escalate any non-conformances, supporting root cause analysis and corrective actions.
• Collaborate with production and engineering teams to uphold continuous improvement in product quality and processes.

Qualifications and Skills required for this Oxfordshire-based Quality Inspector – ISO 13485 role:
• Proven experience in a Quality Inspection or Quality Assurance role within a regulated environment (medical devices preferred).
• Working knowledge of ISO 13485 and GMP requirements.
• Strong attention to detail with excellent documentation and reporting skills.
• Proactive problem-solving approach and ability to work effectively as part of a team.

How to Apply:
If you're ready to join our client’s dynamic team and contribute to the advancement of medical technology, please submit your resume and cover letter to ndrain@redlinegroup.Com
 Or call Nick on 01582 878828 / 07961 158760!