Quality Inspector - ISO 13485

Redline Group Ltd; England; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading medical device company based in Harwell, Oxfordshire seeks a Quality Inspector for ensuring compliance with ISO 13485 standards. The ideal candidate has experience in quality inspection within regulated environments and possesses strong attention to detail. Responsibilities include inspecting medical devices, maintaining records, and collaborating with teams for continuous improvement. Interested candidates should apply via resume and cover letter.

Qualifications

• Proven experience in a Quality Inspection or Quality Assurance role within a regulated environment.
• Working knowledge of ISO 13485 and GMP requirements.
• Strong attention to detail and documentation skills.

Responsibilities

• Inspect and verify medical devices at various stages of production.
• Maintain accurate inspection records and quality documentation.
• Report and escalate any non-conformances.

Skills

Attention to detail

Documentation skills

Team collaboration

Problem-solving

Job description

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 [e-mail]

Or call Nick on 01582 878828 / 07961 158760!