Quality Inspector - ISO 13485

Redline Group Ltd; Wytham; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading medical device company in Harwell, Oxfordshire seeks a detail-oriented Quality Inspector. The role involves ensuring all products comply with ISO 13485 standards. Ideal candidates will have experience in quality inspection within regulated environments and excel in documentation and problem-solving. Join a dynamic team to contribute to the advancement of medical technology.

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 with excellent documentation and reporting skills.

Responsibilities

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

Skills

Attention to detail

Documentation skills

Problem-solving

Job description

Overview

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.

Responsibilities

• 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

• 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 (url removed)

Or call Nick on (phone number removed) / (phone number removed)