Medical Device Quality & Regulatory Engineer

GPW Recruitment; Houghton-le-Spring; On-site; GBP 42,000 - 54,000; Full time

Job summary

GPW Recruitment is seeking a Quality & Regulatory Engineer for a medical device manufacturing site in Durham. This is a full-time, temporary role (12-14 months) with potential shift work.

You will support QA, regulatory affairs, and production to ensure ISO 13485 and MDR compliance, manage technical documentation, conduct product testing and CAPA, and contribute to audits and training across teams.

Qualifications

• Degree in Engineering, Life Sciences or related discipline.
• At least 1 year in medical device regulatory affairs or quality management systems.
• Understanding of QA, QC and regulatory compliance.

Responsibilities

• Support development, implementation and maintenance of quality control systems and procedures.
• Ensure products meet quality, safety and regulatory requirements.
• Support regulatory affairs relating to medical devices.

Skills

Analytical thinking

Problem-solving

Attention to detail

Communication

Team collaboration

Education

Engineering or Life Sciences degree

Job description

GPW Recruitment is seeking a Quality & Regulatory Engineer for a medical device manufacturing site in Durham. This is a full-time, temporary role (12-14 months) with potential shift work.

You will support QA, regulatory affairs, and production to ensure ISO 13485 and MDR compliance, manage technical documentation, conduct product testing and CAPA, and contribute to audits and training across teams.