Quality Engineer – Compliance (Medical Devices / Combination Products)

Cambridge area, UK (Hybrid – 2.5 days onsite per week)

12-month contract | ⏱ 37 hours per week

We are looking for a Quality Engineer – Compliance to support medical device and combination product development programmes within a leading pharmaceutical R&D environment.

Key Responsibilities

• Lead and support design control and risk management activities across device and combination product programmes.
• Prepare and review Design History File (DHF) and risk management documentation .
• Ensure compliance with quality systems and regulatory standards .
• Support design validation activities , including human factors / usability engineering .
• Assist with regulatory submissions, supplier assessments, and quality audits .
• Support investigations relate...