Job Description
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...