Job Description
Overview
12m Contract
Cambridge (2.5 days per week average on site)
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 related to clinical and commercial device manufacturing. Requirements