Job Title: Quality Engineer (Compliance) – Medical Devices

Location: Cambridge, UK (Hybrid)
Job Type: Contract

About the Project

A global biopharma organisation is expanding its Devices Centre of Excellence in Cambridge, UK. We are seeking an experienced contract Quality Engineer (Compliance) to support advanced medical device and drug–device combination product programmes. This is a hands-on, consultative contract role embedded within product development teams, ensuring design controls and risk management activities are completely audit-ready across the lifecycle from early development to clinical supply.

Key Responsibilities & Measurable Goals

Design Controls & Risk Management (Target: 100% compliance across DHF/RMF deliverables)

* Lead design control and risk management activities for assigned programmes, ensuring deliverables are accurate, approved, and maintained.

* Support and facilitate risk management workshops wit...