Found Description
Cambridge (Hybrid – 2.5 days onsite per week)
Contract
Rate £28.20 per hour (PAYE) + holiday entitlement
Atrium (EMEA) is partnering with a leading global biopharma organisation to hire a Quality Engineer. The candidate will provide design control and risk management subject matter expertise to medical device and combination product development programmes throughout the product lifecycle.
Key Responsibilities
- Lead design control and risk management activities for product development programmes
- Ensure compliance with regulatory and quality standards (ISO, FDA, EU MDR)
- Prepare and review design history files and risk management documentation
- Collaborate with external partners, suppliers, and manufacturing sites
- Contribute to regulatory submissions and audit readiness
- Assist with device investigations for clinical and commercial products