Quality Engineer

Cpl Life Sciences

📍 Cambridge, England, United Kingdom 💼 CONTRACT 🕒 Posted June 15, 2026

Apply Now Similar Jobs

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
            
            
Ready to Apply?Submit your application today and join our talented team at Cpl Life Sciences.
Submit Application

Job Details

Location Cambridge, England
Job Type CONTRACT
Category Engineers
Posted Date June 15, 2026
Application Deadline July 25, 2026