We’re seeking a Quality Engineer to join a leading Medical Device company in Cambridgeshire. The role focuses on providing design control and risk management expertise across medical device and combination product development programmes.
Lead design control and risk management activities supporting development, clinical, and commercial programmes.
Ensure compliance with internal and external quality and regulatory standards.
Collaborate with external design and manufacturing partners to support risk management and design verification.
Contribute to human factors engineering and usability assessments.
Support regulatory submissions, audits, and investigations related to device design and manufacturing.
Degree in a relevant science or engineering discipline (BSc/MSc/PhD).
Experience in combination product or medical device development.