Do you have experience working with Medical Devices? Do you have experience in design control and risk management? Are you familiar with device assembling manufacturing processes?
If you answered yes, I might have an exciting role for you!
We are currently working with a brilliant client who is at the forefront of providing process technology, analytical methodology, and support for the development and manufacture of medicines at all phases of clinical development. Being one of the biggest pharmaceutical companies in the world, my client is known for discovering and developing over 150 + medicines and they are currently working on 27 clinical trials across 71 UK sites.
They are currently looking for an Quality Engineer to join their team in Cambridge.
Lead design control and risk management for combination product development, ensuring timely and compliant deliverables for clinical trials and commercial approvals.
Facilitate risk management at external design firms and manufacturing sites.
Ensure compliance with internal and external quality and regulatory standards for product development.
Provide input on design validation, including human factors assessments.
Evaluate external design firms and suppliers for quality systems and procedures.
Support investigations of devices used in clinical and commercial settings.
Contribute to regulatory submissions and content generation for assigned projects.
Assist with internal and external audits of the DCoE Quality Management System
If you would like to hear more, please apply today!