Medical Devices Regulatory Specialist

3 days ago


London, Greater London, United Kingdom Newton Colmore Full time
Key Role in Medical Device Development

A growing medical devices company, Newton Colmore, is seeking an experienced regulatory engineer to assist with the management of regulatory affairs standards and quality management systems on their brand new IVD technology.

This critical role will involve working closely with the quality assurance and design teams within an ISO 13485 environment to ensure the success of the product and help steer future R&D pipeline.

The ideal candidate will have a strong knowledge of regulatory standards within the UK and Europe. A degree in engineering, design, medical, or sciences is desirable, but industry exposure is more important for this role.

In this challenging and engaging position, you will be responsible for managing regulatory affairs documentation, ensuring compliance with relevant standards, and contributing to the development of life-saving and life-improving medical devices.

You will receive an excellent starting salary of £80,000 - £100,000 per annum, depending on experience, as well as a benefits package and opportunities for career progression.

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