This is an exciting and new opportunity to join a clinical software company and take responsibility for the company's ISO13485 (medical devices) quality management system and MHRA compliance; this includes creating and developing a brand new QMS that is ISO 13485 compliant.
The Quality Manager role involves:
This role will be an integral part of the clinical safety team working together to ensure the technical products are compliant with regulations. The role offers interesting and challenging work and long term career opportunity.
To apply please send your CV with details of the relevant experience