UK Regulatory Medical Writer - Clinical Evaluation & Submissions

Mantra Systems Ltd in the UK is seeking a full-time regulatory writer to join our core team in Sheffield. You will contribute to literature reviews, Clinical Evaluation submissions, and the preparation of technical files under EU MDR, IVDR and FDA.

No prior regulatory experience is required, but we seek an exceptional life sciences graduate with a 2:1, strong English, and the ability to learn quickly. The role includes full training and mentorship in a supportive, innovative environment.