Regulatory Lead: Class II Medical Devices (MDR/FDA)

A growing medical device company based in Nottingham seeks a Regulatory Specialist to own regulatory activities for Class II medical devices. This role involves managing submissions, maintaining quality systems, and ensuring compliance with EU MDR and FDA regulations. The ideal candidate will have a Bachelor's degree in a relevant field and 2+ years of hands-on regulatory experience. This position offers the chance to influence and shape regulatory processes in a dynamic environment, contributing to meaningful advancements for individuals managing Tourette Syndrome.