Remote Clinical Regulatory Specialist — MedTech Submissions

A medical technology firm in Carmarthen seeks a Regulatory Affairs Clinical Specialist to ensure compliance with medical device regulations. You will author crucial regulatory documentation, collaborate on clinical trials, and train teams on regulatory requirements. Ideal candidates have an MSc or PhD in Life Sciences and 4-7 years of experience in the medical device industry. This role offers both remote and hybrid work options. #J-18808-Ljbffr