Global Regulatory Specialist (EU MDR, ISO 13485) in Pontypridd

A global medical device company in Pontypridd is seeking a Regulatory Specialist to manage product Technical Files and support regulatory compliance across international markets. The ideal candidate has a degree in a scientific discipline and at least 1 year\’s experience in Regulatory Affairs, with strong knowledge of EU MDR and UK regulations. Additional benefits include 33 days of holiday, pension plans, and life assurance, creating a supportive work environment for career growth. #J-18808-Ljbffr