Regulatory Affairs Specialist EMEA

The Regulatory Affairs Specialist EMEA provides advanced regulatory support for New Product Development, market expansion, and sustaining operations across EMEA, EU/EEA, Middle East, and Africa regions. This role involves managing regulatory submissions, ensuring compliance with global medical device regulations, and collaborating with cross-functional teams to align regulatory requirements with business objectives. The position requires a strong understanding of EU MDR, ISO 13485, and other relevant standards to support product launches and ongoing operations.