EMEA Medical Devices Regulatory Lead

A global medical technology provider in Ireland is seeking a Regulatory Affairs Specialist to support compliance and regulatory activities for medical products within the EMEA region. The role involves ensuring compliance with regulatory requirements, preparation of documentation, and collaboration with cross-functional teams. Ideal candidates will have a degree in Science or Engineering, along with 3 years of experience in the medical device industry. Strong communication and project management skills are essential, making this an exciting opportunity in the healthcare sector.