Senior Regulatory Affairs Specialist – Global Submissions

A global medical technology company in Plymouth is seeking a Regulatory Affairs professional to ensure compliance with healthcare regulations and facilitate product registrations. You will support cross-functional teams, prepare regulatory submissions, and participate in audits. Ideal candidates should possess a Bachelor's degree and relevant industry experience, with skills in project management and strong communication. The role offers a comprehensive benefits package and opportunities for professional growth. #J-18808-Ljbffr