Regulatory Affairs Specialist

A Regulatory Affairs Specialist at Aidoc supports regulatory activities throughout the software development life cycle, including regulatory assessments, worldwide registrations, submissions, and operations to ensure products meet international requirements and industry standards. The role involves leading regulatory impact assessments, driving global regulatory submissions for market expansion, and maintaining product labeling and technical files. This position requires close collaboration with cross-functional teams to ensure compliance, safety, and successful market access for cutting-edge AI healthcare solutions.