Global Regulatory Lead, Medical Devices

PROCEPT BioRobotics Corporation is seeking a Senior Regulatory Affairs Specialist to lead regulatory activities for medical robotics devices. You will guide cross-functional teams on regulatory requirements, develop global strategies, and prepare submissions in the US, EU, and RoW to ensure compliance with FDA and international standards.

Ideal candidates will have 6+ years in regulatory submissions for medical devices, with a strong background in Class II/III devices, ISO 13485, EU MDR, and RAC