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Job description
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
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Worksite address
san jose, CA, 95199, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.