Principal Regulatory Strategy Lead (Medical Devices)

PROCEPT BioRobotics Corporation in Idaho seeks a Principal Regulatory Affairs Specialist to lead regulatory efforts from product development to marketing approval. You will be instrumental in managing submission processes, providing guidance on regulatory issues, and ensuring compliance with quality management systems.

The ideal candidate will have a strong background in the medical device sector, with over 12 years of experience, particularly in FDA510(k) submissions. A Bachelor’s degree is required, with advanced qualifications preferred. The role demands excellent organizational and communication skills.