PROCEPT BioRobotics is a surgical robotics company specializing in urology, offering transformative solutions through its AQUABEAM® and HYDROS™ Robotic Systems. The HYDROS System uniquely combines AI-Powered technology with Aquablation therapy to provide effective, safe, and durable outcomes for men suffering from lower urinary tract symptoms due to benign prostatic hyperplasia (BPH). With over 150 peer-reviewed publications supporting its clinical benefits, PROCEPT BioRobotics stands out in the healthcare industry through innovative robotic technology and a commitment to patient care.
Open Positions
Aquablation Sales Representative - Japan
2+ years of medical sales experience, 5 years of total sales experience, leadership skills, ability to travel
Associate Clinical Representative - Japan
Bachelor’s degree, 1-2 years of sales experience, solid knowledge in science and medical devices industry
Staff Reliability Quality Engineer
Bachelor's or Master's degree in engineering, 6+ years of experience in medical device industry, background in complex electromechanical devices
Senior Regulatory Affairs Specialist
Bachelor's degree, 6 years experience in regulatory submissions for medical devices, and experience in 21 CFR 820, ISO 13485, and Medical Devices Directive
Staff Quality Compliance Engineer
8 years of experience in a medical device industry, Bachelor’s degree in engineering, science, or another technical discipline, Working knowledge of FDA QSR/QMSR, ISO 13485, MDSAP, and EU MDR regulatory requirements
Software Manager
6-12 years of experience developing software for medical devices, with 2 years of experience managing or leading software engineering teams, and a Bachelor's degree in CS/EE or equivalent
Software Manager
Bachelor’s degree in CS/EE or equivalent, 6 years of experience developing software for medical devices, 2 years of experience managing software engineering teams
Staff Quality Compliance Engineer
Bachelor’s degree, 8 years of experience in medical device industry, working knowledge of regulatory requirements, ability to lead project teams
Senior Regulatory Affairs Specialist
5+ years of experience in medical device regulatory affairs and a Bachelor's degree in a scientific or engineering field