Join our team !


Join our fast-growing team of experts dedicated to democratizing chronic heart failure support as problem solvers, game changers and industry leaders.

Regulatory affairs specialist

To own quality and regulatory affairs activities of a medical device class III, including the implementation of a complete Quality Management System (QMS) and pre-market approval pathway to support the development and commercialization of ModulHeart in compliance with applicable regulations in the United States, Canada and Europe. Ambition to scale to a Director position following company growth. Understand the requirements for the verification and validation of the device.

Subscribe to our newsletter




A-419, 1001 Lenoir Street

Montreal, Quebec, H4C 2Z6

Copyright © 2020 Puzzle Medical Devices - All rights reserved

These statements have not been evaluated by the FDA, or any other regulatory agency.