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Career

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.

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Montreal

 

1-514-742-2580

info@puzzlemed.com

A-419, 1001 Lenoir Street

Montreal, Quebec, H4C 2Z6

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