R&d Project Manager

Responsibilities:Contribute to the design and development of new productsCoordinate multiple projects simultaneouslyInteract with the different departments of the company, intervening in the different stages of the projects, from design to product launchContribute to the maintenance of existing product linesEnsure compliance with applicable regulatory requirements ISO, 21CFR Part 820 and MDR 2017/745 (EU)You will be responsible for prototyping and manufacturing test devices in collaboration with internal and external manufacturersEstablish test plan, execute or monitor testsContribute to the design transfer of new productsWrite all associated documentation, perform risk analysis and design verification/validation master plan in accordance with regulatory and quality requirementsManage the design history file (DHF) for the project Your profile:Mechanical engineering degree or equivalent with a minimum of 5 years of experience as a project manager in R&D in the Medical Device industryExperience in implantable Class III Medical Devices mandatoryKnowledge of standards and regulations associated with medical devices such as ISO, 21CFR Part 820 and MDR 2017/745 (EU)Knowledge/experience with SolidWorks is a plusFluent in English ; French is an asset jid20aef59a jit0520a jiy25a