As Medical Device Regulation Project Manager, you will lead cross-functional teams to deliver MDR-related project outcomes across the portfolio (Tube Sets, Pumps, Devices, Insufflators). Specialized in the field of Minimally Invasive Medicine, Novanta develops devices and accessories so that doctors can operate with small cuts. We produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. * Own end-to-end delivery for MDR projects, ensuring the portfolio stays on plan (scope, schedule, dependencies, resourcing). * Devices * Build and maintain integrated project plans for internal MDR requests (incl. milestones, deliverables, risks, actions). * Identify, assess, and mitigate project risks, including resource planning, cost reduction opportunities, and contingency actions for technical challenges
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