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). * 5+ years project management experience in a regulated/technical environment; experience managing multiple parallel projects. * Strong proficiency in project management methodologies and tools (Agile, Waterfall, PMP, Kaizen) This position is part of Novanta's Advanced Surgery (AS) business unit. Specialized in the field of Minimally Invasive Medicine, Novanta develops devices and accessories so that doctors can operate with small cuts. You will drive planning, execution, and timely completion of technical documentation deliverables, proactively manage risks, coordinate internal and external , and ensure alignment to agreed document plans and submission readiness.
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