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). * Identify, assess, and mitigate project risks, including resource planning, cost reduction opportunities, and contingency actions for technical challenges * 3+ years project management experience in a regulated/technical environment like e.g. project launches; experience managing multiple parallel projects. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. 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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