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). 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. * Drive alignment workshops, document review cycles, action tracking, and delivery commitments. * Experience coordinating document-heavy deliverables (documentation plans, review cycles, approvals)
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