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). * Own end-to-end delivery for MDR projects, ensuring the portfolio stays on plan (scope, schedule, dependencies, resourcing). * Coordinate responses and execution for Customers' MDR requests, including impact assessment, planning, and tracking through completion. * Build and maintain integrated project plans for internal MDR requests (incl. milestones, deliverables, risks, actions). * MDR documentation delivery tracking and readiness reporting. * Carrying out change procedures to ensure continuous production and monitor dependency to MDR activities.
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