Sr Program Manager – Global MDR Program Lead

Senior leader overseeing a global MDR regulatory transition program within Medtronic’s Surgical Operating Unit. Drives integration of regulatory, market access, and operational readiness to maintain uninterrupted product availability across international markets. Directs a program team across regulatory affairs, supply chain, operations, quality, marketing, clinical, and enterprise PMO; establishes governance structures, integrated multi-year plans, and risk mitigation. Partners with supply chain and operations to align manufacturing, supply, and lifecycle decisions with regulatory timelines. Leads development of globalization strategy and ensures alignment of registrations, market access planning, and global readiness. Builds and mentors a high-performing program leadership team, enabling autonomous execution while maintaining alignment with strategy and priorities. Responsible for cross-functional planning, execution oversight, and transparent reporting to senior leadership; supports continuous improvement and governance to simplify processes and scale programs. Demonstrates ability to navigate complex and evolving regulatory requirements and industry best practices to ensure program readiness. Must Have Bachelor’s degree with a minimum of 7 years of relevant experience OR advanced degree with a minimum of 5 years of relevant experience; 5+ years in cross-functional program leadership; 5+ years managing budgets; 5+ years stakeholder communications; experience in regulated industries; demonstrated ability to scale programs from concept to execution.