Sr PD Program Manager - EU MDR Leader

We anticipate the application window for this opening will close on - 5 Jun 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the Life                  At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the LifeAs part of the Post Market Development – Compliance PMO within the Surgical Operating Unit, this role leads the EU MDR program and associated Globalization initiatives. The Sr Program Manager is responsible for driving strategy, governance, and cross-functional execution to ensure regulatory compliance and sustained product availability across global markets. This leader will drive the Globalization strategy that aligns regulatory registrations, market access planning, and product supply readiness across regions to ensure sustained product availability for patients and customers worldwide. The role also provides leadership across the broader MDR program through direct management of four program managers responsible for key MDR transition workstreams. The Sr Program Manager ensures alignment across these workstreams, drives program governance, and enables coordinated execution across regulatory, operational, and commercial teams. This position partners closely with Regulatory Affairs, Supply Chain, Operations, Marketing, Quality, Clinical, and PMO teams within the Surgical Operating Unit and across the enterprise to ensure regulatory commitments are met while supporting continued product innovation.  This role plays a critical part in enabling the Surgical Operating Unit to successfully navigate evolving global regulatory requirements while maintaining product availability in key international markets. By driving the EU MDR program and Globalization strategy, this leader helps reduce regulatory and supply risk, strengthen compliance readiness, and support the organization’s ability to deliver safe and effective products to patients worldwide. Additionally, this role helps shape how the Compliance PMO engages with the Surgical Operating Unit and enterprise partners, contributing to the development of durable governance models, scalable execution processes, and transparent reporting mechanisms that support informed decision-making at all levels. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.  You will:Program Strategy and Governance:Define and implement the EU MDR Globalization strategy aligned with regulatory requirements and business priorities.Establish governance structures, decision frameworks, and operating mechanisms to support effective program execution. Ensure alignment and coordination across MDR program workstreams.Program LeadershipLead and develop a team responsible for key MDR transition workstreams, ensuring alignment, accountability, and coordinated execution across the program.Drive alignment across cross-functional teams and manage interdependencies across program workstreams.Provide coaching and leadership to strengthen program management practices across the team.Program Planning and ExecutionDevelop and maintain integrated program plans including milestones, dependencies, and risk mitigation strategies.Monitor program progress and proactively address risks, issues, and constraints.Provide clear recommendations on prioritization, trade-offs, and execution adjustments as conditions evolve.Resource and Financial Management:Lead multi-year resource planning including staffing, tools, and operational capabilities.Manage program budgets and track financial performance against program plans.Stakeholder Engagement and CommunicationPartner with cross-functional leaders to maintain alignment on program priorities and regulatory commitments.Provide clear, consistent program reporting including dashboards, risks, and leadership updates.Performance and Continuous ImprovementDefine and monitor key performance indicators to assess program health and execution effectiveness.Identify opportunities to simplify processes, improve scalability, and strengthen program governance.Maintain awareness of evolving global regulatory requirements and industry best practices.Must Have: Bachelor’s degree with a minimum of 7 years of relevant experienceOR advanced degree with a minimum of 5 years of relevant experience5+ years leading complex cross-functional programs in a matrixed environment5+ years managing multiple concurrent projects or programs of increasing complexity5+ years of experience managing program budgets or financial tracking5+ years leading stakeholder communications across multiple organizational levels5+ years directly managing or mentoring project managers or program team membersExperience working in the medical device, life sciences, or other regulated industryWorking knowledge of global medical device regulatory frameworksDemonstrated ability to build or scale programs from concept through executionAbility to operate effectively in complex and evolving environments Nice to Have:PMP or PgMP certificationExperience supporting EU MDR or other global regulatory transitionsExperience with program planning tools such as Microsoft Project or ResourceFirst/PDWareExperience with Power BI or similar tools to develop program dashboards and reporting       Experience partnering with technical teams to support automation or digital program management toolsFor Baccalaurea