Sr PD Program Manager - EU MDR Leader
$178,400–$267,600 year
On-site · North Haven, Connecticut, United States or Lafayette, Colorado, United States
Job Summary
Senior leader for EU MDR and Globalization within Medtronic’s Post Market Development – Compliance PMO. Drives EU MDR Globalization strategy, governance, and cross-functional execution to ensure regulatory compliance and sustained product availability across global markets. Leads four MDR transition workstreams, aligning regulatory registrations, market access planning, and product supply readiness. Provides program strategy, governance structures, and operational leadership to cross-functional teams (Regulatory Affairs, Supply Chain, Operations, Marketing, Quality, Clinical, PMO) and partners with enterprise functions to meet regulatory commitments, reduce risk, and enable scalable execution. Manages program plans, milestones, risks, budgets, dashboards, and leadership reporting; mentors program managers; and fosters durable governance models and transparent reporting. Requires regular onsite collaboration (minimum 4 days/week). Must have: Bachelor’s degree with substantial program leadership experience; 7+ years’ experience in cross-functional program management; experience in regulated medical device environment; knowledge of global regulatory frameworks; ability to scale programs from concept to execution. Nice to have: PMP/PgMP, EU MDR experience, program planning tools familiarity, Power BI, automation/digital program tools.
Required Qualifications
- 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 of experience leading complex cross-functional programs in a matrixed environment
- 5+ years managing multiple concurrent projects or programs of increasing complexity
- 5+ years of experience managing program budgets or financial tracking
- 5+ years leading stakeholder communications across multiple organizational levels
- 5+ years directly managing or mentoring project managers or program team members
- Experience working in the medical device, life sciences, or other regulated industry
- Working knowledge of global medical device regulatory frameworks
- Demonstrated ability to build or scale programs from concept through execution
- Ability to operate effectively in complex and evolving environments
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.