
Posted a day ago
Sr Program Manager – Global MDR Program Lead
MedtronicSr Program Manager – Global MDR Program Lead
Perks & benefits
Health InsuranceMobile AllowancePaid Leave
Requirements
Bachelor's degree with 7+ years experience, Advanced degree with 5+ years experience, 5+ years leading cross-functional programs, 5+ years managing concurrent programs, 5+ years managing program budgets, 5+ years stakeholder communication, 5+ years managing project managers, Medical device or life sciences experience, Supply chain or manufacturing program experience
Skills
Program ManagementComplianceMedical Devices
About the role
Responsibilities
- Lead the complex EU MDR regulatory transition program for the Surgical Operating Unit to ensure global product availability.
- Define and implement program strategy, governance structures, and decision frameworks aligned with regulatory requirements.
- Manage and develop a team of program leaders responsible for key MDR transition workstreams.
- Integrate regulatory, supply chain, operations, quality, and commercial plans to maintain uninterrupted product supply.
- Develop multi-year program plans, including milestones, dependencies, and risk mitigation strategies.
- Manage program budgets and lead resource planning for staffing and operational capabilities.
- Partner with senior leadership to facilitate decision-making through clear program insights and trade-off analysis.
Requirements
- Bachelor’s degree with 7+ years of relevant experience, or an advanced degree with 5+ years of relevant experience.
- 5+ years of experience leading complex cross-functional programs in a matrixed environment.
- 5+ years of experience managing multiple concurrent programs or projects of increasing complexity.
- 5+ years of experience managing program budgets and financial tracking.
- 5+ years of experience leading stakeholder communications across multiple organizational levels.
- 5+ years of experience directly managing or mentoring project managers or program team members.
- Experience in the medical device, life sciences, or other highly regulated industries.
- Experience supporting supply chain, manufacturing, or operational programs related to product lifecycle or market access.
Preferred Qualifications
- PMP or PgMP certification.
- Direct experience supporting EU MDR or other global regulatory transitions.
- Proficiency with program planning tools such as Microsoft Project or ResourceFirst / PDWare.
- Experience developing program dashboards and reporting using tools like Power BI.
Benefits
- Competitive salary and Medtronic Incentive Plan (MIP).
- Comprehensive health, dental, and vision insurance.
- 401(k) plan with employer contribution and match.
- Paid time off and paid holidays.
- Tuition assistance and reimbursement programs.
- Employee Stock Purchase Plan.
About the Company
Medtronic is a global leader in healthcare technology, dedicated to alleviating pain, restoring health, and extending life. Our mission unites a global team of over 95,000 passionate people working to solve the most challenging health problems facing humanity through engineering excellence and innovation.
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Get started — it's freeSr Program Manager – Global MDR Program Lead
Medtronic · Lafayette
