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Senior PD Program Manager – EU MDR Leader
MedtronicSr Program Manager leading the EU MDR program and globalization initiatives to ensure regulatory compliance. Developing strategies with cross-functional teams in the medical device industry.
Posted 6/2/2026full-timeLafayette • Colorado, Connecticut, Minnesota • 🇺🇸 United StatesSenior💰 $178,400 - $267,600 per yearWebsite
About the role
Key responsibilities & impact- 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.
- Lead 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.
- Develop and maintain integrated program plans including milestones, dependencies, and risk mitigation strategies.
- Monitor program progress and proactively address risks, issues, and constraints.
- Manage program budgets and track financial performance against program plans.
- Partner with cross-functional leaders to maintain alignment on program priorities and regulatory commitments.
- Define and monitor key performance indicators to assess program health and execution effectiveness.
Requirements
What you’ll need- 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 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
Benefits
Comp & perks- Health, Dental and vision insurance
- Health Savings Account
- Healthcare Flexible Spending Account
- Life insurance
- Long-term disability leave
- Dependent daycare spending account
- Tuition assistance/reimbursement
- Simple Steps (global well-being program)
- Incentive plans
- 401(k) plan plus employer contribution and match
- Short-term disability
- Paid time off
- Paid holidays
- Employee Stock Purchase Plan
- Employee Assistance Program
- Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
- Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
program managementbudget managementrisk mitigationperformance indicatorsregulatory complianceproject managementfinancial trackingprogram executionstakeholder communicationcross-functional leadership
Soft Skills
team leadershipstrategic alignmentproblem-solvingcommunicationmentoringcollaborationadaptabilitydecision-makingorganizational skillsaccountability