Sr PD Program Manager - EU MDR Leader

Medtronic

Closes tomorrow Hybrid Actively hiring Posted this week Verified listing
Lafayette, CO Posted 2 days ago $178,400–$267,600 / year
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99+ other roles within 25 mi Near Lafayette, CO

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $187k
This role $223k
$127k most similar roles pay here $283k

This role pays more than 81% of similar roles. Most pay $159,724–$213,687 — the shaded band above. At the midpoint, this role pays about $223k versus about $187k for comparable roles.

Based on 239 similar postings.

Employer

About Medtronic

Medtronic plc is the world's largest medical technology company by revenue, specializing in device-based therapies for over 70 health conditions.

Medtronic currently has 51 open roles on FindRole.

Listed pay typically runs $124,800–$187,200 across 50 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR

As part of the Post Market Development – Compliance PMO within the Surgical Operating Unit at Medtronic, this Senior Program Manager leads the EU MDR program and Globalization initiatives, driving strategy, governance, and cross-functional execution to ensure regulatory compliance and sustained product availability worldwide. The role involves managing a team responsible for key MDR transition workstreams, establishing governance structures, and coordinating efforts across Regulatory Affairs, Supply Chain, Operations, Marketing, Quality, Clinical, and PMO teams. Key responsibilities include program planning, financial management, stakeholder engagement, and continuous improvement to maintain regulatory readiness and support product innovation in the medical device industry. The ideal candidate has extensive experience leading complex programs, managing budgets, and working within regulated industries, with a preference for knowledge of global medical device regulations and tools like Microsoft Project or Power BI.

Skills

Microsoft Project PDWare Power BI EU MDR PMP PgMP CI/CD Agile Waterfall GCP AWS Azure Terraform Python SQL PostgreSQL Jira Confluence Git Docker Kubernetes

What you'll do

  • Define and implement EU MDR Globalization strategy aligned with regulatory requirements.
  • Establish governance structures to support effective program execution across workstreams.
  • Lead a team responsible for key MDR transition workstreams, ensuring coordinated execution.
  • Develop integrated program plans including milestones, dependencies, and risk mitigation strategies.
  • Manage multi-year resource planning, including staffing and operational capabilities.

What we're looking for

  • At least 5 years of experience leading complex cross-functional programs.
  • Proven ability to manage multiple concurrent projects or programs in regulated industries.
  • Experience managing program budgets and financial tracking for multi-year plans.
  • Strong track record of leading stakeholder communications across organizational levels.
  • Demonstrated capability to build, scale, and execute large-scale programs from concept.
  • Bachelor’s degree with 7+ years of relevant experience or advanced degree with 5+ years.
  • Working knowledge of global medical device regulatory frameworks like EU MDR.

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