Senior Engineering Program Manager - Quality Core Team Member

Medtronic

Remote

Quick summary

Work type
Remote
Location
Remote
Salary
$171,200–$256,800 / yr
Posted
3 days ago
Closes
Jun 26, 2026

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $196k
This role $214k
$137k most similar roles pay here $270k

This role pays more than 67% of similar roles. Most pay $166,900–$225,750 — the shaded band above. At the midpoint, this role pays about $214k versus about $196k 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 81 open roles on FindRole.

Listed pay typically runs $124,800–$187,200 across 79 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Senior Engineering Program Manager - Quality Core Team Member

The Senior Engineering Program Manager role within the CardioVascular Surgery team focuses on managing quality and reliability efforts for new product development, ensuring compliance with regulatory standards such as FDA CFR, MDR, and ISO 13485. This position involves coordinating the extended quality team, developing functional strategies, and representing the Voice of Quality across global disciplines. Day-to-day responsibilities include reviewing Design History Files, collaborating with R&D teams to develop robust test methods, and facilitating product risk management. The ideal candidate should have a bachelor’s degree and at least 7 years of relevant experience in quality or engineering, along with expertise in medical device industry standards and proficiency in leading cross-functional teams. Key skills include knowledge of design controls, DRM initiatives, and familiarity with surgical heart valves, cardiac OR solutions, and extracorporeal life support systems.

What you'll do

  • Manage the extended quality team to ensure compliance with regulatory standards from design concept to commercialization.
  • Develop and implement Quality functional strategies, plans, and schedules to meet project goals and manage risks.
  • Review and approve Design History File documentation for assigned products, ensuring compliance with QMS processes.
  • Collaborate with cross-functional teams to develop robust test methods that ensure traceability and reliability of results.
  • Enhance product development processes to improve compliance and guide program teams to compliant quality strategies.
  • Provide guidance, coaching, and training to other employees within CardioVascular Surgery on quality and compliance matters.

What we're looking for

  • Minimum 7 years of relevant experience in quality or engineering, or advanced degree with 5 years.
  • Support and coordinate quality team members to ensure compliance with FDA CFR, MDR, ISO 13485 standards.
  • Develop and manage Quality functional strategies, plans, schedules, and budgets for new product development programs.
  • Collaborate with cross-functional teams including R&D, regulatory affairs, and clinical teams on quality and compliance requirements.
  • Review and approve Design History File and related documentation to ensure reliability and adherence to QMS processes.

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