Engineering Program Manager, QCTM

Medtronic

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Jacksonville, FL
Salary
$142,400–$213,600 / yr
Employment
Full-time
Posted
4 days ago
Freshness
Confirmed live yesterday
Closes
Nov 14, 2026

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $198k
This role $178k
$131k $247k
below market most similar roles pay here above market

This role pays less than 66% of similar roles. Most pay $172,849–$223,430 — the blue band above. At the midpoint, this role pays about $178k versus about $198k for comparable roles.

Based on 240 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 45 open roles on FindRole.

Listed pay typically runs $136,800–$205,200 across 45 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Engineering Program Manager, QCTM

The Engineering Program Manager/QCTM - ENT serves as the Quality Core Team Member for New Product Development programs, acting as the Voice of Quality across design, reliability, supplier, manufacturing, software, and post-market quality functions. This role involves driving quality and reliability strategies, managing risk reduction activities, and leading root cause investigations throughout the product lifecycle. You will partner with cross-functional stakeholders to ensure compliance with regulatory requirements and support deliverables like Design History Files and Device Master Records. Key competencies include experience with risk management, design controls, and product lifecycle management in regulated environments. The role requires knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and IEC 62304. You will ensure product quality requirements are sustained from initial concept through commercialization and post-market transition.

What does a Engineering Program Manager earn?

Median $208650 from 79 postings across 5 companies.

See salary data

What you'll do

  • Lead quality and reliability strategy, plans, metrics, and risk management activities for new product development programs.
  • Manage execution across design, software, supplier, and manufacturing quality functions.
  • Serve as the final quality authority and "Voice of Quality" on cross-functional core teams.
  • Drive Design Reliability and Manufacturability (DRM), Design for Reliability (DfR), and First Time Quality (FTQ) initiatives.
  • Identify quality risks, implement reduction strategies, and lead root cause investigations and corrective actions.
  • Partner with suppliers and manufacturing sites to evaluate risks and ensure readiness for product launch.
  • Lead compliance planning, assessments, audit support, and adherence to regulatory requirements.
  • Support key deliverables including Design History Files, Device Master Records, and regulatory submissions.

What we're looking for

  • Must have a Bachelor's degree with 5 years of technical experience in engineering, quality, technical, or program management.
  • Must have a Master's degree with 3 years of technical experience in engineering, quality, technical, or program management.
  • Must possess unrestricted U.S. work authorization.
  • Must have experience leading cross-functional product development or quality programs.
  • Must have experience applying risk management, quality, and reliability methodologies in regulated product development environments.
  • Must have experience with quality systems, design controls, and product lifecycle management processes.
  • Must have experience supporting compliance with regulated industry requirements and standards.
  • Project Management Professional (PMP) certification (preferred).
  • Design Reliability and Manufacturability (DRM) certification or equivalent experience (preferred).
  • First Time Quality (FTQ) certification (preferred).
  • Experience with medical device product development and software development lifecycle processes (preferred).
  • Knowledge of FDA 21 CFR Part 11, 820, ISO 13485, 14971, and IEC 62304 requirements (preferred).

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