Sr Design Quality Engineer

Medtronic

Remote

Quick summary

Work type: Remote
Location: Lafayette, CO
Salary: $98,400–$147,600 / yr
Posted: 1 day ago
Closes: Jul 17, 2026

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $161k

This role $123k

$87k most similar roles pay here $203k

This role pays less than 86% of similar roles. Most pay $136,182–$186,638 — the shaded band above. At the midpoint, this role pays about $123k versus about $161k 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 56 open roles on FindRole.

Listed pay typically runs $124,800–$187,200 across 55 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Sr Design Quality Engineer

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The Senior Design Quality Engineer role within Acute Care & Monitoring at Medtronic involves driving product quality and regulatory compliance through technical expertise and cross-functional leadership. This position requires partnering with R&D, manufacturing, and program teams to ensure design changes meet internal standards and global regulations such as ISO 13485, EU MDR, and FDA Quality System Regulation. Daily responsibilities include reviewing new designs for safety and reliability, leading risk management documentation development, supporting verification and validation strategies, and applying Design for Reliability methodologies. The ideal candidate has experience in the medical device industry with a strong background in quality management systems, risk management processes, and electronic hardware systems. They should also possess excellent communication skills to collaborate effectively across various technical domains and mentor engineers on quality engineering principles.

Skills

ISO_13485 FDA_Quality_System_Regulation EU_MDR ISO_14971 IEC_60601 CAPA Design_Controls DFMEA Risk_Management Verification_and_Validation Lean_Six_Sigma DMAIC DFSS Minitab HALT_HASS Statistical_Methods PCB_Design Schematics Circuit_Analysis ASQ_Certifications

What you'll do

Critically review product designs to ensure compliance with quality and regulatory standards.
Lead cross-functional teams in developing risk management documentation according to ISO 14971.
Support the creation and review of verification and validation strategies for medical devices.
Apply Design for Reliability, Manufacturability, and DFSS methodologies to enhance product performance.
Drive continuous improvement initiatives focusing on quality, reliability, and manufacturing robustness.

What we're looking for

4+ years of quality experience in medical device or regulated industry.
Working knowledge of ISO 13485, FDA Quality System Regulation, and EU MDR.
Experience applying risk management processes per ISO 14971.
Technical expertise with electronic hardware systems including PCB design.
Demonstrated leadership on complex technical problems and cross-functional projects.
Strong communication skills for effective collaboration across teams.

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