Quality Engineer II

Medtronic

Confirmed live yesterday High trust

Quick summary

Work type: On-site
Location: Minneapolis, MN
Salary: $79,200–$118,800 / yr
Employment: Full-time
Posted: 6 days ago
Freshness: Confirmed live yesterday
Closes: Oct 16, 2026
Nearby: 99+ roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $142k

This role $99k

$68k most similar roles pay here $180k

This role pays less than 88% of similar roles. Most pay $113,750–$169,500 — the shaded band above. At the midpoint, this role pays about $99k versus about $142k 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 77 open roles on FindRole.

Listed pay typically runs $124,000–$186,000 across 73 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Quality Engineer II

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The Quality Engineer II joins the Service and Repair team to ensure compliance, product quality, and continuous improvement across service center and field service operations. This role involves partnering cross-functionally with Engineering, Regulatory, and Supplier Quality teams to maintain quality system requirements and manage the lifecycle of products in a service environment. Key responsibilities include overseeing validation activities, managing nonconformance, leading Corrective and Preventive Action (CAPA) processes, and ensuring audit readiness. The candidate will also monitor supplier performance, conduct audits based on GMP/ISO requirements, and oversee change control documentation. Essential skills include experience with risk management principles, root cause investigation, and process validation. This role addresses the critical challenge of maintaining high quality standards and regulatory compliance for medical devices throughout their service and repair lifecycle in a regulated manufacturing environment.

Skills

ISO 13485 ISO 14971 CAPA GMP PPAP Process Validation Change Control Audit Readiness Supplier Quality Continuous Improvement Risk Management Nonconformance Management

What you'll do

Manage quality system compliance, standards, and controls within the service and repair environment.
Oversee validation activities, nonconformance management, and Corrective and Preventive Action (CAPA) processes.
Investigate quality issues, assess risks, and implement effective corrective actions.
Ensure suppliers provide high-quality parts and materials while managing the change control process.
Conduct audits of current and future suppliers to ensure compliance with GMP and ISO requirements.
Monitor and communicate quality metrics, performance trends, and improvement opportunities to stakeholders.
Lead quality walks to identify gaps and track corrective actions through completion.
Support internal and external audits by coordinating readiness activities for the service organization.

What we're looking for

A Bachelor's degree in Engineering, Science, or a technical field with 2+ years of experience is required.
An Advanced Degree in Engineering, Science, or a technical field is accepted with no experience required.
Candidates with degrees from outside the U.S. must meet specific federal requirements for foreign degree equivalency.
Candidates must possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Quality System Lead Auditor experience (ISO 13485) is preferred.
Working knowledge of ISO 14971 and medical device risk management principles is preferred.
Experience in a regulated industry, preferably the medical device industry, is preferred.
Experience with CAPA, nonconformance management, and root cause investigation methodologies is preferred.

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