Quality Engineer II- Manufacturing Operations

Medtronic

Quick summary

Work type: On-site
Location: Irvine, CA
Salary: $79,200–$118,800 / yr
Posted: 2 days ago
Closes: Jun 27, 2026

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $150k

This role $99k

$67k most similar roles pay here $197k

This role pays less than 96% of similar roles. Most pay $129,000–$170,000 — the shaded band above. At the midpoint, this role pays about $99k versus about $150k 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 73 open roles on FindRole.

Listed pay typically runs $122,400–$183,600 across 73 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Quality Engineer II- Manufacturing Operations

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The Quality Engineer II role at Medtronic’s Global Operations and Supply Chain team in Irvine, California, involves supporting key programs within the Quality Management System to ensure compliance and quality in medical device development and manufacturing. This hands-on position requires developing and maintaining quality standards, collaborating with engineering and manufacturing teams, and implementing inspection methods to evaluate product accuracy and reliability. The ideal candidate will have a strong background in quality engineering principles, analytical skills, and experience managing multiple priorities effectively. Preferred qualifications include a degree in Mechanical Engineering or related fields, knowledge of statistical tools like ANOVA and DOE, and familiarity with medical device regulations such as FMEA and risk management practices.

Skills

Python SQL Excel ANOVAA capability_analysis DOE FMEA Risk_Management NCMRs CAPAs Design_for_Six_Sigma process_validation test_method_validation Minitab JMP

What you'll do

Develop and modify quality standards and protocols for medical device manufacturing.
Implement inspection methods to ensure product precision and accuracy.
Conduct statistical analyses to evaluate nonconformance issues in products or materials.
Design testing procedures and equipment to support quality assurance activities.
Ensure corrective measures meet reliability standards and documentation is compliant.

What we're looking for

Minimum 2 years of relevant Quality experience or Master's degree in related field.
Develop and maintain quality standards and protocols for medical devices.
Implement inspection methods, conduct quality assurance testing, and perform statistical analyses.
Collaborate with engineering and manufacturing teams to ensure compliance with quality standards.
Experience with process validation, test method validation, and FMEA/risk management.

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