Senior Quality Engineer

Medtronic

Closes in 7 days

Quick summary

Work type: On-site
Location: Danvers, MA
Salary: $98,400–$147,600 / yr
Posted: 3 days ago
Closes: Jun 27, 2026 (soon)
Nearby: 99+ roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $164k

This role $123k

$87k most similar roles pay here $205k

This role pays less than 93% of similar roles. Most pay $141,306–$187,118 — the shaded band above. At the midpoint, this role pays about $123k versus about $164k 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 85 open roles on FindRole.

Listed pay typically runs $122,400–$183,600 across 84 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Senior Quality Engineer

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As a Senior Quality Engineer at Medtronic in Danvers, MA, you will collaborate with Engineering, Manufacturing, Operations, and Quality teams to develop and maintain robust quality systems, driving continuous improvement initiatives to ensure products meet regulatory and customer requirements. Your day-to-day responsibilities include leading the implementation of quality standards, developing inspection strategies, analyzing data for root cause investigations, and supporting CAPA activities. You will leverage technical expertise in FDA regulations, ISO 13485, and statistical analysis tools to mentor cross-functional teams on quality principles and best practices. This role requires a Bachelor’s Degree with at least four years of relevant experience or an advanced degree with two years of experience, ideally in medical device manufacturing environments.

Skills

ISO13485 FDA Quality System Regulations CAPA Nonconformance Management Risk Management Statistical Analysis Minitab Six Sigma Lean Manufacturing Quality System Standards GMP ICH Q10 ASQ CQE

What you'll do

Lead the development and maintenance of quality standards, processes, and protocols.
Develop inspection and testing strategies to ensure compliance with regulatory requirements.
Analyze quality data to drive root cause investigations and continuous improvement.
Design and evaluate inspection methods and equipment for product quality assurance.
Support CAPA, nonconformance, complaint, audit, and risk management activities.

What we're looking for

Bachelor’s Degree with at least 4 years of relevant experience in quality management.
Advanced degree with a minimum of 2 years of relevant experience in quality systems.
Experience in medical device or FDA-regulated manufacturing environments.
Strong understanding of quality systems, risk management, validation, and regulatory requirements.
Proficiency in statistical analysis, problem-solving methodologies, and continuous improvement tools.
ASQ Certified Quality Engineer (CQE) or equivalent certification preferred.
Excellent communication, collaboration, and project leadership skills.

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