Senior Quality Engineer

Medtronic

Closes in 4 days

Quick summary

Work type
On-site
Location
North Haven, CT
Salary
$98,400–$147,600 / yr
Posted
2 days ago
Closes
Jun 23, 2026 (soon)
Nearby
32 roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $166k
This role $123k
$87k most similar roles pay here $205k

This role pays less than 93% of similar roles. Most pay $142,250–$190,250 — the shaded band above. At the midpoint, this role pays about $123k versus about $166k 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 74 open roles on FindRole.

Listed pay typically runs $122,400–$183,600 across 74 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’s Surgical Sutures Manufacturing in North Haven, CT, you will play a pivotal role in maintaining the highest standards of quality and compliance within our medical device manufacturing processes. Your responsibilities include developing and implementing quality protocols, collaborating with engineering and manufacturing teams to ensure regulatory adherence, and conducting statistical analyses for continuous improvement. You will specialize in areas such as process validation, root cause analysis, and nonconforming material management, ensuring that all products meet stringent reliability standards. Ideal candidates possess a Bachelor’s degree in Engineering or Science, preferably with experience in FDA-regulated environments, proficiency in tools like Minitab, and the ability to mentor engineers while fostering cross-functional collaboration. This role is crucial for upholding Medtronic's commitment to delivering high-quality medical devices that improve patient outcomes.

Skills

Minitab FDA CFR requirements Engineering drawings Machining Chemical processing Packaging Sterilization Process validation Root cause investigations CAPA development NCMR activities Statistical analysis Continuous improvement Cross-functional collaboration Quality standards Testing mechanisms Precision measurement Accuracy assessment Documentation compliance

What you'll do

  • Develop and modify quality standards and protocols for manufacturing processes.
  • Design inspection methods and equipment to ensure product accuracy and reliability.
  • Conduct quality assurance tests and perform statistical analysis on products.
  • Ensure corrective measures meet acceptable reliability standards and documentation is compliant.
  • Specialize in areas such as design, production control, or research and development.

What we're looking for

  • Bachelor’s Degree in Engineering or Science with 4+ years of relevant experience.
  • Develop and implement quality standards, protocols, and testing methods.
  • Lead root cause investigations, CAPA development, and manage nonconforming material activities.
  • Proficiency in statistical analysis tools for data-driven decision making.
  • Experience in FDA-regulated manufacturing environments with knowledge of CFR requirements.
  • Collaborate effectively across cross-functional teams to enhance product reliability.

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