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Quality Engineer II

Medtronic · North Haven, CT

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Level
Engineer
Team
Quality
Base pay
$79k–$119k
Degree
Required
Experience asked
2+ years
Industry
Medical devices
Posted
Yesterday

The role in 30 seconds

An engineer-level quality role at Medtronic (medical devices) in North Haven, CT. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.

They ask for
2+ years · degree required
Tools it names
Six Sigma, CAPA, Minitab, Validation (IQ/OQ/PQ)
Base pay
$79k–$119k

Read from the posting. The full description is below.

From the plant jobs report · week of November 2, 2026

Quality Engineer roles in Connecticut: typical posted base $82k–$119k. This one lists $79k–$119k.

Median of the low and high ends of 6 live postings that list pay, out of 8 quality engineer openings in Connecticut, read from manufacturers' own careers sites.

Connecticut plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 7 other live quality postings in Connecticut.

Base pay
In line with similar roles

Typical $82k–$119k, from 5 postings that list pay.

Experience asked
Less than usual (2+ vs 4+)

Similar roles usually ask 4+ years.

Skills these teams ask for most

  • ✓ Validation (IQ/OQ/PQ) 88%
  • ✓ Six Sigma 75%
  • Root cause 63%
  • ✓ CAPA 63%
  • FDA / GMP 50%
  • Lean 38%

✓ = this posting asks for it too. % = share of similar postings that mention it.

It asks for 2+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at Medtronic

    We found 5 people at this company and state: 5 in this kind of role. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

    Write to Matthew → (free)
  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: Medtronic in North Haven

3 other open roles at this site · 5 people we found in quality roles at Medtronic.

Quality Engineer II at Medtronic in other locations

Medtronic lists this title in 2 places. Pick the plant you can get to.

Full description from MedtronicAs posted on their careers site.Show

Responsibilities

  • ◆Develop, apply, and maintain quality standards and protocols for manufacturing processes and products.
  • ◆Execute process validation activities across the validation lifecycle, supporting compliant and reliable manufacturing processes.
  • ◆Partner with Engineering and Manufacturing to establish and maintain quality standards and resolve product and process quality issues.
  • ◆Develop and implement inspection, testing, and evaluation methods for products, materials, processes, and production equipment.
  • ◆Perform quality assurance testing and statistical analysis to evaluate process and product performance.
  • ◆Investigate nonconforming products or materials and support corrective and preventive action (CAPA) activities.
  • ◆Ensure corrective measures meet reliability standards and associated quality documentation complies with requirements.
  • ◆Support quality activities across production control, product evaluation, reliability, incoming materials, and process quality.

Required Qualifications

  • ✓Bachelor’s degree in Engineering, Science, or a technical field with 2+ years of Engineering and/or Quality experience OR advanced degree in Engineering, Science, or a technical field with 0 years of Engineering and/or Quality experience

Preferred Qualifications

  • ✓Bachelor’s degree in Chemical, Biomedical, or Mechanical Engineering; advanced degree preferred.
  • ✓Manufacturing environment experience.
  • ✓Process validation experience across the validation lifecycle, including Installation Qualification (IQ), Operational Qualification (OQ), Test Method Validation (TMV), and Performance Qualification (PQ).
  • ✓Corrective and Preventive Action (CAPA) experience.
  • ✓Experience with Minitab statistical software and/or Six Sigma training.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the

requirements

of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

Physical Job

Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required

responsibilities

and skills of this position.

The physical demands described within the

Responsibilities

section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical

requirements

that may be specific to each role.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

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Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:

Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.

Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.

If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.

If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com .

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Medtronic offers a competitive Salary and flexible Benefits Package

A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career an

Show full description ↓

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

The Quality Engineer II supports the Surgical Sutures Manufacturing business within Medtronic’s Surgical Innovations group and Enterprise Operations. The Quality Engineering function supports manufacturing operations through process validation, quality system execution, and maintenance of quality standards for medical device manufacturing.

This role is 100% onsite at the North Haven, CT manufacturing site, five days per week.

The Quality Engineer II provides quality engineering support for manufacturing operations, with a primary focus on process validation and quality system execution. This role partners with Engineering and Manufacturing to maintain product and process quality, execute validation activities, address nonconformances, and ensure required quality documentation is complete and compliant.

Primary

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