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Quality Engineer Medical Device Jobs in Connecticut

Three Point Solutions

Quality Engineer

North Haven, CT · On-site

$50 - $60/hr

Medical Device Manufacturing Industry Duration: 2 Years (Possible Extension) Location: North Haven, CT 06473 Shift: 1st shift | Hybrid (4 days onsite, 1 day remote) Key Responsibilities * Perform ...

LanceSoft Inc

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

Company Description Medical Device Industry. Performs Quality Engineering functions in support of projects associated to product development/change including: design verification (design for six ...

Medtronic

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

Experience in the medical device industry as a supplier quality engineer or manufacturing quality engineer preferred. Responsibilities may include the following and other duties may be assigned.

Medtronic

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

Experience in the medical device industry as a supplier quality engineer or manufacturing quality engineer preferred. Responsibilities may include the following and other duties may be assigned.

Medtronic

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

Experience in the medical device industry as a supplier quality engineer or manufacturing quality engineer preferred. Responsibilities may include the following and other duties may be assigned.

Astrix Inc

Medical Device Assembler

Trumbull, CT · On-site

$17.75 - $21.50/hr

Follow detailed written instructions and assembly procedures to ensure product quality and accuracy ... supervisors Medical Device Assembler Qualifications/Requirements: * High school diploma or ...

Resonetics

Quality Engineer III

Bethel, CT · On-site

$65K - $102K/yr

This Quality Engineer III applies advanced Quality Engineering and scientific method techniques and ... Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ...

Resonetics

Quality Engineer III

Bethel, CT

$74K - $95K/yr

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ... in a Quality Engineering role for a medical device manufacturer and/or start-up company, or ...

Resonetics

Quality Engineer III

Bethel, CT · On-site

$74K - $95K/yr

This Quality Engineer III applies advanced Quality Engineering and scientific method techniques and ... Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ...

LanceSoft Inc

Quality Engineer III

North Haven, CT · On-site

$71K - $92K/yr

... Medical Device industries. We understand the clinical trial process from Phase I through Phase IV. ... Performs Quality Engineering functions in support of projects associated to product development ...

Medtronic

Prin Quality Engineer

North Haven, CT · On-site

$71K - $92K/yr

Medical device industry. * Technical Skills: Proficient in quality management systems, risk ... to engineer the extraordinary. For Baccalaureate degrees earned outside of the United States, a ...

Medtronic

Prin Quality Engineer

North Haven, CT · On-site

$71K - $92K/yr

Medical device industry. * Technical Skills: Proficient in quality management systems, risk ... to engineer the extraordinary. For Baccalaureate degrees earned outside of the United States, a ...

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Showing results 1-20

All JobsQuality Engineer Medical Device JobsQuality Engineer Medical Device Jobs in Connecticut

Quality Engineer Medical Device information

See Connecticut salary details

$20

$34

$67

How much do quality engineer medical device jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for quality engineer medical device in Connecticut is $34.93, according to ZipRecruiter salary data. Most workers in this role earn between $23.56 and $43.65 per hour, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that medical devices meet all regulatory standards and quality requirements. They develop and implement quality assurance processes, perform risk assessments, and conduct inspections and audits to make sure products are safe and effective. Quality Engineers also collaborate with design, manufacturing, and regulatory teams to resolve quality issues and improve product reliability. Their work is crucial for maintaining compliance with standards such as ISO 13485 and FDA regulations.

What are the key skills and qualifications needed to thrive as a quality engineer in the medical device industry?

To thrive as a Quality Engineer in the medical device industry, you need a strong background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and engineering principles, often supported by a relevant engineering degree. Familiarity with quality management systems (QMS), risk analysis tools (like FMEA), and certifications such as CQE (Certified Quality Engineer) are typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills and qualifications are vital to maintain regulatory compliance, uphold product quality, and protect patient safety in a highly regulated environment.

How does a quality engineer in the medical device industry typically collaborate with cross-functional teams to ensure product compliance?

Quality Engineers in the medical device sector work closely with cross-functional teams such as design, manufacturing, regulatory affairs, and supply chain. They participate in design reviews, risk assessments, and process validations to ensure that products meet both internal quality standards and external regulatory requirements (such as FDA or ISO 13485). Regular collaboration involves reviewing documentation, addressing non-conformances, and implementing corrective actions. This teamwork is critical to proactively identify potential issues and maintain continuous product quality throughout the development and production lifecycle.

What is the difference between Quality Engineer Medical Device vs Quality Assurance Specialist Medical Device?

AspectQuality Engineer Medical DeviceQuality Assurance Specialist Medical Device
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, Six Sigma, ASQ certifications
Work EnvironmentDesign, development, manufacturing, and process improvementAuditing, compliance, documentation, and process verification
Employer & Industry UsageMedical device manufacturers, R&D labsMedical device companies, regulatory agencies, consulting firms

While both roles focus on quality in the medical device industry, a Quality Engineer Medical Device primarily works on product design, process development, and continuous improvement. In contrast, a Quality Assurance Specialist Medical Device emphasizes compliance, auditing, and ensuring adherence to regulatory standards. Both roles are essential for maintaining product safety and quality, but they differ in scope and daily responsibilities.

More about Quality Engineer Medical Device jobs

What are the most commonly searched types of Quality Engineer Medical Device jobs in Connecticut?

The most popular types of Quality Engineer Medical Device jobs in Connecticut are:

What are popular job titles related to Quality Engineer Medical Device jobs in Connecticut?

For Quality Engineer Medical Device jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Quality Engineer Medical Device jobs in Connecticut look for?

The top searched job categories for Quality Engineer Medical Device jobs in Connecticut are:

Quality Engineer Medical Device jobs near you
Infographic showing various Quality Engineer Medical Device job openings in Connecticut as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $72,663 per year, or $34.9 per hour.

Manufacturing Quality Engineer - Medical Devices (3+ yrs exp. req.)

#twiceasnice Recruiting

Waterbury, CT • On-site

$90K - $110K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Manufacturing Quality Engineer - Medical Devices (3+ yrs exp. req.)
Location: Near Waterbury, CT
Salary: $90,000-$110,000 + Annual Bonus Potential + Benefits
Benefits: Medical, Dental, Vision, 401(k) w/match, Holidays, PTO
Job Type: Full-Time On-site
Typical Hours: Monday-Friday, 40-45 hours per week
Start Date: ASAP
Sponsorship is not available
Relocation assistance is available

Manufacturing Quality Engineer - Medical Devices Description

Our client in precision manufacturing is looking for a Manufacturing Quality Engineer near Waterbury, CT. You will lead customer quality investigations, support process validation, and improve inspection methods for regulated, precision-molded components. You will work closely with engineering, manufacturing, quality, and metrology teams. This hands-on role includes measurement programming, root-cause analysis, statistical studies, and new-product quality support. To qualify, you must have medical-device manufacturing or ISO 13485 experience. You must also understand injection molding or a comparable precision-manufacturing process. This role offers ownership of varied technical projects and a potential path into quality management, regulatory affairs, or another leadership position.

Manufacturing Quality Engineer - Medical Devices Responsibilities

  • Lead customer complaint, containment, and corrective-action activities
  • Communicate investigation findings and preventive actions to customers
  • Perform root-cause analysis and verify long-term corrective actions
  • Support IQ, OQ, PQ, PPAP, first-article, and product-launch activities
  • Create and analyze CMM or vision-system inspection programs
  • Develop control plans, inspection templates, and measurement methods
  • Apply GD&T when planning measurements, fixtures, and inspection methods
  • Conduct capability studies, GR&R, DOE, and other statistical analyses
  • Support inspectors and metrologists with training and troubleshooting
  • Recommend equipment and automation to improve inspection throughput
  • Design or define gauges, fixtures, and inspection tooling
  • Lead projects that reduce scrap, process variation, labor, and COPQ

Manufacturing Quality Engineer - Medical Devices Qualifications

  • 3+ years of quality experience in medical-device or ISO 13485 manufacturing required
  • Injection-molding or precision-manufacturing experience required
  • Customer complaint, CAPA, root-cause, and defect investigation experience required
  • CMM or vision-system programming experience required
  • IQ/OQ/PQ, PPAP, or process validation experience required
  • Proficiency with GD&T and statistical analysis required
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#twiceasnice Recruiting is a prominent company in the recruitment and staffing industry, based in Boston, MA, US. The company's services are designed to meet all employment needs of its clients, focusing on optimal fits between employers and prospective employees. Ever since its inception, #twiceasnice Recruiting has committed to the goal of providing high quality recruitment services at a swift pace. They have garnered significant acclaim for their innovative approaches and prompt services, leading them to be recognized as a leader in their field.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Boston, MA, US

Year founded

2017

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