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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

$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.

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 · On-site

$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 ...

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 ...

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

$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 ...

Flex Ltd.

Quality Engineer

Manchester, CT · On-site

$72K - $93K/yr

Lead quality engineering activities throughout the product lifecycle, including process and ... Minimum of 1 year of experience in the medical device industry. ISO13485, ISO 14971, FDA * Hands-on ...

CooperCompanies

Design Quality Engineer II

Trumbull, CT · On-site

The Design Quality Engineer II provides Design Quality Engineering support to ensure the successful ... Experience collaborating with cross-functional teams in a medical device development environment.

Flex

Quality Engineer

Manchester, CT

$72K - $93K/yr

Lead quality engineering activities throughout the product lifecycle, including process and ... Minimum of 1 year of experience in the medical device industry. ISO13485, ISO 14971, FDA * Hands-on ...

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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 Aug 31, 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 94% Full Time, and 6% Contract. Highlights an 100% In-person job distribution, with an average salary of $72,663 per year, or $34.9 per hour.

Supplier Quality Engineer

Bridgeport, CT • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 20 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Supplier Quality Engineer

Location: Bridgeport Area, CT

Duration: 6-Month Contract

Position Overview

We are seeking experienced Supplier Quality Engineers to support a medical device quality remediation initiative. This role will focus on supplier quality operations, remediation activities, quality system improvements, and supplier performance management within a regulated medical device environment.

The ideal candidate will have a strong background in supplier quality engineering, remediation projects, injection molding suppliers, and quality system processes including NCMRs, SCARs, and CAPAs.

Key Responsibilities

  • Support supplier quality remediation activities within a medical device manufacturing environment.
  • Lead and manage supplier-related quality investigations, nonconformances, and corrective action initiatives.
  • Review, develop, and maintain Supplier Quality documentation and records.
  • Drive closure of supplier quality issues through effective root cause analysis and corrective actions.
  • Manage and support:
  • Nonconforming Material Reports (NCMRs)
  • Supplier Corrective Action Requests (SCARs)
  • Corrective and Preventive Actions (CAPAs)
  • Collaborate with suppliers to improve quality performance and ensure compliance with regulatory requirements.
  • Support supplier qualification, monitoring, and ongoing quality improvement initiatives.
  • Partner with cross-functional teams including Quality, Manufacturing, Engineering, and Supply Chain.
  • Ensure supplier quality processes align with QMS requirements and remediation objectives.
  • Organize and maintain supplier quality documentation to support audit readiness and compliance efforts.

Required Qualifications

  • 7+ years of Supplier Quality Engineering experience within the Medical Device industry.
  • Proven experience supporting Quality System remediation projects from a Supplier Quality perspective.
  • Hands-on experience managing NCMRs, SCARs, CAPAs, and supplier quality investigations.
  • Strong understanding of FDA Quality System Regulations and ISO 13485 requirements.
  • Experience working with injection molding suppliers and manufacturing processes.
  • Demonstrated experience developing, reviewing, and maintaining supplier quality documentation.
  • Strong problem-solving, root cause analysis, and communication skills.