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Quality Management System Jobs in Connecticut (NOW HIRING)

Aptyx

The Quality Management Systems (QMS) Engineer is responsible for maintaining, improving, and ensuring compliance of the Quality Management System (QMS) within a regulated medical device manufacturing ...

AB SKF

Quality Manager

Winsted, CT · On-site

$111K - $125K/yr

Implements continuous improvement principles within the quality management system to reduce defects and improve operational efficiencies. * Continuously contributes to the development and improvement ...

SKF Group

Quality Manager

Barkhamsted, CT · On-site

$111K - $125K/yr

Implements continuous improvement principles within the quality management system to reduce defects and improve operational efficiencies. * Continuously contributes to the development and improvement ...

SKF

Quality Manager

Winsted, CT · On-site

$111K - $125K/yr

Implements continuous improvement principles within the quality management system to reduce defects and improve operational efficiencies. * Continuously contributes to the development and improvement ...

Actalent

Quality Manager

Milford, CT

$43.26 - $60/hr

Maintain and improve the quality management system to support product quality and compliance requirements. * Lead implementation, maintenance, and continuous improvement of AS9100, ISO 9001, and ...

Actalent

Quality Manager

Milford, CT

$43.26 - $60/hr

Maintain and improve the quality management system to support product quality and compliance requirements. * Lead implementation, maintenance, and continuous improvement of AS9100, ISO 9001, and ...

RBC Aircraft Products, Inc.

Quality Engineer

Torrington, CT

$70K - $90K/yr

This position is responsible for the implementing the Quality Management System under the direction of the Quality Assurance Manager to assure that all products manufactured by the organization meet ...

RBC Transport Dynamics

Quality Engineer

Torrington, CT

$70K - $90K/yr

This position is responsible for the implementing the Quality Management System under the direction of the Quality Assurance Manager to assure that all products manufactured by the organization meet ...

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Quality Management System information

See Connecticut salary details

$51.4K

$93.8K

$146.5K

How much do quality management system jobs pay per year?

As of Aug 12, 2026, the average yearly pay for quality management system in Connecticut is $93,809.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,800.00 and $116,500.00 per year, depending on experience, location, and employer.

What is a quality management system?

A Quality Management System (QMS) job involves developing, implementing, and maintaining an organization's quality policies and procedures to ensure compliance with industry standards and regulations. Professionals in this role oversee audits, process improvements, and corrective actions to enhance product or service quality. They collaborate with various departments to establish best practices, monitor performance metrics, and drive continuous improvement initiatives. QMS roles are crucial in industries like manufacturing, healthcare, and technology to maintain customer satisfaction and operational efficiency.

What are common challenges in managing a quality management system, and how can they be overcome?

Professionals working with Quality Management Systems often face challenges such as ensuring consistent compliance across departments, keeping up with evolving industry standards, and facilitating buy-in from all team members. Overcoming these hurdles typically involves regular internal audits, ongoing training sessions, and effective communication to promote a quality-focused culture throughout the organization. Collaboration with various departments, such as production, engineering, and supply chain, is also essential for identifying root causes of issues and implementing corrective actions. Being proactive and adaptable in your approach will help you address challenges efficiently and foster continuous improvement in the quality process.

What skills and qualifications are needed for a quality management system?

To thrive in a Quality Management System role, you need a comprehensive understanding of quality assurance processes, standards such as ISO 9001, and strong analytical abilities, typically supported by a degree in engineering, quality management, or a related field. Familiarity with quality management software, audit tools, and certifications like Six Sigma or Certified Quality Auditor (CQA) are highly valued. Exceptional attention to detail, problem-solving skills, and the ability to communicate clearly with cross-functional teams set successful professionals apart. These skills are essential to ensure compliance, drive continuous improvement, and maintain high product or service quality standards within an organization.

What are the most commonly searched types of Quality Management System jobs in Connecticut? The most popular types of Quality Management System jobs in Connecticut are:
What are popular job titles related to Quality Management System jobs in Connecticut? For Quality Management System jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Quality Management System jobs in Connecticut look for? The top searched job categories for Quality Management System jobs in Connecticut are:
Quality Management System jobs near you
Infographic showing various Quality Management System job openings in Connecticut as of August 2026, with employment types broken down into 80% Full Time, 13% Part Time, 4% Temporary, and 3% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $93,809 per year, or $45.1 per hour.

Quality Management System (QMS) Engineer

Aptyx

Torrington, CT • On-site

$70K - $100K/yr

Full-time

Re-posted 23 days ago

Job description

The Quality Management Systems (QMS) Engineer is responsible for maintaining, improving, and ensuring compliance of the Quality Management System (QMS) within a regulated medical device manufacturing environment. This role supports quality system processes including CAPA, nonconformance management, document control, internal auditing, and external regulatory and customer audits while ensuring compliance with FDA regulations, ISO 13485, and applicable customer requirements.
The QMS Engineer partners cross-functionally with Operations, Engineering, Manufacturing, Quality, Supply Chain, and Regulatory teams to drive quality system effectiveness, continuous improvement, and regulatory compliance across a medical injection molding and assembly manufacturing facility.
Essential Duties and Responsibilities
Quality Management System Administration
  • Maintain and improve the site Quality Management System in accordance with:
    • FDA 21 CFR Part 820 / QMSR requirements
    • ISO 13485
    • Applicable customer and regulatory requirements
    • Internal corporate quality standards
  • Support development, implementation, revision, and maintenance of quality procedures, work instructions, forms, and records.
  • Ensure QMS documentation remains current, controlled, and compliant.

CAPA Management
  • Lead and coordinate Corrective and Preventive Action (CAPA) activities from initiation through effectiveness verification and closure.
  • Facilitate root cause investigations using structured problem-solving methodologies such as:
    • 5 Why
    • Fishbone/Ishikawa
    • Fault Tree Analysis
    • Risk-based approaches
  • Ensure timely completion of action items and maintain compliance to CAPA metrics and timelines.
  • Monitor CAPA trends and identify systemic improvement opportunities.

Nonconformance & Quality Event Management
  • Manage Nonconformance Reports (NCRs) and related quality events.
  • Support investigation, containment, disposition, and resolution activities for nonconforming material and product.
  • Collaborate with Manufacturing Engineering, Production, and Quality teams to determine appropriate corrective actions.
  • Analyze quality data and trends to drive continuous improvement initiatives.

Document Control
  • Administer document control processes including:
    • SOPs
    • Work instructions
    • Forms
    • Specifications
    • Validation documentation
    • Quality records
  • Ensure proper revision control, approval routing, archival, and retention practices.
  • Support training compliance activities associated with document revisions and implementation.

Audits & Regulatory Compliance
  • Plan, schedule, and perform internal quality system audits.
  • Participate in external audits including:
    • FDA inspections
    • ISO registrar audits
    • Customer audits
    • Supplier audits
  • Support audit preparation activities and coordinate responses to audit findings.
  • Track audit observations through closure and verify effectiveness of corrective actions.

Continuous Improvement
  • Support continuous improvement initiatives focused on quality system effectiveness and compliance.
  • Assist in development and monitoring of quality metrics and KPIs.
  • Participate in Management Review activities and preparation of supporting quality data.
  • Promote a culture of compliance, accountability, and continuous improvement throughout the organization.

Qualifications
  • Bachelor's degree in Engineering, Quality, Life Sciences, or related technical discipline preferred.
  • Minimum 3-5 years of Quality Systems experience in a regulated medical device manufacturing environment.
  • Strong working knowledge of:
    • FDA 21 CFR Part 820 / QMSR
    • ISO 13485
    • Risk management principles
    • Medical device quality system requirements
  • Experience within medical injection molding, plastics manufacturing, or medical device assembly preferred.
  • Hands-on experience managing:
    • CAPAs
    • NCRs
    • Internal audits
    • Document control systems
    • Regulatory and customer audits
  • Experience using electronic QMS systems (eQMS) preferred.
  • Strong root cause analysis and problem-solving skills.
  • Excellent organizational, communication, and technical writing skills.
  • Ability to manage multiple priorities in a fast-paced manufacturing environment.

Preferred Certifications
  • ASQ Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or similar certification preferred.
  • ISO 13485 Internal Auditor or Lead Auditor certification preferred.

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