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Quality Management System Jobs in Connecticut (NOW HIRING)

Insight Global

Quality Manager

Winsted, CT · On-site

$111K - $140K/yr

The facility operates under an accredited quality management system and supports both internal and external audit requirements across a complex, multi-department environment. This is a well ...

New

Altek Electronics, Inc.

Quality Manager

Torrington, CT · On-site

$129 - $175/hr

Provides relevant reporting and recommendations to Management. * Acts as a thought leader for the Altek Quality System and Quality Assurance methodologies, including staying current on techniques ...

ALTEK ELECTRONICS, INC.

Quality Manager

Torrington, CT · On-site

$129K - $175K/yr

Provides relevant reporting and recommendations to Management.   * Acts as a thought leader for the Altek Quality System and Quality Assurance methodologies, including staying current on techniques ...

ImageTek Mfg., Inc.

Assistant Quality Manager

Putnam, CT · On-site

$55K - $75K/yr

Quality Management System * Assist the Quality Manager in developing, maintaining, and continuously improving the Quality Management System. * Support the implementation and ongoing effectiveness of ...

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 · On-site

$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 · On-site

$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 ...

RBC Bearings

Quality Engineer

Torrington, CT · On-site

$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 Sep 6, 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 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 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 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 1% As Needed, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $93,809 per year, or $45.1 per hour.

Senior Manager-Global Quality Systems

CooperCompanies

Trumbull, CT • On-site

Full-time

Posted 17 days ago

Job description


Scope:
The Senior Manager, Global Quality Systems provides leadership and oversight for key elements of CooperSurgical's Global Quality Management System (QMS), including Management Review, Quality System Metrics and Reporting, Regulatory Intelligence, Quality System Impact Assessments, and Quality System integration activities associated with acquisitions and strategic business initiatives. Partners closely with Quality, Regulatory Affairs, Operations, Manufacturing, R&D, Supply Chain, IT, and other functional leaders to ensure QMS remains compliant, effective, scalable, and aligned with evolving regulatory requirements and business objectives. Serves as a key partner to the Director, Global Quality Systems, helping drive quality system performance, governance, inspection readiness, and continuous improvement across the global organization.
Responsibilities
Job Summary:
The Senior Manager, Global Quality Systems is responsible for the leadership, oversight, and continuous improvement of key components of CooperSurgical's Global Quality Management System. This role ensures ongoing compliance with applicable global regulations and standards, including FDA QMSR, ISO 13485, MDSAP, EU MDR, and other relevant requirements. Leads activities related to Management Review, Quality System metrics and reporting, regulatory intelligence, standards management, quality system impact assessments, and merger and acquisition integration efforts. Through effective governance, analytics, and cross-functional collaboration, this role provides visibility into QMS health, identifies compliance risks and opportunities, and ensures regulatory and standards changes are effectively assessed and incorporated into the Quality Management System.
Essential Functions & Accountabilities:
  • Support the governance, effectiveness, and continuous improvement of the global QMS.
  • Drive harmonization, compliance, and operational excellence across global quality system processes.
  • Partner with process owners and cross-functional stakeholders to identify and mitigate quality system risks while ensuring inspection readiness.
  • Lead the global Management Review program, including planning, reporting, action tracking, and continuous improvement.
  • Develop and maintain quality system KPIs, dashboards, and performance reporting to provide visibility into QMS effectiveness, compliance status, and emerging risks.
  • Prepare executive-level reporting on QMS health, quality objectives, risks, and improvement opportunities.
  • Monitor process effectiveness and drive improvements that enhance compliance, efficiency, and user experience.
  • Monitor evolving global regulations, standards, guidance documents, and industry best practices impacting the Quality Management System.
  • Lead quality system impact assessments and gap analyses to determine the effect of regulatory and standards changes on existing QMS processes.
  • Develop and track implementation plans to ensure timely incorporation of regulatory and standards requirements into the QMS.
  • Partner with Regulatory Affairs and Quality leadership to evaluate new or revised regulatory requirements.
  • Lead Quality Systems due diligence, integration planning, and QMS harmonization activities associated with acquisitions and strategic business initiatives.
  • Assess quality system maturity, identify compliance gaps, and implement integration plans that align acquired entities with CooperSurgical processes.
  • Support implementation and optimization of electronic Quality Management Systems (eQMS) and related quality system enhancement initiatives.
  • Support regulatory inspections, audits, and remediation activities as required.
  • Lead, coach, and develop a team responsible for Quality Systems governance, reporting, compliance monitoring, and improvement initiatives.
  • Establish performance expectations, prioritize resources, and foster a culture of quality, accountability, and continuous improvement.
    Travel: This position may require 20% domestic or international travel.

Qualifications
Qualifications
Knowledge, Skills and Abilities:
Required
  • Strong working knowledge of MasterControl, Veeva, Trackwise, or similar eQMS platforms.
  • Solid understanding of 21 CFR 820, ISO 13485, EU MDR, MDSAP.
  • Demonstrated ability to manage and develop teams.
  • Ability to balance operational priorities with compliance requirements.
  • Strong organizational, analytical, and communication skills.
  • Ability to collaborate across global, cross-functional groups.

Preferred
  • Experience participating in or supporting large-scale enterprise software implementations, including data migration and data mapping activities.
  • Advanced proficiency in Excel for data analysis and reporting.
  • Professional certification such as Certified Quality Auditor (CQA) or similar.

Work Environment:
  • Standard office environment with regular use of computer systems and virtual collaboration tools.

Experience:
Required
  • 8+ years of experience in quality management systems, within a regulated med tech industry.
  • 7+ years of people leadership and team development.
  • Experience managing quality systems with ISO 13485 and FDA 21 CFR Part 820, MDSAP, and EU MDR requirements.

Preferred
  • Exposure to other adjacent quality system compliance requirements such as 21 CFR Part 210/211.
  • Prior involvement in supporting external and internal audits.
  • Experience with electronic Quality Management Systems (eQMS) and/or implementation of eQMS, such as Veeva, Trackwise, MasterControl.

Education:
Required
  • Bachelor's degree in a relevant field such as Engineering, Life Sciences, Quality, or a related discipline.

Preferred
  • Professional ASQ certification (CQPA, CQA, CMQ/OE, etc.)
  • Project Management Professional certification (PMP)

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