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Quality System Jobs in Connecticut (NOW HIRING)

NORTHEAST FOODS INC.

Quality Systems Assistant

Dayville, CT · On-site

$17.50 - $22.50/hr

... system. * Ability to lift up to 50 lbs. * Ability to stand on your feet for long periods of time. Attributes: * Self-motivated * Accepts personal accountability. * Passionate about quality and ...

H&S Family of Bakeries

Quality Systems Assistant

CT · On-site

$17.50 - $22.50/hr

... system. * Ability to lift up to 50 lbs. * Ability to stand on your feet for long periods of time. Attributes: * Self-motivated * Accepts personal accountability. * Passionate about quality and ...

W3Global Inc.

Senior Quality Engineer

Avon, CT · On-site

$90K - $100K/yr

Our Client is seeking a Quality Engineer to support the quality system, coordinate project activities, and help ensure products meet customer and regulatory requirements. This role focuses on ...

Building One Facility Services

Quality Engineer

Durham, CT · On-site

$70K - $90K/yr

Support development and implementation of quality systems. Provide strong technical leadership and support to Manufacturing, Procurement, Engineering, and Quality Management to minimize costs and ...

Aquinas Consulting

Quality Engineer

Farmington, CT · On-site

$90/hr

Daily support will include technical problem solving, quality system implementation and auditing, new product launch management and internal/external supplier corrective actions. This position ...

Ametek

Senior Quality Engineer

Bridgeport, CT · On-site

$90K - $122K/yr

You will support and enforce the development of internal systems and procedures to meet ISO standards and FDA quality system regulations. You will develop and implement inspection/validation ...

AMETEK, Inc.

Senior Quality Engineer

Bridgeport, CT · On-site

$90 - $115/hr

You will support and implement systems in the areas of SPC, advanced quality, and design/development. Duties and Responsibilities * Assists in the development and implementation of systems and ...

Ametek

Senior Quality Engineer

Bridgeport, CT · On-site

$90K - $122K/yr

You will support and implement systems in the areas of SPC, advanced quality, and design/development. Duties and Responsibilities * Assists in the development and implementation of systems and ...

Building One Facility Services

Quality Engineer

Durham, CT · On-site

$70K - $90K/yr

Support development and implementation of quality systems. Provide strong technical leadership and support to Manufacturing, Procurement, Engineering, and Quality Management to minimize costs and ...

ebm-papst Inc.

Quality Systems Manager

Farmington, CT · On-site

Formulate and maintain quality objectives complementary to corporate policies and goals. * Manage ... system. * Maintain ISO 9001 continuous improvement. * Manage returns analysis and reporting.

Kimchuk Inc

Quality Engineer

Danbury, CT · On-site

$73K - $94K/yr

This position will also be responsible for maintaining and supporting the quality management system. DUTIES/RESPONSIBILITIES: * Direct interface with manufacturing and QC to resolve manufacturing ...

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Quality System information

What is a quality system?

Quality System jobs involve developing, implementing, and maintaining the processes and standards that ensure a company’s products or services meet regulatory and customer requirements. Professionals in these roles often work with quality management systems (QMS), conduct audits, and ensure compliance with industry regulations like ISO standards. They play a key role in continuous improvement by identifying areas for enhancement and working with other teams to resolve quality-related issues. Quality System jobs are vital across industries such as manufacturing, healthcare, and pharmaceuticals to guarantee product safety, reliability, and effectiveness.

What skills and qualifications are needed to thrive as a quality systems specialist?

To thrive as a Quality Systems Specialist, you need a strong understanding of quality management principles, regulatory standards (such as ISO 9001), and typically a degree in engineering, life sciences, or a related field. Familiarity with quality management software (QMS), document control systems, and relevant certifications like Six Sigma or ASQ are commonly required. Attention to detail, problem-solving abilities, and strong communication skills help ensure compliance and continuous improvement. These skills are essential to maintain product quality, meet regulatory requirements, and support organizational excellence.

What are common challenges faced by professionals working in quality systems, and how can they be addressed?

Professionals in Quality Systems often encounter challenges such as ensuring compliance with evolving regulatory standards, maintaining thorough documentation, and fostering a culture of continuous improvement across departments. Addressing these challenges typically involves staying updated on industry regulations, implementing effective training programs, and utilizing robust digital tools for document management. Additionally, strong communication and collaboration with cross-functional teams are essential to align quality objectives with broader organizational goals.

What is the difference between Quality System vs Quality Assurance?

AspectQuality SystemQuality Assurance
DefinitionFramework of policies, processes, and procedures to ensure quality management across an organization.Part of the quality system focused on preventing defects through planned activities and systematic processes.
FocusOverall quality management and compliancePreventing defects and ensuring product/service quality
CertificationsISO 9001, QS-9000ISO 9001, Six Sigma, CQA
Work EnvironmentCross-departmental, organizational-wideSpecific to quality processes and audits

In summary, a Quality System encompasses the entire framework for managing quality within an organization, including policies and procedures. Quality Assurance is a key component of the Quality System, focusing specifically on preventing defects and ensuring quality through systematic activities.

What are the most commonly searched types of Quality System jobs in Connecticut?

The most popular types of Quality System jobs in Connecticut are:

Quality System jobs near you
Infographic showing various Quality System job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 13% Part Time, 2% Temporary, 5% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Quality System Manager - Remote

Farmington, CT • Remote

The Jackson Laboratory
Biotechnology Research and Development • 1 - 5K employees

8.6

Company rating: 8.6 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

20th of 120 rated laboratories

People enjoy working here

Good employer

Recommended by parents

Learn more about The Jackson Laboratoryexternal

$85.99 - $130K/hr

Full-time

Posted 26 days ago

Job description

This position will direct efforts to harmonize practices across all JAX locations, both domestic and international where applicable, drive organizational change and implement quality improvements. This position will develop and execute JAX-wide strategies to enhance process efficiency, improve risk mitigation, and oversee key quality functions, including internal and external audits, deviation reviews, CAPA facilitation, document control, and change management. Position will be responsible for training and leading the Quality team in industry best practices, and will be responsible for reshaping quality culture across the global organization.

The salary range is $85.987 - $130,000. Salary will be determined based on qualifications and experience.

This role is remote with occasional travel to JAX locations. The ideal candidates will be located on the east coast.

Key Responsibilities (What you contribute):

  • Develop a long-term process development and improvement strategy, focused on assuring quality, and in collaboration with others in the global organization
  • Proactively identify, analyze and leverage quality data to identify trends and risks, manage risk-based assessments and support the implementation of risk mitigation strategies
  • Develop and implement continuous quality improvements in systems to reduce complexity, improve effectiveness, efficiencies and productivity and ensure sustainability and globalization
  • Develop and ensure a high-quality process development and improvement policy is propagated, understood, and implemented organization-wide; provide strategic leadership in a policy setting
  • Determine and implement the quality assurance/quality system subset strategy for global team
  • Co-lead the implementation of quality and regulatory compliance software systems
  • Direct quality personnel by coaching, counseling, and leading employees
  • Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies
  • Other duties as assigned

Minimum Qualifications:

  • Bachelor's degree and 7 years of relevant quality experience
  • Minimum of 2 years supervisory experience.
  • Expertise in risk management tools including Design FMEA, Process FMEA (pFMEA).
  • Proficiency in Root Cause Analysis (RCA), statistical analysis and data-driven decision-making.
  • Experience with MSA/Gauge R&R, quality metrics and performance monitoring.
  • Experience with and knowledge of ISO 9,001 standards.
  • Computer System Validation requirements.
  • Strong knowledge of Quality by Design (QbD) principles and stage-gate product development.
  • Lean/Six Sigma Certification preferred. Quality certifications (CQA, CQM/OE, etc.) a plus.
  • Functional management/leadership experience in a pharmaceutical or biotechnology operation.
  • Research regulatory compliance experience preferred.
  • Grows relationships with key organizational influencers and customers by building credibility and trust.
  • Experience with change management in multi-site, complex environment.
  • Advanced interpersonal skills sufficient for developing complex, dynamic relationships with a diverse variety of individuals representing a broad cross-section of cultures, disciplines, and levels of sophistication.
  • Advanced verbal and written skills sufficient to communicate with the senior leaders in a variety of partner institutions.
  • Ability to formulate, analyze and evaluate complex plans and programs.
  • Ability to keep current on industry practices, regulatory requirements and industry changes.
  • Champion of Lean and continuous improvement .
  • Ability to travel, 10%.

#CA-DS5

About JAX:

The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California),Japan andChina. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health.

Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visitwww.jax.org.

EEO Statement:

The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.

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