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Quality System Manager Jobs in Rhode Island (NOW HIRING)

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Quality Manager Automotive

Cumberland, RI · On-site

$99K - $117K/yr

Quality Management System * Maintain and improve the Quality Management System in compliance with IATF 16949, ISO 14001, customer-specific requirements, and internal standards. * Manage quality ...

Lead the development, implementation, and maintenance of the Quality Management System (QMS) in alignment with industry standards (e.g., ISO 9001). * Lead all aspects of quality control activities ...

Lead the development, implementation, and maintenance of the Quality Management System (QMS) in alignment with industry standards (e.g., ISO 9001). * Lead all aspects of quality control activities ...

Lead the development, implementation, and maintenance of the Quality Management System (QMS) in alignment with industry standards (e.g., ISO 9001). * Lead all aspects of quality control activities ...

Quality Manager

Cranston, RI · On-site

$100 - $125/hr

The Quality Manager is Responsible for ensuring that products/materials/services supplied/provided ... Must be capable of making written recommendations for improving Quality Assurance Systems and ...

Quality Technician

Lincoln, RI · On-site

$28 - $30.25/hr

This is an opportunity to play a key role in maintaining and improving a robust ISO 9001 Quality Management System while working with advanced wire, cable, and compound manufacturing operations. We ...

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

Manufacturing Manager of Quality

Lincoln, RI · On-site

$110K - $140K/yr

Quality Management Systems * Maintain and improve the organization's Quality Management System (QMS). * Ensure compliance with applicable quality standards, customer requirements, and internal ...

Quality Engineer

Warwick, RI · On-site

$72K - $93K/yr

Report to management on quality issues, trends and losses. * Assist in training equipment operators ... Perform internal quality system, manufacturing process, and product audits. * Interface with ...

Quality Engineer

Warwick, RI · On-site

$72K - $93K/yr

Report to management on quality issues, trends and losses. * Assist in training equipment operators ... Perform internal quality system, manufacturing process, and product audits. * Interface with ...

Quality Engineer

West Warwick, RI · On-site

$69K - $90K/yr

Quality Operations Manager Job Function: The Quality Engineer supports quality systems and product quality for a personal care contract manufacturing operation. This role has no direct reports and ...

Quality Engineer

Warwick, RI · On-site

$100 - $125/hr

Report to management on quality issues, trends and losses. * Assist in training equipment operators ... Perform internal quality system, manufacturing process, and product audits. * Interface with ...

Quality Engineer

West Warwick, RI · On-site

$69K - $90K/yr

Quality Operations Manager Job Function: The Quality Engineer supports quality systems and product quality for a personal care contract manufacturing operation. This role has no direct reports and ...

Quality Manager

Rumford, RI · On-site

$125 - $150/hr

Lead and maintain the Quality Management System in accordance with ISO 9001 and other applicable standards. * Develop, implement, and improve quality policies, procedures, work instructions, and ...

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Lead and maintain the Quality Management System in accordance with ISO 9001 and other applicable standards. * Develop, implement, and improve quality policies, procedures, work instructions, and ...

Showing results 21-40

Quality System Manager information

See Rhode Island salary details

$52.9K

$96.6K

$150.8K

How much do quality system manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for quality system manager in Rhode Island is $96,573.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,900.00 and $120,000.00 per year, depending on experience, location, and employer.

What does a quality system manager do?

A Quality System Manager oversees the development, implementation, and maintenance of an organization's quality management systems. They ensure that all processes and products meet established quality standards and comply with relevant regulations. Their responsibilities include auditing processes, managing documentation, training staff on quality procedures, and driving continual improvement initiatives. By monitoring performance and addressing non-conformities, they help organizations deliver consistent, high-quality products or services.

What are the key skills and qualifications needed to thrive as a quality system manager?

To thrive as a Quality System Manager, you need a solid background in quality management principles, regulatory compliance, and process improvement, typically with a degree in engineering, life sciences, or a related field. Familiarity with ISO standards (e.g., ISO 9001), quality management software, and relevant certifications like Six Sigma or ASQ certifications is important. Strong leadership, problem-solving, and communication skills help drive cross-functional initiatives and foster a culture of continuous improvement. These skills ensure effective implementation of quality systems, compliance with industry standards, and sustained operational excellence.

What are some common challenges faced by a quality system manager when implementing new quality standards across an organization?

Quality System Managers often encounter challenges such as resistance to change from staff, aligning new standards with existing processes, and ensuring consistent understanding across departments. Building strong communication channels and providing thorough training are essential to facilitate adoption. Additionally, maintaining regulatory compliance while tailoring the system to the organization's unique needs requires careful planning and collaboration with cross-functional teams.

What is the difference between Quality System Manager vs Quality Assurance Manager?

AspectQuality System ManagerQuality Assurance Manager
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentOversees quality management systems across departmentsFocuses on product quality and testing processes
Industry UsageCommon in manufacturing, aerospace, automotivePrevalent in manufacturing, healthcare, software
Primary FocusMaintaining and improving quality management systemsEnsuring product quality through testing and inspection

The Quality System Manager primarily manages the overall quality management system, ensuring compliance with standards like ISO 9001. The Quality Assurance Manager concentrates on product quality, testing, and inspection processes. Both roles require similar certifications and are vital in manufacturing and related industries, but their focus areas differ—system oversight versus product quality assurance.

What cities in Rhode Island are hiring for Quality System Manager jobs?

Cities in Rhode Island with the most Quality System Manager job openings:

Infographic showing various Quality System Manager job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $96,573 per year, or $46.4 per hour.

Quality Engineering Technician

East Providence, RI • On-site

Evans Capacitor Co
Manufacturing • 11 - 50 employees

$18.25 - $24.50/hr

Full-time

Re-posted 17 days ago


Key responsibilities

  • Administer the Non-Conformance (NC) process, document NCMRs, coordinate containment activities, and support MRB and follow-up activities.

  • Facilitate Corrective Actions (CAs), support root cause analysis, track actions, verify effectiveness, and maintain documentation.

  • Manage supplier NC's and CA's, support customer complaints, and work with cross-functional teams to resolve quality-related issues.


Job description

Description:

About Evans Capacitor Company:

Evans, an electronic components company, is a trusted partner in the military, aerospace, industrial, and commercial markets, with over a century of combined experience as a reliable problem-solver. Being part of the Evans Group portfolio has enabled Evans to continue developing cutting-edge capacitor technology alongside other world-class technology companies that represent the future of mission-critical electronics.

Evans, with sites in East Providence, RI, Sanford, ME, and Phoenix, AZ, manufactures high-energy-density capacitors for demanding, mission-critical applications. We have the most power-dense capacitor technology in the industry and are routinely specified for defense, aerospace, and energy exploration applications where high reliability and SWaP (space, weight, and power) savings are critical design considerations.

Position Summary:

The Quality Engineering Technician is an hourly position that supports the company’s AS9100 and ISO 9001 registered Quality Management System (QMS) in an electronics component manufacturing environment. This role is primarily responsible for facilitating and maintaining the Non-Conformance (NC) and Corrective and Action (CA) programs in accordance with standard requirements. The position ensures proper containment, investigation, root cause analysis, corrective action implementation, and effectiveness verification to support product conformity, regulatory compliance, and continuous improvement.[MD1]  

This role works closely with Quality, Production, Engineering, Purchasing, Customer Quality, and other cross-functional team members to support quality-related activities and help resolve issues, maintain accurate quality records, and support overall quality system effectiveness. Process ownership, approval authority, personnel supervision, customer quality ownership, and final disposition responsibility remain with Quality leadership and assigned functional owners.

Key Responsibilities:

· Non-Conformance (NC) Management: Administer the NC process, document NCMRs, coordinate containment activities, support MRB and follow-up activities ensuring traceability of nonconforming material

· Track NCR/NMR status and support timely closure of records.

· CA Program Facilitation: Facilitate CAs, support root cause analysis, track actions, verify effectiveness, maintain documentation.

· Supplier & Customer Quality: Manage supplier NC’s and CA’s as assigned. Support customer complaints through management of internal CA’s as required.

· Root Cause Analysis & Risk: Support investigations, risk mitigation, and FMEA participation.

· Quality System Support: Maintain quality records, support audits, and help ensure compliance with company procedures, customer requirements, and the registered Quality Management System.

· Traceability & Configuration: Ensure traceability and configuration control in ERP system as well as controlled document databases.

· Data Analysis: Track quality metrics, NCR/NMR status, CAR/CA status, document revisions, and other assigned quality data.

· Document Control: Support creating, reviewing, updating, releasing, and maintaining controlled documents, quality records, and related document revision history.

· Review quality records for accuracy, completeness, and compliance.

· Assist with internal audits, audit preparation, and follow up activities.

· Help identify process improvements and support continuous improvement activities.

· Work with Production, Engineering, Purchasing, the Quality team, Customer Quality, and other cross-functional team members to resolve quality-related issues.

· Ensure quality files and records are organized, accurate, controlled, and readily available for audits or customer review.

· Perform other duties as required.


Requirements:

Qualifications

· High school diploma or equivalent required. Associate degree, technical training, or quality related coursework in a related field preferred.

· Experience in a quality, manufacturing, engineering, inspection, or document control role required.

· Familiarity with ISO 9001, AS9100, or similar quality management systems required.

· ASQ Certified Quality Technician (CQT), Certified Quality Inspector (CQI), Certified Quality Engineer (CQE), or related quality certification preferred.

· Knowledge of CAPA, NC systems, electronics manufacturing, Excel/data analysis, and document control processes.

· Ability to read and understand procedures, work instructions, drawings, specifications, and inspection records.

· Strong attention to detail and organizational skills.

· Good written and verbal communication skills.

· Ability to work independently and as part of a team.

· Proficiency with Microsoft Office and quality management software preferred.

· Experience with IPC standards, FMEA, aerospace background, audit support preferred.

Skills and Competencies

· Document control

· Quality record review

· NC and CAPA support

· Root cause and corrective action support

· Audit preparation

· Process improvement

· Strong attention to detail

· Clear communication

· Time management

· Team collaboration

Work Environment

This position may require work in both an office and manufacturing environment. The employee may occasionally be required to stand, walk, inspect parts, review production areas, and handle quality records or inspection documentation. PPE required on the manufacturing floor.

Physical Requirements

The employee may be required to sit, stand, walk, bend, reach, and use a computer for extended periods. The role may also require occasional lifting of light materials or records in accordance with company safety guidelines.

EEO/AA

Evans Capacitor Company is an affirmative action/equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, work-related mental or physical disability, veteran status, sexual orientation, gender identity, or genetic information. 

We participate in E-Verify. 

EEO Poster in English EEO Poster in Spanish 

U.S. EXPORT CONTROLS

As a U.S. defense manufacturer, Evans Capacitor Company is required to safeguard U.S. defense-related and other export-controlled articles, technologies, and services from unauthorized access, export, or re-export.

The transfer of U.S. export-controlled articles, technologies, or services (including manufacturing processes) to individuals or entities that do not qualify as “U.S. persons,” as defined by 22 CFR 120.62, is prohibited without prior authorization from the appropriate U.S. government agencies, such as the Department of State’s Directorate of Defense Trade Controls (DDTC).

Under 22 CFR 120.62, a “U.S. person” is defined as a lawful permanent resident as per 8 U.S.C. 1101(a)(20), or a protected individual under 8 U.S.C. 1324b(a)(3). It also includes any corporation, business association, partnership, society, trust, or other entity that is incorporated to do business in the United States, as well as governmental entities at the federal, state, or local levels. It does not include foreign persons as defined in § 120.63.

To ensure compliance with U.S. export control regulations, candidates for this position are required to undergo an Export Compliance Assessment. As part of this process, candidates may be asked to provide documentation verifying their status as “U.S. persons” or “foreign persons,” in accordance with U.S. regulation, to determine whether prior authorization is required to perform specific job duties related to this position