Quality Assurance Intern Jobs in Rhode Island
Quality Assurance Intern jobs in Rhode Island concentrate in the state's life sciences, defense manufacturing, and financial services sectors, with Providence, Woonsocket, and Cranston serving as the primary hiring centers. Employers with an established presence in Rhode Island, including CVS Health, Atrion Medical Products, and Raytheon Technologies, regularly bring on quality assurance interns to support regulatory compliance, product testing, and process validation work. The most in-demand specialties are software quality assurance, medical device quality systems, and ISO documentation. Scan the live roles below and apply to whichever ones fit.
Find Quality Assurance Intern JobsOverview
Showing 5 of 16+ Quality Assurance Intern jobs
Westerly, RI, US, 02891
- Perform Contract Review sign-off, including evaluation of customer requirements such as VIRs, test procedures, submittals, and reporting requirements.
- Conduct RFQ (pre-contract) and Purchase Order (PO) reviews to ensure quality requirements are captured and understood.
- Review receiving documentation for completeness and compliance to contract requirements.
- Support Source Inspection at Gemba, including prioritization and visibility of activities.
- Develop, revise, and maintain Incoming Inspection Instructions to ensure accuracy and alignment with requirements.
- Support Receiving Inspection personnel to ensure consistent execution of inspection processes.
- Review inspection records, COCs, and supporting documentation; ensure proper record retention (scan and file).
- Prepare, revise, and maintain Acceptance Test Procedures and Qualification Test Procedures to ensure accuracy and alignment with requirements and submit for approval when required.
- Prepare, review, and revise test reports for WIP and final product.
- Review completed test reports and submit for approval when required.
- Generate and submit data packages, ensuring required documentation is complete and accurate.
- Coordinate and submit Source Inspection requests as required by contract.
- Prepare Certificates of Conformance (CoC) and shipping documentation in accordance with Contract Review and the Purchase Order.
- Support MRB, including Nonconformance Report processing, completion, scanning, and filing.
- Communicate with suppliers regarding missing certifications and vendor-related issues.
- Review and process Engineering Change Notices (ECNs) to ensure continued compliance of product and documentation.
- Maintain accurate quality records and support overall quality system compliance.
- Perform other duties as assigned.
- Bachelor’s degree in engineering, Quality, Manufacturing, or related technical field OR equivalent combination of education and relevant experience.
- Minimum of 3–5 years of experience in a manufacturing or quality engineering role.
- Experience in high-reliability, regulated, or defense-related environments preferred.
- Working knowledge of ISO 9001:2015 Quality Management Systems, including process control, documentation, and record retention.
- Familiarity with contract review processes and requirement flow-down.
- Understanding of controlled documentation and revision control practices.
- Awareness of audit processes (internal, customer, regulatory)
- Demonstrated understanding of:
- Material and certification traceability requirements
- Objective Quality Evidence (OQE) generation and verification
- Data package preparation and completeness validation
- Configuration control and revision integrity
- Familiarity with NAVSEA contract requirements and Level 1 program expectations
- Ability to support or coordinate Government Source Inspection (GSI) activities
- Ability to interpret engineering drawings, specifications and technical requirements (including basic GD&T).
- Experience with:
- Incoming inspection processes and documentation review
- Verification of supplier certifications (CoCs, material certs)
- Development and/or use of inspection instructions or checklists
- Ability to communicate effectively regarding quality requirements such as nonconformances and contractual expectations.
- Strong attention to detail with emphasis on record accuracy and completeness, traceability documentation, and controlled data storage and retention.
- Proficiency in Microsoft Office and Document control systems/QMS tools
- Strong organizational skills and ability to manage multiple priorities.
- High level of accountability for compliance and accuracy.
- Ability to work independently within a controlled, procedure-driven environment.
- Clear, concise technical communication (written and verbal).
Compensation
Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location.
For more information on AMETEK's competitive benefits, please click here.
AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.5 billion.
AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 22,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK is a component of the S&P 500. Visit https://www.ametek.com/careers for more information.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call 1 (866) 263-8359.
Westerly, RI, US, 02891
- Perform Contract Review sign-off, including evaluation of customer requirements such as VIRs, test procedures, submittals, and reporting requirements.
- Conduct RFQ (pre-contract) and Purchase Order (PO) reviews to ensure quality requirements are captured and understood.
- Review receiving documentation for completeness and compliance to contract requirements.
- Support Source Inspection at Gemba, including prioritization and visibility of activities.
- Develop, revise, and maintain Incoming Inspection Instructions to ensure accuracy and alignment with requirements.
- Support Receiving Inspection personnel to ensure consistent execution of inspection processes.
- Review inspection records, COCs, and supporting documentation; ensure proper record retention (scan and file).
- Prepare, revise, and maintain Acceptance Test Procedures and Qualification Test Procedures to ensure accuracy and alignment with requirements and submit for approval when required.
- Prepare, review, and revise test reports for WIP and final product.
- Review completed test reports and submit for approval when required.
- Generate and submit data packages, ensuring required documentation is complete and accurate.
- Coordinate and submit Source Inspection requests as required by contract.
- Prepare Certificates of Conformance (CoC) and shipping documentation in accordance with Contract Review and the Purchase Order.
- Support MRB, including Nonconformance Report processing, completion, scanning, and filing.
- Communicate with suppliers regarding missing certifications and vendor-related issues.
- Review and process Engineering Change Notices (ECNs) to ensure continued compliance of product and documentation.
- Maintain accurate quality records and support overall quality system compliance.
- Perform other duties as assigned.
- Bachelor’s degree in engineering, Quality, Manufacturing, or related technical field OR equivalent combination of education and relevant experience.
- Minimum of 3–5 years of experience in a manufacturing or quality engineering role.
- Experience in high-reliability, regulated, or defense-related environments preferred.
- Working knowledge of ISO 9001:2015 Quality Management Systems, including process control, documentation, and record retention.
- Familiarity with contract review processes and requirement flow-down.
- Understanding of controlled documentation and revision control practices.
- Awareness of audit processes (internal, customer, regulatory)
- Demonstrated understanding of:
- Material and certification traceability requirements
- Objective Quality Evidence (OQE) generation and verification
- Data package preparation and completeness validation
- Configuration control and revision integrity
- Familiarity with NAVSEA contract requirements and Level 1 program expectations
- Ability to support or coordinate Government Source Inspection (GSI) activities
- Ability to interpret engineering drawings, specifications and technical requirements (including basic GD&T).
- Experience with:
- Incoming inspection processes and documentation review
- Verification of supplier certifications (CoCs, material certs)
- Development and/or use of inspection instructions or checklists
- Ability to communicate effectively regarding quality requirements such as nonconformances and contractual expectations.
- Strong attention to detail with emphasis on record accuracy and completeness, traceability documentation, and controlled data storage and retention.
- Proficiency in Microsoft Office and Document control systems/QMS tools
- Strong organizational skills and ability to manage multiple priorities.
- High level of accountability for compliance and accuracy.
- Ability to work independently within a controlled, procedure-driven environment.
- Clear, concise technical communication (written and verbal).
Compensation
Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location.
For more information on AMETEK's competitive benefits, please click here.
AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.5 billion.
AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 22,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK is a component of the S&P 500. Visit https://www.ametek.com/careers for more information.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call 1 (866) 263-8359.
See All 16 Quality Assurance Intern Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
Find Quality Assurance Intern JobsQuality Assurance Intern Jobs by City in Rhode Island
Where Rhode Island roles are concentrated, by current openings.
Quality Assurance Intern Job Market in Rhode Island
A snapshot from current Rhode Island openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Medical Devices
- Healthcare & Medical Services
- Technology & Software
- Electronics & Hardware
What Rhode Island Employers Look For
The qualifications that appear most often in quality assurance intern jobs across Rhode Island.
- Enrollment in a bachelor's or associate program in engineering, science, or a related field
- Familiarity with quality management standards such as ISO 9001 or FDA 21 CFR regulations
- Experience or coursework in testing methodologies, defect tracking, or root cause analysis
- Proficiency with Microsoft Office tools and documentation software used in quality workflows
- Strong written communication skills for drafting inspection reports and nonconformance records
- Ability to work on-site in a regulated manufacturing or laboratory environment in Rhode Island
Quality Assurance Intern Jobs in Rhode Island: Frequently Asked Questions
How do you become a quality assurance intern in Rhode Island?
Most quality assurance intern roles in Rhode Island do not require a state-issued license, so the path runs through academic enrollment and targeted preparation. Employers in Rhode Island's life sciences and defense sectors look for students in engineering, biology, chemistry, or information systems programs at institutions like the University of Rhode Island or Rhode Island College. Building coursework around regulatory standards, completing a relevant lab or technical project, and earning an introductory certification in quality fundamentals strengthens a candidate's standing before applying.
Which companies hire quality assurance interns in Rhode Island?
Rhode Island quality assurance intern roles are posted by ZOLL Medical Corporation, Charcuterie Artisans, and Electro Standards Laboratories and others right now, based on current listings on Migrate Mate as of July 2026. Rhode Island's concentration of life sciences companies and defense contractors means many of these openings involve regulated environments where quality documentation and compliance testing are central to the internship work.
Which Rhode Island cities have the most quality assurance intern jobs?
Cranston, Pawtucket, and Warwick account for the largest share of quality assurance intern openings in Rhode Island. Providence anchors the market as the state's primary commercial and healthcare hub, while surrounding communities like Woonsocket and Cranston draw openings from the manufacturing and medical products employers headquartered or operating there. Smaller postings also appear in the East Bay corridor near defense and technology facilities.
Are there remote quality assurance intern jobs in Rhode Island?
Yes, but they're rare. Quality assurance intern work frequently requires on-site access to production lines, laboratory equipment, or regulated documentation systems, which limits remote options. About 17% of quality assurance intern openings tied to Rhode Island are remote or hybrid as of July 2026, and those tend to be software or data-focused roles rather than manufacturing or medical device positions. Hybrid arrangements are more common at technology-forward companies than in traditional regulated industries.
How can I get hired as a quality assurance intern in Rhode Island with little or no experience?
The most realistic entry path is applying through university cooperative education programs, which connect Rhode Island students directly to employers before graduation. The University of Rhode Island's co-op and experiential learning office partners with life sciences and manufacturing companies across the state. Candidates without prior QA experience can strengthen their applications by completing a coursework project in inspection methods or process documentation, volunteering in a lab setting, or transitioning from a lab technician, research assistant, or manufacturing support role where attention to detail and compliance were part of the work.
Where can I find and apply to quality assurance intern jobs in Rhode Island?
You can find and apply to quality assurance intern jobs in Rhode Island on Migrate Mate, which lists current openings in the state. Search the roles available, identify the ones that match your background and schedule, and apply directly to the positions that fit. No signup is required to see the listings.
See All 16 Quality Assurance Intern Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
Find Quality Assurance Intern Jobs