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Software Qa Engineer Intern Jobs in Woonsocket, RI

PAVmed, Inc.

Quality Assurance Engineer

Foxboro, MA · Remote

The Quality Engineer is responsible for ensuring an efficient and compliant Quality Management System (QMS), including analysis, development and revision of QMS processes, performance monitoring and ...

PAVmed, Inc.

Quality Assurance Engineer

Foxboro, MA · On-site

The Quality Engineer is responsible for ensuring an efficient and compliant Quality Management System (QMS), including analysis, development and revision of QMS processes, performance monitoring and ...

Teleflex

Quality Assurance Engineer II

Mansfield, MA · On-site

$87K - $131K/yr

For more information, please visit Ingenyx.com Position Summary The Quality Assurance Engineer ... Ability in database development, statistical software and analysis, simulation, word processing for ...

Pwc

AIT - AI Quality Assurance Senior Associate

Boston, MA · On-site

$72K - $212K/yr

... engineering to enhance software development and testing processes. Within our Assurance practice, you will leverage your technical skills and creative thinking to deliver innovative software ...

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All JobsSoftware Qa Engineer Intern JobsSoftware Qa Engineer Intern Jobs in Woonsocket, RI

Software Qa Engineer Intern information

See Woonsocket, RI salary details

$12

$24

$37

How much do software qa engineer intern jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for software qa engineer intern in Woonsocket, RI is $24.35, according to ZipRecruiter salary data. Most workers in this role earn between $19.81 and $27.64 per hour, depending on experience, location, and employer.

Is a Software QA Engineer Intern still in demand?

Software QA Engineer Intern positions remain in demand as companies continue to prioritize quality assurance in software development. Interns with skills in testing tools, scripting, and understanding of software development processes are sought after to support quality teams and gain industry experience.

What are the key skills and qualifications needed to thrive in the software QA engineer intern position, and why are they important?

To excel as a Software QA Engineer Intern, you should possess a foundation in computer science, basic understanding of software development and testing methodologies, and a keen attention to detail. Familiarity with test management tools (like JIRA or TestRail), version control systems (such as Git), and some exposure to automation frameworks (like Selenium) is often preferred. Effective communication, teamwork, and analytical thinking set standout candidates apart in this role. These skills are essential to ensure software quality, efficiently identify and resolve defects, and collaborate productively with development teams.

What are the typical responsibilities of a software QA engineer intern?

As a Software QA Engineer Intern, you’ll assist with writing and executing test cases, reporting software bugs, and collaborating with developers to troubleshoot and resolve issues. Your daily work may involve manual and automated testing, documenting results, and participating in agile team meetings. You’ll also learn about industry-standard testing tools and processes, gaining hands-on experience in quality assurance workflows. This role provides an excellent opportunity to build technical skills and understand the software development lifecycle, all while working alongside experienced QA professionals.

What is a software QA engineer intern?

A Software QA Engineer Intern assists in testing software applications to ensure they meet quality standards before release. They help design test cases, execute manual and automated tests, and document defects. Interns collaborate with developers and QA teams to identify and resolve issues, improving software reliability. This role provides hands-on experience with testing tools, methodologies, and industry best practices.

Software Qa Engineer Intern jobs near you
Infographic showing various Software Qa Engineer Intern job openings in Woonsocket, RI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 85% In-person, and 15% Hybrid job distribution, with an average salary of $50,658 per year, or $24.4 per hour.

Quality Assurance Engineer

PAVmed, Inc.

Foxboro, MA • Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago

Job description

The Quality Engineer is responsible for ensuring an efficient and compliant Quality Management System (QMS), including analysis, development and revision of QMS processes, performance monitoring and continuous improvement, ensuring accuracy and compliance with relevant standards. This individual will operate within a small, collaborative and highly driven team focused on improving patient care and saving lives.
PAVmed Inc. is a diversified commercial-stage medical technology company operating in the medical device, diagnostics, and digital health sectors. The company focuses on advancing innovative technologies that address significant unmet clinical needs and improve patient outcomes.
PAVmed’s portfolio includes Lucid Diagnostics, a cancer prevention diagnostics company, and Veris Health Inc., a digital health company focused on personalized cancer care through remote patient monitoring using implantable biologic sensors and connected external devices delivered through the Veris Cancer Care Platform.
Through its portfolio approach, PAVmed supports the development and growth of innovative healthcare businesses across multiple sectors. Every role at PAVmed contributes to strengthening this platform and advancing the company’s long-term strategy.
When you join PAVmed, you become part of a diverse, inclusive, and mission-driven team. We’re committed to creating an environment where you can thrive both professionally and personally.
Here’s what you can expect when you join our team:
  • Comprehensive Benefits: Enjoy top-tier medical, dental, and vision coverage, with 98% of employee healthcare premiums paid by the company, plus company-paid basic life insurance, and short- and long-term disability coverage.
  • Financial Wellness: Build your future with a company 401(k) match (with immediate vesting) and an Employee Stock Purchase Program (ESPP) that lets you share in our success.
  • Rest, Recharge and Give Back: Paid vacation, sick days, 12 company holidays, and a dedicated volunteer day to give back to the causes that matter to you.
  • Professional Growth: Take your career to the next level with ongoing learning opportunities, hands-on training, and clear pathways for advancement.
  • Wellbeing Support: Access employee assistance programs, wellness initiatives, and gym reimbursement to help you feel your best inside and outside of work.
  • A Winning Culture: Proudly recognized as one of GenomeWeb’s 2025 Best Places to Work, we celebrate collaboration, innovation, and shared purpose every day.

Key Responsibilities:
  • Supports and maintains Quality Management System (QMS) processes including audits, complaints, CAPA, and change control activities to ensure compliance with regulatory and company requirements.
  • Owns and manages the Document Control process, including DCO routing, version control, and change order processing, ensuring timely and compliant document lifecycle management.
  • Manages the training program including training matrix maintenance, training record management, and rollout of procedure-based and role-based training to ensure organizational compliance.
  • Supports supplier quality activities including supplier qualification, monitoring of supplier performance, and maintenance of the approved supplier list (ASL) in accordance with QMS requirements.
  • Supports eQMS implementation activities including data migration, validation support, user acceptance testing until go-live, serving as one of the key liaisons between the organization and the eQMS vendor.
  • Reviews and analyzes QMS metrics and performance indicators, preparing reports to identify trends, nonconformances, and opportunities for continuous improvement.
  • Assists in the development, implementation, and revision of QMS procedures, SOPs, work instructions, and quality documentation to maintain compliance with applicable standards and regulations.
  • Participates in risk assessment activities and supports the development of mitigation plans to minimize quality and compliance risks.
  • Contributes to continuous improvement initiatives by identifying process enhancements and supporting implementation of quality system improvements.
  • Collaborates cross-functionally to resolve quality issues, support investigations, and implement corrective and preventive actions.
  • Supports internal and external audits by preparing documentation, coordinating audit activities, and assisting with responses to audit observations.
  • Maintains effective working relationships with internal teams and external stakeholders to support quality objectives and compliance activities.
  • Proactively maintains knowledge of industry standards, regulatory requirements, and company quality procedures.
  • Occasional travel for team meetings, conferences and vendor visits
  • Performs other quality system duties as assigned in support of company quality objective
Qualifications:
  • Education: Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline required.
  • Experience amp; Technical Expertise: 3+ years of experience in FDA-regulated and/or ISO 13485 medical device manufacturing or quality environments.
  • Working knowledge of Quality Management Systems (QMS), including document control, training, CAPA, audits, change control, and nonconformance processes.
  • Experience supporting internal and external audits and maintaining compliance with applicable regulatory and quality standards.
  • Familiarity with CAPA processes, root cause analysis tools, and continuous improvement methodologies.
  • Experience reviewing quality data, metrics, and KPIs to identify trends and support decision-making.
  • Ability to work collaboratively with cross-functional teams and communicate effectively with internal and external stakeholders.
  • Experience maintaining training records, training matrices, or learning management systems is preferred.
  • ASQ-CQE, ISO 13485, or Lead Auditor certification is a plus.
  • Proficient in Microsoft Office applications and quality documentation systems.
  • Hands-on experience with eQMS platforms strongly preferred; experience participating in an eQMS implementation or migration is a plus.
  • Experience with supplier qualification, approved supplier list (ASL) management, or supplier audits preferred.
  • Self-motivated, able to accomplish multiple assignments simultaneously
  • Strong organizational and problem-solving skills
  • Detail-oriented
PAVmed and its subsidiaries are committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We are also committed to compliance with all fair employment practices regarding citizenship and immigration status.

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