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Remote Quality Engineer Jobs in Providence, RI (NOW HIRING)

PAVmed, Inc.

Quality Assurance Engineer

Foxboro, MA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Quality Engineer is responsible for ensuring an efficient and compliant Quality Management ... remote patient monitoring using implantable biologic sensors and connected external devices ...

Harris

(Remote) Software Engineer

Carolina, RI · Remote

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The ideal candidate will be responsible for designing, developing, and maintaining high-quality ... This remote role welcomes candidates anywhere in Canada and the US. Travel is required as needed ...

Harris

(Remote) Software Engineer

Carolina, RI · Remote

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The ideal candidate will be responsible for designing, developing, and maintaining high-quality ... This remote role welcomes candidates anywhere in Canada and the US. Travel is required as needed ...

Harris

(Remote) Technical Engineer

Carolina, RI · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Collaborate with Product, Support, QA, and Engineering teams to improve customer outcomes ... Remote work and more! About MACC: Telecommunication companies of all sizes across the United States ...

Harris

Quality Assurance Analyst

Carolina, RI · On-site +1

$55K - $65K/yr

Ability to work effectively with developers, support staff, product stakeholders, and other cross ... Ability to manage priorities, meet deadlines, and work independently in a remote team environment.

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All JobsQuality Engineer JobsRemote Quality Engineer JobsRemote Quality Engineer Jobs in Providence, RI

Remote Quality Engineer information

See Providence, RI salary details

$45.5K

$84.9K

$120.2K

How much do remote quality engineer jobs pay per year?

As of Aug 18, 2026, the average yearly pay for remote quality engineer in Providence, RI is $84,899.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,700.00 and $94,000.00 per year, depending on experience, location, and employer.

What is a remote quality engineer?

A Remote Quality Engineer is responsible for ensuring the quality and reliability of products or services while working remotely. They develop and execute test plans, identify defects, and collaborate with development teams to improve processes. Their role may involve automation testing, performance testing, or software validation, depending on the industry. Strong analytical skills, attention to detail, and knowledge of quality assurance methodologies are essential.

What does a remote quality engineer do?

A typical day for a Remote Quality Engineer involves reviewing requirements, designing and executing test cases, logging defects, and collaborating with developers and product managers via virtual meetings and online tools. You may also spend time analyzing test results, automating repetitive tests, and verifying bug fixes in different environments. Communication is key, so regular updates and status reports are often shared through team platforms like Slack or Jira. This role is dynamic and may require adapting to evolving project priorities while maintaining high-quality deliverables.

What are the key skills and qualifications needed to thrive as a remote quality engineer?

To thrive as a Remote Quality Engineer, you need a solid background in quality assurance principles, software testing methodologies, and a relevant engineering or computer science degree. Familiarity with automated testing frameworks (like Selenium or JUnit), defect tracking systems, and certifications such as ISTQB or Six Sigma are often expected. Exceptional problem-solving abilities, attention to detail, self-motivation, and effective remote communication skills set top candidates apart. These capabilities are vital for maintaining product quality, collaborating across distributed teams, and ensuring continual process improvement from a distance.

Can remote quality engineers work from home?

Remote quality engineers can work from home, as many companies allow this role to be performed virtually. They typically use tools like test management software, collaboration platforms, and require strong communication skills to coordinate with teams remotely.

Is a remote quality engineer still in demand?

Remote quality engineers are in high demand as companies prioritize software quality and remote work flexibility. Skills in automation tools, testing frameworks, and continuous integration are especially valuable in this role, which often requires collaboration across distributed teams.

Is there a demand for a remote quality engineer?

There is strong demand for remote quality engineers across various industries, as companies seek professionals skilled in testing, automation tools, and quality assurance processes. The role often requires knowledge of programming, testing frameworks, and certifications like ISTQB, with many organizations offering flexible remote work arrangements.

What are the most commonly searched types of Quality Engineer jobs in Providence, RI?

The most popular types of Quality Engineer jobs in Providence, RI are:

What are popular job titles related to Remote Quality Engineer jobs in Providence, RI?

For Remote Quality Engineer jobs in Providence, RI, the most frequently searched job titles are:

What job categories do people searching Remote Quality Engineer jobs in Providence, RI look for?

The top searched job categories for Remote Quality Engineer jobs in Providence, RI are:

What cities near Providence, RI are hiring for Remote Quality Engineer jobs?

Cities near Providence, RI with the most Remote Quality Engineer job openings:

Remote Quality Engineer jobs near you
Infographic showing various Remote Quality Engineer job openings in Providence, RI 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 $84,899 per year, or $40.8 per hour.

Quality Assurance Engineer

PAVmed, Inc.

Foxboro, MA • Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 22 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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