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Remote Quality Management System Jobs in Providence, RI

PAVmed, Inc.

Quality Assurance Engineer

Foxboro, MA · Remote

... remote patient monitoring using implantable biologic sensors and connected external devices ... Supports and maintains Quality Management System (QMS) processes including audits, complaints, CAPA ...

VIVA USA INC

Nurse Case Manager

Woonsocket, RI · On-site +1

Fully remote (never coming onsite) Description: The Case Manager utilizes a collaborative process ... Utilizes case management and quality management processes in compliance with regulatory and ...

VIVA USA INC

Nurse Case Manager

Woonsocket, RI · On-site +1

Fully remote (never coming onsite) Description: The Case Manager utilizes a collaborative process ... Utilizes case management and quality management processes in compliance with regulatory and ...

Harris

(Remote) GIS Developer

Carolina, RI · Remote

Our Outage Management team is dedicated to building resilient, scalable, and mission-critical systems that empower utilities to restore service safely and efficiently. In this role, you will directly ...

Harris

(Remote) GIS Developer

Carolina, RI · Remote

Our Outage Management team is dedicated to building resilient, scalable, and mission-critical systems that empower utilities to restore service safely and efficiently. In this role, you will directly ...

Ourhrconnect

RN Case Management Supervisor

Carolina, RI · On-site +1

... be fully remote . The candidate may be asked to come on-site for training, meetings, or other ... Performs quality control functions for work performed. Develops work plans to improve quality ...

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All JobsQuality Management System JobsRemote Quality Management System JobsRemote Quality Management System Jobs in Providence, RI

Remote Quality Management System information

See Providence, RI salary details

$54.6K

$99.6K

$155.6K

How much do remote quality management system jobs pay per year?

As of Aug 27, 2026, the average yearly pay for remote quality management system in Providence, RI is $99,622.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,300.00 and $123,800.00 per year, depending on experience, location, and employer.

What is a remote quality management system?

A Remote Quality Management System (QMS) is a set of processes and tools that help organizations maintain quality standards for their products or services, even when teams are working remotely or from different locations. It typically involves digital platforms that allow for documentation, tracking, auditing, and continuous improvement activities to be conducted online. This enables companies to ensure compliance with industry regulations, improve efficiency, and maintain product or service quality without the need for on-site supervision. Remote QMS solutions are especially important for distributed teams or organizations with global operations.

What are the key skills and qualifications needed to thrive as a remote quality management system specialist?

To thrive as a Remote Quality Management System Specialist, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 9001), and experience with QMS implementation or auditing. Proficiency with digital QMS platforms (e.g., MasterControl, Veeva), document control systems, and relevant certifications like Certified Quality Auditor (CQA) are typically required. Strong attention to detail, analytical thinking, and clear communication skills help you excel in virtual collaboration and problem-solving. These skills ensure compliance, continuous improvement, and effective maintenance of quality standards in a remote work environment.

How does a remote quality management system professional typically collaborate with cross-functional teams to maintain compliance and quality standards?

As a Remote Quality Management System professional, collaboration with cross-functional teams—such as engineering, regulatory affairs, and production—is primarily facilitated through virtual meetings, shared documentation platforms, and project management tools. You will regularly coordinate with these teams to ensure that quality protocols are followed and that any process improvements or corrective actions are implemented efficiently. Clear communication and proactive follow-up are essential, especially when addressing compliance issues or preparing for audits. Despite working remotely, strong digital collaboration skills help maintain the integrity of the quality system and ensure organizational standards are consistently met.

What is the difference between Remote Quality Management System vs Remote Quality Assurance Specialist?

AspectRemote Quality Management SystemRemote Quality Assurance Specialist
CertificationsISO 9001, CQE, Six SigmaISO 9001, CQE, Six Sigma
Work EnvironmentSoftware-focused, process-orientedProduct-focused, testing and compliance
Industry UsageManufacturing, healthcare, techManufacturing, software, healthcare

Both roles often require similar certifications and work in industries emphasizing quality standards. However, Remote Quality Management System professionals focus on implementing and maintaining quality management software and processes, while Remote Quality Assurance Specialists concentrate on testing, inspections, and ensuring product compliance remotely.

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

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

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

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

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

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

Remote Quality Management System jobs near you

Quality Assurance Engineer

Foxboro, MA • Remote

PAVmed, Inc.
51 - 200 employees
Learn more about PAVmed, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

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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