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Remote Quality Management System Jobs (NOW HIRING)

Role Overview The Senior/Executive Director, Quality Management System (QMS) will be responsible ... Position Location This is a remote role, however, 10-20% travel to team and company events is ...

Plan and execute a risk-based supplier audit program, conducting on-site and remote quality system ... Assess supplier quality management systems for adequacy, compliance, and continuous improvement ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an ... Develop and revise quality system documentation including procedures, work instructions, and change ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an ... Develop and revise quality system documentation including procedures, work instructions, and change ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an ... Develop and revise quality system documentation including procedures, work instructions, and change ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an ... Develop and revise quality system documentation including procedures, work instructions, and change ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an ... Develop and revise quality system documentation including procedures, work instructions, and change ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an ... Develop and revise quality system documentation including procedures, work instructions, and change ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an ... Develop and revise quality system documentation including procedures, work instructions, and change ...

... Management System (QMS) library. To ensure customer growth, aid in completing customer surveys ... This person will work closely with Case Management, Partner Support, and remote Quality Engineering ...

General information Job Posting Title Quality Control Manager (Remote) Date Tuesday, July 7, 2026 ... management system to continuously identify opportunities for improvement while maintaining ...

Maintain and improve the Quality Management System (QMS). * Lead root cause analysis and Corrective and Preventive Action (CAPA) programs. * Develop and maintain global quality procedures and ...

Pleasanton Tech Center 100% Remote *Must be a US Citizen Any Travel for this role? : No Required ... Systems Knowledge Required : Healthcare experience might be good Certifications needed: None ...

Quality Systems Manager

Boston, MA · Remote

$170K - $180K/yr

Responsible for the ongoing management of the electronic Document Management System (eDMS ... Ability to work effectively with communication and office tools in a remote, fast-paced, and ...

Quality Specialist

Parsippany, NJ · Remote

$60K - $85K/yr

Remote - offsite Hours: 40.0 Responsibilities * Support and administer the Electronic Quality Management System (Veeva), including user access, reports, system configuration, validation, and end-user ...

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Remote Quality Management System information

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$54K

$98.6K

$154K

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

As of Jul 11, 2026, the average yearly pay for remote quality management system in the United States is $98,613.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $122,500.00 per year, depending on experience, location, and employer.

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 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.

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 are the key skills and qualifications needed to thrive as a Remote Quality Management System (QMS) Specialist, and why are they important?

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.
More about Remote Quality Management System jobs
What cities are hiring for Remote Quality Management System jobs? Cities with the most Remote Quality Management System job openings:
What are the most commonly searched types of Quality Management System jobs? The most popular types of Quality Management System jobs are:
What states have the most Remote Quality Management System jobs? States with the most job openings for Remote Quality Management System jobs include:
Infographic showing various Remote Quality Management System job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, and 23% Contract. Highlights an 100% Remote job distribution, with an average salary of $98,613 per year, or $47.4 per hour.

Senior/Executive Director, Quality Management System

Jade Biosciences

On-site, Remote

Full-time

Posted 22 days ago


Job description

About Jade Biosciences
Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn.
Role Overview
The Senior/Executive Director, Quality Management System (QMS) will be responsible for driving and delivering the activities necessary to develop, implement, and continuously improve a phase appropriate GxP QMS. This role will be directly involved with both strategy development and day-to-day tactical execution related to QMS processes such as Document Management, Training Management, Change Control, Management Review (MR), Annual Product Quality Review (APQR), Deviation, CAPA, Risk Management, and GxP Computer System Assurance.
The Sr./Exec. Director will be responsible for the maintenance of both paper-based and electronic processes and lead quality initiatives to support the pace and growth of the organization.
This role will maintain and ensure effectiveness of quality programs and documentation to assure compliance and inspection readiness with all applicable quality requirements and regulatory standards.
The ideal candidate brings hands-on expertise in creating and maintaining a GxP QMS, a proactive approach to problem-solving, and the ability to guide and influence cross-functional teams while upholding the highest standards of quality and compliance.
Key Responsibilities
  • Select, implement, manage, and oversee GxP electronic systems including any associated Purchase Orders and contracts.
  • Develop, implement, manage, continuously improve, and oversee processes such as Document Management, Training Management, Change Control, Management Review (MR), Annual Product Quality Review (APQR), Deviation/CAPA/ Risk Management, and GxP Computer System Assurance
  • Guide and support GxP process owners with implementation and improvement /optimization of key functional area processes
  • Establish and improve policies and standard operating procedures for efficient and compliant management of GxP QMS processes
  • Establish, track and report quality metrics for QMS processes and present improvement opportunities at Management Review meetings
  • Implement phase appropriate, risk-based, fit-for-purpose approaches to QMS processes
  • Ensure that QMS processes comply with phase applicable regulatory standards, regulations and guidelines.
  • Maintain awareness of new regulations, technologies, industry trends and best practices and apply them as may be relevant
  • Manage resources to achieve company, department and functional area goals and objectives
  • Contribute to the development and maintenance of a positive team-focused company culture
  • Provide coaching as a manager and team member, make quality decisions and be Quality Approver as appropriate.
  • Act as the primary QMS subject matter expert and point of contact for all related matters and issues.
  • Review and approve (as appropriate) procedures, service provider quality agreements, qualification and onboarding forms and regulatory filings.
  • Champion continuous improvement and simplification across quality systems.
  • Contribute to building a strong quality culture within the organization.
  • Direct and/or deliver yearly training for internal staff as needed.
  • Work closely with Development, Clinical Operations, CMC and other departments to drive inspection readiness and support regulatory interactions.
  • Prepare KPIs, metrics and analysis and present status updates as needed.
  • Provide leadership in inspection preparedness.
  • Apply risk-based thinking to identify the quality activities that meaningfully influence outcomes.
  • Understand when to escalate, when to intervene, and when to let teams move forward.
  • Provide clear, concise guidance that helps teams stay focused, aligned, and inspection ready.

Qualifications
  • Bachelors + 17 or Masters + 14 or PhD + 10 years of related experience within the pharmaceutical industry.
  • Minimum of eight (8) years building, implementing and/or managing Quality Management Systems within the pharmaceutical industry
  • At least five (5) years of experience with Phase 3 and/or commercial product
  • At least three (3) years of experience in an outsourced environment
  • Successful track record of translation and implementation of requirements into operational execution.
  • Extensive knowledge of FDA regulations and practices, ICH guidance, and strong knowledge of global health authority regulations (e.g. EU, China, Japan, Australia) and practices.
  • Must have excellent verbal, written, interpersonal, organizational and communication skills both internally and externally
  • Strong technical understanding and experience in implementing and validating cloud-based (hosted) computer systems
  • The ability to perform at executive levels while collaborating with key stakeholders in an exciting, dynamic environment with a high degree of engagement and enthusiasm.
  • Ability to make timely and sound quality decisions when faced with complex compliance, technical and regulatory considerations. Highly skilled in the ability to work with ambiguity and complexity.
  • Ability to work with minimal supervision, to set priorities to meet timelines, and to manage, motivate and influence others with variable workloads and demanding timelines. Prior management experience is required.
  • Ability to tactically and strategically execute the day-to-day operations to support Jade's goals.
  • Expertise in reviewing, revising, and writing Standard Operating Procedures (SOPs) from scratch.
  • A self-starter and a team player who thrives in a fast-paced dynamic team environment.
  • Proficiency in using SharePoint, Veeva and Microsoft Office applications required (MS Outlook, MS Word, MS Excel, MS PowerPoint).

Position Location
This is a remote role, however, 10-20% travel to team and company events is required.
The anticipated salary range for the Executive Director level is $265,000 - $300,000. The anticipated salary range for the Senior Director level is $250,000 - $280,000 The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography.
As part of the I-9 verification of authorization to work in the United States, Jade Bioscience participates in E-Verify. To learn more about E-Verify please review this poster.
Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.