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Quality Management System Administrator Jobs (NOW HIRING)

The eQMS System Administrator is responsible for the configuration, validation, and ongoing administration of the electronic Quality Management System (eQMS). This role serves as the technical and ...

The System Administrator will manage system operations across the Development, Staging, and Production environments hosted in a secure DoD cloud. The position requires experience with OpenText ...

System Administrator

Honolulu, HI · On-site

$65K - $120K/yr

The C2 System Administrator will provide technical expertise, implementation, maintenance ... Manage NetApp storage arrays, providing high-performance NFS services and efficient volume ...

The C2 System Administrator will provide technical expertise, implementation, maintenance ... Manage NetApp storage arrays, providing high-performance NFS services and efficient volume ...

Quality Management System and Services Lead

Corning, NY · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Quality Management System (QMS). This role ensures effective execution of key quality system ... Serve as primary or delegated administrator for EtQ modules related to document control, training ...

System Administrator

Jessup, MD · On-site

$150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Manage file systems, networking services, and system resources * Troubleshoot operating system and ... We help clients get work done more efficiently and economically, without compromising quality.

Showing results 21-40

Quality Management System Administrator information

See salary details

$41K

$88.9K

$137.5K

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

As of Aug 15, 2026, the average yearly pay for quality management system administrator in the United States is $88,927.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $104,000.00 per year, depending on experience, location, and employer.

What is the difference between Quality Management System Administrator vs Quality Control Coordinator?

AspectQuality Management System AdministratorQuality Control Coordinator
CertificationsISO 9001 Lead Auditor, CQESix Sigma Green Belt, CQE
Work EnvironmentOffice-based, documentation-focusedManufacturing or production floor, inspection-focused
Primary ResponsibilitiesMaintains QMS documentation, audits, compliancePerforms product inspections, tests, defect analysis

The Quality Management System Administrator focuses on maintaining and auditing the company's quality management system, ensuring compliance with standards like ISO 9001. In contrast, the Quality Control Coordinator is more involved in inspecting products and identifying defects during manufacturing. Both roles require quality certifications and work in quality-focused environments, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a Quality Management System Administrator?

To thrive as a Quality Management System Administrator, you need a strong background in quality assurance principles, documentation control, and regulatory compliance, often supported by a relevant degree and experience in quality management. Familiarity with QMS software platforms (such as ISO 9001-compliant systems), database management, and possibly certifications like ASQ Certified Quality Auditor are typically important. Attention to detail, strong organizational skills, and effective communication are vital soft skills for maintaining accurate records and facilitating audits. These skills ensure that quality standards are consistently met, regulatory requirements are adhered to, and continuous improvement is achieved within the organization.

What does a Quality Management System Administrator do?

A Quality Management System (QMS) Administrator is responsible for managing and maintaining an organization’s quality management system, ensuring it complies with relevant standards such as ISO 9001. They oversee document control, facilitate audits, and support continuous improvement initiatives. Their role is crucial in helping organizations maintain high-quality standards, meet regulatory requirements, and streamline processes for better efficiency.

How does a Quality Management System Administrator typically interact with other departments within an organization?

As a Quality Management System (QMS) Administrator, you will regularly collaborate with various departments such as production, engineering, and regulatory affairs to ensure compliance with quality standards. You may coordinate training sessions, facilitate internal audits, and help teams document processes accurately within the QMS. Strong communication skills are essential, as you'll often serve as the point of contact for quality-related inquiries and help resolve issues that span multiple teams. This collaborative environment not only supports continuous improvement but also provides visibility into different organizational functions.
More about Quality Management System Administrator jobs
Infographic showing various Quality Management System Administrator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $88,927 per year, or $42.8 per hour.

QUALITY MANAGEMENT SYSTEM (QMS) SYSTEMS LEAD

HAZELETT STRIP-CASTING CORPORATION

Colchester, VT • On-site

$80K - $108K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 23 days ago


Job description

Description:

POSITION OVERVIEW:

The Quality Management System (QMS) Systems Lead is responsible for leading, maintaining, and continuously improving Hazelett’s Quality Management System to ensure compliance with ISO 9001:2015 and applicable customer, regulatory, and internal requirements. This role serves as the organizational owner of the QMS, working cross-functionally with all departments to promote process discipline, risk-based thinking, and continual improvement. The QMS Systems Lead has no direct reports but exercises significant influence across the organization.


WHAT WILL YOU DO:

Quality Management System Leadership

· Lead and maintain the company’s ISO 9001:2015 compliant Quality Management System, ensuring alignment with business objectives and operational needs.

· Interpret and apply ISO 9001:2015 requirements across the organization, ensuring consistent understanding and implementation.

· Coordinate and support external certification, surveillance, and recertification audits, serving as the primary point of contact with registrars.

· Ensure documented information is established, implemented, maintained, and controlled in accordance with ISO requirements.

· Act as the management representative for the QMS, ensuring system integrity and effectiveness.

· Plan, coordinate, and facilitate management review activities, including preparation of inputs, documentation of outputs, and follow up on assigned actions.


Internal Quality Management

· Develop process control plans including statistical requirements.

· Develop gauges and fixtures needed for proper inspection.

· Define and execute first article inspections.


Internal Auditing

· Develop and maintain the internal audit program, including audit schedules, auditor qualification, and audit execution.

· Plan, conduct, and/or coordinate internal audits to verify QMS conformity and effectiveness.

· Ensure timely documentation of audit results and follow-up on audit findings.


Corrective Action and Risk Management

· Lead the corrective and preventive action (CA) process, ensuring effective root cause analysis and sustainable corrective actions.

· Promote and support risk-based thinking through identification, evaluation, and mitigation of process and system risks.

· Monitor the effectiveness of corrective actions and ensure closure.


Supplier Quality Management

· Maintain and oversee the supplier quality program in alignment with ISO 9001:2015 requirements.

· Establish and maintain criteria for supplier selection, evaluation, reevaluation, and monitoring.

· Support supplier qualification activities, including quality system assessments and risk evaluations as required.

· Review and analyze supplier performance metrics, including quality, delivery, and responsiveness, and work with suppliers to address deficiencies.

· Coordinate and support supplier corrective actions, ensuring effective root cause analysis and verification of corrective action effectiveness.

· Collaborate with Purchasing, Engineering, and Operations to ensure supplier quality requirements are defined, communicated, and maintained.


Incoming Inspection

· Oversee the incoming inspection process for purchased materials and components. Establish inspection criteria, train inspection personnel, and collaborate with engineering and procurement to address supplier quality issues.


Training and Awareness

· Ensure QMS-related training, awareness, and competency requirements are defined and met.

· Provide guidance and training to employees on QMS requirements, procedures, and best practices.


Metrics and Reporting

· Develop, monitor, and report QMS performance metrics, including audit results, nonconformities, corrective actions, supplier performance, and key process indicators.

· Analyze trends and present data-driven insights to leadership to support decision-making.

Requirements:

WHAT YOU WILL NEED:

· Three or more years of experience in quality engineering or manufacturing quality assurance is preferred.

· Expert working knowledge of ISO 9001:2015 requirements and quality management system principles.

· Proficiency in statistical process controls.

· Strong understanding of process-based and risk-based quality management.

· Experience leading internal and external audits.

· Demonstrated ability to influence without direct authority and work effectively across all organizational levels.

· Strong analytical, organizational, and documentation skills.

· Clear, concise written and verbal communication.

· Experience with supplier quality management, auditing, and inspection processes.

· Proficiency in reading engineering drawings and applying geometric dimensioning and tolerancing (GD&T).

· Proficiency with root cause analysis and continuous improvement tools (e.g., 5-Why, Fishbone, PDCA, FMEA).


EDUCATION

· Bachelor's degree in mechanical, manufacturing, or industrial engineering, or equivalent technical experience.

· ISO 9001 Lead Auditor or Internal Auditor certification is preferred.


WORK ENVIRONMENT

The duties of this position are carried out in an office environment, a manufacturing production environment, and at customer and supplier sites, as required. Exposure to fumes, noise, and gases from equipment or machinery might occur. The ability to work in these environments for extended periods of time and to perform moderate lifting are required. Safety shoes and safety glasses must be utilized when working in production areas.


WHAT WE OFFER:

· Hazelett offers 24 plans through its medical coverage and for most of the plans, Hazelett pays 100% of the premiums.

· Hazelett pays 100% of Dental Premiums for one of the best plans in the state.

· Life, AD&D, Short-Term Disability Insurance.

· Matching 401k after 90 days. Fully vested since you start contributing!

· 8 Company Holidays.

· 4 weeks of paid time off.

· On-site Athletic Trainer.

· Free uniforms with cleaning.

· Free use of our company beach on Malletts Bay and boat mooring at a discounted price.

· Opportunities for growth and skill development.


The base pay range for this full-time position is $80,000 – $108,000. Your base pay will depend on your skills, qualifications, experience, and location. In addition, our ranges are determined by role, level, and location.


Hazelett is passionately committed to creating a diverse, equitable, and inclusive work culture. Join us in building a community where differences are our strength, and where everyone has an equal chance to thrive.