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Quality Systems Coordinator Jobs in Riverside, CA

Masimo

Director, Quality Systems

Irvine, CA · On-site

... coordination, timely response, and sustainable corrective actions. * Ensure quality systems align ... with applicable regulatory requirements, including FDA, ISO, MDSAP, and global medical device ...

Masimo

Director, Quality Systems

Irvine, CA · On-site

... coordination, timely response, and sustainable corrective actions. * Ensure quality systems align ... with applicable regulatory requirements, including FDA, ISO, MDSAP, and global medical device ...

BALT Group

Quality System Engineer II

Irvine, CA · On-site

... not limited to, coordination of NCMRs and CAPAs, supporting audit execution, and supporting ... Job Responsibilities Knowledge of quality systems for medical device manufacturing and requirements ...

BALT Group

Quality System Engineer II

Irvine, CA · On-site

... not limited to, coordination of NCMRs and CAPAs, supporting audit execution, and supporting ... Job Responsibilities Knowledge of quality systems for medical device manufacturing and requirements ...

B. Braun Group

Quality Lead I

Irvine, CA · On-site

... coordinates laboratory testing requirements, investigates quality-related issues, and verifies compliance with internal procedures, GMP regulations, and quality system standards. Acting as a key ...

Clariant SE

Quality Lead

Colton, CA · On-site

Leads the Quality Control team in all system management audits, including internal and customer ... Identifies the root cause of quality problems and coordinates modifications or other corrective ...

Jobtailor

Quality Engineer III

Santa Ana, CA · On-site

$74K - $96K/yr

Support MRB and NCR activities, including documentation, disposition coordination, issue ... Ensure NCR records are complete, accurate, current, and closed according to quality system ...

Kirkhill Inc.

Quality Inspector

Brea, CA · On-site

$18 - $25/hr

Carries out and coordinates all inspection and test requirements as outlined in the Quality ... Maintains relevant updated specification, standard and quality systems documents.* Performs ...

Kirkhill, Inc.

Quality Inspector

Brea, CA · On-site

Carries out and coordinates all inspection and test requirements as outlined in the Quality ... Maintains relevant updated specification, standard and quality systems documents. Performs assigned ...

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Quality Systems Coordinator information

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$15

$28

$45

How much do quality systems coordinator jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for quality systems coordinator in Riverside, CA is $28.10, according to ZipRecruiter salary data. Most workers in this role earn between $21.06 and $32.60 per hour, depending on experience, location, and employer.

What is the difference between Quality Systems Coordinator vs Quality Assurance Specialist?

AspectQuality Systems CoordinatorQuality Assurance Specialist
CertificationsISO 9001, ASQ certifications often preferredISO 9001, Six Sigma, ASQ certifications common
Work EnvironmentManufacturing, healthcare, or tech industries focusing on quality management systemsManufacturing, pharmaceuticals, or biotech sectors focusing on product quality testing
Primary FocusMaintaining and improving quality management systems and complianceInspecting, testing, and ensuring product quality
Employer UsageUsed by companies implementing quality standards and systemsUsed by organizations ensuring product and process quality

The main difference is that a Quality Systems Coordinator focuses on managing and improving quality management systems, while a Quality Assurance Specialist concentrates on testing and verifying product quality. Both roles require similar certifications and work in related environments, but their core responsibilities differ in scope and focus.

How much does a quality systems coordinator make?

The average salary for a quality systems coordinator typically ranges from $50,000 to $75,000 per year, depending on experience, industry, and location. Professionals in this role often require knowledge of quality management systems like ISO 9001 and may hold certifications such as CQE or ASQ.

What does a quality systems coordinator do?

A quality systems coordinator manages and maintains a company's quality management system, ensuring compliance with industry standards and regulations. They develop, implement, and monitor quality procedures, conduct audits, and collaborate with teams to improve product or service quality. Proficiency in quality tools like ISO standards and attention to detail are essential for this role.

What is the role of a quality systems coordinator?

A quality systems coordinator manages and maintains a company's quality management system, ensuring compliance with industry standards and regulations. They develop, implement, and monitor quality procedures, often using tools like audits and data analysis, to improve product or service quality. Strong organizational skills and knowledge of quality standards such as ISO are essential for this role.

What are the most commonly searched types of Quality Systems jobs in Riverside, CA?

The most popular types of Quality Systems jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Quality Systems Coordinator jobs?

Cities near Riverside, CA with the most Quality Systems Coordinator job openings:

Infographic showing various Quality Systems Coordinator job openings in Riverside, CA as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $58,452 per year, or $28.1 per hour.

Director, Quality Systems

Irvine, CA • On-site

Masimo
Medical Equipment and Supplies Manufacturing • 1 - 5K employees
Learn more about Masimoexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Job description


Job Summary
The Director, Quality Systems is responsible for leading and advancing the company's Quality Systems strategy, governance, and operational effectiveness to ensure ongoing compliance with global regulatory requirements and industry standards. This role provides leadership and oversight for key quality system functions, including but not limited to Health Hazard Evaluations (HHE), and nonconformance management. This position will support all quality systems processes, including but not limited to computer software assurance (CSA), corrective and preventive actions (CAPA), change control, document control, training, quality metrics and trending, and quality system continuous improvement.
The Director partners cross-functionally with Quality, Regulatory, Engineering, Operations, Clinical, and Information Systems to strengthen quality system performance, mitigate compliance risks, and support product quality and business objectives across the organization. This leader is responsible for driving consistency, accountability, inspection readiness, and continuous improvement while building and developing a high-performing quality systems team.
Duties & Responsibilities
  • Lead and oversee Quality Systems activities to ensure compliance with internal procedures, applicable regulatory requirements, and international quality standards.
  • Provide strategic and operational leadership for core Quality Systems processes, including HHE, nonconformance management, metrics and trending, and management review support.
  • Drive continuous improvement initiatives to strengthen effectiveness, scalability, and efficiency of the Quality Management System (QMS).
  • Monitor quality system performance through data analysis, KPI development, trend reviews, and risk-based metrics to identify opportunities for improvement and proactive mitigation.
  • Partner with Regulatory Affairs, Engineering, Manufacturing, Supply Chain, Clinical, and other cross-functional teams to ensure quality systems are effectively integrated into business and product lifecycle processes.
  • Support internal audits, external audits, customer audits, and regulatory inspections, ensuring readiness, effective coordination, timely response, and sustainable corrective actions.
  • Ensure quality systems align with applicable regulatory requirements, including FDA, ISO, MDSAP, and global medical device regulations.
  • Evaluate and mitigate quality and compliance risks through strong governance, escalation, and risk-based decision-making.
  • Develop, review, and approve policies, procedures, work instructions, and quality system documentation to support compliance and operational excellence.
  • Ensure management is appropriately informed of quality system performance, emerging risks, and improvement opportunities.
  • Drive consistency and harmonization of quality systems practices across sites, functions, and applicable business areas.
  • Lead quality system-related projects, system enhancements, and process improvement initiatives to support growth, efficiency, and regulatory compliance.
  • Collaborate with Information Systems and business stakeholders on validation, implementation, or improvement of systems impacting quality processes.
  • Build, mentor, and develop a high-performing team of quality professionals, fostering accountability, engagement, and continuous development.
  • Provide leadership support for quality-related escalations, issue resolution, and compliance-related decision-making.
  • Perform other duties and special projects as assigned.

Minimum & Preferred Qualifications and Experience:
Minimum Qualifications
  • 10+ years of progressive experience in Quality Assurance, Quality Systems or Quality Compliance within a regulated medical device or life sciences environment.
  • 5+ years of leadership experience managing direct reports, managers, or cross-functional quality teams.
  • Strong knowledge of Quality Management Systems (QMS) principles and regulated quality processes.
  • Deep understanding of applicable regulatory and industry requirements, including but not limited to:
    • FDA 21 CFR Part 820 / Quality System Regulation
    • FDA 21 CFR Part 803 and 806
    • ISO 13485
    • EU MDR
    • MDSAP
    • Risk-based quality methodologies
  • Experience leading HHE and nonconformance processes.
  • Strong experience in CAPA, change control, quality metrics, and process improvement initiatives.
  • Demonstrated ability to analyze quality data, trends, and performance indicators to support risk-based decision-making and process improvements.
  • Strong project leadership experience with cross-functional initiatives and enterprise process improvements.
  • Excellent verbal and written communication skills with the ability to influence and collaborate effectively across all levels of the organization.
  • Strong leadership, organizational, problem-solving, and decision-making skills.
  • Ability to manage multiple priorities in a fast-paced, highly regulated environment.
  • Ability to travel up to approximately 5-10%.

Preferred Qualifications
  • Experience in global or multi-site Quality Systems oversight.
  • Experience supporting enterprise quality system harmonization or transformation initiatives.
  • Experience with electronic quality systems (eQMS), validation activities, and systems impacting regulated processes.
  • Lead Auditor, Certified Quality Auditor (CQA), RAC, or equivalent quality/regulatory certifications preferred.
  • Experience within innovation-driven or high-growth medical device organizations preferred.

Education
Bachelor's degree in Engineering, Life Sciences, Quality, or a related technical discipline required. Master's degree in Engineering, Quality, Regulatory Affairs, Business, or a related field preferred.
Compensation
The anticipated salary range for this position is $170,000 - $210,000 plus benefits. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. This position also qualifies for up to 20% annual bonus based on Company, department, and individual performance. Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Café. All benefits are subject to eligibility requirements.
Language requirements
  • Ability to read, write, and communicate effectively in English.
  • Ability to interpret technical documents, schematics, and written instructions.
  • Ability to clearly document technical findings and communicate with cross-functional team members.

Physical requirements/Work environment
This position primarily works in a laboratory environment. It requires frequent sitting, standing, and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities.
The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodation may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.
Masimo is an Equal Employment Opportunity Commission / Affirmative Action Employer. We encourage Minorities, Females, Disabled and Veterans to apply.
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About Masimo

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Irvine, CA, US

Year founded

1989

Social media

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