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Quality Systems Manager Jobs in Riverside, CA (NOW HIRING)

Quality System Specialist

Tustin, CA · On-site

$42.69 - $53.36/hr

... Systems • CAPA Management • Deviations • OOS Investigations • OOL Investigations • GMP Compliance • Quality Documentation • SOP Development • Batch Production Records (BPRs) • Root ...

Support the Quality department in daily quality assurance and continuous improvement activities. * Assist with the development, revision, and standardization of Quality Management System (QMS ...

Sr. Specialist, Quality Systems

Tustin, CA · On-site

$42.69 - $56.05/hr

The role of the Sr. Specialist, Quality Systems , is to provide technical review of Quality Management System discrepancy reports and CAPAs. In this role, you will participate in the generation and ...

Sr. Specialist, Quality Systems

Tustin, CA · On-site

$42.69 - $53.36/hr

The role of the Sr. Specialist, Quality Systems , is to provide technical review of Quality Management System discrepancy reports and CAPAs. In this role, you will participate in the generation and ...

Showing results 21-40

Quality Systems Manager information

See Riverside, CA salary details

$56.3K

$102.9K

$160.7K

How much do quality systems manager jobs pay per year?

As of Sep 13, 2026, the average yearly pay for quality systems manager in Riverside, CA is $102,880.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,800.00 and $127,800.00 per year, depending on experience, location, and employer.

What does a quality systems manager do?

As a quality systems manager, your primary responsibilities are monitoring the production processes and ensuring factory machinery/goods are within company and industry requirements. Your duties include weighing, sampling, or testing products for quality and functionality. You may also report the results of quality control tests. You monitor the equipment and people involved, and help with the development and implementation of improved management systems. You are also in charge of creating a standard operating procedure for the specific plant where you work. You check that everything is running at full efficiency and the quality of merchandise is standardized.

What are the key skills and qualifications needed to thrive as a quality systems manager?

To thrive as a Quality Systems Manager, you need strong expertise in quality management principles, regulatory compliance, and process improvement, typically supported by a degree in engineering or a related field. Familiarity with ISO standards (like ISO 9001), quality management software, and certifications such as Six Sigma or ASQ Certified Manager of Quality/Organizational Excellence are commonly required. Leadership, analytical thinking, and effective communication are crucial soft skills for coordinating teams and driving continuous improvement. These skills and qualifications are essential to ensure consistent product quality, regulatory adherence, and overall organizational efficiency.

How does a quality systems manager typically collaborate with cross-functional teams to drive continuous improvement?

A Quality Systems Manager works closely with departments such as manufacturing, engineering, regulatory, and supply chain to ensure that quality standards are consistently met and improved. They often lead or participate in cross-functional meetings to identify process gaps, analyze data, and develop corrective and preventive action plans. Effective communication and project management skills are essential, as the role involves aligning diverse teams toward common quality objectives and facilitating training or audits to support compliance and improvement initiatives.

What is the difference between Quality Systems Manager vs Quality Assurance Manager?

AspectQuality Systems ManagerQuality Assurance Manager
Primary FocusDeveloping and maintaining quality management systems and processesOverseeing product testing and ensuring quality standards are met during production
CertificationsISO 9001 Lead Auditor, CQEASQ certifications, QA certifications
Work EnvironmentQuality management departments, compliance teamsProduction lines, testing labs
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

While both roles focus on quality, the Quality Systems Manager primarily manages the overall quality management system and compliance, whereas the Quality Assurance Manager concentrates on product testing and ensuring quality during production. Understanding these differences helps in selecting the right career path or hiring the appropriate professional.

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 are popular job titles related to Quality Systems Manager jobs in Riverside, CA?

For Quality Systems Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Quality Systems Manager jobs in Riverside, CA look for?

The top searched job categories for Quality Systems Manager jobs in Riverside, CA are:

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

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

Infographic showing various Quality Systems Manager job openings in Riverside, CA as of July 2026, with employment types broken down into 84% Full Time, 14% Part Time, 1% Temporary, and 1% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $102,880 per year, or $49.5 per hour.

Quality Systems Complaints Specialist

Irvine, CA • On-site

OrthAlign
Medical Equipment and Supplies Manufacturing • 11 - 50 employees

$30/hr

Full-time

This job post has expired 3 days ago. Applications are no longer accepted.


Job description

OrthAlign, Inc., a Smart Technology, growing medical device company, has an immediate opening for a Quality Systems Complaints Specialist. The Quality Systems Complaints Specialist determines the legitimacy of complaint feedback and processes complaint files. This role works with cross-functional teams to communicate with customers and coordinate complaint product return. This role also reviews complaint device history records, supports complaint investigation, and contributes to the ongoing improvement of the quality system.
NOTE: This is an onsite position and only local candidates will be considered.
You will:
  • Perform initial assessment of customer feedback to determine if the information represents a complaint.
  • Support the investigation of returned complaint product and complaints where product was not returned.
  • Perform reviews of the complaint device history records.
  • Collaborate with Customer Service, Engineering and Operations teams to process complaints in a compliant and timely manner.
  • Communicate with customers as applicable, including issuance of closeout letters.
  • Develop and maintain product knowledge of existing and new products. Identify, propose, and drive opportunities for improvement, including review and revision of procedures and associated documents.

You need:
  • At least 1 year of experience in medical device quality or operations environment
  • Strong proficiency using MS Office Suite (e.g., Word, Excel, Outlook)
  • Familiarity with medical device regulations ISO 13485, 21CFR820 and complaints
  • Strong verbal and written communication skills are essential
  • Experience with problem solving and root cause analysis
  • Strong interpersonal skills including negotiating and relationship management
  • Keen attention to detail and strong organizational skills
  • Experience using an electronic quality management system (e.g. - QCBD, EtQ, etc.) and an electronic document management system/PLM (e.g. - Oracle's Agile, Documentum, etc.)

NOTE: We are unable to provide any type of sponsorship at this time.