ZipRecruiter

Log In

1

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

Avid Bioservices

Sr. Specialist, Quality Systems

Tustin, CA · On-site

$42.19 - $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 ...

Lubrizol Corporation

Senior Quality Manager

Corona, CA · Hybrid

Manage the Quality Engineering team and direct the activities of Quality Engineers, Quality Control ... Analyze Quality Systems data to identify and make recommendations for meeting organizational ...

Lubrizol Corporation

Senior Quality Manager

Corona, CA · Hybrid

Manage the Quality Engineering team and direct the activities of Quality Engineers, Quality Control ... Analyze Quality Systems data to identify and make recommendations for meeting organizational ...

Lubrizol Corporation

Senior Quality Manager

Corona, CA · On-site

Manage the Quality Engineering team and direct the activities of Quality Engineers, Quality Control ... Analyze Quality Systems data to identify and make recommendations for meeting organizational ...

Diamond Wipes International

Quality Manager

Chino, CA · On-site

$110K - $135K/yr

The Quality Manager is responsible for leading and maintaining a robust Quality Management System (QMS) and overseeing daily Quality Assurance operations for cosmetic and OTC drug manufacturing. This ...

CDM Smith

Manager, Quality

Rancho Cucamonga, CA

Develops and commissions quality control systems; applies and analyzes inspection and testing ... Collaborates with management team during project bid and estimating activities to ensure quality ...

next page

Showing results 1-20

People also search for

All JobsQuality Systems Manager JobsQuality Systems Manager Jobs in Riverside, CA

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 May 30, 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, and why are they important?

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.

More about Quality Systems Manager jobs
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:
Quality Systems Manager jobs near you
Infographic showing various Quality Systems Manager job openings in Riverside, CA as of May 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 1% Temporary, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $102,880 per year, or $49.5 per hour.
Manager, Manufacturing Quality Systems

Manager, Manufacturing Quality Systems

Avid Bioservices

Tustin, CA • On-site

$116.85K - $138K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago

Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Manager, Manufacturing Quality Systems position is responsible for overseeing and coordinating the activities of the Manufacturing Quality Systems (MQS) group. They will collaborate with their team in writing records for Avid's Quality Management System (QMS) including, but not limited to, records for the following: Deviations, out-of-tolerance calibration events, out-of-specification (OOS) results, out-of-limit (OOL) results, and out-of-trend (OOT) results. This role coordinates and participates in investigations required to write these records and routing/tracking records from assignment to approval. Identifies and implements corrective and preventive actions (CAPAs), as applicable. Where issues or improvements are identified, this role works with subject matter experts to propose viable solutions including a final product impact assessment. Identifies and implements solutions for elements that can be made more efficient, are potential sources of discrepancies, require 'fine-tuning', or need a complete revision.
Job Duties:
  • Adheres to Good Manufacturing Practice (GMP) regulations (21 CFR, Part 211) and Good Documentation Practices (GDP), as applicable.
  • Identifies technical, procedural, and equipment issues that hinder production and compliance, and improves the manufacturing processes.
  • Leads and conducts root cause investigations for a variety of events, with reference to related source documents including, but not limited to, procedures, protocols, reports, batch records, laboratory data, and calibration data; apply relevant scientific and technical principles during investigation.
  • Write QMS records with excellent attention to detail; ensure records accurately present the facts determined during investigation.
  • Coordinates and plans for the implementation of new procedures, processes, and equipment to be used in Manufacturing.
  • Designs and conducts small scale studies to support GMP compliance of manufacturing processes and deviation root cause investigations.
  • Analyzes process data, writes technical reports and makes technical recommendations/presentations.
  • Proactively interface with witnesses and subject matter experts to gather information; interface with Quality Assurance (QA) on questions related, but not limited, to: GMP compliance, Avid procedures and processes, investigation requirements, and record quality and style.
  • Manage each record from the time it is assigned through closure; work with all stakeholders to ensure record is closed according to defined timelines.
  • Performs specific assignments as requested by VP of Operations.
  • Perform other duties as assigned.

Minimum Qualifications:
  • Related bachelor's degree (i.e. Biology, Biotechnology, Chemical Engineering)
  • 4+ years of cGMP purification experience
  • 1+ years of leadership experience or equivalent

Position Type/Expected Hours of Work:
This role is a full-time, exempt position. Days and hours of work are Monday through Friday, 8:00 AM to 5:00 PM unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $116,850 to $138,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Apply