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Manufacturing Quality Manager Jobs in Riverside, CA

iStaffing

Manufacturing Quality Inspector

Ontario, CA · On-site

$22/hr

Report defects, trends, and process deviations to engineering and management * Perform routine calibration and maintenance of inspection equipment * Work with production teams to resolve quality ...

PRIMALLY PURE LLC

Quality Manager

Murrieta, CA · On-site

$105K - $110K/yr

The Quality Manager partners cross-functionally to ensure sitewide Good Manufacturing Practices (GMPs) are upheld, and is responsible for driving a culture of quality, accountability, and continuous ...

Ametek

Quality Manager

Irvine, CA · On-site

The Quality Manager will lead the Quality Engineering and Quality Inspection teams in our aerospace manufacturing facility. This position will develop the team to ensure compliance with company ...

Balda C Brewer

Quality Manager

Ontario, CA · On-site

$140K - $180K/yr

As a quality manager you will ensure that the manufacturing site meets and applies the Global Quality Policies and Guidelines relating to, ISO 9001 & 13485 standards, FDA 21 CFR 820 regulations ...

KDC One Knowlton

Quality Manager

Walnut, CA · On-site

KDC is a network of best-in-class custom formulators and manufacturers of color cosmetics, skincare ... The Quality Manager carries out management responsibilities in accordance with company policies and ...

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Manufacturing Quality Manager information

See Riverside, CA salary details

$67.8K

$105.1K

$134.1K

How much do manufacturing quality manager jobs pay per year?

As of Jun 13, 2026, the average yearly pay for manufacturing quality manager in Riverside, CA is $105,064.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,200.00 and $120,000.00 per year, depending on experience, location, and employer.

What are the most common challenges a Manufacturing Quality Manager faces in a typical day?

Manufacturing Quality Managers often navigate challenges such as maintaining consistent product quality during high-volume production, investigating and resolving quality issues quickly, and ensuring compliance with changing industry standards. They regularly collaborate with production, engineering, and supply chain teams to implement process improvements and corrective actions. Balancing quality expectations with tight deadlines and cost pressures can be demanding, but effective managers use data-driven strategies and strong teamwork to achieve results. This role is dynamic and requires adaptability, attention to detail, and a commitment to ongoing process optimization.

What does a Manufacturing Quality Manager do?

A Manufacturing Quality Manager ensures that products meet quality standards and regulatory requirements in a production environment. They develop and implement quality control processes, conduct audits, and analyze data to identify areas for improvement. They also collaborate with teams to resolve production issues and enhance efficiency while maintaining compliance. Their role is crucial in minimizing defects, improving customer satisfaction, and ensuring operational excellence.

What are the key skills and qualifications needed to thrive in the Manufacturing Quality Manager position, and why are they important?

To thrive as a Manufacturing Quality Manager, you need strong knowledge of quality assurance processes, regulatory compliance, and manufacturing operations, usually supported by a bachelor's degree in engineering or a related field. Familiarity with quality management systems (like ISO 9001), statistical process control, Six Sigma methodologies, and relevant certifications such as CQE or Lean are commonly required. Strong leadership, problem-solving skills, and effective communication help you excel in team settings and drive continuous improvement initiatives. These competencies ensure consistent product quality, support regulatory requirements, and foster a culture of excellence on the manufacturing floor.

What are popular job titles related to Manufacturing Quality Manager jobs in Riverside, CA? For Manufacturing Quality Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Manufacturing Quality Manager jobs in Riverside, CA look for? The top searched job categories for Manufacturing Quality Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Manufacturing Quality Manager jobs? Cities near Riverside, CA with the most Manufacturing Quality Manager job openings:
Manufacturing Quality Manager jobs near you
Manager, Manufacturing Quality Systems

Manager, Manufacturing Quality Systems

Avid Bioservices

Tustin, CA • On-site

$116K - $138K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Job 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:
TheManager, Manufacturing Quality Systemspositionis responsible foroverseeing 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 andparticipatesin investigationsrequiredto write these records and routing/tracking records from assignment to approval.Identifiesand implements corrective and preventive actions (CAPAs), as applicable. Where issues or improvements areidentified, this role works with subject matter experts to proposeviablesolutions including a final product impact assessment.Identifiesand implements solutions for elements that can be made more efficient,arepotential 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.
  • Identifiestechnical, procedural, and equipment issues that hinder production and compliance, and improvesthe manufacturingprocesses.
  • 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 complianceofmanufacturing processes and deviation root cause investigations.
  • Analyzes process data,writestechnicalreportsand makes technical recommendations/presentations.
  • Proactivelyinterface withwitnesses 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 ensurerecord isclosed 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.
Whoyou 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 thatensurethe smooth running of everything.
  • You are a master at building relationships, capable ofestablishingconnections 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.
Employment Type: Full-Time

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