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Qa Manager Jobs in Riverside, CA (NOW HIRING)

BioPhase Solutions

QA Specialist

Anaheim, CA · On-site

$25 - $35/hr

Work closely with QA management to proactively address the quality of documentation. * Collaborating effectively with operations management to review and approve: SOPs, protocols, reports, equipment ...

FullSteam

QA Supervisor (Cheese Department)

Fontana, CA · On-site

$70K/yr

Quality Assurance Manager FLSA Status: Exempt Shift: TBD Salary: $70,304 per year Benefits: * Medical * Dental * AD&D Insurance Job Summary The Cheese QA Supervisor oversees daily quality assurance ...

Nura

Quality Assurance & Regulatory Manager

Irvine, CA · On-site

$100K/yr

The Quality Assurance & Regulatory Manager provides leadership and day-to-day management of NURA's Quality Assurance and Regulatory functions while supporting the strategic direction established by ...

Nura

Quality Assurance & Regulatory Manager

Irvine, CA · On-site

The Quality Assurance & Regulatory Manager provides leadership and day-to-day management of NURA's Quality Assurance and Regulatory functions while supporting the strategic direction established by ...

Nura

Quality Assurance & Regulatory Manager

Irvine, CA · On-site

The Quality Assurance & Regulatory Manager provides leadership and day-to-day management of NURA's Quality Assurance and Regulatory functions while supporting the strategic direction established by ...

Fujifilm

QA Commercial Manager

Santa Ana, CA

The QA Commercial Manager will oversee communication of quality information to external and internal customers. This may include, but is not limited to: change notifications, surveys, qualifications ...

Fujifilm

QA Commercial Manager

Santa Ana, CA · On-site

The QA Commercial Manager will oversee communication of quality information to external and internal customers. This may include, but is not limited to: change notifications, surveys, qualifications ...

Fujifilm

QA Commercial Manager

Santa Ana, CA

The QA Commercial Manager will oversee communication of quality information to external and internal customers. This may include, but is not limited to: change notifications, surveys, qualifications ...

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All JobsQa JobsQa Manager JobsQa Manager Jobs in Riverside, CA

Qa Manager information

See Riverside, CA salary details

$39.6K

$123.2K

$186.7K

How much do qa manager jobs pay per year?

As of Aug 14, 2026, the average yearly pay for qa manager in Riverside, CA is $123,182.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,600.00 and $150,800.00 per year, depending on experience, location, and employer.

How does a QA manager typically collaborate with development and product teams to ensure software quality?

A QA Manager works closely with both development and product teams to align testing strategies with project requirements and timelines. This collaboration often involves participating in sprint planning meetings, defining acceptance criteria, and facilitating communication to address quality concerns early in the development cycle. By fostering a culture of transparency and continuous feedback, QA Managers help ensure that issues are identified and resolved efficiently, resulting in a higher-quality end product. Effective collaboration also enables QA Managers to advocate for testing best practices and drive improvements across the software development lifecycle.

What is a QA manager?

A QA Manager, or Quality Assurance Manager, is responsible for overseeing the quality assurance processes within an organization. They develop and implement testing strategies, manage QA teams, and ensure that products or services meet established quality standards before reaching customers. QA Managers collaborate closely with development, operations, and product teams to identify defects, improve processes, and maintain compliance with industry regulations. Their work is crucial for minimizing errors, enhancing customer satisfaction, and supporting continuous improvement.

What is a QA manager?

As a QA manager, you oversee the quality assurance (QA) team and make sure that no defective products make it to customers. Your job duties include hiring and training QA inspectors, managing quality control procedures and the operations of the QA department, and ensuring that products meet specifications and are safe for consumer use. As a QA manager, your work is primarily in production and manufacturing, where you ensure the quality of goods like cars, clothes, electronics, and food items.

What are the key skills and qualifications needed to thrive as a QA manager, and why are they important?

To thrive as a QA Manager, you need expertise in quality assurance methodologies, test planning, and process improvement, often supported by a degree in computer science or engineering and relevant experience. Familiarity with test automation tools (like Selenium or JIRA), software development life cycle (SDLC) systems, and certifications such as ISTQB or Six Sigma are typically required. Strong leadership, communication, and problem-solving skills help you manage teams effectively and advocate for quality across departments. These competencies ensure the delivery of high-quality products, foster team productivity, and drive continuous improvement in testing processes.
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The most popular types of Qa jobs in Riverside, CA are:

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

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Qa Manager jobs near you
Infographic showing various Qa Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $123,182 per year, or $59.2 per hour.

QA Specialist

BioPhase Solutions

Anaheim, CA • On-site

$25 - $35/hr

Full-time

Re-posted 7 days ago

Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QA Specialist to work for an Orange County area contract manufacturing company.

Pay Rate: $25-35/hour depending on experience.

Summary:
Review GMP technical documentation to ensure quality standards are met and compliant with applicable SOPs, US FDA 21CFR210, 211, 11 and applicable ICH guidance documents. Develop and revise QA procedures to strengthen cGMP compliance.

Responsibilities:
  • Performing timely review of batch records, test results and supporting technical documentation. Work closely with QA management to proactively address the quality of documentation.
  • Collaborating effectively with operations management to review and approve: SOPs, protocols, reports, equipment qualifications and calibrations, change controls, specifications, and other quality, documentation.
  • Providing assistance during cGMP compliance inspections of the facility by clients, the FDA and/or other regulatory bodies. This includes coordinating the retrieval of quality documents/records/trend data and any other documentation requested during these inspections.
  • Providing support for execution of the supplier assurance program at the site
  • Supporting review and release of raw materials and final product.
  • Providing cGMP compliance guidance and advice as needed.
  • Reviewing and approve deviations.
  • Supporting QA management in gathering data necessary for tracking quality metrics.
  • Maintaining workspace cleanliness by adhering to the 5S method of organization.
  • Abiding by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor.
  • This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary.
Qualifications:
  • Preferred 2 – 3 years industry related work experience.
  • Bachelor's degree or equivalent in scientific discipline required.
  • Proficient experience and knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to contract laboratory and/or aseptic manufacturing operations.
  • Proficient experience and knowledge of USP, Pharm. Eur. (EudraLex) and other applicable standards.
  • Proficient knowledge of root cause investigation and problem solving; experience in the use of 5 Whys and/or other appropriate root cause investigation tools.
  • Proficient experience and knowledge in the use of LIMS and electronic documentation systems (i.e. MasterControl).
  • Works on problems of diverse scope; exercises good judgement in selecting methods and techniques for obtaining solutions while handling Quality Assurance tasks.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, etc.).

Please send resumes to mia@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!