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Quality Assurance Associate Jobs in Rialto, CA (NOW HIRING)

Receiving QA Associate

Rialto, CA

$17 - $20.50/hr

A Day in the Life: In the position of Receiving QA Associate, you will ensure all products meet the quality standards set by the company. Inspect products, identify defects, and recommend ...

Receiving QA Associate

Rialto, CA · On-site

$18 - $20/hr

A Day in the Life: In the position of Receiving QA Associate, you will ensure all products meet the quality standards set by the company. Inspect products, identify defects, and recommend ...

Quality Assurance Manager II

Fontana, CA · On-site

$70K - $115K/yr

Monitor the training and development of site associates to ensure compliance to processes and regulations * Manage Quality Technicians within the site, as applicable. * Hire, train, and develop QA ...

Quality Assurance Manager II

Fontana, CA · On-site

$70K - $115K/yr

Monitor the training and development of site associates to ensure compliance to processes and regulations * Manage Quality Technicians within the site, as applicable. * Hire, train, and develop QA ...

QA Lead

Riverside, CA · On-site

$22 - $24/hr

Description The Quality Assurance Lead is responsible for overseeing daily QA activities, ensuring compliance with regulatory standards, and maintaining the highest quality of products in a fast ...

Jensen Meat Company is seeking a Quality Assurance Supervisor to oversee and enhance food safety and quality assurance programs across both our FDA plant-based and USDA regulated meat production ...

Jensen Meat Company is seeking a Quality Assurance Supervisor to oversee and enhance food safety and quality assurance programs across both our FDA plant-based and USDA regulated meat production ...

QA Specialist

Anaheim, CA · On-site

$25 - $35/hr

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 ...

QA Supervisor

Riverside, CA · On-site

$32 - $35/hr

Jensen Meat Company is seeking a Quality Assurance Supervisor to oversee and enhance food safety and quality assurance programs across both our FDA plant-based and USDA regulated meat production ...

Maintain and organize Food Safety and Quality Assurance daily records. Maintain and monitor inventory product retains and spot-check department documentation for accuracy and compliance. * Monitor ...

Maintain and organize Food Safety and Quality Assurance daily records. Maintain and monitor inventory product retains and spot-check department documentation for accuracy and compliance. * Monitor ...

Supervises QA and Production team members to ensure regulatory compliance in QA and Food Safety processes, adherence to protocols and audit inspections, pre-op, USDA, etc and advises on needed ...

Supervises QA and Production team members to ensure regulatory compliance in QA and Food Safety processes, adherence to protocols and audit inspections, pre-op, USDA, etc and advises on needed ...

The Lead acts as a key partner to the QA Manager by driving quality processes, supporting regulatory readiness, and providing guidance to QA Compliance Associates. Key Responsibilities • Own day-to ...

Supervisor QA

Riverside, CA · On-site

$68K - $73K/yr

Supervises QA and Production team members to ensure regulatory compliance in QA and Food Safety processes, adherence to protocols and audit inspections, pre-op, USDA, etc and advises on needed ...

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Quality Assurance Associate information

See Rialto, CA salary details

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How much do quality assurance associate jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for quality assurance associate in Rialto, CA is $29.37, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $34.47 per hour, depending on experience, location, and employer.

What is the difference between Quality Assurance Associate vs Quality Control Inspector?

AspectQuality Assurance AssociateQuality Control Inspector
CertificationsOften requires certifications like ASQ CQIA or related quality assurance trainingMay require certifications such as ISO auditor or specific industry standards
Work EnvironmentInvolves process audits, documentation, and improving quality systemsFocuses on inspecting products or materials for defects
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and tech industriesPrimarily in manufacturing, food production, and assembly lines

While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.

Which pays more, QA or QC?

In the quality assurance (QA) and quality control (QC) fields, QA roles typically offer higher salaries because they involve broader responsibilities such as process improvement and compliance management. QC positions often focus on inspecting and testing products, which may have lower pay scales. Salary differences can vary based on industry, experience, and certifications like Six Sigma or ISO standards.

What is the role of a quality assurance associate?

A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What are some common challenges faced by Quality Assurance Associates in ensuring consistent product quality?

Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.

What qualifications do you need to be a QA?

To become a Quality Assurance Associate, candidates typically need a high school diploma or equivalent, with many roles preferring a bachelor's degree in a related field such as quality assurance, engineering, or computer science. Strong attention to detail, analytical skills, and familiarity with testing tools or software are important, along with good communication skills. Certifications like ISTQB can enhance prospects but are not always required.

Is QA a good entry level job?

Quality Assurance Associate roles are often suitable for entry-level candidates, as they typically require attention to detail, basic understanding of testing processes, and familiarity with tools like test management software. These positions can provide valuable industry experience and opportunities for skill development in areas such as software testing, documentation, and quality standards.

What does a Quality Assurance Associate do?

A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.

What are the key skills and qualifications needed to thrive as a Quality Assurance Associate, and why are they important?

To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.
What are the most commonly searched types of Quality Assurance jobs in Rialto, CA? The most popular types of Quality Assurance jobs in Rialto, CA are:
What job categories do people searching Quality Assurance Associate jobs in Rialto, CA look for? The top searched job categories for Quality Assurance Associate jobs in Rialto, CA are:
What cities near Rialto, CA are hiring for Quality Assurance Associate jobs? Cities near Rialto, CA with the most Quality Assurance Associate job openings:
Infographic showing various Quality Assurance Associate job openings in Rialto, CA as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $61,094 per year, or $29.4 per hour.
Quality Assurance Associate/QC

Quality Assurance Associate/QC

Intellectt INC

Pomona, CA • On-site

Contractor

Re-posted 9 days ago


Job description

Job Title: Quality Assurance Associate III

Location : Pomona, CA, 91767

Duration : 06 Months
Shift: 8:00 AM – 5:00 PM

Job Summary

Under the supervision of the Supervisor/Manager, this position is responsible for carrying out daily operations in the Batch Record Department and supporting quality system processes.

Responsibilities

  • Carry out assignments in a timely and accurate manner with little or no supervision.
  • Interact effectively with all levels of the organization and perform multiple tasks in a fast-paced environment.
  • Support Quality processes including incoming inspection, change management, records administration, and batch release.
  • Support batch record review and Certificate of Analysis (COA) / Certificate of Conformance (COC) creation and review for material lot release.
  • Work with internal groups to obtain corrections and clarifications to Device History Records (DHR).
  • Facilitate the Change Control process through development, approval, and implementation.
  • Assist others with Change Control processes and provide guidance and best practices.
  • Prepare labeling for finished products and perform product labeling activities.
  • Analyze and interpret proposed changes and guide change initiators in developing accurate change requests.
  • Review SOPs, logs, forms, manufacturing records, work instructions, and other quality records for compliance and documentation accuracy.
  • Utilize databases to perform transactions and verify product information.
  • Generate and/or review Certificates of Conformance and Certificates of Analysis for final products.
  • File and maintain quality records.
  • Communicate issues effectively and collaborate with cross-functional teams to meet compliance requirements.
  • Support organizational improvements related to compliance issues.
  • Troubleshoot issues and improve systems as needed.
  • Coach staff to resolve issues and improve future outcomes.
  • Work on complex assignments requiring judgment, initiative, and problem-solving.
  • Maintain knowledge of applicable regulations including QSRs, ISO 13485, and CMDR.
  • Perform duties in compliance with established business policies.
  • Complete other duties as assigned.

Minimum Qualifications

  • High School Diploma or GED.
  • 3–5 years of related experience.
  • Experience with MS Office.
  • Ability to work on multiple tasks independently and as part of a team.
  • Detail-oriented and self-motivated.
  • Strong communication, problem-solving, and motivational skills.
  • Available for flexible scheduling.

Preferred Qualifications

  • Bachelor’s Degree.
  • Working knowledge of Quality Assurance in a medical device manufacturing environment, preferably in-vitro diagnostics.
  • Knowledge of Quality System Regulations.