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Quality Associate Jobs in Rialto, CA (NOW HIRING)

Quality Specialist

Rialto, CA · On-site

$23.51 - $39.18/hr

High school diploma or GED required; associate degree or technical certification in quality, manufacturing, or engineering preferred. * 3+ years of experience in quality roles within a manufacturing ...

Quality Specialist

Rialto, CA · On-site

$23.51 - $39.18/hr

High school diploma or GED required; associate degree or technical certification in quality, manufacturing, or engineering preferred. * 3+ years of experience in quality roles within a manufacturing ...

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Luxor Staffing is hiring a Quality Coordinator paying $19 per hour. Weekly pay, possible overtime ... Associate's Degree preferred * High school diploma required * Previous experience in food grade ...

... post-Secondary/Associates Degree with a minimum of 2 years of prior related experience ... One-year certificate in a quality related field from college or technical school desired. * ANSI/J ...

Quality Inspector

Colton, CA · On-site

$25.40 - $28.90/hr

... Quality Assurance, System Operator. Administration roles such as Human Resource Clerk and Office ... part-time associates in Walmart and Sam's Club facilities. Programs range from high school ...

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QC Technician

Ontario, CA · On-site

$18/day

Flavor compound QC associate in Ontario CA! **Mus have experience in QC** Monday-Friday 7:30am-4pm Pay: $18 Duties: *Examine shipments of raw materials, components, and finished goods for defects ...

New

Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our ...

PCBA Quality Inspector

Orange, CA · On-site

$32 - $34/hr

Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our ...

Associate degree, technical certificate, or completed coursework in biology, chemistry, food science, quality assurance, or a related scientific field preferred. Experience * Previous experience in ...

Quality Control Clerk

Anaheim, CA · On-site

$18.75/hr

Associate degree, technical certificate, or completed coursework in biology, chemistry, food science, quality assurance, or a related scientific field preferred. Experience * Previous experience in ...

Quality Control Assistant

Walnut, CA · On-site

$20 - $24/hr

High school diploma or GED required; associate degree or relevant coursework a plus * 1+ years of experience in a warehouse, manufacturing, or quality control environment preferred * Strong attention ...

Quality Control Assistant

Walnut, CA · On-site

$20 - $24/hr

High school diploma or GED required; associate degree or relevant coursework a plus * 1+ years of experience in a warehouse, manufacturing, or quality control environment preferred * Strong attention ...

We are seeking an experience quality control asociate to add to our team in our Anaheim warehouse. This is a TEMP TO HIRE POSITION. Position Sumarry: Quality control (production operator) will be ...

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Quality Associate information

See Rialto, CA salary details

$11

$27

$50

How much do quality associate jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for quality associate in Rialto, CA is $27.01, according to ZipRecruiter salary data. Most workers in this role earn between $18.32 and $31.59 per hour, depending on experience, location, and employer.

What are Quality Associates?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

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

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges Quality Associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What Does a Quality Associate Do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

What are the most commonly searched types of Quality jobs in Rialto, CA? The most popular types of Quality jobs in Rialto, CA are:
What job categories do people searching Quality Associate jobs in Rialto, CA look for? The top searched job categories for Quality Associate jobs in Rialto, CA are:
What cities near Rialto, CA are hiring for Quality Associate jobs? Cities near Rialto, CA with the most Quality Associate job openings:
Infographic showing various Quality 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 $56,174 per year, or $27 per hour.
Quality Assurance Associate/QC

Quality Assurance Associate/QC

Intellectt INC

Pomona, CA • On-site

Contractor

Re-posted 5 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.