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Quality Associate Jobs in Riverside, CA (NOW HIRING)

Jeld-Wen Inc.

Quality Specialist

Rialto, CA

$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 ...

Jeld-Wen, Inc.

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 ...

Anduril Industries

Quality Inspector

Santa Ana, CA

Technical or Associates degree in related quality/mechanical/aerospace engineering field * 3+ years experience in a quality assurance or inspection role in a manufacturing/production setting * IPC-A ...

Anduril Industries

Quality Inspector

Santa Ana, CA · On-site

$31 - $40/hr

Technical or Associates degree in related quality/mechanical/aerospace engineering field * 3+ years experience in a quality assurance or inspection role in a manufacturing/production setting * IPC-A ...

ANDURIL INDUSTRIES

Quality Inspector

Santa Ana, CA

$31 - $40/hr

Technical or Associates degree in related quality/mechanical/aerospace engineering field * 3+ years experience in a quality assurance or inspection role in a manufacturing/production setting * IPC-A ...

Agiliti Health, Inc.

Quality Inspector

Corona, CA · On-site

$24.86 - $39.30/hr

Associate degree or equivalent * 1 - 2 years Quality or other manufacturing experience strongly preferred KNOWLEDGE, SKILLS, AND ABILITIES * Basic computer skills, including Microsoft Office programs ...

L3 Harris

Quality Inspector

Anaheim, CA

$52K - $97K/yr

... 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 ...

First Staffing Group

Be Seen First

Quality Control Tech

Anaheim, CA · On-site

$20.75/hr

QUALITY CONTROL TECHNICIAN - PRODUCE COMPANY Anaheim, CA Pay Rate: $20.75 per hour 1st Shift: 4:00 ... Ensure associates follow proper hygiene, handwashing, PPE, and sanitation requirements. * Promote ...

New

L3Harris Technologies

Quality Inspector

Anaheim, CA

$52K - $97K/yr

... 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 ...

Avid Bioservices

Data Reviewer, Quality Control

Tustin, CA · On-site

$31.63 - $42.16/hr

Conduct GMP review of laboratory notebooks, logbooks, and associate forms. * Conduct GMP review of ... Support QC method validation review, as needed. * Perform review of procedural and method revisions ...

Avid Bioservices

Data Reviewer, Quality Control

Tustin, CA

$31.63 - $42.16/hr

Conduct GMP review of laboratory notebooks, logbooks, and associate forms. * Conduct GMP review of ... Support QC method validation review, as needed. * Perform review of procedural and method revisions ...

Pexco

Quality Systems Coord

Yorba Linda, CA · On-site

Job Location Yorba Linda, CA 6:30am-3:30pm $25-$30 DOE Under limited supervision, the QA Associate performs routine quality documentation and administrative activities in support of the Quality team.

SQA Services

PCBA Quality Inspector

Orange, CA

$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 ...

Viant

Quality Inspector II

Upland, CA · On-site

$22 - $26/hr

... quality, life enhancing medical devices ... With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small ...

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All JobsQuality Associate JobsQuality Associate Jobs in Riverside, CA

Quality Associate information

See Riverside, CA salary details

$11

$28

$52

How much do quality associate jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for quality associate in Riverside, CA is $28.10, according to ZipRecruiter salary data. Most workers in this role earn between $19.04 and $32.84 per hour, depending on experience, location, and employer.

Is QA a difficult job?

Quality Associate roles can be challenging as they require attention to detail, understanding of quality standards, and often involve repetitive tasks and strict compliance requirements. Success in the role depends on strong analytical skills, knowledge of testing procedures, and sometimes certifications like Six Sigma or ISO standards.

Is QC a high paying job?

Quality Associate positions typically offer average salaries that are competitive within manufacturing and production industries, but they are generally not considered high-paying roles. Salary levels depend on factors such as experience, location, and industry, with some roles offering opportunities for advancement and certification that can increase earning potential.

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 jobs pay 10,000 a month without a degree?

A Quality Associate typically earns less than $10,000 a month, but high-paying roles in sales, real estate, or skilled trades can reach or exceed that level without a degree. These jobs often require experience, certifications, or specialized skills and may involve variable income or commission-based pay structures.

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 is the job of a quality associate?

A quality associate is responsible for inspecting products, monitoring manufacturing processes, and ensuring compliance with quality standards. They often use testing tools and follow procedures to identify defects and improve product quality. Strong attention to detail and knowledge of quality management systems are essential for this role.

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.

More about Quality Associate jobs
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What are popular job titles related to Quality Associate jobs in Riverside, CA? For Quality Associate jobs in Riverside, CA, the most frequently searched job titles are:
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What cities near Riverside, CA are hiring for Quality Associate jobs? Cities near Riverside, CA with the most Quality Associate job openings:
Quality Associate jobs near you
Quality Control Associate II - Raw Material Inspection (2nd Shift)

Quality Control Associate II - Raw Material Inspection (2nd Shift)

Siegfried

Irvine, CA

$30 - $32/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

Job description

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions-offering long-term opportunities to grow and make an impact.

Your Role:

QC Associate II, Raw Materials - 2nd Shift (2:00 PM - 10:30 PM)
The Quality Control Associate II (Raw Material Inspection), 2nd Shift is an individual contributor within the QC Raw Materials team responsible for supporting raw material receipt, inspection, sampling, physical testing, and release of materials used in the manufacture of sterile drug products. The role supports development, revision, and maintenance of raw material specifications within Labware LIMS 8, ensuring alignment with compendial and regulatory requirements. The position also supports quality investigations such as deviations, OOS, and vendor corrective actions. This role includes hands-on sampling of bulk materials in classified cleanroom environments, physical testing using laboratory instrumentation, and dimensional inspection of components. The associate collaborates cross-functionally with Chemistry, Microbiology, Engineering, Purchasing, Warehouse, and Quality Assurance to ensure materials meet specifications and are released in a timely manner.

Your Profile:

Key Responsibilities

  • Independently execute QC inspection and physical testing activities to support routine manufacturing and development programs.
  • Perform sampling of raw materials for chemistry and microbiology testing in cleanroom classified areas using appropriate aseptic techniques to minimize contamination risk.
  • Support development and improvement of raw material specifications in Labware LIMS 8 in collaboration with cross-functional teams.
  • Perform inspection activities in compliance with applicable GMP and GDP requirements and relevant regulatory standards.
  • Support and participate in internal and external audits, including direct interaction with auditors as needed.
  • Collaborate with Purchasing, QA, and suppliers to resolve issues related to nonconforming raw material lots.
  • Attend production and project meetings to provide updates on raw material testing and release status.
  • Maintain laboratory and sampling areas in a clean and organized state and support quality oversight of warehouse operations.
  • Perform other duties as assigned.

Required Qualifications

  • Bachelor's degree in Chemistry, Biology, or other pharmaceutical-relevant scientific discipline.
  • Minimum of 3 years of experience in QC or QA within an FDA-regulated industry.

Required Skills and Competencies

  • Working knowledge of quality systems and regulatory expectations including FDA and compendial requirements.
  • Familiarity with ANSI/ASQ sampling plans.
  • Ability to perform aseptic sampling, use precision measurement tools, and learn new laboratory instrumentation.
  • Strong written and verbal communication skills with effective documentation practices in a GMP environment.
  • Strong analytical thinking and judgment with the ability to make and defend recommendations.
  • Ability to work effectively in a fast-paced, cross-functional team environment.

Preferred Qualifications

  • Experience performing raw material inspection in a GMP-regulated pharmaceutical or biotechnology environment.

Work Environment

  • This role requires hands-on laboratory and cleanroom work, including sampling of raw materials in classified environments and use of appropriate personal protective equipment.

Target Pay Range: $30-32/hour + 10% Shift Differential working on 2nd Shift

Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.

Your Benefits:

  • Medical, Dental, Vision, Life
  • Voluntary Accident, Hospital, Pet
  • 401K
  • Generous Time Off Structure

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.

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