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Qa Associate Jobs in Riverside, CA (NOW HIRING)

AB InBev

Associate Quality Assurance Manager

Riverside, CA · On-site

$106K - $126K/yr

This position will support Quality and coordinate initiatives in MCC that will ensure integrity in Quality procedures and certifications according to agencies/government regulations/Quality Pillar.

In-N-Out Burger

Senior Software QA Engineer

Irvine, CA · On-site

$107K - $140K/yr

They mentor junior QA associates and serve as a key technical leader in cross-functional initiatives. *This position is full-time, in-office only. Essential Functions * Ability to report to work at ...

In-N-Out Burgers

Senior Software QA Engineer

Irvine, CA · On-site

$107K - $140K/yr

They mentor junior QA associates and serve as a key technical leader in cross-functional initiatives. *This position is full-time, in-office only. Essential Functions * Ability to report to work at ...

VF Corporation

Associate, QA 2nd Shift

Ontario, CA · On-site

$17.82 - $22.28/hr

Associate's degree preferred* One year of experience preferred Knowledge & Application: * Basic ... Accountable for delivery of own tasks to agreed time and quality standards* Typically no awareness ...

F&S PRODUCE WEST LLC

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 ...

Sega of America

QA Lead

Irvine, CA · On-site

$24 - $30/hr

The QA Lead is responsible for coordinating and overseeing QA execution for assigned projects. This role performs most of its time reviewing, vetting, and processing bug reports from the full QA team ...

The North Face

Associate, QA 2nd Shift

Ontario, CA

$17.82 - $22.28/hr

Associate's degree preferred* One year of experience preferred Knowledge & Application: * Basic ... Accountable for delivery of own tasks to agreed time and quality standards* Typically no awareness ...

SEGA OF AMERICA INC

QA Lead

Irvine, CA · Hybrid

$24 - $30/hr

The QA Lead is responsible for coordinating and overseeing QA execution for assigned projects. This role performs most of its time reviewing, vetting, and processing bug reports from the full QA team ...

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Qa Associate information

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How much do qa associate jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for qa associate in Riverside, CA is $30.56, according to ZipRecruiter salary data. Most workers in this role earn between $19.57 and $35.87 per hour, depending on experience, location, and employer.

What are QA Associates?

QA Associates, or Quality Assurance Associates, are professionals responsible for monitoring, inspecting, and proposing measures to improve processes that ensure the quality of products or services in a company. They work closely with production, development, and compliance teams to make sure that products meet required standards and regulations. Their tasks often include reviewing documentation, conducting audits, and reporting on quality metrics. QA Associates play a crucial role in maintaining customer satisfaction and regulatory compliance in industries such as pharmaceuticals, manufacturing, and software.

What are some common challenges faced by a QA Associate, and how can they be addressed?

QA Associates often encounter challenges such as managing tight deadlines, adapting to rapidly changing project requirements, and ensuring thorough test coverage. Effective communication with developers and other team members is crucial to address issues quickly and maintain product quality. Staying organized, using test management tools, and participating in regular stand-up meetings can help QA Associates stay on top of their workload and deliver consistent results.

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

To thrive as a QA Associate, you need a solid understanding of quality assurance methodologies, attention to detail, and often a degree in a scientific or technical field. Familiarity with tools like LIMS, GMP/GLP regulations, and quality management systems, as well as relevant certifications such as ASQ or Six Sigma, is typically required. Strong analytical thinking, effective communication, and problem-solving abilities help you excel within cross-functional teams. These skills ensure product compliance, support continuous improvement, and maintain high standards in regulated environments.
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Qa Associate jobs near you
Quality Assurance Associate - 1st Shift

Quality Assurance Associate - 1st Shift

Siegfried

Irvine, CA

$31 - $34/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago

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:

the Quality Associate supports the Quality Assurance Operation, which consists of QA shop floor supports, and QA batch review and Product Release on the 1st Shift.
1st Shift Hours: 6 AM - 2:30 PM

Your Profile:

Responsibilities

QA Production Floor Support

  • Provide Quality support to Manufacturing personnel on the shop floor for compounding and QA- in-process checks.
  • Perform line clearance verification, sterilization chart review, scale calibration verification, and QA in-process checks including but not limited to visual inspection, CSIT/PID test, weight check, and torque test.
  • Perform AQL and Level II Visual Inspection for Finished products.
  • Prepare in-process samples for submission to the Quality Control laboratory.
  • Support handling of GMP events and initiation of deviation investigations.
  • Read, understand, and follow SOP's and comply with cGMP and GDP. Support the issuance of GMP documentation to the Manufacturing floor.

QA Batch Review and Product Release

  • Review executed batch records for completeness, accuracy and compliance with approved procedures and Good Documentation Practices (GDP) and resolve discrepancies with manufacturing operators or supervisors.
  • Use computerized systems and software such as SAP, LIMS, and TrackWise for data collection and batch record review.
  • Enter and verify data from executed batch records into the Product Log Sheet and maintain the database up to date at all times.
  • Participate in deviation investigation and CAPA implementation.
  • Initiate Certificate of Conformance and prepare executed batch records for product release in a timely manner to meet compliance requirements and business needs.
  • Scan and file batch records (physically & electronically).
  • Assist in writing and/or revising SOPs to ensure compliance with cGMP and other applicable regulations.

Required Knowledge, Skills and Abilities

  • Working knowledge of QA principles In Pharmaceutical and/or other FDA regulated industries required

  • Good computer skills

  • Strong attention to detail

  • Good oral and written communication skills

  • Ability to work overtime and/or work occasionally on weekend as needed

Required Education and Experience

  • BS degree in Biochemistry, Chemistry, Engineering, Biology or closely related discipline required

  • 2-3 years of experience in Quality Assurance / Manufacturing environment in Pharmaceutical or other GMP regulated industries required

  • 3+ years of experience performing Batch Record Reviewing strongly preferred

Target Pay Range: $31-34/hour
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

  • Flexible Spending & HSA Options

  • Life Insurance, Short & Long Term Disability

  • Pet Insurance

  • 401K

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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