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Entry Level Qa Automation Test Engineer Jobs in Riverside, CA

Arrowmac

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Quality Assurance Specialist

Irvine, CA · On-site

$70K - $80K/yr

Our client is seeking a dedicated Quality Assurance Specialist to join their team in a critical ... Ability to read and interpret product specifications, technical drawings, and test results

Arrowmac

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Quality Assurance Specialist

Irvine, CA · On-site

$70K - $80K/yr

Our client is seeking a dedicated Quality Assurance Specialist to join their team in a critical ... Ability to read and interpret product specifications, technical drawings, and test results

Integrated Resources INC

QA inspector

San Dimas, CA · On-site

Performs basic tasks in support of the distribution, retrieval, and filing of controlled documents (SOPs, Specifications, and Test Methods) as well as other Quality Assurance documents). * Solid Dose ...

Integrated Resources INC

QA Inspector

La Verne, CA · On-site

Assists and participates in the distribution, retrieval, and filing of controlled documents (SOPs, specifications, and test methods) as well as other Quality Assurance documents. * May participate in ...

Turion Space

Embedded Test Engineer

Irvine, CA · On-site

$140K - $190K/yr

This Embedded Test Engineer will be responsible for the design and development of Turion's Flight ... to ensure that software meets quality standards and requirements. Provide feedback and ...

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All JobsQa Automation Test Engineer JobsEntry Level Qa Automation Test Engineer JobsEntry Level Qa Automation Test Engineer Jobs in Riverside, CA

Entry Level Qa Automation Test Engineer information

See Riverside, CA salary details

$11

$53

$78

How much do entry level qa automation test engineer jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for entry level qa automation test engineer in Riverside, CA is $53.50, according to ZipRecruiter salary data. Most workers in this role earn between $46.15 and $60.96 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Qa Automation Test Engineer vs Manual Test Engineer?

AspectEntry Level Qa Automation Test EngineerManual Test Engineer
CertificationsBasic testing certifications, automation tools knowledgeBasic testing certifications, focus on manual testing skills
Work EnvironmentAutomated testing tools, scripting environmentsTest case execution, defect reporting
ResponsibilitiesDeveloping and maintaining automated test scriptsExecuting test cases manually and documenting results
Industry UsageCommon in tech companies with automation needsWidespread across various industries for manual testing

While both roles focus on software quality assurance, Entry Level Qa Automation Test Engineers primarily develop automated tests using scripting tools, whereas Manual Test Engineers execute test cases manually. Automation roles require some scripting knowledge, while manual testers focus on detailed test execution. Both are essential for comprehensive testing strategies in tech and software industries.

What are the most commonly searched types of Qa Automation Test Engineer jobs in Riverside, CA? The most popular types of Qa Automation Test Engineer jobs in Riverside, CA are:
What are popular job titles related to Entry Level Qa Automation Test Engineer jobs in Riverside, CA? For Entry Level Qa Automation Test Engineer jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Entry Level Qa Automation Test Engineer jobs in Riverside, CA look for? The top searched job categories for Entry Level Qa Automation Test Engineer jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Entry Level Qa Automation Test Engineer jobs? Cities near Riverside, CA with the most Entry Level Qa Automation Test Engineer job openings:
Entry Level Qa Automation Test Engineer jobs near you
Infographic showing various Entry Level Qa Automation Test Engineer job openings in Riverside, CA as of July 2026, with employment types broken down into 96% Full Time, 2% Part Time, and 2% Contract. Highlights an 82% Physical, 6% Hybrid, and 12% Remote job distribution, with an average salary of $111,271 per year, or $53.5 per hour.
Quality Assurance Associate I - 2nd Shift

Quality Assurance Associate I - 2nd Shift

Siegfried

Irvine, CA • On-site

$30 - $32/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 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 QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which consists of QA Production Floor supports, and QA Product Release.
2nd Shift Hours: 2 PM - 10:30 PM Monday through Friday

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
  • on weekend as needed

Required Education and Experience

  • Bachelor's Degree in Biochemistry, Chemistry, Engineering, Biology or closely related discipline required
  • 1-2 years' experience in Quality Assurance / Manufacturing environment in Pharmaceutical or other GMP regulated industries required

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

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 including PTO, Holidays, Sick & Personal

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 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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