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Contract Qa Jobs in Riverside, CA (NOW HIRING)

Cumming Group

Contracts Administrator I

Murrieta, CA

$29.09 - $36.84/hr

... contract policy and guidelines. Perform rigorous document QA - confirm all referenced agreements/exhibits are present, readable, and fully executed; request missing items through documented @mentions ...

Thales

Senior Quality Engineer

Irvine, CA · On-site

$94K - $128K/yr

Highly experienced within Quality Assurance and Quality Engineering functions across manufacturing environments including Aerospace, Automotive, Electronics, and Contract Manufacturing; strong ...

Thales

Senior Quality Engineer

Irvine, CA

$95K - $128K/yr

Highly experienced within Quality Assurance and Quality Engineering functions across manufacturing environments including Aerospace, Automotive, Electronics, and Contract Manufacturing; strong ...

Cumming Group

Contracts Administrator I

Murrieta, CA · On-site

... contract policy and guidelines. Perform rigorous document QA - confirm all referenced agreements/exhibits are present, readable, and fully executed; request missing items through documented @mentions ...

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All JobsContract Qa JobsContract Qa Jobs in Riverside, CA

Contract Qa information

See Riverside, CA salary details

$15

$46

$67

How much do contract qa jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for contract qa in Riverside, CA is $46.82, according to ZipRecruiter salary data. Most workers in this role earn between $38.12 and $56.92 per hour, depending on experience, location, and employer.

Are contract QA testers still in demand?

Contract QA testers remain in demand as companies seek flexible staffing for software testing projects, especially with the growth of agile development and remote work. Skills in automation tools like Selenium and understanding of testing frameworks increase employability in this field.

What are some common challenges faced by contract QA professionals when working with multiple clients or projects simultaneously?

Contract QA professionals often juggle several projects for different clients at once, which can present challenges in managing varying testing standards, timelines, and communication styles. Staying organized and adapting quickly to each client’s workflow is essential to ensure that all deliverables meet quality expectations without missing deadlines. Additionally, contract QA roles require clear communication skills to coordinate with remote teams and stakeholders, often across different time zones. Building effective collaboration habits and maintaining thorough documentation helps contract QA professionals thrive in these dynamic environments.

What is a contract QA?

Contract QA (Quality Assurance) professionals are specialists hired on a temporary or project basis to evaluate and ensure the quality of products, services, or processes. They typically work with companies to design and execute tests, identify defects, and recommend improvements to meet specific quality standards. Contract QA roles are common in industries like software development, manufacturing, and pharmaceuticals, where quality control is critical. These professionals bring expertise and flexibility, allowing organizations to scale their QA efforts according to project needs. Contract QA workers may operate independently or through staffing agencies.

What is the difference between Contract Qa vs Contract Software Developer?

AspectContract QaContract Software Developer
Required CredentialsQA certifications (e.g., ISTQB), testing tools knowledgeProgramming skills, coding certifications, software development experience
Work EnvironmentTesting labs, collaborative teams, Agile/Scrum settingsDevelopment teams, coding environments, Agile/Scrum settings
Employer & Industry UsageIT companies, software firms, tech startupsIT companies, software firms, tech startups
Common Search & ComparisonYesYes

Contract Qa professionals focus on testing and quality assurance, ensuring software meets standards. Contract Software Developers write and maintain code. While both roles work in tech environments and often overlap in Agile settings, they serve different functions within the software development lifecycle.

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

To thrive as a Contract QA, you need a solid understanding of software testing methodologies, test case creation, and defect tracking, often supported by a degree in computer science or related field. Familiarity with testing tools such as Selenium, JIRA, and knowledge of automation frameworks or ISTQB certification is highly valued. Attention to detail, strong communication, and problem-solving skills help you effectively collaborate with development teams and ensure accurate results. These skills are vital to delivering high-quality products on time and maintaining client satisfaction in project-based environments.
What are the most commonly searched types of Qa jobs in Riverside, CA? The most popular types of Qa jobs in Riverside, CA are:
What are popular job titles related to Contract Qa jobs in Riverside, CA? For Contract Qa jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Contract Qa jobs in Riverside, CA look for? The top searched job categories for Contract Qa jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Contract Qa jobs? Cities near Riverside, CA with the most Contract Qa job openings:
Contract Qa jobs near you
Infographic showing various Contract Qa job openings in Riverside, CA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 8% Part Time, and 6% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $97,376 per year, or $46.8 per hour.

SENIOR QA SPECIALIST - VALIDATION

LGM Pharma, LLC

Irvine, CA • On-site

$75K - $90K/yr

Full-time

Posted 16 days ago

Job description

RESPONSIBILITIES:

  • Prepares equipment validation procedures and protocols for manufacturing equipment (granulation machines, tablet press and incubator sterilizers)
  • Develops and executes matrix type validations where applicable for processes and equipment with adequate supporting rationales.
  • Assists in assuring facility, manufacturing, packaging, and Laboratory equipment are qualified to the required cGMP standards.
  • Authors/approves and executes qualification protocols and reports.
  • Schedules, plans, manages performance qualifications, calibration and maintenance of equipment and utility systems and laboratory Instruments in coordination with operations, Quality Control and maintenance.
  • Assists sourcing and procurement of facility equipment and Laboratory Instruments through completion of following tasks
  • Qualification of Vendors Selected.
  • Input to the development of the URS/FRS/DDS.
  • Assists with the routine calibration and maintenance of the Validation Master Plan for the site.
  • May present qualification studies to Regulatory and Client Auditors as required.
  • Assists with the design, maintenance, and continual improvement of the qualification system in line with cGMP standards.
  • Provides technical expertise and guidance on qualification policies and procedures and the implementation of those within the Production and Quality functional areas.
  • Occasionally supervises specialized contract personnel and outside vendors in the performance of contract services.
  • Summarizes studies and authors qualification reports in compliance with the cGMP standards and in a timely manner.
  • Initiates and investigates exception reports and non-conformances, associated with the qualification studies. Troubleshoots and resolves technical issues.
  • Other responsibilities and special projects will be assigned based on business and customer needs.

QUALIFICATIONS:

  • Bachelor’s degree in sciences or engineering
  • 5+years' experience in a highly regulated pharmaceuticals industry or related field
  • Knowledge of FDA regulations (21 CFR Parts 210,211 standards) to validate pharmaceutical manufacturing equipment
  • Demonstrated experience with qualification commercial processing a packaging equipment.
  • Proven track record of managing projects from start to finish on time and on budget.
  • Strong working knowledge of cGMP and regulatory standards for validation.
  • Experience in writing and reviewing SOPs, GMPs, governmental regulations and/or protocols for accuracy, traceability and compliance.