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Qa Associate Jobs in Riverside, CA (NOW HIRING)

We are currently looking for a QA Specialist to work for an Orange County area contract manufacturing company. Pay Rate: $25-35/hour depending on experience. Summary: Review GMP technical ...

Quality Assurance Manager

Corona, CA · On-site

$110K - $125K/yr

Job Title: Quality Assurance Manager Department: Quality and R&D Reports to: Vice President The ideal candidate will possess and live by Mercer Foods core values. CONTINUOUS IMPROVEMENT ● ...

Pay Rate: $25.00- $26.00 The Quality Assurance Administrator supports the Quality organization by ... High school diploma or equivalent; associate degree or higher preferred * Minimum 2-3 years of ...

Pay Rate: $25.00- $26.00 The Quality Assurance Administrator supports the Quality organization by ... High school diploma or equivalent; associate degree or higher preferred * Minimum 2-3 years of ...

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Are you a detail-oriented QA professional with a passion for digital advertising and creative excellence? We're seeking a sharp, meticulous QA Specialist to ensure every campaign asset is polished ...

Coach and mentor QA Compliance Associates on investigations, documentation, and GMP expectations. Partner cross-functionally with Operations, QC, and other teams to drive a culture of quality and ...

The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... Associate's degree in Business, Communications, Education, Engineering, or related field, Food or ...

The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... Associate's degree in Business, Communications, Education, Engineering, or related field, Food or ...

Showing results 21-40

Qa Associate information

See Riverside, CA salary details

$13

$30

$64

How much do qa associate jobs pay per hour?

As of Aug 11, 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 is a QA associate?

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.

Is a QA associate a difficult job?

A QA associate role involves testing products or software to identify defects, which requires attention to detail, analytical skills, and knowledge of testing tools. The job can be challenging depending on project complexity and deadlines but is generally manageable with proper training and experience.

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 does a QA associate do?

A QA associate is responsible for testing products, software, or processes to ensure they meet quality standards and specifications. They develop test plans, identify defects, document issues, and work with teams to improve quality, often using testing tools and following industry protocols.

Is QA a good entry level job?

A QA Associate role is often suitable for entry-level candidates, as it typically requires basic knowledge of testing processes, attention to detail, and familiarity with testing tools. It provides a good foundation in quality assurance practices and can lead to more advanced positions in software development or testing. However, some roles may prefer candidates with prior experience or certifications in quality assurance or related fields.

What are the key skills and qualifications needed to thrive as a QA associate?

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.
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 cities near Riverside, CA are hiring for Qa Associate jobs? Cities near Riverside, CA with the most Qa Associate job openings:
Infographic showing various Qa Associate job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 26% Part Time, 1% Temporary, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $63,561 per year, or $30.6 per hour.

$25 - $35/hr

Full-time

Re-posted 4 days ago


Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QA Specialist to work for an Orange County area contract manufacturing company.

Pay Rate: $25-35/hour depending on experience.

Summary:
Review GMP technical documentation to ensure quality standards are met and compliant with applicable SOPs, US FDA 21CFR210, 211, 11 and applicable ICH guidance documents. Develop and revise QA procedures to strengthen cGMP compliance.

Responsibilities:
  • Performing timely review of batch records, test results and supporting technical documentation. Work closely with QA management to proactively address the quality of documentation.
  • Collaborating effectively with operations management to review and approve: SOPs, protocols, reports, equipment qualifications and calibrations, change controls, specifications, and other quality, documentation.
  • Providing assistance during cGMP compliance inspections of the facility by clients, the FDA and/or other regulatory bodies. This includes coordinating the retrieval of quality documents/records/trend data and any other documentation requested during these inspections.
  • Providing support for execution of the supplier assurance program at the site
  • Supporting review and release of raw materials and final product.
  • Providing cGMP compliance guidance and advice as needed.
  • Reviewing and approve deviations.
  • Supporting QA management in gathering data necessary for tracking quality metrics.
  • Maintaining workspace cleanliness by adhering to the 5S method of organization.
  • Abiding by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor.
  • This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary.
Qualifications:
  • Preferred 2 – 3 years industry related work experience.
  • Bachelor's degree or equivalent in scientific discipline required.
  • Proficient experience and knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to contract laboratory and/or aseptic manufacturing operations.
  • Proficient experience and knowledge of USP, Pharm. Eur. (EudraLex) and other applicable standards.
  • Proficient knowledge of root cause investigation and problem solving; experience in the use of 5 Whys and/or other appropriate root cause investigation tools.
  • Proficient experience and knowledge in the use of LIMS and electronic documentation systems (i.e. MasterControl).
  • Works on problems of diverse scope; exercises good judgement in selecting methods and techniques for obtaining solutions while handling Quality Assurance tasks.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, etc.).

Please send resumes to mia@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!