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Quality Assurance Associate Jobs in California (NOW HIRING)

Work with QA doc control to ensure accurate issuance of batch record documentation (i.e. lot/media records and labels) to manufacturing. Provide quality assurance support across technical operations ...

Work with QA doc control to ensure accurate issuance of batch record documentation (i.e. lot/media records and labels) to manufacturing. * Provide quality assurance support across technical ...

Excellent employment opportunity for a QA Associate IV in the Fremont, CA area. * This position is on-site, responsible for quality oversight of a GMP manufacturing facility, including manufacturing ...

... Quality Assurance Associate I, you will: Conduct internal audits, documentation, data analysis, control of non-conforming material, authorization of customer returns, and support overall product ...

Showing results 21-40

Quality Assurance Associate information

See California salary details

$12

$28

$61

How much do quality assurance associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for quality assurance associate in California is $28.91, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $33.94 per hour, depending on experience, location, and employer.

What does a quality assurance associate do?

A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.

What skills and qualifications are needed to be a quality assurance associate?

To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.

What are common challenges faced by quality assurance associates in ensuring consistent product quality?

Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.

What is the difference between Quality Assurance Associate vs Quality Control Inspector?

AspectQuality Assurance AssociateQuality Control Inspector
CertificationsOften requires certifications like ASQ CQIA or related quality assurance trainingMay require certifications such as ISO auditor or specific industry standards
Work EnvironmentInvolves process audits, documentation, and improving quality systemsFocuses on inspecting products or materials for defects
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and tech industriesPrimarily in manufacturing, food production, and assembly lines

While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.

Is a Quality Assurance Associate an entry-level job?

A Quality Assurance Associate position is often considered entry-level, suitable for candidates with little to no prior experience in quality assurance or related fields. It typically requires basic knowledge of testing procedures, attention to detail, and may involve training on specific tools or software used in quality control processes.

What is the role of a quality assurance associate?

A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What are the most commonly searched types of Quality Assurance jobs in California?

The most popular types of Quality Assurance jobs in California are:

What are popular job titles related to Quality Assurance Associate jobs in California?

For Quality Assurance Associate jobs in California, the most frequently searched job titles are:

What cities in California are hiring for Quality Assurance Associate jobs?

Cities in California with the most Quality Assurance Associate job openings:

Infographic showing various Quality Assurance Associate job openings in California as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 17% Part Time, 5% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $60,127 per year, or $28.9 per hour.

Quality Assurance Associate

AstraZeneca

Santa Monica, CA • On-site

$55K - $83K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago


Key responsibilities

  • Perform QA batch record review, label review, verifications, and document archival of records.

  • Coordinate and manage timelines for batch record reviews and support quality assurance activities across multiple sites.

  • Review routine manufacturing batch documentation and quality control data to support product disposition and lot closure.


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical


Job description

The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other assigned tasks. You will also be expected to independently coordinate and manage timelines for batch record reviews. You will be expected to provide support for both the Santa Monica, CA and Tarzana, CA sites as needed.

Responsibilities include, but are not limited to: Reviews routine manufacturing batch documentation and quality control data for in-process and finished product to support disposition and lot closure. Review routine material release documentation for quality release of raw materials used for manufacturing and quality control testing. Work with Doc Control to ensure archival of batch records.

Work with QA doc control to ensure accurate issuance of batch record documentation (i.e. lot/media records and labels) to manufacturing. Provide quality assurance support across technical operations functions (i.e

Manufacturing, Facilities & Engineering, Supply Chain, Quality Control, Analytical Development, Product Development/Manufacturing Sciences & Technology) within AZ to assure compliance with the quality manual and maintain collaborative quality relationships. Handle other duties as requested by supervisor/manager to support Quality. Administrative Tracking of QA metrics On the Floor QA support Qualifications: BS in biological sciences or a related field is required.

1-2 years of experience withn GMP regulated industry. Able to work on multiple projects simultaneously and demonstrate organizational, prioritization, and time management proficiencies. Flexibility of occasionally working in weekend or holidays to support lot release.

Ability to take ownership, initiative, and self-accountability. Ability to collaborate, work, and communicate effectively across organizational interfaces in a fast-paced dynamic team setting. Attention to detail and quick learning/application of concepts and information.

Knowledge of cell culture techniques and proficient in MS Word, Excel, Power Point and other applications. Ability to communicate and work in a self-guided manner with scientific/technical personnel. Preferred Qualifications: Experience in Cell or Gene Therapy Well versed in various cell therapy manufacturing processes The annual base pay (or hourly rate of compensation) for this position ranges from $55,920.80 - $83,881.20

Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans. Date Posted 27-Aug-2026 Closing Date 02-Sep-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees

In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.


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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB