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Quality Assurance Associate Jobs in California (NOW HIRING)

QA Associate

Pomona, CA · On-site

$82K - $115K/yr

Job Title: QA Associate (Quality Assurance) Location: Pomona, CA (In-office) Position Type: Full-time Vacancy Status: This position is vacant AI Disclosure in Hiring: We use artificial intelligence ...

Job Title: QA Associate (Quality Assurance) Location:Pomona, CA (In-office) Position Type:Full-time Vacancy Status:This position is vacant AI Disclosure in Hiring:We use artificial intelligence to ...

RH is seeking a Quality Assurance Associate to join our Dmitriy & Co manufacturing location in Los Angeles, CA. This role requires exceptional attention to detail and a passion for craftsmanship ...

New

RH is seeking a Quality Assurance Associate to join our Dmitriy & Co manufacturing location in Los Angeles, CA. This role requires exceptional attention to detail and a passion for craftsmanship ...

New

They are seeking a Quality Assurance Associate to manually test their software and ensure high-quality builds for their neuromodulation device. Responsibilities : • Test the Android app, web ...

QA Associate - Livermore, CA Lobos Staffing is hiring a QA Associate for a temp-to-perm opportunity in Livermore, CA. Schedule: Monday-Friday, 7:00 AM-3:30 PM Pay: $26-$30/hour, DOE Must be available ...

QA Associate - Livermore, CA Lobos Staffing is hiring a QA Associate for a temp-to-perm opportunity in Livermore, CA. Schedule: Monday-Friday, 7:00 AM-3:30 PM Pay: $26-$30/hour, DOE Must be available ...

Role Overview: We're seeking a sharp, detail-oriented Quality Assurance Associate to help us deliver rock-solid, clinic-ready software for our next-generation neuromodulation device. In this role ...

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 ...

Main purpose of the Quality Assurance Associate role: Minimize monetary loss of defective merchandise by identifying the most effective defect recovery process for each item. Major Responsibilities:

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 ...

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 ...

New

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 ...

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Quality Assurance Associate information

See California salary details

$12

$28

$61

How much do quality assurance associate jobs pay per hour?

As of Aug 30, 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

San Diego, CA • On-site

Reva Medical LLC
51 - 200 employees

$24 - $33/hr

Full-time

Posted 20 days ago


Job description

Quality Assurance Associate - Document Control, Training, and Asset Management
Job Purpose
The Quality Assurance Associate supports the effective operation of the Quality Management System through accurate and timely administration of document control, training, equipment calibration/preventive maintenance, and related quality records. The position is responsible for executing established quality system processes, maintaining required logs and records, monitoring routine due dates, and escalating issues in accordance with approved procedures.
The QA Associate works collaboratively with the QA Specialist and Sr. Quality Systems Engineer. The roles are expected to coordinate closely and provide cross-training and backup support for assigned processes; however, the QA Associate does not report to the QA Specialist. The position operates under departmental management and escalates quality decisions requiring independent technical or compliance judgment.
Document Control & Records Administration
  • Administer day-to-day document control activities, including processing document change requests, routing documents for review and approval, issuing effective documents, maintaining controlled copies, and archiving superseded records in accordance with approved procedures.
  • Perform document quality control checks for formatting, required approvals, metadata, references, and completeness; promptly communicate irregularities and coordinate correction prior to release.
  • Maintain controlled Quality System documents and records, including SOPs, Work Instructions, forms, specifications, drawings, batch records, protocols, reports, and other applicable technical documentation.
  • Support authors and process owners with document templates, document numbering, routing requirements, and document control procedures.
  • Maintain external standards and regulatory reference records applicable to manufacturing, quality, and design activities.
  • Support document migration and data verification activities associated with implementation and maintenance of the electronic Quality Management System (eQMS).

Training Administration
  • Administer the training system, including assignment of required training, maintenance of training curricula and records, tracking of completion, and follow-up on overdue training.
  • Coordinate training assignments resulting from new or revised controlled documents and verify completion before or following document effective dates as required by procedure.
  • Support preparation of training status reports and escalate overdue or incomplete training to responsible managers and Quality management.
  • Provide routine user support for the training system and assist with eQMS training administration.

Asset Management - Calibration & Preventive Maintenance
  • Administer the equipment calibration and preventive maintenance program, including maintenance of the asset database, scheduling, due-date tracking, and coordination with internal personnel and outside service providers.
  • Collect and maintain calibration, preventive maintenance, qualification, and service records and perform defined administrative/documentation checks for completeness.
  • Monitor upcoming and overdue calibration and preventive maintenance activities and escalate overdue, missing, or potentially non-conforming equipment records to the QA Specialist, Sr. Quality Systems Engineer, or Quality management as appropriate.
  • Support equipment status labeling and other routine asset-control activities in accordance with approved procedures.

Quality System Support
  • Maintain quality system logs and trackers and support collection of data used for quality metrics and Management Review.
  • Provide administrative support for NCMR, deviation, CAPA, complaint, audit, and other quality system records, including record initiation, routing, tracking, filing, and follow-up as assigned.
  • Support batch release activities through record compilation, document verification, and other assigned activities performed in accordance with approved procedures and authorization levels.
  • Retrieve records and documentation in support of internal, external, customer, Notified Body, and FDA audits or inspections.
  • Support implementation, migration, testing, and ongoing administration of eQMS workflows in coordination with the QA Specialist and Sr. Quality Systems Engineer.
  • Identify recurring administrative issues or opportunities for process improvement and communicate them to process owners and Quality management.
  • Provide backup support for defined QA Specialist activities when trained and authorized.
  • Perform other duties and quality projects as assigned.

Skills / Qualifications
  • Bachelor's degree in a scientific, technical, business, or related discipline preferred; relevant education and experience may be accepted in lieu of a degree.
  • 0-2 years of experience in Quality Assurance, document control, regulated manufacturing, or a related function preferred. Medical device or pharmaceutical experience is desirable.
  • Basic knowledge of, or ability to learn, ISO 13485 and 21 CFR Part 820 (Quality Management System Regulation/QMSR). Exposure to 21 CFR Parts 210/211 and Part 4 for combination products is desirable.
  • Strong attention to detail and demonstrated ability to maintain accurate records, manage multiple due dates, and follow established procedures.
  • Strong written and verbal communication skills and ability to coordinate effectively with employees at all organizational levels.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and electronic document or quality management systems; eQMS experience preferred.
  • Ability to recognize and escalate discrepancies, overdue activities, or situations requiring Quality review.
  • Positive, collaborative, and dependable working style with willingness to cross-train and provide backup support across Quality Assurance activities.