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Quality Associate Jobs in Spring Valley, CA (NOW HIRING)

Erasca

Assoc Director, Quality Assurance GMP

San Diego, CA · On-site

$175K - $210K/yr

Reporting to the Executive Director, Quality Assurance GMP, the Associate Director, Quality Assurance GMP supports GMP clinical manufacturing operations, including product release, analytical data ...

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How much do quality associate jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality associate in Spring Valley, CA is $27.56, according to ZipRecruiter salary data. Most workers in this role earn between $18.70 and $32.21 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

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

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Spring Valley, CA?

The most popular types of Quality jobs in Spring Valley, CA are:

What cities near Spring Valley, CA are hiring for Quality Associate jobs?

Cities near Spring Valley, CA with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Spring Valley, CA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $57,316 per year, or $27.6 per hour.

Associate II, Quality Control Biology (Temporary)

San Diego, CA • On-site

Artiva Biotherapeutics Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about Artiva Biotherapeutics Inc.external

$60 - $80/hr

Other

Posted 22 days ago

Job description

About Artiva:

We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK® is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.

For more information, visit
www.artivabio.com.

Job Summary:

Artiva Biotherapeutics is seeking a skilled and motived QC Associate II, QC Biology (Temporary) who will be reporting to the Associate Director, Quality Control. This individual will perform routine cGMP release and stability testing of Artiva's NK cell therapy products, support laboratory investigations, and contribute to continuous improvement of QC systems. The contract will be through the end of the year with possible extension beyond that.

Duties/Responsibilities:
  • Assist in ordering supplies, reagents and equipment.
  • Write and revise SOPs/Test methods that support Artiva’s cell therapy products.
  • Operate and test ELISA, Flow Cytometers, automated cell counters, and other analytical instruments and equipment, as needed.
  • Support activities for QC equipment IQ/OQ/PQs.
  • Perform routine cGMP release and stability testing of Artiva’s products; including biological tests, biochemistry, chemistry-based tests as needed.
  • Support and as needed evaluate QC systems and/or implement system improvements with supervision.
  • Support laboratory investigations and write reports for deviations and Out of Specification results.
  • Document lab work in a thorough and accurate manner.
  • Perform all work according to company policies, SOPs, and cGMP practices.
  • Assist in planning for GMP release testing, including testing schedules, reviewing biology data and investigating OOS and OOT results.
  • Write technical QC protocols and reports as needed.
  • Assist in analytical qualification and validation, as necessary.
  • Support the transfer and optimization of analytical methods from Analytical Development (or contract laboratories).
  • Develop an in-depth understanding of NK products, testing, and safety.
  • Maintain records and databases in accordance with procedures.
  • Support other special QC projects as needed.
Qualifications:
  • Bachelor’s degree (BS/BA) or relevant scientific field, preferably in biology or related field.
  • Minimum 2 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • Knowledge and experience in supporting cGMP deviations, OOS, etc.
  • Basic knowledge of method transfers, qualifications, and validations; current industry practices; and some experience with guidance interpretation and application
  • Adept at learning critical thinking and technical writing skills.
  • Computer skills required to operate Microsoft Word and Excel programs.

Base Salary: $ 74,000 - $ 85,000. Exact compensation may vary based on level, skills and experience.

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