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

GRIFOLS, S.A.

Sr Quality Assurance Specialist

San Diego, CA · On-site

$87K - $120K/yr

The estimated pay scale for the Senior Quality Associate Specialist role based in San Diego, California, is $108,026.40 to $140,000. Additionally, the position is eligible to participate in up to 8% ...

Grifols

Sr Quality Assurance Specialist

San Diego, CA · On-site

$87K - $120K/yr

The estimated pay scale for the Senior Quality Associate Specialist role based in San Diego, California, is $108,026.40 to $140,000. Additionally, the position is eligible to participate in up to 8% ...

Grifols, S.A

Sr Quality Assurance Specialist

San Diego, CA · On-site

$100 - $125/hr

The estimated pay scale for the Senior Quality Associate Specialist role based in San Diego, California, is $108,026.40 to $140,000. Additionally, the position is eligible to participate in up to 8% ...

Reva Medical LLC

Quality Assurance Associate

San Diego, CA · On-site

$24 - $33/hr

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 ...

BioLegend

Quality Control Associate

San Diego, CA · On-site

Job Summary BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow ...

PCI Pharma Services

QA Associate III

San Diego, CA · On-site

$29.65 - $33.36/hr

Provides quality support for investigations related to quality events associated with GMP ... associates that reflects positively on the company and is consistent with the company's policies ...

Collabera

QC Associate I

San Diego, CA · On-site

Qualifications Education: BS/MS in Biology/Molecular Biology, biochemistry, chemistry or related discipline 2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based ...

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Quality Associate information

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How much do quality associate jobs pay per hour?

As of Sep 8, 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.

Quality Systems Associate (Contract)

ORIC Pharmaceuticals

San Diego, CA

$25 - $33.50/hr

Contractor

Posted 17 days ago

Job description

Company Description

ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn.

Reporting to the Quality Systems Specialist, the Quality Systems Associate will support document control, training, and quality systems activities, providing word processing, archival and electronic system maintenance.  The successful candidate will work closely with Quality Assurance, Technical Operations, Clinical, Regulatory and third-party Contract organizations.   

Job Description
  • Support document processing, review and release of regulated GxP documents .
  • Collaborate closely with document owners to resolve any documentation discrepancies identified during review.
  • Organize review and support activities to ensure timely review and completion of documentation task to meet pre-established timelines.
  • Participate in cross functional program meetings to provide appropriate QA updates.
  • Maintain and update electronic quality systems, documentation files and folders in accordance with written SOPs.
  • Facilitate/coordinate GMP training for internal employees/departments as required.
  • Identify and facilitate continuous improvement of internal Policies, SOPs and Work Instructions, as needed.
  • Provide document support for internal audits and regulatory inspections, as needed.
  • Perform all duties in keeping with ORIC's core values, policies and all applicable regulations.
Qualifications
  • Bachelor's degree or equivalent relevant experience.
  • 0-2 years of relevant experience in Quality Assurance or experience in an academic or regulated environment.
  • Highly polished writing and editing skills.
  • High degree of proficiency in Microsoft Office Suite.
  • Knowledge of GMP regulations and guidance documents is preferred, including but not limited to:
    • 21 CFR Parts 11, 210, 211
    • Applicable ICH Quality Guidelines for Good Manufacturing Practices (GMP)
    • EU EudraLex Volume 4
  • Experience with electronic quality management systems such as Veeva or MasterControl is a plus.
  • Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment that includes external partners. Proven ability to manage multiple priorities and deliver high-quality work.
  • Demonstrated initiative, ownership, problem identification, problem solving, and strategic thinking skills.
  • Demonstrated ability to quickly adapt and find creative solutions to ensure deliverables are met.
  • Excellent verbal and written communication skills
Additional Information

The anticipated hourly rate for candidates who will work on-site at our San Diego location is between $25.00-$33.50 per hour. The final rate offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. This position is not eligible for H-1B visa sponsorship.

ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.

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