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Quality Lab Associate Jobs in Rodeo, CA (NOW HIRING)

Medra

Research Associate - Protein

San Francisco, CA · On-site

$80 - $100/hr

Maintain accurate and detailed experimental records in electronic lab notebooks (ELN), and ... Strong hands‑on experience with high‑throughput protein quality control and biophysical ...

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All JobsQuality Lab Associate JobsQuality Lab Associate Jobs in Rodeo, CA

Quality Lab Associate information

See Rodeo, CA salary details

$14

$24

$37

How much do quality lab associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for quality lab associate in Rodeo, CA is $24.70, according to ZipRecruiter salary data. Most workers in this role earn between $18.85 and $27.60 per hour, depending on experience, location, and employer.

What does a quality lab associate do?

A Quality Lab Associate is responsible for performing laboratory tests and analyses to ensure that products meet established quality standards and regulatory requirements. This role typically involves preparing samples, operating laboratory equipment, recording data, and reporting results to supervisors or quality managers. They may also assist in investigating deviations or non-conformities and help maintain a clean and safe laboratory environment. Quality Lab Associates play a critical role in maintaining product safety and consistency, particularly in industries like pharmaceuticals, food and beverage, or manufacturing.

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

To thrive as a Quality Lab Associate, you need a solid background in laboratory procedures, analytical testing, and quality assurance, usually supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), analytical instruments like HPLC/GC, and relevant certifications such as GMP or ISO standards is often required. Attention to detail, strong organizational skills, and effective communication enable you to identify problems, maintain accurate records, and collaborate with cross-functional teams. These skills ensure the integrity of test results, regulatory compliance, and overall product quality in laboratory environments.

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

Quality Lab Associates often collaborate with production, R&D, and regulatory teams to ensure product quality and compliance. A common challenge in this environment is effectively communicating technical laboratory findings to non-technical stakeholders, which requires clear documentation and presentation skills. Additionally, balancing multiple project deadlines while maintaining strict adherence to quality standards can be demanding. Building strong relationships and understanding the goals of other departments can help overcome these challenges and foster smoother workflows.

What is the difference between Quality Lab Associate vs Quality Control Technician?

AspectQuality Lab AssociateQuality Control Technician
CertificationsOften requires a degree in science or related field; certifications like ASQ are a plusSimilar requirements; certifications like ASQ are common
Work EnvironmentLaboratory setting, performing tests and analysesLaboratory and production environment, conducting inspections and tests
Employer & Industry UsageUsed across manufacturing, pharmaceuticals, food, and biotech industriesCommon in manufacturing, pharmaceuticals, and food industries

Both roles involve testing and ensuring product quality, often requiring similar educational backgrounds and certifications. The main difference lies in their focus: Quality Lab Associates typically perform routine testing and data recording, while Quality Control Technicians may also conduct inspections and troubleshoot quality issues on the production line.

What cities near Rodeo, CA are hiring for Quality Lab Associate jobs?

Cities near Rodeo, CA with the most Quality Lab Associate job openings:

Quality Lab Associate jobs near you
Infographic showing various Quality Lab Associate job openings in Rodeo, CA as of August 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 100% In-person job distribution, with an average salary of $51,377 per year, or $24.7 per hour.

Manager, Quality Control & Analytical Development

Vacaville, CA • On-site

Oath
Non-Profits • 1 - 10 employees
Learn more about Oathexternal

$100K - $130K/yr

Full-time

Posted 14 days ago

Job description

About Oath
Oath is a leading microbial sciences company that utilizes natural soil biology to offer innovative solutions to some of the most critical challenges facing our planet - the climate crisis and the shift to sustainable agriculture. We imagine a world where these crises are not just alleviated, but reversed, replenishing Earth's microbiomes.
Our solution has moved beyond the lab and into real-world deployment, focused on improving farmer livelihoods with teams in Rwanda, Europe, the United States, and expanding. When you join Oath, you become part of a collaborative network that prioritizes high quality scientific work. You will be working alongside trained scientists, talented commercial teams, and a broad network of partners-an ecosystem designed to help you do your best work and grow your capabilities.
Position Summary
We are seeking an experienced Manager, Quality Control & Analytical Development to lead QC and analytical assay development for Oath's live microbial products. This role will own QC methods, specifications, and production batch review and release, while developing and validating fit-for-purpose assays to support manufacturing and product quality. You will ensure microbial products meet quality requirements throughout cultivation, fermentation, downstream processing, formulation, and storage, and translate analytical methods into robust, scalable QC tools for internal and external manufacturing.
Key Responsibilities
Quality Control & Batch Release
  • Own QC review and release of production batches against established specifications.
  • Define and maintain product specifications, release criteria, sampling plans, and QC testing requirements.
  • Review QC data, batch records, COAs/COCs, and supporting documentation.
  • Lead investigations of deviations, out-of-specification results, and product quality issues.
  • Establish stability and shelf-life testing and monitor product quality trends.
Analytical Assay Development & Validation
  • Develop, optimize, and validate quantitative assays supporting manufacturing, QC, and product release.
  • Establish robust methods for microbial titer, viability, sporulation, purity, stability, and other key quality attributes.
  • Apply techniques including CFU methods, qPCR/qRT-PCR, flow cytometry, sequencing, and other relevant analytical methods.
  • Ensure assays are reproducible, scalable, and fit for manufacturing routine QC use.
Manufacturing & Method Transfer
  • Lead transfer and implementation of QC methods at CROs and CMOs/CDMOs.
  • Define testing requirements and ensure consistent execution of Oath methods and specifications.
  • Review external QC data, batch documentation, and technical reports.
  • Partner with manufacturing teams to troubleshoot quality issues and improve QC processes.
Quality Systems & Documentation
  • Develop and maintain QC SOPs, analytical methods, specifications, protocols, and reports.
  • Establish appropriate sample tracking, data management, and QC documentation practices.
Cross-Functional Collaboration
  • Partner closely with Production, Bioprocess Development, R&D, Regulatory, Supply Chain, and Field Science.
  • Provide data-driven recommendations on product quality, manufacturing, formulation, and stability.
  • As the team grows, mentor and manage scientists and research associates.
Qualifications
Required
  • PhD or MS in Microbiology, Biotechnology, Analytical Sciences, Fermentation Science, or a related field, with relevant industry experience.
  • Experience with QC testing, product specifications, method validation, and production batch review/release.
  • Experience developing and validating quantitative assays for microbial, biological, or fermentation-based products.
  • Experience working with manufacturing teams, CROs, CMOs/CDMOs, or external testing laboratories.
  • Strong ownership, communication, documentation, and cross-functional leadership skills.
Preferred
  • Experience in agriculture, agricultural biotechnology, biologicals, or microbial products strongly preferred.
  • Experience with deviations, OOS investigations, stability programs, and quality systems preferred.

Job Type: Full-time, non-exempt position in the United States. At this time, Oath, Inc. is not able to provide visa sponsorship or work authorization support.
Location: Vacaville, CA, 3 days a week with international travel to Europe up to 20%
Compensation: $100,000 - $130,000

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