1

Quality Control Analyst Jobs in Santa Rosa, CA (NOW HIRING)

Be Seen First

... analytical equipment according to manufacturer specifications and CLIA requirements. * Maintain complete and accurate documentation related to calibration, quality control, equipment maintenance ...

Quality Assurance Lead

Petaluma, CA · On-site

$24 - $28/hr

... analysis, and supports the development of SOPs, training, and continuous improvement. In the ... Ensures process control checklists and quality/food safety records are completed accurately and on ...

Clinical Scientist II - C

Santa Rosa, CA · On-site

$47.85 - $52.85/hr

Monitor QC performance for shifts and/or trends and recommend corrective actions as necessary. Clean and maintain analytical equipment to manufacturer specifications, assist with troubleshooting as ...

Monitor QC performance for shifts and/or trends and recommend corrective actions as necessary. * Clean and maintain analytical equipment to manufacturer specifications, assist with troubleshooting as ...

Monitor QC performance for shifts and/or trends and recommend corrective actions as necessary. * Clean and maintain analytical equipment to manufacturer specifications, assist with troubleshooting as ...

Showing results 41-60

Quality Control Analyst information

See Santa Rosa, CA salary details

$18

$30

$44

How much do quality control analyst jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for quality control analyst in Santa Rosa, CA is $30.52, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $33.89 per hour, depending on experience, location, and employer.

What is a quality control analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

What are the key skills and qualifications needed to thrive as a quality control analyst?

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by quality control analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

How much does a quality control analyst earn?

The average salary for a quality control analyst typically ranges from $45,000 to $70,000 per year, depending on experience, industry, and location. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. Many roles also include benefits such as health insurance and paid time off.

What are popular job titles related to Quality Control Analyst jobs in Santa Rosa, CA?

For Quality Control Analyst jobs in Santa Rosa, CA, the most frequently searched job titles are:

What job categories do people searching Quality Control Analyst jobs in Santa Rosa, CA look for?

The top searched job categories for Quality Control Analyst jobs in Santa Rosa, CA are:

What cities near Santa Rosa, CA are hiring for Quality Control Analyst jobs?

Cities near Santa Rosa, CA with the most Quality Control Analyst job openings:

Infographic showing various Quality Control Analyst job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 5% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $63,485 per year, or $30.5 per hour.

Clinical Scientist II - Clinical Laboratory Scientist

Viltis

Santa Rosa, CA • On-site

$50 - $60/hr

Contractor

Retirement

This job post has expired today. Applications are no longer accepted.


Job description

Clinical Scientist II – Clinical Laboratory Scientist

Location: Santa Rosa, California
Job ID: ABOJP00047267
Division: Toxicology Diagnostics
Assignment Dates: August 31, 2026–December 31, 2026
Work Environment: On-site laboratory and office setting

Position Overview

We are seeking a licensed California Clinical Laboratory Scientist to support a toxicology laboratory in Santa Rosa, California. The Clinical Scientist II will perform, review, and certify clinical laboratory testing while ensuring compliance with California laboratory regulations, CLIA requirements, internal procedures, and established quality standards.

The ideal candidate will have experience reviewing mass spectrometry data in a toxicology laboratory and a strong commitment to laboratory safety, regulatory compliance, scientific accuracy, and quality.

Key Responsibilities

  • Perform clinical laboratory testing in accordance with approved standard operating procedures, California requirements, and CLIA regulations.
  • Conduct the final review, certification, and release of laboratory test results.
  • Apply scientific knowledge and sound judgment to evaluate the accuracy, validity, and defensibility of test results.
  • Review calibration and quality-control results to confirm that established specifications have been met before releasing donor test results.
  • Investigate inconsistent or questionable laboratory results and escalate findings to the appropriate teams.
  • Recommend corrective actions when quality-control shifts, trends, or testing inconsistencies are identified.
  • Halt testing or production activities when necessary to protect result quality, patient safety, or regulatory compliance.
  • Review LC/MS/MS and GC/MS analytical data within a toxicology testing environment.
  • Operate, clean, maintain, troubleshoot, and calibrate analytical equipment according to manufacturer specifications and CLIA requirements.
  • Maintain complete and accurate documentation related to calibration, quality control, equipment maintenance, specimen handling, investigations, and result certification.
  • Safely handle hazardous materials and follow all environmental, health, and safety requirements.
  • Promptly report laboratory incidents, near misses, chemical spills, and potential safety concerns.
  • Assist with investigations involving specimen handling, analytical testing, production issues, and other quality events.
  • Support the development, review, and approval of laboratory standard operating procedures and testing protocols.
  • Train, supervise, and support unlicensed testing personnel and document their continued competency in accordance with California requirements.
  • Follow new and revised laboratory procedures as directed by laboratory leadership.
  • Support Quality Assurance and Performance Improvement activities consistent with the Laboratory Quality Plan.
  • Function as a Technical Supervisor under CLIA regulations when required.
  • Provide general or direct supervision of laboratory and clerical personnel in the absence of designated laboratory leadership.
  • Complete continuing education and professional training necessary to maintain an active California CLS license.

Required Qualifications

  • Active California license under the Business and Professions Code as one of the following:
    • Clinical Laboratory Scientist Generalist
    • Clinical Toxicologist Scientist
    • Clinical Chemist Scientist
  • Bachelor’s degree in a scientific discipline.
  • Strong pipetting and general laboratory skills.
  • Proficiency with computers and the ability to learn laboratory information management systems.
  • Knowledge of clinical laboratory quality-control, calibration, documentation, and compliance requirements.
  • Strong commitment to laboratory safety, quality, and regulatory compliance.
  • Excellent written, verbal, and interpersonal communication skills.
  • Ability to coach, train, and provide direction to peers and laboratory personnel.
  • Ability to work effectively in a flexible laboratory and office environment with frequent interruptions and competing requests.
  • High level of accuracy and attention to detail.

Preferred Qualifications

  • At least two years of experience in a toxicology laboratory using mass spectrometry.
  • Experience reviewing and certifying LC/MS/MS and/or GC/MS data.
  • Five or more years of general clinical laboratory experience with demonstrated knowledge of toxicology may be considered in place of direct toxicology laboratory experience.
  • Previous experience functioning as a CLIA Technical Supervisor.
  • Experience supporting laboratory quality investigations, corrective actions, and performance-improvement activities.

Core Competencies

  • Scientific and analytical judgment
  • Quality and compliance focus
  • Risk analysis and problem-solving
  • Attention to detail
  • Adaptability
  • Results orientation
  • Team collaboration
  • Leadership and interpersonal communication

Important Licensing Requirement

Candidates must possess an active and applicable California Clinical Laboratory Scientist license. Applications from candidates who do not meet the California licensing requirement cannot be considered for this position.