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Quality Control Laboratory Jobs in California (NOW HIRING)

TekWissen LLC

QC Laboratory Associate

Vacaville, CA · On-site

$20 - $25/hr

Job Title: QC Associate I / QC Laboratory Associate Location: Vacaville, CA - 95688 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Summary With limited supervision, the QC ...

Astrix Inc

QC Laboratory Technician

Anaheim, CA · On-site

$20.75 - $26.25/hr

Pay Rate Low: 20 | Pay Rate High: 22 Job Summary We are seeking a dependable and detail-oriented Quality Control Laboratory Technician for a full-time role within a growing manufacturing environment.

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Quality Control Laboratory Technician

San Fernando, CA · On-site

$22 - $25/hr

... Quality control background is preferred but not required. · Receive samples and perform laboratory testing in compliance with established specifications and standard operating procedures. · Work ...

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How much do quality control laboratory jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for quality control laboratory in California is $22.32, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $23.70 per hour, depending on experience, location, and employer.

What is a quality control laboratory?

A Quality Control (QC) Laboratory job involves testing and analyzing materials, products, or samples to ensure they meet established quality standards and regulatory requirements. QC lab technicians and analysts perform various tests, document results, and identify deviations from specifications. They work in industries like pharmaceuticals, food production, manufacturing, and environmental science. Their role helps maintain product consistency, safety, and compliance with industry regulations.

What are the typical daily responsibilities of someone working in a quality control laboratory?

Professionals in a Quality Control Laboratory are responsible for conducting routine and non-routine tests on raw materials, in-process samples, and finished products to ensure they meet established quality standards. This typically involves preparing and analyzing samples using various laboratory instruments, accurately documenting results, and reporting findings to supervisors or production teams. You may also assist with troubleshooting equipment, participating in investigations if discrepancies arise, and helping maintain compliance with regulatory requirements. The role often requires collaboration with other laboratory staff and production teams to support continuous quality improvement.

What are the key skills and qualifications needed to thrive in the quality control laboratory position, and why are they important?

Excelling in a Quality Control Laboratory role requires a solid understanding of laboratory testing procedures, attention to detail, and a background in chemistry, biology, or a related science, often supported by a relevant degree. Familiarity with laboratory equipment, analytical instruments (such as HPLC or GC), and quality management systems like ISO standards is essential; certifications such as ASQ may be advantageous. Strong problem-solving abilities, communication skills, and a commitment to teamwork set top professionals apart. These competencies are crucial for ensuring product safety and regulatory compliance while maintaining high standards in testing and reporting.

How to become a quality control laboratory technician?

To become a quality control laboratory technician, candidates typically need a high school diploma or equivalent, with some roles requiring an associate degree or relevant certification in laboratory techniques or quality assurance. Skills in using laboratory equipment, attention to detail, and knowledge of safety protocols are essential; some positions may also require experience in specific industries or with certain testing methods.

Is quality control laboratory a good career?

A career in a quality control laboratory involves testing and analyzing products to ensure they meet safety and quality standards, often requiring knowledge of laboratory techniques and attention to detail. It can offer stable employment, opportunities for advancement, and the chance to work in industries like pharmaceuticals, food, or manufacturing. Certifications such as ASQ or laboratory skills can enhance job prospects and career growth.

What does a quality control laboratory do?

A quality control laboratory is responsible for testing and inspecting products, raw materials, and processes to ensure they meet safety, quality, and regulatory standards. Technicians and scientists use tools like microscopes, spectrometers, and test kits to analyze samples and verify compliance throughout manufacturing. Accurate documentation and adherence to protocols are essential in this role.

What are the most commonly searched types of Quality Control Laboratory jobs in California?

The most popular types of Quality Control Laboratory jobs in California are:

What are popular job titles related to Quality Control Laboratory jobs in California?

For Quality Control Laboratory jobs in California, the most frequently searched job titles are:

What job categories do people searching Quality Control Laboratory jobs in California look for?

The top searched job categories for Quality Control Laboratory jobs in California are:

Quality Control Laboratory jobs near you
Infographic showing various Quality Control Laboratory job openings in California as of August 2026, with employment types broken down into 67% Full Time, 8% Part Time, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $46,423 per year, or $22.3 per hour.

QC Laboratory Associate

Vacaville, CA • On-site

TekWissen LLC
Recruiting and Staffing Services • 501 - 1,000 employees
Learn more about TekWissen LLCexternal

$20 - $25/hr

Contractor

Re-posted 25 days ago

Job description

Overview:  
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  
  
Job Title:     QC Associate I / QC Laboratory Associate
Location:     Vacaville, CA - 95688
Duration:     12 Months    
Job Type:    Temporary Assignment 
Work Type: Onsite
 
 
Summary
 
With limited supervision, the QC Associate I is responsible for performing direct materials testing in compliance with cGMP regulations. Core duties include execution of laboratory testing, trend analysis, documentation review, discrepancy support (OOS, OOT, OOE), and general laboratory support activities. In collaboration with QC leadership, the QC Associate II contributes to achieving departmental and organizational objectives.
 
Responsibilities
  • Perform a broad variety of basic and moderately complex tests with documentation according to GMP
  • Review data and assess against established acceptance criteria
  • Perform technical review of peer-generated data
  • Evaluate data to identify trends and/or establish limits
  • Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed
  • Identify and troubleshoot technical problems
  • Identify gaps in systems and procedures
  • Receive and provide training
  • Participate in assay transfer and assay validation
  • Perform equipment qualification / maintenance
  • Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures
  • Support the maintenance and compliance of operational areas
  • Assure and apply GMP throughout operations
  • Coordinate with customers to support multi-site operational activities
  • Support internal and external audits and regulatory inspections
  • Works to meet schedules, timelines, deadlines
  • Participate in and/or lead group and project teamwork; project and process improvements
  • Write protocols and reports under limited supervision
  • Meets scheduled performance of 95% on time
  • Perform other duties as requested by managers to support Quality activities.
Required Skills
  • B.S./B.A. degree and 1-3 years experience or Master’s Degree plus one year experience or an equivalent combination of education and experience.
  • Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry.
  • Strong verbal and written communication skills, ability to organize and present information both formally and informally.
  • Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
  • Routinely exercises sound judgment, reasoning and problem solving.
  • Capable of working under limited supervision and determining own short term priorities.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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