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Quality Control Laboratory Jobs in California (NOW HIRING)

QC Laboratory Associate

Vacaville, CA ยท 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 ...

QC Laboratory Technician

Anaheim, CA ยท 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.

QC Laboratory Technician

Buellton, CA ยท On-site

$20.25 - $25.75/hr

... Quality Control Laboratory, with preparation, and follow up of CAPA for internal audits and Health Authority inspections, as needed. * Drives continuous improvement initiatives which positively ...

The Quality Control Laboratory Intern supports day-to-day QC lab operations and assists with routine analytical testing under supervision. This internship blends hands-on lab readiness activities ...

QC Laboratory Technician

Buellton, CA ยท On-site

$20.25 - $25.75/hr

... laboratory work, including internal testing and coordinating sample submission to third-party labs. The QC Lab Technician collects, processes, and tests samples from raw materials (RAW), work-in ...

The Quality Control Laboratory Intern supports day-to-day QC lab operations and assists with routine analytical testing under supervision. This internship blends hands-on lab readiness activities ...

QC Laboratory Technician

Buellton, CA ยท On-site

$20.25 - $25.75/hr

... laboratory work, including internal testing and coordinating sample submission to third-party labs. The QC Lab Technician collects, processes, and tests samples from raw materials (RAW), work-in ...

QC Laboratory Technician

Buellton, CA ยท On-site

$20.25 - $25.75/hr

... laboratory work, including internal testing and coordinating sample submission to third-party labs. The QC Lab Technician collects, processes, and tests samples from raw materials (RAW), work-in ...

Ensure world-class safety within the quality control laboratory and Northridge Facility. * Prepare sample solutions, standards, and reagents * Perform wet chemical and instrumental analysis ...

Ensure world-class safety within the quality control laboratory and Northridge Facility. * Prepare sample solutions, standards, and reagents * Perform wet chemical and instrumental analysis ...

Ensure world-class safety within the quality control laboratory and Northridge Facility. * Prepare sample solutions, standards, and reagents * Perform wet chemical and instrumental analysis ...

Ensure world-class safety within the quality control laboratory and Northridge Facility. * Prepare sample solutions, standards, and reagents * Perform wet chemical and instrumental analysis ...

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Showing results 1-20

Quality Control Laboratory information

See California salary details

$13

$22

$30

How much do quality control laboratory jobs pay per hour?

As of Aug 3, 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.

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.

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 is quality control in laboratories?

Quality control in laboratories involves testing and inspecting samples to ensure products meet specified standards and regulations. Laboratory professionals use techniques such as calibration, documentation, and data analysis to maintain accuracy and consistency in testing processes. Certification and adherence to industry protocols are essential for effective quality control.

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.

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.

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 most commonly searched types of Quality Control Laboratory jobs in California? The most popular types of Quality Control Laboratory jobs in California 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:
Infographic showing various Quality Control Laboratory job openings in California as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $46,423 per year, or $22.3 per hour.

QC Analyst, Quality Control Laboratory

Coherus Oncology

Camarillo, CA โ€ข On-site

$90K - $110K/yr

Full-time

Re-posted 19 days ago


Job description

Title: QC Analyst, Quality Control Laboratory
Reports to: Director, Quality Laboratory
Location: Camarillo, CA
Classification: Exempt
Overview:
This laboratory position will be in the Quality Control Department and support activities associated with routine in-process testing, Certificate of Analysis (COA) release testing, and stability program support for biologics. This position will demonstrate strong technical proficiency with analytical methods, operate as a technical leader within the QC team, supporting complex testing, driving investigation quality, and ensuring compliant execution of analytical programs.
In addition, this position will support laboratory investigations, identify and help implement CAPAs, and participate in analytical method lifecycle activities including protocol drafting and execution of method validation, verification, and transfer in accordance with regulatory expectations.
Responsibilities:
  • Perform and review routine in-process, release, and stability testing for biologic drug substances and drug products while adhering to GMP/GDP QC requirements
  • Experience performing plate-based ELISA, ligand binding assays required
  • Execute and troubleshoot a range of analytical methods including HPLC/UPLC (SEC, RP, CEX, Peptide Mapping), capillary electrophoresis testing (cIEF, CE-SDS)
  • Perform compendial methods relevant to large molecule therapeutics (USP/EP/JP)
  • Support laboratory investigations, including OOS, OOT, and atypical result investigations
  • Conduct root cause analysis and identify, implement, and verify effectiveness of CAPAs
  • Draft and oversee protocols for method validation, verification, and transfer
  • Interpret results, perform statistical analyses, and prepare validation reports aligned to ICH Q2 and US FDA expectations
  • Author and review SOPs, test methods, protocols, and technical reports
  • Ensure all work is performed in compliance with cGMP, data integrity principles, and internal QA/QC policies
  • Support regulatory inspections and audits as a subject matter expert
  • Maintain departmental instruments and ensure timely execution of QC quality system records
  • Mentor team members and oversee analytical workflows to meet project goals

Qualifications:
  • Bachelor's or Master's in Biology, Chemistry, Biochemistry, or a related scientific field.
  • Minimum of 3 years of direct, hands-on QC experience in a GMP Quality Control laboratory supporting biologics.
  • Technical proficiency with HPLC, ELISA, capillary electrophoresis, and compendial testing.
  • Background in laboratory investigations, OOS management, and CAPA implementation.
  • Hands-on QC experience with method validation aligned to ICH Q2 and US FDA regulations.
  • Excellent technical writing, documentation, and analytical troubleshooting skills.
  • Ability to work independently while collaborating effectively across QC, QA, and Regulatory.
  • Experience in a commercial-stage or late-phase biologics environment is preferred.
  • Familiarity with LIMS and chromatography data systems (e.g., Chromeleon) is highly desirable.
  • Strong familiarity with GxP requirements.
  • Excellent communication, interpersonal and organizational skills are required.

The Base Salary Range for this position is $90,000 to $110,000. Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.
Coherus provides equal employment opportunities to all employees and applicants for employment and prohibits unlawful discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We also prohibit discrimination based on the perception that anyone has any of these characteristics or is associated with a person who has or is perceived as having any of these characteristics.