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Quality Control Associate Jobs in Anaheim, CA (NOW HIRING)

Nissin Foods (USA) Co., Inc.

QC/SQF Supervisor

Gardena, CA · On-site

$23.50 - $36/hr

Overview Supervisors in Quality Control are responsible for overseeing day-to-day QC operations to ... Associate's degree in business, Engineering, Food Science, or related field, or equivalent work ...

Slope

Supplier Quality Control Supervisor

Costa Mesa, CA · On-site

$86 - $114/hr

ABOUT THE JOB As the Supplier Quality Control Supervisor, you will be instrumental in supporting ... ASQ Certified Quality Engineer, Quality Improvement Associate, or equivalent. * IPC‑A‑610 or ...

New

Bio-Rad Laboratories

Quality Control Technician I

Irvine, CA · On-site

$23.13 - $31.78/hr

Associate's degree or higher in a science field or equivalent clinical lab experience. * Experience working in QC or a clinical laboratory are a plus. * Strong knowledge of Quality Systems and Good ...

Bio-Rad Laboratories

Quality Control Technician I

Irvine, CA · On-site

$23.12 - $33.77/hr

Associate's degree or higher in a science field or equivalent clinical lab experience. * Experience working in QC or a clinical laboratory are a plus. * Strong knowledge of Quality Systems and Good ...

Bio-Rad Laboratories

Quality Control Technician I

Irvine, CA · On-site

$23.13 - $31.78/hr

Associate's degree or higher in a science field or equivalent clinical lab experience * Any experience working in QC or a clinical laboratory are a plus * Strong knowledge of Quality Systems and Good ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Anaheim, CA

Quality Control Associate information

See Anaheim, CA salary details

$12

$26

$40

How much do quality control associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for quality control associate in Anaheim, CA is $26.66, according to ZipRecruiter salary data. Most workers in this role earn between $19.38 and $32.45 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

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

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

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

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Anaheim, CA?

The most popular types of Quality Control jobs in Anaheim, CA are:

What cities near Anaheim, CA are hiring for Quality Control Associate jobs?

Cities near Anaheim, CA with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Anaheim, CA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $55,447 per year, or $26.7 per hour.

QC Microbology Assoc II (Sun-Tues/Wed 5:30pm-5:30am)

B. Braun US Pharmaceutical Manufacturing LLC

Irvine, CA

Full-time

Medical, Retirement

Posted 22 days ago

Job description

B. Braun Medical, Inc.
Company: B. Braun US Pharmaceutical Manufacturing LLC
Job Posting Location: Irvine, California, United States
Functional Area: Quality
Working Model: Onsite
Days of Work: Wednesday, Tuesday, Monday, Sunday
Shift: 3/4 X 12
Relocation Available: No
Requisition ID: 13451

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®.

Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit www.bbraunusa.com


Position Summary

The QC Microbiology Associate II performs microbiological testing and laboratory support activities to ensure compliance with current Good Manufacturing Practices (cGMP), company procedures, and quality standards. This position is responsible for the receipt, preparation, testing, documentation, and review of microbiological samples and results. The Associate II supports laboratory operations through equipment maintenance activities, data integrity practices, and adherence to established quality systems. The role requires a strong attention to detail, the ability to work in a regulated laboratory environment, and a commitment to maintaining safe and efficient laboratory operations. This position reports to the QC Microbiology Supervisor/Manager and is based onsite.

In This Role, You Will Have the Chance To:

  • Perform microbiological testing on finished products, stability samples, environmental monitoring samples, and other laboratory samples in accordance with approved procedures and test methods.
  • Receive, prepare, process, and document samples while maintaining data integrity and compliance with cGMP requirements.
  • Record, review, and compile laboratory results, reports, and supporting documentation to ensure accuracy, completeness, and compliance with established specifications.
  • Support laboratory equipment calibration, qualification, preventive maintenance, troubleshooting, and routine operational activities.
  • Verify test results and ensure compliance with approved procedures, methods, specifications, and quality standards.
  • Assist with the development, revision, and continuous improvement of laboratory procedures, test methods, and documentation practices.
  • Maintain laboratory cleanliness, organization, and compliance with all applicable safety, quality, and regulatory requirements.

Essential Requirements

  • High School Diploma or GED required.
  • Minimum one (1) year of laboratory, microbiology, quality control, or related scientific experience.
  • Strong attention to detail with excellent documentation and recordkeeping skills.
  • Ability to follow written procedures and work effectively within a regulated environment.
  • Proficient in data recording, report preparation, and review of laboratory documentation.
  • Ability to work independently and collaboratively within a team environment.
  • Flexibility to work non-standard hours as business needs require.

Preferred Experience Includes

  • Bachelor's degree in Microbiology, Biology, Chemistry, or a related scientific discipline.
  • Experience working in a pharmaceutical, biotechnology, medical device, or other FDA-regulated environment.
  • Familiarity with cGMP regulations, laboratory quality systems, and microbiological testing methods.
  • Experience supporting laboratory investigations, equipment qualification, or continuous improvement initiatives.

Physical & Work Environment

  • Laboratory-based role requiring frequent standing, walking, bending, and use of laboratory equipment.
  • Ability to lift and carry up to 20 pounds occasionally.
  • Moderate noise levels typical of a laboratory and manufacturing support environment.
  • Required use of appropriate personal protective equipment (PPE) and adherence to all safety procedures.
  • May involve exposure to biological materials, laboratory reagents, and controlled environmental conditions consistent with microbiology laboratory operations.

The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate.

B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com.

Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.

We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here.


All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.

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