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Quality Control Analyst Chemist Jobs in Riverside, CA

Gilead

Senior Manager, Quality Control

La Verne, CA

As the Senior Manager, Quality Control at Gilead you will manage the Quality Control Chemistry or Microbiology laboratory operation, ensuring laboratory processes provide high-quality analytical ...

Astrix Inc

QC Lab Tech- Cosmetics

Chino, CA · On-site

$20 - $25/hr

Prepare and transcribe analytical data for CoA release. * Label specimens accurately and distribute ... Wet chemistry experience. * Able to easily understand complex instructions. * Ability to organize ...

Mapei

Quality Control Technician

San Bernardino, CA · On-site

$20.60/hr

As a Quality Control Technician at MAPEI , you will use your chemistry lab skills to perform tests ... Identify and investigate abnormal test results, conducting root cause analysis. * Prepare and ...

Cynet Systems

Analytical Chemist I

Pomona, CA · On-site

$19.10 - $24.10/hr

Analytical Chemist I Job Location: Pomona CA Job Type: Contract Job Overview: Pay Range: $19.10hr ... Demonstrates commitment to the development, implementation and effectiveness of Quality Management ...

New

Freudenberg

QC/QA Technician (f/m/d)

City Of Industry, CA · On-site

$19 - $24.25/hr

Background in food science, food technology, chemistry, or related field with strong organic ... Strong analytical, investigation, and documentation skills. * Proficiency in ERP systems and ...

Select Source International

Be Seen First

Analytical Chemist I

Pomona, CA · On-site

$20 - $23/hr

Job Title: Analytical Chemist I Location: Pomona, CA, US, 91767 Duration: 06 months of Contract ... Demonstrates commitment to the development, implementation and effectiveness of Quality Management ...

New

Avid Bioservices

Lead Engineer, Quality Control

Tustin, CA · On-site

$105K - $124K/yr

Evaluate and analyze qualification data collected during projects while verifying acceptability of ... Requires a BA/BS in Science (such as Biology, Microbiology, Biochemistry, Chemistry) or other ...

CYNET SYSTEMS

Analytical Chemist I

Pomona, CA · On-site

$19 - $24/hr

Demonstrates commitment to the development, implementation and effectiveness of Quality Management ... Skills: * Analytical Chemistry. * LC-MS/MS. * Sample Preparation. * Pipetting. * Laboratory ...

New

CYNET SYSTEMS

Analytical Chemist I

Pomona, CA · On-site

$19.10 - $24.10/hr

Demonstrates commitment to the development, implementation and effectiveness of Quality Management ... Analytical Chemistry. LC-MS/MS. Sample Preparation. Pipetting. Laboratory Documentation.

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All JobsQuality Control Analyst Chemist JobsQuality Control Analyst Chemist Jobs in Riverside, CA

Quality Control Analyst Chemist information

See Riverside, CA salary details

$18

$32

$47

How much do quality control analyst chemist jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for quality control analyst chemist in Riverside, CA is $32.96, according to ZipRecruiter salary data. Most workers in this role earn between $26.83 and $38.12 per hour, depending on experience, location, and employer.

What does a quality control analyst chemist do?

A Quality Control Analyst Chemist is responsible for testing and analyzing materials and products to ensure they meet established quality and safety standards. They perform laboratory tests on raw materials, in-process samples, and finished products, using various analytical instruments and techniques. Their work helps to identify any deviations or defects, ensuring that only products that meet regulatory and company standards are released. In addition, they document results, maintain lab equipment, and often assist in troubleshooting quality-related issues.

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

To thrive as a Quality Control Analyst Chemist, you need a strong background in chemistry, analytical techniques, and laboratory procedures, typically supported by a bachelor's degree in chemistry or a related field. Familiarity with analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and knowledge of Good Laboratory Practice (GLP) or ISO standards is crucial. Attention to detail, problem-solving ability, and effective communication are essential soft skills for ensuring accurate results and clear reporting. These competencies are vital for maintaining product quality, regulatory compliance, and the integrity of laboratory operations.

What are some common challenges faced by quality control analyst chemists in ensuring product consistency and compliance?

Quality Control Analyst Chemists often encounter challenges such as maintaining accuracy under tight deadlines, managing large volumes of samples, and staying up-to-date with changing regulatory requirements. They must also effectively troubleshoot unexpected results and ensure all testing procedures adhere to strict protocols. Collaboration with production, R&D, and regulatory teams is essential to resolve discrepancies and support continuous improvement in product quality.

What are popular job titles related to Quality Control Analyst Chemist jobs in Riverside, CA?

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

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

The top searched job categories for Quality Control Analyst Chemist jobs in Riverside, CA are:

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Cities near Riverside, CA with the most Quality Control Analyst Chemist job openings:

Quality Control Analyst Chemist jobs near you
Infographic showing various Quality Control Analyst Chemist job openings in Riverside, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $68,556 per year, or $33 per hour.

Technician, Quality Control

JENAVALVE TECHNOLOGY INC

Irvine, CA • On-site

$25 - $33/hr

Full-time

Posted 7 days ago

Job description

Job Title: Technician, Laboratory Quality Control

Supervisor/Manager Title: Senior Manager, Laboratory

Job Description Summary:

  • The laboratory technician is responsible to support sustaining manufacturing by performing microbiological and chemistry testing on various kinds of samples and document the results to assure quality.
  • Responsible for supporting the Quality department with quality control activities related to the manufacture of the THV within the Leeds and Irvine production facilities. To include in-process and final inspection, labelling/packaging, documentation, and environmental monitoring. The role holder will also provide routine reports and communications to provide timely updates on inspection status.

Job Responsibilities:

  • Lab tech role:
    • Comply with company’s policy and procedures on maintenance of personnel hygiene and CEA cleanliness to ensure product safety.
    • Perform microbiological tests, including in-process solutions/water bioburden tests, environmental monitoring, basic microbial characterization such as gram staining.
    • Perform Chemistry testing for solutions, such as pH, concentration, and raw glutaraldehyde test.
    • Responsible for reading plates, recording the test results, and verifying test results meet the specification per standard operating procedure.
    • Responsible for sending samples to the contract lab and any sample preparation if required.
    • Perform sample collections as needed.
    • Assist with investigation for out of specification, above alert, action level results and clean room excursions.
    • Maintains lab supply inventory
    • Responsible for general lab equipment maintenance and overall cleanliness of lab.
    • Perform additional duties as assigned by the laboratory manager.
  • QC inspector role
    • Conduct routine testing on THV, to include functional, visual, and final inspection processes, along with supporting sterilization preparation.
    • Perform Microbiological monitoring on ViVitro (Leeds) or BDC (Irvine) when required.
    • Conduct Preventative Maintenance and calibration of the ViVitro (Leeds) or BDC (Irvine) equipment.
    • Conduct audits on the in-process paperwork associated with the manufacturing process including, but not limited to: manufactured valve DHRs, Jasmine preparation and ancillary logs. Provide support to the Engineering staff by gathering data on clinical product to allow decisions to be made on functionality.
    • Adhere to Quality System and record retention requirements.
    • Comply with all site Health & Safety requirements.
    • Contribute to continuous improvement efforts related to valve manufacture and inspection processes.
    • Inspect final packaging labels and confirm they are applied correctly per the relevant standards and Work Instructions.
    • Support other areas of the business as necessary and applicable to the role.

Required Education and Experience:

  • Bachelor’s degree in a division of Biology, Chemistry or a Biomedical related discipline
  • 2+ year experience in medical device/ pharmaceutical/ nutraceutical microbiology or sterilization and laboratory testing.
  • Must be familiar with 21CFR820 and ISO 13485 requirements. Hands on experience with these requirements is preferred.

Skills and Abilities Required for This Job:

  • Good written and verbal communication skills.
  • Strong cGMP skills.
  • Demonstrate good documentation practices.
  • Knowledge of good laboratory practices and laboratory safety.

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