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Lab Technician

Job in Riverside, Riverside County, California, 92501, USA
Listing for: Green Jeeva LLC
Full Time position
Listed on 2026-10-30
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Production QC/QA
Salary/Wage Range or Industry Benchmark: 52000 - 78000 USD Yearly USD 52000.00 78000.00 YEAR
Job Description & How to Apply Below

We are looking for a detail-oriented and technically skilled Lab Technician to support laboratory testing, sample preparation, analytical instrument operation, and quality control activities. The ideal candidate will have experience working with analytical laboratory equipment, maintaining accurate laboratory records, following established Standard Operating Procedures (SOPs), and ensuring compliance with applicable quality standards and regulatory requirements.

The role involves performing routine and analytical testing of raw materials, in-process samples, and finished products; supporting instrument calibration and maintenance; assisting with laboratory investigations; and maintaining accurate, audit-ready documentation. The candidate should demonstrate strong analytical skills, attention to detail, problem-solving abilities, and a commitment to laboratory safety and data integrity.

What you'll do
  • Perform routine and analytical testing of raw materials, in-process samples, and finished products using appropriate laboratory techniques and equipment.
  • Prepare samples, standards, and reagents for laboratory analysis, following established procedures.
  • Operate analytical instruments such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Visible spectrophotometers, FTIR, pH meters, and dissolution testing equipment, as applicable.
  • Conduct routine instrument calibration, performance checks, maintenance, and basic troubleshooting to ensure reliable analytical results.
  • Assist with analytical method verification, validation, and optimization activities in accordance with approved protocols.
  • Support stability studies by testing samples under specified storage conditions and documenting analytical results.
  • Review, interpret, and record laboratory data accurately, ensuring completeness, traceability, and data integrity.
  • Maintain laboratory documentation, including test records, laboratory notebooks, calibration logs, SOPs, validation documents, and test reports.
  • Follow applicable Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and established laboratory quality procedures.
  • Assist in investigating out-of-specification (OOS) and out-of-trend (OOT) results, deviations, and other laboratory discrepancies.
  • Support root cause analysis and corrective and preventive action (CAPA) activities as required.
  • Maintain laboratory equipment, work spaces, and testing materials in an organized and compliant condition.
  • Coordinate with Quality Assurance (QA), production, research and development (R&D), and other relevant teams to resolve testing issues and support quality objectives.
  • Assist in preparing laboratory records and supporting documentation for internal audits and regulatory inspections.
  • Identify opportunities to improve laboratory workflows, testing efficiency, and sample turnaround time.
What you need

Educational Qualifications

  • A degree in Pharmacy, Biotechnology, Chemistry, Analytical Chemistry, or a related scientific discipline is preferred.
  • Relevant laboratory training or practical experience in analytical testing and quality control is desirable.

Experience

  • Previous experience in laboratory testing, pharmaceutical quality control, analytical chemistry, or a related laboratory environment.
  • Familiarity with testing raw materials, in-process samples, and finished products.
  • Experience with analytical instruments, laboratory documentation, and quality control procedures.
  • Exposure to regulated laboratory environments and quality systems is preferred.

Technical Skills

  • Knowledge of analytical testing techniques, including HPLC, GC, UV-Visible spectroscopy, FTIR, and dissolution testing, as applicable to the role.
  • Understanding of sample preparation, reagent handling, standardization, and analytical testing procedures.
  • Familiarity with instrument calibration, routine maintenance, and basic troubleshooting.
  • Understanding of analytical method validation parameters, including accuracy, precision, linearity, specificity, and robustness.
  • Knowledge of stability testing and laboratory result interpretation.
  • Ability to maintain accurate laboratory records and prepare clear technical reports.
  • Familiarity with laboratory information management systems (LIMS), electronic laboratory notebooks (ELN), and Microsoft Excel is desirable.

Quality and Compliance

  • Understanding of GMP and GLP principles and laboratory quality procedures.
  • Awareness of data integrity principles, including ALCOA+.
  • Familiarity with SOPs, deviation management, OOS/OOT…
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