Temporary Quality Control Data Reviewer

Pyramid Laboratories Inc • Costa Mesa, CA

2d • $32 - $40

About The Position

The QC Data Reviewer supports the Analytical Quality Control department by reviewing laboratory analytical data, testing records, and supporting documentation for accuracy, completeness, and compliance with cGMP requirements and established procedures. The role primarily focuses on timely and accurate review of assigned QC chemistry laboratory records to support manufacturing, product release, stability studies, and other QC testing activities.

Requirements

• Strong attention to detail and ability to work independently, prioritize workload, and maintain accuracy in a fast-paced, high-volume GMP laboratory environment.
• Working knowledge of GMP, GDP, and data integrity principles.
• Familiarity with analytical testing techniques and instruments such as HPLC, UV-Vis, pH, osmolality, water content, conductivity, TOC, and compendial testing.
• Familiarity with laboratory software systems such as LabX, Chromeleon, and Cary WinUV.
• Prior experience reviewing laboratory analytical data, test results, or GMP documentation.
• Approximately 3–5 years of experience in a pharmaceutical, biotechnology, or GMP-regulated QC laboratory.

Nice To Haves

• Bachelor’s degree in chemistry, biochemistry, or a related scientific discipline preferred; equivalent relevant experience may be considered where appropriate.

Responsibilities

• Review QC laboratory analytical data, including raw data, logbooks, calculations, and supporting documentation, for completeness, accuracy, and compliance.
• Review electronic laboratory data, chromatograms, and associated audit trails as applicable to assigned testing.
• Support timely completion of laboratory data reviews in accordance with established priorities.
• Confirm compliance with GDP, cGMP, and data integrity principles.
• Identify documentation discrepancies and communicate findings to QC analysts and supervisors for resolution.
• Verify analytical results against approved specifications, test methods, and established procedures.
• Identify and escalate atypical, OOS/OOT, or potentially noncompliant results according to established procedures.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level