Temp QC Data Reviewer – GMP & Data Integrity

Pyramid Laboratories Inc; Costa Mesa (CA); On-site; USD 44,000 - 55,000; Full time

Job summary

Pyramid Laboratories Inc. is seeking a Temporary Quality Control Data Reviewer to support the Analytical Quality Control team.

The role focuses on timely review of laboratory data, raw data, logbooks, and supporting documents to ensure accuracy and compliance with cGMP procedures. The ideal candidate has 3–5 years in a GMP-regulated QC environment, with hands-on experience in HPLC, UV-Vis, pH, and related testing, and familiarity with LabX or Chromeleon software.

Qualifications

• Bachelor’s degree in chemistry or biochemistry preferred.
• 3–5 years in pharmaceutical QC laboratory.
• Experience reviewing lab data and GMP documentation.
• Familiarity with HPLC, UV-Vis, pH, osmolality, and related tests.

Responsibilities

• Review QC lab data for completeness and accuracy.
• Review electronic data, chromatograms, and audit trails.
• Support timely completion of data reviews per priorities.
• Confirm GDP, cGMP, and data integrity compliance.
• Identify discrepancies and communicate findings.
• Verify results against specs and SOPs.
• Escalate atypical or potentially noncompliant results.

Skills

Attention to detail

GMP GDP knowledge

Data integrity

Lab data review

Independent work

Education

Chemistry degree

Biochemistry degree

Tools

LabX

Chromeleon

Cary WinUV

Job description

Pyramid Laboratories Inc. is seeking a Temporary Quality Control Data Reviewer to support the Analytical Quality Control team.

The role focuses on timely review of laboratory data, raw data, logbooks, and supporting documents to ensure accuracy and compliance with cGMP procedures. The ideal candidate has 3–5 years in a GMP-regulated QC environment, with hands-on experience in HPLC, UV-Vis, pH, and related testing, and familiarity with LabX or Chromeleon software.