Temporary Quality Control Data Reviewer

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

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Temporary Quality Control Data Reviewer

Salary Range: $32.00 To $40.00 Hourly

POSITION SUMMARY:

The QC Data Reviewer will provide support to 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. This position will primarily focus on timely and accurate review of assigned QC chemistry laboratory records to support manufacturing, product release, stability studies, and other QC testing activities.

PRINCIPAL DUTIES:

• 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.

QUALIFICATIONS AND EXPERIENCE:

• 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, compendial testing, etc.
• Familiarity with laboratory software systems such as LabX, Chromeleon, Cary WinUV, etc.
• 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.
• Bachelor’s degree in chemistry, Biochemistry, or a related scientific discipline preferred; equivalent relevant experience may be considered where appropriate.