QC Data Reviewer - GMP Lab (On-site, Costa Mesa)

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

Job summary

Jobot is seeking a QC Data Reviewer to support a GMP-regulated analytical chemistry laboratory in Costa Mesa, CA. The role focuses on reviewing laboratory data and testing records for accuracy, completeness, and compliance, enabling product release, stability testing, and manufacturing support.

Ideal candidates have 3–5 years in GMP QC labs and familiarity with HPLC, UV-Vis, pH and related methods, along with GxP software tools such as LabX, Chromeleon, or Cary WinUV.

Qualifications

• 3–5 years of experience in a pharmaceutical, biotechnology, or GMP-regulated QC laboratory.
• Experience reviewing analytical data, test results, or GMP laboratory documentation.
• Knowledge of cGMP, Good Documentation Practices, and data integrity principles.
• Familiarity with analytical techniques such as HPLC, UV-Vis, pH, osmolality, water content, conductivity, TOC, and compendial testing.
• Familiarity with laboratory software such as LabX, Chromeleon, or Cary WinUV.
• Bachelor’s degree in chemistry, biochemistry, or a related scientific field preferred; equivalent relevant experience will be considered.

Responsibilities

• Review analytical raw data, logbooks, calculations, and supporting documentation.
• Review electronic laboratory data, chromatograms, and audit trails.
• Verify results against approved specifications, test methods, and procedures.
• Confirm documentation follows cGMP, Good Documentation Practices, and data integrity requirements.
• Identify discrepancies and work with QC analysts and supervisors to resolve them.
• Escalate atypical, out-of-specification, or out-of-trend results according to established procedures.
• Complete assigned reviews within required timelines.

Skills

Attention to detail

Prioritization

Education

Bachelor’s degree in chemistry/biochemistry or related field

Tools

LabX

Chromeleon

Cary WinUV

Job description

Jobot is seeking a QC Data Reviewer to support a GMP-regulated analytical chemistry laboratory in Costa Mesa, CA. The role focuses on reviewing laboratory data and testing records for accuracy, completeness, and compliance, enabling product release, stability testing, and manufacturing support.

Ideal candidates have 3–5 years in GMP QC labs and familiarity with HPLC, UV-Vis, pH and related methods, along with GxP software tools such as LabX, Chromeleon, or Cary WinUV.