Senior QC Specialist (GLP Studies – Product Safety Labs)

Eurofins · Bengaluru, India

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Role summary

Senior QC Specialist needed to conduct comprehensive quality control reviews of GLP-compliant preclinical study data, documentation, and records. The role ensures accuracy, completeness, and regulatory readiness while supporting data integrity initiatives and process improvements.

What they're looking for

Bachelor's degree in Toxicology, Biology, Pharmacology, Pharmaceutical Sciences, or related field
8–12 years of experience in GLP-regulated environments, CRO operations, or preclinical research
Strong knowledge of GLP regulations, data integrity principles, and good documentation practices
Master's degree preferred

What you'll be doing

Perform detailed QC reviews of laboratory data, worksheets, protocols, and study records for accuracy and completeness
Identify documentation discrepancies, transcription errors, and data inconsistencies; coordinate corrective actions
Review study trackers, shipping records, and supporting documentation to maintain audit-ready files
Trend recurring quality issues and recommend corrective and preventive actions
Mentor support staff on documentation quality standards and participate in process improvement initiatives

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