Senior QC Specialist (GLP Studies – Product Safety Labs)

About the role

The Senior QC Specialist performs advanced quality control reviews of study data, documentation, and records supporting GLP-compliant preclinical studies. The role ensures study records are accurate, complete, consistent, and inspection-ready before Study Director review while supporting continuous improvement and data integrity initiatives.

What you'll do

• Perform detailed QC reviews of laboratory data ( acute toxicology data ), worksheets, protocols, amendments, and study records
• Conduct first-pass review of complex and long-term study datasets
• Identify documentation discrepancies, omissions, transcription errors, and data inconsistencies
• Coordinate correction and resolution of quality issues and verify completion
• Review study trackers, shipping records, chain-of-custody documents, and supporting study documentation

What you need

• 8–12 yrs of experience
• GLP
• CRO
• Quality control
• Transcription
• Any graduate

Good to have

• Biology
• Pharmacology