Senior QC Specialist (GLP Studies – Product Safety Labs)
BengaluruFull-time8–12 yrsPosted 1 week ago
Leadership mechanical and production role at Eurofins in Bengaluru. Needs 8–12 years.
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
- GLP
- CRO
- Quality control
- Transcription
Good to have
- Biology
- Pharmacology