31 Jul
|
DIFGEN PHARMACEUTICALS PRIVATE
|
India
31 Jul
DIFGEN PHARMACEUTICALS PRIVATE
India
- Review raw analytical data, worksheets, and instrument printouts for accuracy and compliance.
- Review test reports, COAs, and analytical result summaries before release.
- Verify calculations, chromatograms, integration parameters, and result interpretations.
- Ensure adherence to ALCOA+ and data integrity standards.
- Review analytical methods for completeness and compliance.
- Review specifications for raw materials, in‑process materials, intermediates, and finished products.
- Review QC-related deviations, OOS, OOT, incident reports, CAPA, change controls.
- Ensure root cause, impact assessment, and CAPA effectiveness are scientifically justified
M.Pharm and /or any PG
📌 AQA Sr,Executive (India)
🏢 DIFGEN PHARMACEUTICALS PRIVATE
📍 India