AQA Sr,Executive

• 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