Description
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
Qualifications
M.Pharm and /or any PG
📌 Aqa Sr,executive Kukatpally (India)
🏢 Aveva Drug Delivery Systems
📍 India
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