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AQA Sr,Executive

Open 46d

  • 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

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