• Review raw material analytical reports, test results, and laboratory documentation.
• Verify compliance with approved specifications, STPs, SOPs, and pharmacopoeial requirements.
• Review chromatograms, spectra, calculations, and analytical worksheets for accuracy.
• Ensure compliance with ALCOA+ principles and data integrity requirements.
• Review and approve raw material Certificates of Analysis (CoA).
• Coordinate with QC analysts and warehouse for timely material disposition.
• Review deviations, OOS/OOT results, and support investigations as required.
• Ensure GMP and regulatory compliance during documentation review.
• Maintain accurate records in LIMS/ERP or other laboratory systems.
• Participate in internal audits, regulatory inspections, and customer audits.
• Support method verification, laboratory investigations, and continuous improvement initiatives.
• Ensure timely review and release of raw material testing documents to avoid production delays.

📌 Sr Executive-B (India)
🏢 RPG Group
📍 India