To review approval closure rejection drop if required of Quality system documents such as Deviation change control CAPA OOS OOT Re-process Re-work market complaint market returns LIR To ensure handle the investigation for Out of Specification Results OOT Deviations Product failures and Market Complaints are adequately performed and documented with appropriate Quality Risk Assessment activity Corrective and Preventive Actions based on the results of the investigations are identified and implemented To preparation review Approval of Quality system trend To verify In-process Quality Assurance during production activity and sampling at different stages of processing packing as per requirement To review approval of API Analytical Method Transfer Protocol Report and method validation documents Preparation review of Annual Product Quality Review Preparation Review Approval of Hold Time Study Protocol Reports and other study protocols reports Work Experience 7-9 year Education Masters in Science or Pharmaceutical Chemistry Post Graduation in Pharmacy Competencies

📌 Executive (Pithampur)
🏢 LUPIN
📍 Pithampur