Job Description

Initiation and investigation of change control, lab event, deviation, OOS etc in track wiseReview of instrument log books, sample set and method and other analytical recordsEnsure intergrity , accuracy and adequacy of the activity perfomedTo execute applicable SAP transcationsReview of all analytical data generated in the laboratoryCoordinate and priorities analytical data review with the section in charge RM GLP PM and stabilityand schedue review activities as necessary to support manufacturing while minimizing delaysSupport in backup activity of all computer related software used in the QC labProvide troubleshooting support to analysis in the labPreparation and review of SOPs specification and STPSDestruction of samples after completion of analysis and review of dataTo indentify & reporting of deviations , OOT & OOSTo perform the investigations of deviations, OOT & OOSEnsure compliance to cGMP and safety standards in the QC labAssist with analysis for reporting and verification of tgest results/ reportsTo execute applicable SAP transactionsTo perform verification of analytical data as per checklist for verification of anaytical data before submission to QA QC for reviewTo indetify the material for reduced testing and to prepare reduced testing assessment report.To validate the new method in Raman instrumentArchival of all types of records related to QCAny other assigment given by Manager QC from Time to timeTo particiapte and contribute in internal and external audits

Sun Pharmaceutical Industries