VISHWANATH KAMPLI

Accomplished ( Senior executive) with progressive industry background and decisive leadership style. Offers strategic planning abilities, background in change management and forward-thinking mindset. Ready for challenges and focused on meeting future demands.

• Faced FDA, MHRA and WHO Audits
• Responsibilities
• Reviewing of QC records ( Raw material , Semi finished goods and stability reports) in LIMS
• Review of working standard
• Review of Calibration reports ( Analytical Weighing balance, Micro balance
• High performance liquid chromatography, Ion Chromatography, Gas Chromatography UV-spectrophotometer, Osmometer, Karl Fischer titrators, Melting point apparatus, Micropipette, IR Spectrophotometer and Polarimeter )
• Review of Preventive Maintenance of Instruments (High performance liquid chromatography, Gas Chromatography, Karl Fischer titrators, Karl Fischer Coulometer, Ion chromatography)
• Handling of GLP Activities
• Working on SAP for creation of Purchase requisition for laboratory materials and service entries for invoices
• Handling of LIMS
• Audit trial review of Standalone Computerised system
• Periodic log book review
• Handling of QMS activities ( Invalid LIR, OOS, OOT, Breakdowns)
• Instrument qualification ( IQ, OQ and PQ)