Umair Sadiq Email and Phone Number

Self-motivated, energetic and persuasive professional backed by almost 9 years of demonstrated expertise in Quality and validation with extensive knowledge of GMP (Good Manufacturing Practice),GLP (Good Lab Practice) & GDP(Good Documentation Practice),GXP, QMS (Quality Management System), Quality of solid dosage form, Quality of sterile products, Quality of liquid and suspension, In process control, Noncompliance,Deviations ,RCA Rout Cause Analyses,CAPA(Corrective and Preventive Action)… Show more Self-motivated, energetic and persuasive professional backed by almost 9 years of demonstrated expertise in Quality and validation with extensive knowledge of GMP (Good Manufacturing Practice),GLP (Good Lab Practice) & GDP(Good Documentation Practice),GXP, QMS (Quality Management System), Quality of solid dosage form, Quality of sterile products, Quality of liquid and suspension, In process control, Noncompliance,Deviations ,RCA Rout Cause Analyses,CAPA(Corrective and Preventive Action), Sampling of raw material, APQR (Annual Product Review),Releasing of products on SAP,Generat BOM (Bill of Material) ,Amendment of BOM(Bill of Material) on SAP, validation of sterile area. IQ,OQ,PQ. media filling process. Documentation of Validation and Reports. Task-focused professional with expertise in all facets of Quality Assurance; skilled in collaborating with all members of organization to achieve Quality related objectives. Instrumental in streamlining and improving processes, enhancing productivity and implementing QMS, cGMP, GLP and GDP.Acheivemnts:APQR Automation by PowerBI Microsoft . Show less

 Self-motivated, energetic and persuasive professional backed by almost 9 years of demonstrated expertise in Quality and validation with extensive knowledge of GMP (Good Manufacturing Practice),GLP (Good Lab Practice) & GDP(Good Documentation Practice),GXP, QMS (Quality Management System), Quality of solid dosage form, Quality of sterile products, Quality of liquid and suspension, In process control, Noncompliance,Deviations ,RCA Rout Cause Analyses,CAPA(Corrective and Preventive Action)… Show more  Self-motivated, energetic and persuasive professional backed by almost 9 years of demonstrated expertise in Quality and validation with extensive knowledge of GMP (Good Manufacturing Practice),GLP (Good Lab Practice) & GDP(Good Documentation Practice),GXP, QMS (Quality Management System), Quality of solid dosage form, Quality of sterile products, Quality of liquid and suspension, In process control, Noncompliance,Deviations ,RCA Rout Cause Analyses,CAPA(Corrective and Preventive Action), Sampling of raw material, APQR (Annual Product Review),Releasing of products on SAP,Generat BOM (Bill of Material) ,Amendment of BOM(Bill of Material) on SAP, validation of sterile area. IQ,OQ,PQ. media filling process. Documentation of Validation and Reports. Task-focused professional with expertise in all facets of Quality Assurance; skilled in collaborating with all members of organization to achieve Quality related objectives. Instrumental in streamlining and improving processes, enhancing productivity and implementing QMS, cGMP, GLP and GDP. Show less

To ensure GMP,GLP,GDP,To ensure Qulaity of Solid,Liquid/Suspension,Sterile dosage form .To validate new product.To validate qualification of sterile area .To give line clearance of area .In process Control in routine.APR.Annual Product Review.CAPA.corrective and preventive action .Investigation.To maintain Reference store.To maintain Record room.