A well professional QA personnel having 7 years of work experience in different areas of Quality Operation in a team leading position in a world leading multinational pharmaceutical company including other local companies. During my career I have been experiencing corporate GMP audits, have been becoming auditee against cross functional audit and have been representing QO in company EHS and GMP related meetings. Having experience to deal with Deviation, CAPA, Change Management, Quality Risk… Show more A well professional QA personnel having 7 years of work experience in different areas of Quality Operation in a team leading position in a world leading multinational pharmaceutical company including other local companies. During my career I have been experiencing corporate GMP audits, have been becoming auditee against cross functional audit and have been representing QO in company EHS and GMP related meetings. Having experience to deal with Deviation, CAPA, Change Management, Quality Risk Management, EH & S Risk Management. I Have been working on Continual Improvement programs by reviewing all the related data periodically like deviations, Risk Assessments, Market complaints, market returns, investigations, OOS, OOT, In-process Checks, Qualifications, Validations, Annual Product review etc. I have worked in microbiological Laboratory where I have tested BET & TOC of WFI, Microbiological Water Testing, and sterility Testing, Media preparation and Disposal, Raw & FG testing. I have been working on Qualifications and Validations of Instruments and Equipment, Facilities and Products etc. I have been working on the preparation, Archiving, Distribution and control of Documents like SOPs, Batch documents, Protocols etc. cGMP related Trainings on different topics is being carrying out by me on annual basis according to annual training Schedule. Got online training on different topics related to Quality, & Especially "Awareness and Internal Audit to IMS from SGS" that helps me in QMS (ISO 9001, ISO 14001 and ISO 18001) .I have been also working on and off in Quality Control Testing of FG Products. Show less

A well professional QA personnelworking in different areas of Quality Operation as a team player. During my career I have been experiencing GMP related works. Having experience to deal with Deviation, CAPA, Change Management. I Have been working on Continual Improvement programs by reviewing all the related data periodically like deviations, Risk Assessments, Market complaints, market returns, investigations, OOS, OOT, In-process Checks, Qualifications, Validations, Annual Product review etc. I… Show more A well professional QA personnelworking in different areas of Quality Operation as a team player. During my career I have been experiencing GMP related works. Having experience to deal with Deviation, CAPA, Change Management. I Have been working on Continual Improvement programs by reviewing all the related data periodically like deviations, Risk Assessments, Market complaints, market returns, investigations, OOS, OOT, In-process Checks, Qualifications, Validations, Annual Product review etc. I have been working in microbiological Laboratory where I have been testing BET & TOC of WFI, Microbiological Water Testing, and sterility Testing, Media preparation and Disposal, Raw & FG testing. I have been working on Qualifications and Validations of Instruments and Equipment, Facilities and Products etc. I have been working on the preparation, Archiving, Distribution and control of Documents like SOPs, Batch documents, Protocols etc. I have been also working on and off in Quality Control Testing of FG Products. Show less

Worked as Assistant Manager - II grade in Quality assurance & Quality Control department together, where the prime responsibilities were Chemical testing of Raw, Semi Finished & Finished products (Edible Oil). All chemical tests were being performed in the laboratory, More than two methods were developed in R & D laboratory for the analysis of Nickle in nickle Pallets used in hydrogenation and for Quantitative analysis of TBHQ (Anti oxidant) in FG oil samples etc and Learn to operate boiler and… Show more Worked as Assistant Manager - II grade in Quality assurance & Quality Control department together, where the prime responsibilities were Chemical testing of Raw, Semi Finished & Finished products (Edible Oil). All chemical tests were being performed in the laboratory, More than two methods were developed in R & D laboratory for the analysis of Nickle in nickle Pallets used in hydrogenation and for Quantitative analysis of TBHQ (Anti oxidant) in FG oil samples etc and Learn to operate boiler and reverse osmosis plants (sea Water & breakish water treatments) also worked for the chemical analysis of Raw, Semi finished and finished water for the mineral water manufacturing at the plant. Documentation of ISO 9001:2004 is a good learning at the factory. Show less