Total 05 years good hands of experience in QC analysis & QA Activities Working as an Officer-QA, QC in Mega fine Parma (P) Ltd., 3.0 year QA activities experience & 2.0 year QC Analysis experience in Pharmaceutical industries, which are involved in manufacturing of API and Intermediates Got USFDA Approval in March’2008 for Mega fine Parma (P) Ltd & from 30 may 2011 to 03 June 2011, I Face US FDA Audit Actively participated in USFDA Team for implementation of GMP & GLP. Also face WHO audit in Fem care pharmaceutical, Vadivarhe Nashik.ANALYTICAL SOLUTION, PVT LTD, MumbaiWorked with ANALYTICAL SOLUTION, PVT LTD, Mumbai as an Analyst in method validation of API & formulation product of different Pharmaceutical Companies & (Working in Method development & Validation, Rotuine Analysis Department) .current working with Fem care Pharma Ltd as Sr. Officer-QAJob Responsibilities-QA Review of BMRs, review Daily calibration of lab instruments, Product dispatch and customer requirements like marketing samples vendor documents review, specifications follow up.  Ensure the day to day activities looking cGMP implementation in the plant. Review of SOPs. Review of stability study protocol, report and Analytical data sheet. Review of standard test procedures and test procedures. Master production and control record preparation and review. Batch production record review. Review and approval of Executed BMRs. analytical records, dispatch of product, validation protocol and reports, specification/STP, analytical test data sheet.  Responsible for updating the documents as per ISO 9001:2008 such as Quality manual, recording the management review meetings, implementing CAPA and record of Monthly Review meetings etc. Have a long and successful history to give Audits Compliance for leading pharmaceuticals and regulatory authorities inspection  Attaining Regular GMP trainings.