Presently working as Location Head/Laboratory In-Charge for Indore location.

Overall responsible for Quality functions and regulatory compliance. Providing technical and administrative support to team. Monitoring the QMS ,GLP, activities and coordinating with regulatory authorities -state FDA,NABL, APEDA ,MoEF,BIS, USFDA, Imparting training on QMS, Maintaining the lab in compliance state.

Overall responsible for QC functions of 4 locations-Vizag , Tarapur, Mahad,Ambernath.Provided technical and administrative support to team. Was responsible for all labs to maintain the labs in compliance state. Audited the job work sites for QMS and manufacturing, was responsible for outside testing laboratories audit and compliance .

Worked as a corporate QC head for 6 locations-Manglore,Mysore,Vizag,Tarapur,Ambernath,Mahad. Provided tech and admin support to team , Was responsible for QC functions across the sites. Provided the support to all job work sites in their QC function to release the batches.

Was responsible for Quality control functions. Provided the support to the production in achieving the planned target by providing the results on time. Lead the QC team in USFDA inspection and succesfully cleared the audit.Conducted training on cGLP and ICH

Overall responsible for QC functions including micro and AMV. Successfully completed USFDA audits in Dec-2009 & May-2009. EDQM audit in FEB-2010.TGA audit in Aug-2009, GHA audit in FEB-2012 , Achieved ISO/OHSAS certification- a) ISO: 9001 -2008 in July- 2012 b) ISO: 14001:2004 in JAN-2013 c) OHSAS: 180001:2007 in Dec-2012.Ensured activities were performed with written procedures -QCP,s ,QAP,s, CQA,s GTP,s. Supported to release the batches on time and achieve the monthly target. Imparted training to team on QMS, departmental procedures. evaluated the requirements of clients and provided the right quality material on time. Supported RA by providing the quality documents for regulatory submission.

Overall responsible for QC activities -RM/PM,IPQC, IM, FG, stability. worked on instruments-HPLC, GC, IR, UV, potentiometry and common lab equipment's, faced the customer audits, performed the inter section audits and outside lab audits. performed the quality evaluation of competitors samples .Awarded “BRAVO” for targeted production of Nabumentone for Exports in Mar -2008 Certificate of appreciation awarded in appreciation of contribution to USFDA approval of Watson pharma unit –III.(Ambarnath) in JUN-2008Successfully completed the Basic LC maintenance & troubleshooting training at SINGAPORE in Jul-2008 at customer education and training center.

Worked in QC dept , in different sections RM/PM, IPQC, Intermediates and FG testing , stability .Started working as a Jr.analyst , worked in all sections , played role of section incharge, shfit incharge, reviewer , Performed planning of sampling ,testing and release of all materials. hands on all lab instruments. Developed the customers by proving the right quality materials as a reshipment sample/s.1.Certificate of participation received from the The Asian & Mideast insituate of chemist (AMIC) on seminar Entitled “The utility of chemical science in modern industries conducted by Mr. P.S. Ramanthan in 2001.2.Certificate of participation received from the The Asian & Mideast instituate of chemist (AMIC) on seminar Entitled “ HPLC Basic theory , instrumentation and applications in Jun-2002.3.Certificate of participation received from company for paricipiating in the training on implementation of ICH Guidelines held between 19th jan to 24 th Jan-2004 , training was conducted by Dr. Raymont winter. 4.Honored as a team member for successful clearing of USFDA inspection in NOV-1998, Feb- 2002 & Oct-2005

Joined as a trainee , in Food and drugs divisions , Got training in all classical analysis analysis, standardization of volumetric solutions, reagents preparations. Got training on basic lab equipment operations, handling pharmacopeias. Got exposure for different types of materials -Raw materials, excipents and Finished good testing . Got complete external training on GC instrument.

JAN-1992 to MAR-1992 : In plant training In MEYER ORGANICS LIMITED APR-1992 TO JUN-1992 : In plant training In MERIND LIMITED .Got the full time training in these two organization's, this was a part of 2 year,s PG diploma of food drugs and cosmetics.Got Major exposure in the QC dept ,their operations ,instrumentations, sampling area,s . Got exposure to see the activities of cross function teams. Report is prepared based on the traing and submitted to college.