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July 2001 to September 2003
Scientist- Analytical, Vimta Labs Limited, Hyderabad
Job Responsibilities
 Method development and validation as per standard methodologies
 Analysis of different products Food and Agricultural, Drugs and Water.
June 1998 to July 2001
Junior executive in Quality control Aurobindo Pharma Ltd, Unit V Pashamylaram
Job Responsibilities :
 Quality Control
 Bulk Drugs Analysis as per IP, BP, USP
 Analytical Development in deploying chemical & Instrumental Methods
Bulk Drug
 In- Process Control Methodologies for Intermediates & Finished Products
 Implementation of All QA norms applicable to API Industry- Deviations, Change controls,
IQA, Customer Complaints, and Validations etc. Total Process Control (Analytical) on
HPLC for 7-ACCA Production in Plant
 Standardization of HPLC Methods for Intermediates and Finished Products Viz. 6-APA, 7-
ADCA, MAEM, TAC, ACACY and Cephalosporin: Cefalexin, Cefadroxil, Cefradine, Cefixime
trihydrate, Cefuroxime Axetil, Cefuroxime Acid, Cefotaxime acid, Ceftrioxone Disodium,
Cefazolin Sodum Cephalothin Acid, Cefoperozone Acid, Ceftiofur Acid.
 Semi-synthetic penicillin : Ampicillin Trihydrate, Ampicillin Anhydrous etc
 Standardization of GC Methods for analyzing Various Solvent Residues / Recovery
Streams Viz. MDC/HMDO, Toluene / HMDO, Ethylacetoacetate, Methylacetoacetate,
Ethyl acetate / THF, DMF, Acetone etc.