PAC_App_CVs

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.

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