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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