Associate Research Scientist - Catalent Pharma Solution - Somerset, NJ, USA
(2006-10 - 2009-06)
- Analyzing Finished Product testing Dissolution, Assay & Impurity Assay using HPLC
- Analysis of Clinical & Experimental batches
- Conducting Investigations for product quality
Associate Research Scientist - Bristol-Myers Squibb - New Brunswick, NJ, USA
(2006-03 - 2006-07)
- Analysis impurity, assay, content uniformity for Drug Product, impurity and assay for API
- Performing tech-transfer for Drug Product, and basic knowledge for IND & NDA validation, and also familiar with PDLIMS & PDPM
- Troubleshooting of HPLC, FTIR-Spectrophotometer, UV-VIS spectrometer, Dissolution Apparatus
- Following under SOP's, cGMPs and FDA regulation
Analytical Chemist II - Stride Pharmaceutical - Somerset, NJ 08873
(2005-11 - 2006-03)
- Responsible for testing of all finish product (tablets and capsules), R&D samples, Stability, product process validation samples and also media preparation as per USP and in-house methodologies using various analytical techniques with good documentation
- Performing purity and assay analysis on Raw materials, Blends and Finished products using wet chemistry
- Responsible for calibration HPLC, Dissolution, UV Spectrophotometer, IR Spectrophotometer, pH meters, Melting point, Analytical balances, Moistures, Hardness, Friability, Tap density, and Sieve analysis
Analytical Chemist II - Pharmaceutical Formulation Inc - Edison, NJ 08820
(2003-06 - 2005-11)
- Responsible for testing of all finish product (tablets and capsules), R&D samples, Stability, product process validation samples and also media preparation as per USP and in-house methodologies using various analytical techniques with good documentation
- Performing purity and assay analysis on Raw materials, Blends and Finished products using wet chemistry
- Responsible for calibration HPLC, Dissolution, UV Spectrophotometer, IR Spectrophotometer, pH meters, Melting point, Analytical balances, Moistures, Hardness, Friability, Tap density, and Sieve analysis
- Performs method validation for HPLC methods, Stability testing, Process and cleaning validation analysis following under SOP's, cGMPs and FDA regulation