Anil Mahato

Ahmedabad

Summary

I'm Anil Mahato, have over 25 years of experience in pharma industry in analytical development and analytical method validation in API and Formulation. Expertise in Spectral Analysis, Molecular Characterization, NMR, MS, IR Chromatography HPLC, GC, HS.

Work History

DISHMAN Pharma

Ahmedabad

LUPIN Ltd.

Tarapur

TORRENT Research Center

Gandhinagar

SUN Pharma Advanced Research Center

Baroda

CIPLA Pharma

Pune

Education

Ph. D. (Chemistry) -

Hemchandracharya North Gujarat University

01.2020

M. Sc. (Chemistry) -

Nagpur University

01.1996

Skills

NMR Spectroscopy
1D-NMR: Proton NMR, Homo decoupling experiment, Deuterium exchange, 1DNOE, DEPT, 13C-NMR
2D NMR: DQF-COSY, HMQC
NMR Quantification of impurities and API’s by using absolute & relative methods
Method development and validation of drugs and impurities through quantitative NMR in pharma API’s, intermediates, raw materials and its impurity profile through various NMR, IR & Mass spectra tools
Polymorphism Study (using X-ray powder differentiation):
Identification of Polymorphic forms & Solvatomorphs in DS and DP by powder XRD

Quantification of Polymorphic forms & Solvatomorphs in Active pharma ingredients by powder XRD with analytical method validation
High Pressure Liquid Chromatography-Mass-Spectrometry: (HPLC, LC-MS)
Development of analytical method by LC-MS & identification of impurities and their characterization using LC-MS technique coupled with complimentary methods
Quantification of low-level impurities of toxic nature by LCMS
Method development and validation (HPLC, LCMS, NMR, GC):
API, residual solvents impurities, inorganic impurities and genotoxic impurities and its intermediates by various analytical techniques like HPLC, Derivative HPLC, GC, GCHS & IC

Contacts

F91 Tirtha Dham, Ahmedabad, GJ, 380052, INDIA, mahatoanil334@gmail.com, +91 (898) 002-1731

Accomplishments

Successful Method developed for Vitamin D analogues for site in Netherlands by qNMR
Some residual solvents, intermediates and chemicals determined by qNMR
Analytical method developed and validated for Polymorphic quantitative analysis of API.
Potential genotoxic impurities (PGI’s) quantitative method developed.
GLP activities implemented in lab, facility set up in lab, commissioning, and maintenance.

Degree

Ph. D. (Chemistry)

International Work

Amsterdam, Netherlands

Timeline