Senior Scientist
United State Pharmacopeia India.
Total years of experience :17 years, 8 Months
Impurity and Assay Method Development and validation for Drug substance (API) and drug product by HPLC, UPLC, Dissolution, LCMS
Forced degradation study and impurity profiling by LCMS
All wet chemical analysis.
Method Development for Dietary supplement analysis
Preparation and review of Validation protocol, report.
Maintenance and calibration of all equipments
Regularly working on Nugenesis scientific data management system
Working under full GLP Lab practices.
Audit preparation for ISO17025, ISO9001
Previous work experience (Along with above)
HPLC/GC method development and validation.
Method Transfer from R & D to the plant.
Stability study for API
Generate the document for the DMF submission.
Characterization study by XRD, DSC and TGA
Particle size method development and Validation by Malvern Mastersizer 2000.
Audit faced USFDA, ISO17025, ISO9001
Impurity and Assay Method Development and validation for Drug substance (API) and drug product by HPLC, UPLC
All wet chemical analysis.
Preparation and review of Validation protocol, report.
Maintenance and calibration of all equipments
Working under full GLP Lab practices.
Audit preparation for ISO17025, ISO9001
Audit faced USFDA, ISO17025, ISO9001
Impurity and Assay Method Development and validation for Drug substance (API) and drug product by HPLC,
All wet chemical analysis.
Preparation and review of Validation protocol, report.
Maintenance and calibration of all equipments
Working under full GLP Lab practices.
Audit preparation for ISO17025, ISO9001
Audit faced USFDA, ISO17025, ISO9001
All wet chemical analysis.
Maintenance and calibration of all equipments
Working under full GLP Lab practices.
Audit preparation for ISO17025, ISO9001
Secured merit first position in M.Sc. Analytical chemistry in year 2006.