Experience

ENovate Biolife

• United States
• Wellness and Fitness Services
• 1 - 100 Employee

• Sr. Research Associate

  • Jul 2021 - Present

• Research Associate

  • Feb 2021 - Jun 2021



Alkerms Pharmaceuticals Pvt. Ltd

• Delhi, India

• QA/QC

  • Jan 2018 - Feb 2021



Alembic Pharmaceuticals Limited

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Research Scientist

  • Jan 2017 - Nov 2017

  Method development for injectables Stability testing and forced degradation studies. HPLC, UPLC, GC and other instruments handling. Excel validation SOP preparation and to check its proper execution. Documentation and Review Method development for injectables Stability testing and forced degradation studies. HPLC, UPLC, GC and other instruments handling. Excel validation SOP preparation and to check its proper execution. Documentation and Review



Cipla

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Analyst

  • Apr 2013 - Dec 2016

  Method development using sophisticated instrumentation like HPLC, IR & other automated instruments. • Hand on experience on HPLC system, IR, UV spectrophotometers, & other automated instrumentations. • Perform the method development, method validation for no. of pharmaceutical products. • Worked on analysis of different products ranging from tablets, capsules to ophthalmic solutions. Analysis of product wrt their stability testing, forced degradation of products worked in documents review team for project submission Show less



Exotic Naturals

• Mumbai Area, India

• Executive - QC

  • Jul 2011 - Mar 2013

  • To work in collaboration with third party labs for testing of samples wrt actives, stability of products, shelf life, preservatives etc. • To prepare and review the protocol for stability studies for different countries as per guidelines. • Preparation of COA, MSDS for different API, and other generic products. • Sampling of incoming raw materials, intermediates and finished products for QC testing release. • Perform tests and inspections in according with approved procedures and compendia monographs. • Proper documentation for test results and other test related data. • Write, review and update SOP’s at the direction of Management. • Review and check analytical data generated by third party labs. Show less