Experience

Sterling Pharma Solutions

• United Kingdom
• Pharmaceutical Manufacturing
• 500 - 600 Employee

• Analytical Scientist

  • Jul 2022 - Present

  Developing HPLC and GC methods to support non-GMP and GMP projects. Authoring the methods development reports, testing methods, qualification protocols and validation reports. Executing the validation protocols. Analyzing, interpreting data, integrating experimental data with project objectives. Supporting the GMP manufacturing activities. Developing HPLC and GC methods to support non-GMP and GMP projects. Authoring the methods development reports, testing methods, qualification protocols and validation reports. Executing the validation protocols. Analyzing, interpreting data, integrating experimental data with project objectives. Supporting the GMP manufacturing activities.



Advanced Laboratories Inc

• United States
• Consumer Services
• 1 - 100 Employee

• Sr Analytical Chemist

  • Dec 2021 - Jul 2022

  Responsibilities involves analytical approaches for nutraceuticals. Conduct analytical method development and method validation for free amino acid, fat soluble vitamins using UHPLC, HPLC and LC-MS. Coordinate and manage ordering of chemicals, laboratory supplies, and lab equipment. Coordinate and manage disposal of waste. Writing STP, work instruction, and validation protocols. Responsibilities involves analytical approaches for nutraceuticals. Conduct analytical method development and method validation for free amino acid, fat soluble vitamins using UHPLC, HPLC and LC-MS. Coordinate and manage ordering of chemicals, laboratory supplies, and lab equipment. Coordinate and manage disposal of waste. Writing STP, work instruction, and validation protocols.



Young Living Essential Oils

• United States
• Wellness and Fitness Services
• 700 & Above Employee

• Research Scientist II

  • Dec 2019 - Nov 2021

  Responsible in performing Method development, Method validation and Method transfer for Nutritional products using HPLC and UPLC. Finalize STP (Standard Test Procedure), Validation Protocol, and Transfer Protocol through HQMS. Review and upload results in LIMS. Method development for adulteration in essential oils by GCMSMS and LCMSMS using Mass Hunter software. Responsible in performing Method development, Method validation and Method transfer for Nutritional products using HPLC and UPLC. Finalize STP (Standard Test Procedure), Validation Protocol, and Transfer Protocol through HQMS. Review and upload results in LIMS. Method development for adulteration in essential oils by GCMSMS and LCMSMS using Mass Hunter software.



iVeena Delivery Systems

• Salt Lake City, Utah

• Research Analyst

  • Jul 2019 - Dec 2019



Moran Eye Center, University of Utah

• Salt Lake City, Utah

• Research Scientist

  • Sep 2013 - Jun 2019

  Expertise in molecular biology techniques (RNA and DNA purification, PCR, Western Blotting, ELISA, Immuno-precipitation, Immuno-staining, RNA In-situ Hybridization), Bio-molecule conjugation and developing formulation for Ocular drug delivery and developing biomarker for Alzheimer. Lead projects are Keratoconus , Neurotrophic keratopathy, and Angiogenesis. Expertise in molecular biology techniques (RNA and DNA purification, PCR, Western Blotting, ELISA, Immuno-precipitation, Immuno-staining, RNA In-situ Hybridization), Bio-molecule conjugation and developing formulation for Ocular drug delivery and developing biomarker for Alzheimer. Lead projects are Keratoconus , Neurotrophic keratopathy, and Angiogenesis.



Dr. Reddy’s Labs

• Hyderabad Area, India

• Asst. Manager

  • Nov 2010 - Sep 2013

  • Analytical Method development and Validation for Related substance and Assay for drug Products. Analytical Method Development for Cleaning Method for multiple compounds. Routine analysis of Drug Substance and Drug Products. Planning of project on priority basis. Reviewing of Validation and Routine analysis of Drug Products documents. Maintaining Calibration Status for all Laboratory Equipments and review of Calibration Documents (HPLC, GC, Dissolution Apparatus, UV-VIS, Karl-Fisher titrator, auto titrator, and pH meter. Show less



Apotex research Pvt Ltd

• Bangalore, Karnataka India

• Research Scientist-I

  • Apr 2009 - Nov 2010

  Analysis of Exhibit batches as per Stability Protocol. Calibration of HPLC, Dissolution Apparatus and Daily Calibration of Analytical Balance by Lims software. Analysis of Exhibit batches as per Stability Protocol. Calibration of HPLC, Dissolution Apparatus and Daily Calibration of Analytical Balance by Lims software.



Torrent Research Center

• Ahmedabad, Gujarat India

• Scientist II

  • Sep 2006 - Apr 2009

  Analytical Method Development for Drug Substances, Intermediates of Drug Substances and Drug Products of Discovery molecules for Assay, for Related Substance and for Contents of special impurities. Stability studies’ of Drug Substances, Intermediates of Drug Substances and Drug Products of Discovery molecules for Development and Clinical trial batches according to ICH and other Regulatory Guidelines. Preparation, Standardization and Maintenance of Volumetric solutions and Chemical Reagents. Calibrations of analytical instruments like UV-VIS, HPLC, Karl-Fisher titrator, auto titrator, pH meter, etc. Show less