Summary
Overview
Work History
Education
Skills
Declaration
Instruments Handled
Software Handled
Timeline
Generic
Nischal Pandey

Nischal Pandey

Executive -Corporate Quality Assurance
Ghaziabad

Summary

As a dedicated professional with a strong foundation in pharmaceutical chemistry and extensive experience in quality control and regulatory compliance, I aim to leverage my skills and knowledge to contribute to organizational success. I am committed to upholding the highest standards of quality and compliance in all aspects of laboratory operations.

Overview

7
7
years of professional experience
1
1
Language

Work History

Executive – Corporate Quality Assurance

Dabur India Ltd.
01.2025 - Current
  • Ensured laboratory compliance with regulatory requirements and internal quality standards.
  • Prepared and implemented Standard Operating Procedures (SOPs) to standardize and improve laboratory processes.
  • Conducted thorough reviews of analytical and chromatographic data to ensure accuracy, completeness, and compliance.
  • Oversaw the release of Raw Materials (RMs) in SAP, ensuring timely and accurate documentation.
  • Reviewed and approved shelf-life (SL) extensions for Raw Materials across multiple units, maintaining quality and compliance.
  • Designed and executed training programs to enhance analysts’ technical skills and Regulatory awareness.
  • Successfully led Competitor Intelligence review of Dabur products against key competitor to benchmark internal quality standards.

Quality Research and Development Officer

Reckitt India Pvt Ltd
10.2021 - 01.2025
  • Perform internal calibration and maintenance of laboratory instruments, including analytical balances, HPLC, pH meters, and UV-Vis spectrophotometers.
  • Uphold Good Laboratory Practices (GLP) and Good Documentation Practices (GDP) to ensure adherence to regulatory standards.
  • Examine raw materials and finished goods, emphasizing active content assays in products including Dettol liquid handwash, Dettol bar soaps, and Lizol disinfectant liquid.
  • Conducted analytical reviews of data to identify trends and insights. Reviewed audit trails for compliance and accuracy. Performed comprehensive data analysis to enhance decision-making processes. Analyzed audit trails to ensure integrity and traceability of information.
  • Executed IQ, OQ, PQ for analytical instrument installation
  • Administer method transfers for diverse products and collaborate closely with Research & Development (R&D) teams to ensure successful implementation.
  • Develop Standard Operating Procedures (SOPs) and perform stability studies for consumer products.
  • Recorded quality incidents, deviations, and out-of-specifications (OOS), ensuring prompt investigation, resolution, and closure following regulatory and internal timelines.
  • Oversee quality assurance and regulatory compliance of consumer goods, with emphasis on laboratory operations and product analysis.
  • Primary Responsibilities

Research Associate - Analytical API

Mankind Research Centre
03.2020 - 10.2021
  • Engineered and confirmed analytical methods for diverse APIs, intermediates, and key starting materials utilizing techniques such as HPLC, UHPLC, potentiometric titration, Polarimeter, UV-Vis spectrophotometer.
  • Applied spectroscopic methods (UV-Vis, FTIR) to identify and characterize new molecules.
  • Evaluated reactions for diverse APIs including Sugammadex sodium, Ticagrelor, Lasmiditan, Liftegrast, Rosuvastatin calcium, obeticholic acid, and ursodeoxycholic acid utilizing high pressure liquid chromatography
  • Executed analytical method development and validation for diverse Active Pharmaceutical Ingredients (APIs).
  • Core Responsibilities

Officer in Process Validation

Akums Drugs and Pharmaceuticals Ltd
09.2018 - 02.2020
  • Executed process validation for tablets and capsules, incorporating hold time studies utilizing various analytical tests (HPLC, dissolution).
  • Conducted validation of various manufacturing stages and executed analytical assessments utilizing analytical methods.
  • Conducted process validation for solid dosage forms, ensuring adherence to industry and regulatory standards.
  • Primary Duties

Education

Master of Science - Pharmaceutical Chemistry

H.N.B. Garhwal University
01.2018

Bachelor of Science - Physics, Chemistry, Mathematics

H.N.B. Garhwal University
01.2016

Intermediate - Science Stream

Central Board of Secondary Education
01.2012

High School - undefined

Central Board of Secondary Education
01.2010

Skills

MS Office Suite: Completed a 3-month course, acquiring proficiency in Word, Excel, and PowerPoint for data analysis and presentations

Declaration

I hereby declare that the information provided above is true and correct to the best of my knowledge and belief.

Instruments Handled

  • UV-Vis Spectrophotometers: Shimadzu (1800, 1900) and Perkin Elmer Lambda 350.
  • FTIR: Perkin Elmer.
  • HPLC: Waters Alliance e2695(PDA and UV detector) and Agilent Infinity 1260, Agilent 1260 II
  • Karl Fischer Auto Titrator: Mettler Toledo T50.
  • Dissolution Test Apparatus: USP-1 and USP-2.
  • Additional Instruments: Polarimeter, melting point apparatus, friability test apparatus, Refractometer, Ph meter, viscometer.

Software Handled

SAP, Quality One, Master workflow Tool, Technical Documentation System, chromeleon 7.3.1, Open Lab, Empower 3

Timeline

Executive – Corporate Quality Assurance

Dabur India Ltd.
01.2025 - Current

Quality Research and Development Officer

Reckitt India Pvt Ltd
10.2021 - 01.2025

Research Associate - Analytical API

Mankind Research Centre
03.2020 - 10.2021

Officer in Process Validation

Akums Drugs and Pharmaceuticals Ltd
09.2018 - 02.2020

Master of Science - Pharmaceutical Chemistry

H.N.B. Garhwal University

Bachelor of Science - Physics, Chemistry, Mathematics

H.N.B. Garhwal University

Intermediate - Science Stream

Central Board of Secondary Education

High School - undefined

Central Board of Secondary Education
Nischal PandeyExecutive -Corporate Quality Assurance