Summary
Overview
Work History
Education
Skills
Languages
Disclaimer
Personal Information
Seminarsanddevelopmentprograms
Timeline
Generic

MANDA VEERA VENKATA SAI GANGADHARA REDDY

Hyderabad

Summary

Energetic and focused individual, passionate about research and blending laboratory experience with theoretical and practical training to offer solid skills in analytical chemistry, and pharmaceutical research & development. Laboratory-trained scientist offering several years promoting exceptional skills in research and analysis.

Overview

12
12
years of professional experience

Work History

Analytical Scientist III

Aurobindo Pharma Limited Research Centre
Hyderabad
03.2013 - Current
  • Develop and validate stability indicating analytical methods for Dissolution, Assay (stability indicating) and Related Substances for finished products of solid oral dosage forms by HPLC and UPLC as per ICH and USP guidelines
  • Successfully completed DIRECT analytical method transfers in the receiving laboratories (API) and finished products as per FDA regulations and ICH guidelines
  • Provide technical instructions to colleagues on analytical method development by HPLC and UPLC
  • Create/revise documents such as protocols, reports and specifications to support activities in the QC lab
  • Writing and reviewing the protocols, reports and analytical test methods
  • Study of in vitro dissolution profiles in different media of both development samples and innovator sample
  • Support pharmaceutical development and pre-formulation studies with reverse engineering, chromatographic methods, trouble shooting on analytical methods
  • Daily calibration of instruments
  • Review the documents like validation reports, development reports, training analysis documents etc
  • Author/Co-author development reports, protocols, reports and SOPs with senior scientists
  • Carried out stability and bioequivalence study at each stage of formulations development
  • Developed methods and performed routine analysis of stability samples for dissolution and Assay by HPLC
  • Developed analytical methods for Dissolution, Assay (stability indicating) on finished products of solid and semi-solid dosage forms by HPLC
  • Performed validation for Dissolution and Assay by HPLC
  • Regular analysis and online documentation by laboratory notebook
  • Performed stability analysis and compilation of stability data
  • Performed calibration and of analytical equipment's like HPLC coupled with UV-Vis or diode array, dissolution tester, pH meter and Analytical balances
  • Developed and implemented analytical methods to assess product quality.
  • Reviewed laboratory records for accuracy and completeness of data.
  • Conducted research on new analytical techniques to improve testing accuracy and efficiency.
  • Maintained detailed lab notebooks that documented all methods and results obtained from experiments.
  • Interpreted experimental data and communicated results effectively to management team.
  • Developed test plans for validation studies of new analytical methods or existing method modifications.
  • Assisted in troubleshooting various instruments used in the lab when necessary.
  • Provided technical support to other departments regarding analytical procedures or issues related to product quality control.
  • Collaborated with cross-functional teams to develop strategies for improving process efficiency and cost effectiveness.
  • Ensured compliance with Good Laboratory Practices regulations while conducting experiments.
  • Trained junior analysts on proper use of equipment and techniques employed in the lab environment.
  • Optimized existing methods through modification of parameters such as flow rate, temperature, pressure, resulting in improved performance.
  • Documented any changes made to protocols according to established change control procedures.
  • Maintained field equipment and performed troubleshooting techniques to keep tools fully operational.
  • Documented all processes during experiments, keeping meticulous notes of unexpected changes.

Education

M. Pharmacy -

Roland Institute of Pharmaceutical Sciences
Berhampur, Orissa
08.2012

B. Pharmacy -

Roland Institute of Pharmaceutical Sciences
Berhampur, Orissa
06.2010

Intermediate -

SKVS Junior College
Vijayawada, Andhra Pradesh
03.2005

S.S.C -

Bharatiya Vidya Bhavans Residential School
Tadepalligudem, Andhra Pradesh
03.2003

Skills

  • HPLC
  • UPLC
  • Dissolution apparatus
  • UV-Visible Spectrophotometer
  • Fourier Transform Infrared Spectrophotometer
  • Karl-Fischer Titration
  • Waters Empower 3
  • LC Solution

Languages

  • Telugu
  • Hindi
  • Oriya
  • English

Disclaimer

I hereby declare that the information given in this resume is correct to the best of my knowledge.

Personal Information

  • Date of Birth: 09/03/88
  • Marital Status: Married

Seminarsanddevelopmentprograms

  • National Seminar on New Vision in Pharmaceutical Sciences 2009, ASN Pharmacy College, Tenali
  • 62nd Indian Pharmaceutical congress-2010, Manipal University
  • International Conference on Biotechnology in Pharma & Food Industries, Gitam Institute of Pharmacy, Gitam University, Visakapanam-2011

Timeline

Analytical Scientist III

Aurobindo Pharma Limited Research Centre
03.2013 - Current

M. Pharmacy -

Roland Institute of Pharmaceutical Sciences

B. Pharmacy -

Roland Institute of Pharmaceutical Sciences

Intermediate -

SKVS Junior College

S.S.C -

Bharatiya Vidya Bhavans Residential School
MANDA VEERA VENKATA SAI GANGADHARA REDDY