Gobardhan Bal

About Gobardhan Bal

A dedicated and dynamic pharmaceutical professional with a proven ability to collaborate across discovery chemistry, drug substance, drug product, analytical sciences, pharmacokinetics, toxicokinetics, and material science team. Support project teams in identifying optimal drug candidates through comprehensive in-vitro, in-silico, and in-vivo evaluations. Conduct early-stage risk assessments and formulate biopharmaceutical strategies that optimize the relationship between an active ingredient\'s physicochemical properties, its drug product, and its in-vivo performance.Specialized in modeling and simulation (development and validation of PBPK/PBBM, IVIVC), utilizing tools like GastroPlus™ and PK-Sim™ to predict drug absorption and disposition. Design innovative in vitro experimental methods and bio-relevant dissolution studies to establish in vitro-in-vivo correlations.Experienced in evaluating complex generic drug products (oral and non-oral dosage forms, such as MDIs, DPIs, liposomal injections, and ophthalmic formulations), reverse engineering, and Q3 mapping using advanced analytical techniques for drug product characterization. Ensure bioequivalence and regulatory compliance while enabling cutting-edge technologies.Authored/co-authored many scientific publications in top-rated peer-reviewed journals. Demonstrated ability to deliver results within stipulated timelines, with excellent communication and presentation skills.

Experience

1. Senior Expert Science and Technology

   Novartis

   Apr 2025 — Present · Hyderabad, IN

Education

• Roland Institute of Pharmaceutical Sciences (RIPS), Berhampur

  Bachelor of Pharmacy - BPharm, Pharmacy

  2004 — 2008

• Anna University of Technology, Tiruchirappalli - Ariyalur Campus

  Master of Pharmacy, Pharmaceutical Analysis

  2008 — 2010

• Upendra Nath College, Soro, Balasore

  +2 Science

• Chettinad Academy of Research & Education, Kancheepuram

  Doctor of Philosophy - PhD, Pharmaceutical Sciences

  2020 — 2024

Skills

• Ndds
• Pharmaceutics
• Reverse Engineering
• Ich-Gcp
• Regulatory Requirements
• Biopharmaceutics
• Dissolution
• Hplc
• Protein Characterization
• Analytical Methods Development
• Analytical Chemistry
• Good Laboratory Practice (Glp)
• Technology Transfer
• Formulation
• Pharmaceutical Research
• Validation
• Technology
• Science
• Cleaning Validation
• Stability Studies
• Chromatography
• Anda
• Glp
• Regulatory Affairs
• Uv
• Research
• Pharmaceutical Industry
• Sop
• High-Performance Liquid Chromatography (Hplc)
• Gmp
• Uv/Vis
• Standard Operating Procedure (Sop)
• Analytical Method Validation