Vaibhav Chavan

About Vaibhav Chavan

Regulatory Affairs professional with hands-on experience across CMC documentation, lifecycle submissions, and regulatory data processes in leading global organizations—AstraZeneca and GSK. I hold an M.Pharm from Dr. D.Y. Patil, Pune and secured GPAT AIR 240.At GSK, I supported global CMC content delivery, working on renewals, tenders and HAQs while managing end-to-end Module 2 and 3 documentation. My role involved authoring, compiling, formatting and preparing submission-ready CMC content in Veeva Vault, coordinating with global CMC, RA and Quality teams, and ensuring strict alignment with CTD/ICH requirements.Currently at AstraZeneca, I contribute to Regulatory Information Management (RIMS) activities—supporting regulatory data maintenance, documentation workflows and compliance using Veeva Vault and enterprise quality systems. I’m building expertise across regulatory data integrity, structured documentation, and cross-functional regulatory processes.Skilled in Veeva Vault, CMC documentation, Quality documentation, SharePoint, Power BI, MS Office, and collaborative regulatory operations. Passionate about precision, regulatory compliance, and supporting high-quality, timely deliverables across global markets.

Experience

1. Apprenticeship

   GSK

   Aug 2024 — Present · Bengaluru, IN

Education

• DR. D. Y. Patil Vidyapeeth (DPU)

  Masters of pharmacy

• K.K. Wagh College of Pharmacy Nashik

  B. pharm