Full-time

API Regulatory Compliance Lead

Posted by Intas Pharmaceuticals β€’ Odhav, Gujarat, India

πŸ“ Odhav, Gujarat πŸ•’ June 19, 2026

About the Role

We’re hiring API - Regulatory Affairs professionals!

Join us to drive global DMF submissions, regulatory compliance, and strategic market access.


πŸ“ Apply now and grow with a high-impact team. We are seeking a dynamic and detail-oriented professional to manage end-to-end regulatory submissions and lifecycle activities for API dossiers across global markets. The role plays a critical part in ensuring timely approvals, regulatory compliance, and seamless coordination across functions.


Regulatory Submissions & DMF Management :

  • Prepare, review, and submit Drug Master Files (DMFs) in compliance with global regulatory requirements and Manage full DMF lifecycle including amendments, annual updates, and variations
  • Ensure timely submission of regulatory dossiers and responses to health authorities
  • Maintain accurate tracking and documentation of DMFs, LOAs...

Ready to Apply?

Submit your application today and take the next step in your career journey with Intas Pharmaceuticals.

Apply Now