Full-time

Manager - 2

Posted by SUN PHARMA • Tandalja, Gujarat, India

📍 Tandalja, Gujarat 🕒 March 01, 2026

About the Role

Executive and Sr. Executive

  • Review all data and documents related to product registrations for various health authorities.
  • Compile registration dossiers for submission to various health authorities like – China , Canada, Europe, Australia/New Zealand, Japan and Israel.
  • Prepare responses to deficiency letters received from various agencies.
  • Maintain life-cycle / post approval changes for drug product registration dossiers.
  • Provide regulatory support to cross functional departments.
  • Prepare and submit scientific advice to various health authorities.
  • eCTD compilation, verification and submission through electronic gateway
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