Full-time

Manager - 2

Posted by SUN PHARMA • Tandalja, Gujarat, India

📍 Tandalja, Gujarat 🕒 March 01, 2026

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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  

Job Details

Location Tandalja, Gujarat
Job Type Full-time
Category Other-General
Posted March 01, 2026
Deadline April 10, 2026

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