Sun Pharma is the fourth largest specialty generic pharmaceutical company in the world. We provide high-quality, affordable medicines trusted by healthcare professionals and patients in over 150 countries. It is also India’s largest, most trusted and most valuable pharmaceutical company by market capitalization. To keep pace with our growth plan we require young and energetic professionals for our Multiple Locations.
Job description:
1) Review all data and documents related to product registrations for various health authorities ( NON oral is preferable)
2) Compile registration dossiers for submission to various health authorities like US, Canada, Europe, Australia
3) Prepare responses to deficiency letters received from various agencies.
4) Maintain life-cycle / post approval changes for drug product registration dossiers.
5) Provide regulatory support to cross functional departments.
6) Prepare and submit scientific advice to various health authorities.
7) eCTD compilation, verification and submission through electronic gateway
Venue of Interview : Sun Pharmaceutical Inds Ltd, Near Akshar Chowk, Sun Pharma Road, Tandalja – Baroda 390012
Candidates who are unable to attend the interview may send their cvs at : Hr.tandalja@sunpharma.com
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