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Title:Sr. Officer
Date: Nov 11, 2022
Location: Not Applicable
Company: Sun Pharmaceutical Industries Ltd

Job Description:

  • Review all data and documents related to product registrations for various health authorities.
  • Compile registration dossiers for submission to various health authorities like – US-FDA, Health Canada and Europe.
  • 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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Deadline: 12-07-2024

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