Senior Executive - Regulatory Affairs

SUN PHARMA


Date: 1 week ago
City: Vadodara, Gujarat
Contract type: Full time
  • Review all data and documents related to product registrations for various health authorities
  • Compile registration dossiers for submission to various health authorities like – US, Canada, Europe, Australia & China
  • 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

Experience of Non-Orals is preferable.

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