Sr Exe

SUN PHARMA


Date: 18 hours ago
City: Vadodara, Gujarat
Contract type: Full time
  • Compilation , review of dossier for US , EU , AU, Canada & IL market for both solid oral and non-oral dosage form
  • Review of query response prepared and compiled by regulatory associates
  • Manage all the activities pertaining to dossier submission for aforesaid markets .
  • Meet the dossier submission and query response timeline as per given target
  • Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management
  • Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
  • Lifecycle management for US , EU , Canada & IL market
  • Single point contacts for all the regulatory submission activities for IL and Palestine markets
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