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Teva Regulatory Affairs Associate 
India, Karnataka, Bengaluru 
983586233

26.05.2024

שיתוף

התחבר/י כדי להגיש מועמדות
How you’ll spend your day
  • Assessment of change controls for registration impact and implementation of all necessary dossier changes in; Europe and International Market
  • Responsible for compilation of the variations for the products in the product portfolio in collaboration with other stakeholders
  • Compiling variation packages
  • Experienced in managing, regulatory database and Trackwise.
Your experience and qualifications

Academic degree- and thinking level with a chemical/pharmaceutical background.

Experience:

  • 2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market
  • Knowledge on registration procedures and pharmaceutical regulations
  • Interest and capability to work with different software, including Document Management System
  • Accurate, able to prioritize and work according to agreed timelines.
  • Working independently with a moderate level of guidance and direction.
  • Solve complex problems using existing solutions andsupport.
  • Identify & implement process improvements.
  • Team player
Reports To

Sr Manager – CMC Regulatory Affairs

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