Global Regulatory Affairs Specialist

2 weeks ago


Fatih, Istanbul, Turkey dsm-firmenich Full time
Key Responsibilities
  • Develop and manage pharma and food submissions in certain regions or countries, focusing on Russia re-registration activities.
  • Coordinate submission of dossiers to regional authorities and follow up on approval processes.
  • Document and archive submissions and registration statuses in regulatory platforms and applications.
  • Support regulatory teams in answering customer and/or health authority requests related to product submissions.
  • Assist in creating and maintaining global standard product documents.


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