Regulatory Documentation Expert

2 days ago


Fatih, Istanbul, Turkey GlaxoSmithKline Full time
How You Will Contribute

As a Regulatory Affairs Trainee, you will play a critical role in supporting our Regulatory Department.

About Your Role:

  • You will assist in dossier preparations, follow-up activities, and system updates.
  • Updating regulatory databases, files, and correspondence will be an essential part of your responsibilities.
  • You will also assist in preparing regulatory documents and supporting the Regulatory team with MM report preparations.

Responsibilities:

  • Update regulatory databases and files regularly.
  • Assist in preparing regulatory documents.
  • Support the Regulatory team with MM report preparations.
  • Circulate incoming HA letters via the MoHDT system.

Requirements:

  • Minimum 3rd year student in pharmacy or life sciences.
  • Proficiency in computer skills.
  • Good command of English.
  • Strong communication skills.
  • Prone to teamwork.
  • Eager to learn through experience.
  • Able to work at least 3 days/week for min. 6 months.


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