Regulatory Affairs Professional

2 days ago


Fatih, Istanbul, Turkey GSK Full time
Job Description

GSK is seeking a highly motivated Regulatory Affairs Trainee to support the Regulatory Department in various activities.

About the Role

This role involves updating regulatory correspondence files, trackers, and submission archives. You will be responsible for keeping regulatory databases up-to-date, including Veeva updates and MoH submissions. Additionally, you will assist in the maintenance of global and local regulatory databases, ensuring efficient regulatory archive management.

Responsibilities

  • Update regulatory correspondence files, trackers, and submission archives.
  • Keep regulatory databases up-to-date, including Veeva updates and MoH submissions.
  • Assist in the maintenance of global and local regulatory databases.
  • Ensure efficient regulatory archive management.

About You

We are looking for a professional with a strong foundation in pharmacy or life sciences, excellent communication skills, and a good command of English. As a team player, you should be eager to learn through experience and able to work at least 3 days a week for a minimum of 6 months.

Required Skills and Qualifications

  • Min. 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.

What We Offer

GSK offers a dynamic and supportive work environment, where you can grow professionally and personally. If you are a motivated individual looking to start your career in Regulatory Affairs, we encourage you to apply for this exciting opportunity.



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