Regulatory Affairs Specialist

Vor 7 Tagen


Genf, Genf, Schweiz Michael Page Vollzeit

Job Summary

We are seeking a highly skilled Regulatory Affairs Specialist to lead our product registrations management for Asia. As a key member of our team, you will be responsible for managing the maintenance of licenses, reviewing promotional materials for compliance with local regulations, and managing Regulatory Intelligence.

About the Role

This is an exciting opportunity to join a fast-growing medical devices multinational as we enter a new development phase. You will work autonomously and take initiative to drive our product registrations strategy in Asia.

Key Responsibilities

  • Manage the maintenance of licenses for our medical devices in Asia
  • Review promotional materials for compliance with local regulations
  • Manage Regulatory Intelligence to stay up-to-date on changing regulations
  • Collaborate with cross-functional teams to ensure regulatory compliance

Requirements

  • At least 3 years of successful experience in regulatory affairs, preferably in the medical devices sector
  • Business contacts with Asia and a flexible personality
  • Excellent English language skills and good French command

What We Offer

Join Michael Page, a leading recruitment agency, and take advantage of our attractive and fast-paced work environment, as well as good benefits.



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