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Regulatory Affairs Manager

vor 2 Monaten


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 for a seasoned regulatory affairs professional to join our team at Michael Page. As a Regulatory Affairs Specialist, you will have the autonomy to work independently and take initiative to drive results. Your expertise will be essential in ensuring compliance with regulatory requirements and maintaining strong relationships with business contacts in Asia.

Key Responsibilities

  • Manage the maintenance of licenses and ensure compliance with regulatory requirements
  • Review promotional materials for compliance with local regulations
  • Manage Regulatory Intelligence to stay up-to-date on regulatory changes and trends
  • Develop and implement strategies to improve regulatory compliance and efficiency

Requirements

To be successful in this role, you will need to have at least 3 years of experience in regulatory affairs, preferably in the medical devices sector (pharma may be considered). You will also need to have a strong understanding of regulatory requirements in Asia and excellent communication skills. English is a must, and good French command is also required.