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Regulatory Affairs Specialist

vor 2 Monaten

Genf, Genf, Schweiz Michael Page Vollzeit
Product Registration Management for Asia

You will lead the product registrations management for Asia with autonomy and initiative, ensuring compliance with local regulations.

Key Responsibilities:

  • Manage the maintenance of licenses
  • Review promotional materials for compliance with local regulations
  • Manage Regulatory Intelligence

Requirements:

  • At least 3 years of successful experience in regulatory affairs, preferably in the medical devices sector (pharma may be considered)
  • Business contacts with Asia
  • Flexible personality and ability to work in an environment with given responsibility
  • English is a must, and good French command is required