Regulatory Affairs Specialist

vor 4 Wochen


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

As a key member of our team, you will lead the product registrations management for Asia with autonomy and initiative. Your expertise in regulatory affairs will be instrumental in ensuring compliance with local regulations.

Key Responsibilities:

  • Manage the maintenance of licenses and ensure timely renewals
  • Review promotional materials for compliance with local regulations
  • Develop and implement Regulatory Intelligence strategies

Requirements:

  • At least 3 years of experience in regulatory affairs, preferably in the medical devices sector
  • Proven track record of successful product registrations in Asia
  • Excellent communication and interpersonal skills
  • Fluency in English and good command of French

What We Offer:

A dynamic and challenging role with opportunities for growth and development in a leading recruitment agency.



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