International Regulatory Affairs Specialist - Medical Device

29.11.2019 | Employee | 100%

Participate in the registration activities at a global level

International Regulatory Affairs Specialist - Medical Device

International medical device company

Missions

  • Prepare and coordinate various activities to make applications for product licenses
  • Provide an effective follow-up during the registration process to ensure the completion of the product registration
  • Global scope of responsibilities (EU/USA/Rest of the World)

Profil du candidat

  • At least 3 years of experience in a similar role
  • Good command of French and English

Conditions et Avantages

Participate in the registration activities at a global level

29.11.2019
Employee, 100%

Contact

Michael Page Switzerland

Quai de la Poste 12 1204 Geneva

1204 Nyon

Michael Page

Quai de la Poste 12Genève

Industry

Human resources / Personnel services

Michael Page

Quai de la Poste 12Genève

Industry

Human resources / Personnel services
Salary

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