Regulatory Affairs Specialist

Vor 5 Tagen


Geneva, Schweiz Michael Page Vollzeit

You lead with autonomy and initiative the product registrations management for Asia.

Manage the maintenance of licenses.

Review of promotional materials according local regulations.

Manage Regulatory Intelligence.


You have at least 3 years of successful experience in regulatory affairs, ideally in the medical devices sector (pharma might be considered).

You have already had business contacts with Asia.

You have a flexible personality and you enjoy working in an environment where you are given responsibility.

English a must and good French command.



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