Regulatory Affairs Specialist

Geneva Permanent View Job Description
You lead with autonomy and initiative the product registrations management for Asia.

Added 11/09/2024

  • Join a leading and fast growing medical devices multinational
  • The group has an entrepreneurial mindset and offers extended responsibilities

About Our Client

Established and fast growing medical devices multinational, the group has established itself as a key market player and is stepping into a new development phase.

Job Description

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.

The Successful Applicant

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.

What's on Offer

attractive and fast paced environment and good benefits.

Contact
Denis Daniliuc
Quote job ref
JN-092024-6532350

Job summary

Job Function
Healthcare & Life Sciences
Specialisation
Medical Affairs
Industry
Healthcare / Pharmaceutical
Location
Geneva
Contract Type
Permanent
Consultant name
Denis Daniliuc
Job Reference
JN-092024-6532350

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