Swissmedic Regulatory Affairs Expert

Description

Swissmedic Regulatory Affairs Manager - Zug

Our client, a leading pharmaceutical company based in Zug is currently searching Regulatory Affairs Manager to assist them with submission new products in Switzerland.

Requirements

• A degree in the life sciences
• Performing all regulatory activities related to national licences
• Previous experience acting as point of contact to Swissmedic.
• Experience in development of medicinal products (NPD)
• German fluent
• Ability to communicate effectively in German and English both verbally and in writing
• Relevant working/residency permit or Swiss/EU-Citizenship required

I am a specialized recruiter, currently taking care of various projects within the Regulatory Affairs field in Switzerland. If this role is of interest to you or to someone from your network, please send your CV in Word including your hourly rate expectations for immediate consideration.

You can reach me on or at (a.xenitidis'at'realstaffing.com)

Keywords: Regulatory Affairs, German, English, Switzerland, NPD, submissions, Swissmedi