Regulatory Affairs Submission Junior Associate 12 month contract

An opportunity for a Regulatory Affairs Junior Associate has become available in Lausanne, Switzerland, to work with a global pharmaceutical company who is dedicated to improving the quality of life by delivering innovative medical solutions. My Client requires this professional to support the Regulatory Affairs Submissions team for 12-months minimum on a full time contract.

Responsibilities include:

• Coordinate the constitution and/or tracking of registration, variation or renewal dossiers
• Assure timely receipt and dispatch of administrative documents and their legalization (if applicable) necessary for registration, renewal and variation files (including but not limited to Certificate of Pharmaceutical Products, Free Sale Certificates, Letter of Authorization, GMPs, Price certificates)
• Support the team in terms of uploading documentation in our EDMS system, put in place tracker for Regulatory Affairs Database update

Suitable candidates will have:

• 1-2  years’ experience in regulatory affairs, ideally in a global organisation for international countries such as Middle East, CIS or Latin America
• Experience in the pharmaceutical industry and use of Electronic Document
• Management System - Regulatory Affairs Database
• BSc in Scientific or equivalent experience
• Fluent in English; French and/or Spanish is a plus

I specialise in recruiting Regulatory Affairs professionals throughout Europe, if you would like to speak to me regarding one of my current vacancies, or simply be made aware of opportunities as they arise then please call me today on +44 (0)1293 77 66 44 for a confidential discussion.

Alternatively e-mail me on JASmith@barringtonjames.com.  

I look forward to hearing from you soon!

Jasmine Smith

Contract Consultant ~ Regulatory Affairs

+ 44 (0)1293 77 66 44