Analyst Regulatory Affairs - 1 year contract

Entreprise :

Our client is a multinational specialised in the diagnostic industry.

Description du poste :

* Complete product registration projects including but not limited to new product registrations, renewals, notifications, listings and various documentation requests
* Work closely with the manufacturers / legal manufacturer to assess the impact of product design (and other) changes on global registrations
* Stay up-to-date with, interpret and document new and evolving regulatory requirements as they apply in the countries of interest
* Place orders for Certificates of Free Sales from the relevant authorities as required to support product registration activities
* Update and maintain the Global Product Registration Database
* Support sales and marketing teams with regulatory documents

Description du profil :

* A Degree/Diploma in Regulatory Affairs, Sciences or Life Sciences
* A solid knowledge of (IVD) medical devices regulatory frameworks in Middle-East and Africa
* Experience within the highly regulated in vitro diagnostic and/or medical device market for a minimum of 5 years
* Excellent English (written and oral)
* Proven Excel, Word and computer skills
* Attention to detail, rigorous and ability to think critically and outside the box
* Ability to work autonomously and report effectively in an international environment