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Regulatory affairs expert - medicines

Lasne
beBee Careers
Publiée le 13 juin
Description de l'offre

Regulatory Affairs Expert - Medicines

This position is a crucial role within our organization. The Regulatory Affairs Manager occupies a key position and provides critical opinion on issues impacting our members.

The ideal candidate will have the following skills:

* Scientific university degree, ideally in pharmacy (Master)
* Previous experience in Regulatory Affairs (ideally min. 2-3 years, including OTC products)
* Existing network within the industry and with the authorities is a plus
* Fluent in Dutch, French and English (both written and spoken)
* Knowledge of Microsoft Office (Outlook, Word, PowerPoint, Excel)
* Team player, dynamic, autonomous, well-organized, diplomatic, flexible and proactive
* Strong commitment: clearly willing to achieve the agreed objectives
* Environment knowledge: understand how decisions are taken and how changes are approached within the pharmaceutical industry and regarding legislation
* Direct and indirect influence on the external environment to explain members the needs and expectations

About this role

This position involves advising on new policies and legislation, participating in RA meetings with authorities, organizing internal working groups, and participating in interesting trainings/seminars.

Requirements

We are looking for a flexible part-time or full-time employee (min. 60%). The ideal candidate will be able to work independently and as part of a team, and will have excellent communication and interpersonal skills.

What we offer

This role offers the opportunity to work in a dynamic and challenging environment, with a strong focus on regulatory affairs. We offer a competitive salary and benefits package, and opportunities for professional development and growth.

How to apply

If you are a motivated and experienced Regulatory Affairs professional, please submit your application, including your CV and cover letter, to us.

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