Regulatory Affairs Sr Manager - English - Antwerp
A biotech company is looking for a Regulatory Affairs Leader who will support the company with regulatory submissions from the development stage till post-marketing. Here you only need fluency in English so this is the time to shine in a senior role in Belgium, make the most out of your expertise and put their first product on the global market.
- From 8 years of experience in a broad range of regulatory affairs projects in the pharmaceutical/biotech industry
- Good knowledge of international regulatory affairs guidelines (FDA, EMA,…)
- Hands on regulatory experience: IMPD, IND, CMC,…
- Manage multiple projects at the same time
- Fluency in English required, any other language is an advantage
The company works with new techniques which require negotiating with authorities worldwide. This is the best time to join because you will be involved from early in the process and be able to use and expand your global network. The company is specialized in antibodies to put innovative medicines on the market that treat under targeted diseases. In that way you are at the forefront of innovation what makes your role even more interesting.
If this job appeals to you please send me, Annelies De Baere, your most recent CV in Word format to email@example.com or call me on +32 2 403 49 80.
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