Regulatory Leader- Multiple Projects - Antwerp
A clinical-stage biopharmaceutical company is looking for a Regulatory Affairs Leader who will support the company with regulatory submissions for several projects. The company develops own products and develops products in partnership with more established pharmaceutical companies. The projects are in different stages of development so you will have a lot of variety and gain more experience in Regulatory, get all-round knowledge for the whole life-cycle.
- 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,…
- Team Leader skills
- 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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