BeNeLux Regulatory
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Kintiga is seeking an experienced Regulatory Affairs professional to oversee BeNeLux regulatory activities, pharmacovigilance, and medical affairs contributions across Europe. The role emphasizes a strong scientific background, multi-language fluency, and ability to manage multiple priorities in a complex environment.
You will work in a hybrid setup with one day per week in Ghent, collaborating with cross-functional teams and influencing stakeholders to shape the value story of healthcare