Nadia Challouk has extensive experience in the pharmaceutical industry, beginning with an internship as a pharmacist at Zwitserse Apotheek in 2014. Following this, Nadia completed internships at UZA and the Institute of Tropical Medicine in Antwerp, focusing on pre-clinical validation and decontamination processes. Nadia's tenure at Pfizer started in February 2017 as a QA Release Engineer and Trainee Qualified Person, progressing to QP Product Specialist by November 2019 and later serving as a GMP Auditor and Project Engineer in Quality Assurance and Continuous Improvement. Additionally, Nadia gained experience in regulatory affairs at Mundipharma. Academically, Nadia holds a Master in de Geneesmiddelenontwikkeling from Universiteit Antwerpen and an Advanced Master in Industrial Pharmacy from the same institution.
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