Imane Alili

Imane Alili is a regulatory affairs professional with extensive experience in the pharmaceutical industry, having held positions at prominent companies such as Hikma Pharmaceuticals and Pfizer. At Hikma Pharmaceuticals as a Regulatory Affairs Sr. Associate, responsibilities included preparing and compiling eCTD pharmaceutical product dossiers, post-marketing monitoring, and liaising with regulatory authorities. Imane's tenure at Pfizer involved global regulatory operations, focusing on artwork implementation and regulatory compliance for locally manufactured products. Previous roles include a Jr. regulatory affairs consultant at HEALTH CARE SOLUTION, and an Analyst in Product Quality Vigilance at Capgemini Engineering, where product quality complaints were managed according to regulatory guidelines. Imane's educational background includes a Master of Research in Biology & Health and a Bachelor's degree in Life Sciences, with a strong foundation in biochemical and toxicological research.