S Multani

S Multani has extensive experience in pharmacovigilance and quality assurance within the pharmaceutical industry. As Associate Director, GVP QA at Syndax Pharmaceuticals, S Multani applies expertise in quality management. Previous roles include Senior Manager positions in Pharmacovigilance QA at Incyte and Global Safety Submissions at BeiGene, along with managerial positions focused on Safety Records and Global Patient Safety Training and Compliance. Earlier experience at Teva Pharmaceuticals as a Senior Compliance Associate and at Shire as a PV Submissions Manager further contributed to a solid foundation in drug safety and compliance. S Multani holds a degree from Rutgers University.