Claudio Schnyder

Associate Director - Submission Management at Novartis Pharma AG

Speaker

Based in Basel, Switzerland, I am a Regulatory Affairs Operations professional with more than 17 years of experience in the life sciences industry.

Since 2015, I have been working at Novartis Pharma AG, where I currently serve as Associate Director in Global Regulatory Operations, leading major global submissions in close collaboration with key stakeholders.

In addition, I lead and contribute to cross-functional initiatives, including the implementation of global e-submission technical standards, digital transformation pilots / concepts, process improvements, and training activities.

Prior to Novartis, I spent several years at Actelion Pharmaceuticals Ltd, where I held a range of roles within DRA Operations, complemented by earlier experience in Global Quality Management and Global Medical Science.