A leading pharmaceutical company in Switzerland seeks a regulatory affairs professional to support CMC activities for Biologics and Chemicals. The role requires a Master's or Ph.D. in a relevant field and at least 5 years in the pharmaceutical industry. Responsibilities include authoring registration documents, assisting in submissions, and CMC regulatory support throughout development. The company offers a dynamic work environment, flexible hours, and numerous benefits including vacation and travel insurance. #J-18808-Ljbffr