A leading pharmaceutical company in Switzerland is seeking an experienced regulatory affairs professional to join its CMC team. You will support customer activities focusing on Chemistry Manufacturing and Controls for Biologics and Chemistry projects. Key responsibilities include authoring registration documents, conducting regulatory assessments, and collaborating with health authorities. The ideal candidate has at least 5 years of experience in the pharmaceutical industry and a Master's or Ph.D. in a relevant scientific field. Flexible working hours and numerous benefits offered. #J-18808-Ljbffr