A leading medical device company in Switzerland is seeking a Senior Regulatory Affairs Specialist to provide advanced regulatory support for New Product Development and sustaining operations. The ideal candidate will have significant experience in managing regulatory submissions and compliance with EU and global regulations. Responsibilities include leading regulatory efforts, mentoring junior staff, and collaborating with cross-functional teams to ensure adherence to regulatory standards. This role offers an opportunity to contribute to successful product launches and ongoing operations. #J-18808-Ljbffr