Senior Regulatory Affairs Specialist — Rare Disease

Travere Therapeutics in Switzerland is hiring a Senior Specialist, Regulatory Affairs (EU/RoW) to support the preparation, submission and maintenance of regulatory applications, including CTA submissions and post-authorization activities.You will work with regulatory leads, coordinate with external contractors, maintain document management systems such as Veeva Vault, and help implement process improvements across Regulatory Affairs. #J-18808-Ljbffr