Senior Regulatory Affairs Specialist, EU/RoW (RareDisease)

Travere Therapeutics in Switzerland is seeking a Senior Specialist, Regulatory Affairs (EU/RoW) to support regulatory leads with submissions, strategy, and interactions with authorities to advance orphan/rare disease programs. The role involves regional regulatory operations, SOP development, and driving regulatory projects with oversight.The ideal candidate has a biology-related degree, 4+ years of regulatory experience, and strong ability to navigate ICH/EU guidelines, prepare CTAs/MAAs, and #J-18808-Ljbffr