Travere Therapeutics is seeking a Director, Quality Assurance - Technical to provide expert QA and regulatory oversight for GMP CSPs, spanning Drug Substance and Drug Product activities toward Phase 3 and commercialization.
The role requires leading validation, change control, deviations, OOS/OOT, risk management, and supplier qualification while ensuring compliance with CFR/ICH and global guidelines; travel up to 25% domestically and internationally; on-site in San Diego is required.
#J-18808-Ljbffr