CMC Program Lead - Illuccix and Gozellix

Role: CMC Program Lead for radiopharmaceutical assets (Illuccix and Gozellix), responsible for developing and executing CMC strategies to ensure market readiness, regulatory submissions, and lifecycle management. Responsibilities: plan and deliver CMC activities across API, Fill/Finish, and Packaging; coordinate internal teams and external CDMOs/CMOs; manage project timelines, budgets, and risks; lead vendor selection; facilitate cross-functional collaboration; track deliverables; and manage change controls for product launches and process improvements. Requirements: BA/BS in Science, Engineering, or related field; 8+ years in radiopharmaceutical/pharmaceutical CMC with program management experience; strong technical knowledge of radiopharmaceutical manufacturing and regulatory requirements; experience working with cross-functional teams and external partners; proficiency in project management tools (e.g., MS Office, SAP, MS Project). Preferred: experience in late-stage clinical programs, global regulatory submissions, and working in fast-paced, matrix environments. High-Value: radiopharmaceuticals, oncology, late clinical-stage development, regulatory submission readiness, global collaboration, and managing complex CMC projects. WorkSetup: hybrid with 10-20% travel.