Production Operator I

Role: Production Operator I supporting RayzeBio’s radiopharmaceutical manufacturing, responsible for executing clinical and commercial-scale drug product production in compliance with cGMP and aseptic standards. Responsibilities include raw material prep, equipment setup, process validation, inventory management, and maintaining a sterile environment while supporting process improvements and safety protocols. Requirements: 1-4 years GMP-regulated experience, preferably with radiochemistry, radiopharmaceuticals, or working in hot cells/gloveboxes; associate’s or bachelor’s in STEM or equivalent experience; knowledge of GMP practices and radiation safety. High-Value: radiopharmaceutical production, clinical and commercial manufacturing, radiochemistry, GMP, radiation safety, aseptic processing, experience with hot cells/gloveboxes preferred. Work setup: laboratory environment, PPE required; on-site in Indianapolis; no explicit travel mentioned.