Validation Manager, Quality Assurance

A Director of QA for Sterility Assurance leads the qualification and validation program for cGMP radioligand therapy manufacturing facilities and sterile processes. The role ensures compliance with global regulatory requirements for sterile manufacturing and radiation-controlled operations while overseeing equipment, utilities, analytical instruments, and computerized systems. This position collaborates cross-functionally to support the design, commissioning, startup, and day-to-day management of facilities producing personalized medicine.