Telix Pharmaceuticals is seeking a Senior Manager, Development Quality to lead quality activities for radiopharmaceutical development programs. You will oversee GMP compliance, batch release, deviation management, CAPA, change control, and QMS improvements with CDMOs/CMOs, ensuring regulatory readiness across multiple jurisdictions.
The role requires deep industry expertise, mentoring of junior staff, and the ability to influence cross-functional teams in a quick-paced, global setting.