QA Operations Lead

Role: QA Operations Lead supporting radiopharmaceutical manufacturing at Telix, focusing on GMP compliance, quality oversight, and regulatory interactions. Responsibilities: oversee manufacturing, quality control, and supply chain activities; review SOPs, batch records, and QC results; manage deviations, investigations, CAPA, and supplier quality agreements; ensure sterile manufacturing compliance; lead FDA/regulatory interactions; support cross-functional teams in exception management. Requirements: Bachelor’s in Life Sciences or related field; 5+ years in QA or GxP manufacturing experience; strong understanding of quality systems, regulatory requirements, and sterile/Radioactive handling; effective communication and cross-team collaboration skills. Preferred: experience with radiopharmaceuticals or oncology-related products, regulatory submissions, and inspections. High-value: radiopharmaceutical manufacturing, GxP compliance, sterile and radioactive material handling, regulatory interactions, and cross-functional collaboration. Work setup: hybrid or remote; willingness to work with radioactive materials and strict safety protocols.