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Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision…
Quality Assurance CQV Lead providing QA oversight for facility construction, equipment/utility qualification, computerized systems and process validation across Telix's US radiopharmaceutical manufacturing network, ensuring cGMP compliance and GMP site readiness. Advertised as remote but requires 75%+ travel with extended stays at US manufacturing sites.
Leads global development of late-stage radiopharmaceutical therapies for oncology and rare diseases, coordinating clinical, regulatory, CMC, and commercial teams to drive regulatory approvals and commercial readiness.
Leads QA operations at Telix's Angleton radiopharmaceutical manufacturing site, overseeing GMP/GxP compliance, live batch record review and product disposition, deviations/CAPA and change control, supplier quality, aseptic/sterile manufacturing compliance, and FDA regulatory interactions. Requires a life sciences degree, 5+ years in QA, and willingness to work with radioactive materials.
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