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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.
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…
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