Radiochemist - Talent Community

Role: Support development of Telix's clinical-stage radiopharmaceuticals by managing manufacturing and QC procedures compliant with GMP regulations, ensuring readiness for clinical trials, regulatory submissions, and scaling to commercial manufacturing. Responsibilities: interface with external CMOs, develop and validate manual/automated manufacturing and non-compendial QC methods, generate protocols and reports, support regulatory filings (INDs, NDAs, BLAs), and optimize manufacturing scale-up. Requirements: Bachelor's degree plus 5+ years, or Master's/PhD with fewer years, in radiochemistry; practical radiochemistry experience; expertise in developing HPLC, TLC, or GC methods for radiopharmaceuticals; GMP manufacturing experience; strong communication skills. Preferred: radiometals experience, conjugation/radiolabeling of biologics, method development for regulatory submissions. HighValue: radiopharmaceuticals, GMP compliance, clinical-stage assets, regulatory support, radiometal expertise. WorkSetup: hybrid/remote; no travel specified.