
501 - 1000 employees
Founded 2015
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company dedicated to transforming the way cancer and rare diseases are diagnosed and treated. Focusing on the development and commercialization of theranostic radiopharmaceuticals, Telix utilizes targeted radiation to enhance treatment decision-making and deliver personalized therapy. With an extensive pipeline addressing areas such as prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers, Telix has garnered global regulatory approvals for its lead imaging agent, Illuccix®, and is actively conducting numerous clinical trials worldwide.
🔥 28 minutes ago
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501 - 1000 employees
Founded 2015
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company dedicated to transforming the way cancer and rare diseases are diagnosed and treated. Focusing on the development and commercialization of theranostic radiopharmaceuticals, Telix utilizes targeted radiation to enhance treatment decision-making and deliver personalized therapy. With an extensive pipeline addressing areas such as prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers, Telix has garnered global regulatory approvals for its lead imaging agent, Illuccix®, and is actively conducting numerous clinical trials worldwide.
• Support the development of clinical-stage radiopharmaceutical assets. • Manage the development required to ensure manufacturing and QC procedures meet corporate requirements. • Interface with key stakeholders, including external CMOs. • Demonstrate ability to manage multiple CMOs with little oversight. • Manage the development and validation of manufacturing procedures. • Author CMC sections for INDs, NDAs, and other submissions. • Ensure all documentation aligns with Telix QMS and GMP principles.
• Bachelor’s degree plus 8 years experience, or Masters degree plus 6 years experience, or doctorate plus 5 years experience. • Practical radiochemistry experience is required. • Experience developing HPLC, TLC, or GC QC methods for radiopharmaceuticals is required. • Experience working in GMP-compliant manufacturing is required. • Strong written and verbal communication skills. • Experience with conjugation and radiolabeling of biologics is preferred. • Experience of method development to support regulatory filings is preferred.
• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development
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🇺🇸 United States – Remote
💵 $84k - $94k / year
💰 $30M Grant on 2021-10
⏰ Full Time
🟠 Senior
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