Telix Pharmaceuticals Limited
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
501 - 1000 employees
Founded 2015
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Director, Biologics
Job not on LinkedIn
November 26
Telix Pharmaceuticals Limited
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
501 - 1000 employees
Founded 2015
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
📋 Description
• Oversee process development and clinical production of radiolabeled monoclonal antibodies and conjugates. • Guide late-phase development and commercialization strategy. • Manage a team of bioprocess and bioconjugation scientists and engineers. • Ensure readiness for scale-up and manufacturing. • Ensure Biologics deliverables comply with GMP requirements across multiple regions. • Engage in cross-functional program matrix teams by providing options analysis and program timeline input. • Ensure appropriate source documentation to support regulatory filings.
🎯 Requirements
• Bachelor’s degree plus 17 years of experience, or Masters degree or PhD plus 10 years of experience, in bioprocess development, validation, and commercialization. • 5+ years in leadership, ideally managing global teams and external partners (e.g., CDMOs) • 10 years of experience in GMP, quality management system, and CMC compliance and regulation. • Strong written and verbal communication skills are required. • Experience working with radiolabeled antibodies is preferred. • Experience of contributing to regulatory filings is preferred.
🏖️ Benefits
• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development
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