Senior Principal Scientist, Biologics – Translational Medicine

Job not on LinkedIn

November 20

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Logo of Telix Pharmaceuticals Limited

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

• Provide technical and analytical expertise for translational to early phase biologics process development and manufacturing activities • Ensure developability and manufacturability assessments and drug substance intermediates are sufficiently developed to meet program objectives, safety standards, regulatory expectations, and quality compliance. • Manage projects in multiple technology areas (e.g. cell banking, bioprocess/bioconjugation, analytical, formulation, and/or other) at external partners • Contribute to internal cross-functional collaborations to develop and support future preclinical activities, process development, and/or clinical manufacturing. • Act as the Biologics lead for one or more therapeutic programs and communicate with cross-functional teams including governance forums with senior leadership team members in formal settings and third-party meetings.

🎯 Requirements

• Science or engineering degree with minimum relevant experience as applicable: BS with 14 years of experience, MS with 12 years of experience, PhD with 11 years of experience. • Minimum 10 years of experience in translational to early phase GMP, quality management system, and CMC compliance and regulation. • Demonstrated understanding and application of project management principles and tools. • Ability to work in cross-functional, virtual teams. • Travel expectation: 10 – 25% for key in-person meetings, partner site visits, and SME/technical person-in-plant assignments.

🏖️ 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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