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The R&D Project Manager oversees research activities, builds project plans, tracks progress, manages budgets, and coordinates stakeholders to advance clinical projects in oncology and rare diseases.

The Senior Manager, Commercial Product Quality oversees quality leadership for Chemistry, Manufacturing, and Controls activities, ensuring compliance with GMP and enhancing quality systems across product lifecycles.

The Principal Scientist will lead radiochemistry projects, contribute to technology development, provide scientific expertise, and ensure compliance with regulatory standards.

The Director of Marketing Strategy at Telix Pharmaceuticals leads strategic and operational marketing initiatives to drive revenue growth and brand positioning, managing cross-functional partnerships and developing data-driven marketing strategies for oncology products.

The Director of Sustainability will manage the sustainability function at Telix, ensuring compliance with regulations, developing sustainability strategies, and fostering a culture of sustainability within the organization.

The Sustainability Engineer will lead technical support for radiopharmaceutical preparation, manage tech transfer and manufacturing, and ensure regulatory compliance while engaging in continuous improvement efforts.

The QA Operations Lead manages quality-related activities in manufacturing, ensuring compliance with GMP and regulatory standards, while overseeing operational quality assurance and supporting cross-functional collaborations.

The Recruiter is responsible for full life-cycle recruitment for global requisitions, managing hiring processes and collaborating with hiring managers, primarily for cancer and rare disease roles.

The Senior Project Manager oversees the execution of therapeutic programs, ensuring alignment with strategies, managing project development plans, budgets, and cross-functional teams, while mitigating risks and facilitating communication among stakeholders.

Lead global development of PSMA diagnostic products through Phase 3 by creating and executing development and commercialization plans, managing cross-functional teams (clinical, manufacturing, quality, regulatory), overseeing budgets and timelines, tracking risks and documentation, and reporting to senior management to secure product approvals and successful international roll-out.