The Director, Biologics oversees the development and production processes of radiolabeled monoclonal antibodies, managing teams, ensuring compliance, and contributing to regulatory strategies.

Lead cross-functional teams in developing and commercializing novel therapeutic radiopharmaceuticals, focusing on oncology products. Responsible for drug development plans and stakeholder communication.

The Global Development Lead will oversee drug development strategies for radiopharmaceuticals in collaborative environments, ensuring project progress and compliance with budgets and timelines.

Support financial planning, budgeting, and forecasting for R&D projects, partnering with cross-functional teams while ensuring compliance and enhancing FP&A processes.

The Territory Account Manager will drive sales, manage client relationships, conduct market research, and ensure compliance for radiopharmaceutical products.

This role involves leading late-stage biologics process development and manufacturing, ensuring compliance, and managing collaborations with external partners.

The Senior Scientist will manufacture clinical and preclinical radiopharmaceuticals, oversee lab operations in a cGMP environment, execute quality control activities, and support technology transfers. Responsibilities include ensuring compliance with regulatory standards and production protocols, maintaining documentation, and leading team efforts in radiopharmaceutical development.

The Global Employee Equity Lead manages global equity programs, ensuring compliance and accuracy. Key responsibilities include administration, employee support, compliance reporting, process improvement, and supporting global remuneration efforts.

As a Territory Account Manager, you'll drive sales, manage client relationships, develop strategic plans, and ensure compliance in the radiopharmaceutical industry.

The Senior Scientist, Radiochemistry manages laboratory work on radiolabeling and conjugation of antibodies, supports preclinical research, and ensures radiation safety compliance.

The Senior Scientist, Radiochemistry will manage the development of radiopharmaceutical assets, overseeing manufacturing and QC procedures in compliance with GMP regulations, and ensuring documentation aligns with Telix's quality management system.

The Senior Scientist, Radiochemistry will manage clinical-stage radiopharmaceutical asset development, ensuring compliance with GMP regulations and documentation for clinical trials and commercial manufacturing.