Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases.

You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix Scientist II, Analytical Chemistry supports IsoTherapeutics Group’s radiochemistry laboratory by contributing to the development, validation, and technical transfer of analytical methods used in radiopharmaceutical manufacturing. This role is responsible for executing and validating non‑microbiological quality control assays, including HPLC, Radio‑TLC, immunoreactivity testing, and related analytical techniques.

The position involves routine handling of radioactive materials and work within a GMP‑regulated environment, with a strong focus on data integrity, compliance, and method robustness.

Requirements

, HPLC, TLC, spectroscopy) to evaluate the quality and purity of radiopharmaceutical products. Analytical Method Transfer: Assist or lead the technical transfer of analytical methods from external vendors into GMP use at IsoTherapeutics Group Experimental Design and Execution: Plan, execute, and document experiments to support research objectives, ensuring adherence to project timelines.

Instrumentation Maintenance: Operate, calibrate, and maintain laboratory equipment and instruments to ensure reliable and accurate results. Data Analysis and Reporting: Analyze experimental data, interpret results, and prepare technical reports and presentations for internal and external stakeholders. Collaboration: Work closely with cross-functional teams, including quality assurance, production, and R D, to achieve project goals.

Education and Experience: Education: Minimum BS + 5 years, MS + 3 years, PhD + 2 years Experience in handling radioactive material is desired Proficient use with Open Lab (preferred) or similar analytical chemistry software is required Experience in writing and reviewing SOPs and reports is required Experience in coordinating or performing maintenance on routine analytical equipment (HPLC, ICP, etc) is desired Experience operating in a regulated GMP environment preferred.