Senior Scientist, Radiochemistry

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 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 support the international roll‑out of our approved prostate‑cancer imaging agent and help advance our portfolio of late‑clinical‑stage products that address significant unmet need in oncology and rare diseases.

As a Senior Scientist, Radiochemistry you will support the development of clinical‑stage radiopharmaceutical assets. Your role is responsible for managing the development required to ensure manufacturing and QC procedures meet the corporate requirements to support clinical trials, regulatory submissions and transition to commercial‑stage manufacturing.

• Interface with key stakeholders, including external CMOs, to manage the development of manufacturing and QC procedures for clinical‑stage radiopharmaceutical assets in compliance with all applicable GMP regulations.
• Demonstrate the ability to manage multiple CMOs with little oversight from management.
• Manage the development and validation of manual or automated manufacturing procedures as required.
• Manage the development and validation of non‑compendial QC procedures as required.
• Generate development, validation, method transfer and other types of protocols and reports.
• Author CMC sections for INDs, NDAs, BLAs and foreign equivalents.
• Generate SOPs for manufacturing and QC procedures.
• Support method transfers to external manufacturers.
• Participate in streamlining, optimisation and scale‑up of manufacturing procedures in preparation for commercial supply.
• Provide technical support for manufacturing and QC procedures for all Telix products as required.
• Ensure all documentation generated is consistent with Telix QMS and general principles of GMP manufacturing.

• Bachelor’s degree plus 8+ years experience, or Masters degree plus 6+ years experience, or doctorate plus 5+ years experience required.
• Practical radiochemistry experience required.
• Experience developing HPLC, TLC or GC QC methods for radiopharmaceuticals required.
• Experience working in GMP‑compliant manufacturing required.
• Strong written and verbal communication skills.
• Experience with conjugation and radiolabeling of biologics preferred.
• Experience of method development to support regulatory filings preferred.

At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all share a purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being part of a unique, global, interdisciplinary team working to deliver the next wave of precision medicine. We have hybrid and remote employees located around the world. We offer competitive salaries, annual performance‑based bonuses, an equity‑based incentive program, generous vacation, paid wellness days and support for learning and development.

Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.