Radiopharmaceuticals Associate Production Technician

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 As an Associate Production Technician reporting to the Radiopharmaceuticals Production Manager, you will play a pivotal role within our brand-new radiopharmaceutical production facilities.

Responsibilities

will involve assisting in activities related to the manufacturing of radiopharmaceutical products, from development and validation to clinical and commercial use.

Requirements

to ensure the highest quality standards in the production of these crucial medical products.

Supports the (Senior) Production Technicians in the manufacturing of radiopharmaceutical products in accordance with SOPs for development, validation, clinical, and commercial use. This includes aseptic manual and automated radiolabeling and fill-and-finish processing steps. Maintains the GMP production area's environment, including equipment and facility cleaning and environmental monitoring.

Assists in the preparation of assemblies and solutions according to SOPs and aseptic techniques. Assists with in‑process control testing, including radioactivity measurements performed under appropriate guidance. Keeps equipment operating by following operating instructions, troubleshooting breakdowns and calling for repairs.

Contributes to QMS documentation by providing inputs, data, and operational feedback. Manages materials and wastes transfer and inventory management in the production area according to SOPs. Diligently completes all GMP documentation.

Communicates effectively with supervisors and colleagues to provide updates on production status and address matters related to safety, quality, and efficiency. g. EMS, ERP).

Supports continuous improvement initiatives. Works constructively and flexibly within a team. Able to work overtime or out of working hours when required/requested.

Education and Experience: Bachelor’s degree in a relevant field, such as chemistry, radiochemistry, pharmacy, biomedical or a related discipline or equivalent relevant experience. 1+ year of hands-on experience in manufacturing roles in the pharmaceutical or biotech industry. Prior experience in the radiopharmaceutical industry or in aseptic manufacturing processes is a plus.

Key Competencies: Adherence to Procedures: Works with precision in strict accordance with established procedures, rules, and regulations. Can-Do Attitude: Displays a proactive and hands-on approach, approaching tasks with a positive "can-do" attitude. Adaptability: A flexible mindset capable of effectively handling ambiguity and responding energetically and enthusiastically to changes in the work environment.

Self-Motivated and Team Player: A self-motivated and enthusiastic individual who collaborates well within a team, is eager to learn new skills, and mentors junior staff. Proficient in French and intermediate level (B1) in English. Proficient in the use of Microsoft Office applications.