Cyclotron Engineer

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

The Cyclotron Maintenance / Service Engineer is an exempt role that provides service and maintenance for multiple cyclotrons, chemistry modules, and analytical equipment, and provides maintenance oversight for facility equipment serviced by third parties. Working independently, the engineer executes and supports preventative maintenance per SOPs, responds to service calls, and helps maximize equipment uptime for production and analytical systems. The role also supports biomarker manufacturing (cyclotron and chemistry module operation) and quality control processes (TLC, HPLC, GC) under supervision as required by State and Federal law, and works in full compliance with EH&S, cGMP, Radiation Safety, applicable pharmacy laws, DOT, and internal policies.

Key Accountabilities:

Equipment Service & Maintenance

• Provides service maintenance for multiple cyclotrons, chemistry modules, and analytical equipment; works independently to accomplish assigned tasks and responsibilities.
• Provides maintenance oversight for facility equipment service performed by third
• Supports the site in execution of preventative maintenance of cyclotrons, chemistry modules, and QC equipment per SOPs.
• Responds to calls for service support within a reasonable amount of
• Completes and submits work-history tickets in a timely fashion, including all relevant

Production & Quality Control Support

• Performs manufacturing (cyclotron and chemistry module operation) and quality control processes (utilizing analytical equipment — TLC, HPLC, GC), under supervision as required by State and Federal law, as required.
• Participates in routine biomarker production functions as directed by the site
• Supports manufacturing staff in routine logistics functions, including preparing product for shipment, coordinating courier schedules, and documenting as directed.

Reliability, Improvement, & Cost