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

Performs complex radiochemical synthesis, purification, compounding, and quality control functions supporting PET biomarker production at a cyclotron facility, including set-up, operation, routine checks, and preventive maintenance of manufacturing equipment such as cyclotrons and automated chemistry modules. This non-exempt role performs and documents all quality control testing and plays a crucial part in ensuring that manufacturing and QC activities meet cGMP, radiation safety, and applicable State and Federal requirements.

This role is 5 days a week on-site at our Wilkes-Barre, PA location.

Key Accountabilities

Performs complex radiochemical synthesis, purification, and compounding of PET biomarkers, including use of cyclotrons and automated chemistry modules, in accordance with cGMP requirements for PET drug production and applicable radiation safety regulations.
Partners with cross functional teams in process qualification and process improvement initiatives.
Leads commissioning and equipment qualification activities, as necessary.
Lead investigative efforts for manufacturing and process issues to support root-cause analysis and corrective action plan.
Coordinate daily activities of Radiopharmaceutical Production Technicians while ensuring adherence to production schedules and quality requirements.
Provides technical leadership and real-time problem resolution.
Leads the development of manufacturing processes tech transfers and complex projects with communication of timelines to internal and external stakeholders.
Executes quality control testing using analytical instrumentation (TLC, HPLC, GC); analyzes and interprets results against established specifications and documents outcomes in compliance with GxP requirements.
Conducts complex inspections, maintenance, and troubleshooting to support manufacturing and testing processes and equipment.
Implements approved SOP changes to production and quality control processes, helping drive continuous improvement.
Performs daily, weekly, monthly, and quarterly PM checks of cyclotrons, chemistry modules, and QC equipment per SOPs.
Oversees routine logistics functions, including preparing products for shipment, coordinating courier schedules, and documenting as necessary.
Monitor and perform continuous process improvement and waste reduction initiatives.
Maintains a clean, clutter-free facility and a well-organized production area and workflow.
Provide technical coaching to Radiopharmaceutical Production Technician I & II
Provides exemplary customer support.
Other tasks as assigned by supervisor.

Education and Experience

Associates degree or certifications in Chemistry, Radiochemistry, Biochemistry, or a related field required.
4+years of experience in a laboratory setting, preferably in radiopharmaceuticals, or a related industry.
Knowledge of radiochemical synthesis, purification, and safe handling of radioactive materials required.
Advanced understanding of manufacturing processes and quality systems.
Experience interpreting complex engineering documentation
Ability to read and interpret engineering drawings, specifications, and manufacturing work instructions
Strong problem-solving skills and attention to detail.
Ability to work in a team environment and communicate effectively with diverse groups.
Familiarity with regulatory requirements such as GMP and radiation safety practices.