Radiopharmaceutical Production & Development

• Perform routine synthesis, purification, and quality control of a range of PET radiotracers using automated synthesis modules.
  
• Develop and optimize new radiochemistry methods and procedures for novel radiotracers to support clinical and research needs.
  
• Manage the production schedule to efficiently meet clinical demand, coordinating closely with the cyclotron and nuclear medicine teams.
  

Quality Control & Assurance

• Conduct comprehensive QC testing of all produced radiopharmaceuticals, including analyses for radiochemical purity, chemical purity, pH, radio nuclidic identity, and sterility.
  
• Maintain meticulous documentation for all production and QC batches in compliance with Good Manufacturing Practice (GMP) principles.
  
• Manage the QC laboratory, including equipment calibration and maintenance.
  

Radiation Safety & Compliance

• Adhere to and promote strict radiation safety protocols for the handling and disposal of radioactive materials.
  
• Ensure full compliance with all regulations by relevant bodies for radiopharmaceutical production and laboratory safety.
  
• Participate in radiation safety audits and inspections.
  

Research & Innovation

• Actively participate in research and development projects aimed at innovating new radiotracers and improving existing synthesis protocols.
  
• Contribute to clinical trials by providing investigational radiopharmaceuticals and technical expertise.
  
• Publish findings in peer-reviewed journals and present at scientific conferences.
  

Training & Collaboration

• Train and mentor junior radiochemists and technologists on synthesis procedures, QC methods, and safety practices.
  
• Collaborate effectively with cyclotron physicists, nuclear medicine physicians, and radiologists to ensure seamless workflow and high-quality patient care.
  
• Provide technical expertise to multidisciplinary teams on the selection and use of appropriate radiopharmaceuticals.