Radiochemist

Job details

Contract Type

Description
Qualifications
  • Master’s or PhD in Chemistry, Radiopharmaceutical Chemistry, or a closely related field.
  • Certification or formal training in GMP and radio pharmacy is highly preferred.
  • In-depth knowledge of organic chemistry, radiochemistry principles, and analytical techniques (HPLC, GC, TLC).
  • Proven experience with automated radiochemistry synthesis modules and working in a regulated laboratory environment.
  • Strong commitment to quality, safety, and continuous improvement.
  • Minimum of 3-5 years of hands-on experience in a radiopharmaceutical production environment, preferably with PET radiotracers.
  • Demonstrated expertise in GMP-compliant production and quality control of radiopharmaceuticals.
  • Proven track record in method development and optimization of radiochemistry processes.
  • Experience in training or mentoring staff in laboratory techniques and safety procedures is desirable.


Responsibilities

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.


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