Postdoctoral Researcher GMP Formulation Group CONTRACT Hartbeespoort Overview Postdoctoral Researcher to focus on GMP-compliant production and quality control of radiopharmaceuticals, including kit formulations. The role involves translating radiolabelling and QC processes into GMP methodologies for Phase IIII clinical trials. The researcher will contribute to GMP documentation, participate in cleanroom operations, mentor students, present findings, and assist with funding applications. A minimum of two publications per year is expected. Requirements PhD in Pharmaceutical Sciences, ideally specialized in Radiochemistry or Radiopharmacy, obtained within the last 5 years Experience in radionuclide handling, radiolabelling, radiopharmaceutical synthesis, and quality control preferred. Strong publication record (minimum one peer-reviewed paper in last 5 years; additional publications advantageous). Excellent written and spoken English. Strong teamwork, communication, problem-solving, and ability to work independently under GMP/GLP standards.