Postdoctoral Researcher – GMP Formulation Group

SUMMARY:
Postdoctoral Researcher: The role involves translating radio labelling and QC processes into GMP methodologies for Phase I–III clinical trials

POSITION INFO:

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 I–III 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.