Job Description

Summary of duties:

· Extensive knowledge and experience of the production of cyclotron and reactor radiopharmaceuticals according to the international guidelines of Good Manufacturing Practice (GMP).

· Extensive knowledge and experience of the Quality Control (QC) and Quality Assurance (QA) of radiopharmaceuticals according to international regulatory requirements.

· A good track record of writing and reviewing suitable scientific reports & documentation to fulfill radiopharmaceuticals and radiation protection regulatory requirements.

· Extensive experience in the development and validation of novel radiolabeled theranostic agents through pre-clinical studies, and in cyclotron technology.

· Ability of providing knowledge and guidance in the safety and efficacy of the new radiopharmaceuticals to be used clinically.

· Ability to play a key role in research projects with clinician, academic partners and external contract research and development organizations.

Education required:

Doctor of Philosophy (PhD) or equivalent in scientific discipline with a strong background in cyclotron and radiopharmaceuticals from an accredited university/institution is required.

Years of Experience required:

Twelve (12) years post doctorate research experience as an independent professional with at least five (5) years extensive administrative/supervisory experience is required.

Other Requirements:

Research productivity must be demonstrated in a form of publications in reputable relevant peer reviewed journals.