- Supervising the production procedure and quality control of the radiopharmaceuticals
- Inspecting the clean room based on GMP requirements
- Inspecting and adhering to GMP requirements needed for the production line and labs
- Preparing and reviewing the instructions of the related activities
- Preparing the Batch Records and supervising their completion
- Preparing the process validation and clean validation protocols and helping in their implementation
Requirements
- MSc. or PhD in Organic Chemistry, Analytical Chemistry or Applied Chemistry
- Having worked at any pharmaceutical companies
- Familiar with GMP requirements and pharmaceutical standards
- A good command of English in all four skills
- Preferably living in Karaj
- Gender preference: Male
Personality:
Accurate, disciplined, patient, hardworking, interested in teamwork