- 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
- Cooperating in design, implementation and employing quality assurance systems
- Carrying out internal audits
- Preparing documentations
- Editing, monitoring and analyzing process indexes
- Recognizing and evaluating process risks and taking prevention measures
Requirements
- MSc. or PhD in Organic Chemistry, Analytical Chemistry, Applied Chemistry or Industrial Engineering or the related engineering
- Having worked at any pharmaceutical companies or having the related experience for at least 3 years
- Familiar with GMP requirements and pharmaceutical standards
- A good command of English in all four skills
- Familiar with Microsoft Office
- Familiar with management system and product adaptation requirements
- Familiar with recognition and documentation of processes
- Holding an audit certificate related to quality management systems
- Skilled in audit techniques and methods
- Familiar with management system requirements at pharmaceutical industry
- Preferably living in Tehran
Personality:
Accurate, disciplined, patient, hardworking, interested in teamwork