- Building up efficient communication with CMOs, laboratories and MOH to follow up contract manufacturing operations
- Collecting regulatory and QC documentation (such as COA, stability report, PMQC and…) and providing reports
- Supervision of production and providing reports
- Following up some of QA documentation such as preparing SOPs, deviation forms, receiving reports of periodic inspections of MOH or self-inspection in order to correct or eliminate deficiencies (CAPA) and …
Requirements
- Ability to prepare CTD for submission to Iran MOH
- Ability to prepare the contents for leaflet and other packaging materials
- Adequate Knowledge of pharmacopeia and analysis
- Basic knowledge of Iran MOH regulation to prepare the required documents for submission
- Basic knowledge of GMP, GSP & GDP
- Preferably university degree in Chemistry, Pharmacy/ Pharmacology
- Minimum 3 years of experience in pharmaceutical industry
- Highly committed to the job role and follow up of the tasks
- Flexibility for different job roles
- Self-motivated, analyzer & organizer
- English: Intermediate or above
- MS Office and internet: Intermediate or above
- Age range: 25 - 35
- Ready to take short trips out of Tehran to the manufacturing sites