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Job Description
- Coordinate, Prepare, or review regulatory submission for international Projects.
- Maintain Current knowledge base of existing emerging regulations, standards or guidance documents
- Prepare or maintain technical files as necessary to obtain and sustain products approval
- Review products ,labeling ,batch records ,specifications sheet or test methods for compliance with applicable regulations and policies
- Prepare or direct the preparations of additional information or responses as requested by regulatory agencies
- Direct the collection of sample as requested by regulatory agencies
Job Requirements
- BSc of Pharmaceutical science,/Science
- 1-3 years of experience in regulatory affairs
- Broad Knowledge of Pharmaceutical science
- Strong computer skills
- Very good Command of English language
- Having good organizational& communication skills
- Cairo Resident