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Job Description
- Review the distribution cycles all new and updated BOMs.
- Review dispensing orders and production batches to assure compliance with BOMs before delivery of production batch records.
- Creating, reviewing and issuing/update master batch records after delivery from the R&D department.
- Arrangements for hosting the MOH inspectors in order to provide samples and documentation needs of finished products and active raw materials on weekly basis.
- Responsible for archiving system & archiving room and follow up the archiving system in the room.
- Responsible for review batch records received from the production department.
Job Requirements
- Bachelor degree of pharmacy or Science .
- Experience from 6 : 8 years in QA Documentation is a must .
- Pharmaceutical industry experience is must .
- Excellent awareness of the rules and guidance of ISO, GMP and GDP.
- 6th October city resident and nearby are preferred.
