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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.
- Create, review and issue/update master batch records after delivery from the R&D department.
- Arrange for hosting the MOH inspectors in order to provide samples and documentation needs of finished products and active raw materials on weekly basis.
- Be Responsible for archiving system & archiving room and follow up the archiving system in the room.
- Be Responsible for review batch records received from the production department.
Job Requirements
- Bachelor of Pharmacy or Science.
- 3-5 years of experience in QA filed in pharmaceutical industries
- Male is preferred.
- 6th of October resident or nearby areas is preferred.