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Job Description
- Follow up procedures and ISO 9001 Quality Management System
- Handling all issues with QA Department concerning Training, review batches, iso , ect…
- Preparation, issuance & Retrieval and control of Master Production Record (Manufacturing & Packaging).
- Facilitating training program and its documentation.
- Preparing the requirements of the quality system in production area.
- Very good computer skills.
- Complete responsibility for filing and archiving system and for maintaining the documentation system in production department.
- preparing and writing SOPs concerning production department and ISO documentation system.
- Writing of master batch record.
Job Requirements
- BSC pharmaceutical Science OR Science.
- 3-5 years’ experience in a relevant position.
- Male or Female.
- Good English Language.
