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Job Description
- Design overall validation framework- including but not limited to- process and product validation, cleaning validation &, computer system validation and responsible for the overall performance of the system.
- Establish, maintain & continuously improve master plans and procedures for validation activities - including planning, execution, reporting & evaluation - of validation studies to ensure that it fulfill regulatory requirements & company policy.
- Review final validation plan & final validation reports to ensure completeness & participate in assessment of deviations, anomalies & trends prior to final report approval.
- Verify that all changes conducted in site has been registered, assessed & their implementation properly planned prior to execution.
- Establish & maintain system for risk revision for all process to predict process weakness & recommend proper process control.
Job Requirements
- B.Sc. degree in Pharmaceutical Science or in Science.
- From 7 to 10 years of experience in relevant field.
- Excellent Knowledge of English language (Written and spoken).
- Excellent knowledge of MS Office.
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