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Job Description
- Observes the effectiveness of procedure control and in-process checks performed by production staff, according to B.M.R, B.P.R. & SOPs.
- Performs in-process control checks on manufacturing & packaging process randomly
- Check the composition on ORACLE system against the bill of materials details for correctness and readability. & then release for bill of material start up
- Attend dispensing of raw material as wetness checker.
- Identifies & report process changes, incidents & non conformities or any deviations from GMP compliance & follow up the corrective & preventive actions implementation
- Checks and monitors calibrations of equipment & instrument & validation in manufacturing departments.
- Monitor Validation activities & completion of sampling in collaboration with validation officers.
- Review manufacturing & packaging batch records, cleaning & environmental control records and reports his comments to management
- Work with production in setting SOPs, Batch Records & Product improvements.
- Monitors and inspect the rework of batches
Job Requirements
- General : University graduate, Faculty of Pharmacy or Sciences
- Technical: - Preferable one year experience in QA. On pharmaceutical manufacturing.
