Validation Supervisor
Hikma Pharmaceuticals - Other Locations
Total years of experience :14 years, 0 Months
Revision and execution of Production and R&D equipment’s qualification protocols.
2- Revision and execution of Utilities ’s qualification protocols.
3- Preparation, supervise and execution of the Process validation protocols/reports.
4- Preparation, supervise and execution of the Cleaning validation protocols/reports.
5- Environmental Monitoring reports/trends review.
6- Water system documents review.
7- Follow-up the implementation of Calibration system.
8-Validation SOPs preparation and update for relevant tasks.
9- Attend process validation batches and in-process control tests of this batches.
10- participate in committee of batch record update.
1- Perform all testing procedures, inspection and analysis for stability and finished products.
2- Prepare protocol for new products.
3-Also maintain the lab in accordance with SOP’s, c-GMPs, and FDA regulations.
4-Assist in development and validation of analytical methods.
5-Responsible for tools and devices calibration within QC lab.
6-Performing instrumental analysis using HPLC(Waters), UV visible spectrophotometer, Karl Fisher titrator, Dissolution and Disintegration testers and other QC equipments.
hospital military pharmacist
community pharmacist
study chemistry and physics and french
garduate with 97%