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Job Description
- The position holder is responsible for Creation, and the execution of the proper framework that governs the qualification activities for the process validation activities and cleaning validation activities within the organization Quality Management System.
Responsible for execution, monitoring, and reporting of the following:
- All Classified areas Qualification
- Ampoule Machines SIP Validation
- Autoclave Validation
- Steam quality test Qualification
- Compressed Air Quality test Qualification
- Thermal Mapping Studies for warehouses
- Vacuum Chambers Qualification
- Light intensity Qualification
- Media fill aseptic simulation studies on Ampoule Machines
- Cleaning and Process Validation
- equipment qualification
- All Pass Boxes Qualification
- All AHUs reconciliation and Qualification in coordination with the engineering department
- Monitoring all external activities done by the outsourcing and archive reports
- Participate in SOPs creation and revising
- Prepare the Validation calendar Plan and index Annually, validation protocols and reports
- Any Other tasks within the scope of validation department duties assigned by validation supervisor.
Job Requirements
- Bachelor’s degree in Pharmacy, scientific, engineering
- 1-3 years of experience in the field.
- Good command of English language and computer skills
- High communication skills and able to work in a team and able to interact with various priorities
- Active, organized and planner with high attention for details
- High observation skills
