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Job Description
- Implements Operational manuals, production plans and programs.
- Fulfills the monthly and weekly production plans according to the schedule and ensures well execution of production needs.
- Monitors drugs manufacturing activities in compliance with the requirements of cGMP.
- Prepare plan for process validation cleaning validation & execute the validation plan in coordination with validation team.
- Ensures that all operators stick to SOP’s & batch record instructions.
Job Requirements
- Bachelor of Pharmacy.
- 0-4 Years of Experience in Sterile Area in Pharmaceutical Industry.
- Professional knowledge in pharmaceuticals industry principles, method, and applications.
- Detailed knowledge of cGMP and different international standards, ISO standards.
- Knowledge of analytical and instrumental methods.
- Knowledge in related MOH regulations.
- Good Command in English Language
