● Supervise and control the drug manufacturing process, including weighing, granulation, and drug manufacturing.
● Control the documentation and accuracy of the current steps in the production sector.
● Participate in relevant meetings and committees, including new products, domestic and foreign markets.
● Efforts to prevent accidents and occupational diseases.
● Efforts to increase their knowledge in the field of health and personal care regulations and requirements.
Requirements
● Ph.D. in Pharmacy.
● Familiarity with the basic and advanced principles of GMP.
● Full familiarity with the process of production of drug forms and analysis of problems.
● Fluency in English.
● Familiarity with computers and related specialized software.
● No work experience is required.