● Order all the requirements related to the production of technical batch and batch formulation and purchase follow-up.
● Review and research the references of the relevant sites to perform matters related to the formulation unit.
● Comment on items related to raw materials in the manufacture of new products.
● Carry out the necessary planning and coordination for the trial production process of new products.
● Supervise all laboratory work according to current methods.
● Write new formulations and prepare the necessary items to prepare a comprehensive drug file to be sent to the technical unit and quality assurance.
● Efforts to prevent accidents and occupational diseases.
● Efforts to increase their knowledge in the field of health and safety regulations and requirements.
Requirements
● Ph.D. in Pharmacy.
● Familiarity with the basics of GMP.
● Familiarity with different types of CTD preparation.
● Familiarity with drug registration regulations.
● Familiarity with the principles of GLP formulation.
● Familiarity with computers.
● No work experience is required.