● Supervise the preparation and submission of the necessary documents for the issuance of licenses.
● Carry out the necessary follow-ups regarding obtaining approvals such as construction permits, etc.
● Review of new product specifications, manufacturing methods, and materials used and the role of each of them based on the relevant formulation and reference standards.
● Complete a three-page form.
● Perform basic and advanced GMP affairs.
● Write and organize CTD files.
● Review and control of final product analysis results (formulation samples) including the results of chemical, physical and microbial tests and product stability and ensuring their compliance with specified standards.
● Supervise and control the updating of the file of current products and perform the necessary measures and coordination in order to renew their manufacturing license.
Requirements
● Ideal age range: 24 to 45 years old.
● Bachelor's or Master's degree in Chemistry.
● At least 5 years of professional experience.
● Excellent effective communication.
● Responsible.
● Follow up to get results.
● Ability to persuade.