Job Description
● Support regulatory affairs in order to obtain a drug production license.
● Perform basic and advanced GMP affairs.
● Review and perform quality assurance matters.
● Review the specifications of new products, manufacturing methods, and materials used.
● Review and control the analysis of the final product.
● Review and control brochures.
● Monitor and control current product file updates and take the necessary measures and coordination in order to renew their construction license.
