● Regulatory affairs.
● IRCs registration.
● Complying registration file (CTD) regarding to new pharmaceutical production.
● Batch release and control and release of manufacturing and test documentation.
● Coordinate, preparing, executing and post processing inspection by national authorities.
● Registration file compilation in order to submit supplement products.
Requirements
● Fluent in TTAC registration techniques.
● Fluent in quality assurance.
● Fluent in all regulatory affairs in FDO and MOH.
● Fluent in CTD and PMF documentation.
● Fluent in pharmaceutical processes and manufacturing.