Supervise and ensure the implementation of the current Good Manufacturing Processes (cGMP) as well as other set standards to ensure compliance with regulatory requirements. Preparation of CTD FILES. Preparation all documents for pilot Developing Master Batch Production Record File Developing company products file according to ISO 9001.Follow up on team commitment to OHS instructionAny other duty that may be assigned to him /her.Ensures that all activities in his unit or section are done according the relevant Cgmp,EDA and ISO standards Bachelor of PharmacyAt least 7-10 years of experience in R&D FormulationPharmaceutical industry is a mustPreferably October or sheikh zayed resident