Job Description

- Assisting Regulatory Manager on all activities related to the quality of products according to the national and international standards including GMP, GLP, GPS, GMP and etc. - Assist in managing and preparation of all required document, such as guidelines, SOP's, specifications, certifications, and reports for different departments. - Assist in managing the process of registration of products and preparing CTD's and all other requirements. - Assist in planning and communicating with international companies to facilitate import of products. - Assist in all registration related activities, such as preparation of registration documents, gathering of Pharmacovigilance and ARD reports and follow up of submitted dossiers with MOH until successful registration. - Assist in preparing purchase orders and review requisitions for goods. - Assist in coordinating foreign commercial affairs, such as sourcing, correspondence, ordering and all other import process formalities. - Registering PI and invoices in the designated systems and getting necessary approval from Ministry of Health and Ministry of Commerce. - Assist the assigned broker for customs clearance & preparing customs release documents. - Complete order processing cycle, review and track all the orders for complete delivery. - Ensure that purchase goods are delivered on time and as per agreement.