We’re simply looking for Regulatory affairs and partner care (Hearing/ENT/Medical Devices industry)Submit and follow up the necessary documents (shipping files, legal approvals, product documentation, etc.…) with the Ministry of Health ( CAPA- Pharmaceutical Affairs Central Administration) and prepare documents and files to match local registration requirementsMeet with the concerned authorities' personnel and committees to finalize all necessary actions in order to push forward the registration/re-registration procedures & Import permits in a timely manner in order to meet launches dates and customers’ demandsWriting and maintaining procedures for regulatory operationsSubmit required licenses for all different ministries and governmental sectorsSend orders and follow up on the shipping state of each orderPrepare reports related to partners' activitiesReporting and documenting work stuffAttend all meetings and training scheduled by the company