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 requirements
• Meet 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’ demands
• Writing and maintaining procedures for regulatory operations
• Submit required licenses for all different ministries and governmental sectors
• Send orders and follow up on the shipping state of each order
• Prepare reports related to partners' activities
• Reporting and documenting work stuff
• Attend all meetings and training scheduled by the company