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