Regulatory Affairs - Abu Dhabi, United Arab Emirates - Life Medical Equipment

Description

• Ensure that all required documents and actions for Product Classification Registration and Product Registration are available.
• Prepare all required documents to be submitted for Product Classification under MOH.
• Prepare all the Dossiers to be submitted to MOH for medical equipment ,device ,implants ,instruments & consumables.
• Prepare and submit samples to MOH for product registration completion.
• Ensure a quick and accurate release of shipments from MOH to avoid any delays in transporting the products to the warehouse.
• Communicate with the existing and new suppliers regarding MOH importation rules and policies.
• Upload on the MOH importation system any new classifications or registration certificate.
• Monitor the importation payment process and update the finance department regularly with payment records.
• Assist the Warehouse Coordinators with relevant documents when requested.
• Prepare any documentation needed for internal and external audits.
• File all documents in the corresponding files to ensure all are available and are correct.

• Education: Bachelors Degree
• Experience: 2 years of experience.
• Job Specific Skills: Import Permit & Product classification (MOH)
• Preferable : Arabic

• Abu Dhabi: Reliably commute or planning to relocate before starting work (required)