Regulatory Affairs Administrator

Job Description

Under general direction of the Regulatory Affairs Manager, the RA Administrative will do the required registrations on line and all related job requirements including communication with both teams at the supplier's side and inside Amico

Very well OrganizedProfessional attitude. Worked for Medical Device Registration outside Egypt or to register Egyptian products with other countriesMultitasking with time-management skills and ability to prioritize tasks. Excellent Knowledge of MS Office.Fluent in both Arabic and English language nice Communication Skills

Key Responsibilities

• Additional or Desirable Qualifications
• Attending Conference calls with suppliers, prioritizing the requirements, conveying the needed tasks in an understandable manner
• Maintaining the Archive system
• Ability to bridge the communications between Authorities/our local agents in the countries with the supplier
• Understanding the Comments received from the Authorities on any registration and passing it to the supplier in an easily understandable manner.
• Requesting suppliers to provide different documents required for the registration
• Feeding the different governmental systems with the required registration information and uploading needed documents.
• Follow the internal regulations in Amico

Job Requirements

• Professional Certificates
• Bachelor’s degree or equivalent in Biomedical Engineering, Business Administration or Legal
• Knowing the Pharmaceutical registration process, working with SAP and previous experience in registrations in the Gulf will be an added value.
• Having a certificate in Quality or Regulatory Affairs will be an added value as well
• 3 years of experience in Regulatory Affairs