• The RA specialist's role is to prepare dossiers for regulatory submissions, approvals in accordance with the applicable rules and regulations. 
• He/she operationalizes or executes regulatory activities relating to registration requirements, renewals and product life cycle maintenance for Maghreb countries. 
• The RA specialist is expected to act in compliance with country policies and practices to reduce company’s exposure to Regulatory risks.

Qualifications:

• Pharmacy graduate. 
• Experience in the pharmaceutical industry ( 3 years) in regulatory affairs or drug development. 
• QA and PV experience is a plus 
• Good level of English (both writing and speaking)
• Fluent in French and Arabic 
• Proficiency in MS Office tools, especially MS Excel and PowerPoint
• Travel can be required to meet the relevant Distributors & HAs in the concerned countries