Key Responsibilities:
· Prepare and submit all documents required for import approvals, customs release, and exemptions.
· Follow up and respond to Health Authorities’ inquiries until final approvals are granted.
· Handle all Health Authorities visits (EDA & NFSA).
· Stay updated with new Health Authority regulations.
· Support the Marketing team with Health Authority-related inquiries.
· Prepare registration dossiers for company products.
· Maintain records for submitted documents and approvals.
· Issue ACID requests and manage Nafeza platform-related issues.
· Oversee EDA audit visits ensuring compliance and audit readiness.
· Supervise the regulatory team and manage their work plan.
Qualifications: · Bachelor’s degree in Pharmacy. · Fluency in English and Arabic (spoken & written). · 3+ years of Regulatory Affairs experience (Raw Materials; Finished Products preferred). · High level of accuracy. · Strong communication and negotiation skills. · Effective problem-solving and time management abilities.