Regulatory Affairs Supervisor & Specialist

About the role

We are seeking a proactive Regulatory Affairs Supervisor & Specialist to lead our regulatory team in managing import approvals, customs releases, and health authority interactions. The role ensures compliance with evolving health regulations and supports the marketing department with regulatory guidance.

Key responsibilities

• Prepare and submit documentation for import approvals, customs release, and exemptions.
• Respond to health authority inquiries and follow up until final approvals are granted.
• Coordinate health authority visits (EDA & NFSA) and manage audit readiness.
• Maintain up‑to‑date knowledge of health authority regulations.
• Support marketing with health‑authority‑related queries.
• Compile and maintain registration dossiers for company products.
• Issue ACID requests and resolve Nafeza platform issues.
• Supervise the regulatory team, define work plans and ensure compliance.

Required profile

• Bachelor’s degree in Pharmacy.
• Fluency in English and Arabic, both spoken and written.
• 3+ years of regulatory affairs experience, preferably with raw materials and finished products.
• High level of accuracy and strong communication skills.
• Effective problem‑solving and time‑management abilities.

Required skills

What we offer

• Competitive salary.
• Medical insurance.
• Annual bonus.