Responsibilities:

• Manage regulatory submissions and dossier reviews
• Ensure compliance with global and regional regulations
• Liaise with authorities and stakeholders for product registration

Requirements:

• Experience in regulatory affairs in pharma or biotech
• Knowledge of EMA, WHO, and local regulatory guidelines
• Detail-oriented with excellent project coordination skills

What’s on Offer:

• International exposure and strategic project roles
• Work-from-home or hybrid arrangements
• Collaborate with EU suppliers and African/Middle East clients