Key Responsibilities

• Define and execute regulatory strategies to accelerate product approvals and lifecycle management activities.

• Lead registration activities and regulatory submissions across the Novartis portfolio in Egypt.

• Ensure regulatory compliance and implementation of global Regulatory Affairs standards and processes.

• Partner with local, regional, and global stakeholders to support successful product launches.

• Build and maintain influential relationships with health authorities, trade associations, and external partners.

• Lead, develop, and coach a high-performing Regulatory Affairs team to drive functional excellence.

• Monitor regulatory changes and translate insights into impactful business and regulatory strategies.

Essential Requirements

• Bachelor’s degree in Life Sciences or a related scientific discipline.

• Significant experience in pharmaceutical regulatory affairs, drug development, and product registration.

• Proven success developing and executing regulatory strategies across the product lifecycle.

• Strong experience engaging and negotiating with health authorities and external stakeholders.

• Demonstrated leadership experience managing, developing, and coaching high-performing teams.

• Excellent communication, collaboration, and strategic thinking skills within complex matrix organisations.