We are a company inspiring the extraordinary, For more than 70 years, we have led the way with purpose-driven healthcare technology. That history compels us to relentlessly pursue therapies that change lives.

The role is opened to continue our daily milestone in serving our patients & partners and give them the highest level of support & partnership which is aligned with our daily mission to alleviate pain, restore health, and extend life.

In this vital role you will be responsible of setting submission plan for EU MDR changes, driving accountability and operational excellence for execution in compliance with Medtronic standards and national regulatory requirements for Egypt & Libya. You will develop and maintain a broad set of collaborative relationships across the organization and with external stakeholders and partners that will allow you to successfully contribute to achieving organizational goals.

• Directs or performs planning, coordination, and preparation of EUMDR documents for regulatory submissions.
• Dossier review and submission responsibilities for EUMDR changes.
• Promote, maintain, and improve compliance with country regulatory requirements.
• Ensure alignment of regulatory objectives with regional/ global regulatory objectives and commercial plans.
• Monitors and improves tracking / control systems.

• Bachelor’s degree, Pharmaceutical/Medical/ Science background.
• Minimum 1-2 years of related regulatory experience.
• Experience with Egypt Medical Devices regulatory requirements.
• Organizational skills & regulatory project management skills.
• Strong communication skills both verbal and written.
• Self-motivated, proactive, dynamic, organized, and decisive.