✨ AI Summary
The Regulatory Affairs Senior Specialist (Medical Device) role involves developing and executing regulatory strategies for medical devices, ensuring compliance with all applicable regulations, and preparing/submitting regulatory documentation. The position also requires maintaining technical documentation and product registration databases, and supporting the team with regulatory approvals. This is a full-time, on-site position in Cairo, Egypt.
Requirements
At least 3-5 years of experience in regulatory affairs, preferably in the medical device industry.Bachelor’s degree in science.
Description
Develop and execute regulatory strategies for new and existing medical devices.Ensure compliance with local, regional, and international regulations.Prepare and submit regulatory documents.Maintain technical documentation and product registration databases.Support the team with regulatory approvals and documentation.