Regulatory Affairs Intern- Tamheer , Riyadh
Core
Support the entry, maintenance, and accuracy of Unique Device Identification (UDI) data within the Saudi Food and Drug Authority (SFDA) Saudi-DI system.
Role type
Regulatory Affairs Intern
Builds
UDI data submissions and documentation for medical devices in Saudi Arabia
Domain
Medical device regulation in Saudi Arabia
Deliverable
dashboards & analysis
Required skills
Data entry, UDI data management, documentation maintenance, stakeholder coordination, procedural compliance, data accuracy verification
Preferred skills
Familiarity with regulatory requirements, knowledge of medical device industry standards
Technologies
Microsoft Excel, SFDA Saudi-DI system
Responsibilities
Enter and update UDI data in the Saudi-DI system, Maintain UDI trackers and ensure accurate documentation of submissions, Support the regulatory affairs team with UDI-related submissions and updates, Coordinate with internal stakeholders to resolve missing, incomplete, or inconsistent data, Follow established procedures and ensure compliance with quality and regulatory standards, Assist in improving data accuracy and process efficiency where applicable