Regulatory Affairs Intern: UDI Data & Compliance

About the role

The Regulatory Affairs Intern will support the entry, maintenance, and accuracy of Unique Device Identification (UDI) data within the Saudi Food and Drug Authority (SFDA) Saudi-DI system. This internship offers hands‑on experience implementing SFDA MDS-REQ-007 guidance and exposure to regulatory processes in Saudi Arabia. You will collaborate with cross‑functional teams to ensure data integrity and compliance with regulatory requirements.

• Enter and update UDI data in the Saudi-DI system in alignment with SFDA requirements
• 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

• Currently pursuing a bachelor’s degree in regulatory affairs, life sciences, biomedical engineering, or a related field
• Strong attention to detail and organizational skills
• Ability to follow instructions and adhere to established procedures
• Basic proficiency in Microsoft Office tools, including Excel
• Strong communication and collaboration skills

• Familiarity with regulatory requirements or medical device industry standards
• Interest in regulatory affairs and compliance within the healthcare industry