Job Description
Roles & Responsibilities
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
Desired Candidate Profile
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