Regulatory Affairs Intern
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Key skills for this role
About the Role
Support Unique Device Identification data management, ensure compliance with regulatory standards, and collaborate with teams in the healthcare industry.
Key Skills for This Role
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
Requirements
- Currently pursuing or recently completed a degree in a relevant field (e.g., regulatory affairs, life sciences)
- Interest in medical device regulatory affairs
- Attention to detail and data accuracy
- Proficiency in Microsoft Office applications
Full Job Posting
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.
Your 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
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