Regulatory Affairs Intern- Tamheer , Riyadh
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Key skills for this role
About the Role
Boston Scientific is seeking a Regulatory Affairs Intern to support UDI data entry and maintenance in the SFDA Saudi-DI system. This internship offers hands-on experience in regulatory processes within the medical device 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 a bachelor's degree in regulatory affairs, life sciences, biomedical engineering, or 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
Full Job Posting
About the Role
- Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list.
- The Regulatory Affairs Intern will support the entry, maintenance, and accuracy of Unique Device Identification (UDI) data within the SFDA Saudi DI system.
- This internship offers hands on experience implementing SFDA MDS REQ 007 guidance and exposure to regulatory processes in Saudi Arabia.
Your Responsibilities Will Include
- 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
Qualifications
- 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
Preferred Qualifications
- Familiarity with regulatory requirements or medical device industry standards
- Interest in regulatory affairs and compliance within the healthcare industry
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