Regulatory Affairs Intern- Tamheer
Listed on 2026-07-13
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Regulatory Affairs Intern
- Tamheer , Riyadh
Onsite Location(s):
Riyadh, Saudi Arabia
Additional Locations: N/A
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At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.
About the roleBoston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.
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 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
- 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
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