Regulatory Affairs Intern- Tamheer , Riyadh

About Boston Scientific

At Boston Scientific, we are committed to transforming lives through innovative medical technologies that enhance patient health worldwide. As a global leader in medical technology with over 45 years of experience, we drive scientific advancement to address unmet patient needs and reduce healthcare costs. Our diverse portfolio of high-performance solutions empowers physicians to diagnose and treat complex conditions across cardiovascular, respiratory, digestive, oncological, neurological, and urological domains. Recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, we foster a culture of diversity, innovation, and high performance. Join us to harness your potential, collaborate with high-performing teams, and contribute to meaningful advancements in healthcare.

The Opportunity

We are seeking a motivated Regulatory Affairs Intern to support our regulatory compliance initiatives in Riyadh, Saudi Arabia. This internship offers a unique opportunity to gain hands-on experience in implementing regulatory requirements, particularly the Saudi Food and Drug Authority (SFDA) MDS-REQ-007 guidance, while contributing to critical healthcare advancements. You will play a pivotal role in ensuring the accuracy and integrity of Unique Device Identification (UDI) data within the SFDA Saudi-DI system, collaborating with cross-functional teams to maintain compliance and drive process improvements.

Key Responsibilities

• UDI Data Management: Enter, update, and maintain UDI data in the Saudi-DI system in strict alignment with SFDA requirements, ensuring accuracy and completeness.
• Documentation and Tracking: Maintain meticulous UDI trackers and ensure all submissions are accurately documented and compliant with regulatory standards.
• Cross-Functional Collaboration: Support the regulatory affairs team by coordinating UDI-related submissions and updates, liaising with internal stakeholders to resolve data discrepancies or inconsistencies.
• Compliance and Quality Assurance: Follow established procedures and adhere to quality and regulatory standards to ensure data integrity and mitigate risks.
• Process Improvement: Identify opportunities to enhance data accuracy and streamline processes, contributing to the efficiency of regulatory operations.

Qualifications and Skills

To thrive in this role, you should meet the following criteria:

• Education: Currently pursuing a bachelor’s degree in regulatory affairs, life sciences, biomedical engineering, or a related field.
• Core Competencies: Exceptional attention to detail, strong organizational skills, and the ability to follow instructions meticulously while adhering to established procedures.
• Technical Proficiency: Basic proficiency in Microsoft Office tools, particularly Excel, to support data management and reporting tasks.
• Soft Skills: Excellent communication and collaboration abilities to effectively engage with cross-functional teams and stakeholders.

Preferred Qualifications

While not mandatory, the following qualifications will enhance your candidacy:

• Familiarity with regulatory requirements or medical device industry standards, particularly within the Saudi Arabian healthcare landscape.
• A demonstrated interest in regulatory affairs and compliance, with a passion for contributing to healthcare innovation.

This internship is an exceptional opportunity to gain practical experience in a dynamic and impactful industry, working alongside industry leaders to shape the future of healthcare. If you are eager to develop your skills, contribute to meaningful projects, and grow within a supportive and innovative environment, we encourage you to apply.