Regulatory Affairs Intern at Boston Scientific, Saudi Arabia | Life Sciences Candidates Eligible

Regulatory Affairs Intern at Boston Scientific, Saudi Arabia | Life Sciences | Apply Now

If you are a motivated life sciences student, an aspiring biomedical engineer, or a recent graduate looking to secure a high-impact corporate footprint in the medical device industry, this full-time internship at Boston Scientific is an exceptional opportunity. Located at our regional office in Riyadh, Saudi Arabia, and structured as a hybrid engagement under the national Tamheer framework, this position places you at the center of medical device compliance, data integrity, and local regulatory strategy. For organized, early-career specialists tracking a competitive Regulatory Affairs Intern opening, this role provides practical exposure to the Saudi Food and Drug Authority (SFDA) databases and medical device regulations. It serves as an elite corporate milestone to launch an exceptional career with a global market leader and stands out as a premier selection for individuals looking to lock in a prestigious Life Sciences Internship or a flexible Regulatory Affairs Internship in Saudi Arabia.

About The Company

Boston Scientific is a world-leading global developer, manufacturer, and marketer of innovative medical devices used across a broad array of interventional medical specialties. Recognized globally as a Glassdoor Best Place to Work in 2026 (ranking No. 15 on the Top 100 list), Boston Scientific shapes the future of healthcare by designing high-performance therapies that treat complex cardiovascular, respiratory, digestive, oncological, and neurological conditions. The Riyadh-based regulatory team functions as the primary gatekeeper ensuring all life-saving medical devices entering the Kingdom comply fully with national healthcare policies. This internship is aligned with the Tamheer Program—Saudi Arabia’s specialized on-the-job training scheme for local university graduates. Joining Boston Scientific through this track embeds you within an advanced corporate ecosystem where you receive direct mentorship from regulatory executives while helping execute complex compliance portfolios that impact real patient outcomes across the region.

Regulatory Affairs Intern – Key Responsibilities

The Regulatory Affairs Intern functions as a vital data management engine, taking direct operational ownership over product identification records, data integrity tracking, and cross-functional regulatory updates.

Your core regulatory tracking, data entry, and database compliance duties include:

• Saudi-DI System Administration: Reviewing, formatting, entering, and updating Unique Device Identification (UDI) product data fields within the official SFDA Saudi-DI database.
• MDS-REQ-007 Implementation: Applying the precise regulatory directives outlined in the SFDA MDS-REQ-007 guidance documents to guarantee all active medical device profiles match national mandates.
• UDI Document Repository Maintenance: Creating, updating, and performing continuous quality reviews on internal regulatory UDI trackers to ensure data alignment and audit readiness to advance this Regulatory Affairs Intern assignment.
• Internal Data Triage Collaboration: Partnering with cross-functional supply chain, quality, and engineering teams to resolve missing, incomplete, or inconsistent raw product data points.
• Regulatory Submissions Support: Assisting full-time Regulatory Affairs Associates in compiling and submitting routine update documentation to local health authorities to maximize your Life Sciences Internship milestones.
• Process Efficiency Optimization: Adhering strictly to established corporate standard operating procedures (SOPs) while actively identifying ways to optimize data accuracy and process velocity within the local division.

Qualifications & Profile Requirements For Regulatory Affairs Intern

Boston Scientific seeks a detail-oriented, collaborative professional who demonstrates a strong passion for healthcare compliance and an ability to follow rigorous data entry instructions.

• Required Academic Foundations:
• Educational Enrollment: Currently pursuing or recently completed a formal Bachelor’s degree in Regulatory Affairs, Life Sciences, Biomedical Engineering, or a closely related natural science/healthcare discipline.
• Tamheer Program Eligibility: Eligibility to participate in the national Tamheer training scheme framework in Riyadh to qualify for this Regulatory Affairs Internship in Saudi Arabia.
• Core Technical & Professional Competencies:
• Basic, foundational proficiency using standard Microsoft Office applications, with a specific comfort level executing data tracking tasks in Microsoft Excel.
• Highly developed natural attention to detail, strong organizational habits, and the ability to systematically review alphanumeric product keys with zero errors.
• Effective written and verbal communication traits, enabling comfortable collaboration across a diverse team environment.
• An active, demonstrable interest in medical device industry standards, clinical compliance pathways, or healthcare operations.

In short, the Regulatory Affairs Internship under the Tamheer program at Boston Scientific is a definitive route to transitioning your biomedical or life sciences background into a high-value corporate compliance asset. Securing an appointment here allows you to move past general observation tracks and take direct, hands-on operational charge of the SFDA database registries, UDI tracking parameters, and localized compliance metrics that clear life-saving medical tech for hospital distribution. If you reside in Riyadh, match the bachelor’s science baseline, and possess an analytical, error-free approach to data governance, apply via the portal today to secure this premier choice in a Regulatory Affairs Intern trajectory, jumpstart an exceptional corporate path, and lock in this outstanding Life Sciences Internship milestone.

APPLY ONLINE HERE