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

BioTecNika Global; Riyadh; On-site; SAR 33,480 - 55,800; Full time

Job summary

Boston Scientific, Riyadh, invites a Regulatory Affairs Intern to support data governance, product data entry and regulatory activities under the Tamheer program. The hybrid internship engages you with SFDA databases, regulatory team collaboration and documentation for local health authorities.

The role emphasizes attention to detail, teamwork across regulatory, quality and engineering functions, and building exposure to medical device compliance pathways in a fast‑paced environment.

Qualifications

• Pursuing or recently completed a formal Bachelor’s degree in Regulatory Affairs, Life Sciences, Biomedical Engineering or a closely related health‑care discipline.
• Tamheer Program Eligibility: Eligibility to participate in the national Tamheer training scheme in Riyadh.

Responsibilities

• Saudi‑DI System Administration: Review, format, enter and update UDI product data fields within SFDA Saudi‑DI database.
• MDS‑REQ‑007 Implementation: Apply SFDA MDS‑REQ‑007 guidance to ensure active medical device profiles meet national mandates.
• UDI Document Repository Maintenance: Create, update and quality‑review internal UDI trackers for data alignment and audit readiness.
• Internal Data Triage Collaboration: Collaborate with cross‑functional teams to resolve missing or inconsistent product data points.
• Regulatory Submissions Support: Assist associates in compiling and submitting routine documentation to local health authorities.
• Process Efficiency Optimization: Follow SOPs and identify ways to improve data accuracy and velocity within the division.

Skills

Excel

Attention to detail

Written communication

Verbal communication

Cross-functional collaboration

Education

Bachelor’s degree in Regulatory Affairs

Bachelor’s degree in Life Sciences

Bachelor’s degree in Biomedical Engineering

Tools

Microsoft Excel

Job description

Regulatory Affairs Intern at Boston Scientific, Saudi Arabia

If you are a motivated life‑sciences student, an aspiring biomedical engineer, or a recent graduate, this full‑time internship at Boston Scientific offers a high‑impact corporate opportunity within the medical device industry. Located at our regional office in Riyadh and structured as a hybrid engagement under the national Tamheer framework, the role places you at the center of medical device compliance, data integrity, and local regulatory strategy.

As an early‑career specialist, you will gain practical exposure to the Saudi Food and Drug Authority (SFDA) databases and medical device regulations, working directly with the regulatory team that ensures all life‑saving medical devices entering the Kingdom comply fully with national policies.

Boston Scientific is a world‑leading global developer, manufacturer and marketer of innovative medical devices used across a broad array of interventional specialties. The Riyadh‑based regulatory team functions as the primary gatekeeper for medical device compliance, and this internship aligns with the Tamheer Program—Saudi Arabia’s specialized on‑the‑job training scheme for local university graduates.

Key Responsibilities

• Saudi‑DI System Administration: Review, format, enter and update Unique Device Identification (UDI) product data fields within the official SFDA Saudi‑DI database.
• MDS‑REQ‑007 Implementation: Apply the regulatory directives outlined in the SFDA MDS‑REQ‑007 guidance documents to guarantee that all active medical device profiles match national mandates.
• UDI Document Repository Maintenance: Create, update and perform continuous quality reviews on internal regulatory UDI trackers to ensure data alignment and audit readiness.
• Internal Data Triage Collaboration: Partner with cross‑functional supply chain, quality and engineering teams to resolve missing, incomplete or inconsistent raw product data points.
• Regulatory Submissions Support: Assist full‑time Regulatory Affairs Associates in compiling and submitting routine update documentation to local health authorities.
• Process Efficiency Optimization: Adhere strictly to established SOPs while identifying ways to improve data accuracy and process velocity within the local division.

Qualifications & Profile Requirements for Regulatory Affairs Intern

• 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 health‑care discipline.
  • Tamheer Program Eligibility: Eligibility to participate in the national Tamheer training scheme in Riyadh.
• Core Technical & Professional Competencies:
  • Basic proficiency using standard Microsoft Office applications, with a specific comfort level executing data‑tracking tasks in Microsoft Excel.
  • Highly developed attention to detail, strong organizational habits and the ability to systematically review alphanumeric product keys with zero errors.
  • Effective written and verbal communication, enabling collaboration across a diverse team.
  • An active interest in medical‑device industry standards, clinical compliance pathways or healthcare operations.

In short, this Regulatory Affairs internship under the Tamheer program at Boston Scientific provides a definitive pathway to transition your biomedical or life‑sciences background into a high‑value corporate compliance role. 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 to secure this premier opportunity in Saudi Arabia.