Regulatory Affairs Intern - Medical Device Compliance

BioTecNika Global; Riyadh; Hybrid; 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

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.