About this role
¿Dónde quiSIERAS trabajar? Legal, Compliance & Regulatory Affairs Medical Device Regulatory Data & AI Intern - Países Bajos - Hoofddorp - Hybrid - Temporary Full-Time - 6 months - Publicado: 6 Jul 2026 Sobre el trabajo In this internship, you will design, build and maintain a structured, scalable regulatory compliance database supporting global registrations for a portfolio of medical devices. The role combines regulatory knowledge with data, digitalization and AI to improve compliance, accelerate local registrations, facilitate participation in tenders and automate tracking across global markets. Responsibilities: • Collect and align the need in collaboration with regulatory stakeholders across all key markets. • Build and maintain a centralized regulatory database • Track Medical device documentation (CE marking, Notified Body certificates, Declarations of Conformity, and product labelling). • Map and monitor country registrations across EU and international markets. • Implement automated tracking systems for expiries and renewals. • Develop a structured intake and tracking system for regulatory requests. KPI's: • Completeness of regulatory documentation (>90%). • Database accuracy and usability. • Timely identification of expiring certificates • Stakeholder satisfaction and response time. • Automation level achieved (alerts, dashboards, workflows). Meet your future manager! Your manager will be Barthélémy Arman, Senior Global Regulatory Affairs Manager. Learn more about them: Barthélémy Arman | LinkedIn Sobre ti Two complementary profiles are welcome: - Regulatory / Medical Device Profile: - Background in regulatory affairs, life sciences or biomedical field. - Understanding of EU MDR, CE marking and documentation requirements. - Strong interest in data structuring, digital tools and AI applications. - Technical / Digital Profile: - Background in data science, software engineering or similar. - Experience ...