Role Overview
As a Compliance Intern, you will support Nuclivision’s quality and regulatory efforts by maintaining our ISO 13485 certification, contributing to the ISO 27001 setup, and gaining hands-on experience with EU MDR and FDA regulatory documentation for AI-based Software as a Medical Device (SaMD). Key tasks include:
- Assisting in the maintenance and improvement of the Quality Management System (QMS) to uphold ISO 13485 standards.
- Supporting the implementation of information security policies for ISO 27001 compliance.
Required Qualifications
- Bachelor’s degree (or ongoing studies) in biomedical engineering, regulatory affairs, health sciences, computer science, law, or a related field.
- Interest in medical device regulations, quality management systems, and cybersecurity compliance.
- Strong analytical, organizational, and documentation skills.
- Full proficiency in English.
- Detail-oriented and able to work independently.
What We Offer
- Work from the Wintercircus campus in Ghent at least one day per week.
- A dynamic startup environment with direct exposure to MedTech compliance processes.
- The opportunity to apply and develop academic knowledge in real-world regulatory settings.
- Hands-on experience in ISO 13485, ISO 27001, EU MDR, and FDA regulatory landscapes.
- A young, driven, and collaborative team to work with.
Location: Ghent, Belgium
Duration: 1 to 6 months
How to Apply
Please complete the form below and indicate in your motivation letter if you intend to undertake this internship as part of your student curriculum (for ECTS credits).
