Internship - Medical Device Standards & Certification Preparation

Internship

Etterbeek

Job description

👉 You'll support the early-stage implementation of an ISO 13485 and/or FDA MD-compliant quality system by:

Mapping the standard's requirements to our current operations
Identifying documentation and process gaps
Assisting in the creation of SOPs, risk analysis files, traceability matrices, QMS, etc.
Supporting alignment across teams (product, software, operations)

Profile

Engineering, biomedical
Structured, detail-oriented, and able to synthesize standards
Interest in medical devices, regulatory affairs, or quality systems 👌

Why apply?

Full immersion in product, ops, and quality topics
Hands-on learning in a fast-moving femtech startup 🚀
A collaborative and supportive environment in the heart of Brussels

Conduct of interviews

First of all, we will contact you via email to schedule an online call. We'll get to know each other and discuss what you're looking for 🔎
☕️ Then, if the feeling goes well, we will go for a coffee together to deepen the topics that interest you.
And then, if it's a game, we'll go and create a breast pump from the space together 🚀

Diversity, inclusion and equal opportunities are important to us. Applicants are therefore selected on the basis of their qualities and skills, without distinction as to age, religion, origin, disability, sex or gender.

If you have a disability, learning difficulty or illness and would like to benefit from reasonable accommodation as part of the selection procedure, please mention this on your application. Just say so in your application. The conditions will be adapted as best we can so that you can apply in the best possible circumstances.