Engineering Intern – Regulatory

The Regulatory Intern will play a key role in strengthening Medifab’s regulatory compliance and technical documentation by building well-structured Device Master Records (DMRs) and CE technical files. This role focuses on collecting, organising, and indexing critical documents so that product information can be accessed at the device, family, and SKU levels. In addition, the intern will support material compliance by reviewing risk files, compiling a controlled materials register, and linking specifications and test evidence to products. By ensuring documentation is complete, traceable, and aligned with regulatory expectations, the Regulatory Intern will help lay the foundation for robust submissions, smoother audits, and long-term product compliance.