Overview
Hands-on role supporting quality management and regulatory compliance in med-tech.
Ideal candidate should be studying Biomedical Engineering or similar with knowledge of ISO standards.
2k eur / monthhybridentry-leveltemporaryfull-timeFrenchEnglish
Locations
France, Île-de-France, Paris
Requirements
Studying in Biomedical Engineering or similar Good knowledge of ISO standards Detail-oriented and organized
Responsibilities
Assist with regulatory submissions Collaborate with R&D teams
Benefits