I am working with a highly innovative biotech company based in Barcelona, specializing in the development of groundbreaking medical devices. We are looking for a Regulatory Affairs & Quality Assurance Specialist to join their team.

Ideal Profile:
Experience in regulatory strategies and documentation preparation for CE Marking and FDA submissions.
Implementation of Quality Management Systems (ISO 13485, MDR).
Project management in Class IIa medical devices.
What the Role Offers:
The opportunity to be part of a biotech company developing high-impact medical technology for cardiovascular disease prevention.
Hybrid work model (remote/in-office in Barcelona).
A dynamic and innovative environment with a competitive salary.