About WERFEN:

WERFEN is a global leader in specialized diagnostics in the fields of hemostasis, acute care, autoimmunity, transfusion, and transplantation. Our core business focuses on the research and development, manufacturing, and distribution of innovative diagnostic systems for hospitals and clinical laboratories, with the purpose of improving patient care. We are a family-owned company founded in 1966 in Barcelona, Spain.

We have direct presence in more than 30 countries and distribute our products in over 100 countries worldwide.

Our purpose: to contribute to the advancement of patient care globally through specialized and innovative diagnostics. The patient is always at the center of our strategies, decisions, and everything we do.

Our DNA: we are passionate about our work, and everything we do is dedicated to serving the healthcare community.

More than 7,000 employees are part of our family. Join us and let’s continue growing together.

Responsibilities

• Maintenance and updating of regulatory dossiers.
• Participation in internal improvement projects, contributing to the optimization of department processes.
• Preparation and review of the documentation required for international registrations of medical devices.

Educational Objective of the Position

• Enable the student to become familiar with the complete lifecycle of medical device registrations, from preparation to ongoing maintenance.
• Provide a practical understanding of the daily work carried out by a Regulatory Affairs team, enhancing learning in a real professional environment.

Profile

• Bachelor’s degree in any business‑related field (or equivalent).