We are a world leader in plasma‑derived medicines with a presence in more than 100 countries, and a growing global team of over 20,000 people. That’s why we need a Quality Auditor like you.

Misión del Rol

The role involves overseeing and conducting routine Good Manufacturing Practice (GMP) audits, as well as technical and specialized audits related to current products and potential licensing agreements. It also includes providing regulatory compliance guidance and support to the entire Quality organization, delivering training, and leading multidisciplinary teams and initiatives.

What Your Responsibilities Will Be

• Generate study protocols, reports, and standard departmental documentation.
• Review analytical results and related processes for assigned projects.
• Ensure knowledge and application of applicable working standards (GMP, SOPs, internal guidelines, GLP, etc.) in line with established procedures.