This position contributes to the implementation and maintenance of the local Quality Management System, including document management, training, change controls, deviations, CAPAs, complaints, and audit readiness. The role also supports product launches, supplier quality activities, quality agreements, inspections, and key quality reporting, using electronic QMS tools such as Veeva, TrackWise, or similar digital platforms.
The specialist works closely with cross-functional teams including Regulatory Affairs, Supply Chain, and Quality colleagues across Iberia. Responsibilities may also include support for market release activities, controlled substance permits, plasma product submissions, and health authority communications when assigned, requiring strong collaboration and attention to detail in a complex, regulated environment.