Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking an experienced Quality Assurance Specialist in Spain . Responsible for batch release, GMP compliance, quality systems management, supplier oversight, audit support, and continuous improvement initiatives to ensure product quality and regulatory compliance. Although the primary location for this role is Madrid , the selected candidate will be required to work 100% on site in Azuqueca de Henares (Madrid) for the duration of the project. Review and approve specifications for APIs, raw materials, packaging components, bulk products, and finished products. Approve or reject raw materials, packaging materials, bulk, and finished product batches in SAP. Issue and approve Certificates of Analysis (CoA) and release documentation for commercial and regulatory purposes. Monitor and assess deviations, non-conformities, OOS/OOT investigations, and related quality events affecting batch disposition. Review stability protocols, retention samples, and stock-control status to support product release decisions. Support customer requests, quality technical agreements, product registration activities,



and supplier complaint management. Quality Systems & Compliance Manage Change Controls, CAPAs, deviations, complaints, root-cause investigations, and trend analysis activities. Oversee document control processes, including issuance, distribution, archival, and management of controlled GMP documentation. Support GMP training programs and provide guidance on quality compliance matters. Prepare and review Annual Product Reviews (APR/PQR) and other quality system reports. Participate in supplier qualification, certification, performance monitoring, and audit activities. Review environmental, microbiological, temperature, and pressure monitoring data to ensure GMP compliance. Support quality investigations, recalls, and Qualified Person (QP) activities. Manage quality relationships with suppliers and third parties, ensuring compliance with technical and quality agreements. Act as a subject matter expert by training and mentoring new team members on quality processes and GMP requirements. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.

📌 Quality and Training Technician (Madrid)
🏢 Pqe Group
📍 Madrid