General Responsibility Plan, review, record, edit and answer questions from the work of analysts in the laboratory and, when appropriate, open OOS or deviations and notify Quality Assurance and plan, create tables, studies SAP introducing in climatic chambers and monitor samples of each batch; according to GMP regulations, operating procedures, Methods of Analysis, Good Laboratory Practices, Protocols and guidelines Stability direct superior; so that the results areconsistent, to apply actions to correct deviations, duly recorded anomalous results, the study of stability, keeping the team updated and informed and, ultimately, confirm that batches behave like and registered. All this taking into
📌 Técnico Estabilidades Control De Calidad (España)
🏢 Chemo
📍 España