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Grifols Worldwide Operations seeks a QA Manufacturing Analyst to establish the Environmental Monitoring programme for aseptic manufacturing and water systems. You will report to the Quality Assurance Monitoring Supervisor and perform aseptic sampling and environmental monitoring across the site.
The role requires a B.Sc degree and 1–2 years in aseptic pharma/medical devices, with strong regulatory knowledge and experience in Grade C/D environments.
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
The QA Manufacturing Analyst is required for a new purification and aseptic filling plant for the blood protein albumin at Grifols Worldwide Operations (GWWO). Reporting directly to the Quality Assurance Monitoring Supervisor of GWWO, the role is for an experienced analyst who will perform aseptic sampling and environmental monitoring as part in the establishment of the Environmental Monitoring programme for aseptic manufacture and water systems for the manufacturing operations at GWWO.