Gitte Neess Eir is a Senior QA Engineer at AFRY, leveraging over 30 years of experience in the pharmaceutical industry, particularly in validation and GxP compliance. They have worked with risk-based validation approaches for the past four years, focusing on developing user requirement specifications, validation plans, and conducting risk assessments. Gitte has held various validation roles in organizations such as Novo Nordisk and Statens Serum Institut, and they have a background in chemical engineering, having studied at Laborantskolen i Hovedstadsområdet and Aarhus Teknisk Skole.
Location
Copenhagen, Denmark
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