She graduated in Chemistry at the University of Barcelona and has over twenty year’s professional experience in the pharmaceutical industry as QC and R&D manager. This background in managing quality and development teams in multinational companies has enabled her to acquire an overview of the regulatory requirements and the needs of drugs manufacturing.
She is a third party qualified auditor in GMP/ GDP/ GLP for drugs, APIs, medical devices food supplements and also CRO’s (bioequivalence studies).
In 2004 she began her career as a consultant. Since then she has delivered about one hundred projects for forty different companies .
As a passionate of quality she became a Six Sigma Black B...
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pharmaceuticalqbdichq10ichq9ichq8validationsix sigmaqualityquality by designbiotechnology and pharmaceuticalsdevelopmentpharmaknowledge managementrisk managementgmpengineeringfarma consultor validaciones
She graduated in Chemistry at the University of Barcelona and has over twenty year’s professional experience in the pharmaceutical industry as QC and R&D manager. This background in managing quality and development teams in multinational companies has enabled her to acquire an overview of the regulatory requirements and the needs of drugs manufacturing.
She is a third party qualified auditor in GMP/ GDP/ GLP for drugs, APIs, medical devices food supplements and also CRO’s (bioequivalence studies).
In 2004 she began her career as a consultant. Since then she has delivered about one hundred projects for forty different companies .
As a passionate of quality she became a Six Sigma Black B...
Marcadores
pharmaceuticalqbdichq10ichq9ichq8validationsix sigmaqualityquality by designbiotechnology and pharmaceuticalsdevelopmentpharmaknowledge managementrisk managementgmpengineeringfarma consultor validaciones
