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Validate computerised systems and data integrity, so software and automated systems meet regulatory requirements. Computer System Validation (CSV) in pharma.
Onze klant is een internationale organisatie gespecialiseerd in de farmaceutische verpakkingssector. In deze rol ben je verantwoordelijk voor het op niveau brengen en houden van de validatiestatus van systemen, processen en installaties conform de geldende farmaceutische wet- en regelgeving.
You do your work. We take care of the rest. Clear agreements and real support.
One dedicated Talent Manager who knows you, coaches you and thinks along with your next step. Before, during and after every project.
From an electric company car to 32 days of holiday. We discuss your expectations openly in the first conversation.
Decades of trusted relationships with leading pharmaceutical players give you access to projects you would not reach on your own.
Workshops, masterclasses and training, from Lean Six Sigma to project management, at your own pace.
Life Sciences projects tend to run long, which gives you stability. We plan your next step well before a project ends.
You make sure the systems and data behind production meet strict regulatory and data integrity requirements.
"I sit right where software, data and compliance meet. No two systems are the same."
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For most validation roles, yes, usually at master's level.
CSV proves that software, automated systems and data flows work as intended and meet data integrity and regulatory requirements.
Often, yes. Consultants move into CSV from validation, QA or digital backgrounds.
Yes. We propose concrete projects, you approve or decline. Only then do you meet the client.
We are happy to answer your questions or help you find your next project as a CSV Engineer.
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