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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, een vooraanstaande organisatie binnen de farmaceutische sector, is op zoek naar een MBR Editor om de digitalisering van productieprocessen te ondersteunen. De rol focust op het vertalen van operationele processen naar geavanceerde beheersystemen in nauwe samenwerking met diverse projectteams.
Onze klant, een toonaangevend farmaceutisch bedrijf, is op zoek naar een Pas-X MBR Design Specialist voor een grootschalig IT-moderniseringsproject. De rol richt zich op de overgang van legacy-systemen naar een geavanceerd MES-platform door het ontwerpen en implementeren van conforme elektronische batchdocumentatie.
Our client, a leading global healthcare organization, is seeking a specialist to manage logistics quality compliance and deviation management. The role focuses on driving the full lifecycle of non-conformances and root cause investigations to ensure operational excellence within a regulated supply chain environment.
Our client, a leading pharmaceutical organization, is seeking a professional to manage and execute validation activities for computerized systems. The project involves ensuring that all cGMP-critical software packages remain compliant with regulatory and user requirements.
Our client, a leading pharmaceutical company, is seeking a CSV Engineer to support the validation of cGMP-critical computerized systems. The role focuses on ensuring systems remain compliant with applicable regulatory and quality requirements through hands-on validation activities.
Our client, a leading pharmaceutical company, is seeking a CSV Engineer to support the validation of cGMP-critical computerized systems. The role focuses on ensuring systems remain compliant with applicable regulatory and quality requirements through hands-on validation activities.
Our client, a leading organization in the life sciences sector, is seeking a professional to support computer system validation activities. The role focuses on ensuring that computerized and automated systems in GxP-regulated environments are fit for purpose and comply with both regulatory requirements and internal standards.
Our client is seeking a Project Documentation & Validation Coordinator to join their engineering team. The role involves managing project documentation and executing validation activities to ensure compliance across various engineering disciplines.
Our client, a leading manufacturer of pharmaceutical production equipment, is seeking validation professionals to support their automated systems. The project focuses on testing complex machinery on both physical and simulated platforms within a strictly regulated environment.
Our client, a prominent pharmaceutical organization, is looking for a hands-on Production Engineer to provide first-line technical support. This role ensures the continuity of the production line by troubleshooting process issues and coordinating team activities within a regulated environment.
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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