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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.
Our client, a leading pharmaceutical company, is seeking a professional to manage product and project lifecycles within their technical services department. The role focuses on providing end-to-end validation support and managing quality investigations to ensure seamless production and new product introductions.
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 Compliance Engineer to serve as the primary point of contact for quality and compliance matters within their technical operations. This role bridges the gap between engineering, maintenance, and qualification by ensuring all processes align with rigorous quality standards.
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.
Our client, a leading pharmaceutical organization, is seeking a professional to ensure the end-to-end validation of new products across formulation, filling, and packaging. This role focuses on supporting product launches through rigorous documentation, production follow-up, and quality investigations within a dynamic project environment.
Our client, a leading pharmaceutical company, is seeking a Project Engineer to manage validation aspects for new product introductions. The role involves ensuring regulatory compliance and successful implementation across the product lifecycle, with a specific focus on assembly and packaging processes.
Onze klant, een toonaangevend bedrijf in de life sciences, is op zoek naar een coördinator om validatieactiviteiten binnen complexe projecten te sturen. De rol focust op het aansturen van projectteams en het waarborgen van tijdige oplevering van systeem- en equipmentvalidatie.
Our client, a leading biotechnology company specializing in advanced therapies, is seeking a professional to lead manufacturing investigations. The role focus on driving root cause analysis and ensuring process robustness within a cell and gene therapy environment.
Our client, a leading pharmaceutical organization, is looking for a Cleaning Validation Engineer to support their production site. This role focuses on ensuring that cleaning processes for equipment and systems are properly documented and validated in compliance with strict quality standards.
Our client, a leading pharmaceutical organization, is seeking an Equipment Validation Engineer to ensure the reliable and compliant operation of production systems. The role focuses on managing validation documentation and testing for mechanical equipment within multidisciplinary engineering and production projects.
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.
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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