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Qualify process and lab equipment through IQ, OQ and PQ, and make sure installations are ready for reliable production. Prove that machines and installations do what they should.
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.
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.
Onze klant, een toonaangevende organisatie binnen de biotechnologie, is op zoek naar een professional voor de kwalificatie van diverse procesinstallaties. In deze rol draagt men bij aan het projectvalidatieteam door systemen zoals bioreactoren, chromatografiekolommen en clean utilities tijdig te kwalificeren.
Our client is seeking a professional to support commissioning and qualification activities within a highly regulated environment. The role focuses on ensuring project compliance and managing periodic activities autonomously to meet technical standards.
Our client, a leading organization in the life sciences sector, is seeking a professional to ensure manufacturing processes are validated, documented, and maintained in compliance with global standards. This role involves collaborating across departments to validate new and existing processes, supporting product introductions, and maintaining a validated state throughout the lifecycle.
Our client, a prominent life sciences organization, is seeking an professional to manage the qualification and testing of Master Batch Records. The role focuses on the development, writing, and execution of test protocols within a manufacturing execution system to ensure compliance with industry standards.
Our client, a leading biopharmaceutical company, is seeking an experienced Site/Construction Supervisor for a large-scale new-build project. The role focuses on overseeing the construction and fit-out phase of a state-of-the-art production facility, ensuring all technical systems and cleanroom environments meet industry standards.
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 take equipment from installation through IQ, OQ and PQ until it is proven ready for production.
"Every qualification I sign off means the line can run with confidence."
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For most validation roles, yes, usually at master's level.
Yes, validation is documentation heavy: writing and reviewing protocols, reports and risk assessments, combined with on site checks and execution.
Often, yes. Consultants move into validation from QA, lab or engineering 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 an Equipment Validation Engineer.
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