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Design and validate cleaning procedures that prevent cross contamination between products, using sampling strategies, worst case assessments and residue limits, all in line with GMP.
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.
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 international pharmaceutical organization, is seeking an autonomous expert to oversee cleaning validation strategies across multiple production units. This role focuses on high-level expertise and the strategic revamp of documentation structures within a dynamic and fast-paced site environment.
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 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, 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 leading pharmaceutical organization, is seeking a senior expert to support their production and supply chain facility. This role focuses on providing quality oversight and acting as a subject matter expert for cleaning validation activities to ensure regulatory compliance and reliable supply.
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.
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.
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.
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.
Your work makes sure no residue carries over between products. It is quality and patient safety in practice.
"It is detailed work, but knowing it keeps products safe makes it worth it."
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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 a Cleaning Validation Engineer.
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