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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 organization in the pharmaceutical and biotechnology sector, is seeking a Validation Engineer to support the validation of equipment, systems, and processes. This role ensures that facilities, utilities, and computerized systems remain compliant with regulatory and quality requirements throughout their entire lifecycle.
Onze klant, een toonaangevend farmaceutisch bedrijf, zoekt een ervaren professional voor de opstart van een nieuwe productieomgeving. De focus van deze rol ligt op de kwalificatie van diverse apparatuur volgens de geldende GMP-standaarden binnen een grootschalig project.
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 seeking a QA Qualification Engineer to provide quality oversight for process and laboratory equipment. This role focuses on managing qualification activities throughout the system lifecycle to ensure strict compliance with international regulations and quality standards.
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 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.
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, a leading biotechnology organization, is seeking a professional to support the start-up of a new production facility. The project focuses on technical transfers, sterilization validation, and equipment introduction to expand therapeutic manufacturing capacity. This role ensures that all manufacturing processes are developed and validated according to the highest industry standards.
Our client, a leading life sciences organization, is seeking an expert to oversee validation activities for transport and CMO-manufactured products. This role ensures the compliance of validation lifecycles, protocols, and risk assessments while serving as a key technical point of contact for regulatory submissions and audits.
Onze klant, een toonaangevende organisatie binnen de farmaceutische sector, is op zoek naar een ingenieur voor het ontwikkelen en vastleggen van technische specificaties en normen. De focus van deze functie ligt op het opstellen van lastenboeken voor nieuwe projecten en het vertalen van procesvereisten naar concrete technische criteria.
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.
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.
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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