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Civil Engineer →
The same engineering craft inside a regulated environment. You calculate the loads, design and follow up the works, and document every step to prove it holds up.
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The Civil roles we recruit for on pharmaceutical sites.
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The same engineering craft inside a regulated environment. You calculate the loads, design and follow up the works, and document every step to prove it holds up.
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You supervise the works on site, from civil works to cleanroom builds, coordinating trades, tracking progress and enforcing safety and quality standards every step of the way.
Civil engineering stays civil engineering. It is the environment around it that asks something extra.
Far more has to be recorded and proven. That asks for a certain kind of person, with the patience to document as carefully as they build.
Building a cleanroom is its own discipline. Earlier cleanroom experience is often required for those projects.
Not every project sits in the regulated zone. A new hall outside it asks nothing extra, and purely civil work such as stairs or bridges asks no pharma background at all.
Filter by role, location or contract type. Or click through to a specific role above.
Onze klant, een vooraanstaande organisatie in de farmaceutische sector, is op zoek naar een Project Engineer Co-Development om de introductie van nieuwe molecules te faciliteren. Deze rol richt zich op het begeleiden van producten van laboratoriumfase tot lancering, met een sterke focus op process design en projectmanagement. Het doel is de ontwikkeling van robuuste processen en de tijdige oplevering van klinisch materiaal binnen een innovatieve omgeving.
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.
Onze klant, een vooraanstaande organisatie binnen de life sciences sector, is op zoek naar een deskundige voor de ondersteuning van diverse investerings- en verbeteringsprojecten. De focus ligt op het coördineren en opvolgen van alle validatie- en kwalificatieactiviteiten voor cleanrooms en technische installaties binnen een multidisciplinaire omgeving.
Onze klant, een toonaangevend bedrijf in de farmaceutische sector, is op zoek naar een gedreven professional voor het onderzoek naar analytische afwijkingen binnen laboratoriumomgevingen. De rol richt zich op het waarborgen van productkwaliteit door middel van diepgaande root cause analyses en het implementeren van structurele verbeteringen.
Onze klant, een toonaangevend bedrijf binnen de farmaceutische sector, is op zoek naar een professional voor het beheer van validatie-aspecten bij de introductie van nieuwe producten. De rol richt zich op de succesvolle implementatie en regelgevende naleving gedurende de volledige productlevenscyclus. Een pragmatische, proactieve en resultaatgerichte aanpak staat centraal binnen dit project.
Our client, a leading biotechnology organization, is seeking an experienced professional to manage quality investigations and process improvements. This role is responsible for driving excellence in compliance and manufacturing within a highly regulated environment.
Our client, a leading pharmaceutical organization, is seeking a professional to provide commercial manufacturing support and process optimization. The role focuses on technology transfer activities to facilitate the introduction of new products and processes within a large-scale manufacturing environment.
Our client, a leading organization in the pharmaceutical sector, is seeking a professional to support engineering and construction projects at a GMP-regulated site. This role involves taking ownership of safety aspects during the design and realization phases, ensuring both process and construction safety for diverse project scopes.
Onze klant, een toonaangevende speler in de farmaceutische industrie, is op zoek naar een expert voor het leiden van veiligheidsstudies. Deze rol richt zich op het faciliteren van complexe risicoanalyses en het waarborgen van de procesveiligheid binnen een hoogtechnologische omgeving.
"Technically it is the work I have always done. What I had to get used to is that here you also prove it, step by step."
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Honest answers to the questions civil profiles really ask.
Usually not, and it depends on the project. A lot of this work is straightforward civil engineering, and experience from food or another industry counts fully.
Stricter regulation and much more documentation. The building is the same; the proof around it is not.
On cleanroom projects it is often required. Outside the regulated zone it makes no difference.
Yes. The same roles exist in our Engineering competence center, for other industries. The vacancies are kept separate, so if you are open to both it is worth looking at the Engineering pages as well.
Not every project runs on a pharmaceutical site. Our Engineering colleagues place the same profiles in infrastructure, industry and energy. Follow the link to see what is open there.
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