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Project Engineer Pharma Production →
You manage several projects across different phases at once, from planning and resources to validation, in the pilot plant.
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The production roles we recruit for.
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You manage several projects across different phases at once, from planning and resources to validation, in the pilot plant.
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You sit between quality and assurance, keeping production documentation and processes compliant on the floor.
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You keep one production line running and improving, as the point of contact between operators, planning and management.
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You set up, upgrade and validate new formulation and filling lines, from specifications to FAT and SAT.
Production runs across several stages, each with its own pace and kit.
Where new production methods are developed, proven at scale and transferred between sites without losing capacity.
Set up, upgrade and validate the equipment and lines behind production, from compounding to packaging.
Validate, improve, coordinate and implement new processes once production runs at full scale.
Filter by role, location or contract type. Or click through to a specific role above.
Onze klant, een vooraanstaande organisatie binnen de life sciences, zoekt een gedreven professional voor de installatie en kwalificatie van technische projecten. De focus ligt op het beheren van multidisciplinaire trajecten van de ontwerpfase tot de finale oplevering binnen een streng gereguleerde productieomgeving.
Our client, a pharmaceutical organization, is seeking an experienced professional to ensure quality readiness and compliance for the startup of a new production facility. The role coordinates quality-related activities during the facility qualification phase to ensure a seamless transition from construction to operational status. This position maintains full regulatory compliance and GMP standards throughout the commissioning process.
Onze klant, een toonaangevende organisatie in de medische technologie, zoekt een ervaren projectmanager voor het leiden van strategische automatiseringsinitiatieven. De rol richt zich op het handhaven van strikte projectcontroles, budgetbewaking en leveranciersbeheer voor grootschalige investeringen in distributiecentra. De focus ligt op de uitvoering van projectmanagementprocessen terwijl het engineeringteam de technische verantwoordelijkheid behoudt.
Our client, a leading global biopharmaceutical company, is seeking a strategic leader to drive evidence generation strategies. This role focuses on designing and implementing real-world evidence and outcomes research to support product value and regulatory submissions within a specific disease area.
Notre client, une entreprise leader dans le secteur des sciences de la vie, recherche un profil pour évaluer les risques chimiques des matériaux en contact avec les produits. Le projet consiste à définir les standards techniques pour les systèmes à usage unique, les filtres et les matières entrantes.
Our client, a global pharmaceutical leader, is seeking a Microbiology Expert – Small Molecules to support clinical and lifecycle management programs. This role involves coordinating global microbiology activities and providing scientific expertise in method qualification and validation within an R&D environment.
Onze klant, een vooraanstaande organisatie binnen de farmaceutische sector, is op zoek naar een Data Integrity Consultant. De focus van deze rol ligt op het uitvoeren van compliance reviews voor analytische systemen en computerized toepassingen binnen productie- en kwaliteitsafdelingen.
Our client, a leading biopharmaceutical organization, is seeking an expert to join their analytical science and technology department. The role focuses on driving analytical excellence by developing and implementing critical methods to ensure the quality and consistency of cell culture-based manufacturing processes.
Our client, a leading organization in the pharmaceutical sector, is looking for a Process Engineer to optimize their highly automated production facilities. The project involves driving technical improvements, overseeing equipment updates, and managing new product introductions to ensure seamless manufacturing processes.
Our client, a leading life sciences organization, is seeking a specialist to provide quality oversight and functional governance for computerized systems. The role combines independent QA-CSV validation support for manufacturing automation with the site-wide implementation of a digital checklist management system.
Not necessarily. Bio, industrial or civil engineer all fit, and biomedical, biotech or pharma backgrounds are welcome too. What really counts is how you think.
It is possible, but your profile needs to stand out. Most roles ask for a master's and ideally one to two years of experience. For graduates, strong soft skills and things like taking the lead in a student club or the scouts can make the difference.
For production roles, often yes: early and late shifts, with a shift premium. Weekend and night work stay exceptional, and we are upfront about it from the start.
There is no remote work in the first year. After that, one day a week is standard, regardless of performance. We are transparent about this from the start.
Projects run for at least a year and are often extended to three or four. That gives you real stability.
It is a proper learning school with modern kit. You specialise, build real expertise and grow from there.
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