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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 speler in de farmaceutische sector, is op zoek naar een Project Engineer Automation voor de uitvoering van automatisatieprojecten binnen equipment- en utilitiesomgevingen. De focus ligt op het volledige traject van specificatie en design tot de uiteindelijke oplevering van hoogwaardige process automation systemen.
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.
Onze klant, een toonaangevend farmaceutisch bedrijf, is op zoek naar ondersteuning voor batch-gerelateerde documentatie binnen een GMP-omgeving. De focus van het project ligt op data-integriteit van kleine apparatuur en het beheren van kwaliteitsdocumentatie zoals deviaties en CAPA's.
Our client, a leading biopharmaceutical organization, is seeking a Complaint Corporate Process Owner to manage and optimize global complaint management systems. This role ensures process compliance with international regulations while driving operational excellence through cross-functional collaboration and strategic oversight.
Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een Quality Specialist Operations om de operationele kwaliteitsnormen te waarborgen. De focus ligt op het ondersteunen van productie- en QC-afdelingen bij het naleven van wettelijke vereisten en interne standaarden.
Our client, a leading biopharmaceutical organization, is seeking a professional to support their biological development activities. This role combines operational shop floor presence with administrative quality assurance tasks to ensure compliance during the manufacturing of early-stage biologics. The project requires high adaptability in a dynamic environment where priorities can change frequently.
Our client, a leading global biopharmaceutical company, is looking for a professional to bridge the gap between business stakeholders and digital technology teams. The role involves evaluating, selecting, and implementing innovative digital solutions within a clinical development and regulatory context.
Onze klant, een vooraanstaand farmaceutisch bedrijf, is op zoek naar een Project Engineer Filling om engineeringprojecten voor formulatie-apparatuur te ondersteunen. De rol richt zich op het beheren van upgrades en nieuwbouwprojecten binnen aseptische productieprocessen om een betrouwbare levering van geneesmiddelen te waarborgen.
Our client, a leading pharmaceutical company, is seeking a Project Engineer to manage validation aspects for new product introductions. The role involves ensuring regulatory compliance and successful implementation across the product lifecycle, with a specific focus on assembly and packaging processes.
Onze klant, een internationale speler in de farmaceutische industrie, zoekt een Site Coordinator voor de begeleiding van diverse bouwprojecten. Deze rol focust op de coördinatie van multidisciplinaire brownfield projecten op een actieve productiesite.
Our client, a leading pharmaceutical organization, is seeking a Data Integrity Quality Lead to provide strategic leadership for their global data integrity maturity models. The role focuses on ensuring that all data generated and processed across GxP environments complies with international regulatory requirements and industry best practices while integrating new digital technologies.
Notre client, un leader international du secteur pharmaceutique, recherche un Project Coordinator pour soutenir le lancement d'un nouveau projet stratégique. Ce rôle se concentre sur la coordination opérationnelle et la gestion documentaire au sein d'une unité de production de pointe.
Honest answers to questions production consultants really ask.
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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