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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 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.
Our client, a leading pharmaceutical organization, is seeking an Analyst for their raw materials laboratory. The role focuses on executing analytical tests and reporting results to ensure the highest quality standards for materials used in production.
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 prominent pharmaceutical organization, is seeking a Quality Specialist Operations to focus on quality oversight and project support. The role involves managing operational quality tasks and ensuring compliance within a strictly regulated production environment.
Our client, a leading pharmaceutical organization, is seeking a QA Officer to provide quality documentation support and operational quality assurance. This role focuses on maintaining high standards through risk assessments and documentation review while staying connected to the shop floor.
Our client, a leading organization in the life sciences sector, is seeking a dedicated professional to join their laboratory team. The role involves performing and evaluating complex analytical and microbiological tests within a strictly regulated quality control environment.
Our client, a leading life sciences organization, is seeking a specialist to assess and enhance a quality management system in alignment with EU GMP requirements. The role supports inspection readiness and a manufacturing import authorization project to enable compliant processes for clinical product certification.
Our client, a leading life sciences organization, is seeking an expert to lead comprehensive regulatory dossier assessments and file gap analyses. The project focuses on identifying compliance risks and developing scientific justifications to support regulatory submissions and health authority responses.
Our client is a specialized knowledge partner based in the province of Limburg, guiding international suppliers through the registration of biocidal products on the EU market. You'll be joining a small, ambitious team where in-house regulatory expertise is the core of what they do and where there's real room to take ownership as the organization grows into adjacent regulatory frameworks and international markets.
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.
Onze klant, een toonaangevende organisatie binnen de life sciences, is op zoek naar een PLC Technicus om de operationele betrouwbaarheid van elektrische installaties en instrumentatie te waarborgen. De focus ligt op het uitvoeren van onderhoud en technische optimalisaties binnen een hoogtechnologische productieomgeving.
Onze klant, een toonaangevende organisatie binnen de farmaceutische sector, is op zoek naar versterking voor een langdurig project op een productiesite. De focus ligt op het opstarten en kwalificeren van PLC-gestuurde systemen en mechanische installaties binnen een gereguleerde omgeving. De rol biedt de mogelijkheid om onder begeleiding van ervaren specialisten expertise op te bouwen in commissionering en kwalificatie.
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.
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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