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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 prominent life sciences organization, is seeking an professional to manage the qualification and testing of Master Batch Records. The role focuses on the development, writing, and execution of test protocols within a manufacturing execution system to ensure compliance with industry standards.
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 life sciences organization, is seeking a Learning Operations Coordinator to provide hands-on support for their learning technology ecosystem. This role focuses on user enablement, ticket management, and ensuring system compliance during a transition period. The professional will manage platform housekeeping and coordinate with third-party vendors to maintain service levels.
Our client, a leading organization in a regulated industry, is looking for a Data Operations & Orchestration Specialist to manage critical master data elements. This role ensures that data integrity within the project enables optimal material planning, production, and financial processes through efficient coordination and system maintenance.
Our client, a leading pharmaceutical organization, is seeking a MBR Coordinator to support the startup of a new production facility. The project focuses on ensuring quality readiness, operational excellence, and regulatory compliance during the commissioning phase. This role is essential for managing the transition to operational status through meticulous batch record oversight and GMP adherence.
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.
Our client, a fast-growing MedTech organization, is seeking a professional to establish their quality foundations and guide their initial regulatory submission. This role focuses on building a robust quality framework for an innovative surgical software platform.
Onze klant, een toonaangevend farmaceutisch bedrijf, is op zoek naar een Quality Project Associate. In deze rol is men verantwoordelijk voor de kwaliteits- en productregistratieactiviteiten om de introductie van nieuwe producten te ondersteunen.
Onze klant, een toonaangevend farmaceutisch bedrijf, zoekt een Project Engineer Filling om engineeringprojecten voor farmaceutische formulatie-apparatuur te ondersteunen. Deze rol richt zich op de realisatie van zowel upgrades als nieuwbouwprojecten binnen een aseptisch productieproces.
Our client, a pharmaceutical organization, is seeking a Quality Operational Readiness Officer for the start-up of a new production facility. This role focuses on ensuring quality readiness and compliance during the transition from construction to operational status. The position coordinates qualification activities and maintains high GMP standards throughout the commissioning phase.
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.
"It is detailed work, but knowing it keeps products safe makes it worth it."
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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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