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Equipment Validation Engineer →
You qualify process and lab equipment through IQ, OQ and PQ, and make sure installations are ready for reliable production.
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The validation roles we recruit for.
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You qualify process and lab equipment through IQ, OQ and PQ, and make sure installations are ready for reliable production.
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You design and validate cleaning procedures that prevent cross contamination between products, in line with GMP requirements.
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You validate computerised systems and data integrity, so software and automated systems meet regulatory requirements.
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You prove that manufacturing processes consistently meet their specifications, across design, qualification and ongoing verification.
Validation covers several areas. You can specialise in one or work across them.
Qualify machines and installations through IQ, OQ and PQ, from arrival to production readiness.
Prove that cleaning removes residues to safe limits between products and batches.
Validate software, automated systems and data integrity against regulatory requirements.
Prove that established production processes consistently meet their specifications over time.
Filter by role, location or contract type. Or click through to a specific role above.
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 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.
Our client, a leading biotechnology organization, is seeking a professional to support the start-up of a new production facility. The project focuses on technical transfers, sterilization validation, and equipment introduction to expand therapeutic manufacturing capacity. This role ensures that all manufacturing processes are developed and validated according to the highest industry standards.
Our client, a leading pharmaceutical organization, is seeking a professional to ensure the end-to-end validation of new products across formulation, filling, and packaging. This role focuses on supporting product launches through rigorous documentation, production follow-up, and quality investigations within a dynamic project environment.
Our client, a leading pharmaceutical company, is seeking a professional to manage product and project lifecycles within their technical services department. The role focuses on providing end-to-end validation support and managing quality investigations to ensure seamless production and new product introductions.
Our client, a prominent organization in the life sciences sector, is looking for a specialist to bridge the gap between IT and Quality Assurance. The role involves ensuring IT systems and processes remain compliant with GxP regulations through audit leadership, CAPA management, and document control.
Our client, a leading life sciences organization, is seeking an expert to oversee validation activities for transport and CMO-manufactured products. This role ensures the compliance of validation lifecycles, protocols, and risk assessments while serving as a key technical point of contact for regulatory submissions and audits.
Our client, a leading pharmaceutical organization specialized in innovative cell therapies, is seeking a CAR-T QA C&Q Engineer. This role focuses on ensuring the qualification status of critical production assets and managing compliance for facilities, utilities, and process equipment. The position involves acting as a quality process expert and supporting international regulatory inspections.
Our client, a leading biotechnology company specializing in advanced therapies, is seeking a professional to lead manufacturing investigations. The role focus on driving root cause analysis and ensuring process robustness within a cell and gene therapy environment.
Onze klant, een toonaangevend farmaceutisch productiebedrijf, is op zoek naar een ervaren professional voor de strategische aansturing van C&Q-activiteiten. De focus van deze rol ligt op het bepalen van de aanpak voor complexe PLC-, automatisatie- en mechanische systemen binnen een gereguleerde omgeving.
Onze klant, een vooraanstaande farmaceutische producent, is op zoek naar een C&Q Engineer om een omvangrijk project te ondersteunen. De rol focust op het volledige traject van commissioning en kwalificatie voor zowel automatisatie- als mechanische systemen, van testplan tot turnover package.
Honest answers to questions validation consultants really ask.
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.
Yes. You can focus on equipment, cleaning or computer system validation, or work across all three.
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.
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