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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.
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.
Our client, a leading organization in the pharmaceutical and biotechnology sector, is seeking a Validation Engineer to support the validation of equipment, systems, and processes. This role ensures that facilities, utilities, and computerized systems remain compliant with regulatory and quality requirements throughout their entire lifecycle.
Onze klant is een internationale organisatie gespecialiseerd in de farmaceutische verpakkingssector. In deze rol ben je verantwoordelijk voor het op niveau brengen en houden van de validatiestatus van systemen, processen en installaties conform de geldende farmaceutische wet- en regelgeving.
Our client, a leading organization in the life sciences sector, is seeking a professional to ensure manufacturing processes are validated, documented, and maintained in compliance with global standards. This role involves collaborating across departments to validate new and existing processes, supporting product introductions, and maintaining a validated state throughout the lifecycle.
Our client, a leading pharmaceutical organization, is seeking an Equipment Validation Engineer to ensure the reliable and compliant operation of production systems. The role focuses on managing validation documentation and testing for mechanical equipment within multidisciplinary engineering and production projects.
Our client, a leading pharmaceutical organization, is looking for a Cleaning Validation Engineer to support their production site. This role focuses on ensuring that cleaning processes for equipment and systems are properly documented and validated in compliance with strict quality standards.
Our client, a leading organization in the life sciences sector, is seeking a professional to support computer system validation activities. The role focuses on ensuring that computerized and automated systems in GxP-regulated environments are fit for purpose and comply with both regulatory requirements and internal standards.
Onze klant, een toonaangevende organisatie binnen de biotechnologie, is op zoek naar een professional voor de kwalificatie van diverse procesinstallaties. In deze rol draagt men bij aan het projectvalidatieteam door systemen zoals bioreactoren, chromatografiekolommen en clean utilities tijdig te kwalificeren.
Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een Production Technician voor de technische en administratieve ondersteuning van het productieproces. De functie combineert praktische werkzaamheden aan de lijn met nauwkeurige documentatie en effectieve communicatie met interne technische afdelingen.
Our client, a prominent pharmaceutical organization, is looking for a hands-on Production Engineer to provide first-line technical support. This role ensures the continuity of the production line by troubleshooting process issues and coordinating team activities within a regulated environment.
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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