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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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Work in Validation
You design and execute IQ, OQ and PQ protocols that prove that equipment, processes and systems perform as intended, keeping production reliable and compliant.
The roles in this domain
The validation roles we recruit for.
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Cleaning Validation Engineer →
You design and validate cleaning procedures that prevent cross contamination between products, in line with GMP requirements.
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CSV Engineer →
You validate computerised systems and data integrity, so software and automated systems meet regulatory requirements.
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Process Validation Engineer →
You prove that manufacturing processes consistently meet their specifications, across design, qualification and ongoing verification.
The types of validation
Validation covers several areas. You can specialise in one or work across them.
- Equipment validation
Qualify machines and installations through IQ, OQ and PQ, from arrival to production readiness.
- Cleaning validation
Prove that cleaning removes residues to safe limits between products and batches.
- Computer System Validation (CSV)
Validate software, automated systems and data integrity against regulatory requirements.
- Process validation
Prove that established production processes consistently meet their specifications over time.
View our open vacancies
Filter by role, location or contract type. Or click through to a specific role above.
Filters
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26
Jobs foundProject Engineer Co-Development
Life Sciences
Validation and Qualification
Onze klant, een vooraanstaande organisatie in de farmaceutische sector, is op zoek naar een Project Engineer Co-Development om de introductie van nieuwe molecules te faciliteren. Deze rol richt zich op het begeleiden van producten van laboratoriumfase tot lancering, met een sterke focus op process design en projectmanagement. Het doel is de ontwikkeling van robuuste processen en de tijdige oplevering van klinisch materiaal binnen een innovatieve omgeving.
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, On-site
MBR Designer
Life Sciences
Validation and Qualification
Bachelor, Master
Advanced (5+)
Onze klant, een toonaangevend farmaceutisch bedrijf, is op zoek naar een Pas-X MBR Design Specialist voor een grootschalig IT-moderniseringsproject. De rol richt zich op de overgang van legacy-systemen naar een geavanceerd MES-platform door het ontwerpen en implementeren van conforme elektronische batchdocumentatie.
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, On-site
"You prove that a process does exactly what it should, batch after batch. That certainty is what protects the patient, and it is what makes validation work so rewarding."
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Life Sciences Consultant
Validation
FAQs
Honest answers to questions validation consultants really ask.
- Do I need a master's degree?
For most validation roles, yes, usually at master's level.
- Is validation mostly desk work?
Yes, validation is documentation heavy: writing and reviewing protocols, reports and risk assessments, combined with on site checks and execution.
- Can I specialise in one type of validation?
Yes. You can focus on equipment, cleaning or computer system validation, or work across all three.
- Can I switch into validation from another role?
Often, yes. Consultants move into validation from QA, lab or engineering backgrounds.
- Do I have a say in which project I do?
Yes. We propose concrete projects, you approve or decline. Only then do you meet the client.
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Ready to get started?
Validation and CSV engineers: here you find all the open roles.