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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
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20
Jobs foundJunior Process Improvement Engineer - Steriele Afdeling
Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)
Onze klant, een vooraanstaande organisatie in de farmaceutische sector, zoekt een junior profiel voor procesverbetering om de operationele organisatie te versterken. De rol richt zich op het observeren, analyseren en standaardiseren van operationele processen binnen een steriele productieomgeving middels Lean-principes.
Heist-op-den-Berg, Antwerp
Consultancy
Fulltime, On-site
Junior Validation Engineer
Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)
Our client is seeking a professional to support commissioning and qualification activities within a highly regulated environment. The role focuses on ensuring project compliance and managing periodic activities autonomously to meet technical standards.
Ghent, East Flanders
Consultancy
Fulltime, On-site
Senior MES Designer (Werum PAS-X)
Life Sciences
Validation and Qualification
Master
Senior (7+)
Our client, a leading pharmaceutical organization, is seeking an experienced professional for a strategic digital transformation initiative. The project involves replacing legacy systems with a global standard to establish the future of manufacturing execution. The role focuses on defining design principles that will shape technical solutions for years to come.
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, Hybrid
Process Validation Engineer
Life Sciences
Validation and Qualification
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.
Antwerp, Antwerp
Consultancy
Fulltime
Equipment Validation Engineer
Life Sciences
Validation and Qualification
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.
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime
Cleaning Validation Engineer
Life Sciences
Validation and Qualification
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.
Antwerp, Antwerp
Consultancy
Fulltime, Hybrid
CSV Engineer - MES Systems Integration
Life Sciences
Validation and Qualification
Bachelor, Master
Senior (7+)
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, Hybrid
Computer System Validation (CSV) Engineer
Life Sciences
Validation and Qualification
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.
Antwerp, Antwerp
Consultancy
Fulltime
Graduate role: MBR Qualification Engineer
Life Sciences
Validation and Qualification
Master
Junior (0+)
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.
Ghent, East Flanders
Consultancy
Fulltime, On-site
Project Engineer Cleanroom Validation
Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)
Onze klant, een vooraanstaande organisatie binnen de life sciences sector, is op zoek naar een deskundige voor de ondersteuning van diverse investerings- en verbeteringsprojecten. De focus ligt op het coördineren en opvolgen van alle validatie- en kwalificatieactiviteiten voor cleanrooms en technische installaties binnen een multidisciplinaire omgeving.
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, On-site
CQV Engineer
Life Sciences
Validation and Qualification
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.
Geel, Antwerp
Consultancy
Fulltime
Production Technician
Life Sciences
Validation and Qualification
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.
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime
"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.