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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 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.

30
Jobs found

Junior C&Q Engineer – Automatisatie & Mechanisch

Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)

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.

Geel, Antwerp
Consultancy
Fulltime, On-site
Apply now

Process Validation Engineer Cell Therapy

Life Sciences
Validation and Qualification
Bachelor, Master
Advanced (5+)
Ghent, East Flanders
Consultancy
Fulltime, Hybrid
Apply now

Validation Engineer

Life Sciences
Validation and Qualification

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.

Antwerp, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

QA Officer Validation

Life Sciences
Validation and Qualification
Bachelor, Master
Advanced (5+)

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.

Hamont-Achel, Limburg
Consultancy
Fulltime, Hybrid
Apply now

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
Apply now

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
Apply now

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
Apply now

CSV Engineer - MES Systems Integration

Life Sciences
Validation and Qualification
Bachelor, Master
Senior (7+)
Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

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
Apply now

Commissioning & Qualification 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
Apply now

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
Apply now

Production Engineer

Life Sciences
Validation and Qualification

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.

Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime
Apply now

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.

Worker in protective gear using a tablet in an industrial facility with large stainless steel tanks in the background.

Ready to get started?

Validation and CSV engineers: here you find all the open roles.