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Process Validation Engineer jobs in Belgium

Verify that manufacturing processes consistently produce results meeting predefined specifications, through stages of process design, process qualification and continued process verification.

20
Jobs found

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
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Junior 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
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MBR Editor

Life Sciences
Validation and Qualification

Onze klant, een vooraanstaande organisatie binnen de farmaceutische sector, is op zoek naar een MBR Editor om de digitalisering van productieprocessen te ondersteunen. De rol focust op het vertalen van operationele processen naar geavanceerde beheersystemen in nauwe samenwerking met diverse projectteams.

Geel, Antwerp
Consultancy
Fulltime
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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
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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
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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
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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

Launch Excellence Project Engineer

Life Sciences
Validation and Qualification

Onze klant, een toonaangevend bedrijf binnen de farmaceutische sector, is op zoek naar een professional voor het beheer van validatie-aspecten bij de introductie van nieuwe producten. De rol richt zich op de succesvolle implementatie en regelgevende naleving gedurende de volledige productlevenscyclus. Een pragmatische, proactieve en resultaatgerichte aanpak staat centraal binnen dit project.

Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime
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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
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Project 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
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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
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Project Validation Coordinator

Life Sciences
Validation and Qualification

Onze klant, een toonaangevend bedrijf in de life sciences, is op zoek naar een coördinator om validatieactiviteiten binnen complexe projecten te sturen. De rol focust op het aansturen van projectteams en het waarborgen van tijdige oplevering van systeem- en equipmentvalidatie.

Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime
Apply now

What you can expect as a Process Validation Engineer

You do your work. We take care of the rest. Clear agreements and real support.

A dedicated Talent Manager

One dedicated Talent Manager who knows you, coaches you and thinks along with your next step. Before, during and after every project.

How our Talent Managers work →

A tailored salary package

From an electric company car to 32 days of holiday. We discuss your expectations openly in the first conversation.

The doors we open

Decades of trusted relationships with leading pharmaceutical players give you access to projects you would not reach on your own.

Pauwels Academy

Workshops, masterclasses and training, from Lean Six Sigma to project management, at your own pace.

Discover the Academy →

Project stability

Life Sciences projects tend to run long, which gives you stability. We plan your next step well before a project ends.

Established processes, proven again

You revalidate processes already in production and validate the changes as production evolves.

"Process validation is where deep pharma knowledge really pays off."

Scientist in a white lab coat using a microscope in a modern laboratory, with lab equipment and a colleague working in the background.
Life Sciences Consultant
Process Validation Engineer

FAQs

Do I need a master's degree?

For most validation roles, yes, usually at master's level. Process validation in particular suits more experienced validation profiles.

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 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.

Talk to an expert

We are happy to answer your questions or help you find your next project as a Process Validation Engineer.