CQV Engineer
Life Sciences
Validation and Qualification
Geel, Antwerp
Consultancy
Fulltime
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Equipment Validation Engineer jobs in Belgium
Qualify process and lab equipment through IQ, OQ and PQ, and make sure installations are ready for reliable production. Prove that machines and installations do what they should.
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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
Automation Engineer
Life Sciences
Electromechanical
Bachelor, Master
Advanced (5+)
Courcelles, Hainaut
Consultancy
Fulltime, Hybrid
Cleanroom Construction Specialist
Life Sciences
Civil and Construction
Master
Senior (7+)
Our client, a leading pharmaceutical company, is seeking an expert to support the construction and revamping of classified manufacturing environments. The role focuses on overseeing the technical fit-out and internal finishes of facility upgrades to ensure operational excellence.
Geel, Antwerp
Consultancy
Fulltime, Hybrid
QA Operational Readiness Officer
Life Sciences
QA
Bachelor, Master
Medior (3+)
Our client, a pharmaceutical organization, is seeking a Quality Operational Readiness Officer for the start-up of a new production facility. This role focuses on ensuring quality readiness and compliance during the transition from construction to operational status. The position coordinates qualification activities and maintains high GMP standards throughout the commissioning phase.
Geel, Antwerp
Consultancy
Fulltime, Hybrid
Young Master Graduate
Life Sciences
QA
Master
Junior (0+)
Beerse, Antwerp
Consultancy
Fulltime, Hybrid
What you can expect as an Equipment 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.
- 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.
- Project stability
Life Sciences projects tend to run long, which gives you stability. We plan your next step well before a project ends.
- From arrival to production ready
You take equipment from installation through IQ, OQ and PQ until it is proven ready for production.
"Every qualification I sign off means the line can run with confidence."
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Life Sciences Consultant
Equipment Validation Engineer
FAQs
- 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 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 an Equipment Validation Engineer.
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