Qualification & Validation Specialist
Location
: Hybrid, Belgium
Type
: Full-time
Are you the kind of person who won't rest until every system, process, and piece of equipment runs exactly as it should — and can prove it? We're looking for
a Qualification & Validation Special
ist who's passionate about quality, precision, and ensuring that life-saving products are backed by rock-solid complianc
e.
In this role, you'll play a vital part in guaranteeing that critical equipment and systems meet the highest standards — from installation to performance. If you thrive on structure, enjoy solving technical challenges, and want to make a real impact in the pharmaceutical or life sciences world, then this could be the perfect next step in your ca
re
**er.
What's in it for**
* youMake a real
impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical dev
* icesGrow within a community of e
xperts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your exper
* tiseBuild a meaningful
career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life scie
* ncesA fair, competitive p
ackage: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be va
**lued
What you'll be**
* doingSuppo
rting the qualification of lab and production equ
ipment (e.g., installation, operational, and performance qualification activi
* ties).Reviewin
g and developing qualification documen
tation such as risk assessments, protocols, and reports in compliance with regulatory require
* ments.Participati
ng in the design and execution of validation strat
egies and ensuring alignment with quality and compliance
stan
* dards.Performing and reviewing test
activities (e.g., user acceptance testing) and ensuring proper documentation and traceab
* ility.Supporting change control, deviation management, and CAPA proc
esses related to equipment qualific
* ation.Providing training and guidance to end-users on qualification procedures and compliance expect
**ations
**
Who
* you ar
eYou have a bachelor or master's
degree in engineering, technological, pharmaceutical or chemical sc
* iences.You have a strong interest in or initial expe
rience with equipment qualification, validation, or data int
egrity within a GxP-regulated envir
* onment.You are fl
uent in the Dutch or the
English la
* nguage.You show a resilient attitude to to tackle any challenge with a positive m
* indset.You are able to communicate effectively and work collaboratively in diverse team envir
* onment.You show an eye for details and strong technical ap
* titude.You have a genuine passion for contributing to the mission of ensuring quality and compliance in the life sciences i
**ndustry
**
About usWe support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and
pharma.We believe in JPEG:Joy. Partnership. Going the Extra Mile. Getting Thin
gs Done.You won't just be taking a job — you'll be joining a community where people grow, laugh, build, and contribute to something
**bigger
Interested? Le**
* t's talk.Send us your CV and motivation letter. You could be the next one to join the Qb
D family.