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 Specialis
t who's passionate about quality, precision, and ensuring that life-saving products are backed by rock-solid compliance.
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 caree
r.
What's in it for you
* Make a real impa
ct: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices
* Grow within a community of exper
ts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise
* Build a meaningful care
er: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences
* A fair, competitive packa
ge: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued
What you'll be doing
* Supporting
the qualification of lab and production equipment
(e.g., installation, operational, and performance qualification activities).
* Reviewing and
developing qualification documentation
such as risk assessments, protocols, and reports in compliance with regulatory requirements.
* Participating in
the design and execution of validation strategies
and ensuring alignment with quality and compliance standa
rds.
* Performing and reviewing test activi
ties (e.g., user acceptance testing) and ensuring proper documentation and traceability.
* Supporting change control, deviation management, and CAPA proces
ses related to equipment qualification.
* Providing training and guidance to end-users on qualification procedures and compliance expectations
Who yo
u are
* You ha
ve a bachelor or master's degree
in engineering, technological, pharmaceutical or chemical sciences.
* You have a strong interest in or initial experience
with equipment qualification, validation, or data integrity
within a GxP-regulated environment.
* You are fluent in
the Dutch or the English
language.
* You show a resilient attitude to to tackle any challenge with a positive mindset.
* You are able to communicate effectively and work collaboratively in diverse team environment.
* You show an eye for details and strong technical aptitude.
* You have a genuine passion for contributing to the mission of ensuring quality and compliance in the life sciences industry
About us
We 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 Things 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? Let's talk.
* Send us your CV and motivation letter. You could be the next one to join the QbD family.