Computer System Validation (CSV) Specialist
Do you want to contribute to cutting-edge projects in the Life Sciences while specializing in Computer Software Validation (CSV)? We’d love for you to join our expanding Software and Services division
Join us!
🔍 Computer System Validation (CSV) Specialist
📍
Location
: Hybrid
🕓
Type
: Full-time
QbD Group’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in
Software Solutions.
💡 What’s in it for you?
Make a real impact:
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 experts:
Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.
Build a meaningful career:
As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
A fair, competitive package:
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
As a Software Validation Consultant, you will play a critical role in
managing and overseeing project deliverables
for a variety of cutting-edge applications, such as:
Automated systems
Software as a Medical Device (SaMD)
Mobile apps
From
preparation and project design to implementation and follow-up
, you will provide full-cycle support to clients, ensuring the successful delivery of projects.
You will also contribute to the
integration and implementation
of our proprietary QbD quality management software at client sites. With your knowledge of
data integrity and quality management
, you will support companies across the Life Sciences, including pharmaceuticals, biotech, medical devices and healthcare—from large, established firms to the most innovative start-ups.
💪 What you bring
You hold a
master’s degree in a scientific or engineering field
(e.g., bio-engineering, bioinformatics, industrial engineering, civil engineering, etc.).
You have some
experience in the Life Sciences industry or with software-related projects
.
You have a strong affinity with IT, software, and systems.
You have knowledge of
data integrity
.
You are detail-oriented, eager to learn, and adaptable to new challenges.
You possess strong technical and project management skills.
You are responsible, with a strong analytical mindset and excellent problem-solving abilities.
🫵 Who you are
Our culture is driven by values If this sounds like you, you’ll fit right in:
You’re
resilient
and tackle challenges with a positive mindset
You’re
curious
and always up for learning something new
You have a
no non-sense approach
honest, clear, respectful
You’re
innovative
and bring ideas, not just opinions
And above all, you’re
serious about your work, but not too serious about yourself
✨ 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
Service
Software Solutions & Services
Role
Software Validation Specialist
Locations
QbD Spain (Barcelona), QbD Wallonia, QbD Flanders (HQ)
Remote status
Hybrid