- Location
- Thuin, Belgium
- Contract type
- CDI — 38h / week
Your next challenge
Ready to make a difference? Here's what awaits you.
As a Computerised System Validation (CSV) Specialist, you’ll play a key role in ensuring that our laboratory systems meet the highest regulatory standards. Your expertise will help secure compliance and support the development of life-changing therapies. You’ll join a dedicated team of three professionals and report directly to the Team Leader, working on projects that truly matter for patients worldwide.
Your key responsibilities
Here's what you'll be in charge of:
- Define and implement validation strategies for laboratory computerised systems
- Draft, review and execute CSV documentation (URS, DQ, IQ, OQ, validation reports, archiving)
- Monitor suppliers during system installation and ensure compliance with international standards (FDA, GAMP) and internal procedures
- Collaborate with IT, Quality Assurance and Operations teams to guarantee project compliance
- Manage system changes and assess their impact on validation
- Support users during onboarding and troubleshooting
- Participate in internal audits to maintain quality standards
Skills you'll need to bring
To succeed in this role, you'll demonstrate:
- Strong affinity with both scientific (laboratory) and IT environments
- Previous experience in a similar role within a regulated environment
- Excellent communication skills and a customer-focused mindset
- High level of organisation and attention to detail
- Ability to work independently while thriving in a team setting
- Analytical thinking and problem-solving skills
- Proficiency in written English; spoken English is a plus
- Knowledge of software validation principles and quality standards
Our commitment to you
Join us and make a real impact on patients’ lives while growing your career in a supportive, innovative environment.
Here's why you'll love working with us.
- A competitive salary package aligned with the sector, plus extra-legal benefits (meal vouchers, hospitalisation and outpatient care insurance, group insurance, bonus)
- A comprehensive onboarding and training programme to boost your expertise from day one
- Real opportunities for career progression: in 2024, 30 colleagues were promoted internally
- A collaborative, respectful and supportive work culture where your voice matters
- A vibrant social life at work: afterworks, sports sessions, team buildings, family events and more
- Everyday perks that make a difference: free fitness classes, fresh fruit, up to 4 car washes per year, and practical services like lunch delivery
Who we are
And why it matters
We are a leading Belgian Contract Research Organisation (CRO) supporting the pharmaceutical industry with the full range of analytical services required by EMA and FDA regulations.
From early development to drug registration and beyond, we design analytical protocols, develop methods, and perform studies that ensure the safety, efficacy and quality of innovative medicines.
With 280 experts, state-of-the-art technologies, and all labs centralised on one site in Donstiennes, Belgium, we combine scientific excellence with human values to shape the future of medicine faster, smarter, together.