Location
Thuin, Belgium
Contract type
CDI  — 38h / week

Your next challenge

Ready to make a difference? Here's what awaits you.

As analytical project leader, you’ll be the trusted partner for our clients, ensuring their projects move forward seamlessly in a regulated environment.

Your role is central: you’ll coordinate analytical studies that demonstrate the quality, safety and efficacy of innovative medicines. Every decision you make will help accelerate access to life-changing therapies.

Apply now

Your key responsibilities

Here's what you'll be in charge of:

  • Being the main point of contact for clients throughout their project lifecycle
  • Drafting technical agreements and ensuring compliance with protocols and contracts
  • Driving project execution to meet timelines in close collaboration with laboratory teams
  • Monitoring sample and reference standard availability
  • Communicating progress clearly to clients and internal teams
  • Reviewing final reports, including trend analyses and compliance checks
  • Managing project-related quality documentation with the laboratory and Compliance department
  • Maintaining accurate document tracking for all dossiers
  • Participating in client visits and audits

Skills you'll need to bring

To succeed in this role, you'll demonstrate:

  • Scientific background: PhD, Master’s degree or engineering diploma
  • Minimum 2 years’ experience in analytical project management within a regulated environment (GMP, GLP, GcLP), ideally in the pharmaceutical industry
  • Clear and effective communication in French and English (B2 level minimum)
  • Strong client orientation and service mindset
  • Adaptability in a fast-changing environment
  • Ability to anticipate risks and solve problems proactively
  • Rigour and attention to detail

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.

Join us now