- Location
- Thuin, Belgium
- Contract type
- CDI — 38h / week
Your next challenge
Ready to make a difference? Here's what awaits you.
As a Laboratory Projects Specialist, you will be at the heart of analytical projects that support the development of new medicines. Acting as the link between internal laboratory teams and project requirements, you will coordinate analytical activities, ensure high-quality deliverables and contribute to keeping projects on track. Through your work, you will help accelerate access to innovative therapies for patients around the world.
Your key responsibilities
Here's what you'll take ownership of:
- Coordinate project implementation with laboratory teams while ensuring timelines, protocols and contractual requirements are respected
- Monitor the availability of samples and reference standards throughout project execution
- Communicate analytical progress to internal stakeholders
- Ensure the review of analysis reports and certificates of analysis
- Maintain quality documentation in collaboration with laboratory and compliance teams
Skills you'll need to bring
To succeed in this role, you'll demonstrate:
- Scientific background at Master's level or Engineering degree
- First experience in project management within a regulated environment such as GMP, GLP or GcLP, ideally within the pharmaceutical industry
- Fluency in French and English (minimum B1 level)
- Customer-focused mindset
- Adaptability in a changing environment and multitasking capability
- Risk awareness and problem-solving ability
- Attention to detail and commitment to deadlines
- Team-oriented approach
Our commitment to you
Here's why you'll love working with us.
As a Laboratory Projects Specialist, you will have a meaningful role contributing to the development of safe and effective therapies, with exposure to diverse international projects in a highly regulated scientific environment.You will benefit from:
- A collaborative culture built on respect, trust and knowledge sharing
- Modern laboratories equipped with advanced analytical technologies
- A balanced work environment supporting your well-being and performance
Who we are
And why it matters
Quality Assistance is a leading European CRO focused on analytical sciences for innovative drug development. Based in Belgium and GxP-certified, the company provides EMA- and FDA-compliant services from a fully integrated, single-site facility equipped with a comprehensive suite of state-of-the-art technologies.
With over 40 years of experience and 280 professionals, it supports the development of complex modalities such as biologics, oligonucleotides, peptides, cell and gene therapies, vaccines and nanomedicines. Having contributed to more than 2,000 drug candidates, we are now more than doubling our capacity with a new facility and investing in the development of our people through an internal Pharma Academy. At the same time, we continue to expand internationally while remaining anchored in scientific excellence, regulatory reliability, and operational rigor.