Laboratory Projects Specialist

Description de l'entreprise

We secure the drug development while reducing time-to-patient for life-changing therapies.

Quality Assistance is a leading European CRO (Contract Research Organisation) exclusively focused on analytical sciences for innovative medicines. Based in Belgium, our company brings together 280 experts under one roof with over four decades of experience in delivering analytical excellence. Our single-site model enables agility and collaboration, while rigorous regulatory compliance ensures the highest standards of quality and reliability.

Our scientific experts provide GxP and security compliant analytical data that contribute to demonstrate quality, safety, and efficacy at every stage of drug development. From preclinical phases to regulatory approval and beyond, we provide the full range of analytical services required by the EMA and FDA regulations, acting as a trusted partner committed to excellence. Together, we shape the future of medicine through precision, reliability, and a shared commitment to improving patients’ lives.

Vos missions

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

Votre profil

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

Description de l'offre

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