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 bring: 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 As an Analytical Project Leader, you will have a meaningful role contributing to the development of safe and effective therapies, having an exposure to diverse and 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, nanomedicines, mRNA, and cell and gene therapies. Having contributed to more than 2,000 drug candidates, Quality Assistance is now more than doubling its capacity with a new facility and internal Pharma Academy, while expanding internationally and remaining anchored in scientific excellence, regulatory reliability, and operational rigor.