Analytical Project Leader

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 an Analytical Project Leader, you will play a central role in turning complex analytical studies into reliable data that drives life-changing therapies forward. Acting as the key point of contact for your clients, you will guide them through each stage of their project while ensuring scientific rigor, regulatory compliance and effective coordination with laboratory teams. Your work will directly support critical decisions in drug development and help bring innovative treatments closer to patients.

Your key responsibilities
Here's what you'll take ownership of:

• Draft clear and comprehensive technical agreements
• Coordinate project activities to meet defined timelines with laboratory teams
• Ensure compliance with protocols and contractual commitments
• Monitor the availability of samples and reference standards
• Communicate project progress clearly with clients and internal stakeholders
• Maintain accurate and up-to-date project documentation
• Review final reports including trend analyses, conclusions and QA compliance
• Manage quality documentation in collaboration with laboratory and compliance teams
• Support client visits and contribute to audit preparation

Votre profil

Skills you'll need to bring
To succeed in this role, you'll demonstrate:

• Scientific background (PhD, Master’s degree or Engineering)
• Minimum 2 years’ experience in analytical project management within a regulated environment (GMP, GLP or GcLP), ideally in the pharmaceutical industry
• Fluency in French and English (minimum B2 level)
• Customer-focused mindset
• Adaptability in a changing environment
• Problem-solving and risk anticipation skills
• Accuracy and attention to detail
• Team-oriented approach

Description de l'offre

Our commitment to you
Here's why you'll love working with us.

As an Analytical Project Leader, you will have a meaningful role contributing to the development of safe and effective therapies. We give you the environment and support to succeed in a project leadership role:

• Real project ownership with direct client interaction and decision-making responsibility
• A structured organisation that supports efficient delivery and clear prioritisation
• Exposure to diverse and international projects in cutting-edge therapies
• Close collaboration with experts in analytical sciences, QA and regulatory compliance
• A culture that values accountability, trust and knowledge sharing
• Access to continuous development through our Pharma Academy
• A balanced work environment that supports focus, flexibility and well-being