Analytical Project Leader

Quality Assistance; Henegouwen; Sur place; EUR 50 000 - 70 000; Plein temps

Avantages offerts par ce poste

Access to continuous development through Pharma Academy

Balanced work environment that supports focus and well-being

Résumé du poste

Quality Assistance in Belgium is seeking an Analytical Project Leader to transform complex studies into reliable data that advances life-changing therapies. You will coordinate projects, ensure compliance, and guide clients through each stage while supporting critical decisions in drug development.

The ideal candidate has a strong scientific background and at least 2 years of project management experience in a regulated environment. Join us to contribute to innovative treatments in a supportive, flexible work setting.

Qualifications

• 2+ years of experience in analytical project management within a regulated environment.
• Scientific knowledge in drug development.

Responsabilités

• Draft comprehensive technical agreements.
• Coordinate project activities with laboratory teams.
• Ensure compliance with protocols and commitments.
• Communicate project progress to clients.

Connaissances

Scientific background (PhD, Master’s degree or Engineering)

Minimum 2 years’ experience in analytical project management

Fluency in French and English (minimum B2 level)

Customer-focused mindset

Adaptability in a changing environment

Problem-solving and risk anticipation skills

Formation

PhD, Master’s degree or Engineering

Description du poste

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.

• 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

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

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

Who we are

And why it matters

At Quality Assistance, we operate as a fully integrated analytical partner, allowing our project leaders to work in a streamlined environment where decisions translate quickly into action.

From our GxP-certified site in Belgium, we bring together scientific expertise, regulatory rigour and operational execution under one roof. This means fewer silos, clearer communication and stronger control over project outcomes.

With over 40 years of experience and more than 2,000 drug candidates supported, we continue to grow internationally while investing in new capacities and technologies. For you, this means leading projects that are both technically challenging and directly connected to bringing new treatments to patients.