Analytical Project Leader (H/F/X)

QUALITY ASSISTANCE; Henegouwen; On-site; EUR 60,000 - 90,000; Full time

Job summary

Quality Assistance is seeking an Analytical Project Leader to turn complex analytical studies into reliable data that advances life-changing therapies. You will act as the main client contact, guiding projects through each stage with scientific rigor, regulatory compliance, and close coordination with lab teams.

You will support critical drug development decisions, ensure quality control, manage project documentation, and communicate progress to clients and internal stakeholders.

Qualifications

• 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

Responsibilities

• 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

Job description

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