Analytical Industrial Lead Associate

Are you an energetic life sciences professional with a strong background in analytical chemistry and pharmaceutical project management?

We are currently seeking an Analytical Project Coordinator/Industrial Lead Associate to join a global biopharmaceutical leader operating in the pharmaceutical / biopharmaceutical industry based in Braine-l'Alleud (hybrid setup).

This position is offered as a long‑term project contract (employee or freelance) starting ASAP until December 31, 2027.

In this role, you will play a key operational and coordination role within the Center of Expertise Analytical. You will bridge strategy, laboratory operations (QC), and project execution for commercial products—supporting them from late‑stage development through their full lifecycle across global supply networks.

Key Responsibilities

• Project Management & Support : provide analytical expertise and end‑to‑end coordination for specific technical projects (e.g., implementing new regulatory requirements, coordinating stability studies to support process changes).
• Lifecycle Management : implement analytical lifecycle plans and integrated technical solutions using structured project management frameworks.
• Cross-Product Processes : take ownership of cross‑product business processes and operational activities within the department.
• Operational Interface : build and maintain seamless communication interfaces between central teams and operational entities, including QC testing laboratories.
• Problem Solving : apply a pragmatic, proactive, and dynamic mindset to resolve complex technical challenges within a matrix environment.

Requirements & Qualifications

• Master’s Degree in Analytical Chemistry, Life Sciences, or a related scientific discipline.
• Proven experience in the pharmaceutical or biopharmaceutical industry, with direct exposure to analytical chemistry (QC, stability, method transfers, or CMC).
• Demonstrated ability in project management, planning, monitoring, issue resolution, risk mitigation, and reporting.
• Strong knowledge of GMP (Good Manufacturing Practices), Quality Assurance, and Regulatory Affairs applied to analytical testing.
• Fluency in both English and French is essential.
• Customer- and results-oriented, highly autonomous, with strong problem-solving capabilities and a dynamic mindset.

What We Offer

We offer a long‑term project engagement until December 31, 2027, with flexible contract options depending on experience:

• Employee : gross monthly salary up to €5,100/month (commensurate with experience) + comprehensive package of extra‑legal benefits.
• Freelance : daily rate up to €650/day (commensurate with experience).