Raw Material Scientist
Contracting – Brabant Wallon
Your Responsibilities:
· Map and monitor all raw materials used in Biologics and Gene Therapy development projects.
· Lead risk assessments related to quality, regulatory compliance, and supply chain continuity.
· Oversee mitigation plans and ensure proper execution across cross-functional teams.
· Implement a Quality by Design (QbD) approach focusing on Critical Material Attributes (CMA).
· Create templates, guidelines, and best practices for raw material management during development phases.
· Collaborate daily with Procurement, Quality, Regulatory, and Clinical Manufacturing departments.
· Partner closely with upstream and downstream experts to ensure technical alignment.
Your Profile:
· At least 5 years of experience in a biopharmaceutical environment, ideally in process development.
· Solid background in risk analysis, project management, and prioritization of technical activities.
· Strong understanding of upstream/downstream bioprocesses. Expertise in downstream processing is a strong asset.
· General knowledge of antibody purification, including affinity chromatography techniques.
· Autonomous and structured professional with excellent stakeholder collaboration skills.
· Fluent in English (written and spoken); French is a plus but not required.
Our offer:
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]
