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Raw Material Scientist (M/F/D)
Tasks:
Mapping all raw materials used in Biologics and Gene Therapy
Monitoring mitigation plans
Risk analysis (quality, regulatory, supply chain, etc.)
Implementing a Quality by Design (QbD) strategy around Critical Material Attributes (CMA)
Drafting templates, guidelines, and recommendations for raw material management during the development phase
High level of interaction with:
Procurement, Quality, Regulatory, Clinical Manufacturing
Process teams in Braine, Slough (UK), and Levallois (FR)
Regular collaboration with upstream and downstream experts
Qualification:
Minimum of 5 years’ experience in a biopharma environment, preferably in process development
Experience in risk analysis, project management, structuring and prioritizing actions
Understanding of upstream/downstream bioprocesses
General knowledge of antibody purification and techniques such as affinity chromatography
Autonomy, structured approach, ability to collaborate and engage with various stakeholders
English required (written, spoken, meetings, documentation)
Requirements:
Start: 02.06.2025
Duration: 6 months
Capacity: 5 days per week
Location: Braine, Belgium
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