Embark on an exceptional adventure with a global biopharmaceutical company, driven by an unwavering passion to meet the crucial needs of people affected by serious diseases.
The group’s objective is to provide cross-functional expertise on raw materials, excluding cell banks and plasmids.
🎯 Main Missions
- Mapping all raw materials used in Biologics / Gene Therapy projects.
- Risk analysis (quality, regulatory, supply chain, etc.).
- Monitoring mitigation plans.
- 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.
👥 Interactions & Stakeholders
High level of interaction with:
- Procurement, Quality, Regulatory, Clinical Manufacturing.
- Process teams in Braine, UK, and France.
- Regular collaboration with upstream and downstream experts.
👤 Experience:
Minimum of 5 years’ experience in a biopharma environment, preferably in process development.
Experience in risk analysis, project management, structuring and prioritizing actions.
⚒️ Technical skills:
- Understanding of upstream/downstream bioprocesses.
↪ A downstream background is a plus to complement the current team
- General knowledge of antibody purification and techniques such as affinity chromatography.
⚙️ Soft skills:
- Autonomy, structured approach, ability to collaborate and engage with various stakeholders.
🗣️Language:
- English required (written, spoken, meetings, documentation).
📝For this position of Raw Material Scientist, we offer an attractive salary with the following benefits :
A rate as a freelancer is also possible.