For a project within a pharmaceutical production environment, you will temporarily join the Material Life Cycle Management team. You will contribute to the onboarding, compliance, and optimization of materials and services. In this role, you will combine data analysis, stakeholder management, and process improvement. You will have a high degree of autonomy and be involved in projects that have a direct impact on quality, continuity, and cost control.
What you will do.
- Onboarding and maintaining new materials and services
- Performing compliance checks for supplier changes
- Identifying quality and process improvements within GMP environments
- Developing solutions for supply continuity and alternative materials
- Optimizing processes via Excel and Power BI
- Analyzing cost structures and formulating optimization proposals
- Supporting change controls and transfer projects
Profile
You enjoy working independently and maintaining an overview when multiple priorities converge. Additionally, you dare to ask critical questions, take initiative, and communicate smoothly with various stakeholders. You feel comfortable in an environment where change and collaboration are central.
What they ask
- Bachelor's or master's degree in a scientific or technical field
- Minimum 2 years of experience within a pharmaceutical or life sciences environment
- Knowledge of GMP and quality systems within production environments
- Strong knowledge of Excel and experience with Power BI
- Fluent in Dutch and English
How to apply
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