You will be responsible for New Material Introduction, defining and maintaining the Material Control Strategy, and driving continuous process improvements across both clinical and commercial CAR-T manufacturing
Job Summary
You will be responsible for New Material Introduction, defining and maintaining the Material Control Strategy, and driving continuous process improvements across both clinical and commercial CAR-T manufacturing.
You will act as key interface between Operations, Quality, Procurement and external suppliers to ensure material robustness, compliance and process reliability.
We provide an inclusive work environment where each person is considered as an individual.
Matching Summary
You will be responsible for New Material Introduction, defining and maintaining the Material Control Strategy, and driving continuous process improvements across both clinical and commercial CAR-T manufacturing.
Skills & Requirements
Must-have
Material Control Strategy
GMP-regulated environment
material robustness
process reliability
supplier investigations
Nice-to-have
structured project management skills
proactive and hands-on
Key Requirements
Master’s degree in Biotechnology, Chemistry, Engineering, Life Sciences, or a related scientific discipline
Minimum 3 years of experience in the pharmaceutical or biopharmaceutical industry
Experience in GMP-regulated clinical and/or commercial manufacturing environments