↳Bachelor’s or Master’s degree in a scientific, engineering, or technical discipline.
↳Solid experience in GMP-regulated biologics manufacturing, quality systems, compliance, technical operations, or a related area.
↳Proven ability to solve complex problems and lead investigations with minimal guidance.
↳Strong knowledge of GMP expectations, quality systems, documentation standards, and risk-based decision-making.
↳Experience working cross-functionally with Manufacturing, Quality, Engineering, and MSAT.
↳Ability to lead projects or workstreams and influence stakeholders within assigned scope.
↳Strong communication skills in German and English.
