nemensis ag in Luzern, Switzerland, is seeking a dedicated Specialist Clinical Supplies Quality to ensure GMP-compliant processes in clinical drug supply. The ideal candidate holds a relevant university degree and has 2-3 years of experience in a GMP-regulated setting.
Responsibilities include batch record review, inspection of packaging components, and regulatory review, all while maintaining rigorous quality standards. This role offers an opportunity to work in a dynamic team committed to patient safety.
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