Downstream GMP Associate Specialist – 12 Months

CK QLS is seeking an Associate Specialist for Downstream Operations in Luzern. This full-time position supports the manufacturing of early-phase clinical therapies, requiring on-site presence in a GMP environment. Key responsibilities include setting up downstream processes, ensuring compliance with GMP, and participating in continuous improvement. Candidates should possess relevant experience, effective communication skills in German and English, and flexibility under pressure. A bachelor's or master's degree is preferred.
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