06.09.24 | Vollzeit | Luzern | Randstad Schweiz AGActivities include, but are not limited to - Creation of label text translations using a translation database and approval of the translations regarding study-specific, company-internal, and country-specific regulatory requirements. - Create and monitor project schedule and coordinate projects from
Später ansehen28.08.24 | Vollzeit | Luzern | Randstad Schweiz AGRequired, ideally in biotechnology, biology or pharmaceutical studies. Master’s Degree in clinical research, clinical data or clinical analysis is also advantageous. - Minimum of 2-years’ experience in GMP environment within the pharmaceutical business or comparable. - Experience in batch record review
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