18.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGIn the biotechnology or pharmaceutical industry - Fluent in French and English (C1 written and spoken) - Extensive experience with validation life cycle requirements for cGMPs laboratory systems - Experience with project management and/or leadership enabling cross functional engagement to deliver project goals
Später ansehen06.08.24 | Vollzeit | Le Locle | Randstad Schweiz AGEnsure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements. - Support and address comments and suggestions associated with validation and engineering documentation. - Protocol, Deviation, and summary report generation and approval
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