11.04.25 | 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
Später ansehen28.03.25 | Vollzeit | Neuchâtel | Randstad Schweiz AGFDA, EMA, etc.) - Validation Report Review - Evaluate test results to confirm all protocol requirements are met - Identify deviations and propose appropriate corrective actions - Quality Support - Collaborate with cross-functional teams (Production, Engineering, Validation) to ensure quality
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