07.05.25 | Vollzeit | Cressier (NE) | RandstadAnd written communication, negotiation, and multitasking abilities, coupled with strong organizational skills. - Good understanding of biotechnological, pharmaceutical, or diagnostic products. - Knowledge of quality standards (GMP, ISO 13485, ISO 9001). - Understanding of production and supply constraints
Später ansehen02.04.25 | Vollzeit | Le Locle | RandstadAnd final test sequencing. - Ensure 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
Später ansehen11.04.25 | 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 ansehen27.03.25 | Vollzeit | Le Locle | Randstad Schweiz AGAnd requirements across the company - Knowledge or experience working in an FDA and/or European regulatory environment - Thorough understanding of GMP (Good Manufacturing Practices)/ISO (International Organization for Standardization) regulations - Written and verbal effective communication skills in English
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