20.06.24 | Vollzeit | Neuchâtel | NonStop Consulting | Responsibility is to perform activities related to the production of active pharmaceutical ingredients. Key Responsibilities - Adhere to cGMP, BDP, and EHS standards. - Execute routine and nonroutine manufacturing processes, including completion planning. - Identify and report technical or organizational
Später ansehen14.05.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGHe/she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements. General information - Start date asap - Planned duration of employment 8 months - Workplace Neuchatel - Workload 100
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