08.05.24 | Vollzeit | Neuchâtel | RM Group AGProtocols for CIP, SIP processes, including surface sampling, thermal mapping, and handling of Bioindicators Your experience/knowledge - 5+ years of experience in validation CIP, SIP, and Equipment qualification within the pharmaceutical industry - Extensive experience with filling equipment
Später ansehen07.05.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGOf SAT protocol, - Writingexecution of IOQ protocol - Writing, execution of performance qualification CIP, SIP (surface sampling, thermal mapping, Bioindicators handling). - Writing of traceability matrix - Revision of risk analysis, validation plan when applicable. Your profile - 5-10 years
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