29.02.24 | Teilzeit | Friesoythe | Vet Pharma Friesoythe GmbHProcedures Remain abreast of and assure GMP compliance with applicable worldwide regulatory standards Responsible for all testing and release activities including raw materials, components, intermediates and final product Responsible for the Quality management systems (documentations, deviations, complaints
Später ansehen05.03.23 | Vollzeit | Garrel | www.hoegemann.deAnd maintenance of databases - Automation of processes for machine control - Development of interfaces to software systems - Creation of software documentation Our requirements - Completed studies or training in IT - Professional experience - Knowledge of English - Ability to work in a team Our benefits That's
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