17.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Biopharmaceutical production sites in Switzerland. Operating 24 hours a day, 7 days a week, the site employs a wide range of professionals trained in biotechnologies and their application in industrial production. With more than twenty nationalities, Takeda Neuchâtel offers an international, diverse and innovative
Später ansehen16.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Of professionals trained in biotechnologies and their application in industrial production. With more than twenty nationalities, Takeda Neuchâtel offers an international, diverse and innovative working environment within a company that is firmly rooted and committed to its local ecosystem. Takeda Neuchâtel
Später ansehen15.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 And improvements. Proactively assist business partners in expressing their needs to provide adapted solutions and collaborate with global teams. User Support and Capability Building Process user account requests for various systems, train superusers, and manage the associated training toolkits. QMS performance
Später ansehen15.09.24 | Vollzeit | Le Locle | JobLeads GmbH | CHF 80’000 - CHF 100’000 And laboratories - Supporting risk assessments from a contamination control perspective - Providing training for personnel to ensure that the requirements of the environmental monitoring program are met - Supporting the internal team in the commissioning and maintenance of controlled environments and finishing
Später ansehen15.09.24 | Vollzeit | St-Sulpice (NE) | JobLeads GmbH | CHF 125’000 - CHF 150’000 In decision making. - Ensure department staff is properly trained, per designated training plan, before assuming job responsibilities. - Ensure department’s adherence to company policies, including privacy/GDPR, as well as other legal and regulatory directives. YOU'RE AWESOME AT - Demonstrated experience
Später ansehen18.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGURS-FS-SDCS). - Author plans, protocols, and reports - Execute and document Equipment & Software validation. - Oversee validation and qualification activities executed by analysts, provide training and support. - Assure cGMP compliant and timely implementation and maintenance of validated status
Später ansehen11.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGActivities Validation and Qualification Activities - Author transfer protocols and reports for assays - Author qualification plans and reports for critical reagents - Oversee validation and qualification activities executed by analysts, provide training and support - Execute and documents experiments
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