22.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Activities - Author specification documents (URS-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
Später ansehen22.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Job Responsibilities - Support and interface with process owners of systems and take part in daily activities upon request (provide technical and statistical support) - Execute and document Equipment & Software validation - Oversee validation and qualification activities executed by analysts
Später ansehen21.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Integrity deployment in the department following cGMP, company policies and EHS requirements - Authoring specification documents, including URS-FS-SDCS, plans, protocols, and reports - Overseeing validation and qualification activities executed by analysts, providing training and support - Executing
Später ansehen21.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Integrity deployment in the department following cGMP, company policies and EHS requirements - Authoring specification documents, including URS-FS-SDCS, plans, protocols, and reports - Overseeing validation and qualification activities executed by analysts, providing training and support - Executing
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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