21.09.24 | 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 ansehen17.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 And associated contingency plans, and prepare executive progress reports. The PM is required to work in a cross-functional and dynamic setting where project assumptions and scenarios may change. The PM must quickly adapt to changes and manage communications at different levels in the organization. Duties
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 ansehen17.09.24 | Vollzeit | Itingen | Swatch StoreWith cutting-edge equipment. Job description - Team member of a R&D project. - Organic synthesis and polymer synthesis (lab scale). - Weekly reporting on results and planification of the project step. - Carrying out the various stages of research - such as literature survey, reagents ordering, formulation
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
Später ansehen06.08.24 | Vollzeit | Le Locle | Randstad Schweiz AGEnsure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements. - Support and address comments and suggestions associated with validation and engineering documentation. - Protocol, Deviation, and summary report generation and approval
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