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 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 ansehen19.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 100’000 - CHF 125’000 Strategy and driving the evolution of all FM roles, in alignment with overall business/Therapeutic Area (TA) goals and customer needs. Key Responsibilities 1. Reports to the Head of Field Medical Excellence within the Medical Excellence team 2. Serves as a member of the FME Leadership Team 3. Develops
Später ansehen19.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 With multiple reporting lines. 2. Excellent knowledge of the ultra low power IoT technology and market, with strong network in the industry. 3. Fluent in oral/written English language is a must. #J-18808-Ljbffr
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 | Boudry | JobLeads GmbH | CHF 100’000 - CHF 125’000 Experience (FM CX) strategy and driving the evolution of all FM roles, in alignment with overall business/Therapeutic Area (TA) goals and customer needs. Key Responsibilities 1. Reports to the Head of Field Medical Excellence within the Medical Excellence team 2. Serves as a member of the FME Leadership Team
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 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
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