17.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Product impact assessment in protocols/studies deviations related to product, - process/ equipment improvement projects including technology transfer, - small scale/scale down product validation activities, - writing of reports /review of documents and reports. - Manage documentation associated
Später ansehen16.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 In protocols/studies deviations related to product, - process/ equipment improvement projects including technology transfer, - small scale/scale down product validation activities, - writing of reports /review of documents and reports. - Manage documentation associated with laboratory activities. - Control
Später ansehen15.09.24 | Vollzeit | St-Sulpice (NE) | JobLeads GmbH | CHF 125’000 - CHF 150’000 For the design development, modification and evaluation of parts, components, mechanical systems, equipment and packaging, electrical systems, sensing systems or optical systems; in collaboration with the Program Management team. - Work in close collaboration with the Director, Software Engineering to ensure
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 ansehen06.08.24 | Vollzeit | Le Locle | Randstad Schweiz AGFluency in French and good command of English - Demonstrates excellent organizational and communication skills. - Experience with qualifying medical devices, manufacturing equipment or external components. - Excellent technical writing skills with a thorough understanding of good documentation practice
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