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 And documenting Equipment and Software validation - Conducting and participating in risk assessments, root cause analysis and investigations Your experience/knowledge - 5+ years of relevant validation experience in the biotechnology or pharmaceutical industry - Solid skills in Data Integrity requirements
Später ansehen21.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 And documenting Equipment and Software validation - Conducting and participating in risk assessments, root cause analysis and investigations Your experience/knowledge - 5+ years of relevant validation experience in the biotechnology or pharmaceutical industry - Solid skills in Data Integrity requirements
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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