25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalEmployment application is true to the best of my knowledge. Job Description A propos du rôle Le/La Manufacturing Project Engineer est chargé(e) de soutenir les unités de production du site dans le processus d’implémentation de projets et amélioration sur les lignes de production. Il/elle dirige
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalEmployment application is true to the best of my knowledge. Job Description A propos du rôle Le/La Manufacturing Project Engineer est chargé(e) de soutenir les unités de production du site dans le processus d’implémentation de projets et amélioration sur les lignes de production. Il/elle dirige
Später ansehen27.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor different responsibilities, including Regulatory Compliance activities, Interaction with Authorities, External inspections and internal audits, Quality projects. How you will contribute Regulatory compliance - Be responsible for biological product manufactured on site and act as an expert for all
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf activities all along the manufacturing and release process. How you will contribute QA Expert Act as QA(Quality Assurance) representative for both routine GMP (Good Manufacturing Practice) activities and Takeda projects. Act as the Quality partner within Production Unit Team and the Quality Control
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor different responsibilities, including Regulatory Compliance activities, Interaction with Authorities, External inspections and internal audits, Quality projects. How you will contribute Regulatory compliance Be responsible for biological product manufactured on site and act as an expert for all
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor different responsibilities, including Regulatory Compliance activities, Interaction with Authorities, External inspections and internal audits, Quality projects. How you will contribute Regulatory compliance Be responsible for biological product manufactured on site and act as an expert for all
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf activities all along the manufacturing and release process. How you will contribute QA Expert Act as QA(Quality Assurance) representative for both routine GMP (Good Manufacturing Practice) activities and Takeda projects. Act as the Quality partner within Production Unit Team and the Quality Control
Später ansehen08.05.24 | Vollzeit | Neuchâtel | RM Group AGAnd process performance, reliability, and compliance - Revising risk analysis and validation plans as needed based on project requirements - Overseeing the execution of SAT protocols, ensuring compliance with regulatory standards and company guidelines - Developing and executing performance qualification
Später ansehen23.05.24 | Vollzeit | Lausanne | Michael Page InternationalButton - Information Technology 43 - IT Support 10 - Systems Administration 8 - IT Development 4 - ERP 3 - IT Data Analysis 3 - Senior IT Management 3 - Infrastructure 2 - IT Architecture 2 - IT Business Analysis 2 - Technology consultancy 2 - Consulting 1 - IT Project & Programme Management 1 - Networks
Später ansehen16.05.24 | Vollzeit | Neuchâtel | Michael Page InternationalIn coordinating the social media channels and presence, including Instagram, Facebook, Twitter, TikTok, LinkedIn, and any additional channels - Work closely and collaboratively with the marketing agency to conceptualise, plan, personal produce and execute content and content-driven projects that resonate
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