06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalDe respecter les normes cGMP (Good Manufacturing Practice) et EHS (Environment, Health, Safety). Vous réalisez les activités process de routine. Vous réalisez quelques activités hors routine. Vous êtes responsable de remonter les problématiques techniques et/ou organisationnelles. Vous êtes responsable
Später ansehen06.06.24 | 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 ansehen06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor a dynamic, autonomous, continuous improvement minded and change agile professional to embrace a team-based culture and more specifically within the Quality Unit team within a world-class Biotech manufacturing environment. The scope of the role is to manage the day-to-day and the medium to long-term
Später ansehen06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOversight and quality assurance (QA) support to partners (QA, manufacturing, projects). They actively participates to internal and external inspections. How you will contribute Quality Management of Systems Follow and implement changes in project/process or operational mode, depending on the perimeter
Später ansehen06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor products manufactured at Neuchâtel facility. Participate in GMP (Good Manufacturing Practice) tours of facility to ensure inspection ready status. Interaction with authorities Act as a “Subject Matter Expert” (SME) in the creation and modification of regulatory license sections for products manufactured
Später ansehen06.06.24 | 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 ansehen06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor a dynamic, autonomous, continuous improvement minded and change agile professional to embrace a team-based culture and more specifically within the Quality Unit team within a world-class Biotech manufacturing environment. The scope of the role is to manage the day-to-day and the medium to long-term
Später ansehen06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOversight and quality assurance (QA) support to partners (QA, manufacturing, projects). They actively participates to internal and external inspections. How you will contribute Quality Management of Systems Follow and implement changes in project/process or operational mode, depending on the perimeter
Später ansehen06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor products manufactured at Neuchâtel facility. Participate in GMP (Good Manufacturing Practice) tours of facility to ensure inspection ready status. Interaction with authorities Act as a “Subject Matter Expert” (SME) in the creation and modification of regulatory license sections for products manufactured
Später ansehen06.06.24 | Vollzeit | Zug | Michael Page InternationalBiotechnology company in Solothurn, we are currently looking for a motivated Manufacturing Associate, working in shifts. The assignment will be temporary for the next 12 months, to start as soon as possible. Depending on the performance and motivation, the possibility of an extension or permanent takeover
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