1622 Emplois pour Manufacturing

Sap Quality Management Consultant AD

...Manufacturing industry is a strong plus.(SAP QM, SAP Quality Management)#SAPQM #SAPQualityManagement #SAPWM #SAPWarehouseManagement

Sap Quality Management Consultant AD

...Manufacturing industry is a strong plus.(SAP QM, SAP Quality Management)#SAPQM #SAPQualityManagement #SAPWM #SAPWarehouseManagement

Sap Quality Management Consultant AD

...Manufacturing industry is a strong plus.(SAP QM, SAP Quality Management)#SAPQM #SAPQualityManagement #SAPWM #SAPWarehouseManagement

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Responsable Affaires Réglementaires - spécialiste produits combinés

...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...

Sap Quality Management Consultant AD

...Manufacturing industry is a strong plus.(SAP QM, SAP Quality Management)#SAPQM #SAPQualityManagement #SAPWM #SAPWarehouseManagement

Sap Quality Management Consultant AD

...Manufacturing industry is a strong plus.(SAP QM, SAP Quality Management)#SAPQM #SAPQualityManagement #SAPWM #SAPWarehouseManagement