2028 Emplois pour manufacturing %252F production %252F operations

Buyer/Planner AD

...operations team. With recent regulatory clearance and ambitious growth plans, they are rolling out transformative technology across Europe and the US. To support this expansion and ensure seamless pro...

JD Edward's Consultant AD

...production L1 L2 support.Should possess a deep understanding of factory production operations and production line processes along with strong incident and problem management skills for JDE production ...

Buyer/Planner AD

...operations team. With recent regulatory clearance and ambitious growth plans, they are rolling out transformative technology across Europe and the US. To support this expansion and ensure seamless pro...

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 Manufacturing Consultant AD

...operations continue. The need is for a mid-level SAP PP Consultant to work onsite supporting users in small activities related to production planning. This site is running S/4HANA , though using ECC-s...

SAP Consultant Manufacturing Industry AD

...operations continue. The need is for a mid-level SAP PP Consultant to work onsite supporting users in small activities related to production planning. This site is running S/4HANA , though using ECC-s...