2480 Emplois pour manufacturing %2525252525252525252525252f production %2525252525252525252525252f 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...

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...

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, ...

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...

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...