1826 Emplois pour manufacturing %252F production %252F operations

Head of Tooling AD

...production and testing of aircraft parts.Operating in a fast-paced environment with high expectations on turnaround time, your ability to bring structure, drive process, and create consistency across ...

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...

Chef d’équipe/Cheffe d’équipe AD

...Manufacturing en collaboration avec le Responsable Operations Excellence. Le profil Expérience d’au moins 2 ans dans le management d’une équipe, de préférence dans le secteur de la production alimenta...

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, ...

Method Transfer & Validation Specialist AD

...manufacturing and purification technologies, with operations in southwest France, is urgently seeking an experienced Freelance Method Transfer & Validation Specialist for a 6-month assignment near Pau...

Method Transfer & Validation Specialist AD

...manufacturing and purification technologies, with operations in southwest France, is urgently seeking an experienced Freelance Method Transfer & Validation Specialist for a 6-month assignment near Pau...