2238 Emplois pour manufacturing %25252525252F production %25252525252F operations

Head of Operations AD

...Operations to lead a newly established business unit focused on highly regulated sectors and heavy engineering manufacturing . Based at a 1 million sq. ft industrial facility in Normandy, this is a ca...

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...

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...

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...

Responsable Méthodes et Industrialisation H/F (CDI) AD

...Manufacturing -Fournir les dossiers de fabrication et l'ensemble des standards nécessaires à la production. -Participer à l'ordonnancement de la production pour optimiser les coûts de fabrication. -Êt...