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Deutschland - Senior Manager Document Management (m/f)

Pharmazeutische Industrie - Produktion, Herstellung - Abteilungsleiter / Manager

Resource planning and allocation of functional resources in order to meet timelines, budgets and expected quality level of AbbVie's clinical programs. Ensure that staff and trial master files are compliant with ICH, GXP, OEC and AbbVie SOPs by conducting quality control checks of assigned Therapeutic Are a studies, including but not limited to the following key activities: investigational product (IP) release to clinical sites, audit/inspection readiness, archival of the TMF identify. Identify, implement and maintain strategic process improvements and standards for Document Management functional area designed to reduce cycle time and improve productivity. Provide feedback, coaching, and coun ...

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