1262 offres d'emploi Associate Director, Product Management - |
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Lieu : Ghent Flanders Société : Argenx The role will play a critical role across the product life cycle and will be a key advisor and enabler of successful product launches and commercialization...
Postuler | Plus d'offres Associate Director/Director, Regulatory Plus d'offres - Ghent |
Lieu : Ghent Flanders Société : Argenx ..argenx is looking for an Associate Director/Director Regulatory Affairs,..to support the rapid growth needed for successful commercialization.Key Accountabilities and Responsibilities:The Associate Director/Director Regulatory Affairs is a key me..
Postuler | Plus d'offres Associate Director/Director, Regulatory Plus d'offres - Ghent |
Lieu : Ghent Flanders Société : Argenx to support the rapid growth needed for successful commercialization.Key Accountabilities and Responsibilities:The Associate Director/Director Regulatory Affairs is a key member of the global regulatory team...
Postuler | Plus d'offres Associate Director/Director, Regulatory Plus d'offres - Ghent |
Lieu : Ghent Flanders Société : Argenx The role will play a critical role across the product life cycle and will be a key advisor and enabler of successful product launches and commercialization...
Postuler | Plus d'offres Associate Director/Director, Regulatory Plus d'offres - Ghent |
Lieu : Brussels Brussels Société : Eurofins traceability and purity of biological substances and products...you will work to ensure that Eurofins’ unique structure as a network of independent companies is reflected in the management of two important IT System,..
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Lieu : Brussels Brussels Société : Eurofins and act as a point of contact for enquiries around federated access management...Project Management experience;..
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Lieu : Brussels Brussels Société : Eurofins You will take responsibility for our Identity Lifecycle Management system,..and act as a point of contact for enquiries around federated access management...
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Lieu : Brussels Brussels Société : Eurofins You will take responsibility for our Identity Lifecycle Management system,..It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products...
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Lieu : Brussels Brussels Société : Eurofins pharmaceutical and cosmetic product testing and in discovery pharmacology,..Working knowledge on Identity and Access Management protocols and technologies:..
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Lieu : Brussels Brussels Société : Eurofins Single-sign-on (SSO) and usage of proprietary Windows Authentication and Authorisation protocols (Kerberos NTLM). Working knowledge in IT Service Management and respective processes on Incident,..
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Lieu : Brussels Brussels Société : Eurofins You will take responsibility for our Identity Lifecycle Management system,..As an IT Director & Programme Manager,..
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Lieu : Brussels Brussels Société : Eurofins along with setting goals and targets for team members. Organisational and time-management skills...As an IT Director & Programme Manager,..
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Lieu : Beerse Flanders Société : Johnson and Johnson and control the Active Pharmaceutical Ingredient (API) solid state form and form attributes and drug product solid state for each phase of development...
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Lieu : Beerse Flanders Société : Johnson and Johnson * Develop the solid-state control strategy for both API and drug product,..* Demonstrated strategic thinking and the ability to help define a vision for the future * Good understanding of the drug development process from early through late development and an appreciation of how Pha..
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Lieu : Beerse Flanders Société : Johnson and Johnson The group provides solid state support for projects at all stages of the product life cycle starting at the preclinical stage...
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Lieu : Beerse Flanders Société : Johnson and Johnson You will be responsible to develop the right API and drug product control strategy...* Develop the solid-state control strategy for both API and drug product,..
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Lieu : Beerse Flanders Société : Johnson and Johnson * Experience and profound knowledge in solid state sciences and characterization of API's and drug product,..In Belgium (Beerse) there is a vacancy for an Associate Director in Solid State Sciences & Characterization ...
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Lieu : Société : BeiGene the Employee is responsible for the following tasks in Belgium and Luxembourg :Regulatory affairs:Verification of the translation compliance of the SPC and the leaflets.The RIP must sign the “Declaration of Conformity” for registration of variations on a marketing authorization (Circul..
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Lieu : Société : BeiGene collection and analysis of KPI for major pharmaceutical activities)Drug safety management :Implementation of the local pharmacovigilance processDesignation as local Qualified Persons responsible for PharmacovigilanceInteraction with European Qualified Person responsible for Pharmaco..
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Lieu : Société : BeiGene etc.)Participation to early access programs managementMarketing monitoring (report to health authority on initial marketing date,..
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Lieu : Société : BeiGene Gathers and analyzes information skillfully.Project Management – Communicates changes and progress;..report and follow-up of adverse eventsFollow-up of local scientific and medical literature for pharmacovigilance relevant informationLocal Signal detectionParticipation to Periodic..
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Lieu : Société : BeiGene prohibition or restriction decisions or any information that can influence the benefit to risk assessment)Review of Medical advertising and medical information processesParticipation to local training processPharmaceutical documentation archiving managementParticipation to Regulator..
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Lieu : Société : BeiGene the Employee is responsible for the following tasks in Belgium and Luxembourg :Regulatory affairs:Verification of the translation compliance of the SPC and the leaflets.The RIP must sign the “Declaration of Conformity” for registration of variations on a marketing authorization (Circul..
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Lieu : Société : BeiGene Gathers and analyzes information skillfully.Project Management – Communicates changes and progress;..responds to management direction;..
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Lieu : Société : BeiGene Gathers and analyzes information skillfully.Project Management – Communicates changes and progress;..etc.) and business continuity plan implementationMonitoring of local pharmaceutical vendorsMedical information management :Collaboration with the Medical information departm..
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