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1262 offres d'emploi Associate Director, Product Management -


Associate Director/Director, Regulatory

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


Associate Director/Director, Regulatory

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


Associate Director/Director, Regulatory

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


Associate Director/Director, Regulatory

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


IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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,..

Postuler


IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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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IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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...

Postuler


IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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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IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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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IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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,..

Postuler


IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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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IT Director & Programme Manager Federated Access Management and Identity Lifecycle Management

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,..

Postuler


Associate Director in Solid State Sciences & Characterization

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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Associate Director in Solid State Sciences & Characterization

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..

Postuler


Associate Director in Solid State Sciences & Characterization

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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Associate Director in Solid State Sciences & Characterization

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,..

Postuler


Associate Director in Solid State Sciences & Characterization

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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Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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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Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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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Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

Lieu :
Société : BeiGene

etc.)Participation to early access programs managementMarketing monitoring (report to health authority on initial marketing date,..

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Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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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Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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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Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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..

Postuler


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

Lieu :
Société : BeiGene

Gathers and analyzes information skillfully.Project Management – Communicates changes and progress;..responds to management direction;..

Postuler


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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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