1262 offres d'emploi Associate Director, Product Management - |
|
Lieu : Ghent Flanders
Société : Argenx
argenx is looking for an Associate Director/Director Regulatory Affairs,..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,..among others.Your primary areas of focus are:Provide strategic,..
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
pharmaceutical and cosmetic product testing and in discovery pharmacology,..stakeholder management...both of which are a fundamental part of the Identity and Access Management functionalities at Eurofins...
Postuler |
Lieu : Brussels Brussels
Société : Eurofins
It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products...
Postuler |
Lieu : Brussels Brussels
Société : Eurofins
It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products...
Postuler |
Lieu : Brussels Brussels
Société : Eurofins
along with setting goals and targets for team members. Organisational and time-management skills...and act as a point of contact for enquiries around federated access management...
Postuler |
|
Lieu : Brussels Brussels
Société : Eurofins
traceability and purity of biological substances and products...You will have the chance to be part of an international setting with high visibility and impact by attending critical meetings with high-level management and leading the discussion on security changes. Success ..
Postuler |
Lieu : Brussels Brussels
Société : Eurofins
Project Management experience;..As an IT Director & Programme Manager,..includes workflow management capabilities,..
Postuler |
Lieu : Brussels Brussels
Société : Eurofins
traceability and purity of biological substances and products...pharmaceutical and cosmetic product testing and in discovery pharmacology,..
Postuler |
Lieu : Brussels Brussels
Société : Eurofins
includes workflow management capabilities,..You will lead the design and deployment of Identity and Access Management technologies,..
Postuler |
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...
Postuler |
Lieu : Beerse Flanders
Société : Johnson and Johnson
* 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 Pharmaceutical & Drug Product Development contributes to R&D,..
Postuler |
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...
Postuler |
Lieu : Beerse Flanders
Société : Johnson and Johnson
..As an Associate Director,..and control the Active Pharmaceutical Ingredient (API) solid state form and form attributes and drug product solid state for each phase of development...
Postuler |
Lieu : Beerse Flanders
Société : Johnson and Johnson
Understanding how API form attributes impact the drug product manufacturing process and co-drive particle engineering efforts in the right direction...
Postuler |
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..
Postuler |
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 |
Lieu :
Société : BeiGene
Gathers and analyzes information skillfully.Project Management – Communicates changes and progress;..collection and analysis of KPI for major pharmaceutical activities)Drug safety management :Implementation of the local pharmacovigilance processDesignation as local Qualifie..
Postuler |
Lieu :
Société : BeiGene
lean environment is preferredIn depth knowledge and understanding of the regulatory system and challenges and opportunitiesHands-on experience and successful track record in contacts with regulatory authoritiesDemonstrated success and experience supporting product pre-launch,..
Postuler |
Lieu :
Société : BeiGene
etc.)Participation to early access programs managementMarketing monitoring (report to health authority on initial marketing date,..
Postuler |
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..
Postuler |
Lieu :
Société : BeiGene
etc.)Participation to early access programs managementMarketing monitoring (report to health authority on initial marketing date,..
Postuler |
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..
Postuler |
|
