1163 offres d'emploi Associate Director Director, Regulatory - |
|
Lieu : Heist-op-den-Berg Flanders Société : Organon it is expected that you will visit the Oss site once every other week.ResponsibilitiesTakes a leading role in CMS projects executed independently or in close collaboration with fellow CMS team members and provides mentoring or coaching to the CMS team or internal customers throughout all p..
Postuler |
Lieu : Heist-op-den-Berg Flanders Société : Organon including associated vaccination prerequisitesFlexible Work Arrangements:Shift:Valid Driving License:Hazardous Material(s):Number of Openings:..
Postuler |
Lieu : Heist-op-den-Berg Flanders Société : Organon including associated vaccination prerequisitesFlexible Work Arrangements:Shift:Valid Driving License:Hazardous Material(s):Number of Openings:..
Postuler |
Lieu : Heist-op-den-Berg Flanders Société : Organon it is expected that you will visit the Oss site once every other week.ResponsibilitiesTakes a leading role in CMS projects executed independently or in close collaboration with fellow CMS team members and provides mentoring or coaching to the CMS team or internal customers throughout all p..
Postuler |
Lieu : Heist-op-den-Berg Flanders Société : Organon it is expected that you will visit the Oss site once every other week.ResponsibilitiesTakes a leading role in CMS projects executed independently or in close collaboration with fellow CMS team members and provides mentoring or coaching to the CMS team or internal customers throughout all p..
Postuler |
Lieu : Heist-op-den-Berg Flanders Société : Organon Job DescriptionAssociate Director – Quantitative Sciences Consultant (Data Science / Statistics)This position is ideally located at our manufacturing sites in Oss (The Netherlands) or Heist- op-den-Berg (Belgium).The positionBy joining the Center for Mathematical Sci..
Postuler |
Lieu : Société : BeiGene The Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical affairs Associate Director is responsible for medical information and publicity in Belgium and Luxembourg.As Pharmaceutical Affairs Associate Director,..
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 Regulatory..
Postuler |
|
Lieu : Société : BeiGene The Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical affairs Associate Director is responsible for medical information and publicity in Belgium and Luxembourg.As Pharmaceutical Affairs Associate Director,..
Postuler |
Lieu : Société : BeiGene The Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical affairs Associate Director is responsible for medical information and publicity in Belgium and Luxembourg.As Pharmaceutical Affairs Associate Director,..
Postuler |
Lieu : Société : BeiGene The Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical affairs Associate Director is responsible for medical information and publicity in Belgium and Luxembourg.As Pharmaceutical Affairs Associate Director,..
Postuler |
Lieu : Société : BeiGene The Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical affairs Associate Director is responsible for medical information and publicity in Belgium and Luxembourg.As Pharmaceutical Affairs Associate Director,..
Postuler |
Lieu : Société : BeiGene etc.)Implementation of change control after regulatory approvals (marketing authorization,..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 si..
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 ..
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 Regulatory..
Postuler |
Lieu : Brussels Brussels Société : AXA and where individual differences are valued...for each other,..including life,..Data & Operations) is one of AXA Group Operation’s key strategic efforts in the coming years...
Postuler | Plus d'offres TDO Program Director Plus d'offres - Brussels |
Lieu : Brussels Brussels Société : AXA Increase Operational Efficiency),..and report directly to AXA Group Operations’ Deputy CEO,..Main responsibilities·Lead and manage the TDO Program team,..
Postuler | Plus d'offres TDO Program Director Plus d'offres - Brussels |
Lieu : Leuven Flanders Société : Sotera Health and regulatory guidance to processing facilities within Europe and Asia and has responsibility for the quality oversight of Sterigenics’ quality system implementation and execution.DUTIES AND RESPONSIBILITIES:..
Postuler | Plus d'offres Director RA/QA EMEAA Plus d'offres - Leuven |
Lieu : Brussels Brussels Société : AXA but also achieve economies of scale and synergies when necessary.At AXA Group Operations,..Main responsibilities·Lead and manage the TDO Program team,..
Postuler | Plus d'offres TDO Program Director Plus d'offres - Brussels |
Lieu : Leuven Flanders Société : Sotera Health Ensure compliance with global regulatory bodies,..the Director of Quality Assurance and Regulatory Affairs – EMEAA,..
Postuler | Plus d'offres Director RA/QA EMEAA Plus d'offres - Leuven |
Lieu : Brussels Brussels Société : AXA Group political and matrixed environment.·Experience in following up on business cases to identify value realization and monitor progress towards a defined goal·Strong track record of successfully delivering large-scale technology programs,..
Postuler | Plus d'offres TDO Program Director Plus d'offres - Brussels |
Lieu : Leuven Flanders Société : Sotera Health and regulatory guidance to processing facilities within Europe and Asia and has responsibility for the quality oversight of Sterigenics’ quality system implementation and execution.DUTIES AND RESPONSIBILITIES:..
Postuler | Plus d'offres Director RA/QA EMEAA Plus d'offres - Leuven |
Lieu : Brussels Brussels Société : AXA Group including the ability to develop and manage budgets and financial plans.·Experience with project portfolio management (PPM) tools and methodologies to prioritize and manage a portfolio of technology projects.Soft skills / transversal skills ·Strong change management skills with practica..
Postuler | Plus d'offres TDO Program Director Plus d'offres - Brussels |
Lieu : Ottignies-Louvain-la-Neuve Walloon Region Société : Zoetis We are currently seeking to fill a new position to support our growing biopharmaceutical portfolio. POSITION SUMMARYThe Project Director shall manage the design,..
Postuler | Plus d'offres MSG Project Director Plus d'offres - Ottignies-Louvain-la-Neuve |
Lieu : Leuven Flanders Société : Sotera Health The Director of Quality Assurance and Regulatory Affairs – EMEAA is a permanent member of both the Global Quality Leadership Team and the cross-functional EMEAA Regional Leadership Team EDUCATION,..
Postuler | Plus d'offres Director RA/QA EMEAA Plus d'offres - Leuven |
|