1163 offres d'emploi Associate Director Director, Regulatory - |
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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
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
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..
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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..
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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..
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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,..
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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 ..
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
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 ..
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Lieu :
Société : BeiGene
the above responsibilities could be separated and executed by different persons and/or departments.Qualifications:A minimum of 10 years of pharmaceutical industry/biotech in regulatory affairs in Belgium (and Lux is a plus)Fluent in English,..
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Lieu :
Société : BeiGene
..etc.)Implementation of change control after regulatory approvals (marketing authorization,..The Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical affairs Associate Director is responsible for medical information and publicity i..
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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 Regulatory..
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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,..
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Lieu : Brussels Brussels
Société : AXA
Scale Existing Date & AI,..Job position pitch The role is an exciting opportunity to lead a newly created team at the heart of AXA Group Operations' largest strategic efforts...
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Brussels Brussels
Société : AXA
and progress monitoring of AXA's largest technology program to date.·Oversee the organization of AXA Group's efforts across all three streams (Consolidate Foundations,..
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Leuven Flanders
Société : Sotera Health
Must complete all required training for a “Quality Assurance Director” outlined in the training program...
Postuler | Plus d'offres Director RA/QA EMEAA
Plus d'offres - Leuven |
Lieu : Brussels Brussels
Société : AXA
sourcing,..LGBT+,..disabled persons,..and report directly to AXA Group Operations’ Deputy CEO,..Know you can.About the EntityAXA is becoming a sustainable tech-led company and at AXA Group Operations we are one of the major catalysts for this transformation. We set the tone by triggerin..
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
Power BI or Tableau.·Understanding of insurance products,..sourcing,..You will be responsible for ensuring that deliverables are managed in a timely and structured manner with the necessary quality...
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
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 |
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
schedule management and risk management.Ensure project safety and environmental compliance.Obtain all necessary permits and regulatory approvals for site construction and commissioning.Select and manage key external parties for the project (including engineering consultants,..
Postuler | Plus d'offres MSG Project Director
Plus d'offres - Ottignies-Louvain-la-Neuve |
Lieu : Leuven Flanders
Société : Sotera Health
Track and understand all applicable Quality and Regulatory regulations that impact Sterigenics operations in our Europe and Asia facilities...
Postuler | Plus d'offres Director RA/QA EMEAA
Plus d'offres - Leuven |
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