1163 offres d'emploi Associate Director Director, Regulatory - |
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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 : 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..
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 : 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..
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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
..etc.)Implementation of change control after regulatory approvals (marketing authorization,..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..
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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
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 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
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
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,..
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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..
Postuler |
Lieu : Brussels Brussels
Société : AXA
Increase Operational Efficiency) and ensure consistency and value realization for each initiative is captured and accurately reported.·Identify program-wide risks and issues and manage these with minimal impact to the program.·Follow up on business cases to identify value realization and..
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Brussels Brussels
Société : AXA
but also achieve economies of scale and synergies when necessary.At AXA Group Operations,....We leverage technology,..health,..
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,..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..
Postuler | Plus d'offres Director RA/QA EMEAA
Plus d'offres - Leuven |
Lieu : Brussels Brussels
Société : AXA
Scale Existing Date & AI,..and proactively identify and mitigate potential roadblocks.·Communicate complex concepts to non-technical stakeholders in a clear and concise manner.·Develop and manage budgets and financial plans for the TDO Program.·Build and maintain strong relationships wi..
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 Group
to ensure alignment,..such as JIRA or Trello.·Demonstrated ability to effectively manage risks and issues,..This is your chance to build the tomorrow you want...
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 has indirect responsibility for the QA Managers within the EMEAA facilities...
Postuler | Plus d'offres Director RA/QA EMEAA
Plus d'offres - Leuven |
Lieu : Brussels Brussels
Société : AXA Group
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 : 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,..The Director of Quality Assurance and Regulatory Affairs – EMEAA has indirect responsibility for the QA Managers within the EMEAA facilities...
Postuler | Plus d'offres Director RA/QA EMEAA
Plus d'offres - Leuven |
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