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..
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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 : 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
improving product and process robustness,..A better and healthier every day for every woman.As an equal opportunity employer,..
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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:..
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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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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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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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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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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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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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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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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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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 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 : Brussels Brussels
Société : AXA
The TDO Program (Technology,..and managing these with minimal impact to the program.Where will you be in the organization?The division The TDO Program team will be part of AXA Group Operations’ COO Office.The department / team The TDO Program team is a project focused team that will belo..
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Brussels Brussels
Société : AXA
push boundaries and benefit people in critical moments of their lives...we want to be recognized in three fields of action:..
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Leuven Flanders
Société : Sotera Health
Ensure compliance with global regulatory bodies,..Experience with Quality Systems and applying Regulatory Standards...
Postuler | Plus d'offres Director RA/QA EMEAA
Plus d'offres - Leuven |
Lieu : Brussels Brussels
Société : AXA
..coordination,..Inclusion and diversity link closely with our values,..The team will have a leading role in organizing AXA Group’s efforts across the all three streams (Consolidate Foundations,..
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
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 |
Lieu : Brussels Brussels
Société : AXA Group
ideally in the financial services or insurance industry.·Experience with agile methodologies and tools,..and where individual differences are valued...
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
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 |
Lieu : Brussels Brussels
Société : AXA Group
such as JIRA or Trello.·Demonstrated ability to effectively manage risks and issues,..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
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
the Director of Quality Assurance and Regulatory Affairs – EMEAA,..Directly Supervised by the Global VP Of Quality Assurance and Regulatory Affairs. Indirectly reports to the Regional VP of Operations...
Postuler | Plus d'offres Director RA/QA EMEAA
Plus d'offres - Leuven |
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