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 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 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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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 : 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,..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..
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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 ..
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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 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 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,..lean environment is preferredIn depth knowledge and understanding of the regulatory system and challenges and opportunitiesHands-on experience and successful track record in contacts..
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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 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 : Brussels Brussels Société : AXA 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 : Brussels Brussels Société : AXA We leverage technology,..disabled persons,..property and casualty,..we act for human progress by protecting what matters...
Postuler | Plus d'offres TDO Program Director Plus d'offres - Brussels |
Lieu : Leuven Flanders Société : Sotera Health Work with local regulatory agencies on new and existing permits,..The responsibility for a successful project includes meeting applicable regulatory and quality system requirements...
Postuler | Plus d'offres Director RA/QA EMEAA Plus d'offres - Leuven |
Lieu : Brussels Brussels Société : AXA 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 with key stakeholders through..
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 negotiation and influencing skills to achieve results in a matrix management environment·Recognized as a strong team leader with a collaborative and growth mind-set·Strong multi-cultural understanding and application·Ability to build collaborative relationships with both internal projec..
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 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 : Ottignies-Louvain-la-Neuve Walloon Region Société : Zoetis contractors and regulatory authorities to ensure smooth handover and operation of the new site...equipment vendors and contractors).Coordinate with the Operational Readiness leader to provide a seamless delivery of the manufacturing capacity.Work closely with local government and 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 |
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