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
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
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
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
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 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 :
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
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 ..
Postuler |
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,..
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..
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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,..
Postuler |
Lieu : Brussels Brussels
Société : AXA
or people of different origins) and to promoting Diversity & Inclusion by creating a work environment where all employees are treated with dignity and respect,..
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Brussels Brussels
Société : AXA
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
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
LGBT+,..cultural diversity and creativity of over 8,000 employees worldwide and we’re committed to equal opportunities in all aspects of employment (gender,..
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Leuven Flanders
Société : Sotera Health
..Experience with Quality Systems and applying Regulatory Standards...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
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
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
property and casualty,..coordination,..Inclusion and diversity link closely with our values,..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 : Ottignies-Louvain-la-Neuve Walloon Region
Société : Zoetis
........the Project Director shall lead a team of engineering consultants,..construction managers and SMEs to ensure the quality and timely completion of the project within budget.POSITION RESPONSIBILITIES Manage the Project Management Delivery TeamEnsure the project is deliv..
Postuler | Plus d'offres MSG Project Director
Plus d'offres - Ottignies-Louvain-la-Neuve |
Lieu : Leuven Flanders
Société : Sotera Health
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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