1163 offres d'emploi Associate Director Director, Regulatory - |
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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..
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..
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..
Postuler |
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 in ..
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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 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
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 w..
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 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,..
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
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 : Brussels Brussels
Société : AXA
you will be responsible for overseeing the daily operations of the team and to ensure that the team ultimately delivers on its obligations...
Postuler | Plus d'offres TDO Program Director
Plus d'offres - Brussels |
Lieu : Brussels Brussels
Société : AXA
health,..LGBT+,..and monitoring progress of AXA’s largest technology program to date.About the jobJob purpose As Head of the TDO Program team,..
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,..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 |
Lieu : Brussels Brussels
Société : AXA
and report directly to AXA Group Operations’ Deputy CEO,..and together we’re nurturing a culture ofrespect,..disabled persons,..
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...Ensure compliance with global regulatory bodies,..
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,..to ensure alignment,..Inclusion and diversity link closely with our values,..
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 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
for each other,..The team will be fully dedicated to ensuring alignment,..are included and can thrive...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
contractors and regulatory authorities to ensure smooth handover and operation of the new site...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
Ensure compliance with global regulatory bodies,..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 |
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