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Associate Director – Quantitative Sciences Consultant (Data Science / Statistics)

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


Associate Director – Quantitative Sciences Consultant (Data Science / Statistics)

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


Associate Director – Quantitative Sciences Consultant (Data Science / Statistics)

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


Associate Director – Quantitative Sciences Consultant (Data Science / Statistics)

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


Associate Director – Quantitative Sciences Consultant (Data Science / Statistics)

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


Associate Director – Quantitative Sciences Consultant (Data Science / Statistics)

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


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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..

Postuler


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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..

Postuler


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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..

Postuler


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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


Qualified Person Responsible Information and Publicity (QP RIP) and Pharmaceutical Affairs Associate Director - BeLux

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


TDO Program Director

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


TDO Program Director

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


Director RA/QA EMEAA

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


TDO Program Director

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


Director RA/QA EMEAA

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


TDO Program Director

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


Director RA/QA EMEAA

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


TDO Program Director

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


MSG Project Director

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


Director RA/QA EMEAA

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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