Supplier Quality Data Specialist

In this capacity, you will manage processes for Supplier Quality data- and document management, user access management, digital reporting, that are necessary to monitor manufacturing and development activities with a focus on QA SystemsIn collaboration with internal stakeholders, you ensure that supplier and material data is accurate, harmonized, visible and...

In this capacity, you will manage processes for Supplier Quality data- and document management, user access management, digital reporting, that are necessary to monitor manufacturing and development activities with a focus on QA SystemsIn collaboration with internal stakeholders, you ensure that supplier and material data is accurate, harmonized, visible and...

In this capacity, you will manage processes for Supplier Quality data- and document management, user access management, digital reporting, that are necessary to monitor manufacturing and development activities with a focus on QA SystemsIn collaboration with internal stakeholders, you ensure that supplier and material data is accurate, harmonized, visible and...

You will be working closely with internal and external stakeholders, leading strategic projects to enable fast Product Launches for our Life Science Business, finding innovative, tailored solutions and pathways to ensure compliant first to market statusYou must have a general understanding of laws and regulations across the globe, governing for example GHS,...

You will be working closely with internal and external stakeholders, leading strategic projects to enable fast Product Launches for our Life Science Business, finding innovative, tailored solutions and pathways to ensure compliant first to market statusYou must have a general understanding of laws and regulations across the globe, governing for example GHS,...

You will be working closely with internal and external stakeholders, leading strategic projects to enable fast Product Launches for our Life Science Business, finding innovative, tailored solutions and pathways to ensure compliant first to market statusYou must have a general understanding of laws and regulations across the globe, governing for example GHS,...

You will be working closely with internal and external stakeholders, leading strategic projects to enable fast Product Launches for our Life Science Business, finding innovative, tailored solutions and pathways to ensure compliant first to market statusYou must have a general understanding of laws and regulations across the globe, governing for example GHS,...

You are in charge of regulations on chemicalsYou will be responsible for classification and labelling of hazardous chemicals and Safety Data SheetsYou assess hazardous properties of products and you derive secondary information required for the Safety Data Sheet and labelYou will maintain and analyze regulatory data in our central product safety data base...

Responsibility for wide-ranging technical and strategic EHS management activitiesEvaluation and optimization of organizational design and (work) processesFocus on ensuring that the regulatory content in the System is current with respect to global requirementsCoordination of efficient and timely execution and delivery of the mass updates of regulatory master...

Responsibility for wide-ranging technical and strategic EHS management activitiesEvaluation and optimization of organizational design and (work) processesFocus on ensuring that the regulatory content in the System is current with respect to global requirementsCoordination of efficient and timely execution and delivery of the mass updates of regulatory...

Responsibility for wide-ranging technical and strategic EHS management activitiesEvaluation and optimization of organizational design and (work) processesFocus on ensuring that the regulatory content in the System is current with respect to global requirementsCoordination of efficient and timely execution and delivery of the mass updates of regulatory master...

Responsibility for wide-ranging technical and strategic EHS management activitiesEvaluation and optimization of organizational design and (work) processesFocus on ensuring that the regulatory content in the System is current with respect to global requirementsCoordination of efficient and timely execution and delivery of the mass updates of regulatory...

Supporting the authorization of biocidal products and other regulatory activities under the regime of the EU BPR and under comparable jurisdictions in other target markets (e.g. US FIFRA, K-BPR)Assessment of the respective country specific regulatory status and implementation of registration strategies Support of active substance registration dossiers to...

Supporting the authorization of biocidal products and other regulatory activities under the regime of the EU BPR and under comparable jurisdictions in other target markets (e.g. US FIFRA, K-BPR)Assessment of the respective country specific regulatory status and implementation of registration strategies Support of active substance registration dossiers to...

Supporting the authorization of biocidal products and other regulatory activities under the regime of the EU BPR and under comparable jurisdictions in other target markets (e.g. US FIFRA, K-BPR)Assessment of the respective country specific regulatory status and implementation of registration strategies Support of active substance registration dossiers to...

Supporting the authorization of biocidal products and other regulatory activities under the regime of the EU BPR and under comparable jurisdictions in other target markets (e.g. US FIFRA, K-BPR)Assessment of the respective country specific regulatory status and implementation of registration strategies Support of active substance registration dossiers to...

Creation and maintenance of project and study plans in iMAP/PlaniswareDevelopment of plans and study protocols into a meaningful, robust project plan, which is captured on a project management platformTracking project and study progress through reporting and ensure that plans are a reliable source of information for senior management and decision...

Creation and maintenance of project and study plans in iMAP/PlaniswareDevelopment of plans and study protocols into a meaningful, robust project plan, which is captured on a project management platformTracking project and study progress through reporting and ensure that plans are a reliable source of information for senior management and decision...

Creation and maintenance of project and study plans in iMAP/PlaniswareDevelopment of plans and study protocols into a meaningful, robust project plan, which is captured on a project management platformTracking project and study progress through reporting and ensure that plans are a reliable source of information for senior management and decision makersClose...

Creation and maintenance of project and study plans in iMAP/PlaniswareDevelopment of plans and study protocols into a meaningful, robust project plan, which is captured on a project management platformTracking project and study progress through reporting and ensure that plans are a reliable source of information for senior management and decision makersClose...