2143 offres d'emploi Regulatory Specialist - |
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Lieu : Deerlijk Flanders Société : Michael Page As a successful Regulatory Affairs Specialist - Pharma - BeNeLux you will have the following responsibilities:Prepare,..
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Lieu : Deerlijk Flanders Société : Michael Page maintain and record technical and regulatory documentationEnsure up to date EMEA document management systemCollect information on products to create and update the product regulatory informationInterpret regulatory requirements to ensure compliance of the products Prov..
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Lieu : West Flanders Flanders Société : Michael Page ..French is a plusAs the successful Regulatory Affairs Specialist - Pharma - BeNeLux,..and standardsSupport Change Control process Maintain communication and relation with regulatory stakeholders As a successful Regulatory Affairs Specialist - Pharma - Be..
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Lieu : Ghent Flanders Société : Michael Page they are approximately 4,500 passionate professionals operating in more than 100 markets around the world...As a company built on innovation,..
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Lieu : Ghent Flanders Société : Michael Page prepare regulatory & risk assessments,..you will have the following responsibilities:Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on EuropeCollect needed scientific data,..
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Lieu : Ghent Flanders Société : Michael Page they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally...
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Lieu : Ghent Flanders Société : Michael Page ..prepare regulatory & risk assessments,..As the successful Regulatory Affairs Specialist,..MSDS,..
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Lieu : Ghent Flanders Société : Michael Page they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally...
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Lieu : Ghent Flanders Société : Michael Page they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally...
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Lieu : Ghent Flanders Société : Michael Page or equivalent A minimum of 1-3 years' experience in Regulatory Affairs (dossier preparation & submission,..you will have the following responsibilities:Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on EuropeCo..
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Lieu : Ghent Flanders Société : Michael Page they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally...
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Lieu : Ghent Flanders Société : Michael Page they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally...
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Lieu : Ghent Flanders Société : Michael Page or equivalent A minimum of 1-3 years' experience in Regulatory Affairs (dossier preparation & submission,..As the successful Regulatory Affairs Specialist,..
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Lieu : Ghent Flanders Société : Michael Page they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally...
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Lieu : Ghent Flanders Société : Michael Page The chance to work in a dynamic stimulating environment with a young and highly motivated team RA specialist role - key & central role within the team Based in Ghent region Our client has the vision to make sustainable food production possible...
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific and current regulatory guidelines as applicable to services providedKeys to Success:Bachelor's degreeProven elated experience or equivalent combination of education,..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific ensures alignment of submission process for sites and study are aligned to the critical path for site activationMay work with CRA(s) to prepare the regulatory compliance review packages,..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.Our Clinical Operations team in Belgium is expanding and we are currently looking for a Country Approval Specialist who will be working fro..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific Country Approval Specialist (Submissions) - BelgiumAt Thermo Fisher Scientific,..local regulatory submissions (MoH,..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific local regulatory submissions (MoH,..Country Approval Specialist (Submissions) - BelgiumAt Thermo Fisher Scientific,..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific ensures alignment of submission process for sites and study are aligned to the critical path for site activationMay work with CRA(s) to prepare the regulatory compliance review packages,..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific under guidance local regulatory strategy advice (MoH &/or EC) to internal clientsProvide project specific local start up services and coordination of these projectsMay have contact with investigators for submission related activitiesKey-contact at country level for either Ethical or..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.Our Clinical Operations team in Belgium is expanding and we are currently looking for a Country Approval Specialist who will be working fro..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.Our Clinical Operations team in Belgium is expanding and we are currently looking for a Country Approval Specialist who will be working fro..
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Lieu : Brussels Brussels Société : Thermo Fisher Scientific Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.Our Clinical Operations team in Belgium is expanding and we are currently looking for a Country Approval Specialist who will be working fro..
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