117 offres d'emploi Regulatory Affairs Consultant - |
|
Lieu : Puurs Flanders
Société : Akkodis
Manufacturing & Controls (GCMC) in order to support the introduction of new products.Scope of work:Support regulatory submissions (CTD,..
Postuler | Plus d'offres Regulatory Affairs Consultant
Plus d'offres - Puurs |
Lieu : Puurs Flanders
Société : Akkodis
global regulatory colleagues (Global Chemistry,..Manufacturing & Controls (GCMC) in order to support the introduction of new products.Scope of work:Support regulatory submissions (CTD,..
Postuler | Plus d'offres Regulatory Affairs Consultant
Plus d'offres - Puurs |
Lieu : Puurs Flanders
Société : Akkodis
we have close to 1000 experts active in different technical fields.Job descriptionAs a Regulatory Affairs Consultant,..
Postuler | Plus d'offres Regulatory Affairs Consultant
Plus d'offres - Puurs |
Lieu : Zaventem Flanders
Société : Parexel
you will be responsible for providing expertise in registration Regulatory Affairs,..and Luxembourg.Demonstrate knowledge of EU and country-specific regulations and be familiar with document management systems.Understand the Regulatory processes required to update labe..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
and Luxembourg.Demonstrate knowledge of EU and country-specific regulations and be familiar with document management systems.Understand the Regulatory processes required to update labelling of a product,..
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
there's no limit to what we can achieve. We are seeking an experienced Regulatory Affairs Consultant to join our team...
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
you will be responsible for providing expertise in registration Regulatory Affairs,..As a Regulatory Affairs Consultant,..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
you will be responsible for providing expertise in registration Regulatory Affairs,..and Luxembourg.Demonstrate knowledge of EU and country-specific regulations and be familiar with document management systems.Understand the Regulatory processes required to update labe..
Postuler |
|
Lieu : Zaventem Flanders
Société : Parexel
As a Regulatory Affairs Consultant,..with a focus on Global Regulatory (Clinical/Safety) and Global Labelling...
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
and Luxembourg.Demonstrate knowledge of EU and country-specific regulations and be familiar with document management systems.Understand the Regulatory processes required to update labelling of a product,..
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
with a focus on Global Regulatory (Clinical/Safety) and Global Labelling...and Luxembourg).Job ResponsibilitiesUtilize your previous experience in registration Regulatory Affairs to support Global Regulatory (Clinical / Safety) and Global Labeling processes.Comp..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
with a focus on Global Regulatory (Clinical/Safety) and Global Labelling...and Luxembourg.Demonstrate knowledge of EU and country-specific regulations and be familiar with document management systems.Understand the Regulatory processes required to update labelling of a produc..
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
and Luxembourg.Demonstrate knowledge of EU and country-specific regulations and be familiar with document management systems.Understand the Regulatory processes required to update labelling of a product,..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
As a Regulatory Affairs Consultant,..you will be responsible for providing expertise in registration Regulatory Affairs,..
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
....As a Regulatory Affairs Consultant,..with a focus on Global Regulatory (Clinical/Safety) and Global Labelling...
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
As a Regulatory Affairs Consultant,..3-5 years in registration Regulatory Affairs to support Global Regulatory (Clinical / Safety) and Global Labeling processes.Client-focused approach to workExcellent interpersonal and intercultural communication ..
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
there's no limit to what we can achieve. We are seeking an experienced Regulatory Affairs Consultant to join our team...
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
and Luxembourg.Demonstrate knowledge of EU and country-specific regulations and be familiar with document management systems.Understand the Regulatory processes required to update labelling of a product,..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity?..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team!..
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
you will play a vital role in our company's worldwide post-approval regulatory activities,..and mitigate risks associated with regulatory procedures and activities.Experience and Knowledge Requirements:University-level education,..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
and annual reports.Assess change controls and provide regulatory assessments of quality changes in production and quality control.Review study reports from the quality control and production departments to ensure compliance with regulatory requirements.Coordinate submission p..
Postuler |
Lieu : Zaventem Flanders
Société : Parexel
and annual reports.Assess change controls and provide regulatory assessments of quality changes in production and quality control.Review study reports from the quality control and production departments to ensure compliance with regulatory requirements.Coordinate submission p..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
..you will play a vital role in our company's worldwide post-approval regulatory activities,..within the pharmaceutical industry.Strong understanding of CMC and post-approval regulatory requirements.Experience in writing CMC (technical) sections of regulatory documents..
Postuler |
Lieu : Wavre Wallonia
Société : Parexel
within the pharmaceutical industry.Strong understanding of CMC and post-approval regulatory requirements.Experience in writing CMC (technical) sections of regulatory documents such as registration files or variations.Knowledge of biological processes.Background in validation/..
Postuler |
|
