Drug Regulatory Affairs Jobs in Ingelheim am Rhein
1 - 10 von 10
Suchergebnisse - Drug Regulatory Affairs Jobs in Ingelheim am Rhein
SCHOTT AG-Ingelheim am Rhein
Serve as the go-to advisor and trainer for internal SCHOTT-Pharma-specific regulatory topics, such as National Product Registrations and Drug Master Files (DMFs)
• Roll out and oversee standards and central specifications for Dossier-structures across...
Boehringer Ingelheim-Ingelheim am Rhein
The Position
Step into the dynamic world of pharmaceuticals as a Regional Regulatory Lead for EUCAN in Human Pharma. This pivotal role, nestled within our regulatory affairs excellence team, is the driving force behind our development projects...
myability.jobs -
SCHOTT AG-Bingen am Rhein, 13 km von Ingelheim am Rhein
Serve as the go-to advisor and trainer for internal SCHOTT-Pharma-specific regulatory topics, such as National Product Registrations and Drug Master Files (DMFs)
• Roll out and oversee standards and central specifications for Dossier-structures across...
Boehringer Ingelheim-Ingelheim am Rhein
of Drug Regulatory Affairs, are highly welcomed
• In-depth knowledge in pharmacology and/or medicine, preferably with a focus on drug development
• Several years professional experience in Regulatory Affairs or other relevant discipline, e.g...
myability.jobs -
SCHOTT Pharma AG & Co. KGaA-Mainz, 15 km von Ingelheim am Rhein
contributions to the business
• Serve as the go-to advisor and trainer for internal SCHOTT-Pharma-specific regulatory topics, such as National Product Registrations and Drug Master Files (DMFs)
• Roll out and oversee standards and central specifications for...
stepstone.de -
Boehringer Ingelheim-Ingelheim am Rhein
Epidemiology and Medical Affairs to develop safety-focused post-authorisation studies.
• Interpret clinical trial safety data for clinical trial reports and submission documents
• Review and provide medical-scientific input to regulatory documents (e.g. IBs...
myability.jobs -
SCHOTT AG-Mainz, 15 km von Ingelheim am Rhein
Serve as the go-to advisor and trainer for internal SCHOTT-Pharma-specific regulatory topics, such as National Product Registrations and Drug Master Files (DMFs)
• Roll out and oversee standards and central specifications for Dossier-structures across...
Boehringer Ingelheim-Ingelheim am Rhein
Global Epidemiology and Medical Affairs to develop safety-focused post-authorization studies
• Interpret clinical trial safety data for clinical trial reports and submission documents
• Review and provide medical-scientific input to regulatory documents...
myability.jobs -
Barrington James Limited-Frankfurt, 45 km von Ingelheim am Rhein
and contribute to submission strategy, regulatory dossiers, and safety issues.
You proactively identify the need for studies that need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan...
appcast.io -
Veeva Systems, Inc.-Frankfurt, 45 km von Ingelheim am Rhein
experience working with life sciences or healthcare companies performing system implementation experience either as a consultant, business or IT representative
• In-depth knowledge of drug development processes and regulatory submissions; including, Labeling...
appcast.io -
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