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Drug Regulatory Affairs Jobs in Hessen

1 - 15 von 15
1 - 15 von 15
Suchergebnisse - Drug Regulatory Affairs Jobs in Hessen
CSL Behring-Marburg
For our Global Regulatory Affairs department, we are looking for a Global Regulatory Affairs CMC Manager / Senior Manager (100%) in the Immunology & Immunoglobulins Team (m/f/x) R-248105 Fulltime / permanent/ non-tariff Do you want to work in a...
CSL Behring-Marburg
For our Global Regulatory Affairs department, we are looking for aGlobal Regulatory Affairs CMC Manager / Senior Manager (100%) in the Immunology & Immunoglobulins Team (m/f/x)R-248105Fulltime / permanent/ non-tariffDo you want to work in a global...
BioNTech IMFS-Frankfurt
Senior Director Global Regulatory Affairs CMC Mainz, Germany; Cambridge, US; London, United Kingdom | full time | Job ID:7050 In this position, you will lead all aspects of Global Regulatory Affairs CMC for the mRNA-based individualized neoantigen...
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STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
STADA Arzneimittel AG-Bad Vilbel
in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions  •  You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g...
CSL-Marburg
foundation of product labelling and other forms or communicating value propositions for patients, physicians and payersDefinition and content of product business cases that deliver both regulatory approval (meeting worldwide health authority needs...

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