Drug Jobs in Hessen
1 - 15 von 31
Suchergebnisse - Drug Jobs in Hessen
Aenova Group-Marburg
Drug Regulatory Affairs Manager (w/m/d)
für den Standort Marburg, Deutschland
Sie möchten einen wertvollen Beitrag für die Gesundheit von Patient*innen leisten? Und eigenverantwortlich etwas wirklich Sinnvolles bewirken? Dann freuen...
stepstone.de -
ARCONDIS AG / GmbH-Frankfurt
strong focus on FDA processes.
• In-depth knowledge of FDA regulations, guidelines, and submission processes for both medical devices and pharmaceutical products.
• Demonstrated success in managing submissions and gaining device and drug approvals...
appcast.io -
Sanofi-Aventis Deutschland GmbH-Frankfurt am Main
und Gebrauchsinformation)
• für das Lifecycle-Management bestehender (EU) Zulassungen
• bei der Beantwortung regulatorischer Fragestellungen
• der Mitarbeit von Projekten
Anforderungen & Qualifikationen
• Du bist im Master of Drug Regulatory Affairs eingeschrieben...
myability.jobs -
Veeva Systems, Inc.-Frankfurt
life sciences industry, committed to making a positive impact on its customers, employees, and communities.
The Role
Help us transform and bring innovation to Drug Safety and Pharmacovigilance!
Veeva is looking for senior system implementation...
appcast.io -
CureVac SE-Wiesbaden
CureVac SE is a global biopharmaceutical company researching and developing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on prophylactic vaccines, innovative cancer immunotherapies and protein-based therapies...
stepstone.de -
CSL Behring-Marburg
including indication selection, drug design and lead candidate selection, assay development and validation, mechanism of action, establishment of animal models, efficacy and safety, and comparison of in-house and competitor drug candidates.
You will work...
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...
jobspreader.com -
Global Regulatory Affairs CMC Manager / Senior Manager (100%) in the Immunology & Immunoglobulins...
CSL Behring-Marburg
regulatory
• experience is an advantage.
• Good knowledge of pharmaceutical drug development, and CMC regulations / guidelines governing the development and the lifecycle management of pharmaceuticals / biotechnology products.
• Excellent communication...
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...
jobspreader.com -
Resolute Digital, a Weber Shandwick Company-Frankfurt
wissenschaftliche Zusammenhänge und brennen dafür, diese in Geschichten umzusetzen, die Menschen interessieren und miteinander verbinden. Ob für Fachkreise oder Patient:innen, medizinisch komplexe Themen, RX, Orphan Drugs, hoch kompetitive Gesundheitsbereiche...
appcast.io -
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...
jobspreader.com -
LEO Pharma GmbH-Neu-Isenburg
similar role
• Minimum of 10 years demonstrable experience, within the pharmaceutical industry, in medical affairs and or in clinical research and development
• Solid knowledge of drug development, safety, regulatory, market access and reimbursement...
stepstone.de -
BDH-Klinik Braunfels gGmbH-Braunfels
Hormondiagnosstik, therapeutisches Drug-Monitoring, PCR, Liquor-Zytologie und Urindiagnostik selbständig durch
• Die Probeneingangskontrolle und Auftragserfassung wird von Ihnen eigenverantwortlich bearbeitet
• Alle Messungen und Qualitätskontrollen...
maxime-media.de -
Randstad-Frankfurt am Main
Tools or Six Sigma Green Belt certification is highly preferred
• Excellent knowledge of relevant regulatory requirements related to medical devices, drug-device-combination products as per e.g. 21 CFR 820, ISO 13485, EU Medical Device Regulation, ISO...
randstad.com -
Wiesbaden
critical data points when planning for each assigned protocol
• Develop Quality Control strategies for team member projects
• Perform clinical duties (e.g. Drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope...
icims.com -
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