Junior Expert Drug Regulatory Affairs (m/w/d)
Bad Homburg vor der Höhe
Vollzeit
Fresenius Medical Care
… in the ever-evolving medical technology industry? As a Junior Expert in Drug Regulatory Affairs, you'll play a crucial role in ensuring that … medical technology industry? As a Junior Expert in Drug Regulatory Affairs, you'll play a crucial role in ensuring that cutting-edge medical … the ever-evolving medical technology industry? As a Junior Expert in Drug Regulatory Affairs, you'll play a crucial role in ensuring that cutting-edge medical …Junior Expert Drug Regulatory Affairs StellenangeboteEU-QPPV & Head QPPV Office (d/f/m)
Holzkirchen
Vollzeit
Sandoz
… a 24-hour basis and manage/cascade safety related requests for systems or drug safety related information to ensure any requests are answered fully and … To ensure timely and quality preparation (together with PV, Regulatory Affairs (RA) and Medical Safety) the appropriate medical input to PV reports … as required. To ensure timely and quality preparation (together with PV, Regulatory Affairs (RA) and Medical Safety) the appropriate medical input to PV …Junior Drug RegulatoryRA Manager Medicine and Global Labelling (m/w/d)
Freiburg
Vollzeit
Dr. Falk Pharma GmbH
… Abgleich mit den jeweils gültigen regulatorischen Anforderungen. Orphan Drug Designations, Paediatric Investigation Plans (PIPs) und Briefing-Dokumente … Naturwissenschaftler*in Mehrjährige Berufserfahrung in Bereich Regulatory Affairs, optimalerweise über 10 Jahre jedoch mindestens 7 Jahre. Vertiefte … Naturwissenschaftler*in Mehrjährige Berufserfahrung in Bereich Regulatory Affairs, optimalerweise über 10 Jahre jedoch mindestens 7 Jahre. Vertiefte …Expert Drug Regulatory
Senior Pharmakovigilanz Manager (m/w/d)
Greifswald
Vollzeit/Teilzeit
Dr. Haney Pharma GmbH
… Apothekern und Medizinern, die in unserem Unternehmen als Drug Safety Manager oder Regulatory Affairs Manager arbeiten. Ihre Aufgaben … die in unserem Unternehmen als Drug Safety Manager oder Regulatory Affairs Manager arbeiten. Ihre Aufgaben sind äußerst abwechslungsreich und richten … und Medizinern, die in unserem Unternehmen als Drug Safety Manager oder Regulatory Affairs Manager arbeiten. Ihre Aufgaben sind äußerst abwechslungsreich und …Junior Expert Regulatory AffairsApotheker / Pharmazeut (m/w/d)
Schwäbisch Gmünd
Vollzeit
Weleda
… Enge Zusammenarbeit mit den Bereichen Arzneimittelherstellung, Drug Regulatory Affairs und Analytische Entwicklung Mitarbeit in … Zusammenarbeit mit den Bereichen Arzneimittelherstellung, Drug Regulatory Affairs und Analytische Entwicklung Mitarbeit in interdisziplinären Projektteams … Enge Zusammenarbeit mit den Bereichen Arzneimittelherstellung, Drug Regulatory Affairs und Analytische Entwicklung Mitarbeit in interdisziplinären …Junior Expert Regulatory AffairsEngagement Manager - R&D (Remote)
Berlin
Vollzeit
Veeva Systems
… areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You’ll Do Lead multiple project … on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You’ll Do … you will focus on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What …Junior AffairsW2-Professur Arzneimittelqualität- und zulassung
Pirmasens
Vollzeit
Hochschule Kaiserslautern
… in mindestens einem sollen diese tiefgehend und weitreichend sein: Drug Regulatory Affairs (EU, USA) Qualitätsmanagement und Qualitätssicherung … einem sollen diese tiefgehend und weitreichend sein: Drug Regulatory Affairs (EU, USA) Qualitätsmanagement und Qualitätssicherung Eigene … in mindestens einem sollen diese tiefgehend und weitreichend sein: Drug Regulatory Affairs (EU, USA) Qualitätsmanagement und Qualitätssicherung Eigene …Junior Regulatory Affairs StellenangeboteProcurement Lead Clinical Development (f/m/d)
Aachen
Vollzeit
Grünenthal
… all other categories in the R&D Development area (e.g. Reg. Affairs, Drug Safety, CMC, CTS, Data Science, etc.) Gain and deliver on a comprehensive … and support all other categories in the R&D Development area (e.g. Reg. Affairs, Drug Safety, CMC, CTS, Data Science, etc.) Gain and deliver on a … organization Experience in categories close to clinical trials (e.g. Regulatory Affairs, CMC, CTS, Drug Safety, Medical Writing, Biosampling, Data …Expert Drug AffairsGlobal Head Infection Prevention (m/f/d)
Hamburg
Vollzeit
Olympus Europa SE & Co. KG (OEKG)
… - CDC, European Centre for Disease Prevention and Control -ECDC, US Food & Drug Administration – FDA, or equivalent), and/or Country, Regional, State, or … Medical Officer, and other senior leaders within Medical and Scientific Affairs to share best practices and ensure consistent patient safety for all … European Centers for Prevention & Disease Control, notified bodies, regulatory agencies, and public health authorities worldwide Create and chair the …Regulatory Affairs StellenangeboteAssociate Director Regulatory Affairs
Aachen
Home Office
PAION Pharma GmbH
… M3 documentation. In addition, the job holder establishes and maintains Drug Master Files in various non-European territories in cooperation with local … Your tasks The Associate Director Regulatory Affairs is responsible for establishing and implementing the regulatory CMC … Your tasks The Associate Director Regulatory Affairs is responsible for establishing and implementing the Regulatory …Junior DrugScientist
Biberach an der Riß
Vollzeit
BI Pharma GmbH&Co.KG
… transfer documents will be one of your main tasks. Your good knowledge in drug regulatory affairs will help you in authoring submission documents and … will be one of your main tasks. Your good knowledge in drug regulatory affairs will help you in authoring submission documents and answer questions from … documents will be one of your main tasks. Your good knowledge in drug regulatory affairs will help you in authoring submission documents and answer …Expert DrugHead of Regulatory Affairs*
Deutschland
Vollzeit
AiCuris GmbH & Co. KG
… infectious diseases in immunocompromised patients. Our front-runner drug Prevymis®, a prophylactic treatment for CMV infection in transplant … Your mission We are seeking a dynamic and experienced Head of Regulatory Affairs to lead NDA and MAA filings of our lead candidate Pritelivir. As Head of … Your mission We are seeking a dynamic and experienced Head of Regulatory Affairs to lead NDA and MAA filings of our lead candidate Pritelivir. As …Junior Expert Drug Affairs Stellenangebote(Junior) Pharmacovigilance Officer (w/f/d) Global Drug Safety
Frankfurt am Main
Vollzeit
Merz Therapeutics
… is appreciated Willingness to engage in ongoing training for current drug safety practices and GVP implementation Confident handling of Microsoft … the UK (e.g., AMG, AMWHV, GVP) Basic knowledge in the field of Regulatory Affairs for medicinal products is appreciated Willingness to engage in ongoing … "Stufenplanbeauftragte". Tracking and analysis of updates in legal and regulatory PV requirements and the development of implementation initiatives and PV …Expert DrugJunior Clinical Research Associate
München
Vollzeit
AstraZeneca
… to learn relevant Alexion Therapeutic AreasGood understanding of the drug development processExcellent understanding of Clinical Study Management … and assisting with feasibility activitiesCollaborating with local Medical Affairs and other internal stakeholders, as neededFollowing quality issue … some countries, as required, CRAs are accountable for study startup and regulatory maintenance; tasks may include collection, preparation, review and …Expert Drug Affairs