Aktuelle Jobs im Zusammenhang mit Specialist Corporate Drug Regulatory Affairs - Frankfurt Am Main - Viatris
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Drug Regulatory Affairs Manager
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Aenova Group VollzeitDrug Regulatory Affairs Manager (w/m/d)Wir suchen einen erfahrenen Regulatory Affairs Manager, der unsere Marke Aenova in der Branche der Medizinprodukte und Arzneimittel weiterentwickelt. Als wichtiger Teil unseres Teams werden Sie sich um die strategische Planung und Umsetzung von Regulierungsstrategien kümmern, um sicherzustellen, dass unsere Produkte...
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Drug Regulatory Affairs Manager
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Aenova Group VollzeitDrug Regulatory Affairs Manager (w/m/d)Wir suchen einen erfahrenen Regulatory Affairs Manager, der unsere Marke Aenova in der Branche der Medizinprodukte und Arzneimittel weiterentwickelt. Als wichtiger Teil unseres Teams werden Sie sich um die strategische Planung und Umsetzung von Regulierungsstrategien kümmern, um sicherzustellen, dass unsere Produkte...
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Regulatory Affairs Specialist
vor 2 Wochen
Monheim am Rhein, Nordrhein-Westfalen, Deutschland Elanco VollzeitAbout ElancoAt Elanco, we are a global leader in animal health, dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. Our vision is to 'Food and Companionship Enriching Life' and our approach to sustainability – the Elanco Healthy Purpose – is to advance the health of animals, people, the...
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Regulatory Affairs Specialist
vor 2 Wochen
Monheim am Rhein, Nordrhein-Westfalen, Deutschland Elanco VollzeitAbout ElancoAt Elanco, we are a global leader in animal health, dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. Our vision is to 'Food and Companionship Enriching Life' and our approach to sustainability – the Elanco Healthy Purpose – is to advance the health of animals, people, the...
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Regulatory Affairs Specialist
vor 1 Woche
Monheim am Rhein, Nordrhein-Westfalen, Deutschland Elanco VollzeitAbout ElancoAt Elanco, we're driven by a passion for innovation and a commitment to delivering high-quality products and services that improve the lives of animals and people.We're a global leader in animal health, dedicated to advancing the health of animals, people, and the planet through our Elanco Healthy Purpose.Job SummaryWe're seeking a highly skilled...
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Regulatory Affairs Specialist
vor 1 Woche
Monheim am Rhein, Nordrhein-Westfalen, Deutschland Elanco VollzeitAbout ElancoAt Elanco, we're driven by a passion for innovation and a commitment to delivering high-quality products and services that improve the lives of animals and people.We're a global leader in animal health, dedicated to advancing the health of animals, people, and the planet through our Elanco Healthy Purpose.Job SummaryWe're seeking a highly skilled...
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Regulatory Affairs Specialist
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland Merz Therapeutics VollzeitAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Merz Therapeutics. As a key member of our regulatory affairs department, you will play a critical role in ensuring the compliance of our medicinal products with global regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory strategies to...
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Regulatory Affairs Specialist
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland Merz Therapeutics VollzeitAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Merz Therapeutics. As a key member of our regulatory affairs department, you will play a critical role in ensuring the compliance of our medicinal products with global regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory strategies to...
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Regulatory Affairs Specialist Eu
vor 4 Monaten
Frankfurt am Main, Deutschland Clinglobal Group Vollzeit**Regulatory Affairs Specialist - European Union** Clinglobal is an Animal Health Contract Research Organisation and supports our global operations in various countries. We are currently looking for a** Regulatory Affairs Specialist** based in the EU to join our growing Regulatory Affairs team at Clinglobal. This position offers the opportunity to work...
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Regulatory Affairs Specialist
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland elemed VollzeitJob Description:Job Title: Regulatory Affairs SpecialistJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Elemed. As a key member of our quality management team, you will be responsible for maintaining and improving our Quality Management System (QMS), leading audits, and driving regulatory compliance at product...
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Regulatory Affairs Specialist
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland elemed VollzeitJob Description:Job Title: Regulatory Affairs SpecialistJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Elemed. As a key member of our quality management team, you will be responsible for maintaining and improving our Quality Management System (QMS), leading audits, and driving regulatory compliance at product...
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Regulatory Affairs Specialist
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Grifols VollzeitRegulatory Affairs ManagerGrifols is seeking a highly skilled Regulatory Affairs Manager to support the Technical Director in the development and implementation of the strategic regulatory plan. The successful candidate will have primary responsibility for European wide registrations and license maintenance to ensure timely approvals in alignment with...
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Regulatory Affairs Specialist
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Grifols VollzeitRegulatory Affairs ManagerGrifols is seeking a highly skilled Regulatory Affairs Manager to support the Technical Director in the development and implementation of the strategic regulatory plan. The successful candidate will have primary responsibility for European wide registrations and license maintenance to ensure timely approvals in alignment with...
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Regulatory Affairs Specialist
vor 1 Monat
Frankfurt am Main, Hessen, Deutschland Merz Therapeutics GmbH VollzeitPosition: (Junior) Specialist Regulatory Affairs (m/w/d)In dieser Rolle sind Sie verantwortlich für die Aktualisierung und Pflege von regulatorischen Dokumenten. Sie sorgen dafür, dass alle Daten korrekt im Regulatory Information Management System (RIMS) eingegeben werden.Zusätzlich verwalten Sie die Zugriffsrechte für RIMS sowie die EMA-Portale. Ihre...
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Regulatory Affairs Director
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Biocon Biologics VollzeitBiocon Biologics is shaping the future of healthcare through its end-to-end expertise in biologic and biosimilar development. We are seeking a seasoned regulatory affairs professional to lead our European regulatory strategy. The ideal candidate will have a strong background in European regulatory affairs, excellent leadership and communication skills, and...
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Regulatory Affairs Director
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Biocon Biologics VollzeitBiocon Biologics is shaping the future of healthcare through its end-to-end expertise in biologic and biosimilar development. We are seeking a seasoned regulatory affairs professional to lead our European regulatory strategy. The ideal candidate will have a strong background in European regulatory affairs, excellent leadership and communication skills, and...
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Regulatory Affairs Specialist
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Merz Therapeutics VollzeitRegional Regulatory Affairs ManagerAt Merz Therapeutics, we are seeking a highly skilled Regional Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will play a critical role in ensuring compliance with regulatory and legal requirements in the assigned region.Key Responsibilities:Develop and maintain...
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Regulatory Affairs Specialist
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Merz Therapeutics VollzeitRegional Regulatory Affairs ManagerAt Merz Therapeutics, we are seeking a highly skilled Regional Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will play a critical role in ensuring compliance with regulatory and legal requirements in the assigned region.Key Responsibilities:Develop and maintain...
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Regulatory Affairs Specialist
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Biocon Biologics VollzeitAbout Biocon Biologics:We are a leading company in the biosimilars revolution, where patients come first. Our ambition is to impact a billion lives by fostering a culture of affordable innovation, patient centricity, and disruptive thinking. We have a long-term commitment to bring high-quality, affordable biosimilars to patients worldwide.Job Description:The...
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Regulatory Affairs Specialist
vor 1 Woche
Frankfurt am Main, Hessen, Deutschland Biocon Biologics VollzeitAbout Biocon Biologics:We are a leading company in the biosimilars revolution, where patients come first. Our ambition is to impact a billion lives by fostering a culture of affordable innovation, patient centricity, and disruptive thinking. We have a long-term commitment to bring high-quality, affordable biosimilars to patients worldwide.Job Description:The...
Specialist Corporate Drug Regulatory Affairs
vor 4 Monaten
9118 Meda Pharma GmbH & Co KG
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We do so via:
Access - Providing high quality trusted medicines regardless of geography or circumstance;
Leadership - Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership - Leveraging our collective expertise to connect people to products and services.
Jeden Tag aufs Neue nehmen wir die Herausforderung an, einen Unterschied in der Welt zu machen. Im Folgenden erfahren Sie, inwiefern Ihre Position als Specialist Corporate Drug Regulatory Affairs (m/w/d) Ihren Teil dazu beitragen kann:
Zu den wesentlichen Verantwortungsbereichen dieser Position zählen:
- Bearbeitung, zusammentragen von Informationen und Versand von monatlichen Reports und Anfragen
- Rechnungsmanagement und -tracking
- Beantragung und Verwaltung von POs (Purchase Orders)
- Bearbeiten der Aufgaben in den jeweiligen Systemen, u.a. SAP, Cora, Smart Source, Amazon, Insight, LCM, Concur
- Vertragsmanagement inklusive tracking, LCM
- Unterstützung der regulatorischen Aktivitäten der Abteilung
- Kontakte mit Behörden und anderen Firmen
- Koordination von Schulungen und Fortbildungen
- Koordinierung, Prüfung und Verwaltung von Vollmachten
- Koordination von CPPs und Legalisierung von Dokumenten
- Bearbeitung und Durchführung von einzelnen Sonderprojekten
- Büroorganisation (Bestellungen Büromaterial, Hardware, etc., Postbearbeitung, Reiseorganisation, Reisekostenabrechnung, Koordination Arbeitsplätze Mitarbeiter*Innen, Termine und Besprechungen, externe Consultants)
- Unterstützung des Abteilungsleiters (u.a. Budgetplanung, Vorbereitung und Durchführung von Abteilungsbesprechungen und Regional Regulatory Management Meetings)
- Unterstützung bei SOPs / Aktualisierung des Organigramms
- Verwaltung der zentralen CDRA-Ablage
- Koordination / Betreuung der Archive
Im Rahmen dieser Position sind die folgenden Mindestanforderungen zu erfüllen:
- Erfolgreich abgeschlossene kaufmännische Ausbildung
- Kommunikationsgeschick, Durchsetzungsfähigkeit und eine strukturierte Arbeitsweise sowie gute Umgangsformen und Teamfähigkeit
- Koordination und Durchführung Sekretariats
- und Abteilungsaufgaben
- mindestens 3 Jahre Berufserfahrung (in der pharmazeutischen Industrie wäre wünschenswert)
- Sehr gutes Englisch in Wort und Schrift
- Sicherer Umgang mit den gängigen MS-Office Programmen
At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.
Viatris is an Equal Opportunity Employer.
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