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Pharmazie: 20 Jobs in Dettingen an der Erms

Berufsfeld
  • Pharmazie
Branche
  • Pharmaindustrie 19
  • Sonstige Branchen 1
Berufserfahrung
  • Mit Berufserfahrung 20
  • Ohne Berufserfahrung 5
  • Mit Personalverantwortung 2
Arbeitszeit
  • Vollzeit 20
Anstellungsart
  • Feste Anstellung 20
Pharmazie

Mitarbeiter Validierung & pharmazeutische Projekte (m/w/d)

Sa. 21.05.2022
Eckwälden
Die WALA ist ein mittelständischer Hersteller von Arzneimitteln, Präparaten zur Gesundheitspflege und Kosmetika aus Natursubstanzen auf der Basis der anthroposophischen Natur- und Menschenerkenntnis. Wir suchen einen Mitarbeiter Validierung & pharmazeutische Projekte (m/w/d)Zusammen mit rund tausend Kolleginnen und Kollegen leisten Sie Ihren Beitrag zu Wohl und Wachstum unseres Unternehmens. Sie engagieren sich für den Erfolg von WALA Arzneimitteln und Dr. Hauschka Kosmetik in aller Welt. Eigenständig im Sinne des Ganzen bringen Sie sich vor allem in folgende Bereiche ein: Koordination, Planung, Durchführung und Dokumentation von Prozess- und/oder Reinigungsvalidierungen bzw. Prozessentwicklungs- und -Optimierungsstudien für alle zugeordneten Herstellungsbereiche Sicherstellung einer sach- und termingerechten Umsetzung der Validierungsaktivitäten in der Herstellung unter Berücksichtigung der internen und externen Schnittstellen in enger Abstimmung mit dem Vorgesetzten und den betroffenen Stellen Sicherstellung eines reibungslosen Informationsflusses innerhalb des Verantwortungsbereichs und der betroffenen Schnittstellen sowie Weitergabe der gewonnenen Erkenntnisse und Erfahrungen zur Qualitätssicherung und –steigerung Erstellung der für die Aufgabe notwendigen bzw. angeforderten Berichte, Statistiken und GMP-Dokumentationen Laufende Überprüfung der Machbarkeit und Realisierung gem. Master-Validierungsplan und Information des Vorgesetzten Vorbereitung und Teilnahme an behördlichen Inspektionen Gesellschaft und Umwelt, Gesundheit und Schönheit sind Ihnen genauso ein Anliegen, wie wirtschaftlicher Erfolg. Eine dialogische Unternehmenskultur macht Ihnen Freude. Für die hier ausgeschriebene Aufgabe setzen wir außerdem voraus: Abgeschlossenes technisches oder naturwissenschaftliches Studium (z.B. der Pharmazie) oder technische bzw. pharmazeutische Ausbildung (z. B: Pharmakant), Berufserfahrung von Vorteil Wenn möglich, Erfahrungen im Validierungs-/Qualifizierungsumfeld GMP-Kenntnisse Sehr gute Kenntnisse in Office-Programmen (i. B. Word und Excel) Wir bewerben uns um Ihre Mitarbeit in einem Stiftungsunternehmen, das seit 1935 das Beste aus der Natur für den Menschen gewinnt. Das seinen Werten verpflichtet ist und Niemandem sonst. Dessen Mitarbeitende ambitionierte Ziele in einem spannenden Wettbewerbsumfeld haben. Aber auch ein Leben neben der Arbeit.
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Data Analytics Manager (f/m/d) Process Development Drug Product

Do. 19.05.2022
Tübingen
CureVac AG 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. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Data Analytics Manager (f/m/d) Process Development Drug Product Management of process and analytical data Maintenance and further development of (process) databases  Coordination and development of department expertise for raw material specifications Support for process development teams in the establishment of new analytical methods Participation in cross-functional projects and committees Completed university degree in a relevant field, e.g., pharmacy, bioprocess engineering, biotechnology, chemistry, or a comparable qualification Several years of professional experience in process development and data management, ideally in a pharmaceutical company Knowledge of statistical design of experiments (DoE), data analysis and profound experience with MS Excel and database creation desirable Ideally experience in project management   Strong teamwork and communication skills Ability to work in a dynamic and fast-paced environment Very good written and spoken English required; German skills are an advantage We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
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Scientist Process Development (f/m/d) Drug Product

Do. 19.05.2022
Tübingen
CureVac AG 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. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Scientist Process Development (f/m/d) Drug Product Development, optimization and upscaling of GMP-compliant manufacturing processes for formulated RNA products Planning, execution, interpretation and documentation of experiments Contribution to the development of bio- and physicochemical characterizations of formulated nucleic acids and process-related impurities Characterization and development of excipients and packaging materials Support of process development at C(D)MOs as well as technology transfers to GMP production sites Preparation of development reports, risk analyses, laboratory instructions, training documents and SOPs Participation in interdisciplinary project teams PhD in the field of biotechnology, pharmacy or chemistry, or a comparable qualification Professional experience in process development, ideally in a pharmaceutical company First relevant experience in the production of biopharmaceutical formulations as well as their characterization is preferred Experience in drug product manufacture, e.g., filtration, formulation, filling, drying, as well as characterization of biomolecules, e.g., by HPLC, DLS, viscometry, gel electrophoresis, UV/Vis spectroscopy Knowledge of statistical experimental design and data analysis (DoE) is a plus Proactive, structured and independent way of working Strong communication skills and team orientation Fluency in English is a must, additional German skills are preferred We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
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Senior Process Expert (f/m/d) Process Development Drug Product

Do. 19.05.2022
Tübingen
CureVac AG 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. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Senior Process Expert (f/m/d) Process Development Drug Product Project management and coordination of process development activities with internal and external partners Successful execution of process transfers through efficient planning Coordinate and assist in the preparation of risk analyses, plans and reports Preparation of laboratory instructions, training documents, SOPs, non-disclosure agreements, and material transfer agreements Exchange and cooperation with interdisciplinary project teams Completed university degree or a comparable qualification, preferably in the field of Biotechnology, Pharmacy or Chemistry Extensive experience in the field of project management with various business partners and stakeholders Knowledge of the production of biopharmaceutical formulations as well as their characterization is an advantage Ideally knowledge in statistical experimental design and analysis Proactive and structured working style in a dynamic environment Strong communication skills, self-organization and team orientation Fluent English; German is a plus We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
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Scientist (f/m/d) Oncology Research

Do. 19.05.2022
Tübingen
CureVac AG 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. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Scientist (f/m/d) Oncology Research Exploration and discovery of novel RNA-based therapeutic approaches in the field of cancer immunotherapy Planning, execution, interpretation and documentation of experiments to develop and assess these approaches Devise and evaluate research strategies with a strong focus on further clinical development and intellectual property protection Written and oral presentation of research results at scientific meetings Coordinate collaborations with academic, industrial and funding partners Support cross-functional projects within the various teams PhD or equivalent degree in Life Sciences with a strong research background in immunology, preferably with a focus on cancer immunotherapy Several years of professional experience of independent research in the industry or as a postdoctoral fellow FELASA B qualification is a must Relevant knowledge in the field of Bioinformatics / Computational Life Science is a plus Proactive, structured, efficient and independent way of working in a dynamic environment Excellent team spirit, communication and presentation skills Fluency in English is a must, German is a plus We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
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Team Lead (f/m/d) Process Development Drug Substance

Mi. 18.05.2022
Tübingen
CureVac AG 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. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Team Lead (f/m/d) Process Development Drug Substance Technical and disciplinary management of a team responsible for the development, optimization and upscaling of GMP-compliant manufacturing processes for RNA products Planning, execution, interpretation and documentation of experiments Overseeing and steering the development of biochemical characterizations of nucleic acids Subject Matter Expert (SME) for process development topics at C(D)MOs as well as technology transfers to GMP production sites Preparation of development reports, risk analyses, laboratory instructions, training documents and SOPs Participation in interdisciplinary project teams PhD in the field of biotechnology, pharmacy or chemistry, or a comparable qualification Extensive professional experience in process development of scalable and efficient biopharmaceutical processes; ideally in a pharmaceutical company Several years of relevant professional experience in the production of biopharmaceutical drug substances and process characterization Ideally previous experience in leading international teams Knowledge in bioreactor handling or tangential flow filtration Relevant knowledge in statistical experimental design and data analysis (DoE) Proactive, structured, efficient and independent way of working in a dynamic environment Strong communication skills and team-oriented work style Ability to independently devise research projects but also to work in an interdisciplinary team Fluency in English; German is a benefit We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
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External Manufacturing Manager (f/m/d)

Mi. 18.05.2022
Tübingen
CureVac Corporate Services GmbH, a wholly owned subsidiary of CureVac AG, combines the central functions of the CureVac business group. CureVac is a global biopharmaceutical company in the field of mRNA technology, with more than 20 years of expertise in researching, developing and optimizing the versatile biological molecule for medical purposes. Our focus is on prophylactic vaccines, innovative cancer immunotherapies, and protein-based therapies. All RNA people are striving to achieve our main joint goal: To bring multiple best-in-class mRNA medicines to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit an External Manufacturing Manager (f/m/d) The Digital Strategy & Governance function is responsible for defining and driving CureVac's ambitious Digital Transformation Agenda. As IT Business Partner with focus on the needs of our R&D functions, you will be responsible for collaborating and interacting with the key stakeholders from strategy to execution and you will thereby drive the continuous evolution of our application roadmap and complex projects in these functional areas. Ensure an on-time and uninterrupted supply of clinical and commercial high complexity products Support the execution of CureVac's clinical and commercial manufacturing strategy Build a strong relationship between CMO and CureVac for efficient and fast-tracked collaboration Lead all activities related to selected Contract Manufacturing Organizations (CMO) for clinical and commercial supply for Drug Substance, Drug Product, fill and finish steps Be the central point of contact for all CV functions working with CMOs and vice versa: Ensure alignment across all functions and units in the interaction with CMO Support and coordinate the implementation of harmonized governance structures across CMO accounts, organize governance meetings for CMOs and follow up with internal and external stakeholders Plan and track budget adherence together with finance, accounting and procurement; be accountable for the budget for the CMO Manage Change Controls and support the resolution of deviations to ensure on-time batch release Contribute to technology transfer and improvement projects with the CMOs Drive process and operational improvements, and ensure adherence to standards and GMP Establish and execute operational excellence and lean approaches to drive continuous efficiency gains in supplier interactions Plan for future improvements of the CureVac CMO network Coordinate and contribute to contract establishment and vendor selection procedures in collaboration with procurement Analyze and understand accounts' business strategy, future product plans and expansion activities University degree (M.Sc. or Ph.D. or similar relevant degree) in scientific, technical or pharmaceutical manufacturing field 3+ years of relevant experience in technical/project management roles in the pharmaceutical or other regulated industry– project management certification is a plus Experience in CMO and key account management, preferably in an international environment Strong communication and coordination skills, working in a matrix organization, people-oriented and team player Proven understanding of biotechnology process (upstream and downstream) and technology transfers is preferred Ability to equally handle broader business topics and technical details, and to engage with senior leaders and technical experts Experience in GMP manufacturing and/or quality roles, with supply chain, planning, financial management in manufacturing is a plus Influencing skills, accountability, reliability and detailed orientation Ability to travel up to 20 % Action-oriented and hands-on working skills Ability to translate strategy into operational execution Fluency in English; German is a plus We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
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Projektmanager CMC (w/m/d) RNA Printer®

Mo. 16.05.2022
Tübingen
Die CureVac AG ist ein globales biopharmazeutisches Unternehmen, das neuartige Medikamente auf Basis des Botenmoleküls Messenger RNA (mRNA) erforscht und entwickelt. Unsere Schwerpunkte liegen auf prophylaktischen Impfstoffen, innovativen Krebsimmuntherapien sowie proteinbasierten Therapien. Aktuell engagieren sich alle RNA people dafür, unser großes Ziel zu erreichen: Wir wollen mehrere Best-in-Class mRNA-Arzneimittel auf den Markt bringen. Zur Unterstützung unseres Teams am Standort Tübingen bei Stuttgart suchen wir zum nächstmöglichen Zeitpunkt Sie in der Position als Projektmanager CMC (w/m/d) RNA Printer® Sie betreuen die CMC-bezogenen Projektaktivitäten des RNA Printer® für die automatisierte Herstellung von mRNA Sie managen Projektaktivitäten wie Technologie- / Prozessentwicklung, Transfer, GMP-Herstellung sowie Qualitätskontrolle und arbeiten mit den Managern der CureVac-Programme zur Arzneimittelentwicklung zusammen Sie sind für den kompletten Projektmanagement-Zyklus von der Planung bis zum Abschluss verantwortlich und entwickeln neue Projektpläne gemeinsam mit den Projektpartnern Sie steuern die Teamarbeit mit Ihren Kollegen der betreffenden Abteilungen: R&D, Manufacturing, Quality, Regulatory, Intellectual Property und Legal Sie koordinieren und überprüfen die C(D)MO-Aktivitäten, insbesondere die Einhaltung der qualitätskonformen Herstellung, Timelines und des Budgets Sie konsolidieren die projektspezifischen Informationen und sind verantwortlich für das Reporting an das Management Sie identifizieren Risiken, überprüfen den Projektreifegrad und entwickeln mit Ihren Projektpartnern Maßnahmen, um herausfordernde Projektziele zu erreichen Sie gestalten einen wachsenden Unternehmensbereich mit und unterstützen damit die Leitungsfunktionen Naturwissenschaftlichen oder medizintechnischen Hochschulabschluss als Pharmazeut, Biologe bzw. Chemiker oder Weiterbildungsabschluss als staatlich geprüfter Techniker (m/w/d) der Fachrichtung Medizintechnik Einschlägige Berufserfahrung mit der Leitung von komplexen Projekten in der biotechnologischen oder pharmazeutischen Industrie oder mehrjährige praktische Erfahrung im Bereich der Herstellung und Abfüllung flüssiger Arzneimittel Kenntnisse der relevanten ICH- und GMP-Richtlinien und Erfahrung in der Herstellung von klinischen Prüfpräparaten von Vorteil Exzellente Kommunikation, Durchsetzungsvermögen und soziale Kompetenz sowie die Motivation, effektiv in einer Team-/Matrixumgebung zu arbeiten Schnelle Auffassungsgabe und Lösungsorientierung Serviceorientierte Denkweise, flexible und proaktive Einstellung gegenüber sich schnell ändernden Anforderungen Projektmanagement-Zertifizierungen wünschenswert Verhandlungssichere Deutsch- und Englischkenntnisse Wir bieten Ihnen eine herausfordernde und abwechslungsreiche Tätigkeit in einem innovativen und dynamischen Unternehmen, das auf Wachstumskurs ist. Mit viel Herzblut und Verantwortungsbewusstsein arbeiten wir gemeinsam an einer medizinischen Revolution. Dabei pflegen wir ein vertrauensvolles Miteinander, das von der Offenheit für Neues und ständigem Fortschritt geprägt ist. Gegenseitiger Respekt, Verlässlichkeit und Eigeninitiative sind für uns selbstverständlich. Gestalten Sie bei uns Ihre Zukunft – werden Sie Teil der RNA people!
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Specialist Hygiene (w/m/d) Qualitätsmanagement

Sa. 14.05.2022
Tübingen
Die CureVac Real Estate GmbH, eine 100-prozentige Tochter der CureVac AG, ist ein biopharmazeutisches Produktionsunternehmen, das neuartige Medikamente auf Basis des Botenmoleküls Messenger RNA (mRNA) herstellt. Unsere Schwerpunkte liegen auf prophylaktischen Impfstoffen, innovativen Krebsimmuntherapien sowie proteinbasierten Therapien. Aktuell engagieren sich alle RNA people dafür, unser großes Ziel zu erreichen: Wir wollen mehrere Best-in-Class mRNA-Arzneimittel auf den Markt bringen. Zur Unterstützung unseres Teams am Standort Tübingen bei Stuttgart suchen wir zum nächstmöglichen Zeitpunkt Sie in der Position als Specialist Hygiene (w/m/d) Qualitätsmanagement Definition, Umsetzung und Nachverfolgung hygienerelevanter Anforderungen in den Bereichen Produktion, Lager und (Qualitäts-)Labore Kontinuierliche Verbesserung bestehender Hygienemanagement-Systeme sowie Erstellung und Änderung relevanter Vorgabe-, Nachweis- und Schulungsdokumente Planung und Durchführung von Unterweisungen und Hygieneschulungen, u. a. für Reinraumpersonal, inklusive Prüfung und Freigabe der Qualifizierung von Mitarbeitern Fachliche Anleitung des (Reinigungs-)Personals bei der Durchführung von Reinigungs- und Desinfektionsaktivitäten Auswahl geeigneter Materialien und Geräte zur Durchführung von Reinigungs- und Desinfektionsarbeiten Planung, Koordination und Durchführung von Hygienekontrollen und Risk Assessments in Herstellbereichen sowie Ableitung entsprechender Maßnahmen Unterstützung bei Audits und Inspektionen in Zusammenarbeit mit dem Qualitätsmanagement nach GMP Funktion als Erstkontakt zum Thema Hygiene Naturwissenschaftlichen Hochschulabschluss mit Schwerpunkt Hygiene, erfolgreichen Abschluss als Industriemeister (w/m/d) der Fachrichtung Pharmazie oder eine vergleichbare Qualifikation Einschlägige Berufserfahrung im Bereich Hygiene / Mikrobiologie und Kenntnisse der Anforderungen nach GMP, vorzugsweise in der biotechnologischen bzw. pharmazeutischen Produktion Erfahrung in den Bereichen Reinigung, Desinfektion und Umgebungsmonitoring in Reinräumen im GMP-Umfeld Sicheren Umgang mit MS Office, Erfahrungen im Umgang mit SAP wünschenswert Ausgeprägte Kommunikations- und Präsentationsfähigkeit Selbstständige und strukturierte Arbeitsweise in einem dynamischen Umfeld Freude an Teamarbeit und abteilungsübergreifender Zusammenarbeit Fließende Deutsch- und sehr gute Englischkenntnisse Wir bieten Ihnen eine herausfordernde und abwechslungsreiche Tätigkeit in einem innovativen und dynamischen Unternehmen, das auf Wachstumskurs ist. Mit viel Herzblut und Verantwortungsbewusstsein arbeiten wir gemeinsam an einer medizinischen Revolution. Dabei pflegen wir ein vertrauensvolles Miteinander, das von der Offenheit für Neues und ständigem Fortschritt geprägt ist. Gegenseitiger Respekt, Verlässlichkeit und Eigeninitiative sind für uns selbstverständlich. Gestalten Sie bei uns Ihre Zukunft – werden Sie Teil der RNA people!
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Senior Scientist Pharmaceutical Development (f/m/d)

Fr. 13.05.2022
Tübingen
CureVac AG 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. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Senior Scientist Pharmaceutical Development (f/m/d) Technical and disciplinary management of a team responsible for the development, optimization for formulations and pharmaceutical presentations of RNA products (LNP-based and peptide adduct-based RNA liquid formulations, especially lyophilisates) Planning, execution, interpretation and documentation of experiments Overseeing and steering the development of biochemical characterizations of formulated nucleic acids, excipients and process-related impurities in the DP formulation Characterization and development of excipients and packaging materials Subject Matter Expert (SME) for formulation topics Preparation of development reports, risk analyses, laboratory instructions, training documents and SOPs Participation in interdisciplinary project teams PhD in the field of biotechnology, pharmacy or chemistry, or a comparable qualification Extensive professional experience in formulation development, ideally in a pharmaceutical company Several years of relevant professional experience in the production of biopharmaceutical formulations and their characterization, ICH stability studies Knowledge in filtration, filling, drying, freezing and characterization of formulated biomolecules Relevant knowledge in statistical experimental design and data analysis (DoE) Proactive, structured, efficient and independent way of working in a dynamic environment Strong communication skills and team-oriented work style Fluency in English is a must, additional German skills are preferred We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
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