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Beliebte Jobs
- Account Manager
- Content Management
- Fraud Management
- Study Coordinator
- Dokumentationsbeauftragter
- Documentation Manager
- International Officer
- Manager CRM
- Operations Lead
- Case Management
- Mitarbeiter/in Case Management
- Dokumentenmanagement
- Customer Care Agent
- Customer Care
- Archivierung
- Document Management
Standorte
- Frankfurt am Main
- Darmstadt
- Neu-Isenburg
- Eschborn
- Dreieich
- Dietzenbach
- Idstein
- Friedberg, Hessen
- Hattersheim
- Kelsterbach
- Rosbach vor der Höhe
- Großwallstadt
- Budenheim
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Bayern
- Rheinland
- Hessen
- Rhein-Main-Gebiet
- Taunus
- Eifel
- Odenwald
- Vogelsberg
- Main-Taunus
Home-Office-Optionen
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Beliebte Jobs
- Account Manager
- Content Management
- Fraud Management
- Study Coordinator
- Dokumentationsbeauftragter
- Documentation Manager
- International Officer
- Manager CRM
- Operations Lead
- Case Management
- Mitarbeiter/in Case Management
- Dokumentenmanagement
- Customer Care Agent
- Customer Care
- Archivierung
- Document Management
Standorte
- Frankfurt am Main
- Darmstadt
- Neu-Isenburg
- Eschborn
- Dreieich
- Dietzenbach
- Idstein
- Friedberg, Hessen
- Hattersheim
- Kelsterbach
- Rosbach vor der Höhe
- Großwallstadt
- Budenheim
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Bayern
- Rheinland
- Hessen
- Rhein-Main-Gebiet
- Taunus
- Eifel
- Odenwald
- Vogelsberg
- Main-Taunus
47 Treffer für Document Manager Jobs in Dreieich im Umkreis von 30 km
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Dokumentenmanager / Document Manager (m/w/d)
Dokumentenmanager / Document Manager (m/w/d)
VTU Engineering Deutschland GmbH
Hattersheim a.M., Berlin, Braunschweig, Rheinbach, Neu-Ulm, Penzberg, Burghausen, Hamburg, DD, DO
Teilweise Home-Office
Als Dokumentenmanager (m/w/d) unterstütz Du unsere Projektmanagement- und Ingenieurteams in organisatorischen, administrativen und kommunikativen Aufgaben.
Als Dokumentenmanager (m/w/d) unterstütz Du unsere Projektmanagement- und Ingenieurteams in organisatorischen, administrativen und kommunikativen Aufgaben.
Noch nichts dabei? Es gibt 46 weitere Jobs, die zu deiner Suche passen könnten
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The Product Manager prefilters for Cytiva is responsible for Creating and maintaining the prefilter portfolio business plan, including product strategy, new product developments, pricing, all stages of a product family's lifecycle, Cross functional communication including operational involvement. * Excellent oral and written communications skills to deliver content for documents and presentations.
The Product Manager prefilters for Cytiva is responsible for Creating and maintaining the prefilter portfolio business plan, including product strategy, new product developments, pricing, all stages of a product family's lifecycle, Cross functional communication including operational involvement. * Excellent oral and written communications skills to deliver content for documents and presentations.
NEU
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Legal Compliance Manager (m/f/d)
Legal Compliance Manager (m/f/d)
Industrial and Commercial Bank of China Limited Frankfurt Branch
Frankfurt am Main
Schnelle Bewerbung
Review and assess the legality and feasibility of major business activities, decisions, documents, and contracts of the branch. * Draft, review, and finalize agreements, contracts, and other legal documents to safeguard the branch's legal rights and ensure compliance with applicable laws. * Relevant certifications like Certified Regulatory Compliance Manager (CRCM) or Certified Anti-Money Laundering Specialist (CAMS).
Review and assess the legality and feasibility of major business activities, decisions, documents, and contracts of the branch. * Draft, review, and finalize agreements, contracts, and other legal documents to safeguard the branch's legal rights and ensure compliance with applicable laws. * Relevant certifications like Certified Regulatory Compliance Manager (CRCM) or Certified Anti-Money Laundering Specialist (CAMS).
UBS is the world's largest and the only truly global wealth manager. • document and communicate audit issues, root causes and risks, and prepare reports of audit findings for UBS Group and UBS Europe SE senior management
UBS is the world's largest and the only truly global wealth manager. • document and communicate audit issues, root causes and risks, and prepare reports of audit findings for UBS Group and UBS Europe SE senior management
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Strategic Pitch Senior Manager Europe (m/w/d)
Strategic Pitch Senior Manager Europe (m/w/d)
Linklaters LLP
Frankfurt am Main, Berlin, Düsseldorf, Hamburg und München
Ensure that feedback and lessons learnt are documented and made available on Salesforce. * Define and shape requirements with the Pitch Development Manager for pitch improvement initiatives.
Ensure that feedback and lessons learnt are documented and made available on Salesforce. * Define and shape requirements with the Pitch Development Manager for pitch improvement initiatives.
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Control and maintain records for all revenue accountable documents such as tickets and MCOs ensuring that usage is monitored in order to provide necessary accounts at the end of the day/shift.
Control and maintain records for all revenue accountable documents such as tickets and MCOs ensuring that usage is monitored in order to provide necessary accounts at the end of the day/shift.
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Territory Telecom and Multimedia Coordinator (all genders) in BNP Paribas Territory Functions
Territory Telecom and Multimedia Coordinator (all genders) in BNP Paribas Territory Functions
BNP Paribas S.A.
Frankfurt am Main, München, Nürnberg
Please send us your application documents exclusively via our online portal.
Please send us your application documents exclusively via our online portal.
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Rite-Hite GmbH * Frankfurt am Main * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Über uns - Die Rite-Hite GmbH ist eine Tochtergesellschaft der amerikanischen Rite-Hite Corporation, die mit weltweit mehr als 3000 Mitarbeitenden und einem globalen Netzwerk aus Produktionen und Niederlassungen zu den führenden Unternehmen in der Entwicklung, Fertigung und dem Vertrieb von Produkten und Lösungen im Bereich Intralogistik zählt. Am Entwicklungs- und Produktionsstandort in Volkmarsen, der zugleich die europäische Firmenzentrale ist, werden hydraulische Überladebrücken, Torabdichtungen, LKW-Wegfahrsperren und weitere Produkte gefertigt, die in aller Welt dafür Sorge tragen logistische Prozesse sicherer und energieeffizienter zu machen. Zum europäischen Netzwerk der Rite-Hite GmbH gehören neben der Service-Zentrale im rheinland-pfälzische
Rite-Hite GmbH * Frankfurt am Main * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Über uns - Die Rite-Hite GmbH ist eine Tochtergesellschaft der amerikanischen Rite-Hite Corporation, die mit weltweit mehr als 3000 Mitarbeitenden und einem globalen Netzwerk aus Produktionen und Niederlassungen zu den führenden Unternehmen in der Entwicklung, Fertigung und dem Vertrieb von Produkten und Lösungen im Bereich Intralogistik zählt. Am Entwicklungs- und Produktionsstandort in Volkmarsen, der zugleich die europäische Firmenzentrale ist, werden hydraulische Überladebrücken, Torabdichtungen, LKW-Wegfahrsperren und weitere Produkte gefertigt, die in aller Welt dafür Sorge tragen logistische Prozesse sicherer und energieeffizienter zu machen. Zum europäischen Netzwerk der Rite-Hite GmbH gehören neben der Service-Zentrale im rheinland-pfälzische
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Legal, GBM - Fixed Income, Currency and Commodities Lawyer, Associate/Vice President, Frankfurt/Paris
Legal, GBM - Fixed Income, Currency and Commodities Lawyer, Associate/Vice President, Frankfurt/Paris
Goldman Sachs AG MesseTurm
Frankfurt, Germany
Assisting with the structuring, negotiation and drafting of client and transactional documents, including coordination with external
Assisting with the structuring, negotiation and drafting of client and transactional documents, including coordination with external
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Schnelle Bewerbung
• Ensure familiarisation and compliance with contract documents and procedures. • Manage, deliver and obtain approval on relevant project Mechanical Cx documents such as Test Scripts, Compl iance statements etc
• Ensure familiarisation and compliance with contract documents and procedures. • Manage, deliver and obtain approval on relevant project Mechanical Cx documents such as Test Scripts, Compl iance statements etc
Schnelle Bewerbung
• Ensure familiarisation and compliance with contract documents and procedures. • Manage, deliver and obtain approval on relevant project Electrical Cx documents such as Test Scripts, Compl iance statements etc
• Ensure familiarisation and compliance with contract documents and procedures. • Manage, deliver and obtain approval on relevant project Electrical Cx documents such as Test Scripts, Compl iance statements etc
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By submitting your application, you consent to the sharing of your submitted documents (including your CV and any other uploaded materials) with affiliated companies within the Hyundai Motor Group for the purpose of processing your application. * Developing cost models with Product Managers and local branches
By submitting your application, you consent to the sharing of your submitted documents (including your CV and any other uploaded materials) with affiliated companies within the Hyundai Motor Group for the purpose of processing your application. * Developing cost models with Product Managers and local branches
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Associate Principal/Principal Medical Writers (F, M or D)
Associate Principal/Principal Medical Writers (F, M or D)
Trilogy Writing & Consulting GmbH
Frankfurt am Main
Function as a lead writer to prepare a variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) in collaboration with members of client authoring teams and supported by other , as appropriate. - Ensure that all documents are produced according to agreed timelines, monitor and manage project budgets, adhere to relevant SOPs, and meet the requirements of Trilogy as well as the company's clients. - Be responsible for providing document-specific advice to clients. - Oversee and coordinate other and assisting with documents under your responsibility. - Project manage the timelines and review cycles of your documents. - Work in the client's regulatory
Function as a lead writer to prepare a variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) in collaboration with members of client authoring teams and supported by other , as appropriate. - Ensure that all documents are produced according to agreed timelines, monitor and manage project budgets, adhere to relevant SOPs, and meet the requirements of Trilogy as well as the company's clients. - Be responsible for providing document-specific advice to clients. - Oversee and coordinate other and assisting with documents under your responsibility. - Project manage the timelines and review cycles of your documents. - Work in the client's regulatory
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Review and interpret electrical drawings, schematics, and technical documents. Laboratory Manager - Robotarium - EC&I Construction Manager
Review and interpret electrical drawings, schematics, and technical documents. Laboratory Manager - Robotarium - EC&I Construction Manager
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IT-Service Manager (m/w/d) 80% Remote
IT-Service Manager (m/w/d) 80% Remote
EICS Group GmbH Engineering Solutions
Frankfurt am Main
Teilweise Home-Office
Kontext: Der Service Manager ist für die Bereiche E-Mail Communication, File Service und Document and Content Management beheimatet.
Kontext: Der Service Manager ist für die Bereiche E-Mail Communication, File Service und Document and Content Management beheimatet.
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Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
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Senior Consultant Data Analytics & Business Insights (m/w/d)
Senior Consultant Data Analytics & Business Insights (m/w/d)
Deloitte
Berlin, Düsseldorf, Frankfurt (Main), Hamburg, München
Teilweise Home-Office
Anschreiben nicht erforderlich
Dokumentation & Weiterbildung: Du unterstützt bei der Erstellung von Documents wie Data Books und Due-Diligence-Berichten und entwickelst dein Wissen zu neuen Technologien und Methoden kontinuierlich weiter.
Dokumentation & Weiterbildung: Du unterstützt bei der Erstellung von Documents wie Data Books und Due-Diligence-Berichten und entwickelst dein Wissen zu neuen Technologien und Methoden kontinuierlich weiter.
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Supporting legal drafting and review of letters, contracts and other IT law or data protection-related documents for the European region
Supporting legal drafting and review of letters, contracts and other IT law or data protection-related documents for the European region
Supporting legal drafting and review of letters, contracts and other IP law or litigation-related documents for the European region
Supporting legal drafting and review of letters, contracts and other IP law or litigation-related documents for the European region
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Collaboration will be key as you work closely with internal to gather the necessary documents and technical solutions for bid submissions. A core part of your responsibilities will involve compiling, refining, and owning the final proposal documents, showcasing your ability to present technical content and designs in a professional and concise manner.
Collaboration will be key as you work closely with internal to gather the necessary documents and technical solutions for bid submissions. A core part of your responsibilities will involve compiling, refining, and owning the final proposal documents, showcasing your ability to present technical content and designs in a professional and concise manner.
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Research Assistant in Membrane Protein Biochemistry (f/m/d)
Research Assistant in Membrane Protein Biochemistry (f/m/d)
Max-Planck-Institut für Biophysik
Frankfurt am Main
Max-Planck-Institut für Biophysik * Frankfurt am Main * Befristeter Vertrag * Vollzeit - Sei einer der ersten Bewerber - The Max Planck Institute of Biophysics is a leading international research center that develops biophysical, biochemical and computational methods to investigate the structure, dynamics and function of cellular systems at molecular scale. It consists of about 200 employees from more than 25 countries, and is located at the Campus Riedberg in Frankfurt am Main. Within the Department of Molecular Sociology, led by Martin Beck, we investigate large macromolecular assemblies using state-of-the-art in situ structural biology. Our work spans nuclear transport systems, protein complex assembly, protein homeostasis, and membrane protein complexes and membrane remodeling, as well as in situ studies of viruses, including SARS-CoV‑2 and virus-like particles.
Max-Planck-Institut für Biophysik * Frankfurt am Main * Befristeter Vertrag * Vollzeit - Sei einer der ersten Bewerber - The Max Planck Institute of Biophysics is a leading international research center that develops biophysical, biochemical and computational methods to investigate the structure, dynamics and function of cellular systems at molecular scale. It consists of about 200 employees from more than 25 countries, and is located at the Campus Riedberg in Frankfurt am Main. Within the Department of Molecular Sociology, led by Martin Beck, we investigate large macromolecular assemblies using state-of-the-art in situ structural biology. Our work spans nuclear transport systems, protein complex assembly, protein homeostasis, and membrane protein complexes and membrane remodeling, as well as in situ studies of viruses, including SARS-CoV‑2 and virus-like particles.
By submitting your application, you consent to the sharing of your submitted documents (including your CV and any other uploaded materials) with affiliated companies within the Hyundai Motor Group for the purpose of processing your application.
By submitting your application, you consent to the sharing of your submitted documents (including your CV and any other uploaded materials) with affiliated companies within the Hyundai Motor Group for the purpose of processing your application.
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We look forward to receiving your application documents in English
We look forward to receiving your application documents in English
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You will pick-up, assign or process (draft), review and provide feedback on corporate documents drafted for all stages of company lifecycle, i.e. from company incorporation through to dissolution, for clients worldwide in accordance to legal requirements with agreed deadlines;
You will pick-up, assign or process (draft), review and provide feedback on corporate documents drafted for all stages of company lifecycle, i.e. from company incorporation through to dissolution, for clients worldwide in accordance to legal requirements with agreed deadlines;
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As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. * Develop regulatory documents for submission to regulatory agencies globally, including Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring standards, as applicable, in adherence with study/project timelines and corporate objectives. * Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents. * Review other documents associated with the assigne
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. * Develop regulatory documents for submission to regulatory agencies globally, including Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring standards, as applicable, in adherence with study/project timelines and corporate objectives. * Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents. * Review other documents associated with the assigne
Beliebte Jobs
Standorte
- Frankfurt am Main
- Darmstadt
- Neu-Isenburg
- Eschborn
- Dreieich
- Dietzenbach
- Idstein
- Friedberg, Hessen
- Hattersheim
- Kelsterbach
- Rosbach vor der Höhe
- Großwallstadt
- Budenheim
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Bayern
- Rheinland
- Hessen
- Rhein-Main-Gebiet
- Taunus
- Eifel
- Odenwald
- Vogelsberg
- Main-Taunus