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Marketing in Bad Homburg (Höhe)

Hier finden Sie Marketing Kleinanzeigen in Bad Homburg (Höhe). Bitte klicken Sie auf eine Anzeige für mehr Informationen.

(Senior) Manager (m/f/d) Medical Device Safety

/ er with a purpose / - creating a future worth living for patients worldwide every day more than four decades of experience in dialysis innovative research the global leader in dialysis services and products - that is com (senior) manager (m/f/d) device safety within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company maintains and receives its marketing authorizations (eg ce-marks or drug registrations) having identified legal requirements and regulations for the company qrem works with different departments and regions guiding them and ensuring that regulatory compliance and regulatory prerequisites for devices & drugs are met within qrem the device safety department is responsible for the device vigilance system and to ensure that possible product risks are identified assessed and appropriate corrective actions are taken more within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company maintains and receives its marketing authorizations (eg ce-marks or drug registrations) having identified legal requirements and regulations for the company qrem works with different departments and regions guiding them and ensuring that regulatory compliance and regulatory prerequisites for devices & drugs are met within qrem the device safety department is responsible for the device vigilance system and to ensure that possible product risks are identified assessed and appropriate corrective actions are taken your assignments as a senior manager (m/f/d) you will make significant contribution to the safety of our devices in the market by defining implementing maintaining and improving processes of the device vigilance system while conducting post market surveillance and carrying out required reporting to competent authorities your task will also include the preparation and submission of authority notifications for device incidents and field safety corrective actions define and maintain processes indicators and tools with regards to device vigilance collect information on product risks and document assessment criteria assess product risk and health hazard assessments and initiate field safety corrective action as required report and notify incidents and related capa to competent authorities compile post market surveillance summaries and psursfunctional lead of local safety officers report to corporate safety officer preparation of monthly and quarterly kpis (eg incidents fsca & msi (major safety issue)) liaise with various functions involved in the product risk assessments your profile graduate degree in technical or scientific studies or similar educational background several years of professional experience in device vigilance or leading position in device quality/risk management or device regulatory affairs expertise in device regulations and standards sound understanding of vigilance processes and organizational structures moderation and presentation competence with conflict management skills strong communication skills with the ability to handle confidential information while interacting with different business functions high language proficiency in german and english (oral and written) apply now send via email print this page at a glance er level: professional experienced job category: quality management / environment regulatory affairs / drug safety working condition: permanent contract / full-time business segment: location: bad homburg / hessen closing date for applications: none - we look forward to your application apply now send via email print this page your contact gmbh bad homburg ref number: 32953 about er with a purpose: over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com   one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons   the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits your contact gmbh bad homburg ref number: 32953 erfmc-agcom er level: professional experienced job category: quality management / environment regulatory affairs / drug safety working condition: permanent contract / full-time business segment: location: bad homburg / hessen closing date for applications: none - we look forward to your application about over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits (Senior) Manager (m/f/d) Medical Device Safety Define and maintain processes indicators and tools with regards to medical device vigilance collect information on product risks and document assessment criteria assess product risk and health hazard assessments Bad Homburg

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61348 Bad Homburg (Höhe)

23.05.2019

Marketing, Medien, PR

Kundenbetreuer (m/w/d) im angestellten Versicherungsau​ßendienst einer Allianz Agentur in der Region Bad Homburg / Oberursel

</p><p>Allianz Beratungs- und Vertriebs-AG Geschäftsstelle Gießen<br/>Gießen</p> Kundenbetreuer (m/w/d) im angestellten Versicherungsaußendienst einer Allianz Agentur in der Region Bad Homburg / Oberursel Festanstellung Vollzeit Allianz Beratungs- und Vertriebs-AG Region Bad Homburg, Oberursel Versicherung Finanzberatung,Versicherungen,Marketing, PR,Außendienst,Kundenbetreuer Kaufmännisch/Handel allgemein,Kaufmann/-frau für Versicherungen und Finanzen,Versicherungskaufmann/-frau Festanstellung Vollzeit Berufseinsteiger Die Allianz ist einer der erfolgreichsten Finanzdienstleister weltweit und führender Versicherer in Deutschland.

61348 Bad Homburg (Höhe)

24.05.2019

Recht, Finanzen, Steuern

Vertragssachbea​rbeiter (m/w/d) Flotte

deutsche-leasing.com Mehr im Blick Vertragssachbearbeiter (m/w/d) Flotte Festanstellung Vollzeit Deutsche Leasing AG Bad Homburg Außenhandel Außenhandelsassistent Betriebswirt Bürokaufmann Büromanagement CRM Customer Direktmarketing Einzelhandel Fachkaufmann Fachwirt Groß Handelsfachwirt Industriekaufmann Kaufmann Kundenberatung Kundenbetreuung Logistikdienstleistung Management Onlinemarketing Relationship Sachbearbeiterin Sales Spedition Speditionskaufmann Strukturvertrieb Vertragsmanagement Vertrieb Vertriebsmarketing Vertriebsstrategie Bank & Finanzdienstleistung Sachbearbeitung Kaufmann/-frau für Büromanagement,Kaufmann/-frau für Bürokommunikation Festanstellung Vollzeit Mit Berufserfahrung Die Experten der Deutschen Leasing machen das Mögliche machbar – ob Leasing, Mietkauf, Investitionskredite oder weitere Finanzierungslösungen sowie ergänzende Services.

61352 Bad Homburg (Höhe)

24.05.2019

Verwaltung, Assistenz

(Junior) Manager (m/f/d) Medical Device Vigilance

/ er with a purpose / - creating a future worth living for patients worldwide every day more than four decades of experience in dialysis innovative research the global leader in dialysis services and products - that is com (junior) manager (m/f/d) device vigilance within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company maintains and receives its marketing authorizations (eg ce-marks or drug registrations) having identified legal requirements and regulations for the company qrem works with different departments guiding them and ensuring that regulatory compliance and regulatory prerequisites for devices & drugs are met within the company qrem holds different regulatory functions and one lies within drug regulatory affairs & product safety more within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company maintains and receives its marketing authorizations (eg ce-marks or drug registrations) having identified legal requirements and regulations for the company qrem works with different departments guiding them and ensuring that regulatory compliance and regulatory prerequisites for devices & drugs are met within the company qrem holds different regulatory functions and one lies within drug regulatory affairs & product safety your assignments as a "(junior) manager (m/f/d) device vigilance " you will make an important contribution to the safety of our devices you will record and document device risks and will identify and document product safety indicators create post market surveillance & periodic safety update reports and process product incidents your task will also include recording and documenting of risks concerning devices while reporting device incidents to the authorities you will compile risks of devices for clinical evaluation and will draft product safety indicators process optimization for vigilance of devices and maintenance of security databases will be part of your responsibility your profile if you have a graduate degree in technical or scientific studies or equivalent qualification with relevant experience in a similar function then you would be on the right track we would surely appreciate your application if you have professional expertise in eu devices law (incl meddev guidelines) and experience in management system standards (iso 13485 iso 14971) if you enjoy using your analytical evaluation and decision-making skills then this position would be worth your while on a personal level you would convince us if you are keen on demonstrating your strong communication and conflict management competence and if you capable of handling confidential information and of interacting across all levels of business functions in this role as a "(junior) manager (m/f/d) device vigilance we expect you to have high language proficiency in german and english (written and spoken) to interact within our international working environment apply now send via email print this page at a glance er level: professional experienced graduates job category: regulatory affairs / drug safety working condition: permanent contract / full-time business segment: location: bad homburg / hessen closing date for applications: none - we look forward to your application apply now send via email print this page your contact gmbh bad homburg ref number: 31700 about er with a purpose: over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com   one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons   the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits your contact gmbh bad homburg ref number: 31700 erfmc-agcom er level: professional experienced graduates job category: regulatory affairs / drug safety working condition: permanent contract / full-time business segment: location: bad homburg / hessen closing date for applications: none - we look forward to your application about over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits (Junior) Manager (m/f/d) Medical Device Vigilance You will make an important contribution to the safety of our medical devices You will record and document medical device risks and will identify and document product safety indicators create post market surveillance & periodic safety update reports Bad Homburg

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61348 Bad Homburg (Höhe)

23.05.2019

Ingenieur, Techniker

Manager (m/f/d) Document Control

/ er with a purpose / - creating a future worth living for patients worldwide every day more than four decades of experience in dialysis innovative research the global leader in dialysis services and products - that is com manager (m/f/d) document control within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company receives and maintains its marketing authorizations (eg ce-marks or drug registrations) more within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company receives and maintains its marketing authorizations (eg ce-marks or drug registrations) your assignments as a manager (m/f/d) document control you will help implement and develop the electronic document control system and help qualify document owners by giving them trainings on regulatory issues concerning integrated management system (ims) documentations you will be a member of a team of four and will build your network within the company reaching out to different departments  to align their documentation processes with the required document quality standards of as an expert you will monitor and analyze new regulatory requirements for the ims documentation system and ensure that document owners / stakeholders understand and meet these requirements in their daily documentation processes if needed you will carry out document change requests document review and even improve ims default documents your profile if you have strong verbal communications skills the ability to influence with knowledge of legal requirements governing the devices industry you are on the right track it will be the right job for you if you enjoy translating requirements into a language all stakeholders understand and influencing them to exercise these policies we believe you will even master it if you have had some experience in the document control systems in the past and if you have a degree in scientific or technical studies or have completed a comparable vocational training with some years' experience apply now send via email print this page at a glance er level: professional experienced job category: other quality management / environment working condition: permanent contract / full-time business segment: location: bad homburg closing date for applications: none - we look forward to your application apply now send via email print this page your contact gmbh bad homburg ref number: 30699 about er with a purpose: over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com   one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons   the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits your contact gmbh bad homburg ref number: 30699 erfmc-agcom er level: professional experienced job category: other quality management / environment working condition: permanent contract / full-time business segment: location: bad homburg closing date for applications: none - we look forward to your application about over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits Manager (m/f/d) Document Control You will help implement and develop the electronic document control system and help qualify document owners by giving them trainings on regulatory issues concerning Integrated Management System (IMS) documentations Bad Homburg

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61348 Bad Homburg (Höhe)

23.05.2019

Medizin, Gesundheit

Drug Safety Associate (m/f/d)

/ er with a purpose / - creating a future worth living for patients worldwide every day more than four decades of experience in dialysis innovative research the global leader in dialysis services and products - that is com drug safety associate (m/f/d) within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company maintains and receives its marketing authorizations (eg ce-marks or drug registrations) having identified legal requirements and regulations for the company qrem works with different departments guiding them and ensuring that regulatory compliance and regulatory prerequisites for devices & drugs are met more within the qrem department (quality regulatory affairs & management systems) has the key responsibility to ensure that the company maintains and receives its marketing authorizations (eg ce-marks or drug registrations) having identified legal requirements and regulations for the company qrem works with different departments guiding them and ensuring that regulatory compliance and regulatory prerequisites for devices & drugs are met your assignments as a drug safety associate (m/f/d) you will handle the registration of medicinal product risks (eg adverse event (ae) adverse drug reaction (adr)) enter and feed medicinal product risks information into the global drug safety database while distributing relevant cases to partners and subsidiaries you will also report individual case safety reports to authorities and archive documents and information your role will include screening of the database for quality complaints documenting "periodic safety update report" as well as case report related compliance data you will handle queries and extract information from the global drug safety database for reporting purposes you will also render administrative support to the drug safety manager in maintaining the pharmacovigilance system master file your profile as a drug safety associate (m/f/d) we expect you to have completed vocational training as a documentation officer or an equivalent education further on you bring appropriate professional experience and expertise in drug safety demonstrating your superb computer skills particularly in databases and adr recording systems is something you enjoy doing dealing with database queries and extracting information from databases for reporting purposes is a part of your professional experience you are keen on working in a team and are capable of identifying and carrying out tasks independently if you have an eye for detail with a structured working approach then this role would be just right for you in order to work in the international setting that we operate in we expect your level of english to be proficient orally and in writing apply now send via email print this page at a glance er level: professional experienced graduates job category: regulatory affairs / drug safety working condition: permanent contract / full-time business segment: location: bad homburg / hessen closing date for applications: none - we look forward to your application apply now send via email print this page your contact gmbh bad homburg ref number: 32565 about er with a purpose: over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com   one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons   the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits your contact gmbh bad homburg ref number: 32565 erfmc-agcom er level: professional experienced graduates job category: regulatory affairs / drug safety working condition: permanent contract / full-time business segment: location: bad homburg / hessen closing date for applications: none - we look forward to your application about over 270000 people across the globe work at to provide better medicine for more people our independent business segments kabi helios and vamed offer a wide spectrum of products and services in the health sector we offer you the opportunity to make a difference with your er - and to become part of our impressive growth story ercom com one of ' strengths: our corporate culture for "entrepreneurs in an enterprise" where you can quickly take on responsibility more reasons the benefits we offer: profit-sharing long-term accounts for your future plans and other benefits which meet individual needs more benefits Drug Safety Associate (m/f/d) As a Drug Safety Associate (m/f/d) you will handle the registration of medicinal product risks (eg Adverse Event (AE) Adverse Drug Reaction (ADR)) enter and feed medicinal product risks information into the global drug safety database Bad Homburg

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61348 Bad Homburg (Höhe)

23.05.2019

Medizin, Gesundheit

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