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- Medizinischer Dienst
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- Medical advisor
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- Medical Information
- Clinical Application
- Medical Director
- Medical Adviser
Standorte
- München
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- Garching bei München
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- Gilching
- Ismaning
- Fürstenfeldbruck
- Ottobrunn
- Unterschleißheim
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1.019 Treffer für Clinical Support Jobs in Weßling im Umkreis von 30 km
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Medizintechnikplaner (m/w/d) für Bildgebende Verfahren (MRT, CT, Ultraschall)
Medizintechnikplaner (m/w/d) für Bildgebende Verfahren (MRT, CT, Ultraschall)
Birkholz und Partners - Ingenieure und Fachplaner für Medizin- und Informationstechnik GmbH
Munich
Schnelle Bewerbung
Mehrjährige Berufserfahrung in der medizinischen Bildgebung als Clinical Support Specialist, im Clinical Sales, im Product Management oder als Fachplaner in einem Planungsbüro.
Mehrjährige Berufserfahrung in der medizinischen Bildgebung als Clinical Support Specialist, im Clinical Sales, im Product Management oder als Fachplaner in einem Planungsbüro.
Noch nichts dabei? Es gibt 1018 weitere Jobs, die zu deiner Suche passen könnten
Define and manage clinical studies and investigations to support product innovation and regulatory approvals * Represent the company in communications with regulatory authorities related to clinical strategy, investigations and submissions * Define and lead the global Clinical Affairs strategy for Brainlab's global surgery portfolio, ensuring alignment with product, regulatory and commercial objectives / teams * Lead and develop an international Clinical Affairs team responsible for clinical evaluation, clinical research and scientific marketing communication * Ensure clinical compliance with EU MDR, FDA and other regulatory requirements * Build and maintain a strong clinical network of investigators, key opinion leaders and research partners * Act as Process Owner for clinical evaluation and validation, training authors and evaluators to ensure regulatory compliance
Define and manage clinical studies and investigations to support product innovation and regulatory approvals * Represent the company in communications with regulatory authorities related to clinical strategy, investigations and submissions * Define and lead the global Clinical Affairs strategy for Brainlab's global surgery portfolio, ensuring alignment with product, regulatory and commercial objectives / teams * Lead and develop an international Clinical Affairs team responsible for clinical evaluation, clinical research and scientific marketing communication * Ensure clinical compliance with EU MDR, FDA and other regulatory requirements * Build and maintain a strong clinical network of investigators, key opinion leaders and research partners * Act as Process Owner for clinical evaluation and validation, training authors and evaluators to ensure regulatory compliance
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(Senior) Product Support Specialist – Cranial & Functional Planning Applications
(Senior) Product Support Specialist – Cranial & Functional Planning Applications
Brainlab
München
Teilweise Home-Office
As a (Senior) Product Support Specialist “Cranial & Functional Planning Applications”, you are responsible for the of our world-wide customer care teams and providing effective technical & clinical knowledge transfer from our development teams into the world-wide support organization as well as representing the support perspective as a stakeholder in product development and helping to continuously improve the quality and performance of our treatment planning application. As an interface between , R&D and product management, you are playing a key role in ensuring successful development and preparation of support related documentation for the release of our software products. You are responsible for 3rd level customer support incl. root cause analysis, managing and resolving customer complaints incl. * Improve product design and service concept as a support stakeholder ...
As a (Senior) Product Support Specialist “Cranial & Functional Planning Applications”, you are responsible for the of our world-wide customer care teams and providing effective technical & clinical knowledge transfer from our development teams into the world-wide support organization as well as representing the support perspective as a stakeholder in product development and helping to continuously improve the quality and performance of our treatment planning application. As an interface between , R&D and product management, you are playing a key role in ensuring successful development and preparation of support related documentation for the release of our software products. You are responsible for 3rd level customer support incl. root cause analysis, managing and resolving customer complaints incl. * Improve product design and service concept as a support stakeholder ...
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All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together. You will collaborate closely with the global and local organizations, particularly in growth markets, in order to address customers' needs (surgeons, clinical staff) to further drive business growth of ZEISS SMILE pro. * Steering of relevant project partners for launch campaigns: you will work with product management, communication departments and clinical regulatory stakeholders to steer and implement integrated marketing plans for global launches
All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together. You will collaborate closely with the global and local organizations, particularly in growth markets, in order to address customers' needs (surgeons, clinical staff) to further drive business growth of ZEISS SMILE pro. * Steering of relevant project partners for launch campaigns: you will work with product management, communication departments and clinical regulatory stakeholders to steer and implement integrated marketing plans for global launches
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Pharmazeutisch-kaufmännische/r Angestellte/r (PKA, m/w/d) in Vollzeit
Pharmazeutisch-kaufmännische/r Angestellte/r (PKA, m/w/d) in Vollzeit
Medizone Germany GmbH
Fürstenfeldbruck
Teilweise Home-Office
Unsere Kernkompetenzen: Analytical Samples for Clinical Trails – wir beschaffen genau die Präparate, die für Forschung und Studien benötigt werden. Du packst mit deiner Allround-Support-Qualität die Aufgaben an, die gerade anstehen
Unsere Kernkompetenzen: Analytical Samples for Clinical Trails – wir beschaffen genau die Präparate, die für Forschung und Studien benötigt werden. Du packst mit deiner Allround-Support-Qualität die Aufgaben an, die gerade anstehen
All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together. It makes digital adoption easy, providing one ecosystem connecting devices, data and applications that enable a streamlined workflow, clinical planning, education, and optimization of clinical procedures. Especially, your outstanding experience in Java software development for medical industry will guide and support the entire team locally and internationally. * Support agile planning and refinement
All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together. It makes digital adoption easy, providing one ecosystem connecting devices, data and applications that enable a streamlined workflow, clinical planning, education, and optimization of clinical procedures. Especially, your outstanding experience in Java software development for medical industry will guide and support the entire team locally and internationally. * Support agile planning and refinement
The CSA collaborates closely with the Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country. * End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the Clinical Trial Management System (CTMS) and other general trial support in the country or region as delegated or per assigned trials. * Collaborating with PMCO, CRAs, SSU manager and study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information - The Clinical Study Administrator (CSA) assists in the coordination of study ...
The CSA collaborates closely with the Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country. * End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the Clinical Trial Management System (CTMS) and other general trial support in the country or region as delegated or per assigned trials. * Collaborating with PMCO, CRAs, SSU manager and study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information - The Clinical Study Administrator (CSA) assists in the coordination of study ...
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Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment - Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. * Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring * Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management * Minimum 4 years of R and R Shiny programming experience in Clinical/Pharmaceutical domain - Actual position's title: Clinical Data
Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment - Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. * Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring * Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management * Minimum 4 years of R and R Shiny programming experience in Clinical/Pharmaceutical domain - Actual position's title: Clinical Data
All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together. Our light, electron and X-ray microscopes as well as software solutions that utilize AI technology enable groundbreaking discoveries in life science, materials and industrial research as well as for education and clinical practice.
All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together. Our light, electron and X-ray microscopes as well as software solutions that utilize AI technology enable groundbreaking discoveries in life science, materials and industrial research as well as for education and clinical practice.
Schnelle Bewerbung
Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information - You will contribute to statistical activities related to global clinical trials and work closely with international teams of , and , including the role of biostatistics project lead * Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis * Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information - You will contribute to statistical activities related to global clinical trials and work closely with international teams of , and , including the role of biostatistics project lead * Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis * Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies * Provide support to medical data review
Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies * Provide support to medical data review
NEU
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Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies - Support of the departments in the area of shipping and logistics - Support for data maintenance and data collection - General office activities and support of in-house administrative processes - You are reliable, and ambitious to learn new skills achieving the best you can in support of your team.
Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies - Support of the departments in the area of shipping and logistics - Support for data maintenance and data collection - General office activities and support of in-house administrative processes - You are reliable, and ambitious to learn new skills achieving the best you can in support of your team.
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Medical Science Liaison Manager, Neurology, Northern Germany, fixed-term until April 2027
Medical Science Liaison Manager, Neurology, Northern Germany, fixed-term until April 2027
Alexion Pharma Germany GmbH
Germany - Munich
Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives * In conjunction with EMEA clinical operations perform clinical study feasibility and support effective study implementation. The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion's scientific platform and product/s across the product/s life cycle. The MSL combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally. * Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries * Identify and implement appropriate high-impact medical research projects to support the business objectives
Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives * In conjunction with EMEA clinical operations perform clinical study feasibility and support effective study implementation. The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion's scientific platform and product/s across the product/s life cycle. The MSL combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally. * Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries * Identify and implement appropriate high-impact medical research projects to support the business objectives
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Supervises and provides support to the , including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. The Project Manager (PM) is an important member of the Alira Health Clinical team. * Manages clinical research studies to ensure studies are conducted in accordance with approved scope of work/budget, ICH GCP guidelines, and FDA regulations and within established timelines. * Manages clinical study functions, which may include investigational supply, IWRS/IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. * Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/form templates, study manuals and plans, site binders, etc. * Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones.
Supervises and provides support to the , including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. The Project Manager (PM) is an important member of the Alira Health Clinical team. * Manages clinical research studies to ensure studies are conducted in accordance with approved scope of work/budget, ICH GCP guidelines, and FDA regulations and within established timelines. * Manages clinical study functions, which may include investigational supply, IWRS/IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. * Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/form templates, study manuals and plans, site binders, etc. * Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones.
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We are looking for a highly skilled Senior AI/ML Engineer (AI Lead) to take ownership of Custom Surgical's AI technical direction and help translate real-world clinical data into robust, scalable AI systems. You will design, build, and guide AI/ML solutions across computer vision, multimodal models, and emerging AI capabilities, working closely with Engineering, Product, and clinical stakeholders. * Design, implement, and maintain computer vision and multimodal ML systems for real-world clinical data; * Mentor and support junior and mid-level AI/ML engineers through reviews, guidance, and technical leadership;
We are looking for a highly skilled Senior AI/ML Engineer (AI Lead) to take ownership of Custom Surgical's AI technical direction and help translate real-world clinical data into robust, scalable AI systems. You will design, build, and guide AI/ML solutions across computer vision, multimodal models, and emerging AI capabilities, working closely with Engineering, Product, and clinical stakeholders. * Design, implement, and maintain computer vision and multimodal ML systems for real-world clinical data; * Mentor and support junior and mid-level AI/ML engineers through reviews, guidance, and technical leadership;
Collaborate closely with Marketing, Support, and Product teams to ensure an excellent customer experience; * Strong experience in Medical devices, ideally in ophthalmology (clinical, sales, medical devices, or related);
Collaborate closely with Marketing, Support, and Product teams to ensure an excellent customer experience; * Strong experience in Medical devices, ideally in ophthalmology (clinical, sales, medical devices, or related);
Reliability, performance, and scalability are critical, as these applications are used daily in real clinical environments. You will contribute to technical decisions, help shape the software architecture, and support other as the team grows. * Direct impact on mission-critical software used in clinical workflows worldwide;
Reliability, performance, and scalability are critical, as these applications are used daily in real clinical environments. You will contribute to technical decisions, help shape the software architecture, and support other as the team grows. * Direct impact on mission-critical software used in clinical workflows worldwide;
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Schnelle Bewerbung
To support this rapid growth and long-term integration, we are hiring a Head of Network Strategy and Post-Merger Integration. Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply. Founded in 2020, Adragos Pharma has rapidly grown through an ambitious buy & build strategy, supported by FSN Capital.
To support this rapid growth and long-term integration, we are hiring a Head of Network Strategy and Post-Merger Integration. Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply. Founded in 2020, Adragos Pharma has rapidly grown through an ambitious buy & build strategy, supported by FSN Capital.
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Trainer / Clinical Educator (m/w/d) Tracheotomie / Laryngektomie – Großraum Bayern
Trainer / Clinical Educator (m/w/d) Tracheotomie / Laryngektomie – Großraum Bayern
Coloplast GmbH
München, Augsburg, Nürnberg, Fürth, Erlangen, Ingolstadt, Regensburg, Bayreuth, Bamberg, Würzburg
Teilweise Home-Office
Zur Verstärkung für unser Commercial Development Team suchen wir zum nächstmöglichen Zeitpunkt einen Trainer / Clinical Educator (m/w/d) Tracheotomie / Laryngektomie – Großraum Bayern
Zur Verstärkung für unser Commercial Development Team suchen wir zum nächstmöglichen Zeitpunkt einen Trainer / Clinical Educator (m/w/d) Tracheotomie / Laryngektomie – Großraum Bayern
NEU
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Als Service Engineer (w/m/d) - Support stellst Du sicher, dass die IT-Systeme der ADAC Luftrettung zuverlässig und reibungslos arbeiten. * Support und Problemlösung - Du bearbeitest Störungen und Serviceanfragen im lst-und 2nd-Level-Support, dokumentierst sie im ITSM System und löst technische Probleme in den Bereichen Hard- und Software, Netzwerke und Benutzerrechte eigenständig. Bei Bedarf eskalierst Du an den 3rd-Level-Support oder externe Dienstleister. Zudem erstellst und pflegst Du Supportdokumentationen sowie technische Konzepte und stellst die Einhaltung von Compliance- sowie IT-Sicherheitsstandards sicher. * Berufserfahrung - Idealerweise kannst Du bereits mehrjährige Berufserfahrung im IT-Support/Service Desk oder in der Anwendungsbetreuung nachweisen.
Als Service Engineer (w/m/d) - Support stellst Du sicher, dass die IT-Systeme der ADAC Luftrettung zuverlässig und reibungslos arbeiten. * Support und Problemlösung - Du bearbeitest Störungen und Serviceanfragen im lst-und 2nd-Level-Support, dokumentierst sie im ITSM System und löst technische Probleme in den Bereichen Hard- und Software, Netzwerke und Benutzerrechte eigenständig. Bei Bedarf eskalierst Du an den 3rd-Level-Support oder externe Dienstleister. Zudem erstellst und pflegst Du Supportdokumentationen sowie technische Konzepte und stellst die Einhaltung von Compliance- sowie IT-Sicherheitsstandards sicher. * Berufserfahrung - Idealerweise kannst Du bereits mehrjährige Berufserfahrung im IT-Support/Service Desk oder in der Anwendungsbetreuung nachweisen.
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Manager Clinical & Regulatory Affairs Software (m/w/d)
Manager Clinical & Regulatory Affairs Software (m/w/d)
Meierhofer AG
Leipzig, München, Berlin, Hannover
Teilweise Home-Office
Meierhofer AG * Leipzig, München, Berlin, Hannover * Feste Anstellung * Homeoffice möglich, Vollzeit - Unsere Standorte - Wir suchen dich zur Verstärkung unseres Qualitätsmanagement-Teams an einem unserer Standorte in Leipzig, Berlin, Hannover, München oder im Home Office - Dein zukünftiges Team - Wir suchen Unterstützung rund um das Thema Zulassung unserer Medizinprodukte mit Schwerpunkt klinische Bewertung und technische Dokumentation! Als Manager für klinische und regulatorische Angelegenheiten bist du zuständig für die Betreuung der technischen Dokumentation sowie die Aktualisierung der klinischen Bewertungen unserer Medizinprodukte (Softwarelösungen). Du übernimmst eine zentrale Rolle in unserem Unternehmen. Du arbeitest eng mit deiner (/BoL), der Geschäftsführung, deinen Team-Kolleg*innen sowie Spezialist*innen aus anderen relevanten Bereichen zusammen. Das erwartet dich bei uns
Meierhofer AG * Leipzig, München, Berlin, Hannover * Feste Anstellung * Homeoffice möglich, Vollzeit - Unsere Standorte - Wir suchen dich zur Verstärkung unseres Qualitätsmanagement-Teams an einem unserer Standorte in Leipzig, Berlin, Hannover, München oder im Home Office - Dein zukünftiges Team - Wir suchen Unterstützung rund um das Thema Zulassung unserer Medizinprodukte mit Schwerpunkt klinische Bewertung und technische Dokumentation! Als Manager für klinische und regulatorische Angelegenheiten bist du zuständig für die Betreuung der technischen Dokumentation sowie die Aktualisierung der klinischen Bewertungen unserer Medizinprodukte (Softwarelösungen). Du übernimmst eine zentrale Rolle in unserem Unternehmen. Du arbeitest eng mit deiner (/BoL), der Geschäftsführung, deinen Team-Kolleg*innen sowie Spezialist*innen aus anderen relevanten Bereichen zusammen. Das erwartet dich bei uns
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Werkstudent IT Second Level Support & Helpdesk (m/w/d)
Werkstudent IT Second Level Support & Helpdesk (m/w/d)
Baader Bank AG
Unterschleißheim bei München
Teilweise Home-Office
Der Bereich Helpdesk & Second Level Support kümmert sich dabei um die effiziente Unterstützung unserer , das Lösen technischer Störungen sowie die Weiterentwicklung unserer IT‑Systeme * Du bringst Grundkenntnisse in Windows‑Betriebssystemen, Office 365 und IT‑Grundlagen mit und hast Interesse an IT‑Support, Serverumgebungen und moderner Microsoft‑Technologie
Der Bereich Helpdesk & Second Level Support kümmert sich dabei um die effiziente Unterstützung unserer , das Lösen technischer Störungen sowie die Weiterentwicklung unserer IT‑Systeme * Du bringst Grundkenntnisse in Windows‑Betriebssystemen, Office 365 und IT‑Grundlagen mit und hast Interesse an IT‑Support, Serverumgebungen und moderner Microsoft‑Technologie
NEU
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Für unser Team in München suchen wir ab sofort in Vollzeit einen IT Support Specialist (m/w/d). * Support von Computer-Hardware und -Software in enger Zusammenarbeit mit unserem internationalen IT-Team * Support bei der Administration von Telefonanlagen sowie Mobile-Device-Management-Systemen * Erfassung und Nachverfolgung von Supportanfragen und Systemfehlern über unser Ticketsystem * Eskalation komplexer IT-Probleme an 2nd- und 3rd-Level-Support, inklusive Follow-up und Kommunikation mit den * Anwendersupport in der Windows-Umgebung, insbesondere für Microsoft-Office-Produkte und Konferenzsysteme * Abgeschlossene Ausbildung im IT-Bereich oder vergleichbare Qualifikation wünschenswert – alternativ mindestens 3 Jahre Berufserfahrung im IT-Support
Für unser Team in München suchen wir ab sofort in Vollzeit einen IT Support Specialist (m/w/d). * Support von Computer-Hardware und -Software in enger Zusammenarbeit mit unserem internationalen IT-Team * Support bei der Administration von Telefonanlagen sowie Mobile-Device-Management-Systemen * Erfassung und Nachverfolgung von Supportanfragen und Systemfehlern über unser Ticketsystem * Eskalation komplexer IT-Probleme an 2nd- und 3rd-Level-Support, inklusive Follow-up und Kommunikation mit den * Anwendersupport in der Windows-Umgebung, insbesondere für Microsoft-Office-Produkte und Konferenzsysteme * Abgeschlossene Ausbildung im IT-Bereich oder vergleichbare Qualifikation wünschenswert – alternativ mindestens 3 Jahre Berufserfahrung im IT-Support
NEU
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Mitarbeiter Technischer Support - Heiztechnik oder Lüftungs- und Klimatechnik (m/w/d)
Mitarbeiter Technischer Support - Heiztechnik oder Lüftungs- und Klimatechnik (m/w/d)
Hoval GmbH
Frankfurt am Main, Hoyerswerda, München, Stuttgart
Teilweise Home-Office
In dieser anspruchsvollen Position bist du verantwortlich für eine lösungsorientierte Supporttätigkeit im Bereich Heiztechnik. * Idealerweise hast du schon erste Berührungspunkte im Bereich Technischer Support
In dieser anspruchsvollen Position bist du verantwortlich für eine lösungsorientierte Supporttätigkeit im Bereich Heiztechnik. * Idealerweise hast du schon erste Berührungspunkte im Bereich Technischer Support
NEU
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Praktikant HR Transformation & PMO Support (m/w/d)
Praktikant HR Transformation & PMO Support (m/w/d)
Rohde & Schwarz GmbH & Co. KG
München
Teilweise Home-Office
Rohde & Schwarz GmbH & Co. KG * München * Praktikum * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Bei Rohde & Schwarz entwickeln und produzieren wir Lösungen in den Bereichen Test & Measurement, Technology Systems sowie Networks & Cybersecurity – mit der Vision einer sicheren und vernetzten Welt. Von der Software bis zur Endfertigung gestalten unsere über 15.000 Mitarbeitenden Produkte und Systeme, die die technologische Souveränität unserer Kunden aus Wirtschaft, Behörden und hoheitlichem Umfeld sichern und weltweit Standards setzen. Unser Headquarter liegt zentral in München und ist zugleich unser Hauptentwicklungsstandort. Der Firmensitz ist in München. In Asien und Amerika steuern starke regionale Hubs in Singapur und Columbia, Maryland, die Geschäfte. Verstärke unseren Bereich Personal in München (Deutschland) zum nächstmöglichen Zeitpunkt. Aufgaben
Rohde & Schwarz GmbH & Co. KG * München * Praktikum * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Bei Rohde & Schwarz entwickeln und produzieren wir Lösungen in den Bereichen Test & Measurement, Technology Systems sowie Networks & Cybersecurity – mit der Vision einer sicheren und vernetzten Welt. Von der Software bis zur Endfertigung gestalten unsere über 15.000 Mitarbeitenden Produkte und Systeme, die die technologische Souveränität unserer Kunden aus Wirtschaft, Behörden und hoheitlichem Umfeld sichern und weltweit Standards setzen. Unser Headquarter liegt zentral in München und ist zugleich unser Hauptentwicklungsstandort. Der Firmensitz ist in München. In Asien und Amerika steuern starke regionale Hubs in Singapur und Columbia, Maryland, die Geschäfte. Verstärke unseren Bereich Personal in München (Deutschland) zum nächstmöglichen Zeitpunkt. Aufgaben
NEU
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