Schnelle Bewerbung
87
Erscheinungsdatum
Home-Office-Optionen
Pendelzeit
Bewerbungsart
Sprache
Fähigkeiten
Berufsfeld
Branche
Region
Städte
Berufserfahrung
Anstellungsart
Arbeitszeit
Filter
SortierungRelevanz
Standorte
- Berlin
- Hamburg
- München
- Frankfurt am Main
- Köln
- Düsseldorf
- Stuttgart
- Hannover
- Leipzig
- Bremen
- Essen
- Dortmund
- Karlsruhe
- Mannheim
- Kiel
- Freiburg im Breisgau
- Ulm
- Wiesbaden
- Paderborn
- Bautzen
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Niedersachsen
- Mitteldeutschland
- Hessen
- Rhein-Main-Gebiet
- Ruhrgebiet
- Sachsen
Home-Office-Optionen
Gehalt
Leg fest, wie viel du mindestens verdienen willst.
Pendelzeit
Bewerbungsart
Sprache
Fähigkeiten
Berufsfeld
Branche
Region
Städte
Berufserfahrung
Anstellungsart
Arbeitszeit
Standorte
- Berlin
- Hamburg
- München
- Frankfurt am Main
- Köln
- Düsseldorf
- Stuttgart
- Hannover
- Leipzig
- Bremen
- Essen
- Dortmund
- Karlsruhe
- Mannheim
- Kiel
- Freiburg im Breisgau
- Ulm
- Wiesbaden
- Paderborn
- Bautzen
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Niedersachsen
- Mitteldeutschland
- Hessen
- Rhein-Main-Gebiet
- Ruhrgebiet
- Sachsen
297 Treffer für Process Safety Specialist Jobs
Noch nichts dabei? Es gibt 297 weitere Jobs, die zu deiner Suche passen könnten
){kind=logo}
Fachkoordinator und Fachkraft (m/w/d) für Arbeitssicherheit
Fachkoordinator und Fachkraft (m/w/d) für Arbeitssicherheit
amedes Medizinische Dienstleistungen GmbH
bundesweit
Anschreiben nicht erforderlich
Schnelle Bewerbung
Eingebettet in den Bereich Process Excellence unterstützen Sie mit der Datengrundlage der Arbeitssicherheit die Analyse, Auswertung und Überwachung der Optimierungsprozesse
Eingebettet in den Bereich Process Excellence unterstützen Sie mit der Datengrundlage der Arbeitssicherheit die Analyse, Auswertung und Überwachung der Optimierungsprozesse
){kind=logo}
Head of Global Safety Product Leads - Risk & Label Management (m/f/d)
Head of Global Safety Product Leads - Risk & Label Management (m/f/d)
Dr. Falk Pharma GmbH
Freiburg
Teilweise Home-Office
Team management of a group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. * Preparation of periodic safety reports - Supporting the of Global Safety / EU/UK QPPV / Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including * Ensuring an adequate quality management system to fulfill all relevant pharmacovigilance obligations of Dr. Falk Pharma GmbH by establishing suitable working methods and processes as well as procedural instructions for the quality assurance of results * Collection and systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases.
Team management of a group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. * Preparation of periodic safety reports - Supporting the of Global Safety / EU/UK QPPV / Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including * Ensuring an adequate quality management system to fulfill all relevant pharmacovigilance obligations of Dr. Falk Pharma GmbH by establishing suitable working methods and processes as well as procedural instructions for the quality assurance of results * Collection and systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases.
){kind=logo}
Strict compliance with quality, occupational safety, and environmental regulations and implementation of instructions from quality/environmental management officers and occupational safety specialists * Initiating and actively participating in measures for process improvement, standardization, waste elimination, etc. * Active participation in the innovation process
Strict compliance with quality, occupational safety, and environmental regulations and implementation of instructions from quality/environmental management officers and occupational safety specialists * Initiating and actively participating in measures for process improvement, standardization, waste elimination, etc. * Active participation in the innovation process
NEU
){kind=logo}
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement * Strict compliance with the quality, occupational safety and environmental regulations.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement * Strict compliance with the quality, occupational safety and environmental regulations.
Strict adherence to quality, occupational safety and environmental regulations and implementation of the instructions of quality/ environmental management officers and occupational safety specialist * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement
Strict adherence to quality, occupational safety and environmental regulations and implementation of the instructions of quality/ environmental management officers and occupational safety specialist * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement
){kind=logo}
Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.
Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.
){kind=logo}
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
NEU
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement * Strict compliance with the quality, occupational safety and environmental regulations.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement * Strict compliance with the quality, occupational safety and environmental regulations.
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management officers and the occupational safety specialist. * Technical management of the technical project components and content-related support for the associated work packages (target definition, DoD) together with the project manager and the specialist departments * Support of the production processes up to the series (NPI); technical support of production (PE) * Initiation and active participation in measures for synchronisation processes, further development of processes in the area * Active participation in the innovation process * Knowledge of the relevant norms and standards as well as the approval process (FDA; CE)
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management officers and the occupational safety specialist. * Technical management of the technical project components and content-related support for the associated work packages (target definition, DoD) together with the project manager and the specialist departments * Support of the production processes up to the series (NPI); technical support of production (PE) * Initiation and active participation in measures for synchronisation processes, further development of processes in the area * Active participation in the innovation process * Knowledge of the relevant norms and standards as well as the approval process (FDA; CE)
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management representatives and the occupational safety specialist Technical management of the technical project components and content-related support of the associated work packages (target definition, DoD) together with the project manager and the specialist departments - Support of manufacturing processes up to the series (NPI); Technical support of production (PE) Initiation and active participation in measures for synchronization processes Active participation in the innovation process
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management representatives and the occupational safety specialist Technical management of the technical project components and content-related support of the associated work packages (target definition, DoD) together with the project manager and the specialist departments - Support of manufacturing processes up to the series (NPI); Technical support of production (PE) Initiation and active participation in measures for synchronization processes Active participation in the innovation process
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) * Focusing on Medical Affairs related processes such as PMS, PMCF, Clinical Evaluation, Risk Management, Change Management and Nonconformance/Corrective and Preventive Action ...
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) * Focusing on Medical Affairs related processes such as PMS, PMCF, Clinical Evaluation, Risk Management, Change Management and Nonconformance/Corrective and Preventive Action ...
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc.
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management representatives and the occupational safety specialist As a Senior Regulatory Affairs Specialist, you'll be working to obtain government approval for new products. Your responsibilities will include analyzing compliance regulations and ensuring product and process compliance. * Contribute to the execution of the risk management process, clinical evaluation and usability file as part of the design steering process. * Processing of change processes and checking for relevance to approval * General inquiries regarding RA and contact person for interpretation of standard requirements e.g. for steri-validation, biocompatibility, electrical safety etc. Handling of safety-related complaints in cooperation with the QM team
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management representatives and the occupational safety specialist As a Senior Regulatory Affairs Specialist, you'll be working to obtain government approval for new products. Your responsibilities will include analyzing compliance regulations and ensuring product and process compliance. * Contribute to the execution of the risk management process, clinical evaluation and usability file as part of the design steering process. * Processing of change processes and checking for relevance to approval * General inquiries regarding RA and contact person for interpretation of standard requirements e.g. for steri-validation, biocompatibility, electrical safety etc. Handling of safety-related complaints in cooperation with the QM team
from quality/environmental management officers and the occupational safety specialist. * Technical management of the technical project components and content-related support for the associated work packages (target definition, DoD) together with the project manager and the specialist departments * Support of the production processes up to the series (NPI); technical support of production (PE) * Initiation and active participation in measures for synchronisation processes, further development of processes in the area * Active participation in the innovation process * Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions * Very good knowledge of manufacturing processes of sterile tubing sets (bonding, welding, packaging, etc.) * Knowledge of the relevant norms and standards as well as the approval process (FDA; CE)
from quality/environmental management officers and the occupational safety specialist. * Technical management of the technical project components and content-related support for the associated work packages (target definition, DoD) together with the project manager and the specialist departments * Support of the production processes up to the series (NPI); technical support of production (PE) * Initiation and active participation in measures for synchronisation processes, further development of processes in the area * Active participation in the innovation process * Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions * Very good knowledge of manufacturing processes of sterile tubing sets (bonding, welding, packaging, etc.) * Knowledge of the relevant norms and standards as well as the approval process (FDA; CE)
Strict adherence to quality, occupational safety and environmental regulations and implementation of the instructions of quality/ environmental management officers and occupational safety specialist * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement
Strict adherence to quality, occupational safety and environmental regulations and implementation of the instructions of quality/ environmental management officers and occupational safety specialist * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement * Strict compliance with the quality, occupational safety and environmental regulations.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. * Coordination with other on processes, interfaces and cross-sectional tasks * Active participation in the innovation process & continuous improvement * Strict compliance with the quality, occupational safety and environmental regulations.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. Based on market needs and voice of customer, the employee develops product requirements, and actively manages the related portfolio from product idea until discontinuation, and develops all necessary documentation following PM-related regulative processes and sustaining activities. * Create and own NPVs and contribute to phase gate process * Contribution and support of risk management process * Coordination of sustaining activities and PM-related Regulatory Processes as Clinical Evaluation, Post Market Surveillance, Post Market Clinical Follow-up, Usability * Strict compliance with the quality, occupational safety and environmental regulations. Exercises primarily technical and some process leadership.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist. Based on market needs and voice of customer, the employee develops product requirements, and actively manages the related portfolio from product idea until discontinuation, and develops all necessary documentation following PM-related regulative processes and sustaining activities. * Create and own NPVs and contribute to phase gate process * Contribution and support of risk management process * Coordination of sustaining activities and PM-related Regulatory Processes as Clinical Evaluation, Post Market Surveillance, Post Market Clinical Follow-up, Usability * Strict compliance with the quality, occupational safety and environmental regulations. Exercises primarily technical and some process leadership.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) * Focusing on Medical Affairs related processes such as PMS, PMCF, Clinical Evaluation, Risk Management, Change Management and Nonconformance/Corrective and Preventive Action ...
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) * Focusing on Medical Affairs related processes such as PMS, PMCF, Clinical Evaluation, Risk Management, Change Management and Nonconformance/Corrective and Preventive Action ...
NEU
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management officers and the occupational safety specialist. * Technical management of the technical project components and content-related support for the associated work packages (target definition, DoD) together with the project manager and the specialist departments * Support of the production processes up to the series (NPI); technical support of production (PE) * Initiation and active participation in measures for synchronisation processes, further development of processes in the area * Active participation in the innovation process * Knowledge of the relevant norms and standards as well as the approval process (FDA; CE)
Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions from quality/environmental management officers and the occupational safety specialist. * Technical management of the technical project components and content-related support for the associated work packages (target definition, DoD) together with the project manager and the specialist departments * Support of the production processes up to the series (NPI); technical support of production (PE) * Initiation and active participation in measures for synchronisation processes, further development of processes in the area * Active participation in the innovation process * Knowledge of the relevant norms and standards as well as the approval process (FDA; CE)
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) * Focusing on Medical Affairs related processes such as PMS, PMCF, Clinical Evaluation, Risk Management, Change Management and Nonconformance/Corrective and Preventive Action ...
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) * Focusing on Medical Affairs related processes such as PMS, PMCF, Clinical Evaluation, Risk Management, Change Management and Nonconformance/Corrective and Preventive Action ...
){kind=logo}
Health, Safety & Environment Specialist (m/w/d) für Kundenprojekte
Health, Safety & Environment Specialist (m/w/d) für Kundenprojekte
NVL B.V. & Co. KG
Hamburg, Lemwerder, Bremen
Teilweise Home-Office
NVL B.V. & Co. KG * Hamburg, Lemwerder, Bremen * Feste Anstellung * Homeoffice möglich, Vollzeit - Schiffbau voller Leidenschaft, hochspezialisierte Marineschiffe, Innovation und Teamwork: Dafür steht die NVL. Wir sind eine privat geführte, unabhängige Werftengruppe mit vier renommierten Werftstandorten in Norddeutschland und internationalen Standorten mit mehr als 1.700 hochqualifizierten Mitarbeitenden. Unseren Kunden bieten wir maßgeschneiderte, intelligente und kosteneffiziente Schiffbaulösungen sowie umfangreiche Services und unterstützen damit die Einsatzbereitschaft der Deutschen Marine und von Navies weltweit. Kommen Sie an Bord! Aufgaben - Als zentrale Schnittstelle zwischen Kundenprojekten, Projektleitung und unserer HSE-Organisation tragen Sie dazu bei, Arbeits-, Gesundheits- und Umweltschutz entlang des Projektverlaufs sicherzustellen.
NVL B.V. & Co. KG * Hamburg, Lemwerder, Bremen * Feste Anstellung * Homeoffice möglich, Vollzeit - Schiffbau voller Leidenschaft, hochspezialisierte Marineschiffe, Innovation und Teamwork: Dafür steht die NVL. Wir sind eine privat geführte, unabhängige Werftengruppe mit vier renommierten Werftstandorten in Norddeutschland und internationalen Standorten mit mehr als 1.700 hochqualifizierten Mitarbeitenden. Unseren Kunden bieten wir maßgeschneiderte, intelligente und kosteneffiziente Schiffbaulösungen sowie umfangreiche Services und unterstützen damit die Einsatzbereitschaft der Deutschen Marine und von Navies weltweit. Kommen Sie an Bord! Aufgaben - Als zentrale Schnittstelle zwischen Kundenprojekten, Projektleitung und unserer HSE-Organisation tragen Sie dazu bei, Arbeits-, Gesundheits- und Umweltschutz entlang des Projektverlaufs sicherzustellen.
){kind=logo}
Analyse, Aufbereitung und Reporting relevanter Health-&-Safety-Kennzahlen (z. B. Unfallstatistiken, Abwesenheiten) sowie Steuerung kontinuierlicher Verbesserungsprozesse
Analyse, Aufbereitung und Reporting relevanter Health-&-Safety-Kennzahlen (z. B. Unfallstatistiken, Abwesenheiten) sowie Steuerung kontinuierlicher Verbesserungsprozesse
){kind=logo}
Schnelle Bewerbung
CMBlu Energy AG * Alzenau * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Wir sind die Pioniere organischer Batterien - CMBlu Energy befindet sich auf der spannenden Reise hin zu einem globalen Cleantech-Unternehmen. Unsere Mission: Unbegrenzte Energiespeicherung nach dem Vorbild der Natur ermöglichen – und das für alle, weltweit. Was sind SolidFlow-Batterien? SolidFlow-Batterien speichern Energie in organischen Molekülen. Der Verzicht auf explosive Materialien macht sie sicher, der Einsatz von sozial und ökologisch konfliktfreien Rohstoffen nachhaltig und die nahezu unbegrenzte Materialverfügbarkeit skalierbar und günstig in der Beschaffung. Das macht unsere patentierte SolidFlow-Technologie zu einem Gamechanger im Aufbau eines globalen klimaneutralen Energiesystems. Vom Start-up zum Scale-up: Gemeinsam packen wir es an
CMBlu Energy AG * Alzenau * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Wir sind die Pioniere organischer Batterien - CMBlu Energy befindet sich auf der spannenden Reise hin zu einem globalen Cleantech-Unternehmen. Unsere Mission: Unbegrenzte Energiespeicherung nach dem Vorbild der Natur ermöglichen – und das für alle, weltweit. Was sind SolidFlow-Batterien? SolidFlow-Batterien speichern Energie in organischen Molekülen. Der Verzicht auf explosive Materialien macht sie sicher, der Einsatz von sozial und ökologisch konfliktfreien Rohstoffen nachhaltig und die nahezu unbegrenzte Materialverfügbarkeit skalierbar und günstig in der Beschaffung. Das macht unsere patentierte SolidFlow-Technologie zu einem Gamechanger im Aufbau eines globalen klimaneutralen Energiesystems. Vom Start-up zum Scale-up: Gemeinsam packen wir es an
Beliebte Jobs
Standorte
- Berlin
- Hamburg
- München
- Frankfurt am Main
- Köln
- Düsseldorf
- Stuttgart
- Hannover
- Leipzig
- Bremen
- Essen
- Dortmund
- Karlsruhe
- Mannheim
- Kiel
- Freiburg im Breisgau
- Ulm
- Wiesbaden
- Paderborn
- Bautzen
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
- Ostdeutschland
- Bayern
- Baden-Württemberg
- Rheinland
- Neckarland-Schwaben
- Niedersachsen
- Mitteldeutschland
- Hessen
- Rhein-Main-Gebiet
- Ruhrgebiet
- Sachsen