Act as a Senior Finance Business Partner for R&D, Quality/Regulatory, and Medical Affairs, providing financial insights and decision support to senior stakeholders Lead project controlling for R&D projects and clinical studies, including budgeting, forecasting, cost tracking, and performance analysis Ensure transparency of project costs, resource utilization, and key cost drivers to enable effective financial steering of development activities Drive the standardization and continuous improvement of controlling processes, KPIs, and reporting tools across the organization Serve as SAP Key User for CO and PS, supporting project structures, cost allocation logic, and reporting, as well as contributing to SAP ECC6 and S/4HANA implementation and optimization initiatives Degree in Business Administration, Finance, Controlling, or a related field Robust experience in controlling, preferably within the Life Sciences, MedTech, or Pharmaceutical industry Strong background in project controlling for R&D projects or clinical studies, including business case evaluation and financial performance management Advanced SAP expertise, particularly in SAP CO and PS, with experience using SAP BW / Analysis for Office and advanced Excel reporting Proven business partnering and stakeholder management skills, with the ability to challenge senior leaders in a constructive manner; fluent English and solid German skills required Challenging and varied tasks in a promising and innovative industry Flat hierarchies Individual development opportunities Ihr Kontakt Referenznummer 865253/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Act as a Senior Finance Business Partner for R&D, Quality/Regulatory, and Medical Affairs, providing financial insights and decision support to senior stakeholdersLead project controlling for R&D projects and clinical studies, including budgeting, forecasting, cost tracking, and performance analysisEnsure transparency of project costs, resource utilization, and key cost drivers to enable effective financial steering of development activitiesDrive the standardization and continuous improvement of controlling processes, KPIs, and reporting tools across the organizationServe as SAP Key User for CO and PS, supporting project structures, cost allocation logic, and reporting, as well as contributing to SAP ECC6 and S/4HANA implementation and optimization initiatives Degree in Business Administration, Finance, Controlling, or a related fieldRobust experience in controlling, preferably within the Life Sciences, MedTech, or Pharmaceutical industryStrong background in project controlling for R&D projects or clinical studies, including business case evaluation and financial performance managementAdvanced SAP expertise, particularly in SAP CO and PS, with experience using SAP BW / Analysis for Office and advanced Excel reportingProven business partnering and stakeholder management skills, with the ability to challenge senior leaders in a constructive manner; fluent English and solid German skills required Challenging and varied tasks in a promising and innovative industry Flat hierarchies Individual development opportunities Ihr Kontakt Referenznummer 865253/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Löwenstein Medical SE & Co. KG sucht in eine/n Controller (m/w/d) (ID-Nummer: 13753104)
ALPRO MEDICAL GMBH sucht in St. Georgen eine/n Controller (m/w/d) (ID-Nummer: 13685082)
MED-EL Medical Electronics sucht in Innsbruck eine/n Group Controller (m/w/d) (ID-Nummer: 13728235)
Löwenstein Medical SE & Co. KG sucht in eine/n Supply Chain Controller (m/w/d) (ID-Nummer: 13753388)
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
Selbstständige Planung, Durchführung, Auswertung und Dokumentation von Integrationstests im BSL-1 Labor in unterschiedlichsten ProjektphasenAbstimmung der Integrationstests mit internen Schnittstellen und regelmässige Kommunikation an relevante Stakeholder über den Fortschritt der IntegrationstestsVerantwortlich für den Fortschritt der Systems Testing Aktivitäten innerhalb des Projektes gemäss der definierten ArbeitspaketeSie erstellen die erforderlichen technischen Dokumentationen in englischer SpracheSelbständiges Auswerten, Interpretieren und Präsentieren der Testergebnisse nach Regulatorischen und Projektspezifischen AnforderungenIdentifikation, Minimierung, Verfolgen und Reporten von Risiken und Issues nach Prozess und / oder ProjektdefinitionenReview von Produktanforderungen/Requirements hinsichtlich Testbarkeit und die Erstellung von Testfällen für die Verifikation dieser AnforderungenHinterfragen bestehender Laborprozesse, Identifikation von Optimierungsbedarf aus technischer und naturwissenschaftlicher Sicht und anschließende selbstständige Umsetzung Bachelor/Master Abschluss oder Ausbildung mit fundierter ErfahrungErste Test Erfahrung, idealerweise im Medical Device UmfeldSichere Programmierkenntnisse: entwickeln von internen Test-Frameworks und Analyse-Tools weiter mit Unterstützung von Git als Versionierung ToolPython Expertise (z.
Selbstständige Planung, Durchführung, Auswertung und Dokumentation von Integrationstests im BSL-1 Labor in unterschiedlichsten Projektphasen Abstimmung der Integrationstests mit internen Schnittstellen und regelmässige Kommunikation an relevante Stakeholder über den Fortschritt der Integrationstests Verantwortlich für den Fortschritt der Systems Testing Aktivitäten innerhalb des Projektes gemäss der definierten Arbeitspakete Sie erstellen die erforderlichen technischen Dokumentationen in englischer Sprache Selbständiges Auswerten, Interpretieren und Präsentieren der Testergebnisse nach Regulatorischen und Projektspezifischen Anforderungen Identifikation, Minimierung, Verfolgen und Reporten von Risiken und Issues nach Prozess und / oder Projektdefinitionen Review von Produktanforderungen/Requirements hinsichtlich Testbarkeit und die Erstellung von Testfällen für die Verifikation dieser Anforderungen Hinterfragen bestehender Laborprozesse, Identifikation von Optimierungsbedarf aus technischer und naturwissenschaftlicher Sicht und anschließende selbstständige Umsetzung Bachelor/Master Abschluss oder Ausbildung mit fundierter Erfahrung Erste Test Erfahrung, idealerweise im Medical Device Umfeld Sichere Programmierkenntnisse: entwickeln von internen Test-Frameworks und Analyse-Tools weiter mit Unterstützung von Git als Versionierung Tool Python Expertise (z.
Was Sie mitbringen: Optimalerweise Medizinprodukteberater nach MPG, Pharmareferent mit Vertriebserfahrung im Medical Bereich und/oder Neueinsteiger mit medizinischen oder kaufmännischen Kenntnissen aus dem Medical Bereich (OP Pfleger/in, Einkäufer/in aus Kliniken oder Einkaufsgemeinschaften)Mehrjährige Erfahrung in vergleichbarer Position von Vorteil (Vertragsverhandlungen, Bonuskonzepte und DRG System)Großes Maß an Selbstständigkeit und EigeninitiativeHohes Maß an TeamfähigkeitFreude daran, kreative Gedanken, neue Ideen und Ansätze zuzulassen und mit einzubringenFähigkeit und Bereitschaft, sich selbst zu hinterfragen und die eigene Arbeit und Lösungsansätze zu prüfen und ggfls. zu adaptierenFührerschein und Reisebereitschaft (inkl. vereinzelt mit Übernachtung) Wir passen zu Ihnen.
Löwenstein Medical Technology GmbH + Co. KG sucht in eine/n IT-Systemadministrator (m/w/d) Virtualisierung & Citrix (ID-Nummer: 13673711)
Sie beobachten Markt- und Wettbewerbsentwicklungen und bringen Ihre Erkenntnisse aktiv in die Weiterentwicklung unserer Vertriebsstrategie ein. Sie passen zu uns. Was Sie mitbringen: Erfahrung im Medical-Bereich, z. B. als Medizinprodukteberater (MPG), Pharmareferent mit Vertriebserfahrung oder aus einem klinischen Umfeld (z. B. OP-Pflege, Einkauf im Krankenhaus oder in Einkaufsgemeinschaften).
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
Main Accountabilities: ·Collection and analysis of data ·Identify areas of opportunity or problems within a supply chain environment ·Determine & analyze all costs to enable the daily management of effective & efficient deliveries so as to meet the pre agreed to KPI's ·Build models and run "what-if" analysis ·Provide support to teams to drive cost containment and/or cost reductions, delivery flexibility through development of comprehensive transport performance metrics ·Act as consultant to the design team during design phase for new business ·Translate defined strategies into specific goals, objectives and responsibilities ·Identify, review and implement processes to ensure operational efficiency and increased productivity Requirements: ·Ability to review and analyse data/results ·TMS experience would be an advantage ·Fixed and dynamic routing experience ·Advanced Microsoft suite knowledge ·Ability to function on a strategic level ·Excellent communication skills both verbally and written ·Business and financial acumen ·Build and maintain excellent relationships ·Fluent English ·Readiness to travel We offer: ·Work with professionals full of passion and willing to share knowledge ·A friendly workplace ·Real opportunities for development ·Private medical care ·Co-funded sport card ·Preferred life insurance conditions ·Co-funded vacation ·Christmas vouchers ·Participation in events supporting the local community
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
Purpose As a Therapeutic Strategy Lead, you’ll develop and implement effective delivery strategies tailored to customer needs during the RFP/Bid Defense cycle. You’ll bridge the gap between sales, medical, and operational teams to ensure seamless project execution and support sales teams throughout the Business Development process.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
Together, we ensure that our patients receive professional support, hands-on guidance, and reliable delivery of essential medical supplies. We are looking to strengthen our team and are seeking a Head of Continuous Improvement (m/w/d) (Certified Master Black Belt) - 25% travel to join us.
Previous experience in a project-driven and international environment within a medical company. Ambu – a visionary and international workplace where your efforts matter Ambu is a company that expands rapidly and has ambitious growth targets.
YOUR TASKS You consistently enforce HSE and safety requirements on site and intervene immediately in case of deviations You provide technical coordination and supervision of external contractors during mechanical installation activities You ensure quality, quantity, and compliance of installation work and initiate corrective actions when requirements are not met You ensure timely completion of work as the basis for proper commissioning of the wind turbine systems You review turbine-related reports and documentation for completeness, accuracy, and up-to-date status You actively participate in project and site meetings and contribute your expertise as a Mechanical Supervisor You identify missing or defective components and promptly report requirements to the site management YOUR PROFILE Completed technical vocational training, for example as a mechatronics technician or industrial mechanic, or an equivalent qualification gained through long-term experience in the wind energy sector Willingness to undertake multi‑week assignments on construction sites as well as regular Saturday work High willingness to travel mainly within Germany, with occasional assignments in Austria and the Netherlands Medical fitness for working at heights as well as confined working space and good physical condition for work on wind turbines Confident PC user skills, especially in MS Office Good command of English, both written and spoken, for collaboration in international teams High resilience, structured problem-solving skills, and clear, transparent communication Valid driving license class B We provide the opportunity for further qualification as an industrial electrician.
YOUR TASKS You consistently enforce HSE and safety requirements on site and intervene immediately in case of deviations You provide technical coordination and supervision of external contractors during mechanical installation activities You ensure quality, quantity, and compliance of installation work and initiate corrective actions when requirements are not met You ensure timely completion of work as the basis for proper commissioning of the wind turbine systems You review turbine-related reports and documentation for completeness, accuracy, and up-to-date status You actively participate in project and site meetings and contribute your expertise as a Mechanical Supervisor You identify missing or defective components and promptly report requirements to the site management YOUR PROFILE Completed technical vocational training, for example as a mechatronics technician or industrial mechanic, or an equivalent qualification gained through long-term experience in the wind energy sector Willingness to undertake multi‑week assignments on construction sites as well as regular Saturday work High willingness to travel mainly within Germany, with occasional assignments in Austria and the Netherlands Medical fitness for working at heights as well as confined working space and good physical condition for work on wind turbines Confident PC user skills, especially in MS Office Good command of English, both written and spoken, for collaboration in international teams High resilience, structured problem-solving skills, and clear, transparent communication Valid driving license class B We provide the opportunity for further qualification as an industrial electrician.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
Are you able to take responsibility for the development of novel medical devices? Do you see your strength in creating a trusting and open cooperation with external partners? And do you want to join a successful company in rapid growth?
As a subject matter expert, the Medical Strategy Lead will drive thought leadership activities including presentations, publications, and interactions with the medical scientific community.
As a subject matter expert, the Medical Strategy Lead will drive thought leadership activities including presentations, publications, and interactions with the medical scientific community.