PSURs).Du unterstützt klinische Strategien in Zulassungs- und Entwicklungsprojekten.Du bist in Risikomanagementprozesse eingebunden.Du gestaltest aktiv mit: Vorlagen, SOPs und Arbeitsanweisungen entwickelst Du eigenverantwortlich weiter.Du kommunizierst mit Behörden, Fachkreisen und internationalen Partnern.Ausbildung/ Studium: Du bringst ein abgeschlossenes Masterstudium in Medizin, Naturwissenschaften, Medizintechnik oder einem vergleichbaren Bereich mit.Fachwissen:Erste Erfahrung mit wissenschaftlichem Arbeiten, idealerweise mit Fokus auf Medical Writing, klinische Datenanalyse oder klinische Bewertung.Kenntnisse relevanter Regularien (MDR, ISO 14155, MDCG) sind ein Plus.Idealerweise bringst Du Produktkenntnisse in der Endoprothetik mit.Soft-Skills: Du arbeitest strukturiert, bist analytisch starkDu bist kommunikationsstark und ein echter TeamplayerSprachkenntnisse: Du sprichst und schreibst Deutsch und Englisch mindestens auf C1-Niveau.Unsere Stellenausschreibung gibt Dir einen Einblick in die Anforderungen der Position.
For our esteemed client in the pharmaceutical industry, we are looking for a Supplier Quality Engineer Packaging (m/f/d) based in Bad Homburg. Become part of a globally leading company in medical devices and pharmaceuticals and take responsibility for qualifying packaging suppliers and driving the global harmonization of packaging standards.
Ihre Aufgaben: Montage und Prüfung von Kleinkomponenten im Bereich Medical ElectronicsUmsetzung des Produktionsplanes HochspannungsprüfungenSelbstständige Analyse und Reparatur bei fehlerhaften KomponentenBearbeitung von Rückwaren und Dokumentation anfallender Reparaturen in SAP Dokumentation von Arbeitsfortschritten und Seriennummern Ihre Qualifikation: Abgeschlossene Ausbildung als Feinwerkmechaniker (m/w/d) oder vergleichbare QualifikationErste Berufserfahrung vorzugsweise aus der IndustrieMontageaffinitätHandwerkliches GeschickPC-AnwenderkenntnisseSchichtbereitschaft Ihr Vorteil: Qualifikationsübergreifende Einstiegsmöglichkeiten Übertarifliche BezahlungWeitere Zusatzleistungen und optionale Zulagen Urlaubs- und Weihnachtsgeld Kostenlose, persönliche SchutzausrüstungKantinennutzungChance auf Übernahme durch unseren Kunden Arbeitsplatzbezogene WeiterbildungsmöglichkeitenIndividuelle Begleitung und Beratung im Bewerbungsprozess und im Kundeneinsatz Arbeitsmedizinische und sicherheitstechnische Betreuung Ihr Kontakt zu Hofmann: Zögern Sie nicht und bewerben Sie sich noch heute.
Benefits Vergütung nach dem GVP inklusive Zulagen und Branchenzuschlägen (IG Metall) bis zu 25,23€ brutto/StundeUrlaubs- und WeihnachtsgeldModerne und hochwertige Arbeitskleidung von Engelbert StraussSichere und langfristige Perspektive bei einem namhaften KonzernÜbernahmemöglichkeit in eine FestanstellungGute Anbindung an öffentliche VerkehrsmittelPersönliche Betreuung und Unterstützung während Ihres gesamten Einsatzes Aufgaben Löten von Flachbaugruppen Reparaturlöten von SMD-Bauteilen Optische Kontrolle von SMD-bestückten Flachbaugruppen Montage und Prüfung von Kleinkomponenten im Bereich Medical Electronics Verantwortung für die Umsetzung des Produktionsplans unter Berücksichtigung der Produktionsqualität Durchführung der Montage und Prüfung in Fertigungsinseln, sowohl softwaregestützt als auch manuell an Handprüfplätzen Selbständige Analyse und Reparatur fehlerhafter Komponenten Profil Mehrjährige Berufserfahrung in der Elektronikfertigung mindestens 2 JahreErfahrung im Löten Hohe Fingerfertigkeit, handwerkliches Geschick Bereitschaft zur Arbeit im Dreischichtsystem Arbeitszeit: 35 Stunden pro Woche Arbeitsort: Erlangen Anstellungsart: Arbeitnehmerüberlassung Klingt nach Deinem nächsten Job?
Ihr Arbeitszeitmodell: 3-Schichtbetrieb Ihre Aufgaben: Löten von FlachbaugruppenReparaturlöten von SMD BauteilenOptische Kontrolle von SMD bestückten FlachbaugruppenMontieren und prüfen von Kleinkomponenten im Bereich Medical Electronics ProzesskontrolleVerantwortlich für die Umsatzung des Produktionsplanes unter Berücksichtigung der ProduktionsqualitätSoftwaregestützte Montage und Prüfung Selbständige Analyse und Reparaturen von Komponenten Ihre Qualifikation: Mehrjährige Berufserfahrung im Bereich ElektronikfertigungVorzugsweise Erfahrung im LötenHohe FingerfertigkeitGutes technisches Verständnis und präzise ArbeitsweiseBereitschaft zur Arbeit im Dreischichtmodell Ihr Vorteil: Wir sind eine internationale Unternehmensgruppe mit über 20.000 Mitarbeitern in Deutschland, Österreich, Tschechien, Slowakei, Schweiz, Italien, Ungarn und den USA.
These technologies are paving the way for advancements in telecommunications, autonomous vehicles, and medical diagnostics. Our company-wide goal is to set up top-notch technology that facilitates our customers from around the world in building tomorrow’s optoelectronic devices.
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.
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.
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
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
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.
To supervise and assist in the preparation and care of the patient and her partner before, during and after the above procedures. To demonstrate initiative and provide support in assisting medical staff with procedures e.g. performing transvaginal ultrasound guided oocyte retrieval. To work within the legal framework as laid out by the 1990 Human Fertilisation and Embryology Act of Parliament and Care Quality Commission To manage difficult situations with competence, taking appropriate action, utilising relevant protocols and supporting the patient, their relatives and members of the multidisciplinary team as required.
To supervise and assist in the preparation and care of the patient and her partner before, during and after the above procedures. To demonstrate initiative and provide support in assisting medical staff with procedures e.g. performing transvaginal ultrasound guided oocyte retrieval. To work within the legal framework as laid out by the 1990 Human Fertilisation and Embryology Act of Parliament and Care Quality Commission To manage difficult situations with competence, taking appropriate action, utilising relevant protocols and supporting the patient, their relatives and members of the multidisciplinary team as required.
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.
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
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.
To supervise and assist in the preparation and care of the patient and her partner before, during and after the above procedures. To demonstrate initiative and provide support in assisting medical staff with procedures e.g. performing transvaginal ultrasound guided oocyte retrieval. To work within the legal framework as laid out by the 1990 Human Fertilisation and Embryology Act of Parliament and Care Quality Commission To manage difficult situations with competence, taking appropriate action, utilising relevant protocols and supporting the patient, their relatives and members of the multidisciplinary team as required.
These technologies are paving the way for advancements in telecommunications, autonomous vehicles, and medical diagnostics. Our company-wide goal is to set up top-notch technology that facilitates our customers from around the world in building tomorrow’s optoelectronic devices.
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.
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?
Proactive participation in all phases of software development from feasibility studies through design,development, testing and bug fixing and maintenanceCollaboration within the Scrum-TeamsIndependent interaction with internal framework manufacturersBased on requirements and models, definition of software architecture, design and specifications, ultimately leading to implementationParticipation in the definition of work packages, their estimation and planning in a sprint-based agile environmentAdherence to a software development process including contribution to written deliverables and documentation Degree in a software related field such as software or electrical engineering or similarHands-on experience as Software Engineer, preferred in the regulated environment such as the medical device industryYears hands- on experience with C++ and Linux from the last project or positionStrong with Linux DockersExperience with CAN busSoftware architecture would be advantageous Internal career opportunities World-renowned biotech company Ihr Kontakt Referenznummer 865145/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
WIR BIETEN IHNEN Direkte Festanstellung bei unserem Kundenunternehmen Eine attraktive Vergütung auf Basis des Chemietarifs Ein Firmenfahrzeug zur privaten Nutzung, verfügbar ab dem ersten Arbeitstag 30 Tage Erholungsurlaub zur Förderung einer ausgewogenen Work-Life-Balance Unterstützung durch ein professionelles Innendienstteam, das Sie umfassend bei Ihren Aufgaben begleitet Zugang zu etablierten und hochwertigen Medikamenten im OTC-Bereich IHRE AUFGABEN Sie betreuen eigenverantwortlich Ärztinnen und Ärzte verschiedener Fachrichtungen und vermitteln den Nutzen der Produkte für Patienten und das Gesundheitssystem Sie führen fundierte Fachgespräche und erläutern Diagnose- und Therapieansätze praxisnah Sie klären medizinische Fragen, optimieren gemeinsam mit den Ärzten die Diagnostik und stellen therapeutische Möglichkeiten transparent dar Sie bauen langfristige Beziehungen zu relevanten Facharztpraxen auf und pflegen diese kontinuierlich Sie setzen die Vertriebs- und Kommunikationsstrategien um und stimmen sich eng mit den Bereichen Marketing, Medical Affairs und Vertrieb ab Sie dokumentieren Ihre Aktivitäten strukturiert und beobachten Markt- und Wettbewerbsentwicklungen IHR PROFIL Sie verfügen über ein abgeschlossenes Studium in Medizin, Pharmazie, Biologie, Biochemie, über eine erfolgreich abgeschlossene Weiterbildung zum geprüften Pharmareferenten / zur geprüften Pharmareferentin oder eine vergleichbare Qualifikation mit erworbener „Sachkenntnis nach § 75 AMG" Sie haben bereits langjährige Erfahrung im Außendienst eines pharmazeutischen Unternehmens oder im Facharztaußendienst gesammelt Sie bringen fundiertes medizinisches Wissen mit und treten sicher im fachlichen Austausch mit Ärzten auf Sie verfügen über sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Sie arbeiten strukturiert, eigenverantwortlich und lösungsorientiert Sie sind hochmotiviert, neue Indikationen aufzubauen und Themen im Markt zu etablieren IN NUR 2 MINUTEN ZU IHREM NEUEN JOB Nutzen Sie unser Online-Formular und laden Ihre vollständigen Bewerbungsunterlagen (inklusive aussagekräftigen Lebenslauf, Zeugnisse, Zertifikate, etc.) einfach hoch – ein Anschreiben ist nicht erforderlich.
WIR BIETEN IHNEN Direkte Festanstellung bei unserem Kundenunternehmen Eine attraktive Vergütung auf Basis des Chemietarifs Ein Firmenfahrzeug zur privaten Nutzung, verfügbar ab dem ersten Arbeitstag 30 Tage Erholungsurlaub zur Förderung einer ausgewogenen Work-Life-Balance Unterstützung durch ein professionelles Innendienstteam, das Sie umfassend bei Ihren Aufgaben begleitet Zugang zu etablierten und hochwertigen Medikamenten im OTC-Bereich IHRE AUFGABEN Sie betreuen eigenverantwortlich Ärztinnen und Ärzte verschiedener Fachrichtungen und vermitteln den Nutzen der Produkte für Patienten und das Gesundheitssystem Sie führen fundierte Fachgespräche und erläutern Diagnose- und Therapieansätze praxisnah Sie klären medizinische Fragen, optimieren gemeinsam mit den Ärzten die Diagnostik und stellen therapeutische Möglichkeiten transparent dar Sie bauen langfristige Beziehungen zu relevanten Facharztpraxen auf und pflegen diese kontinuierlich Sie setzen die Vertriebs- und Kommunikationsstrategien um und stimmen sich eng mit den Bereichen Marketing, Medical Affairs und Vertrieb ab Sie dokumentieren Ihre Aktivitäten strukturiert und beobachten Markt- und Wettbewerbsentwicklungen IHR PROFIL Sie verfügen über ein abgeschlossenes Studium in Medizin, Pharmazie, Biologie, Biochemie, über eine erfolgreich abgeschlossene Weiterbildung zum geprüften Pharmareferenten / zur geprüften Pharmareferentin oder eine vergleichbare Qualifikation mit erworbener „Sachkenntnis nach § 75 AMG" Sie haben bereits langjährige Erfahrung im Außendienst eines pharmazeutischen Unternehmens oder im Facharztaußendienst gesammelt Sie bringen fundiertes medizinisches Wissen mit und treten sicher im fachlichen Austausch mit Ärzten auf Sie verfügen über sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Sie arbeiten strukturiert, eigenverantwortlich und lösungsorientiert Sie sind hochmotiviert, neue Indikationen aufzubauen und Themen im Markt zu etablieren IN NUR 2 MINUTEN ZU IHREM NEUEN JOB Nutzen Sie unser Online-Formular und laden Ihre vollständigen Bewerbungsunterlagen (inklusive aussagekräftigen Lebenslauf, Zeugnisse, Zertifikate, etc.) einfach hoch – ein Anschreiben ist nicht erforderlich.
In addition, our online learning platform gives you access to a wide range of training courses and seminars.Well taken care of: You benefit from comprehensive social benefits such as a company pension scheme, Christmas gifts for employees’ children, employee gifts, a company cafeteria offering healthy meal options, and various employee discounts.Stay fit: We offer a variety of programs to support your health and well-being, including Wellpass, our Vital Workshop, and company sports groups.Health services: For health-related matters, you can consult our on-site occupational physicians and medical staff, as well as use our Orthopaedics Express Service. In addition, we provide a free external counselling service for you and your family members – whether you need support with everyday concerns or more serious professional or personal challenges.Gerne beantworte ich deine Fragen.
Mein Arbeitgeber Our client is a globally recognized leader in the medical technology and diagnostics industry. The Rotkreuz site focuses on the development and testing of advanced laboratory instruments used worldwide in highly regulated environments.
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.
Mein Arbeitgeber Our client is a globally recognized leader in the medical technology and diagnostics industry. The Rotkreuz site focuses on the development and testing of advanced laboratory instruments used worldwide in highly regulated environments.
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.
Working in an interdisciplinary team of engineers to develop and improve designs and manufacturing processes for thick film sensors Improve and maintain the data infrastructure and pipeline for production and process control data from various sources and ensure timely data availability Act as a technical interface between R&D and Production and between various R&D departments to harmonize data handling and standards Improve and maintain data visualization tools (dashboards, interactive charts) and support in routine data analysis Support in defining and improving image analysis methods and tools to derive quantitative feature values from images Extend the data infrastructure with additional information, e.g. from sensor performance characterization Data driven improvements of manufacturing processes Completed technical training in process engineering, data science, bioinformatics, or similar professional education Professional experience in industrial R&D or manufacturing environment, ideally in the medical device industry or a comparable regulated environment Experience in building and maintaining data pipelines (ETL processes) from diverse sources such as SQL databases, CSV, and machine log files Ability to create interactive dashboards and visualization tools with a solid understanding of applied statistics (e.g. correlation analysis, cluster analysis) to support the development teams Skills in digital image processing, object-oriented programming (OOP) in Python, and knowledge of SQL are a strong advantage, adding significant value to this opportunity Good communication skills in a multicultural and multidisciplinary environment A thorough way of working and documentation Motivated team player with passion in promoting and driving fast-paced and ambitious projects Aptitude to understand and improve the underlying technical processes Proficiency in both English and German Unlimited project contract Fascinating, innovative environment in an international atmosphere Ihr Kontakt Ansprechpartner Jannik Fabio Eichin Referenznummer 865639/1 Kontakt aufnehmen E-Mail: jannik.eichin@hays.ch Anstellungsart Freiberuflich für ein Projekt
Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical softwareEnsure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomesCommunicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teamsEmpower your team members to take ownership of their work and leading by example to foster teamwork and mentorship Degree or equivalent practical experience in a specialized field related to software development or engineeringProven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx).Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis to resolve complex technical challengesExcellent communication skills with the ability to foster an inclusive and diverse environment as well as collaborate effectively within and across teamsEnglish fluency is a prerequisite, German is advantageous Internal career opportunitiesWorld-renowned medical devices company Ihr Kontakt Referenznummer 858105/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
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.
Working in an interdisciplinary team of engineers to develop and improve designs and manufacturing processes for thick film sensorsImprove and maintain the data infrastructure and pipeline for production and process control data from various sources and ensure timely data availabilityAct as a technical interface between R&D and Production and between various R&D departments to harmonize data handling and standardsImprove and maintain data visualization tools (dashboards, interactive charts) and support in routine data analysisSupport in defining and improving image analysis methods and tools to derive quantitative feature values from imagesExtend the data infrastructure with additional information, e.g. from sensor performance characterizationData driven improvements of manufacturing processes Completed technical training in process engineering, data science, bioinformatics, or similar professional educationProfessional experience in industrial R&D or manufacturing environment, ideally in the medical device industry or a comparable regulated environmentExperience in building and maintaining data pipelines (ETL processes) from diverse sources such as SQL databases, CSV, and machine log filesAbility to create interactive dashboards and visualization tools with a solid understanding of applied statistics (e.g. correlation analysis, cluster analysis) to support the development teamsSkills in digital image processing, object-oriented programming (OOP) in Python, and knowledge of SQL are a strong advantage, adding significant value to this opportunityGood communication skills in a multicultural and multidisciplinary environment A thorough way of working and documentationMotivated team player with passion in promoting and driving fast-paced and ambitious projectsAptitude to understand and improve the underlying technical processesProficiency in both English and German Unlimited project contractFascinating, innovative environment in an international atmosphere Ihr Kontakt Ansprechpartner Jannik Fabio Eichin Referenznummer 865639/1 Kontakt aufnehmen E-Mail: jannik.eichin@hays.ch Anstellungsart Freiberuflich für ein Projekt
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.
Multiple career opportunities; Free Parking; Further training and education; International assignments; Medical, Dental and Vision coverage; Talent development; Team Events Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
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.
Your Qualifications Bachelor in computer or electrical engineering with good mechanical skills or comparable education/training Extensive knowledge of machinery for the beverage / packaging industry and work experience of at least 2 years Analytical thinking for solving technical tasks Programmable Logic Controller’s (PLC) experience, electrical and/or mechanical Flexibility, assertiveness and organizational skills Self-confidence and friendly appearance Willingness to travel up to 90% of the time Passport or willingness to obtain a passport Benefits Innovative and international working environment Competitive wages Medical, Dental, Vision insurance offered at 30 days of employment Generous Educational Reimbursement program Company sponsored Life and Disability Insurance Paid Time Off Ten (10) Paid Holidays per year 401K with Company Match Location: Waukesha ǀ Wisconsin ǀ USA
Aktuelle Forschungsschwerpunkte sind: Robot- und KI-gestützte Diagnose- und Interventionssysteme Fortschrittliche und personalisierte Assistenztechnologien Intelligente mechatronische Systeme für die regenerative Medizin Diese Stelle richtet sich nicht an Profile aus der Medical Data Science oder Medical Image Analysis. Wir suchen ausdrücklich Forschende mit einem ingenieurwissenschaftlichen und systemorientierten Hintergrund.
Your Qualifications Bachelor in computer or electrical engineering with good mechanical skills or comparable education/training Extensive knowledge of machinery for the beverage / packaging industry and work experience of at least 2 years Analytical thinking for solving technical tasks Programmable Logic Controller’s (PLC) experience, electrical and/or mechanical Flexibility, assertiveness and organizational skills Self-confidence and friendly appearance Willingness to travel up to 90% of the time Passport or willingness to obtain a passport Benefits Innovative and international working environment Competitive wages Medical, Dental, Vision insurance offered at 30 days of employment Generous Educational Reimbursement program Company sponsored Life and Disability Insurance Paid Time Off Ten (10) Paid Holidays per year 401K with Company Match Location: Waukesha ǀ Wisconsin ǀ USA
International assignments; Exclusive employee benefits/discounts; Further training and education; Medical, Dental and Vision coverage; Multiple career opportunities; Talent development; Team Events; Trust-based working time; paid vacation days, holidays and sick time Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
We know: motivated and committed employees are the precondition for the success of our company. Medical, Dental and Vision coverage; Multiple career opportunities; Talent development; Team Events Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
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.
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.
API Services • Web Skills o Understanding of Internet standards including HTTP, DSP, FTP, SMTP/POP3, and TCP/IP o HTML, JavaScript, WML, XML, JQuery, AJAX, JSON Databases o Oracle11g/10g, MS SQL Server2005/2000 and MYSQL o Skilled in the use of SQL, stored procedures, connection pooling, and transaction processing Operating Systems o UNIX (GNU/Linux), Windows Server/XP, 2003, 2008 and DOS File Transfer Tools & Protocols o MFT, FTP, FTPS and SFTP, Cyclone, AS2, IBM MQ, VAN, VPN, RNIF, XML PI Version Controls o PVCS, CVS and VSS Knowledge on cloud-Based B2B IntegrationSound knowledge of international EDI industries standard specification – EDIFACT, ANSI X12, XML, Rosettanet, SAP IDOC, CSV, XSLT, JSON Knowledge on Supply Chain business industry B2B EDI integration development tools, B2B communications protocol and standards WHAT YOU WILL GET FROM US Great team of IT professionals with global working exposure On-going professional and technical training and certifications Global internal job opportunities available within DPDHL A multicultural environment in modern offices Meal Card and Flexible Benefits – customized according to individual needs Choose any day for your vacation from earned public holiday (Saturday and ad hoc) Smart casual dress code everyday Unlimited Outpatient Medical Home office possibilities Sounds good? Start your application now! DHL IT Services IT Services is the internal provider of specialized IT Build services and industrialized IT Run services to Deutsche Post DHL (DPDHL) Group: Supports over 260,000 DPDHL e-mail users; Runs more than 7700 servers; Supports more than 2000 global services and applications; Processes 9 million shipment information messages per day; 200000 man days per year of development application.