Monitoring aktueller wissenschaftlicher Literatur, Publikationen und Kongressbeiträge im Bereich respiratorischer Infektionen (Schwerpunkt RSV). Cross‑funktionale Zusammenarbeit, Enge Kooperation mit Medical Affairs, Commercial Teams, globalen und regionalen Medical‑Teams. Unterstützung bei der Erstellung und Aktualisierung wissenschaftlicher Materialien und Trainingsinhalte.
Unsere Klinik ist in allen Fachbereichen renommiert und folgt mit dem Medical-Wellness-Angebot konsequent dem Präventionsgedanken. Unser Hauptaugenmerk ist es, ein zuverlässiger und fairer Arbeitgeber zu sein.
Löwenstein Medical Technology GmbH + Co. KG sucht in eine/n IT Operations Manager (m/w/d) (ID-Nummer: 13723269)
About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care.
Unsere Klinik ist in allen Fachbereichen renommiert und folgt mit dem Medical-Wellness-Angebot konsequent dem Präventionsgedanken. Unser Hauptaugenmerk ist es, ein zuverlässiger und fairer Arbeitgeber zu sein.
A Bachelor's programme in Computer Science in Culture and Health and a Master's programme in Applied Computer Science are offered.The teaching assignment is in Bachelor's and Master's degree programmes of the department at the University in Berlin. Focal points of the Department of Health Informatics are: Medical information systems and image data processing Mobile applications in health care Analysis of high-throughput data and machine learning Legal aspects of digitalisation in the health sectorHiring requirements for professors (Berlin Higher Education Act): 5 years of relevant professional experience, including 3 years outside of university.
Für die Professur für Clinical Medical Imaging Research an der Klinik für diagnostische und interventionelle Radiologie und Neuroradiologie suchen wir zum nächstmöglichen Zeitpunkt in Vollzeit, für zwei Jahre befristet, einen wissenschaftlichen Mitarbeiter (m/w/d).
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.
Prüfung von Sponsoring-Anfragen auf FSA-Konformität, Transparenzvorgaben und interne Standards Herstellung vollständiger Dokumentation gemäß Lilly-ProzessenAbgleich der Anfragen mit strategischen Prioritäten der BrandsBudgetmonitoring sowie Erstellung monatlicher Reports für Business, Finance und Compliance.Enge Abstimmung mit Brand Teams, Medical, Legal und ComplianceAnsprechpartner für interne Stakeholder und externe Dienstleister (inkl. Vertragsrückfragen)Unterstützung bei System- und ProzessverbesserungenMitarbeit bei der Weiterentwicklung digitaler Tools, Templates und Dashboards Abgeschlossene kaufmännische Ausbildung oder vergleichbarer AbschlussBerufserfahrung in der Pharmaindustrie oder einem anderen regulierten UmfeldSehr gute Deutsch- und EnglischkenntnisseHohe Genauigkeit, Verlässlichkeit und OrganisationsfähigkeitSicherer Umgang mit Office-Tools (v.a.
ARNOWA GmbH sucht in Salzkotten eine/n Account Manager Sales (m/w/d) - Medical & Care (ID-Nummer: 13315587)
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.
What makes you stand out Proven experience in RPA development (minimum 3 years) using tools like UiPath, Automation Anywhere, or Blue Prism.Strong programming skills in languages such as C#, .NET, Java, or Python.Knowledge of software development methodologies, Agile frameworks, and version control.Experience with process mapping and business process analysis.Strong problem-solving and debugging skills.Excellent communication skills, with the ability to collaborate effectively with cross-functional teams.Bachelor’s degree in Computer Science, Information Technology, or a related field. What we offer: Attractive benefits packageRegina Maria medical subscription for you and your family according with internal policeMeal vouchersSpecial discounts for gymsAdditional days offDKV card with discount for fuel valid in 25 countriesWhen you are in the office can have free facilities like massage, fruits, coffeeFlexible working hours with home office and flextimeContinuous training and much more...
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.
regenold GmbH sucht in eine/n Regulatory Affairs Manager (m/f/d) in-vitro diagnostic medical devices / CDx I 80-100% (ID-Nummer: 13764773)
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.
Ärztliche Gesellschafterversammlung und Geschäftsführung sowie unser Medical Board sichern den Fokus auf eine medizinische Ausrichtung und Entwicklung für unsere Patient:innen und Mitarbeitenden. Die Radiologische Allianz ist Gründungspartnerin der Starvision Service GmbH und steht für eine nachhaltige Digitalisierung.
Ärztliche Gesellschafterversammlung und Geschäftsführung sowie unser Medical Board sichern den Fokus auf eine medizinische Ausrichtung und Entwicklung für unsere Patient:innen und Mitarbeitenden. Die Radiologische Allianz ist Gründungspartnerin der Starvision Service GmbH und steht für eine nachhaltige Digitalisierung.
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
About us Your Contribution Develop and progress into a technical expert for specialty vials and ready-to-use [RTU] vials, supporting growth with our innovative productsCollaborate within a global, cross-functional team (sales, product management, quality, pharma services)Design and execute targeted roadshows with market intelligence, sales, and marketing in biotech hubs across the United States Act as a technical expert to introduce high-value products to the biotech sectorIdentify and acquire new customers; support cross-selling of high-value products to established accountsUnderstand the drug formulation for clients, along with their challenges, while providing technical solutionsFollowing all Company policies, procedures, along with Code of Conduct and safety guidelines Your Profile Bachelor’s Degree in natural science (Chemistry, Physics, Biology, Pharmacy, Biotechnology) or EngineeringAt least 3 years of experience in business development or related roles in a B2B environment within an international organizationExperience in pharmaceutical packaging, medical devices, or biotechnology, strongly preferredProven project management, analytical, and conceptual skillsFluent in English (additional languages are a plus)Willingness to travel up to 60%Strong analytical skillsDemonstrated project management skill, along with conceptual skillsWell-organized and highly motivated Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election 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.
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.
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.
Erreichung vertrieblicher Zielvorgaben wie Marktanteil, Umsatz, Kontaktvorgaben, -frequenz und Gebietsabdeckung, sowie qualitativer Ziele mit regelmäßigem Monitoring und Reporting der verantworteten Ergebnisse an den bzw. die Vorgesetzten Besuche/Kontakte der im Zuge des Targetings ausgewählten und/oder zugewiesenen Zielkunden im niedergelassen, ambulanten und/oder stationären Bereich mit effizienter Frequenz, sowie selbständiger, zahlenorientierter Erfolgsmessung- und Steuerung Erreichung einer optimalen Vertriebsbreite durch Nutzung von Omnichannel Aufbau und Ausbau von Netzwerk/Beziehungen zu Schlüsselkunden und Meinungsbildnern Enge Zusammenarbeit und Abstimmung mit anderen Vertriebslinien (z.B. Medical Liaison Manager, Klinik) Wir suchen im Gebiet Bayreuth/Dresden/Chemnitz/Frankfurt a.d. Oder/Greifswald
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.
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.
IQVIA CSMS GmbH sucht in Mannheim eine/n Medical Scientific Liaison Manager (m/w/d) bundesweit - verschiedene Indikationen (ID-Nummer: 10574436)
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.
BEC Medical GmbH sucht in eine/n Innovativer Qualitätsmanager / Regulatory Affairs Manager Medizinprodukte (Mensch) (ID-Nummer: 13669004)
About us Our Business Unit Lighting and Imaging offers smart solutions for light delivery and image transmission in demanding environments — from medical devices, industrial, and safety applications to aviation and automotive. With manufacturing sites in Europe and North America, and supported by SCHOTT’s global sales network, we are a leading supplier of high-quality fiber optic and LED components.
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
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.
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectivesDesign and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regionsBuild and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutionsConduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiativesContribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical dataOversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL DirectorAct as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentationPlan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical OfficerRepresent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencersServe as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic communityCollaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groupsFull professional proficiency in English, both spoken and writtenStrong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflowsExperience with product launches, advisory boards, and post-approval studies is highly advantageousRelevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned companyOther Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
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.
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectives Design and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regions Build and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutions Conduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiatives Contribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical data Oversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL Director Act as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentation Plan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical Officer Represent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencers Serve as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic community Collaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groups Full professional proficiency in English, both spoken and written Strong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflows Experience with product launches, advisory boards, and post-approval studies is highly advantageous Relevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned company Other Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
About us Our Business Unit Lighting and Imaging offers smart solutions for light delivery and image transmission in demanding environments — from medical devices, industrial, and safety applications to aviation and automotive. With manufacturing sites in Europe and North America, and supported by SCHOTT’s global sales network, we are a leading supplier of high-quality fiber optic and LED components.
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.
Tasks Assisting with surgical procedures, including instrument preparation and intraoperative support Confident handling of medical and technical equipment Patient related administration and accurate documentation Preparation and post-processing of materials and instruments for surgical procedures Supporting the positioning of patients Profile Completed education as a Surgery Technology Assistant (OTA) obtained abroad Recognition notice (Anerkennungsbescheid) issued by the Bavarian State Office for Nursing (Bayerisches Landesamt für Pflege) German language skills at a minimum level of B2, with a willingness to continuously improve your language proficiency Motivation and enthusiasm to work as part of our team and provide support to our patients Friendliness, a strong sense of responsibility, and professionalism Good interpersonal skills in dealing with patients High willingness to learn Motivation and discipline to complete your recognition process in a timely manner Our Offer Support from the Office for International Professionals, assisting you with organizational and administrative matters, as well as preparing for the knowledge examination (Kenntnisprüfung) Accompanied German language course offered during the recognition process Practical trainers specifically assigned to staff undergoing the recognition procedure, ensuring structured onboarding and knowledge development to prepare you for your professional responsibilities Additional qualified and personalized training by your team of experienced colleagues Long-term career perspective at Augsburg’s largest employer, including a permanent employment contract upon recognition Remuneration according to the collective agreement for public service (TV-L), including bonuses for work on Sundays, public holidays, and night shifts Company pension scheme and annual special payment 30 vacation days per year, plus up to 6 additional days for shift work Regulated working hours (38.5 hours/week) with working time account and collectively agreed salary increases Contact Frau Ulrike Kurz, Center Manager, 0821/400-168713 Herr Alexander Wagner, Nursing Educator - Recognition of OTA, 0821/400-168665 Frau Marina Klisanin, Head of Field Office - International Qualified Employees (IFAP), 0821/400-3401 Application Deadline Please upload your documents and submit your application.
Associate Director, Biostatistics - Permanent - w /m / d Global Biostatistics Home-Based/Hybrid: Germany Join us on our exciting journey! The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.
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.
About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care.
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.
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.