Medical Director \- Diabetes/AID Systems (m/f/d) Medical Director – A Unique Leadership Role for Physicians in MedTech Introduction Our client, headquartered in central Switzerland is a global MedTech company focused on integrated solutions for people with diabetes. The growing organization offers a challenging and dynamic environment characterized by a clear strategic direction, ambitious growth objectives, and a high degree of personal accountability. These factors create exciting opportunities for the successful candidate in the newly created position Medical Director – Diabetes/AID Systems (m/f/d) Your responsibilities The Medical Affairs department connects clinical science, medical expertise, and real\-world application to support the successful development, differentiation, and adoption of innovative diabetes technologies. Through clinical evidence, scientific engagement, medical strategy, training and education, as well as collaboration with internal and external stakeholders, the department enables safe, effective, and patient\-centric solutions worldwide. At the core of your role is ensuring the safe, effective, and consistent clinical application of our client’s innovative AID system across global markets. You will own the development and continuous evolution of the global Training \& Education strategy, ensuring that healthcare professionals, affiliates, and internal stakeholders are equipped to support the optimal use of the company’s technologies. Through close collaboration with the key departments, including Product Management, Research \& Development, Regulatory Affairs, Commercial, and external experts, you will translate clinical expertise into best practise, support product differentiation, and contribute to the successful adoption of our client’s solutions globally. Beyond educational leadership, you will also serve as a trusted medical authority and sparring partner to key departments. Your medical insights will help shape product innovation and development, clinical differentiation, and long\-term medical strategy. As an ambassador for the organization, you will represent the company at national and international congresses, scientific meetings, advisory boards, and further professional forums. In your role as a medical/scientific spokesperson you will build and maintain strong relationships with healthcare professionals, KOLs, scientific societies, and other external stakeholders, further strengthening the company’s scientific reputation and market position. As the leader of the Global Training \& Education and Clinical Application team, you will play a pivotal role at the intersection of clinical science, product development, and commercial execution. Reporting directly to the Head of Global Medical Affairs, you will be based at the company's Swiss headquarters, with a flexible hybrid working model. The role requires approximately 20% international travel. Your identity We are seeking a dynamic and entrepreneurial physician with substantial experience in diabetes technology, including AID systems, CGM, and digital diabetes solutions. You hold a medical degree and a certification in Endocrinology/Diabetology and have developed a strong track record either in clinical settings or within the MedTech industry. Your strategic mindset, analytical approach, and ability to communicate complex medical concepts make you an effective partner for both, internal and external stakeholders. You are confident in working across functions, creating alignment between stakeholders, and influencing decisions in collaboration with the key departments, and senior leadership. Your prospects The fascinating environment of a globally expanding industry leader offering challenging opportunities and a high degree of self\-responsibility in an environment of highly motivated top\-class professionals awaits you, allowing you to significantly contribute to the company’s further growth and success as a global player. In addition to a highly visible international leadership role, there may be flexibility to maintain selected clinical responsibilities on a part\-time basis. If you can identify yourself with the requirements of this challenging position, we kindly ask you to send us your application and CV indicating the reference 3120618\. For further information please contact Dr. . Contact oprandi \& partner ag, personnel recruitment, KONNEX Building Brown Boveri Strasse 7, CH\-5400 Baden Phone \+41 79 408 68 64, [Write an email](<>), oprandi \& partner is an international group with numerous branches in Europe and the UAE / Dubai Apply jpidb681712jm jit0728jm jiy26jm

Director, Integrated Product Medical Lead (m/f/d) At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Director, Integrated Product Medical Lead (m/f/d) YOUR TASKS AND RESPONSIBILITIES The Integrated Product Medical Lead (IPML) is crucial for advancing the Oncology early development portfolio. As an IPML, you create a significant impact through the successful progression of global development programs and the expansion of our pipeline. You set the vision and strategic direction for assigned programs, ensuring a medically and clinically sound end\-to\-end development strategy for our products across various modalities, biologies, and indications, representing the full value chain from pre\-D1 up to hand\-over to late\-stage drug development. You build an end\-to\-end clinical strategy and are responsible for executing development programs on behalf of Early Clinical Development Oncology (ECDO), providing clinical\-scientific leadership for one or more global development programs with full decision\-making authority. Collaborating with cross\-functional IPT members, you drive the creation and maintenance of a target product and target value profile to maximize the clinical success of development programs, significantly shaping the value of the product. You co\-lead the incorporation of novel assets into the pipeline through supporting internal and external innovation efforts. Additionally, you play a vital role in shaping functional excellence within ECDO by driving core project, people, and innovative clinical development topics under a peer\-reviewed setting, pushing the boundaries of drug development in collaboration with internal and external researchers. Key tasks: Act as the clinical leader and primary clinical representative for global programs, ensuring high quality and speed of functional deliverables. Develop a clinical vision for addressing unmet medical needs, considering the molecule's scientific hypothesis. Accountable for timely delivery of milestones, mitigating roadblocks, and empowered to take decisions to effectively execute the clinical strategy. Support preclinical evaluation and validation of new oncology assets in line with the Research and Early Development Oncology (RED ONC) strategy. Guide preclinical asset development to enable informed clinical development, facilitating go/no\-go decision making. Review key study documents, ensuring alignment with clinical development plans and target product profiles. Provide comprehensive knowledge of the scientific, development, and regulatory landscape to enable state\-of\-the\-art early precision drug development. Proactively interact with academic and industry partners, health authorities, key opinion leaders, and patient advocacy groups. Lead and drive ECDO\-initiated strategic initiatives in support of overall ECDO, RED\-ONC, Oncology, and Bayer strategy. Independently lead self\-empowered matrix teams, promoting a creative and innovation\-friendly collaboration between clinicians and scientists. Foster a culture of ownership and empower others, driving peer accountability across portfolio deliverables. WHO YOU ARE Medical excellence: M.D. with 5\+ years in direct patient care and board certification within oncology/hematology or associated subspecialties. Scientific excellence demonstrated by a track record of relevant research documented in peer\-reviewed publications. Outstanding drug development expertise with 3\-5 years of experience, including 2\+ years in early drug development. Expertise across different biologies and modalities, including small and large molecules. Relevant global health authority interactions and current knowledge of regulatory review and responses. Ability to independently develop a sound medical strategy and teach others to do so. Strong communication and leadership skills, strategic thinking, and good business and external trends insights. High energy with focus and vision; self\-motivated with a high sense of ownership and proactive, solution\-oriented approach. Fluency in English is mandatory; command of a second major European language, especially German, would be an asset. jpid94d3b8fjm jit0728jm jiy26jm

RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. Are you a driven regulatory professional who enjoys ownership, collaboration and working close to product development? This could be the role for you. Apply and help shape the future of medical device software at RaySearch. About the role We are looking for an experienced and driven Regulatory Lead to own the regulatory strategy and lifecycle oversight for one of RaySearch's products. In this role, you will be the regulatory point of contact for the product, working closely with key stakeholders in the Development, Corporate Strategy and Sales teams. You will help shape product strategy, guide development activities, drive market access, and ensure compliance throughout the product lifecycle. This is a highly visible role for someone who enjoys combining deep regulatory expertise with strategic thinking, project coordination, and collaboration across the organization. What you'll do Own and drive the global regulatory strategy for your product throughout its lifecycle. Lead the preparation, review, and maintenance of Technical Documentation and regulatory submissions, including EU MDR. Act as the regulatory expert within development projects and ensure regulatory requirements are integrated throughout the design and development process. Coordinate and oversee multiple projects, priorities, and submission timelines while maintaining a long-term view of the product roadmap. Partner closely with Development, Corporate Strategy, Sales and other key stakeholders to support product development and market access. Support inspections, audits, post-market activities, and continuous improvements. Your profile You are a proactive and pragmatic regulatory professional who enjoys taking ownership and driving things forward. You are technically strong, comfortable working with development teams, and able to translate complex regulatory requirements into practical solutions. You like having oversight of the full product picture—from early development and regulatory strategy to submission and post-market activities—and you thrive in a collaborative, fast-paced environment where you can make a real impact. Requirements Bachelor's or Master's degree in Engineering, Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field. Several years of Regulatory Affairs experience within the medical device industry. Strong experience preparing and reviewing Technical Documentation under EU MDR. Experience working with medical device product development and design control processes. Experience with medical device software Strong knowledge of IEC 62304, IEC 60601 and ISO 14971 Strong project management and stakeholder management skills. Ability to manage multiple activities and timelines while maintaining the bigger picture. Proficiency in English. Meriting experience US regulatory experience, Experience with FDA submissions, including eSTAR/510(k). Experience with IEC 62366 and ISO 14155 Experience with Cybersecurity requirements for medical devices. Experience with AI/ML-enabled medical devices. Our Culture Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care. Our Offer At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package. Application Please apply to the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.

Are you interested in medical images, image analysis and leading projects? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI), Positron Emission Tomography (PET), and Dual-energy X-ray (DXA) to design and deliver clinical studies for decision making and differentiation in drug development. We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 140 employees working at our offices in Mölndal, Uppsala, and Lund, and we are continuously growing and developing. As a part of our growth journey, we are looking for a quality-focused and communicative Project Lead Corelab with good organisational skills to join our Corelab Team in Mölndal. As a Project Lead Corelab, you will be part of a project team where you are responsible for the analysis and delivery of data according to the project’s timeline, as well as to our quality requirements and ICH-GCP. You will also to some extent work with quality control and analysis of images from MR, PET and DXA investigations and communicate with national and international imaging centres. As part of your on-boarding you will receive a mentor and undergo an extensive training programme. Your main responsibilities will be: Ensure that systems for data handling in the project are set up and configured Development and maintenance of documentation for data handling in project Planning and follow-up of analysis and delivery of data to customer according to the project’s timeline Delivery of data and reports to customer Quality control of the images and documentation from the MR, PET and DXA investigations in the clinical trials Segmentation and analysis of images from the MR, PET and DXA investigations including documentation of this Communication with national and international imaging centres on image quality Who are we looking for? We emphasize personal suitability and believe that you are a structured and thorough person with attention to quality. We further believe that you are a positive and service-oriented person with good communication skills who enjoys collaborating with others. We are happy to see that you have an interest in images, technology, and medicine. You also enjoy working on multiple tasks simultaneously and to plan, coordinate, and follow-up on work in projects. We are also happy to see that you like to work with systems. Desired qualifications and skills: University degree or relevant higher education, such as in engineering, biomedicine, pharmacy, biomedical laboratory science or similar Good computer proficiency Good knowledge of spoken and written English Experience from project management and programming are an advantage, however not a requirement. Are you interested? Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than July 31st 2026. Interviews can take place during the advertisement period. For more information about the position, please contact Anna Ringheim Cadete, Head of Corelab, at anna.ringheim@antarosmedical.com The recruitment refers to permanent full-time employment. We only handle applications via our recruitment system Teamtailor. The recruitment if managed by Antaros Medical. We kindly decline any contact from recruitment- or staffing firms. About Antaros Medical At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicine Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com. Our culture is our people, and our values makes us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even more: Our culture - Antaros Medical.

Rejoignez notre Centre de Santé Dentaire à Millau ! Le Centre de Santé Dentaire fait partie d'Altriane, le réseau de services et de soins de la Mutualité Française Aveyron. Altriane c'est : 800 collaborateurs, 19 activités réparties au sein de 60 structures dans le département. Nous proposons une offre de santé globale (soins, accompagnement, hébergement, formation, produits et services, etc.) au service du parcours de vie des Aveyronnais. A ce jour, Altriane compte 4 centres de santé dentaire répartis sur le département de l'Aveyron, assurant des soins accessibles, modernes et coordonnés, au service de la santé bucco-dentaire de tous. Pourquoi nous rejoindre ? - Vous bénéficierez des moyens du réseau Altriane, reconnu et localement implanté depuis des années. - Vous travaillerez dans un environnement bienveillant et stimulant, basé sur la solidarité et l'entraide, avec des missions utiles, au service de la santé et du bien-être de tous - Nous vous accompagnerons tout au long de votre parcours professionnel : vous pourrez bénéficier d'actions de formations régulières et acquérir de nouvelles compétences voire de nouvelles qualifications. - Vous bénéficierez d'un accompagnement systématique, dès votre arrivée, grâce à un système de tutorat - Notre CSE propose des avantages intéressants pour améliorer votre quotidien Vous avez le sens du service et l'esprit d'équipe ? Nos valeurs sont aussi les vôtres : rejoignez-nous ! ****DIPLOME SECRETAIRE MEDICO-SOCIAL OBLIGATOIRE***** ou *****EXPERIENCE EN SECRETARIAT MEDICAL EXIGÉ**** Missions : Rattaché.e à la responsable d'activités des centres de santé dentaire, vous exercez les fonctions suivantes : : - Assurer l'accueil téléphonique et physique de la patientèle : tenue des agendas des chirurgiens-dentistes, prise de rendez-vous, identification des urgences - Assurer la gestion administrative du centre de santé dentaire : dossier administrations et médical des patients, prise en charge mutuelle, factures et encaissements des honoraires. Profil : - Formation : Diplôme de niveau 4 : secrétaire médico-sociale - maîtrise des outils informatiques - Qualités : excellent relationnel, goût du travail en équipe, organisé(e) et réactif(ve), capacité d'adaptation - La connaissance de l'activité dentaire serait un plus. Statut : Employé(e) E4 - convention collective de la mutualité Contrat : CDI à temps plein - poste à pourvoir au 1er septembre. Salaire : salaire mensuel brut à partir de 1867.02 € (rémunération conventionnelle variable selon profil et expérience) Avantages : prise en charge de la mutuelle à 93% (soit minimum 4,40 €/mois à votre charge); CSE (chèques vacances, chèques Cadhoc, tarifs préférentiels cinéma, achats groupés ou remise dans certaines enseignes, etc.) ; carte « avantages » pour les salariés en CDI (réduction dans les magasins du réseau) ; Compte Epargne Temps ; accords d'entreprise : PEE et PERECO en vigueur (accessible à partir de 3 mois d'ancienneté) Convaincus que la diversité est une source de richesse pour nos collaborateurs et notre entreprise, nos offres s'adressent à toutes et tous !

Gi Group, prima agenzia per il lavoro italiana con oltre 200 filiali sul territorio nazionale e più di 1800 professionisti impegnati ogni giorno ad orientare, formare e accompagnare le persone verso nuove (le migliori) opportunità lavorative RICERCA per Azienda Ospedaliera del settore Sanità Pubblica: TECNICO SANITARIO DI LABORATORIO BIOMEDICO (TSLB) La risorsa selezionata sarà inserita all'interno di un team strutturato e sarà chiamata ad occuparsi di tutte le attività legate alle analisi, assicurando i turni previsti dalle modalità organizzative già in atto presso l'azienda. Mansioni e responsabilità - Analizzare le richieste del medico inviante - Valutare metodi e strumenti a disposizione - Eseguire test, raccogliere i dati emersi ed elabora il referto Requisiti richiesti - Laurea in Tecnico di Laboratorio Biomedico - Iscrizione all'ordine professionale - Disponibilità immediata Si offre: contratto a tempo determinato con possibilità di proroghe, CCNL COMPARTO SANITARIO. Retribuzione lorda mensile 2172. Sede di lavoro: Muravera Facciamo parte di Gi Group Holding (www.gigroupholding.it ) la prima multinazionale italiana del lavoro, nonché una delle principali realtà a livello mondiale nei servizi dedicati allo sviluppo del mercato del lavoro. Il nostro Gruppo è attivo nei seguenti campi: lavoro temporaneo, Permanent e Professional Staffing, Ricerca e Selezione, Consulenza HR, Formazione, Outsourcing, supporto alla ricollocazione e attività complementari. Siamo presenti in più di 30 Paesi in Europa, Asia e America con un team di oltre 6000 persone. I valori che ci contraddistinguono: attenzione, passione, apprendimento continuo e innovazione, collaborazione, sostenibilità, responsabilità. Consulta tutti i nostri annunci su www.gigroup.it Gi Group S.p.A. è autorizzata ad operare dal Ministero del Lavoro (Aut. Min. 26/11/2004 PROT. 1101 - SG). L'offerta si intende rivolta a candidati ambosessi, nel rispetto del D.Lgs. n. 198/2006 e ss.mm.ii. e dei Decreti Legislativi n. 215 e n. 216 del 2003 sulle parità di trattamento. I candidati sono invitati a leggere l'informativa privacy ai sensi degli artt. 13 e 14 del Reg. EU 679/2016 al seguente indirizzo www.gigroup.it/privacy-candidati

Ihre zukünftige Arbeitsstelle: Unsere Kundenfirma ist ein innovatives globales Gesundheitsunternehmen, das zur nachhaltigen Entwicklung der Gesellschaft beiträgt. Das Unternehmen erforscht, entwickelt und liefert neue Standards in der Gesundheitsversorgung, um die Lebensqualität der Menschen weltweit zu verbessern. Mit mehr als 120 Jahren Erfahrung nutzt unsere Kundenfirma seine erstklassige Forschung und Technologie, um neue Behandlungsmethoden und innovative Medikamente für Menschen mit Krebs, Herz-Kreislauf- und anderen Erkrankungen zu entwickeln, für die es bisher nur unzureichende oder keine Behandlungsmöglichkeiten gibt. Ihre Aufgaben: Angaben zur Tätigkeit: In dieser Funktion arbeiten Sie mit einem Team aus Medical Scientific Liaison (MSL) Managern in projektbasierten Prozessen zusammen. Sie unterstützen die Planung, Organisation, Durchführung und Nachbereitung verschiedenster regionaler medizinisch-wissenschaftlicher Projekte und Prozesse. Ihr Aufgabenbereich: - ProjektmanagementProjektbasierte Zusammenarbeit mit dem MSL-TeamPlanung, Überwachung und Organisation verschiedener Projekte bis zur FertigstellungKoordination des Onboardings neuer MitarbeiterOrganisationVertragsmanagementRechnungsmanagement inkl. sachlicher Prüfung/Freigabe elektronischer Rechnungen Bestellanforderung sowie Bearbeitung in SAP, Lieferantenanlagen und FreigabenUnterstützung der Dokumentation und Abrechnung von regionalen Veranstaltungen Planung, Organisation und Unterstützung von Meetings, Tagungen und Kongressen – sowohl regional, national als auch international – einschließlich Eventmanagement, Kommunikation, Angebotseinholung sowie Koordination mit internen Teams und externen Partnern.Unterstützung der Dokumentation und Abrechnung von regionalen Veranstaltungen Dokumentation aller Aktivitäten unter Beachtung des Pharmacodex und rechtlicher Anforderungen Ihr Profil: Medical Liaison Project Coordinator (m/w/d) Angaben zur Tätigkeit: In dieser Funktion arbeiten Sie mit einem Team aus Medical Scientific Liaison (MSL) Managern in projektbasierten Prozessen zusammen. Sie unterstützen die Planung, Organisation, Durchführung und Nachbereitung verschiedenster regionaler medizinisch-wissenschaftlicher Projekte und Prozesse. Ihr Aufgabenbereich: - ProjektmanagementProjektbasierte Zusammenarbeit mit dem MSL-TeamPlanung, Überwachung und Organisation verschiedener Projekte bis zur FertigstellungKoordination des Onboardings neuer Mitarbeiter - OrganisationVertragsmanagementRechnungsmanagement inkl. sachlicher Prüfung/Freigabe elektronischer Rechnungen Bestellanforderung sowie Bearbeitung in SAP, Lieferantenanlagen und FreigabenUnterstützung der Dokumentation und Abrechnung von regionalen Veranstaltungen Planung, Organisation und Unterstützung von Meetings, Tagungen und Kongressen – sowohl regional, national als auch international – einschließlich Eventmanagement, Kommunikation, Angebotseinholung sowie Koordination mit internen Teams und externen Partnern.Unterstützung der Dokumentation und Abrechnung von regionalen Veranstaltungen Dokumentation aller Aktivitäten unter Beachtung des Pharmacodex und rechtlicher Anforderungen Fachliche Anforderungen: - Kaufmännischer Abschluss oder abgeschlossene medizinische Berufsausbildung (z.B. MTA) - erste Vertriebs- oder Projekterfahrung in der pharmazeutischen Industrie von Vorteil - Sehr gute Kenntnisse in SAP im Zusammenhang mit der Erstellung von Verträgen und Bestellungen (POs) - umfangreiche Vorkenntnisse mit Budgetabrechnungsprogrammen - Gute Kenntnisse in MS Office - Hohes Interesse an medizinischen Themen - Erfahrung im Organisieren von Veranstaltungen und Events erwünscht - Sehr gute Deutschkenntnisse, gute Englischkenntnisse in Wort und Schrift Persönliche Anforderungen: - Freude am Organisieren und Kommunizieren - Selbstständige Arbeitsweise - Hohe Eigenmotivation & Zielorientierung - Ausgeprägte Fähigkeit in einem Team zu arbeiten - „Hands on“ Mentalität Bewerbung und Rückfragen: Wir freuen uns auf Bewerbungen (unter Angabe von Verfügbarkeit und Gehaltsvorstellung) gerne per E-Mail an bewerbung.donau-isar@orizon.de oder über unser Bewerbungsmodul auf dieser Seite.Für Fragen steht Frau Kamp gerne unter der Telefonnummer +49 841 9534712 zur Verfügung. Beim hier angegebenen Gehalt sind unter Umständen nicht alle Bestandteile (bspw. Branchenzuschläge, Weihnachtsgeld, Schicht-Boni o.ä.) berücksichtigt. Das verbindliche Gehalt ist im persönlichen Gespräch zu klären. Weitere Informationen finden Sie unter orizon.de Wir nehmen den Schutz Ihrer personenbezogenen Daten ernst: www.orizon.de/de/datenschutzvereinbarungen

Die Medical Park-Gruppe ist bundesweit Qualitätsführer im Bereich Rehabilitation und Arbeitgeber für mehr als 3.650 Mitarbeiterinnen und Mitarbeiter. Zu unserer Gruppe gehören 13 Fachkliniken und zwei ambulante Therapie- und Rehazentren. Unsere Fachklinik Medical Park Bad Camberg liegt am Rande des Rhein-Main-Gebiets zwischen Wiesbaden, Limburg und Frankfurt. Wir sind seit 20 Jahren auf das gesamte Spektrum neurologischer Erkrankungen spezialisiert und gewährleisten 200 Patienten der Phasen B, C und D eine optimale Betreuung. 400 Mitarbeiterinnen und Mitarbeiter setzen sich Tag für Tag dafür ein, unsere Patienten bei der Wiedererlangung ihrer verlorenen Fertigkeiten zu unterstützen und sie nach Möglichkeit in ein selbstständiges Leben zurückzuführen. Wirksam zu helfen ist unser gemeinsamer Anspruch!   Ihre Aufgaben   Betreuung unserer Patienten im Akutbereich mit Monitorüberwachung einschließlich tracheotomierter Patienten Anwendung intensivmedizinischer Methoden und Fertigkeiten Untersuchung und Behandlung neurologischer Patienten der Rehabilitationsphasen B, C und D Durchführung der Funktionsdiagnostik und Elektrophysiologie Teilnahme am Bereitschaftsdienst    Ihre Qualifikation   Approbation Berufsanfänger und Ärzte (m/w/d) mit Berufserfahrung sind gleichermaßen willkommen Ausgeprägter Teamgeist mit hoher sozialer Kompetenz Freunde an der Arbeit in einem motivierten, interdisziplinären Behandlungsteam Zuverlässigkeit, Engagement und Eigeninitiative   Unser Angebot   Eine verantwortungsvolle und abwechslungsreiche Aufgabe in einem gesunden und renommierten Unternehmen Selbstständige Arbeitsweise und Eigenverantwortlichkeit Ein hoch motiviertes und engagiertes Umfeld geregelte Arbeitszeiten, z.B. durch Teilzeitarbeit 5 Fortbildungstage pro Jahr Regelmäßige interne Fortbildungen Förderung passgenauer Fort- und Weiterbildungsmöglichkeiten, inklusive Kostenübernahme und Freistellung Zuzahlung zur betrieblichen Altersversorgung in Höhe von 15 % der Gehaltsumwandlung (Ausnahme: Arbeitnehmer über der Beitragsbemessungsgrenze) Zuschuss zum VWL-Vertrag Kinderbetreuungszuschuss und Kooperation mit einer ortsansässigen Kindertagesstätte Hilfe bei der Wohnungssuche Vergünstigtes Mittagsessen   Haben wir Ihr Interesse geweckt?   Nehmen Sie Kontakt zu uns auf. Ihre Ansprechpartner Panagiotis Kostopoulos (Chefarzt), Tel. +49 6434 919 504 und Dr. med. Julia Hemberger (Lt. Oberärztin) stehen Ihnen gerne zur Verfügung. Wir freuen uns auf Sie!  

Medical Concierge & Health Guide (m/w/d) – Schnittstelle Gästebetreuung & Medical Spa Anstellungsart: Vollzeit / Teilzeit • Region: Überregional / Deutschlandweit • Ab sofort • Haus: Neuausrichtung 4* Superior Einzigartiges Konzept – Einzigartige Aufgabe: Das Allgäu Resort verbindet High-End-Hotellerie mit modernster Regeneration, apparativer Kosmetik, Biohacking und interdisziplinärer Medizin. Unsere anspruchsvollen, oft internationalen Gäste erwarten eine hochkompetente, diskrete und individuelle Begleitung ihrer Health- und Wellness-Programme. Als Medical Concierge sind Sie der exklusive Ansprechpartner für die gesamte „Health-Journey" des Gastes im Haus. Das ist Ihre Aufgabe – Kompetenz & Premium-Service - Individuelle Begleitung: Sie koordinieren die Behandlungs-, Biohacking- und Regenerationspläne unserer Gäste in enger Abstimmung mit unseren Ärzten und Therapeuten vor Ort. - Internationale Schnittstelle: Kompetente Beratung und Betreuung unserer ausländischen Gäste bei allen Fragen rund um ihre Health- und Wellness-Programme. - Gäste-Glow: Betreuung der exklusiven Lounge- und Beratungsbereiche im Medical Spa. Das bringen Sie mit – Perfekt für ausländische Ärzte & MFA - Sie verfügen über ein abgeschlossenes medizinisches Studium (z. B. ausländische Ärzte in der Anerkennungsphase / im Approbationsprozess) oder eine fundierte Ausbildung als Medizinische Fachangestellte (MFA) bzw. im gehobenen Gesundheitsmanagement. - Sprachprofil: Fließende Englischkenntnisse und gute bis sehr gute Deutschkenntnisse sind zwingend erforderlich. Ihre Herkunftssprache und jede weitere internationale Sprache (z. B. aus dem osteuropäischen, arabischen oder asiatischen Raum) setzen wir gezielt für unsere internationalen Gäste ein. - Ein hohes Maß an Empathie, Diskretion und Freude am Umgang mit einem anspruchsvollen Publikum. Das erwartet Sie bei uns - Ein Karrieresprung mit Perspektive: Ein hochattraktives, akademisches und wertschätzendes Arbeitsumfeld abseits des klassischen, stressigen Klinik- oder Praxisalltags. - Der Mallorca-Joker: Option auf zukünftige Einsätze in unseren internationalen Projekten im Süden nach erfolgreicher Einarbeitung. - Wohnungs-Joker: Volle Unterstützung beim Einleben im Allgäu durch bereitgestellten Wohnraum. Bewerbung in nur 1 Minute – ohne Papierkram! Tragen Sie sich einfach in unser Express-Formular ein https://www.allgäuresort.info/#card-recldai2o5lv1lw oder schreiben Sie uns direkt mit Angabe der Anzeigennummer 0017 im Betreff eine kurze E-Mail an: jobs@allgaeuresort.info (https://mailto:jobs@allgaeuresort.info) — Allgäu Resort Bad Grönenbach • Team HR / Recruiting • Vertraulichkeit im Bewerbungsprozess ist für uns selbstverständlich.

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Your Role: We are seeking an experienced Global Regulatory Lead to drive the regulatory strategy for our class III implantable neurostimulation devices focused on Vagus nerve stimulation within our Company's portfolio. You will define, develop, and lead global regulatory strategies for clinical investigations and submissions to achieve approvals for active implantable medical devices. You will prepare and lead health authority interactions, including FDA, Notified Bodies, and EMA advisory groups, building productive relationships to secure favorable regulatory outcomes worldwide. You will act as a key member and sole GRA representative for Governance meetings, guiding the Global Regulatory Affairs Strategy Team to ensure a unified regulatory voice. You will author, oversee, and review device documentation for HA submissions, applying global regulatory strategies, standards, and guidelines. You will share knowledge and coach colleagues across Regulatory Affairs and related functions. You will participate in audits in accordance with QMS ISO 13485 and 21 CFR 820 to maintain ongoing compliance. You will identify opportunities to build trust and scientific credibility with internal and external stakeholders, accelerating development through early engagement. You will work effectively within a matrixed organization to deliver an aligned and successful regulatory strategy. You will demonstrate fluency in English and lead with a collaborative, cross-functional mindset to achieve regulatory milestones. Key selling points include the opportunity to shape the regulatory pathway for cutting-edge implantable neurostimulation technology, direct interaction with major health authorities, and a leadership role that influences a global regulatory voice within a high-impact portfolio. This position is based in Germany. Who You Are: - MSc or higher in Life Science or a related discipline (PhD preferred). - 10 to 15 years in medical-device regulatory affairs with at least 5 years of recent experience on active-implantable devices. - Proven track record in IDE/510(k)/PMA filings, eSTAR processes, and quality systems application (ISO 13485, software validation, human factors, design verification/validation). - Strong understanding of clinical development, trial design, and regulatory frameworks (ICH, GCP, ISO 14155, EU-MDR, MPDG, MDCG). - Demonstrated ability to build and execute global regulatory strategy, including EU and US submissions; experience with global dossiers is strongly preferred. - Proven capability to engage health authorities through scientific advice meetings and serve as a credible, influential spokesperson. - Solid knowledge of EU/US regulatory frameworks for medical devices and combination products (QMS, MDSAP, ISO 13485, MDCG guidelines). - Excellent collaboration and communication within multidisciplinary teams and across functions. - Ability to lead and prioritize in a global, matrixed environment and work autonomously. - Fluency in English is mandatory. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!