Medical Research Engineer 80 \- 100 % (w/m/d) For more than 40 years, Hamilton Medical has shaped the future of mechanical ventilation. We develop Intelligent Ventilation solutions that support clinicians in critical moments. Our Hamilton ventilators are used in intensive care units, during emergency transport, and in MRI environments. They help medical teams care for adult, pediatric, and neonatal patients worldwide. Here, your work has real impact. Every improvement you make supports better respiratory care for patients around the globe. How you can make a difference: As a Medical Research Engineer, you join the Clinical Data Science team within Digital Health Solutions, Hamilton Medical's Software as a Medical Device (SaMD) business. Digital Health Solutions develops cloud\-based applications including a Clinical Decision Support System (CDSS) for critical care ventilation; our team develops data\-driven features and applications for it. You take ownership of your topics in a startup\-like setting and help us grow these capabilities further as the products scale. Building ona solid understanding of ventilation principles, you design, develop, andvalidatesignal processingand machine learning algorithms that address a wide range of challenges across mechanical ventilation. You own problems from research question through to product\-readysolutions, working hands\-on with clinical experts and engineers to move prototypes into clinical validation and, ultimately, intoproducts that reach the bedside. Yourkeyresponsibilities Design, implement, and rigorously evaluate signal processing, data science, and machine learning algorithms across mechanical ventilation Take ownership of research topics end\-to\-end, from problem framing and data exploration tovalidated, product\-oriented solutions Build and run data analyses and complete ML workflows using our Azure\-based cloud data platform Developreproducible, well\-engineered pipelines that support fast iteration while meeting the traceability and documentation needs of a regulated environment Work closely with clinical experts, software engineers, and product stakeholders across disciplines That's what you bring along: Must\-have A PhD in a relevant engineering or scientific field (biomedical engineering, computer science, physics, or related), or equivalent industry experience Several years of experience developing and validating data science / machine learning solutions Strong programming skills in ; solid grounding in data and signal processing Experience with cloud\-based data and ML tooling Analytical, independent, and meticulous work style Openness to interdisciplinary collaboration and a product\-oriented mindset Beneficial Prior experiencedeveloping medical\-device software, ideally through to production Working knowledge of Microsoft Azure (Azure Databricks, Azure Machine Learning) Familiarity withMLOpspractices (experiment tracking, model deployment, monitoring) How to apply: Learn more about career opportunities at Hamilton at Jobs \| Hamilton Medical. Do you share our values and feel at home in a cooperative, innovative,and down\-to\-earth environment? At Hamilton, we not only offer a motivating working environment, but also purposeful workand modern working conditions. Our interactions at eye level encourage open communication and a pleasant working environment. Become part of a team where your skills are valued and innovative ideas are fostered. Interested? Then apply online using the "Apply now" button. If you have any questions, please contact us at [Write an email](<>) with the following details: Reference: JR\-5973\-fjm/Contact: Juli Applications by post or e\-mail can unfortunately not be considered. jpid15fa94ejm jit0731jm jiy26jm

Wir suchen ab Vereinbarung Frauen mit einem Zertifikat in **medizinischer Thai-Massage** Anforderungen: - Ausbildung aus Thailand, vorzugsweise mit der staatlichen Anerkennung „National Skill Standards Assessment Certificate“ - mindestens ein Jahr Berufserfahrung Wir freuen auf Ihren Kontakt.

The AO is a medically guided, not-for-profit organization, a global network of surgeons, and the world's leading education, innovation, and research organization specializing in the surgical treatment of trauma and musculoskeletal disorders. We are home to people from all over the world, from different backgrounds, with diverse talents and specialist areas. What binds us together is our passion for excellence, our dedication to our mission of improving patient care, and our understanding that we are stronger together: we are one AO. For more information, visit: https://www.aofoundation.org/ The AO Innovation Translation Center (AO ITC) streamlines and drives innovation projects. Its activities include the development of clinical solutions with our industrial partner, innovation gathering, proof-of-concept studies, strategic investment in intellectual property, technology, or companies, and evidence creation through clinical research. As part of the AO ITC, Clinical Operations is the AO’s service provider for clinical research. Our clinical research specialists deliver clinical insights that are highly relevant to current surgical practice and enable better patient care by planning and conducting global clinical trials. The Head of Medical Scientific Affairs provides strategic and scientific leadership for AO's clinical evidence generation ecosystem and ensures that clinical research investments translate into meaningful improvements in patient care. He/she serves as a trusted scientific advisor to AO leadership, governance committees, and clinical divisions and represents AO ITC in internal and external scientific initiatives, partnerships, and expert forums. The role is accountable for developing a high-impact portfolio of clinical studies across Trauma, CMF, Spine,TC, Veterinary, and related orthopedic disciplines, ensuring optimal allocation of resources, scientific excellence, and supporting effective translation of evidence into clinical practice. The position serves as a key interface between surgeons, researchers, clinical operations, governance bodies, industry partners, and educational stakeholders to maximize the generation, dissemination, and adoption of evidence-based innovations within the AO ecosystem. Main Responsibilities: Lead the Medical Scientific Affairs team Provide scientific, strategic and operational leadership to the Medical Scientific Affairs team with two direct reports, fostering a high-performing, collaborative, and service-oriented culture. Define team objectives, priorities, and performance expectations aligned with the organization's strategy and portfolio needs. Recruit, develop, coach, and evaluate team members to support professional growth, ensuring the appropriate scientific, clinical, and operational competencies are in place. Close collaboration with Clinical Operations in the resource planning and allocation across studies, programs, and stakeholder requests to meet organizational objectives. Build effective collaboration between surgeons, governance bodies, Clinical Operations, NCR, AO Education Institute, AO Research Institute, educators, and external partners to advance the Clinical Research activities in the AO. Drive continuous improvement of Medical Scientific Affairs processes, standards, and capabilities to enhance quality, efficiency, and impact and establish a culture of scientific excellence, integrity, compliance, and evidence-based decision-making across all Medical Scientific Affairs activities. Lead the Clinical Science Advisory Commission (CSAC). Lead the AO ITC Clinical Research Fellowship Program. Support the AO PEER program. Clinical Study Design & Scientific Support Develop clinical study protocols addressing important knowledge gaps and clinical needs in close collaboration with surgeons, industry partners, governance bodies and Network Clinical Research and Clinical Operations. Review and provide medical-scientific assessment of adverse events and safety-related findings throughout study conduct. Provide expert advice on medical and scientific questions arising during study execution and support preparation of scientific publications, clinical reports, congress abstracts, and other dissemination activities. Close collaborate with Clinical Operations in study planning, implementation, and monitoring activities. Support interpretation of results in close collaboration with surgeons, investigators, governance bodies, and Clinical Operations. Drive excellence in scientific publication strategies, congress presentations, and dissemination activities. Clinical Research Portfolio Strategy Lead scientific discussions regarding future evidence needs. Develop and maintain a strategic clinical research portfolio in collaboration with the Research Commissions and internal stakeholders which is aligned with AO's mission and priorities. Establish and continuously refine portfolio prioritization frameworks balancing available research funding, knowledge gaps, patient impact, scientific significance, feasibility, cost-effectiveness and translational potential and risk-benefit considerations in collaboration with the Research Commissions and internal stakeholders. Monitor portfolio performance with regards to strategic objectives and adapt research priorities based on emerging evidence, and clinical needs. Provide scientific leadership across the full research lifecycle, ensuring methodological rigor, clinical relevance, regulatory compliance, and ethical conduct. Collaborate with Clinical Operations in establishing a grant acquisition strategy and strengthen industry partnerships and drive grant acquisition. Support Knowledge Translation activities to ensure clinical evidence generated by AO is effectively translated into education, clinical guidelines, decision support tools, and clinical practice. Collaborate closely with Clinical Operations, NCR, AO Education, AO Clinical Divisions, community development and governance bodies to facilitate adoption of new evidence. Lead implementation of health economic and outcomes research initiatives. Main Requirements: Professional & Technical Skills Advanced expertise in clinical research methodology. Strong understanding of orthopedic clinical practice and research. Advanced expertise in clinical study design, statistical principles, and evidence synthesis. Experience in designing and executing industry sponsored clinical studies as a CRO. Experience in health economic evaluation and outcomes research. Excellent scientific grant and publication writing and presentation skills. Sound understanding of regulatory requirements, Good Clinical Practice (GCP), and clinical research governance. Education & Qualifications Medical Degree (MD) required. PhD, MSc, or equivalent advanced scientific qualification highly desirable. Formal training in clinical epidemiology, research methodology, biostatistics, or related disciplines is advantageous. Professional Experience Minimum 10 years of experience in clinical research within orthopedics, trauma, spine, CMF, sports medicine, or related disciplines. Experience in multicenter clinical studies from concept generation to publication and dissemination. Experience in developing and managing research portfolios and clinical research strategies. Strong track record of peer-reviewed scientific publications and grant acquisition. Experience in line management and leading interdisciplinary and cross-functional teams. Demonstrated ability to collaborate effectively with surgeons and international clinical research networks. CRO services are of advantage. We offer: An interesting and varied job in an exciting and innovative organization The opportunity to be part of a highly committed international team Modern infrastructure High degree of flexibility regarding working hours and location (depending on operational requirements) Generous package of social benefits, including supplementary vacation days and pension scheme contributions Internal skills training opportunities and support for continued education

About the role: - Provide strategic program leadership for the most critical and complex Medical priorities, ensuring that enterprise Medical strategies are translated into executable portfolio plans, governed effectively, and delivered with visibility, accountability, and disciplined decision-making. - Serve as a senior PMO partner to Therapeutic Area and Medical leaders, shaping execution models, governance architecture, and cross-functional alignment for major programs, portfolios, launches, transformations, and lifecycle priorities. - Improve enterprise execution confidence by integrating milestone management, dependency control, risk signaling, budget visibility, and escalation leadership across highly matrixed Medical environments. - Strengthen the Medical PMO operating model by defining standards, mentoring talent, and advancing data-enabled, GCM-forward execution practices that improve speed, transparency, and consistency at scale. How you will contribute: - Lead end-to-end execution management for the most strategically important Medical portfolios or programs, establishing integrated roadmaps, governance structures, milestone frameworks, and escalation pathways that support enterprise delivery confidence. - Partner with senior Medical leaders to shape execution strategy for complex initiatives, ensuring that portfolio priorities are converted into realistic, sequenced plans with clear accountabilities, resource assumptions, interdependency management, and decision forums. - Provide enterprise-level visibility into execution health for assigned scope, synthesizing milestones, budget implications, risks, dependencies, and organizational constraints into clear leadership narratives and recommended actions. - Drive portfolio-level governance and decision-making by facilitating high-value leadership discussions, surfacing trade-offs, aligning stakeholders around choices, and ensuring timely closure of critical decisions. - Own the most complex risk and issue management topics within assigned scope, including systemic barriers, cross-program conflicts, resourcing tensions, and execution risks that require senior intervention or enterprise coordination. - Guide prioritization and scenario planning with Medical leaders and PMO leadership, helping determine where to accelerate, sequence differently, de-scope, or escalate in order to protect enterprise objectives and delivery credibility. - Provide strategic oversight of budget and resource implications for assigned portfolios, partnering with Finance and business leaders to assess execution feasibility, spending pressures, and trade-offs linked to critical path delivery. - Shape and improve the Medical PMO operating model through refinement of standards, decision-rights, governance cadences, reporting frameworks, and digital or automation-enabled execution practices. - Model Takeda values and reinforce a culture of integrity, scientific credibility, inclusion, accountability, and continuous improvement in all PMO activities. Skills and qualifications: - Bachelor's degree required; advanced degree in science, business, operations, engineering, or management preferred. - 12-14+ years of relevant experience in pharmaceutical, biotech, healthcare, or other regulated environments, including extensive leadership of complex global programs or portfolios. - Proven experience partnering with senior leaders to shape execution strategy and guide major portfolio decisions in matrixed organizations. - PMP, PgMP, change management certification, or comparable advanced PM/portfolio credentials preferred. - Strategic execution leadership: translates enterprise priorities into delivery models, governance, and portfolio control mechanisms. - Enterprise portfolio insight: identifies patterns, trade-offs, and systemic execution risks across multiple programs. - Executive communication: frames status, implications, options, and recommendations in a concise, leadership-ready manner. - Organizational influence: aligns senior stakeholders and drives action through credibility, judgment, and structured facilitation. - PMO leadership and talent development: strengthens standards, coaches others, and advances a data-enabled, future-ready execution model. - Digital enablement mindset for PMO: Embeds a digital enablement mindset across the PMO, leading adoption of digital tools, automation, and data-driven practices to transform operations, improve decision-making, and drive scalable execution.

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

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.

Vielfalt gestalten. Wissen nutzen. Verantwortung tragen. Sicherheit geben. Auch nach über 190 Jahren entwickeln wir unsere Inspektions-, Klassifikations- und Zertifizierungslösungen permanent weiter. Mit messbarem Erfolg: Heute vertrauen mehr als 400.000 Unternehmen weltweit darauf, dass wir ihre Welt sicherer machen. Tag für Tag, mit mehr als 85.000 Personen in über 140 Ländern. (mehr erfahren) In unserem Geschäftsbereich Consumer Products Services verbessern wir die Sicherheit, Qualität und Konformität der Produkte unserer Kunden im Konsumgüterbereich. (mehr erfahren) Deutschlandweit an unseren Standorten sind wir stets auf der Suche nach Fachkräften zur Bereicherung unseres kollegialen und aufgeschlossenen Teams von mehr als 250 Mitarbeiter/innen. Aktuell suchen wir: Sales Manager Medical (w/m/d) YOUR MISSION:✓ Erfolgreiche Weiterentwicklung, Steuerung und Umsetzung unserer Vertriebsstrategie✓ Gewinnung und Aufbau von Neukunden ✓ Intensive Markt- und Wettbewerbsbeobachtung✓ Eigenverantwortliche Erstellung von Markt- und Portfolio-Analysen sowie Entwicklung von innovativen Marktbearbeitungsansätzen✓ Begeisterung für das Erlernen neuer Themen, insbesondere im Bereich Nachhaltigkeitsinitiativen und Regulierungen wie z.B. dem EU Green Deal, CSRD und SBTi etc. ✓ Konzeption, Planung, Durchführung YOUR SKILLS:✓ Erfolgreich abgeschlossenes wirtschaftswissenschaftliches Studium oder abgeschlossene kaufmännische Ausbildung✓ Fundierte Berufspraxis in der TIC-Industrie oder einer ähnlichen Branche✓ Leistungsbereitschaft, eigenverantwortliche, strukturierte und ergebnisorientierte Arbeitsweise✓ Verhandlungssicher in Deutsch und Englisch OUR OFFER:✓ Wertebasierte und internationale Unternehmenskultur mit flachen Hierarchien und einem dynamischen und zukunftsorientierten Arbeitsumfeld✓ Nachhaltige und langfristig ausgerichtete Einarbeitung, Integration sowie Förderung der beruflichen und persönlichen Weiterentwicklung✓ Kollegiales, aufgeschlossenes und inklusives Team✓ Interessante Sozialleistungen (Vermögenswirksame Leistungen, betr. Altersvorsorge, Corporate Benefits)✓ Firmenevents✓ KITA-Zuschuss von bis zu 100 EUR pro Monat und pro Kind✓ BV-Kreditkarte mit einem monatlichen Ladebetrag von bis zu 50 EUR✓ Jubiläumsgratifikationen✓ Weiterbildungsmöglichkeiten✓ Vorsorgeuntersuchungen und jährliche Grippeschutzimpfungen✓ Bio-Obst an den Standorten✓ JobRad✓ Gleitzeit✓ Homeoffice✓ Dienstwagen und Dienst Smartphone✓ 30 Tage Erholungsurlaub bei einer 5 Tage Woche sowie Sonderurlaub Haben wir Ihr Interesse geweckt? Bewerben Sie sich jetzt! Bitte schicken Sie uns Ihre aussagekräftigen Unterlagen inkl. Ihres Gehaltswunsches und Ihrer Verfügbarkeit. Entweder über unser Online Portal oder per Mail an [E-Mail Adresse gelöscht]. Wir freuen uns auf Sie. Ihr HR – Team Leave Your Mark! Bureau Veritas Consumer Products Services Germany GmbH Human Resources

Ihr Beitrag - Aktive Mitarbeit in interdisziplinären Teams bei der Entwicklung von Produkten der Löwenstein Medical Technology mit Fokus auf elektronische Komponenten, insbesondere Leiterplatten - Betreuung medizinischer Geräte innerhalb des Qualitätsmanagements über den gesamten Produktlebenszyklus hinweg - Realisierung von Prüfkonzepten für elektronische Bauteile in enger Abstimmung mit der Produktentwicklung - Begleitung von Post-Market-Surveillance-Maßnahmen und Designtransfers in die Produktion - Optimierung der Prozesse des Produktlebenszyklus sowie Unterstützung bei deren Umsetzung in Hinsicht auf die Elektronikentwicklung - Sicherstellung einer vollständigen und normgerechten technischen Dokumentation Das bringen Sie mit - Abgeschlossener technischer Bildungsweg in Bereichen wie Elektrotechnik, Medizintechnik, Mechatronik, Maschinenbau oder einer vergleichbaren Fachrichtung - Mehrjährige Berufserfahrung im Qualitätsmanagement, vorzugsweise im Umfeld der Medizintechnik - Praktische Erfahrung in der Entwicklung oder qualitätsseitigen Begleitung elektronischer Produkte und Baugruppen sowie den damit verbundenen normativen Vorgaben - Sicherer Umgang mit regulatorischen Anforderungen an Medizinprodukten (bspw. EN 60601-1, wünschenswert ISO 13485) - Hohes Qualitätsbewusstsein sowie eine strukturierte und eigenverantwortliche Arbeitsweise - Ausgeprägte analytische Fähigkeiten und Problemlösungskompetenz - Zuverlässigkeit und Freude an der Arbeit mit interdisziplinären Teams - Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Das können Sie von uns erwarten - Flexible Arbeitszeiten (Gleitzeit), unbefristete Anstellung - Homeoffice gemäß aktueller Betriebsvereinbarung möglich - 30 Tage Urlaub pro Jahr - Bezahlung nach Tarifvertrag, ggf. Prämien- und Bonuszahlungen - Attraktive Zuschüsse: - Mittagessen - Deutschlandticket - betriebliche Altersvorsorge (bAV) - JobRad - Corporate Benefits, Preisnachlässe auf ausgewählte Produkte bekannter Marken - Freizeitangebote wie Spieleabende und After-Work-Fußballrunden - Individuelle Teamevents, z. B. Firmenläufe, Frisbee-Turniere u.v.m. - Führendes und kontinuierlich wachsendes Unternehmen der Medizintechnik - Viele Möglichkeiten zur Mitgestaltung sowie zur persönlichen und fachlichen Weiterentwicklung - Anspruchsvolle und abwechslungsreiche Projekte Warum Löwenstein Medical Technology? **Neue Wege gehen.**Aber nie vergessen, wo man herkommt. Löwenstein Medical Technology ist ein mittelständisches Unternehmen unter dem Dach der international aufgestellten Löwenstein Gruppe. Als Kompetenzträger für respiratorische Diagnostik und Therapie entwickeln und produzieren wir in Deutschland hochwertige Medizinprodukte „Made in Germany“ für den weltweiten Einsatz in der Schlaf- und Beatmungsmedizin. Wir investieren in Mitarbeiter, die unsere zentralen Werte Eigenverantwortung, Begeisterung, Kreativität und Leistung in den Fokus ihres Schaffens stellen.

Wir suchen aktuell: Personalberater / Personaldisponent (m/w/d) Medical in Kaiserslautern Sie kennen die Personaldienstleistung, verbinden Menschen und Unternehmen mit einem klaren Blick für den Markt und möchten Ihren nächsten Schritt in Kaiserslautern, Rheinland-Pfalz gehen? Für meinen Mandanten besetze ich im Rahmen der Direktvermittlung die Position Personalberater / Personaldisponent (m/w/d) Medical. Sie gestalten Kunden- und Kandidatenbeziehungen aktiv und übernehmen Verantwortung für nachhaltige Besetzungen. Ihre zukünftigen Aufgaben - Bewerbermanagement und Rekrutierung von qualifiziertem Personal - Mitarbeiterführung und -betreuung - Kundenbetreuung und Neukundenakquise - Vertragsmanagement und Stammdatenpflege - Platzierung von Kandidaten bei Kunden - Einsatzplanung und -steuerung von externen Mitarbeitern in Kaiserslautern Das bringen Sie mit - Abgeschlossene Berufsausbildung im kaufmännischen oder medizinischen Bereich - Erste Berufserfahrung als Personalberater / Personaldisponent (m/w/d) im Bereich Medizin, Pflege oder Pädagogik - Begeisterung für Vertrieb und Kundenkontakt - Versierter Umgang mit MS Office Das dürfen Sie erwarten - Attraktives Gehaltspaket mit Erfolgsbeteiligung - Einen Firmenwagen zur privaten Nutzung - Unbefristetes Arbeitsverhältnis und strukturierte Einarbeitung - Motiviertes Team und angenehmes Arbeitsumfeld in Frankfurt a. Main - Flache Hierarchien für starken Zusammenhalt im Unternehmen - Mitarbeiter-Rabatte, Teamevents und Weiterbildungsmöglichkeiten Vertraulichkeit ist die Grundlage jeder Zusammenarbeit. Ihre Unterlagen und Wechselmotivation behandle ich diskret und bespreche eine Weitergabe ausschließlich mit Ihnen. Sie erhalten eine persönliche Rückmeldung von Julius Oscar Lorr. In einem vertraulichen Erstgespräch klären wir Ihre Ziele und die wichtigsten Rahmendaten. Passt die Position, begleite ich Sie transparent durch den gesamten Auswahlprozess – verbindlich und ohne unnötige Schleifen. Vertraulich. Persönlich. Klar. Passt die Position zu Ihrem nächsten Schritt? Dann bewerben Sie sich direkt – Ihr Lebenslauf genügt. Ein Anschreiben ist nicht erforderlich. Für eine vertrauliche Vorabfrage können Sie mich persönlich kontaktieren.

Wir suchen aktuell: Personalberater / Personaldisponent (m/w/d) Medical in Frankfurt am Main Sie kennen die Personaldienstleistung, verbinden Menschen und Unternehmen mit einem klaren Blick für den Markt und möchten Ihren nächsten Schritt in Frankfurt am Main, Hessen gehen? Für meinen Mandanten besetze ich im Rahmen der Direktvermittlung die Position Personalberater / Personaldisponent (m/w/d) Medical. Sie gestalten Kunden- und Kandidatenbeziehungen aktiv und übernehmen Verantwortung für nachhaltige Besetzungen. Ihre zukünftigen Aufgaben - Bewerbermanagement und Rekrutierung von qualifiziertem Personal - Mitarbeiterführung und -betreuung - Kundenbetreuung und Neukundenakquise - Vertragsmanagement und Stammdatenpflege - Platzierung von Kandidaten bei Kunden - Einsatzplanung und -steuerung von externen Mitarbeitern in Frankfurt a. Main Das bringen Sie mit - Abgeschlossene Berufsausbildung im kaufmännischen oder medizinischen Bereich - Erste Berufserfahrung als Personalberater / Personaldisponent (m/w/d) im Bereich Medizin, Pflege oder Pädagogik - Begeisterung für Vertrieb und Kundenkontakt - Versierter Umgang mit MS Office Das dürfen Sie erwarten - Attraktives Gehaltspaket mit Erfolgsbeteiligung - Einen Firmenwagen zur privaten Nutzung - Unbefristetes Arbeitsverhältnis und strukturierte Einarbeitung - Motiviertes Team und angenehmes Arbeitsumfeld in Frankfurt a. Main - Flache Hierarchien für starken Zusammenhalt im Unternehmen - Mitarbeiter-Rabatte, Teamevents und Weiterbildungsmöglichkeiten Vertraulichkeit ist die Grundlage jeder Zusammenarbeit. Ihre Unterlagen und Wechselmotivation behandle ich diskret und bespreche eine Weitergabe ausschließlich mit Ihnen. Sie erhalten eine persönliche Rückmeldung von Julius Oscar Lorr. In einem vertraulichen Erstgespräch klären wir Ihre Ziele und die wichtigsten Rahmendaten. Passt die Position, begleite ich Sie transparent durch den gesamten Auswahlprozess – verbindlich und ohne unnötige Schleifen. Vertraulich. Persönlich. Klar. Passt die Position zu Ihrem nächsten Schritt? Dann bewerben Sie sich direkt – Ihr Lebenslauf genügt. Ein Anschreiben ist nicht erforderlich. Für eine vertrauliche Vorabfrage können Sie mich persönlich kontaktieren.