FMTC logo Amsterdam - Instructor Medical Frist Aid & Medical Care - On-site - - Amsterdam , Noord-Holland , Netherlands - €2,800 - €4,000 per month Job description Do you thrive on inspiring others, sharing knowledge, and making a real impact through hands-on training? Are you someone who takes ownership, embraces variety, and feels at home in an international and fast-moving environment? Who Are We? At FMTC Safety, everything revolves around people and safety. We are a fast-growing, global organization preparing professionals to work safely in some of the world's most demanding environments: from offshore platforms and wind farms to ships and industrial sites. Job requirements You don't just deliver courses, you create impactful learning experiences that truly prepare people for real-life offshore emergencies. What will you do? No two days are the same and that's exactly what excites you. You take full ownership of your trainings and: Why FMTC? Because here, you don't just join a company, you become part of a journey.

FMTC logo Amsterdam - Instructor Medical Frist Aid & Medical Care - On-site - - Amsterdam , Noord-Holland , Netherlands - • Schiphol , Noord-Holland , Netherlands • +1 more Job description Do you thrive on inspiring others, sharing knowledge, and making a real impact through hands-on training? Are you someone who takes ownership, embraces variety, and feels at home in an international and fast-moving environment? For our training center in Amsterdam , we are looking for a driven and passionate Medical First Aid & Medical Care Instructor (m/f/d) who wants to enable people to work safely and optimally prepare them for emergency situations in offshore environments. Who Are We? At FMTC Safety, everything revolves around people and safety. We are a fast-growing, global organization preparing professionals to work safely in some of the world's most demanding environments: from offshore platforms and wind farms to ships and industrial sites. What makes us different? We go where our clients need us. With training centers strategically located around the world, we offer maximum flexibility: in timing, location, and delivery. Our mindset is simple: we make it happen . Even if there's only one participant, the training goes ahead. This requires more than just knowledge, it requires passion, flexibility and a true customer-first mentality. And that's exactly what defines our instructors. Job requirements Your Role as a Medical First Aid & Medical Care As a Medical First Aid & Medical Care Instructor (m/f/d) in Amsterdam , you are at the heart of our training center. You don't just deliver courses, you create impactful learning experiences that truly prepare people for real-life offshore emergencies. What will you do? No two days are the same and that's exactly what excites you. You take full ownership of your trainings and: - Deliver Medical First Aid and Medical Care courses - Guide practical exercises, such as life-saving a...

Bienvenue chez Form'aou, centre de formation & CFA situé à Saint-André et Saint-Louis. Nous proposons des formations en continu et en alternance, allant du niveau CAP au BAC+2. - Postes à pourvoir en alternance uniquement ! (1 jour de formation/semaine) Le poste : FORMAOU, centre de formation et CFA basé à Saint-Louis, proposant des formations du niveau BAC à BAC+2, recrute en URGENCE- pour renforcer son équipe de formateur, un.e formateur.trice en administratif / secrétariat. Vos missions : - Concevoir et actualiser des contenus et supports de formation - Animer des sessions en présentiel - Mettre en place des mises en situation professionnelles et des évaluations des acquis - Adapter les parcours en fonction des objectifs professionnelsType de contrat : indépendant Rémunération et conditions déterminées lors de l'entretien. Lieux d'intervention : Saint?Louis centre. Objectif : garantir la montée en compétences opérationnelles des stagiaires et la qualité des prestations de formation, en veillant au respect des référentiels et des obligations réglementaires. Profil recherché : - Bac+2 en assistanat/secrétariat ou équivalent - 1 à 3 ans d'expérience en formation d'adultes - Maîtrise des outils bureautiques (Word, Excel, Outlook) et aptitude à concevoir des supports pédagogiques. - Compétences pédagogiques, animation de groupe, sens du relationnel, rigueur et autonomie. - Expérience pratique en secrétariat et gestion administrative appréciée; adaptabilité et communication professionnelle indispensables.DISPONIBLE IMMÉDIATEMENT ? Savoir-faire demandés : - Adapter l'enseignement à un groupe cible - Adapter l'enseignement aux capacités des étudiants - Aider des étudiants dans leur apprentissage - Coopérer avec des professionnels de l'enseignement - Évaluer des étudiants Savoir-être demandés : - Adaptabilité - Compréhensif - Confiant

Specialist Medical Center Operations Das kannst du bewegen Als MPA bist du die erste Kontaktperson für unsere Patientinnen und Patienten und sorgst für eine angenehme Praxiserfahrung. Medbase bietet dir ein dynamisches Team, das Wert auf Qualität und Kollegialität legt. Empfang und Betreuung von Patientinnen und Patienten, inklusive Agendaplanung und Terminkoordination Durchführung von Laboruntersuchungen, EKGs und Röntgenaufnahmen Assistenz bei kleinchirurgischen Eingriffen Verwaltung und elektronische Abrechnung der Patientenakten Sicherstellung reibungsloser Praxisabläufe Kooperation mit dem Team bei administrativen Aufgaben Was du mitbringst Ausbildung als Med. Praxisassistent/in EFZ Bereitschaft zur Weiterbildung als Berufsbildner/in und/oder in Röntgentechnik Organisationstalent und Freude an der Patientenbetreuung Empathie und Flexibilität Teamfähigkeit und Humor in herausfordernden Situationen Gute Deutschkenntnisse (mind. B2 Niveau) Bewirb dich noch heute Für Fragen stehen wir dir unter der Telefonnummer gerne zur Verfügung. Über uns Mit unseren innovativen und effektiven pharmazeutischen Lösungen setzen wir bei Zur Rose alles daran, das Leben der Menschen positiv zu beeinflussen. Unser Team von 500 Mitarbeitenden mit Hauptsitz in Frauenfeld verfolgt das gemeinsame Ziel, die Zukunft des Gesundheitswesens zu verbessern. Da Qualität, Komfort und Effektivität bei uns besonders grossgeschrieben werden, können Patientinnen und Patienten ihre Gesundheit einfach, und sicher selbst in die Hand nehmen. Unser Anspruch ist es, künftige Anforderungen im Gesundheitswesen zu prognostizieren. Bei der Entwicklung unserer Lösungen und Arzneimittel setzen wir auf ein hohes Mass an Zuverlässigkeit und Effizienz und kümmern uns um die komplexen Themen, damit unsere Kundinnen und Kunden sich entspannt zurücklehnen können. Die funktionsübergreifende Teamarbeit wird durch unsere Unternehmenskultur gefördert, sodass jedes Teammitglied gleichermassen geschätzt und darin bestärkt wird, sich am Entscheidungsprozess aktiv zu beteiligen. Offene Kommunikation und Empathie stehen bei uns an erster Stelle. Dabei versuchen wir stets, einen gemeinsamen Nenner zu finden und somit Kompromisse zu vermeiden. Unsere Leidenschaft bei Zur Rose besteht darin, die Welt positiv zu beeinflussen. Teilst du dieselben Werte und möchtest auch du das Leben der Menschen verbessern? Dann würden wir uns freuen, dich als Teil unseres Teams zu begrüssen. jpide522e74jm jit0625jm jiy26jm

Role Purpose As Medical Director in Sweden, you will be the principal medical authority across our Swedish sites. Accountable for clinical performance, governance, quality, team leadership, and the credibility of Neko’s clinical model. You will report to the Medical Director, Europe and work closely with the international medical leadership team. You will have a visible, active presence in the clinics. Hold the clinical standard with consistency and clarity and build a strong clinical team culture together with the Swedish clinical leads. Beyond the clinics, you are Neko’s medical voice in Sweden. You will engage with academic institutions, regulatory bodies, professional networks, and public health discourse. Representing a model of preventive care that is evidence-based, and genuinely different from what the system currently offers. What You’ll Deliver in the First 6–12 Months Clinical Leadership and Team Performance Set and hold the clinical standard for Neko’s Swedish operations. Lead, develop, and performance-manage Sweden's clinical leads. Create a culture of clinical excellence, high expectations, and honest feedback. Partner closely with Sweden's operational and clinical teams to ensure the two sides of the business move in the same direction without friction. Ensure clinical KPIs. Clinical Governance and Quality Own the Swedish clinical governance framework: policies, protocols, escalation pathways, incident review, and risk management, aligned to Neko’s global standards and Swedish regulatory requirements. Own Sweden’s clinical quality composite and drive it consistently to benchmark. Lead Neko Sweden’s continuous quality assurance efforts across patient safety and medical quality. Contribute actively to the global medical quality framework, bringing Swedish market insight into shared standards and improvement initiatives. Regulatory and Compliance Leadership Responsible for ensuring that all Swedish Neko clinics operate in compliance with applicable Swedish healthcare laws and regulations. Maintain Neko’s relationship with relevant Swedish regulatory and professional bodies. Ensure clinical documentation, consent frameworks, and protocols are compliant with Swedish healthcare law, EU MDR, and GDPR. Ensure Neko’s Swedish clinical operations are prepared for regulatory inspection at all times. Clinical Evidence and Medical Community Engagement Help build the clinical case for Neko’s preventive model in Sweden’s medical and public health discourse. Engaging with academic institutions, research bodies, and clinical networks. Ensure that the clinical claims Neko makes are grounded in evidence. Build and maintain Neko’s clinical credibility in the Swedish medical community. Be a recognized and respected voice on preventive medicine, population health, and the clinical value of early detection. Engage with Swedish academic medicine, public health institutions, and professional bodies. Represent Neko at medical conferences, academic and policy forums, and in media engagement on preventive health. Minimum Qualifications Swedish medical license issued by Socialstyrelsen. 10+ years of clinical experience, including 3–5 years in a senior clinical leadership role with direct management of clinical teams. Demonstrable track record of managing, developing, and performance-managing clinicians. Strong knowledge of Swedish healthcare regulations. A senior physician with a standing in the Swedish medical community. A genuine belief in preventive medicine and early detection. Fluency in Swedish and English. Preferred Experience in technology-enabled, consumer-facing, or multi-site private healthcare environments. Familiarity with Swedish private healthcare, Företagshälsovård, and corporate wellness markets. Track record of external profile-building: published clinical or scientific work, speaking engagements, advisory roles, or media presence on population health. Experience leading a clinical function through significant growth or operational scaling.

In order to work in Ireland a non-EEA National, unless they are exempted, must hold a valid employment permit. Please review the Eligibility and requirements for an employment permit if you are unsure of your eligibility to apply for this vacancy.
Position: Initial Medical Service Driver Location: Connacht Contract: Full-Time, Permanent, 39 Hours Per Week. Salary: €29,800 per annum, Paid Monthly The Driver Role As a service driver, you will travel to and from our customers to collect and dispose of their hazardous waste items. Key responsibilities include: Visiting a number of different customer sites servicing their hazardous waste facilities such as sharp bins, poisons, dental waste and other types of waste - don’t worry, we have a world-class accident rate! Ensuring that your vehicle is safe at all times and that you take care on the road and follow our RI Drive Smart guidance Providing exceptional customer service and upholding a professional image at all times Requirements Driver Requirements: Full Irish driving licence held for more than two years, with no more than six penalty points. You will need to be comfortable working in a very manual role as you will be loading and unloading units and bins An ADR certificate would be great but this is not essential Demonstrate excellent customer service and communication skills Flexibility with working patterns to support business needs Ability to use own initiative and have a positive ‘can do’ attitude You may be required to pass a DBS check depending on the role you have applied for Benefits Driver Benefits: Access to a company vehicle and fuel card. Salary grading system - linked to performance for those keen to develop their career within our business. Comprehensive Field Based Training Enrolment in our company pension scheme. Exciting discounts and cashback offers from over 3,000 retailers with RI Rewards. Overtime opportunities - potential to earn extra in overtime to meet the needs of our customers. Leads Commission scheme available - although this isn’t a sales job, we appreciate and reward you for passing on sales leads. Employee Assistance Programme (EAP) - free to access and available 24/7 to you, your family, and friends. Long service recognition - includes an extra five days of annual leave entitlement after five years of service. Refer a Friend - earn up to €1,000 for referring someone to work for Rentokil Initial. If you would like the chance to work in this exciting role for an innovative company, please apply. For more information on the Rentokil Initial family, please visit our website Rentokil Initial is an equal opportunities employer and is committed to creating a diverse working environment. To find out how we process your data, view our privacy policy here.

Head of Medical Safety GCSP At Bavarian Nordic, we are committed to saving and improving lives by unlocking the power of the immune system. Our commercial portfolio includes market\-leading vaccines against smallpox/mpox, rabies, tick\-borne encephalitis, typhoid fever, and cholera. We excel in R\&D innovation, manufacturing, and commercialization\-working every day to protect people's health and quality of life and protecting our tomorrow. We are looking for an experienced Head of Medical Safety GCSP providing medical leadership across Global Clinical Safety \& Pharmacovigilance (GCSP). The position reports to the Head GCSP \& EU/UK QPPV and can be based in either Germany or Switzerland \- travel up to \~20% within Europe should be expected. The roleAs our Head of Medical Safety GCSP, you will be accountable for all medical safety related aspects of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects in your area of expertise. In this role, you will manage and mentor a team of six (Sr) Safety Physicians and (Sr) Safety Scientists. Key responsibilities Lead and develop the medical safety team and ensure that appropriate tools and skillsets are available/developed Ensure high quality clinical safety contributions to development programs and for the life\-cycle management of marketed products in compliance with regulations, guidelines, BN operating procedures (SOPs) Serve as member of the GCSP Leadership Team and in governance committees as assigned Ensure medical safety support for GCP and GVP audits and inspections Contribute to company strategic initiatives and innovations Stay abreast of innovative technologies, tools, innovations, and regulations concerning area of expertise What you bringTo become a success in this role, you bring a Medical Doctor (MD) degree combined with leadership experience within clinical safety and pharmacovigilance. You are recognized for setting direction, taking accountability, and leading teams with passion, clarity and empathy in a highly regulated, global environment. You balance strategic oversight with confident decision?making and strong ethical stakeholder engagement. 10\+ years of experience across clinical safety and pharmacovigilance, including senior Medical Safety roles Deep regulatory expertise across global safety activities, including signal management and risk minimization You bring solid knowledge of global clinical safety and pharmacovigilance regulations including GCP, GVP, and ICH guidelines, along with hands\-on experience in CTD compilation and MAAs/BLAs submissions to major health authorities. Besides this, you communicate fluently in English with solid written, verbal, and presentation skills using medical and regulatory terminology. You are highly proficient in relevant IT tools and database applications and are a self\-driven, positive team player who helps to build and sustain high performance and team cohesion. Most importantly, you thrive in change; your judgment, integrity, and resilience help safeguard patient safety and support our transition from development to full commercialization in a fast\-moving, life\-science environment. Please note an advanced degree is required, and an MD qualification is mandatory for this role. Why this roleThis role offers a unique opportunity to take end?to?end responsibility for all medical safety activities within clinical safety and pharmacovigilance in a science driven organization with a strong purpose. You will mentor a team, work closely with global stakeholders, contribute directly to regulatory submissions and patient safety, and have real influence on how safety processes and risk management activities are shaped and executed. It is a role with both strategic impact and hands?on responsibility, ideal, if you want to grow your expertise while making a meaningful difference. In this role, you will have the platform to make a lasting impact on public health, advance our mission, and set new benchmarks for medical excellence in a dynamic, growth\-oriented biotechnology environment. ApplicationIf you are ready to take on a pivotal role in a growing organization and drive meaningful change in healthcare, apply now and join Bavarian Nordic in our mission to improve health outcomes and foster sustainable growth. Please note that we do not support any relocation package for this role. We kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position. Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit jpid589a182jm jit0623jm jiy26jm

Associate Director, Medical Affairs Obesity Medical & Scientific Affairs, International Operations Strategic Office Zurich, Switzerland If you’re driven by a desire to translate cutting-edge science into real-world clinical impact, elevate standards of care, thrive through collaboration, and help reshape how the world understands obesity—this is your moment. At Novo Nordisk we are looking for an Associate Director, Medical Affairs – Obesity, to help lead the evolution of one of the most transformative therapy areas in modern medicine—and one of the greatest healthcare challenges of our time. Your New Role As Associate Director, Medical Affairs – Obesity, you’ll play a pivotal role in advancing Novo Nordisk’s global obesity strategy across International Operations (IO)—covering all markets outside the U.S. You’ll operate at the scientific forefront, turning the latest research into meaningful medical advances, while ensuring our approach to obesity and related conditions is rooted in evidence, empathy, and excellence. You’ll serve as a trusted scientific partner across regions and functions—shaping how we engage with healthcare professionals, key opinion leaders, and patients. Your work will directly influence how obesity is understood, treated, and prioritized in more than 190 countries. Your key responsibilities will be: Lead the execution of medical strategy and tactics for obesity and related conditions across IO, incl. new product launches ensuring tight alignment with global medical and development priorities. Champion obesity as a serious, chronic disease, while integrating insights across the broader cardiometabolic portfolio. Partner with regional and affiliate Medical Affairs teams to strengthen medical education, scientific exchange, and patient journey insights. Represent market and regional perspectives in global forums—to shape clinical development and communication strategies. Drive high-impact scientific engagement with thought leaders, academic institutions, and professional societies to elevate the global narrative around obesity. You will also support RWE and data generation initiatives in collaboration with global and local teams, aligning with medical and access goals. Operate effectively in a global, matrixed environment, partnering across Medical, Clinical, Commercial, and Access functions. This is a role for someone who brings both intellectual rigor and relentless dedication—someone ready to go the extra mile to deliver strong results and make a lasting difference, all within a supportive, values-driven environment that champions sustain-able high performance. Please note: For Zurich-based roles at this level within IO Strategic Operations, international mobility within a three-five year horizon is expected. Your New Team You’ll join the IO Cardiometabolic Medical & Scientific Affairs team—a dynamic, mission-driven group at the heart of Novo Nordisk’s fastest-growing therapeutic area. Reporting to the Director, Medical Affairs Obesity, you’ll be part of a global network of medical leaders shaping the future of care for people living with obesity and related conditions. Based in Zurich, Switzerland, you’ll work from our International Operations Strategic Office—a hub for innovation, talent development, and cross-regional collaboration. As part of Novo Nordisk’s Talent Incubator, this role offers exceptional exposure to global strategy and the chance to build an international network that can accelerate your career. Your Skills & Qualifications We’re looking for a scientifically rigorous, strategically agile, and highly collaborative leader who thrives where medicine, science, and business impact intersect. What you bring: MD preferred, or an advanced scientific degree with 7+ years of experience in the pharmaceutical industry – ideally, though not mandatorily, in obesity, endocrinology, or cardiometabolic diseases. Proven track record in Medical Affairs, including experience in pre-launch planning, scientific communication, and stakeholder engagement. Solid understanding of clinical development pathways, regulatory frameworks (EMA/FDA), and real-world evidence generation. Demonstrated ability to lead cross-functional initiatives and influence without formal authority in a global matrix. Exceptional scientific communication, analytical thinking, and presentation skills—with the ability to distill complex data into clear, compelling narratives. A proactive, solutions-oriented mindset and deep commitment to improving outcomes for people living with obesity. Above all, you combine scientific depth with strategic execution, and you believe—wholeheartedly—that obesity deserves the same seriousness, investment, and innovation as any other chronic disease. Working at Novo Nordisk At Novo Nordisk, we don’t just treat diseases—we redefine what’s possible. For over a century, our “unordinary” mindset has driven us to challenge conventions, champion patients, and pursue science with purpose. We know careers aren’t linear—and lives aren’t one-size-fits-all. That’s why we foster a culture of mutual respect, curiosity, and sustainable high performance, where your growth matters as much as our mission. Here, dedication is valued. You’ll be part of a global community united by a simple truth: Together, we’re life-changing. What We Offer Beyond a competitive compensation package, we offer continuous learning, global mobility opportunities, and a people-first culture. Our benefits are thoughtfully designed to support both your professional ambitions and personal well-being—at every stage of your journey. Ready to Make an Impact? If you’re ready to lead with science, collaborate with purpose, and help transform the future of obesity care, we’d love to hear from you. To submit your application, please upload your CV in English (click on Apply and follow the instructions).

Berlin-Chemie entwickelt, produziert und vertreibt moderne Arzneimittel aus Berlin für Menschen in aller Welt. Durch den Einsatz unserer 5.000 Mitarbeitenden verbessern wir die Lebensqualität von Patient:innen und ermöglichen ihnen ein gesünderes Leben - mit Qualitätsbewusstsein, Leidenschaft und dem Rückhalt eines starken, verlässlichen Teams. Unsere 130-jährige Unternehmensgeschichte zeigt, dass wir stetige Veränderung mit Beständigkeit und einem stabilen Arbeitsumfeld verbinden können. Als Ausbildungsunternehmen und familienfreundlicher Arbeitgeber in Berlin sind wir seit Generationen bewährt.Berlin-Chemie entwickelt, produziert und vertreibt moderne Arzneimittel aus Berlin für Menschen in aller Welt. Durch den Einsatz unserer 5.000 Mitarbeitenden verbessern wir die Lebensqualität von Patient:innen und ermöglichen ihnen ein gesünderes Leben - mit Qualitätsbewusstsein, Leidenschaft und dem Rückhalt eines starken, verlässlichen Teams. Unsere 130-jährige Unternehmensgeschichte zeigt, dass wir stetige Veränderung mit Beständigkeit und einem stabilen Arbeitsumfeld verbinden können. Als Ausbildungsunternehmen und familienfreundlicher Arbeitgeber in Berlin sind wir seit Generationen bewährt. Als International Pharmacovigilance Coordinator sind Sie zuständig für die Koordination von Pharmakovigilanz-Aktivitäten zur Gewährleistung der Patientensicherheit innerhalb der International Division der Berlin-Chemie AG. Von unserer Unternehmenszentrale in Berlin aus arbeiten Sie eng mit unseren lokalen Drug Safety Units in Osteuropa und in Ländern der CIS-Region sowie mit unserer italienischen Muttergesellschaft Menarini zusammen. International Pharmacovigilance Coordinator (m/w/d) Unternehmen: Berlin-Chemie AG Bereich: Naturwissenschaftliche Berufe Einsatzort: Berlin Arbeitsmodell: hybrides Arbeiten Arbeitszeit: Vollzeit Nachverfolgung und kontinuierliche Bewertung des Nutzen-Risiko-Verhältnisses ausgewählter Arzneimittel Monitoring und Auswertung internationaler Fachliteratur im Hinblick auf sicherheitsrelevante Erkenntnisse Durchführung und Unterstützung der Signal Detection auf Basis von ICSR-Analysen und Literatur-Monitoring Koordination regulatorischer Aktivitäten im Bereich Arzneimittelsicherheit Begleitung sicherheitsrelevanter SmPC-Variations sowie Sicherstellung fristgerechter Einreichungen Pharmakovigilanz-Expertise in der Erstellung und Aktualisierung von RSI-Dokumenten Unterstützung des ICSR-Managements mit medizinischer Expertise Mitwirkung bei Inspektionen sowie internen und externen Audits Erstellung, Überarbeitung und Pflege von Standard Operating Procedures und Working Instructions Koordination von Qualitätssicherungsmaßnahmen zur weiteren Stärkung der Patientensicherheit Abgeschlossenes Studium der Humanmedizin oder einer anderen relevanten naturwissenschaftlichen Disziplin Mehrjährige Erfahrung im Bereich Arzneimittelsicherheit Erfahrung in der Auswertung medizinischer Fachliteratur sowie ein sicherer Umgang mit relevanter medizinischer Terminologie Gute Kenntnisse der Arzneimittelregulierung und von Zulassungsprozessen Kenntnisse in der Risikobewertung und Risikominimierung Hohes Qualitätsbewusstsein sowie ein sicherer Umgang mit komplexen medizinischen und regulatorischen Fragestellungen Strukturierte, sorgfältige und eigenverantwortliche Arbeitsweise Hohe Zuverlässigkeit sowie ausgeprägtes Verantwortungsbewusstsein Sehr gute Englischkenntnisse, insbesondere in der schriftlichen Anwendung und der medizinischen Fachterminologie Finanzielles: Markt- und leistungsgerechtes Vergütungspaket, Urlaubs- und Weihnachtsgeld, Verpflegungszuschuss, betriebliche Altersvorsorge, anlassbezogene Sonderzahlungen, Rabatte über Plattform Corporate Benefits Work-Life-Balance: Zeiterfassung, Gleitzeit & Überstundenausgleich, anteiliges mobiles Arbeiten, 30 Tage Urlaub, Möglichkeit auf zusätzliche freie Tage, Angebote zur flexibleren Arbeitszeitgestaltung in unterschiedlichen Lebensphasen bei z... Homeoffice: Umfang: Nach Vereinbarung

Willkommen bei der Allianz In der Position als Medical Risk Analyst gestaltest Du aktiv das Privatkundengeschäft der Allianz Privaten Krankenversicherung (APKV) mit, indem Du die medizinische Risikoprüfung prozessual weiterentwickelst und einfache, effiziente Versicherungslösungen ermöglichst. Arbeite in einem dynamischen, agilen Umfeld, das es Dir ermöglicht, flexibel und schnell auf Marktveränderungen zu reagieren und innovative Prozesse zu gestalten. Die agile Arbeitsweise fördert Kreativität und Zusammenarbeit, sodass Du maßgeblich zur Stabilität und Weiterentwicklung unserer Risikoprüfungsprozesse beiträgst. Besonders in den Bereichen Vollversicherungen, inklusive Beihilfe und Zusatzversicherungen, die für den Erfolg der APKV von großer Bedeutung sind, bringst Du Deine medizinische und prozessuale Expertise ein. Aktive Gestaltung der Risikoprüfung: Du bist maßgeblich an der prozessualen Entwicklung und Weiterentwicklung der medizinischen Risikoprüfung beteiligt, indem Du neue Prozesse aktiv gestaltest und bestehende Abläufe optimierst. In Projekten wie der „Risikoprüfung4Future" bringst Du Deine Expertise ein und setzt kreative Lösungen um. Medical Underwriting: Du übersetzt medizinische Erkenntnisse in wirtschaftlich sinnvolle, kundenfreundliche und risikoadäquate Entscheidungen. Du definierst fachliche Anforderungen und entwickelst gemeinsam im Team innovative Lösungen für Antrags- und Entscheidungsprozesse im Neugeschäft. Fundierte Entscheidungsvorbereitung: Du arbeitest analytisch und strukturiert, um sicherzustellen, dass Entscheidungen auf fundierten Grundlagen basieren. Du bereitest Informationen und Analysen so auf, dass sie als solide Basis für strategische Entscheidungen dienen und arbeitest proaktiv Handlungsoptionen für zukünftige Weichenstellungen vor Marktbeobachtung und Innovation: Du beobachtest Markt- und Technologietrends und verwandelst diese in konkrete Innovationschancen für die Allianz. Deine medizinische Expertise hilft dabei, komplexe Sachverhalte in verständliche und umsetzbare Informationen zu verwandeln und die Risikoprüfung kontinuierlich zu verbessern. Fachliche Analyse: Du setzt moderne Analysetools ein, um neue Impulse zu geben und den Einsatz von KI weiter voranzutreiben. So prägst Du das Erlebnis unserer Kund:innen, Mitarbeiter:innen und externen Stakeholdern beim ersten Kontakt mit der Allianz Privaten Krankenversicherung-AG nachhaltig. Qualifikation: Abgeschlossenes Studium in Humanmedizin, medizinischer Informatik oder einem vergleichbaren Fachgebiet Prozesserfahrung: Nachweisbare Erfahrung in der Entwicklung und Implementierung von Risikoprüfungs- und Antragsprozessen - nicht nur Anwendung, sondern aktive Konzeption Datenanalyse: Fundierte Erfahrung in der Analyse großer Datenmengen, Identifikation relevanter Fragestellungen und Überführung in belastbare Risikomodelle (z. B. mit SQL oder vergleichbaren Tools) KI & Digitalisierung: Erfahrung im Einsatz moderner Analyse-Tools und datenbasierter Methoden, idealerweise KI-gestützter Technologien zur Prozessoptimierung Arbeitsweise: Analytisch, strukturiert und proaktiv - mit dem Anspruch, evidenzbasierte Entscheidungsgrundlagen zu schaffen und innovative Impulse voranzutreiben Sprachkenntnisse: Sehr gute Deutsch- und gute Englischkenntnisse in Wort und Schrift Branchenwissen (wünschenswert): Erfahrung im Krankenversicherungswesen, in der Versicherungsbranche mit medizinischem Bezug und/oder in der Projektleitung Gesundheit & Wohlbefinden: Eine betriebliche Krankenversicherung, Sport- und Gesundheitsangebote sowie Präventionsmaßnahmen legen den Grundstein für körperliche und mentale Gesundheit. Vergütung: Tarifliche Sonderzahlungen, betriebliche Altersvorsorge, vermögenswirksame Leistungen und Mitarbeiteraktien machen die Vergütung besonders attraktiv. Außerdem werden Mitarbeiter am Unternehmenserfolg beteiligt. Zeit & Flexibilität: Mit unserem Modell „Neues Arbeiten“ können Beruf und Privatleben noch ... Homeoffice: Umfang: Nach Vereinbarung