descriptif du postePrêt(e) à jouer un rôle clé dans un cabinet médical en tant que Secrétaire médical(e) ?Vous jouerez un rôle clé en assurant un accueil chaleureux et en coordonnant efficacement les activités administratives quotidiennes d'un établissement médical. - Accueillir les patients avec courtoisie et les renseigner pour garantir un service de qualité - Gérer la planification des rendez-vous et interventions tout en s'adaptant aux imprévus - Fa

For an international company specialized in clinical trials, we're looking for a Medical Technologist.

As Lab Technician you'll perform essential laboratory procedures including sample processing, testing, and analysis while maintaining the highest standards of quality and safety. 

Your Key Responsibilities:

• Performs, reviews, and interprets complex, esoteric, and routine chemical, hematological, coagulation, renal, lipid, and hormonal analyses by manual, automated, and/or microscopic means.
• Integrates analytical results with specific and highly varied clinical trial protocols to evaluate credibility, appropriateness and accuracy of test results in order to facilitate entry or exclusion of subjects from research programs.
• Operates, maintains, troubleshoots and repairs clinical laboratory equipment, including routine preventative maintenance, calibrations, and safety checks.
• Recognizes and pursues instrument problems and resolutions.
• Evaluates analytical reagents, calibrators, and QC standards to ensure the accuracy of analytical results.
• Evaluates quality control procedures, evaluates results, and implements corrective action when indicated.
• Assists in carrying out ongoing statistical data anal

We're looking for someone with a Bachelor's degree in a science-related field, such as Biology, Medical Technology, or Chemistry. Fluent knowledge of English is a must, as all company communication and documents will be issued in English. Prior experience as a Med. Tech in a laboratory is essential.

Required skills, KNnwledge:

• Demonstrated knowledge of laboratory safety protocols and aseptic techniques
• Proficiency in handling and processing biological specimens and hazardous materials
• Experience with Laboratory Information Management Systems (LIMS) preferred
• Ability to operate standard laboratory equipment and analytical instruments
• Strong organizational and time management abilities to handle multiple tasks
• Excellent written and verbal communication skills in English
• Physical ability to lift up to 50 lbs and work in temperature-controlled environments
• Knowledge of GMP/GLP practices preferred
• Ability to stand for extended periods and perform repetitive tasks
• May require working in cold environments with exposure to dry ice and liquid nitrogen
  

Flex Logo, Blue - Werken bij Flex - Cultuur Customer Focus Team (CFT) Employee Medical 32 - 40 uur v.a. € 2.590,- Venlo, Heierhoevenweg Jouw nieuwe baan bij Flex Customer Focus Team (CFT) Employee Medical Wij zijn op zoek naar een CFT Employees die verantwoordelijk is voor de planning, communicatie en andere administratieve taken voor één van onze medical klanten. Jij zorgt ervoor dat de goederen van de klant op tijd in ons warehouse aankomen en weer vertrekken. Je wordt onderdeel van een team voor onze huidige of onze nieuwe klant. In deze functie rapporteer je aan de Account Manager. Wat ga je doen? - Je bent het eerste aanspreekpunt voor klanten via e-mail, telefoon, chat en andere communicatiekanalen; - Je levert uitstekende klantenservice door accurate, volledige en tijdig informatie te verstrekken; - Beheer van klantorders, retouren, replacements, klachten, klantfeedback en accountvragen; - Monitoren van klantfeedback en identificeren van terugkerende problemen; - Volg klantverzoeken op met betrekking tot urgente orders, werkorders en andere kwesties; - Ondersteun procesverbeteringen die de klantervaring verbeteren; - Beheer en prioriteer de dagelijkse workload om service level agreements te halen of te overtreffen; - Monitor de voortgang van je eigen afdeling en van het warehouse; - Werk nauw samen met andere afdelingen; - Monitor de KPI's en identificeer tijdig afwijkingen; - Neem deel aan dagelijkse en wekelijkse interne en externe voortgangsvergaderingen; - Stel diverse rapportages op; - Breng veelvoorkomende problemen in kaart, los deze op en denk mee over procesoptimalisatie; - Houd werkinstructies up-to-date Wat heb je nodig? - Opleiding en/of ervaring gelijkwaardig aan MBO+ niveau; - Ervaring in een internationale Customer Service omgeving is een vereiste; - Administratieve vaardigheden; - Ervaring met WMS/ERP-systemen en zeer goede kennis van MS Office; - Goede communicatieve vaardigheden in het Engels; - Fle...

For an international company specialized in clinical trials, we're looking for a Medical Technologist.

As Lab Technician you'll perform essential laboratory procedures including sample processing, testing, and analysis while maintaining the highest standards of quality and safety. 

Your Key Responsibilities:

• Performs, reviews, and interprets complex, esoteric, and routine chemical, hematological, coagulation, renal, lipid, and hormonal analyses by manual, automated, and/or microscopic means.
• Integrates analytical results with specific and highly varied clinical trial protocols to evaluate credibility, appropriateness and accuracy of test results in order to facilitate entry or exclusion of subjects from research programs.
• Operates, maintains, troubleshoots and repairs clinical laboratory equipment, including routine preventative maintenance, calibrations, and safety checks.
• Recognizes and pursues instrument problems and resolutions.
• Evaluates analytical reagents, calibrators, and QC standards to ensure the accuracy of analytical results.
• Evaluates quality control procedures, evaluates results, and implements corrective action when indicated.
• Assists in carrying out ongoing statistical data anal

We're looking for someone with a Bachelor's degree in a science-related field, such as Biology, Medical Technology, or Chemistry. Fluent knowledge of English is a must, as all company communication and documents will be issued in English. Prior experience as a Med. Tech in a laboratory is essential.

Required skills, KNnwledge:

• Demonstrated knowledge of laboratory safety protocols and aseptic techniques
• Proficiency in handling and processing biological specimens and hazardous materials
• Experience with Laboratory Information Management Systems (LIMS) preferred
• Ability to operate standard laboratory equipment and analytical instruments
• Strong organizational and time management abilities to handle multiple tasks
• Excellent written and verbal communication skills in English
• Physical ability to lift up to 50 lbs and work in temperature-controlled environments
• Knowledge of GMP/GLP practices preferred
• Ability to stand for extended periods and perform repetitive tasks
• May require working in cold environments with exposure to dry ice and liquid nitrogen

Le Centre Hospitalier de Saint-Tropez est en direction commune avec le Centre Hospitalier Intercommunal de Frejus Saint-Raphael et l'établissement pour personne âgée dépendante (EHPAD) Peirin de Cogolin. II assure la prise en charge des Urgences et dispose de 167 lits et places d'hospitalisation et d'hébergement. Depuis janvier 2022, il intègre l'établissement d'hébergement pour personne âgée dépendante (I'EHPAD de Grimaud) qui est fusionné avec le Centre Hospitalier. Avantages : * RTT * Possibilité de restauration sur place le midi (self) * Possibilité de logements temporaires * Parking gratuit * Formation * Remboursement des transports publics à 50% CDI/MUTATION MISSIONS PRINCIPALES * Participation à la conception, à l'élaboration et à la mise en uvre des décisions dans le domaine RH * Encadrement des agents du service des ressources humaines (4 personnes) * Participation au pilotage des RH et de la masse salariale * Coordonner les affaires médicales en lien avec l'adjoint des cadres en charge du personnel médical MISSIONS SPECIFIQUES * Gestion des effectifs : suivi des mobilités internes, suivi des tableaux de bords * Statistiques : RSU, études et enquêtes diverses * Dialogue social : LDG, gestion des droits syndicaux, rédaction de protocole d'accord... * Gestion administrative des personnels : avancements, évaluations, retraites, positions statutaires * Coordonner et superviser les processus de gestion RH des personnels affectés au site : - Organiser le suivi des affectations et des changements de statut des personnels du site, - Veiller à la conformité des processus de gestion du temps de travail sur le site, gestion des absences au travail des personnels du site (arrêts de travail, autorisations d'absence, absences injustifiées, grève, ), - Garantir la conformité du processus de paie des agents affectés sur le site (saisie et contrôle des éléments variables de paie et de l'ensemble des évènements impactant la rémunération), * Gestion des concours et examens professionnels * Participation et suivi du CSE * Veille juridique : recueil et analyse des documents et textes relevant du service RH * Gestion et suivi des procédures disciplinaires et des contentions agents * Participation à des groupes de travail : égalité H/F, qualité de vie au travail... * Coordination avec le GHT83 : marché, réunions... * Pilotage des effectifs et de la masse salariale en lien avec la DAF Vous êtes titulaire d'un diplôme de niveau Bac + 3 à bac + 5 en gestion des ressources humaines, droit social, droit public, gestion et administration des établissements de santé, gestion des entreprises et des administrations ou d'un diplôme d'IEP, d'IPAG ou d'écoles de management ou de gestion avec spécialisation RH ou service public ou avez validé le Cycle de formation des attachés d'administration hospitalière (EHESP) Une 1ère expérience d'encadrement dans un établissement hospitalier ou en ressources humaines dans le secteur public est souhaitée Savoir faire : * Capacité d'organisation et savoir prioriser les action * Capacité à gérer des dossiers/situations urgentes de manière appropriée * Capacité à transmettre les informations * Capacité rédactionnelle * Maitrise des logiciels bureautiques * Capacité d'animation d'équipe, conduite de réunion * Sens des responsabilités Cécile CRAVERO * * Contrat : CDI;Détachement;Mutation

The successful candidate will: Design and deliver engaging, high-quality teaching across the MBBS programme;

Other Remarks:
For details applicaton - https://form.jotform.com/250784338080358 - Closing date of Application - 18th May 2026

Head of Quality Operations Medical Präzision, die Leben schützt \- gestalte die Qualität von morgen. Seit mehr als 130 Jahren steht die Gruppe für Präzision. Heute sind wir ein global aufgestelltes, dynamisches Familienunternehmen mit 9 Standorten weltweit. In der Division Medical entwickeln und produzieren wir Komponenten, bei denen Qualität keine Option, sondern eine Verpflichtung ist. Um unseren hohen Standard am Standort weiter auszubauen, suchen wir eine führungsstarke Persönlichkeit als Head of Quality Operations Medical. In dieser Rolle berichtest du direkt an den Head of Quality und führst die Teams Quality Engineering sowie Quality Support. Head of Quality Operations Medical Aufgaben In dieser Schlüsselposition stellst du sicher, dass unsere Prozesse und Produkte die regulatorischen Anforderungen erfüllen und gleichzeitig operative Exzellenz gelebt wird Du leitest und coachst die Teams Quality Engineering und Quality Support. Du förderst eine Kultur der Eigenverantwortung und kontinuierlichen Verbesserung Du verantwortest die Qualitätssicherung entlang des gesamten Produktlebenszyklus – von der Bemusterung bis zur Serienfertigung Du stellst die strikte Einhaltung der ISO 13485 sicher und führst Audits sowie komplexe Validierungsprozesse Du bist der Sparringspartner für Produktion, Engineering und Kunden bei qualitätsrelevanten Fragestellungen und sorgst für eine reibungslose Interaktion innerhalb der Matrix\-Organisation Du überwachst Qualitätskennzahlen, leitest bei Abweichungen gezielte Massnahmen ein und treibst Risikoanalysen (FMEA) sowie Ursachenanalysen (8D, Ishikawa) voran Voraussetzungen Du bist ein Profi im regulierten Umfeld, der es versteht, Normen pragmatisch in den Alltag zu integrieren, ohne den Blick für die Effizienz zu verlieren Abgeschlossenes Studium im Bereich Ingenieurwesen, Medizintechnik oder eine vergleichbare technische Ausbildung mit höherer Fachweiterbildung Mehrjährige Berufserfahrung im Qualitätsmanagement der Medizinaltechnik (ISO 13485\). Erfahrung in der Automobilindustrie (IATF 16949\) ist ein willkommenes Plus Du bringst ausgewiesene Führungserfahrung mit und verstehst es, Teams zu motivieren und fachlich weiterzuentwickeln Versierter Umgang mit Q\-Tools (CAPA, Validierungen IQ/OQ/PQ, MSA, SPC) Verhandlungssichere Deutsch\- und sehr gute Englischkenntnisse Du agierst durchsetzungsstark, entscheidungsfreudig und behältst auch in komplexen Situationen den Überblick Wir bieten Ein langfristig ausgerichtetes Familienunternehmen mit modernster Infrastruktur Du bist nicht nur Verwalter, sondern aktiver Gestalter unserer Qualitätsprozesse am Werkplatz Kurze Entscheidungswege, ein dynamisches Team und eine offene Kommunikation auf Augenhöhe Attraktive Anstellungsbedingungen und Unterstützung bei deiner beruflichen Weiterentwicklung Bereit für den nächsten Schritt? Wenn du die Qualität unserer Medizinalprodukte auf das nächste Level heben möchtest, freuen wir uns auf deine Bewerbung. Sende uns deine Unterlagen direkt online zu. Kontakt Charly Baggenstos Head of HR Switzerland Federn AG Telefon: jidcb81932jm jit0518jm jiy26jm

PhD Position in Medical Entomology (100%) The Swiss Tropical and Public Health Institute (Swiss TPH) is a world\-leading institute in global health with a particular focus on low\- and middle\-income countries. Associated with the University of Basel, Swiss TPH combines research, education and services at local, national and international level. Around 1000 staff and students from 96 nations work at Swiss TPH focusing on climate change, environment and health, infectious and non\-communicable diseases, societal and cultural context, and health systems and policies. The Vector Biology Group is inviting applications for a PhD Position in Medical Entomology (100%) Our research group investigates the biology, surveillance and control of insect vectors of human pathogens. We are offering a PhD position to study the behaviour and ecology of the invasive Asian tiger mosquito, Aedes albopictus, and to evaluate innovative, community\-based control strategies – including large\-scale adult mosquito trapping – in Basel, Switzerland, as part of a cluster\-randomised controlled trial. YOUR VARIOUS RESPONSIBILITIES INCLUDE: Plan and conduct field experiments on mosquito behaviour and ecology Collect, manage and analyse entomological and environmental data Contribute to the development and evaluation of community\-based vector control strategies Support the implementation of a cluster\-randomised controlled trial Publish results in peer\-reviewed journals and present findings at scientific conferences YOU SHOULD HAVE THE FOLLOWING EXPERIENCES AND SKILLS IN: Master’s degree in biology, ecology, epidemiology, entomology or a related field Strong interest in vector biology, applied entomology and public health Experience with fieldwork and experimental design Ability to work independently and as part of an interdisciplinary team Quantitative skills and experience with statistical analysis (e.g. R) are an advantage Excellent communication skills in English; knowledge of German is an asset WHAT WE OFFER: PhD position within a dynamic and interdisciplinary research environment The candidate will be registered with the University of Basel Remuneration is according to the Swiss National Science Foundation salary scheme for PhD students Opportunities to contribute to applied public health research with real\-world impact Access to modern research infrastructure and international collaborations Training and career development opportunities JOB CONDITIONS: Start Date: 1 July 2026 Duration: 3 years Percentage: 100% Location: Allschwil, Switzerland Travel required: No Internal job title: PhD student HOW TO APPLY: Please submit your application onlinewith: CV Motivational letter including names and contact information (email or phone) of 1 – 2 references Reference letters and diploma Swiss TPH is committed to fostering an inclusive and diverse workplace that values and respects differences across gender, race, ethnicity, disability, sexual orientation, and socio\-economic background. We believe that diversity strengthens our work, and we are dedicated to providing equal opportunities for all. Please note that we can only accept applications via our online recruiting tool . As long as the position is online on our company website, we are open to new applications. Applications via e\-mail or external recruiter/agency will not be considered. Join us in improving people’s health and well\-being worldwide – we look forward to receiving your application. CONTACT: Viviane Brodmann, Student Help Recruiting, Tel: Tel: jid05fd2ebjm jit0418jm jiy26jm

Position: Medical Imaging Specialist – CT Segmentation & Ground Truth Annotation Location: Uppsala, Sweden Employment: Fixed-term, 12 months, full-time (100%) Salary: 35,000 SEK/month Start date: By agreement About CarcinoQuant AB CarcinoQuant AB is a Swedish medtech company developing an automated tool for quantitative analysis of CT images in oncology. Our platform is designed to measure tumour volume and track tumour growth over time, providing clinicians and researchers with objective, reproducible metrics for monitoring cancer progression. We are building the next generation of AI-driven decision support for oncology imaging, and we are now looking for a skilled medical imaging specialist to support the development of our AI models. About the role You will perform expert manual segmentation of tumours in CT images, creating high-quality ground truth datasets used to train and validate CarcinoQuant's automated AI models for cancer analysis. The work requires precision, domain knowledge, and an understanding of radiological imaging in oncology. Your contributions will directly determine the quality and clinical validity of our AI system. The role will also comprise LLM training and programming work but the primary work to be undertaken will be the aforementioned annotation work. Responsibilities Manual delineation and segmentation of tumours in CT image datasets Quality control and review of segmentation outputs Contributing to the development of annotation protocols and guidelines Collaborating with the technical team on iterative model improvement Requirements Degree in medical imaging, radiography, medical physics, or a related field At least two years of practical experience with CT imaging in an oncological or radiological setting Solid understanding of tumour morphology and radiological anatomy Proficiency in English (working language) Experience with segmentation software or medical image annotation tools Familiarity with AI/ML workflows in medical imaging Experience with DICOM data

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).