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📑 About the role: The Medical Affairs Manager will be responsible for executing high quality scientific activities in accordance with the medical strategies for the company’s portfolio. Responsibilities will span across data dissemination, maintaining relationships with key partners, contribution to therapy and brand strategy b ...

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📑 Are you studying science, medicine or nutrition and would like to gain practical experience in an international healthcare company during your studies? Then support our Medical-Scientific Affairs & Liaison Clinical Nutrition department from June 2024, which is part of the global Clinical, Medical and Scientific Affairs team, Pharma & Nutrition. ...

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📑 We’re looking for people who are determined to make life better for people around the world. Be part of our team in Bad Homburg near Frankfurt am Main and start as soon as possible as: Senior Advisor Clinical Research (m/f/d) - Hematology What challenges await you? Busines ...

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📑 Chemie-Scientific Technical Specialist (m/w/d) Anstellung bei der Hays Professional Solutions GmbH In Bad Homburg Startdatum: sofort Referenznummer: 495168/1 Diesen Job teilen oder drucken Ihre Aufgaben Selbstständige termingerechte Durchführung, Auswertung ...

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📑 We’re looking for people who are determined to make life better for people around the world. Lilly has a long history of research/development in the therapy area of Oncology, and of bringing innovative products to market that improve the lives of patients with oncologic diseases. Be part of our team in Bad Homburg near Frankfur ...

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📑 Sie studieren im Bereich der Naturwissenschaften, Medizin oder Ernährungswissenschaften und möchten bereits während des Studiums praktische Erfahrungen in einem internationalen Gesundheitsunternehmen sammeln? Dann unterstützen Sie ab Juni 2024 unsere Abteilung Medical-Scientific Affairs & Liaison Clinical Nutrition, welche ein Teil des globalen ...

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📑 Patienten, Ärzte und Apotheker stehen im Mittelpunkt unseres Denkens und Handelns. An ihren Bedürfnissen orientieren wir uns. Mit unseren Spezialpharmazeutika und Biosimilars eröffnen wir schwer und chronisch erkrankten Patienten Zugang zu hochwirksamen, wirtschaftlichen Behandlungsmöglichkeiten. Mit innovativen Therapie- und Service-Angeboten i ...

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📑 Sie studieren Medienwissenschaften, Graphic Design, Digitales Business oder auch Marketing und möchten bereits während des Studiums hinter die Kulissen eines internationalen Gesundheitsunternehmens blicken sowie Ihr erlerntes Wissen direkt mit Kreativität in die Praxis umsetzen? Dann unterstützen Sie ab sofort unser Team Education & Trainin ...

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📑 Meda Pharma GmbH & Co KG At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing ...

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📑 Fresenius Medical Care is the world’s leading provider of products and services for individuals with renal diseases of which around 3.9 million patients worldwide regularly undergo dialysis treatment. We care for more than 344,000 dialysis patients and provide our products in around 150 countries. With a strong focus on innovation, qual ...

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📑 Fresenius Medical Care is the world’s leading provider of products and services for individuals with renal diseases of which around 3.9 million patients worldwide regularly undergo dialysis treatment. We care for more than 344,000 dialysis patients and provide our products in around 150 countries. With a strong focus on innovation, qual ...

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📑 Sie haben eine sorgfältige Arbeitsweise und Spaß an der Archivierung von Dokumenten? Dann unterstützen Sie zum nächstmöglichen Zeitpunkt unser Office Administration Team im Bereich Clinical Trials & Data Management / Medical Scientific Affairs! Im Rahmen Ihres Einsatzes erhalten Sie interessante Einblicke in die Arbeit eines medizinisch-wissens ...

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📑 Main tasks: Material compliance: Evaluation of raw materials as well as finished products concerning regulatory EHS-requirements on substances and materials (REACH, POP, MDR, CLP, Packaging Directive etc.) Contact person to external supplier concerning the before mention ...

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📑 Your assignments: Driving clinical application collaboration Serves as a “customer relationship manager” point of contact with external partners (e.g. hospitals, ICUs, HCP) to monitor emerging trends in clinical practice; communicates that information to project teams in a form that is concise and understandable for ...

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📑 Your Job Ensure vendor/supplier qualifications are carried out in line with company policy and procedure Work cross functionally to resolve supplier related issues and drive continuous improvement Complete vendor/supplier questionnaires on behalf of the QA function against agreed timeframes <l ...

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📑 We’re looking for people who are determined to make life better for people around the world. The demand for high quality health economic and outcomes research (HEOR) and real-world evidence (RWE) to support drug development, health technology assessment/access decisions, product differentiation, and clinical decision making continues t ...

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📑 Medical Director Here at Fresenius Medical Care, we pride ourselves for being the leading provider of dialysis services to the NHS and are looking for a Medical Director to support with our Clinical Vigilance and Pharmacovigilance matters within our Nephrocare business. We are looking for somebody who is already a m ...

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📑 In your role as Regulatory Affairs Manager (m/f/d) you will support product registrations, provide design input and assess changes to ensure regulatory product availability on global markets. Your assignments: Obtain and sustain global registrations for product portfolio as per Regulatory Strategy and product roadmap <li ...

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📑 Caring for People's Health as a Trusted Partner - This mission motivates us at STADA every day to improve the health of people worldwide. With our wide range of generics, consumer health products and specialty pharmaceuticals, we offer patients, doctors and pharmacists a wide range of therapeutic options. Around 13,000 employees live o ...

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📑 Your assignments in the Product group “Concentrates and Disinfectants”: Product Quality expertise Coordination of major quality issue management including root cause analysis, CAPA and follow up analysis Monitoring and reporting of quality KPIs analyzing trends and failure trend analysis Preparation and p ...

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📑 Your Tasks: Creation and maintenance of non-clinical documentation for medicinal products, e.g., CTD modules 2.4 and 4 in alignment with Global Drug Regulatory Affairs and other relevant stakeholders Responsibility for the content of the above-mentioned regulatory information (subject matter e ...

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📑 In your role as Assistant Medical, Safety & Post Market Surveillance (m/w/d) you will be responsible for effective administrative support for the supervisors and managers of the System, Quality and Regulatory department with a focus on the Medical, Safety & PMS department. Your tasks Planning and coordination of inte ...

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📑 PURPOSE AND SCOPE: Develops regulatory strategies for assigned products/product lines. Prepares regulatory submissions required to market new or modified medical devices in the domestic and international clinical markets. Develops and maintains procedures and systems designed to ensure the product development process addresses ...

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📑 The ideal candidate should have US Advertising and Promotion experience. This position can be fully remote. PURPOSE AND SCOPE: Ensures company products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post-marketing compliance. Develops, coordinates, reviews a ...

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📑 This position can be fully remote Global Regulatory experience needed. Demonstrated project management experience needed. PURPOSE AND SCOPE: Ensures company products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post-marketing compliance. Develops, ...

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