Drug Regulatory Affairs Manager

Company Overview:Meda Pharma GmbH & Co KG, part of Viatris, is dedicated to transforming healthcare by addressing the evolving needs of patients worldwide. We strive to empower individuals to lead healthier lives at every stage.Role Overview:The Corporate Drug Regulatory Affairs Manager plays a crucial role in ensuring compliance and excellence in our...

Company Overview:Meda Pharma GmbH & Co KG is part of Viatris, a company that envisions healthcare as it should be. We are committed to providing stability in a rapidly changing healthcare landscape.Role Overview:The Corporate Drug Regulatory Affairs Manager plays a pivotal role in ensuring compliance and excellence in regulatory practices within the...

Company Overview: Meda Pharma GmbH & Co KG, part of Viatris, envisions healthcare as it should be, acting decisively to meet the evolving needs of the healthcare landscape. Our mission is to empower individuals globally to lead healthier lives at every stage. Role Overview: The Corporate Drug Regulatory Affairs Manager plays a pivotal role in ensuring...

Company Overview:Meda Pharma GmbH & Co KG, a part of Viatris, is dedicated to transforming healthcare to meet the evolving needs of patients globally. We are committed to providing high-quality, trusted medications and fostering partnerships that enhance patient health.Role Overview:The Corporate Drug Regulatory Affairs Manager plays a pivotal role in...

Company Overview:At Viatris, we envision healthcare not merely as it exists but as it ought to be. We take bold steps and are uniquely positioned to provide stability in a landscape of shifting healthcare demands.Our Mission:Viatris empowers individuals globally to lead healthier lives at every stage of their journey.Our Approach:We achieve this...

Are you driven by the desire to influence the healthcare landscape? Siemens Healthcare Diagnostics Products GmbH is seeking a Director of Regulatory Affairs based in Marburg to uphold the excellence of our offerings for clients worldwide.Your Key Responsibilities:Oversee the Regulatory Affairs division in Marburg, managing global product registrations for...

Are you ready to influence the future of healthcare? Siemens Healthcare Diagnostics Products GmbH is seeking a Director of Regulatory Affairs in Marburg to uphold the integrity and quality of our offerings for clients worldwide.Your Key Responsibilities:Oversee the Regulatory Affairs division in Marburg, managing global product registrations for hematology,...

Are you driven by the desire to influence the healthcare landscape? Siemens Healthcare Diagnostics Products GmbH is seeking a Director of Regulatory Affairs in Marburg to uphold the excellence of our offerings for clients worldwide.Key Responsibilities:Oversee the Regulatory Affairs division in Marburg, managing global product registrations for hematology,...

Company Overview: At Viatris, we envision healthcare not merely as it exists, but as it ought to be. We act with determination and are uniquely positioned to provide stability in a landscape of changing healthcare demands.Our Mission: Viatris empowers individuals globally to lead healthier lives at every stage of their journey.Our Approach: We achieve this...

Job SummaryFresenius Medical Care is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for ensuring that our products meet regulatory requirements and comply with relevant laws and regulations.Key ResponsibilitiesProvide regulatory assessment and support to ensure...

Are you ready to influence the healthcare landscape? Siemens Healthcare Diagnostics Products GmbH is seeking a Director of Regulatory Affairs in Marburg to uphold the excellence of our offerings for a global clientele.Your Key Responsibilities:Oversee the Regulatory Affairs division in Marburg, managing worldwide registrations for hematology, hemostasis, and...

Über ViatrisBei Viatris betrachten wir das Gesundheitswesen nicht so, wie es ist, sondern so, wie es sein sollte. Wir handeln mutig und sind einzigartig positioniert, um eine Quelle der Stabilität in einer sich wandelnden Gesundheitslandschaft zu sein.Unsere MissionViatris befähigt Menschen weltweit, in jeder Lebensphase gesünder zu leben. Dies erreichen...

Your Responsibilities: Develop and manage non-clinical documentation for pharmaceutical products, ensuring compliance with CTD modules and aligning with Global Drug Regulatory Affairs and pertinent stakeholders. Act as the subject matter expert for the regulatory content mentioned above. Serve as the non-clinical authority for CTD module inquiries. Address...

Ihre AufgabeErstellung, Prüfung und Einreichung von nationalen und internationalen Zulassungsunterlagen für MedizinprodukteKommunikation mit benannten Stellen sowie mit nationalen und internationalen ZulassungsbehördenRegulatorische Begleitung der Neu- und Weiterentwicklung von Produkten und GerätenUnterstützung für das Risikomanagement im Lebenszyklus...

Ihre AufgabeErstellung, Prüfung und Einreichung von nationalen und internationalen Zulassungsunterlagen für MedizinprodukteKommunikation mit benannten Stellen sowie mit nationalen und internationalen ZulassungsbehördenRegulatorische Begleitung der Neu- und Weiterentwicklung von Produkten und GerätenUnterstützung für das Risikomanagement im Lebenszyklus...

Join Fresenius Medical Care as a Change Expert in Regulatory ComplianceKey Responsibilities:Overseeing global teams engaged in regulatory and compliance initiativesFacilitating the execution of projects to meet regulatory standardsServing as a liaison among various departmentsCoordinating communication on an international scaleAssisting in quality monitoring...

About the RoleWe are seeking a highly experienced Senior Manager to lead our Clinical Trial Supply Chain team. As a key member of our organization, you will be responsible for managing the end-to-end supply chain for assigned clinical studies, ensuring compliant, on-time delivery of study medication and ancillary materials to patients.Key...

About the RoleWe are seeking a highly experienced Senior Manager to lead our Clinical Trial Supply Chain team. As a key member of our organization, you will be responsible for managing the end-to-end supply chain for assigned clinical studies, ensuring compliant, on-time delivery of study medication and ancillary materials to patients.Key...

About the RoleWe are seeking a highly experienced Senior Manager to lead our Clinical Supply Chain team. As a key member of our organization, you will be responsible for managing the end-to-end supply chain for assigned clinical studies, ensuring compliant, on-time delivery of study medication and ancillary materials to patients.Key ResponsibilitiesSupply...

About the RoleWe are seeking a highly experienced Senior Manager to lead our Clinical Supply Chain team. As a key member of our organization, you will be responsible for managing the end-to-end supply chain for assigned clinical studies, ensuring compliant, on-time delivery of study medication and ancillary materials to patients.Key ResponsibilitiesSupply...