Principal Medical Device Regulatory Specialist

Principal Device Technical Regulatory Specialist page is loadedPrincipal Device Technical Regulatory SpecialistApply locations Northern Cross, Dublin, Ireland time type Full time posted on Posted Today job requisition id R5660652 McDermott Laboratories LimitedAt VIATRIS, we see healthcare not as it is but as it should be.We act courageously and are uniquely...

Principal Device Technical Regulatory SpecialistMcDermott Laboratories LimitedViatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing high quality trusted medicines regardless of geography or circumstance; Leadership – Advancing sustainable operations and innovative solutions to improve patient health;...

Principal Device Technical Regulatory Specialist page is loadedPrincipal Device Technical Regulatory SpecialistApply locations Northern Cross, Dublin, Ireland time type Full time posted on Posted Today job requisition id R McDermott Laboratories LimitedAt VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely...

Principal Device Technical Regulatory Specialist page is loadedPrincipal Device Technical Regulatory SpecialistPostuler locations Northern Cross, Dublin, Ireland time type Temps plein posted on Offre publiée il y a 9 jours job requisition id R5660652 McDermott Laboratories LimitedChez Viatris, nous envisageons la santé non pas telle qu'elle est mais telle...

Job SummaryThe role of Regulatory Affairs Specialist is crucial for the post-market activities of medical devices, supporting departmental regulatory processes and procedures, strategies, authoring, reviewing, and supporting global registrations.Main Responsibilities:Support regulatory strategies for OUS medical devices and combination products, ensuring...

Regulatory Specialist for Medical DevicesThis position requires a subject matter expert in the application of FDA, EU and ISO standards, regulations and guidance related to design control and regulatory compliance.The successful candidate will maintain detailed awareness and understanding of current regulations and regulatory guidance in regions of interest...

Regulatory Affairs ExpertiseThe Senior Specialist in Regulatory Affairs is responsible for post-market activities for medical devices, supporting departmental regulatory processes and procedures. Main Responsibilities:Develop and execute regulatory strategies for OUS medical devices and combination products.Create regulatory documentation such as CIAs,...

Regulatory Support RoleWe are seeking a highly organized and detail-oriented professional to provide administrative and regulatory support within our Medical Devices department.Key Responsibilities:Process regulatory cases, correspondence, and certificates of free saleManage data entry, updates, and document control for compliance with EU and national...

At the core of our mission to improve patient lives, we're a dedicated team connected by a shared purpose.Job SummaryThis role is pivotal in supporting our regulatory processes and procedures, strategies for worldwide post-market surveillance activities, and maintaining knowledge of current US, EU, and international regulations/guidelines/policies related to...

Senior Regulatory Affairs SpecialistAs a Senior Regulatory Affairs Specialist, you will be responsible for leading post-market activities for Administration and Safety System medical devices.Key Responsibilities:Complete global Post Market Surveillance (PMS) activities and assignments for Administration and Safety System medical devices in West's...