Device Development Regulatory Strategist

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,...

Job Title: Senior Regulatory StrategistThis position involves developing and maintaining strategic relationships with the Central Bank of Ireland (CBI).Key Responsibilities:Regulatory Liaison: Act as a primary liaison with regulators to ensure regulatory deliverables are met within CBI timeframes.Assist in making regulatory notifications and drafting...

Global Regulatory Affairs StrategistAre you a seasoned professional in regulatory affairs looking to take on a leadership role? We are seeking an Associate Director Regulatory Affairs to join our team and contribute to the development of global regulatory strategies for assigned products.

Senior Portfolio StrategistIn a rapidly evolving mobile technology landscape, you will spearhead the development and execution of a competitive device and future technology product portfolio across consumer and business segments.About This Role:Create comprehensive product portfolios that cater to diverse customer needsDemonstrate in-depth knowledge of...

Regulatory Compliance ExpertiseThis role makes a significant impact by:Providing subject matter expertise in the application of FDA, EU, and ISO standards, regulations, and guidance related to design control and regulatory compliance.Offering expert advice to the EU regulatory function on the device constituent of drug-device combination products, in...

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...

Job OverviewThis role is responsible for leading the technical regulatory compliance of medical devices and drug-device combination products. The successful candidate will have a strong understanding of FDA, EU, and ISO standards, regulations, and guidance related to design control and regulatory compliance.Key ResponsibilitiesMaintain awareness of current...

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...