Edwards Lifesciences
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Recently posted jobs
Healthtech • Pharmaceutical
Lead and oversee enterprise-scale programs from initiation through closure. Create and manage milestone plans, control scope/schedule/cost, coordinate resources, track risks/issues, communicate status to stakeholders, mentor project managers, drive PMO continuous improvement, and ensure program benefits and regulatory compliance within a medical device business unit.
Healthtech • Pharmaceutical
Develop and maintain a mission-critical hybrid Angular web application using Angular best practices. Build responsive, cross-browser UI/UX, implement complex reactive forms, fix performance and functional issues, write automated and manual tests, perform code reviews, document solutions, and collaborate within CI/Git workflows to deliver quality software integrated with backend APIs and Salesforce.
Healthtech • Pharmaceutical
Develop and own cardiac CT segmentation protocols and standardized annotations to support TAVR algorithm and AI development. Build Python tools for DICOM processing, define algorithmic measurement requirements, evaluate segmentation/analysis tools, and collaborate with clinicians to deliver end-to-end R&D solutions.
Healthtech • Pharmaceutical
Provide clinical and technical support for the Cordella PA Sensor System across Georgia. Support and attend implant procedures, deliver on-site training, troubleshoot devices, analyze data, liaise with physicians and hospital staff, lead site and cross-functional meetings, and help improve customer experience and product adoption.
Healthtech • Pharmaceutical
Supervise manufacturing employees, manage performance reviews, ensure staffing and training, monitor production metrics, and lead improvement projects.
Healthtech • Pharmaceutical
The Territory Manager drives sales for Edwards' TAVI in Tuscany and Umbria, managing relationships with heart centers, physicians, and hospital staff, and implementing strategic account plans to enhance business growth.
Healthtech • Pharmaceutical
Lead clinical input and lifecycle management for Class II/III transcatheter heart valve projects. Design and execute pre-clinical and first-in-man evaluations, develop clinical trial strategy and investigator brochures, support site training and regulatory submissions, perform literature reviews and clinical design control documentation, assess field performance and imaging, and guide cross-functional teams on clinical risk assessments and validation activities.
Healthtech • Pharmaceutical
Manage engineering teams and operations, ensure project deliverables, oversee equipment maintenance and improvements, and integrate financial metrics into projects.
Healthtech • Pharmaceutical
The Senior Engineer will develop and deploy machine learning models and workflows, mentor junior engineers, and collaborate with cross-functional teams to improve patient care through innovative solutions.
Healthtech • Pharmaceutical
Lead design, development, and support of enterprise data pipelines, ETL/ELT, Snowflake objects, Airflow workflows, and Power BI assets. Partner with IT and business teams to deliver secure, scalable data products, mentor engineers, produce technical documentation, and drive automation and quality improvements within a regulated environment.
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Healthtech • Pharmaceutical
Sell transcatheter mitral and tricuspid therapies in São Paulo; act as primary contact for territory, build long-term customer relationships, identify and close new business, meet sales targets, develop and execute annual regional plans, and apply clinical knowledge of cardiovascular anatomy and hemodynamic monitoring to influence customer decisions.
Healthtech • Pharmaceutical
The Senior Analyst, Process Excellence analyzes end-to-end processes using mining and analytics, builds KPI dashboards, and documents processes to identify improvement opportunities.
Healthtech • Pharmaceutical
Lead and execute multi-year strategic account plans for Germany's most strategic hospital accounts, coordinating cross-functional teams to grow sales, protect profitability, improve customer experience, and deploy tailored value-based solutions across business units.
Healthtech • Pharmaceutical
As a Principal Engineer, NPD Quality, you'll ensure compliance with quality standards, lead product development, and optimize engineering processes in medical device manufacturing.
Healthtech • Pharmaceutical
Supervise multiple production areas to ensure continuous manufacturing operations. Manage staffing, performance reviews, training, productivity, quality, scheduling, and materials. Lead improvement projects, partner with engineering on investigations and corrective actions, and maintain documentation and metrics for management and cross-functional stakeholders.
Healthtech • Pharmaceutical
Lead Quality Engineering for new product development of transcatheter heart valve devices. Apply design control, risk management, test method development, verification/validation, failure investigations, and transfer to manufacturing. Mentor direct reports, collaborate cross-functionally, ensure regulatory compliance, and implement inspection and test mechanisms to support successful product launches.
Healthtech • Pharmaceutical
The role involves developing and executing product marketing strategies, managing product launches, building relationships, and overseeing marketing collateral and compliance with regulatory requirements.
Healthtech • Pharmaceutical
Lead development and execution of the German transcatheter mitral and tricuspid therapies marketing strategy aligned with EU plans. Drive market development, product launches, events, KOL engagement, segmentation, and cross-functional collaboration to achieve local business goals and measure impact.
Healthtech • Pharmaceutical
The role entails executing label change packages, supporting updates to procedures, and ensuring compliance with established guidelines while collaborating cross-functionally.
Healthtech • Pharmaceutical
Perform field monitoring for clinical trials ensuring GCP and protocol compliance, validate device accountability and regulatory documentation, train and mentor staff, contribute to protocol/CRF development, verify source data and adverse event reporting, and provide oversight and process improvements for trial activities.


