Jobs at Edwards Lifesciences

The Senior Coordinator, Documentation supports Product Configuration Services by managing documentation changes, conducting audits, and providing training logistics. Responsibilities include creating reports, improving processes, and ensuring compliance with medical device regulations.

The role involves ensuring compliance with quality system processes, driving regulatory compliance, and improving quality processes through analysis and audits.

The Key Account Manager builds relationships with medical professionals, manages customer networks, develops business opportunities, and meets sales targets in the medical devices sector.

Support EEMEA regional growth by enabling new-country HR setups, ensuring compliant HR operations (payroll, benefits, visas), partnering on recruitment and capability-building, and managing vendor relationships.

The Senior Analyst, Data Analytics manages data pipelines and analytical models, delivering analytics and reporting to stakeholders. This role involves translating business needs into data requirements, building automated ETL processes, and ensuring data quality and governance.

The Senior Mechanical Design Engineer leads complex design projects, develops automated equipment, ensures compliance with standards, and mentors engineers while improving processes.

The Territory Manager is responsible for managing customer relationships, achieving sales targets, and developing new business opportunities in the medical devices sector, specifically focusing on cardiovascular products.

Lead business expansion in the TMTT unit by developing clinical content strategies, enhancing customer relations, and providing promotional training to sales teams.

The Senior Manager, Market Development is responsible for leading marketing strategies, managing teams, and overseeing market expansion plans for cardiovascular medical devices. This role requires collaboration with internal and external stakeholders and prioritizing resources for profitable growth opportunities.

The Senior Director of Plant Operations oversees site performance, ensuring compliance and quality in manufacturing while leading operations and engineering teams toward strategic objectives and operational excellence.

The Associate Specialist, Sales Training will develop and execute educational programs for healthcare providers and manage training logistics while overseeing lab materials and resources.

The Quality Engineer II investigates product quality issues, manages NCRs and CAPAs, collaborates on process validation, and ensures regulatory compliance.

Develop and enhance AI/ML solutions to improve patient care by collaborating with cross-functional teams and deploying machine learning models in production.

The Internship Program allows early-career professionals to gain experience in the medical device industry, focusing on Engineering, Quality, and Supply Chain Management over 6 months. Interns work in teams, enhancing patient lives while developing their skills.

The Senior Distinguished Engineer in R&D will lead product development for catheter delivery systems, solve complex engineering problems, mentor engineers, and ensure technical rigor while partnering across various departments.

The role involves strategic planning, performance management, and execution enablement in sales operations, focused on driving excellence in medical device sales.

Responsible for managing moderately complex congresses and event elements, including planning, contract negotiation, budgeting, and project management. Oversees onsite execution and supports communications with stakeholders in the healthcare industry.

The Sr Specialist in Clinical Imaging will analyze imaging modalities for case planning in TMTT, train healthcare teams, and improve imaging processes.

Manage clinical imaging for Transcatheter Mitral and Tricuspid Therapies, providing analysis, training, and improving imaging processes for optimal patient outcomes.

Manage regulatory affairs for Transcatheter Heart Valve products, ensuring compliance with global regulations and preparing submissions for regulatory agencies.