Jobs at Edwards Lifesciences

Supports Edwards TAVI procedures across Eastern Canada by providing clinical and technical expertise to physicians, heart centers, and hospital teams. Responsibilities include proctoring, product training, cath lab and OR support, CT imaging interpretation, procedure planning, disease education, and customer relationship management. Requires cardiac cath lab or operating room experience, strong cardiovascular knowledge, French fluency, communication skills, MS Office proficiency, and willingness to travel 50%. This is a 14-month contract based in Montreal.

Analyzes 3D CT and other cardiovascular imaging modalities for transcatheter mitral and tricuspid therapy case planning. Produces imaging reports, performs advanced CT reconstructions, tracks planning workflows, enters measurements into CRM systems, trains field teams and healthcare providers, develops educational content, supports quality assurance, and recommends process improvements. The role requires extensive clinical echocardiography or cardiac sonography experience, relevant imaging certification, cardiovascular imaging expertise, and up to 15% U.S. travel.

Owns strategy and roadmaps for a data product and platform domain, as well as a defined clinical modeling research area. Writes detailed data and platform requirements, makes prioritization decisions, measures product outcomes, and partners technically with data engineers and data scientists. The role requires expertise in data product management, analytics, data contracts, service levels, schemas, pipelines, data quality, semantic definitions, and regulated clinical data governance.

Own product strategy and roadmap for a technical software product area within a regulated medtech organization. Translate marketing needs into detailed technical requirements, define acceptance and verification criteria, prioritize features and technical debt, evaluate architecture and API tradeoffs with engineering, conduct customer discovery, and measure business and technical outcomes. The role requires strong software product management expertise, technical depth, and familiarity with regulated software design controls, including 21 CFR 820.30 and IEC 62304.

Leads UX design direction for a medical device product area, owning design systems, accessibility, prototyping, and usability engineering. Plans formative and summative testing, conducts use-error analysis, and contributes human factors evidence for SaMD regulatory submissions. Partners with product, engineering, clinical, quality, and regulatory teams while mentoring designers and driving product strategy.

Represent Regulatory Affairs on medical device manufacturing and product development teams. Review technical documentation, guide regulatory strategy, prepare and oversee domestic and international submissions, support agency interactions and audits, monitor global regulations, and ensure labeling and product documentation comply with applicable requirements. The role focuses on Class II and III transcatheter heart valve devices and requires extensive regulatory submission experience.

Drives sales growth and market share for Edwards’ Transcatheter Heart Valve business across Sydney South and southern NSW. Manages customer relationships, identifies and closes new business, develops territory plans, and provides clinical expertise on structural heart therapies. The role requires knowledge of cardiovascular anatomy, pathology, physiology, medical devices, and competitive products, along with the ability to influence complex customer environments and achieve sales targets.

Supports JAPAC Business Operations by coordinating governance activities, operating cadences, strategic initiatives, portfolio tracking, capability management, stakeholder alignment, executive reporting, and continuous improvement across Digital Enablement, Analytics, and Data Governance teams.

Leads clinical data management for complex, multi-site studies, including defining data collection requirements, developing eCRFs and edit checks, coordinating user acceptance testing, creating data management plans, analyzing data quality trends, administering database access, resolving collection issues, and maintaining SOPs and training materials in compliance with clinical research regulations.

Leads enterprise marketing technology solutions across the MarTech stack. Responsibilities include gathering requirements, configuring and integrating platforms, developing roadmaps and documentation, managing enhancements and small-to-medium projects, testing systems, supporting governance and training, and partnering with IT, marketing, sales, stakeholders, and vendors. The role also evaluates emerging technologies, develops functional specifications, and provides system administration and business analysis support.

Leads clinical safety analytics, including dashboard design, safety data reconciliation, regulatory reporting, data quality control, and signal detection support. Manages a safety analytics team, partners with biostatistics, clinical data management, medical safety, and engineering teams, and translates reporting needs into technical requirements. Oversees process improvement, talent development, stakeholder communications, and corrective actions while ensuring compliant and timely clinical safety reporting.

Leads global training operations projects for TMTT programs, managing scope, timelines, risks, stakeholders, reporting, process improvements, training systems, content governance, certification workflows, product launch readiness, inventory planning, and training logistics. Partners across global functions and regions to improve scalability, compliance, operational efficiency, and training effectiveness.

Leads development, integration, validation, site transfer, and optimization of laser-based and optical tissue manufacturing processes for structural heart valves. Defines system architectures and specifications, manages technical workstreams and suppliers, troubleshoots equipment, executes experiments and process characterization, and supports regulatory-compliant qualification and production ramp-up. Mentors engineers and technicians while advancing laser safety, automation, yield, throughput, and quality across global manufacturing sites.

Leads the design, delivery, and continuous improvement of learning and development programs supporting commercial, clinical, leadership, selling, account management, and technical capabilities across Canada. Partners with business leaders, HR, talent, and regional stakeholders to align programs with strategic goals, drive Salesforce adoption, measure effectiveness, and support change management. Provides project leadership for strategic initiatives and promotes leadership ownership of sustainable workforce development.

Leads end-to-end plant operations, manufacturing engineering, site support, financial performance, workforce development, and operational strategy. Owns safety, quality, delivery, cost, inventory, capacity, compliance, continuous improvement, capital planning, and organizational effectiveness. Oversees manufacturing and engineering leaders, drives Lean and Six Sigma initiatives, supports product transfers and site growth, and maintains regulatory, audit, environmental, and EHS readiness in a regulated medical device manufacturing environment.

Provides attorney-supervised legal support through research, analysis, issue spotting, drafting memoranda and legal documents, and developing preliminary recommendations. Partners with attorneys, outside counsel, and business stakeholders on routine to moderately complex matters, business initiatives, legal processes, templates, and training materials. The role requires a J.D. from an ABA-accredited law school; bar admission is not required at hire. This is a full-time onsite position in Irvine, California.

The EDI Operations Analyst serves as the subject matter expert for electronic customer ordering, EDI connectivity, GHX integration, and hospital trading partner onboarding. Responsibilities include gathering requirements, troubleshooting transaction and order issues, analyzing process metrics, testing system changes, documenting workflows, coordinating stakeholders, training users, and supporting continuous improvement to increase electronic order adoption and reduce manual processing.

Supports and sustains manufacturing of transcatheter heart valve delivery systems. Optimizes processes, equipment, tools, and fixtures; conducts root cause analysis, experiments, testing, qualification, and validation; resolves compliance issues; develops documentation and training; coordinates technicians; and drives continuous improvement across production in collaboration with Quality, Operations, Complaints, and New Product Development teams.

Performs sewing and assembly steps for medical device valves using specialized tools and microscopes. Follows detailed work instructions, SOPs, GMP and clean room requirements; verifies completed work, records traceability information, maintains housekeeping, and follows safety and quality guidelines. Requires strong hand-eye coordination, basic computer skills, teamwork, and successful completion of ongoing assembly-process training.

Leads Edwards’ Germany country marketing strategy for transcatheter heart valves, translating European priorities into local execution and driving business growth. Oversees product and indication launches, localized marketing, therapy development, events, and KOL engagement. Leads the country marketing team and collaborates with Sales, Clinical, Training, Market Access, Governmental Affairs, and European Marketing. Requires strong MedTech marketing expertise, market analysis, clinical knowledge, stakeholder influence, fluent German and English, and 30–40% travel.