Jobs at Edwards Lifesciences

Conducts advanced materials testing and characterization for medical device R&D, including method development, equipment validation, troubleshooting, data analysis, and failure-mode investigation. Maintains and calibrates laboratory equipment, develops fixtures and technical documentation, implements process improvements, and supports engineering change requests. Serves as a subject matter expert, collaborates with R&D and Quality teams, works with vendors, and trains lower-level employees.

Leads manufacturing quality investigations, CAPAs, nonconformance reviews, root cause analyses, and corrective actions. Drives Lean and Six Sigma continuous improvement, risk management, process optimization, documentation, validation, and compliance initiatives. Provides technical guidance, coordinates testing, supports engineering projects, and mentors technicians while collaborating across Manufacturing, Quality, and Engineering teams in a regulated medical device environment.

Supports training systems through LMS user assistance, training assignment configuration, employee profile and transcript data entry, data auditing and cleanup, reporting support, and resolution of routine customer support tickets. The role also assists with regulatory audit reporting and maintains data quality, confidentiality, and compliance with company and quality procedures.

Designs, develops, configures, tests, maintains, and supports ServiceNow HRSD solutions. Partners with HR, IT, and business stakeholders to translate requirements into scalable technology solutions, including case and knowledge management, Employee Center Pro, lifecycle events, integrations, document management, NowAssist, and Moveworks. Troubleshoots issues, supports automation and AI-enabled self-service, conducts training, and recommends improvements to increase case deflection and HR service delivery efficiency.

Leads end-to-end supply chain readiness for new product launches across EMEA. Manages launch plans, timelines, risks, dependencies, inventory, distribution, warehousing, systems, regulatory, and commercial readiness. Coordinates cross-functional teams, tracks milestones and performance, resolves issues, drives continuous improvement, and strengthens launch governance through lessons learned.

Sustains and improves the Application Lifecycle Management platform in a regulated medical device environment. Partners with quality, engineering, validation, IT, manufacturing, and vendor stakeholders to gather requirements, define workflows, manage enhancements, support testing and validation, maintain traceability and documentation, troubleshoot issues, facilitate governance, and drive user adoption through training and communication.

Coordinates regulatory submission deliverables, documentation packages, records, databases, and tracking tools for global medical device regulatory activities. Supports process improvements, compliance assessments, audits, inspections, and regulatory documentation maintenance. Collaborates with regulatory affairs teams and cross-functional stakeholders while ensuring accuracy, data integrity, and adherence to global requirements for medical devices.

Design, develop, test, debug, and deploy scalable cloud-native software in a regulated medical-device environment. Lead architecture, coding, prototyping, APIs, microservices, distributed systems, and full-stack development while applying Generative AI, LLMs, RAG, and AI agents. Provide technical leadership through code reviews, design discussions, mentoring, and cross-functional collaboration with product, clinical, quality, systems, and cybersecurity teams.

Leads architecture and full-stack development for scalable, secure, AI-enabled, cloud-based software supporting regulated medical-device products. The role drives system architecture, roadmaps, software validation, risk management, DevOps, Agile practices, and cross-functional collaboration while mentoring engineering teams. It requires expertise across web, mobile, distributed systems, cloud platforms, generative AI, medical-device software standards, and the full software development lifecycle.

Develop the transcatheter heart valve market across Washington, D.C. and Northern Virginia by selling medical devices, building provider relationships, supporting site launches, training clinicians, presenting patient selections, forecasting sales, managing inventory, and executing marketing strategies. The role requires advanced interventional cardiology knowledge, technical medical sales expertise, leadership, and frequent travel.

Lead design, implementation, operation, and maintenance of enterprise security architectures with emphasis on cloud and AI security. Provide technical leadership for security solutions, design secure architecture frameworks and patterns, guide integrations, support delivery lifecycle, and act as business liaison. Mentor colleagues and document build guides and configurations.

Manages and coaches medical device sales teams to achieve territory targets. Promotes transcatheter heart valve products, builds relationships with cardiologists and healthcare decision-makers, supports complex sales activities, and leads short- and long-term territory plans. Requires expertise in cardiovascular anatomy and medical device sales, with experience in patient activation, reimbursement, market development, and preferably cardiac or interventional devices.

Leads Edwards Lifesciences’ TMTT business across EEMEA, driving regional growth, therapy adoption, innovation launches, market access, reimbursement strategies, distributor performance, and patient access. Builds high-performing geographically dispersed teams, develops Centers of Excellence and key stakeholder networks, and partners across global, regional, clinical, and commercial functions to execute strategic priorities.

Provides specialist HR solutions and shared-services support across JAPAC. Responsibilities include employee data management, HR case escalation, troubleshooting, audits, system testing, process improvement, vendor management, standardized HR process delivery, stakeholder support, team coaching, and recommendations to improve employee experience. Requires collaboration with HRBPs, country HR teams, technology partners, third-party providers, and functional leaders.

Supports people development and learning initiatives, including facilitator programs, individual development plans, onboarding analysis, training improvement, and communications. Also develops dashboards, reports, SharePoint solutions, data architecture, and scalable technology-enabled processes using learning, workforce, and development data.

Applies quality engineering principles to medical device manufacturing and distribution. Investigates complaints, NCRs, CAPAs, ECRs, audits, and quality issues; oversees product release, MRB disposition, material controls, and equipment validations. Supports process validation, risk management, PFMEAs, quality metrics, manufacturing transfers, and continuous improvement using Six Sigma and Lean methods. Develops production documentation and training, coordinates technician activities, and collaborates with engineering, manufacturing, vendors, and project stakeholders to maintain regulatory and quality-system compliance.

Leads therapy development and product marketing for transcatheter heart valve programs across EEMEA. Converts clinical awareness into referrals and procedures through market strategy, patient and physician activation, referral planning, budget management, KPI ownership, and cross-functional coordination with Medical Affairs and Sales. Builds patient advocacy partnerships, supports field execution, ensures approvals and best-practice adoption, and influences regional stakeholders across multiple markets.

Leads Quality Engineering for medical device manufacturing operations, managing engineers and overseeing compliance, CAPAs, nonconformance investigations, validations, audits, quality metrics, supplier issues, and continuous improvement under ISO 13485 and 21 CFR Part 820.

Lead enterprise Developer Experience and cloud architecture strategy across Edwards Lifesciences. Design secure, scalable, compliant cloud solutions; establish developer platforms, DevSecOps capabilities, software delivery standards, infrastructure-as-code practices, and secure SDLC guardrails. Guide disaster recovery, high availability, architecture reviews, cloud governance, vendor relationships, and cross-functional initiatives. Mentor architects and support cloud-based product development in regulated manufacturing and quality environments.

Manage cost center finances, month-end close, reporting, budgeting, forecasting, variance analysis, compliance, and financial planning. Partner with business leaders on resource allocation, strategy execution, special projects, audits, and risk mitigation. Provide financial guidance, develop business-unit reports, support revenue and cost planning, and lead finance-related initiatives while ensuring compliance with GAAP, SOX, SEC, IRS, and Sunshine Act requirements.