Jobs at Medela

Leads global Amazon and digital shelf performance across Amazon, Walmart, Target, and other retailers. Manages PDP optimization, Salsify content operations, syndication, localization, catalog issue resolution, SEO, analytics, testing, and content deployment. Partners cross-functionally with marketing, sales, product, IT, regulatory, regional teams, agencies, and vendors to improve product discoverability, conversion, content quality, and eCommerce execution.

Lead complex, cross-functional medical device development projects from initiation through commercialization. Responsibilities include defining objectives, maintaining integrated plans, managing risks and dependencies, coordinating multidisciplinary stakeholders, facilitating decisions, overseeing governance, communicating with leadership, and improving R&D project management practices. The role requires strong influence, accountability, strategic thinking, and execution within a regulated product development environment.

The Verification Engineer will lead system and subsystem verification for electromechanical medical devices. Responsibilities include defining V&V strategies, developing test plans and protocols, conducting software integration and acceptance testing, analyzing verification data, preparing regulatory documentation, resolving anomalies, validating test methods, and verifying cloud-connected and IoT features. The role collaborates with system architects and R&D engineers and serves as the technical project leader for verification activities.

Leads Amazon eCommerce growth through performance analysis, forecasting, promotional effectiveness, assortment and pricing optimization, competitive intelligence, margin improvement, and digital shelf recommendations. Serves as the Amazon 1P and Vendor Central expert, translating data into commercial actions while partnering with Sales, Finance, Marketing, Supply Chain, Demand Planning, Analytics, and IT. Builds scalable reporting, automation, and global Amazon capabilities.

Leads system architecture, requirements development, integration, verification, validation, risk management, and technical documentation for complex electromechanical medical devices. Collaborates across mechanical, electrical, software, and cross-functional teams to define interfaces, connected-device technologies, and technical direction. Supports FDA-regulated product development, design controls, audits, and international market requirements while providing hands-on systems engineering leadership.