Designer

• Drive the evolution of Medtronic’s product development processes to set new industry-leading standards serving as a domain expert in Design Control
• Lead our team by coaching internal customers across our diverse product portfolio, to elevate Design Control capabilities throughout the organization
• Proactively identify and implement large-scale initiatives that enhance rigor, productivity and user experience by leveraging cutting-edge technologies and innovative methodologies
• Lead enterprise-wide initiatives with emphasis on Design, Reliability & Manufacturability (DRM) to ensure product quality, regulatory compliance and operational excellence across all Medtronic Operating Units (OU)
• Apply your technical expertise to Put Patients First every day
• Apply Design for Reliability and Design for Manufacturability principles to reduce risk, improve First Time Quality (FTQ), and enable efficient design transfer
• Guide cross-functional teams through the Product Development Process (PDP) with a strong focus on positive design control outcomes and regulatory adherence
• Serve as a subject matter expert in CAPA and Post-Market Surveillance (PMS), ensuring field performance insights are incorporated into early design phases
• Apply systems engineering principles to coordinate complex, multi-disciplinary product development efforts from concept through commercialization
• Leverage biomedical engineering knowledge to ensure designs meet functional, safety, and efficacy requirements in compliance with medical device standards
• Maintain deep familiarity with FDA 21 CFR Part 820, ISO 13485, and other design-controlled regulations, providing expert guidance on compliance throughout the development lifecycle
• Partner closely with R&D and Quality colleagues to embed best practices in technical rigor, simplify execution, and bring forward individual perspectives that strengthen decision-making and solution design

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