Jobs at Stryker

Develops complex medical devices from concept through commercialization by translating clinical and stakeholder needs into system requirements and architectures. Leads interface management, risk management, integration, verification, and validation across software, electrical, and mechanical disciplines. Supports trade studies, modeling, simulations, design assessments, and product risk activities. Creates design documentation, collaborates with clinical, quality, regulatory, manufacturing, and engineering teams, and mentors team members on development procedures and medical device standards.

Leads strategic sourcing for new product introduction projects, including supplier identification, evaluation, selection, negotiation, contracting, and performance management. Partners with engineering and cross-functional teams on product launches, cost reduction, supply continuity, supplier risk mitigation, and make-versus-buy analyses. Communicates sourcing strategies and recommendations to stakeholders and leadership while leveraging supplier capabilities and best practices across the organization.

Develops advanced medical device concepts, prototypes, mechanical and electromechanical assemblies, testing methods, engineering drawings, and design verification strategies. Translates clinical and user needs into technical specifications, applies design-for-manufacturability principles, materials and manufacturing knowledge, and supports risk management, quality documentation, regulatory compliance, and product development through launch.

Provides system-level technical leadership for commercial medical devices across commercialization and sustaining engineering. Leads requirements, architecture, risk management, reliability assessments, integration, verification testing, and complex product issue investigations. Partners with engineering, quality, manufacturing, regulatory, service, and operations teams to maintain safe, reliable, compliant products. Mentors engineers and guides systems engineering practices, design controls, and industry standards.

Leads technology-focused internal audits and risk advisory engagements, including IT risk and SOX compliance assessments. Evaluates IT general controls, automated controls, key reports, and control effectiveness across ERP and enterprise applications. Identifies technology risks and control gaps, develops remediation recommendations, coordinates audit workstreams, coaches analysts, and prepares audit reports. Uses data analytics and audit technologies to improve testing and risk coverage while advancing audit methodologies and team capabilities.

Executes technology-focused internal audit and risk advisory engagements, including SOX compliance testing, IT general and automated control testing, system implementation reviews, risk assessments, operational audits, and SOC report reviews. The role evaluates control design and effectiveness, documents audit findings, supports remediation, and advises stakeholders on technology risk across enterprise applications, infrastructure, and cloud environments.

Leads national commercial marketing strategy for Stryker’s Mako SmartRobotics and Mako RPS portfolio, targeting hospital executives and administrative decision-makers. Develops integrated campaigns, economic value tools, ROI calculators, business cases, and executive-focused content to influence capital purchasing decisions. Builds executive reference networks, partners with sales and health economics teams, and drives adoption through customer engagement, value messaging, and coordinated go-to-market programs.

Mechanical Engineering Intern supporting Stryker’s research and development teams in new product development, product engineering, or test lab activities. Responsibilities may include CAD and FEA work, prototype development, product improvement, fixture design, root cause analysis, design verification testing, process documentation, and presenting technical findings while collaborating with cross-functional teams.

Mechanical Engineering Interns support research and development teams in new product development, product engineering, or test lab activities. Responsibilities include researching technologies and customer needs, designing or improving medical products, developing prototypes and test fixtures, conducting design verification, performing root cause analysis, documenting processes, and presenting findings. Interns collaborate cross-functionally and apply classroom knowledge in a fast-paced medical technology environment.