Jobs at Stryker

Oversee daily manufacturing across assembly, inspection, material handling, and packaging. Supervise approximately 20 employees, manage scheduling and performance, develop production plans, and coordinate with Engineering, Quality, Supply Planning, Finance, Purchasing, and R&D. Drive production, safety, quality, productivity, downtime, waste, compliance, and schedule-attainment metrics while ensuring adherence to validated processes and work instructions.

Lead trade show and events marketing strategy and execution for Stryker’s Peripheral Vascular business. Manage event logistics, project plans, exhibits, budgets, vendors, agencies, customer engagements, and cross-functional coordination. Develop pre-show briefings, facilitate lead tracking, analyze post-show results, and identify sponsorship and event opportunities aligned with business priorities. The role requires approximately 30–40% travel and is remote.

Designs and implements in-circuit, functional, and electromechanical manufacturing tests for medical device products. Performs process verification, equipment qualification, validation, Gauge R&R, DOE, and capability analysis. Develops fixtures, schematics, instrumentation, and documentation; troubleshoots manufacturing issues; and supports design-for-testability, design-for-manufacturing, new product introduction, and process transfers with engineering, suppliers, and manufacturing partners.

Leads downstream marketing strategy and execution for a neurovascular portfolio, including brand positioning, campaigns, portfolio roadmaps, customer engagement, KOL development, product lifecycle management, forecasting, education programs, and cross-functional collaboration. Manages marketing personnel and partners with sales, supply chain, global marketing, customers, and clinical stakeholders to drive growth, market share, profitability, and brand performance.

Supports product launches and lifecycle management by maintaining accurate master data across PLM, ERP, and global item management systems. The role monitors data integrity, resolves discrepancies, supports data governance and regulatory procedures, analyzes trends, and recommends process improvements. It partners with project management, operations, supply chain, quality, and commercial teams, while contributing to documentation, training, and scalable data management practices in a regulated medical device environment.

Manage product master and transactional data across PLM, ERP, and global item management systems. Support product launches, lifecycle changes, and discontinuations while ensuring data accuracy, integrity, regulatory compliance, and operational readiness. Monitor and resolve discrepancies, analyze trends, improve data processes, maintain documentation and training materials, and collaborate with project managers and cross-functional stakeholders on system setup and change requests.

Biomedical Engineering interns support research and development teams in new product development or product engineering. Responsibilities include researching technologies, customer needs, regulations, and product performance; using CAD, FEA, test labs, and root cause analysis; designing or improving medical products; documenting processes; collaborating cross-functionally; and presenting findings.

Lead product and portfolio strategy for a Workflow Engine and integrations within the SmartCare platform. Define vision, roadmaps, and investment priorities; partner with engineering, architecture, UX, sales, and customers; drive discovery, requirements, go-to-market, and lifecycle management; ensure scalability, security, interoperability, and business performance; gather market and customer insights; evaluate partnerships and competitive landscape; mentor teams and influence cross-functional stakeholders.

Supports supply chain projects across purchasing, business planning, distribution, demand planning, product lifecycle management, and PMO functions. Responsibilities may include procurement, inventory planning, production scheduling, forecasting, demand analysis, product portfolio analysis, process improvement, and executive reporting. Interns collaborate cross-functionally to improve efficiency, cost, customer service, and operational decision-making while documenting processes and presenting findings.

Supports Sales Support initiatives through AI and automation exploration, process improvement, data analysis, dashboard and report development, knowledge management, training documentation, tool testing, and project execution. Partners with sales leaders and cross-functional teams to document requirements, improve workflows, present findings, and support data-driven decisions.

Supports global medical-device regulatory affairs through regulatory intelligence, international submission preparation, new product development meetings, post-market reporting, and change-notification strategies. The intern collaborates with R&D, Supplier Quality, Marketing, and Clinical Affairs teams while documenting complex processes, assessing regulatory requirements, and helping ensure product safety, compliance, and continued market approvals.

Manage and maintain accounting systems and controllership functions (GL, AR, AP, revenue reconciliation, cash flows) ensuring GAAP and SOX compliance. Coordinate audits, perform monthly financial statement and balance sheet reviews, oversee ERP controls with IT, respond to corporate compliance inquiries, and partner with finance leadership to implement accounting policy changes.

This internship provides hands-on exposure to orthopedic medical device sales and field operations. Responsibilities include shadowing sales and operations teams, preparing sales presentations and target account strategies, learning selling processes and surgical instrument techniques, assisting with kit deliveries and warehouse preparation, interacting with cross-functional teams, and supporting special projects.

This internship provides hands-on exposure to orthopedic medical device sales and field operations. Responsibilities include shadowing sales and operations teams, preparing sales presentations and target-account or marketing strategy projects, learning selling and instrument-use techniques, assisting with kit deliveries and warehouse preparation for surgeries, collaborating across product teams, and supporting special projects.

Quality Engineering interns support medical device development and sustainment across advanced, process, supplier, and product quality teams. Responsibilities may include risk management, statistical analysis, reliability engineering, design verification and validation, root cause analysis, corrective actions, supplier quality, CAD fixture design, LabVIEW, compliance, continuous improvement, and complaint handling. Interns collaborate with cross-functional teams, suppliers, sales, regulatory groups, and customers.

Mechanical Engineering interns support Stryker’s Research and Development teams in new product development, product engineering, or test lab work. Responsibilities include researching technologies and customer needs, designing and improving products, using CAD and FEA, building test fixtures, conducting design verification testing, performing root cause analysis, documenting processes, and presenting findings. Interns collaborate cross-functionally while applying classroom knowledge to medical technology projects.

Supports quality assurance and regulatory processes for medical device products, including Quality Management System activities, nonconformance investigations, corrective and preventive actions, documentation review, audits, quality metrics, compliance, and continuous improvement. Collaborates with manufacturing, engineering, regulatory affairs, supplier quality, and operations teams while gaining hands-on experience in product and process quality.

Supports upstream marketing and marketing communications initiatives for medical technology products. Responsibilities may include product development support, customer insights, strategic marketing, creation of customer-facing materials, digital and advertising communications, product launches, trade shows, and sales meetings. Interns collaborate with internal teams, external vendors, and stakeholders while documenting processes and presenting information clearly.

Software Engineering interns support Stryker teams across quality, research and development, testing, and manufacturing. Responsibilities may include product development, design verification and validation, prototype testing, root cause analysis, process improvement, documentation, and collaboration with cross-functional teams and suppliers. Interns apply their technical education to improve medical products, manufacturing processes, reliability, and quality while developing professional and communication skills.

Supports downstream marketing and commercialization initiatives, including campaign development, messaging, positioning, customer insight gathering, and commercial model validation. The intern collaborates with sales members, surgeons, internal stakeholders, and external contacts while documenting processes, presenting information, and managing multiple priorities. The role provides practical experience in medical technology marketing and requires strong communication, organization, leadership, and problem-solving skills.