Jobs at Stryker

Develop secure, scalable backend APIs, cloud data-ingestion pipelines, and distributed systems supporting AI-enabled healthcare applications. Build systems handling clinical data such as images, videos, STL files, and CT scans; integrate AI models; contribute to web applications; conduct code reviews and automated testing; and collaborate with product, security, regulatory, QA, and engineering teams in a regulated environment.

Leads a centralized team delivering data analytics, reporting, automation, and governance across regulatory affairs, quality assurance, and clinical functions. Establishes data ownership, metric standards, dashboards, data lineage, automation intake, and support models. Develops divisional strategies, manages portfolios and resources, partners with business and technology stakeholders, and scales analytics and automation solutions to improve data integrity, operational efficiency, and decision-making.

Summer interaction design internship supporting UX and UI design for mobile and web emergency care applications. The intern will collaborate with experienced designers, engineering, marketing, and clinical teams; create user flows, prototypes, interaction models, and design-system elements; conduct user research; maintain visual brand language; and advocate for end users in product development.

Quality Assurance 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, regulatory complaint handling, CAD fixture design, and continuous improvement. Interns collaborate with cross-functional teams, suppliers, sales, and customers while documenting processes and presenting findings.

Supports manufacturing process improvements using Lean Six Sigma, mistake-proofing, automation, sensing, fixture development, assembly optimization, ergonomics, safety, and process validation. Collaborates with manufacturing, design, and operations teams to reduce defects, rework, and process escapes while documenting processes and presenting findings. Works under mentorship on projects that improve manufacturing efficiency and product launch execution.

Supports medical device research and development through new product development or product engineering projects. Interns collaborate cross-functionally to research technologies, customer needs, regulations, product performance, and business requirements. Responsibilities may include product concept development, product improvement, CAD and FEA work, testing, root cause analysis, process documentation, presentations, and reporting. The role targets students in human factors, industrial, cognitive psychology, or biomedical engineering programs.

Mechanical Engineering Interns support Stryker’s research and development teams in new product development, product engineering, or testing. Responsibilities may include researching technologies and customer needs, designing and improving medical 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 developing technical, communication, leadership, and problem-solving skills.

Biomedical engineering interns support post-market quality and product engineering initiatives in medical technology. Responsibilities may include researching product performance, customer feedback, technologies, and regulations; conducting root cause analysis; documenting complex processes; presenting findings; and collaborating with cross-functional teams to improve product safety, efficacy, and quality. Interns may also use CAD, FEA, and test labs while developing professional communication, leadership, and organizational skills.

Summer intern supporting orthopedic medical device sales in a field-based Seattle territory. Responsibilities include shadowing sales and operations teams, preparing sales presentations and target account or marketing strategies, learning selling and instrument-use techniques, assisting with surgical instrument kits and warehouse operations, supporting deliveries, and completing special projects. The role requires strong communication, organization, leadership, analytical skills, and proficiency with Microsoft Office.

Supports medical device post-market surveillance, complaint and adverse event evaluation, regulatory reporting, field actions, risk assessments, CAPA, investigations, audits, and technical documentation. Collaborates with Quality, Engineering, Clinical, Marketing, customers, and regulatory stakeholders to assess patient harm, maintain compliance, and support product safety and performance.

Supervise Quality Technicians executing incoming, in-process, and final inspections; assign and balance daily workload; track and report quality and operational metrics; oversee inspection methods and sampling plans; lead MRB and non-conformance disposition; support audits and training; drive root cause analysis and corrective/preventive actions to improve processes.

Field-based sales rep responsible for promoting and selling craniomaxillofacial products, building clinician relationships, conducting product evaluations in OR and office settings, managing territory and sample inventory, meeting sales targets, and providing product training and onsite problem resolution.

Lead second-shift production of Class III medical devices, managing daily operations, staffing, quality, safety, and delivery. Drive Lean/6S continuous improvement, monitor performance metrics, ensure regulatory compliance, and implement corrective actions to meet production objectives.

Lead and define research vision for Emergency Care, manage a team of scientists/engineers, oversee strategic planning, budgeting, talent development, cross‑functional collaboration, external KOL engagement, IP creation, and scientific publications to advance long-term product and business objectives.

Provide intraoperative clinical support by managing, troubleshooting, and maintaining Stryker and related surgical equipment; anticipate device needs, record procedure and monthly metrics, maintain account and credentialing information, comply with HIPAA and facility policies, support varied shifts including on-call and occasional travel, and train/educate OR staff on products and disposables.

Provide nationwide, field-based coverage for neurosurgical product sales and leave coverage. Educate OR staff on product use, conduct evaluations and demos, support territory planning and customer relationships, resolve product issues, and adhere to OR/OSHA/GMP regulations. Requires extensive overnight travel.

Lead quality operations for Emergency Care division: manage quality systems, investigations, CAPA, metrics, audits, cross-functional partnerships, continuous improvement, budgeting, and team development to ensure regulatory compliance and product safety.