Jobs at Stryker

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.

Manage and execute international regulatory strategies and submissions for medical products. Assess regulatory classification, interpret global requirements, support cross-functional teams, prepare filings, interact with authorities, review clinical/quality documentation, and improve submission planning and metrics to ensure compliant market access.

Provides onsite clinical support during surgical procedures by managing, troubleshooting, and maintaining Stryker and related medical equipment. Anticipates equipment needs, supports surgeons and operating-room personnel, records procedure and account data, provides product information, and follows hospital, vendor credentialing, and HIPAA requirements. The role requires rotating, on-call, overnight, weekend, and occasional travel coverage, along with the ability to work under pressure and handle physical demands.

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.

Supports Upper Extremities medical device sales by partnering with sales representatives, attending surgical cases, educating healthcare professionals, managing inventory and product sets, identifying opportunities, processing purchase orders, and supporting customer relationships. The role requires product training, field calls, compliance with AdvaMed and applicable regulations, and achievement of territory sales targets.

Designs, validates, troubleshoots, and improves manufacturing processes for medical devices. Develops equipment, tooling, fixtures, tests, and process alternatives; analyzes data; supports product development, sustaining engineering, risk management, and design controls. Collaborates with production, quality, suppliers, and cross-functional teams to resolve manufacturing issues, manage engineering projects, train operators, and ensure product safety, quality, compliance, and delivery.

Leads global regulatory strategy and compliance for a peripheral vascular medical device portfolio across the full product lifecycle. Oversees regulatory submissions, labeling, product and manufacturing change assessments, audits, inspections, metrics, and authority interactions. Partners with product development, quality, clinical, and business teams while building and managing a high-performing Regulatory Affairs organization. The role also drives regulatory training, process improvement, compliance programs, budgeting, resource planning, and strategic business guidance.

Lead continuous improvement across medical device production value streams. Responsibilities include facilitating value stream mapping and kaizen events, designing lean systems, implementing process improvements, reducing waste, monitoring operational metrics, quantifying cost reductions, coaching teams, identifying root causes, and supporting new product introduction and product ramp-up activities.

Leads environmental health and safety strategy, compliance, risk reduction, emergency response, incident investigations, security oversight, budgeting, and continuous improvement across manufacturing operations. Manages the EHS team, develops performance culture, partners with plant and business leadership, coordinates stakeholders, supports capital projects, and ensures regulatory compliance and effective site security.

Leads global standards and regulations compliance for medical devices and quality systems. Monitors regulatory changes, interprets requirements, performs impact assessments and standards gap analyses, and develops compliance action plans. Provides technical guidance to product development, sustaining engineering, and quality teams; supports documentation, audits, and regulatory conformity reviews. The role requires expertise in medical device regulations, design controls, risk management, and quality management systems.

Creates 24-month supply and production plans, capacity plans, inventory targets, and safety-stock strategies. Partners with manufacturing, procurement, finance, quality, engineering, and IBP teams to execute plans, identify supply risks, address bottlenecks and backorders, and improve planning processes. Maintains ERP master data, monitors supply chain KPIs, evaluates financial and operational performance, communicates mitigation strategies, and drives continuous improvement.

Supports statistical programming for clinical research studies by creating and reviewing deliverables, processing and standardizing clinical data, implementing endpoint algorithms, coordinating requirements, and conducting exploratory analyses for publications and abstracts. Collaborates with statisticians, clinicians, and internal and external project teams while documenting processes and managing project priorities.

Leads a quality assurance team supporting product quality, process performance, audit readiness, regulatory compliance, and continuous improvement in a regulated medical device manufacturing environment. Oversees quality systems, CAPA, change management, validation, investigations, audits, quality metrics, training, supplier quality, and field-action communications. Partners with manufacturing, regulatory, global quality, and suppliers while supporting strategic planning, acquisitions, and budgeting.

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.

Leads advanced manufacturing and operations engineering for new product development, commercialization, process scale-up, technology transfer, and operational readiness. Drives manufacturability, continuous improvement, equipment qualification, process validation, automation, lean manufacturing, and cross-functional technical projects. Partners with R&D, Quality, Supply Chain, Manufacturing, Regulatory Affairs, and other stakeholders to deliver successful product launches and improve safety, quality, delivery, and cost performance.

Summer internship supporting orthopedic medical device sales in a field-based role. Responsibilities include shadowing sales and operations teams, preparing sales presentations and target account or marketing strategy projects, learning selling and instrument-use techniques, delivering surgical kits, assembling instrument kits, preparing products for surgery, collaborating with teams, and assisting with special projects. The role requires 40% travel and offers corporate housing or a living stipend depending on location.

Leads supply planning across a 24-month horizon, developing resource and capacity plans, managing inventory strategies, identifying risks, and coordinating production, purchasing, demand planning, and product launches. Monitors supply chain metrics, resolves disruptions and backorders, maintains planning data, evaluates financial impacts, drives process improvements, and coaches planners.

Leads development of electro-mechanical and fluidic systems for Class II and III vascular medical devices. Responsibilities include system architecture, CAD/CAE modeling, prototyping, sensor-data acquisition, automated verification and validation testing, fixture development, stress testing, design controls, risk management, cross-functional collaboration, technical mentorship, and transferring products from R&D into high-volume manufacturing.

Provides quality engineering support across medical device manufacturing, products, and processes. Owns nonconformances, CAPAs, MRB activities, supplier quality issues, validations, audits, complaints, and corrective actions. Analyzes quality metrics using statistical methods, develops quality documentation and inspection procedures, supports risk assessments and regulatory compliance, and drives continuous improvement with cross-functional teams and suppliers.

Promote and sell Stryker ENT products in field, operating room, and office settings. Conduct product evaluations and demonstrations, build customer relationships, track territory progress, achieve sales goals, and provide product-use guidance and troubleshooting to doctors, nurses, and staff. Requires customer-focused service, strong communication, independent judgment, organization, and approximately 30% travel with a valid driver’s license.