Jobs at Stryker

Provides field-based clinical and technical support for robotic and manual joint replacement procedures. Responsibilities include CT-based preoperative planning, implant sizing, instrumentation checks, system setup, intraoperative troubleshooting, surgeon and OR staff support, inventory coordination, product demonstrations, customer training, documentation, and account collaboration. The role requires extensive travel, on-call coverage, physical handling of instruments and equipment, and composure in fast-paced surgical environments.

Leads manufacturing engineering projects and process improvements, resolves manufacturing and equipment issues, and supports new product introduction. Applies Lean, Six Sigma, statistical methods, and GMP principles to improve yield, throughput, quality, and safety. Designs, qualifies, and implements fixtures, tooling, and equipment using IQ/OQ/PQ protocols. Performs failure analysis, manages engineering changes, develops technical documentation and work instructions, and trains teams on product launches and process changes.

Performs account reconciliations, investigates outstanding balances, prepares journal entries, analyzes financial statements, and supports month-end close activities for international entities. The role maintains documentation, escalates unusual activity, and ensures compliance with US GAAP, local accounting standards, and corporate policies. It requires bilingual English and Spanish fluency, Excel proficiency, financial reporting systems experience, and an accounting or business degree.

Provides field-based operating room support for Stryker and related surgical equipment. Sets up, tests, adjusts, troubleshoots, cleans, maintains, and stages equipment used in minimally invasive procedures. Educates OR and sterile processing staff, supports connectivity and image routing, records procedure metrics, maintains account information, and ensures compliance with hospital and company policies. The role requires flexible rotating shifts, on-call coverage, occasional overnight travel, and collaboration with surgeons, OR personnel, biomedical teams, and central processing staff.

Provides technical leadership for manufacturing processes, CNC machining, equipment qualification, process validation, troubleshooting, and continuous improvement in a regulated production environment. Leads validation documentation, risk assessments, corrective actions, engineering changes, Lean initiatives, and production training while partnering with quality, operations, suppliers, and engineering teams.

Supports orthopedic surgeons during robotic and manual joint replacement procedures. Responsibilities include CT-based preoperative planning, implant sizing, instrument and equipment setup, intraoperative technical support, troubleshooting, inventory and account coordination, customer training, case documentation, and surgeon relationship management. The role requires on-call coverage, extensive travel, physical stamina, and composure in fast-paced operating-room environments.

Leads the design, development, testing, and integration of complex electro-mechanical medical device systems. The role guides electrical, mechanical, and systems architecture decisions; leads prototyping, verification, validation, and technical problem-solving; mentors engineers; supports regulatory and quality compliance; and collaborates with clinical, manufacturing, marketing, and cross-functional R&D teams to commercialize innovative products.

Sell Stryker Foot & Ankle medical devices to surgeons and healthcare professionals in a field-based territory. Responsibilities include product consultations and training in operating room environments, competitor and product expertise, customer relationship management, inventory management, sales meetings, and compliance with healthcare regulations. The role requires 30% travel and is compensated through 100% commission, with bonuses and benefits.

Sell orthopaedic instruments and surgical products across an assigned territory. Develop territory plans, achieve quotas, build relationships with surgeons, hospital staff, supply chain teams, and administrators, conduct product demonstrations and evaluations, support launches and implementations, train clinical staff, grow the pipeline, analyze sales metrics, and provide real-time support in surgical environments.

Supports Upper Extremities sales representatives in a field-based territory by attending surgeries, educating healthcare professionals, promoting Stryker products, managing inventory and product sets, identifying sales opportunities, processing purchase orders, supporting customer relationships, and meeting business targets while following regulatory and ethical compliance requirements.

Leads clinical evidence workflows, including systematic reviews, data extraction, quality control, reporting, and evidence repository management. Translates clinical, regulatory, reimbursement, and business questions into structured analyses and recommendations. Generates insights from literature, real-world evidence, registries, and claims data while supporting clinical evaluation reports, post-market activities, publications, and regulatory submissions. Partners with cross-functional stakeholders and technical teams to scale evidence-management processes, automate workflows, and prioritize evidence-generation investments.

Leads a team of four sales professionals across Southern Mexico to achieve orthopedic portfolio targets. Develops regional commercial strategies, expands market presence, manages customers and distributors, drives direct and indirect sales, forecasts performance, advances key accounts, and supports robotic-assisted technology initiatives. Partners cross-functionally while ensuring regulatory, quality, policy, and ethical compliance.

Lead Joint Replacement sales across Yorkshire and the North East, managing regional revenue, costs, forecasting, customer service, and a high-performing sales and service team. Coach and develop employees, support Mako product specialist onboarding and training, coordinate clinical case coverage, build surgeon and hospital relationships, expand procedural volume, and collaborate with commercial, compliance, service, and finance teams. The role is home-based with regular regional travel, overnight stays, and occasional head-office visits.

Complete Mako clinical specialist training and certification while supporting robotic-assisted orthopedic procedures. Provide clinical and technical assistance before, during, and after surgeries; educate surgeons and hospital teams; assist with imaging review and preoperative planning; support new account launches; coordinate training, workshops, and certification activities; and ensure equipment readiness, procedural logistics, regulatory compliance, and quality standards.

Leads microbiology, biocompatibility, sterilization, and reprocessing activities for medical device development and lifecycle management. Develops testing strategies, protocols, validation plans, risk assessments, and regulatory documentation. Supports sterilization validations, equipment qualifications, monitoring programs, audits, CAPAs, supplier changes, and regulatory submissions. Partners with R&D, Quality, Regulatory Affairs, Manufacturing, suppliers, and external laboratories to ensure biological safety, compliance, product quality, and patient safety.

Leads quality management system integration for a regulated medical device environment. Responsibilities include assessing current-state processes, performing QMS gap assessments, harmonizing procedures and documentation, identifying compliance risks, supporting future-state implementation, coordinating training and document control, verifying QMS changes, and maintaining compliance with FDA, ISO, MDSAP, EU MDR, and other applicable requirements.

Leads EMEA treasury core operations, including bank account openings and closures, KYC refreshes, signatory updates, banking resolutions, and M&A-related integrations. Oversees activities across multiple countries, entities, and banking partners while identifying risks and maintaining business continuity. Drives process improvements involving account rationalization, bank connectivity, payment files, statement integration, automation, and KPI tracking. Collaborates with Treasury, Finance, Legal, HR, IT, business stakeholders, and banks.

Leads early-stage mechanical and system-level design for future medical devices, including research, prototyping, testing, design optimization, technical problem-solving, and invention development. Collaborates across R&D, quality, manufacturing, regulatory, clinical, marketing, and project management teams. Applies medical device standards, develops engineering documentation, supports customer-focused design and market strategy, mentors engineers, and drives technical excellence through commercialization.

Provides technical leadership for automated manufacturing and engineering projects from concept through implementation. Leads process improvement, equipment qualification, validation, statistical studies, risk assessments, supplier evaluation, and production troubleshooting. Develops manufacturing procedures and control plans, supports enterprise-system integration, and trains engineers and operators. Requires expertise in regulated, high-volume manufacturing, industrial automation, quality methodologies, and process validation. Occasional supplier and project travel may be required.

Leads complex, cross-functional R&D projects involving digital health, connected devices, software delivery, and new product development. Owns scope, schedules, milestones, dependencies, risks, resources, and budgets across concurrent workstreams. Facilitates planning and stakeholder alignment, communicates status to leadership, resolves obstacles, and drives execution without direct authority. Improves project management processes and applies traditional, Agile, or hybrid methodologies in a fast-paced product environment.