Jobs at Inari Medical

Supports joint replacement product sales by assisting sales representatives, covering surgical cases, conducting product evaluations, resolving onsite product issues, educating medical staff, maintaining inventory, developing territory relationships, and providing customer service. The role includes business development, sales tracking, required training, certifications, and on-call support during evenings, weekends, and holidays.

Develop complex medical devices from concept through commercialization. Translate clinical and stakeholder needs into system requirements, architectures, interfaces, and verification strategies across mechanical, electrical, and software disciplines. Lead integration, verification, validation, risk management, design assessments, and technical issue resolution. Create design documentation, apply medical device standards and design controls, collaborate with clinical, quality, regulatory, manufacturing, and engineering teams, and mentor team members.

Lead strategic sourcing for new product introduction projects, including supplier identification, selection, negotiation, contracting, performance management, cost reduction, and supply chain risk mitigation. Partner with engineering and cross-functional stakeholders to support product launches, conduct cost and make-versus-buy analyses, and communicate sourcing strategies and recommendations to leadership.

Develops advanced medical device concepts, prototypes, mechanical and electromechanical assemblies, and testing methods. Translates clinical and user needs into design requirements, creates engineering drawings and models, applies GD&T and design-for-manufacturability principles, and supports verification, risk management, quality documentation, and product launches. Collaborates with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams.

Provides system-level technical leadership for commercial medical devices across design changes, lifecycle management, reliability, risk management, requirements, integration, verification, and complex issue resolution. Partners with multidisciplinary teams across engineering, quality, manufacturing, regulatory, service, and operations. Requires regulated-industry engineering experience, with preferred medical device post-commercialization expertise and knowledge of systems engineering, reliability methods, design controls, and medical device standards.

Leads technology-focused internal audits and risk advisory engagements involving ITGCs, automated controls, key reports, ERP systems, cloud solutions, and SOX compliance. Assesses control design and effectiveness, identifies risk exposures, develops remediation recommendations, oversees audit workstreams, coaches analysts, prepares audit documentation, and improves audit methodologies and testing approaches.

Executes technology-focused internal audits and risk advisory engagements, including SOX compliance testing, IT control assessments, system implementation reviews, and technology risk assessments. Tests IT general controls, automated controls, and key reports across SAP, enterprise applications, infrastructure, and cloud environments. Reviews audit evidence and third-party SOC reports, documents deficiencies, prepares workpapers, recommends remediation, and validates corrective actions with management.

Leads commercial marketing strategy for Stryker’s Mako SmartRobotics portfolio, targeting hospital executives and administrative decision-makers. Develops integrated campaigns, economic value tools, ROI calculators, business cases, executive engagement programs, and customer-facing content. Partners with sales, health economics, medical education, commercial excellence, and marketing teams to influence capital purchasing decisions, accelerate adoption, and support portfolio growth. Requires substantial marketing and people-management experience, with medical device and healthcare marketing experience preferred.

Mechanical Engineering interns support medical device research and development through new product design, product improvements, prototype testing, design verification, fixture development, CAD, FEA, test labs, and root cause analysis. Interns collaborate cross-functionally, document complex processes, research technologies and customer needs, and present findings while gaining practical industry experience.

Mechanical Engineering Interns support Stryker’s research and development teams in new product development, product engineering, or test labs. 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 applying classroom knowledge to healthcare technology projects.