Jobs at Inari Medical

Provide finance support including employee reimbursement checks, prepare cash disbursement/receipt documents, verify AP documentation, file vouchers and finance records, assist the COE team, and ensure GMP and regulatory compliance. Perform other tasks as assigned by supervisor.

Lead technical engineering support for manufacturing projects: ensure GMP/ISO13485 compliance, drive process validation (IQ/OQ/PQ), PFMEA/PPAP/Control Plans, continuous improvement using SPC/Six-Sigma, manage CAPA/NC, support equipment acquisition/validation, train staff, and lead cross-functional process improvements to reduce cost and ensure product quality.

Support Suzhou finance team and ensure GMP/regulatory compliance. Prepare daily European intercompany and public reports (Absorption & COGS, Scrap & Production, Engineering hours & Productivity, WIP Aging & E&O). On-site at least four days weekly for a minimum six-month internship. Requires good Office skills, English, logical thinking, and strong communication.

Lead clinical safety oversight across studies including identification, assessment, adjudication, coding, and reporting of adverse events. Author event narratives, partner with cross-functional teams, coordinate with sites/CROs, present safety findings, and drive process improvements to ensure regulatory compliance and data quality.

Lead sourcing strategy for new product introductions, selecting and negotiating with suppliers, managing RFQs/contracts, and mitigating supply, cost, quality, and delivery risks. Partner cross-functionally to track project costs, support business cases, and ensure launch readiness and transition to sustaining procurement for long-term value.

Lead cross-functional teams to plan and execute new product introduction projects for a neurosurgical console. Manage scope, schedule, budget, risks, suppliers, and stakeholder communications to deliver compliant manufacturing readiness and high-quality launches.

Lead HR digital and technology strategy as the senior advisor to HR and EDT leadership. Define multi-year roadmaps, prioritize investments, govern portfolio value, drive architecture harmonization, and lead cross-functional teams to deliver scalable, compliant solutions that align with enterprise priorities and business outcomes.

Lead full-cycle recruiting for Manufacturing Engineering and related technical roles across North America. Partner with hiring managers to define requirements, build sourcing strategies, assess candidates, manage the ATS and candidate pipeline, present evaluations, and improve recruiting processes and reporting to meet hiring goals.

Lead cross-functional teams to plan, execute, monitor, and close new product launch projects at the Anngrove facility. Manage stakeholders, schedules, risks, and reporting; ensure manufacturing readiness, compliance, and quality. Drive problem-solving, continuous improvement, and alignment across engineering, operations, quality, supply chain, digital/IT, and commercial teams.

Field-based role supporting daily onsite surgical operations: manage and troubleshoot Stryker and third-party endoscopy equipment, lead on-the-job training/onboarding, coordinate staffing, ensure compliance, record metrics, and build relationships with OR staff and hospital stakeholders. Requires flexible scheduling and frequent travel.

Field-based sales role promoting and selling craniomaxillofacial products. Performs OR and office product demonstrations, manages territory accounts, resolves product issues, cross-sells, tracks metrics, attends meetings, and trains or mentors associates to meet sales goals.

Support surgical teams by preparing, maintaining, and decontaminating endoscopy equipment; troubleshoot devices; perform function testing and sterilization prep; document usage and performance metrics; collaborate with OR, SPD, and biomedical staff; provide flexible on-call and overnight coverage and occasional travel.

Lead clinical quality and compliance for neurovascular clinical research: manage quality programs, audits, inspections, vendor audits, risk controls, SOPs, corrective actions, training, and inspection readiness across global clinical activities.

Lead electrical hardware design for handheld cranial and spinal medical devices. Own system requirements, prototyping, verification/validation, testing, and design tradeoffs. Collaborate cross-functionally, evaluate emerging technologies, drive regulatory-compliant documentation, and contribute to IP and customer-centric design activities.

Design, build, and optimize CI/CD pipelines; manage build and release processes for .NET and embedded software; troubleshoot deployments; drive DevOps automation and best practices; partner with global engineering teams to improve development efficiency and track metrics.

Field-based territory manager responsible for achieving sales targets across the Gold Coast, building relationships with orthopaedic surgeons and hospital stakeholders, providing in-theatre support for hip and knee replacements, driving MAKO and implant adoption, delivering product training, and managing pipeline and territory forecasts.

Support surgeons in hip and knee replacement procedures by providing clinical and technical support in operating theatres, assisting with MAKO robotic-assisted surgery, preparing cases and instruments, executing territory plans with Territory Managers, and supporting account management and sales growth.

Own site quality performance and KPIs, lead supplier containment and CAPA activities, support PPAP and manufacturing transfers for new products, participate in cross-functional product development, apply root-cause problem solving (5-Why, 8D, DMAIC, FMEA), analyze quality data to drive improvements, manage engineering change with suppliers, and promote continuous improvement methodologies like Lean, Six Sigma, SPC, MSA, pFMEA and poka-yoke.

Design, develop, prototype, and test mechanical components for medical devices under supervision. Support root-cause analysis, documentation (Design History File), design controls, and cross-functional project work while learning regulatory-aligned engineering and quality processes.

Provide in-theatre technical and clinical support for robotic knee and hip procedures, perform pre-op CT segmentation and planning, train and support theatre staff, manage case documentation, collaborate on scheduling and inventory, and feed usage insights to product teams.