Jobs at Inari Medical

Designs, validates, troubleshoots, and improves manufacturing processes, equipment, tooling, and fixtures for medical devices. Supports production quality, safety, compliance, experiments, risk management, design controls, supplier collaboration, and engineering projects. Trains operators on process changes and partners with cross-functional teams to resolve manufacturing issues and optimize performance.

Lead complex, cross-functional cost reduction and operational excellence projects across global quality and operations. Manage project scope, schedules, budgets, resources, risks, governance, stakeholder communications, and supplier coordination. Drive initiatives involving sterilization optimization, manufacturing capacity, process automation, data systems, scrap reduction, and productivity improvements while ensuring compliance with quality standards and delivering measurable business results.

Leads complex, cross-functional cost reduction and operational excellence initiatives across quality and operations. Responsibilities include managing project scope, schedules, budgets, resources, risks, governance, stakeholder communications, procurement coordination, and supplier relationships. The role drives sterilization optimization, capacity improvements, automation, systems initiatives, scrap reduction, and process optimization while ensuring quality-system compliance and delivering measurable business results.

Leads a Quality Operations and Quality Engineering team in a regulated manufacturing environment. Oversees compliance with quality standards and regulatory requirements, audits, inspections, quality systems, nonconformances, CAPAs, deviations, and risk mitigation. Drives continuous improvement, monitors quality metrics, supports product and process quality, and recruits, develops, and retains high-performing talent while partnering with manufacturing and cross-functional leaders.

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, authority interactions, compliance programs, metrics, and regulatory training. Partners with product development, quality, clinical, and business teams while building and managing a high-performing Regulatory Affairs organization, including talent development, budgeting, resource planning, and performance management.

Lead continuous improvement across medical device production value streams. Responsibilities include value stream mapping, Kaizen events, lean system design, future-state implementation, process optimization, root-cause analysis, cost reduction, coaching, quality and safety compliance, and support for new product introduction and product ramp-up.

Leads trade show and event marketing strategy and execution for Stryker’s Peripheral Vascular business. Responsibilities include selecting priority events, managing logistics, exhibits, budgets, vendors, agencies, briefing materials, lead tracking, VIP engagements, sponsorship opportunities, and post-event performance analysis. Partners with marketing and cross-functional teams, develops project plans, negotiates with service providers, and travels approximately 30–40%.

Leads downstream marketing strategy and execution for a neurovascular medical device portfolio. Responsibilities include brand positioning, annual and long-range planning, marketing campaigns, customer and KOL engagement, product lifecycle management, demand forecasting, portfolio development, market analysis, pricing, medical education, and team leadership. Partners with sales, local and global marketing, supply chain, education, and other cross-functional stakeholders to drive portfolio growth, profitability, market share, and brand performance.

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 site safety culture, partners with plant and regional leadership, oversees regulatory requirements, and supports production, capital projects, and operational changes.

Oversee first-shift medical device manufacturing operations, leading production teams and ensuring safety, quality, GMP compliance, productivity, yield, cost, and documentation objectives. Manage capacity, inventory traceability, equipment utilization, workforce planning, and employee development. Drive Lean and continuous improvement initiatives, support audits, budgeting, manufacturing transfers, new product introductions, and operational readiness while partnering with Engineering, Quality, Materials, and other cross-functional teams.

Provides technical leadership for global medical device standards and regulations compliance. Monitors regulatory changes, interprets requirements, conducts impact assessments and standards gap analyses, and implements compliance action plans across products and quality systems. Partners with cross-functional teams on documentation and conformity activities, supports audits, and reviews technical documentation, test protocols, and reports for regulatory compliance.

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, mitigate supply risks, and improve service levels, capacity utilization, inventory performance, and backorder results. Maintains ERP planning data, tracks KPIs, analyzes performance gaps, and drives corrective actions and continuous improvement.

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

Leads quality assurance activities for a medical device manufacturing portfolio, managing quality systems, audits, investigations, CAPA, change management, validation, metrics, training, supplier quality, and continuous improvement. Develops a quality team and partners with Operations, Regulatory Affairs, Global Quality, and suppliers to maintain compliance, audit readiness, product quality, and process performance.

Supports quality assurance and regulatory compliance activities for medical device products. Responsibilities include maintaining Quality Management System activities, investigating nonconformances, supporting corrective and preventive actions, organizing quality documentation, contributing to continuous improvement, and assisting with audits and quality metrics. The intern collaborates with Manufacturing, Engineering, Regulatory Affairs, Supplier Quality, and Operations teams.

This internship provides field-based exposure to orthopedic medical device sales. Responsibilities include shadowing sales and operations teams, preparing sales presentations and target-account or marketing projects, learning selling and instrument-use techniques, delivering surgical kits, assembling instrument kits, preparing products for surgery, collaborating across teams, and supporting field operations projects.

Leads advanced manufacturing and operations engineering for new product development, commercialization, and product launches. Drives process development, scale-up, technology transfer, manufacturability, operational readiness, equipment qualification, and process validation. Leads continuous improvement, lean manufacturing, automation, and cross-functional technical projects involving R&D, Quality, Supply Chain, Manufacturing, Regulatory Affairs, and other stakeholders.

Manage supply planning across complex product portfolios and multiple sites over a 24-month horizon. Develop resource and capacity plans, identify risks, optimize inventory and safety stock, monitor execution, and coordinate production and purchasing teams. Partner cross-functionally on demand alignment, launches, phase-outs, master data, and process improvements. Analyze performance metrics, implement corrective actions, lead strategic initiatives, and coach supply planners.

Leads systems engineering for Class II and III vascular thrombectomy devices, including fluid-control architecture, sensor feedback, CAD modeling, prototyping, automated verification and validation, and data acquisition. Coordinates cross-functional R&D, quality, manufacturing, regulatory, and clinical teams through design controls, risk management, product development, and transfer to high-volume manufacturing. Mentors engineers and drives technical and process improvements.

Provides onsite operating room, sterile processing, case cart, inventory, and liaison support for Stryker surgical equipment and instruments. Responsibilities include equipment setup, intraoperative troubleshooting, post-procedure breakdown, cleaning, reprocessing, inventory management, staff education, data reporting, and coordination with OR, SPD, biomedical, and hospital leadership. The role supports rotating, on-call, overnight, weekend, and regional coverage while maintaining compliance with hospital, HIPAA, IFU, HSPA, and AAMI requirements.