Jobs at Enovis

Leads global product strategy and lifecycle management for orthopedic enabling technologies, including robotics, navigation, augmented reality, and data-driven surgical solutions. Owns portfolio roadmaps, product requirements, launches, commercial positioning, adoption plans, financial modeling, and capital strategy. Partners with engineering, clinical, regulatory, sales, and marketing teams while engaging surgeons and key opinion leaders. The role requires global cross-functional leadership, competitive intelligence, and travel for customer meetings, education, trade shows, and training programs.

Supports finished-goods shipping activities by coordinating with transportation providers, answering routine shipment questions, verifying invoices and charges, entering order information, maintaining records, distributing paperwork, and preparing reports. The role is performed under close supervision and is intended for someone with little or no prior experience.

Lead technical architecture and execution for medical device mechatronic systems—integrating software, electronics, optics, sensors, and algorithms. Guide cross-functional teams through design, verification, regulatory compliance, risk management, and commercialization while mentoring engineers and evaluating emerging enabling technologies.

Manages sustaining engineering and product development for medical devices, including project prioritization, resource allocation, mentoring engineers, prototyping, testing, design documentation, 3D CAD modeling, design history files, vendor coordination, and regulatory submissions. The role supports mechanical instrumentation, electronic hardware, and related software while collaborating with manufacturing, quality, marketing, purchasing, and regulatory teams.

Leads U.S. downstream marketing strategy for resident and fellowship programs in orthopedic adult reconstruction. Responsibilities include developing strategic partnerships, managing fellow and resident databases, driving acquisition and retention, coordinating communications and events, managing budgets, defining KPIs, analyzing market and customer insights, optimizing lifecycle marketing, and presenting performance to leadership. The role collaborates with marketing, sales, medical education, product development, professional affairs, compliance, and analytics teams.

Leads regional medical device sales execution across Foot & Ankle markets. Coaches sales representatives, manages distributor partnerships, oversees pipeline forecasting and inventory efficiency, coordinates surgeon education and trade events, supports account contracting, troubleshoots field challenges, and collaborates with marketing, operations, legal, supply chain, and customer service. The role requires regular field engagement and travel of up to 75% within the assigned region.

Supports sustaining engineering and new product development for medical devices. Responsibilities include CAD modeling, engineering documentation, nonconformance and CAPA investigations, complaint handling, failure analysis, design transfer, verification and validation, and regulatory compliance. Collaborates with quality, manufacturing, regulatory, purchasing, product development, and marketing teams to improve product reliability and performance.

Operates CNC mills and lathes to manufacture complex prototype and production surgical instruments and orthopedic implants. Creates Mastercam programs, interprets engineering drawings, establishes machine setups, inspects precision parts, adjusts processes for accuracy, maintains equipment, completes records, and recommends process improvements. Collaborates with engineering and manufacturing teams and may train less experienced staff.

Supports global medical-device post-market surveillance and vigilance, including complaint intake and triage, adverse-event reporting, PMS data analysis, trend monitoring, dashboards, PSURs, benefit-risk evaluations, and health-hazard assessments. Maintains complaint records and regulatory documentation, supports SOP updates, and collaborates with Regulatory Affairs, Quality, Clinical Affairs, Risk Management, R&D, Manufacturing, and international affiliates to ensure compliance and identify emerging product risks.

Manage moderate-complexity manufacturing operations projects from initiation through completion. Develop project charters, plans, budgets, communication strategies, and risk mitigation plans. Coordinate Operations, Engineering, Quality, Regulatory, and Marketing stakeholders to deliver projects on time and within budget. Lead project teams and meetings, track progress, provide status reporting, resolve issues, and communicate project goals and updates to management.

Drives Foot and Ankle medical device sales across the United States by supporting surgeons, distributors, and representatives in operating rooms, sales calls, labs, and trade shows. Provides technical product training, develops prospects and pipelines, supports strategic sales initiatives, gathers product feedback, and serves as a field liaison to corporate teams. The role is remote but field-based, requiring frequent domestic travel, overnight stays, and routine car and air travel.

Manages technical documentation and regulatory submissions for medical devices under EU MDR 2017/745. Coordinates with product development, quality, clinical, and manufacturing teams; assesses product and process changes; communicates with notified bodies and competent authorities; prepares responses to deficiencies; and improves internal regulatory processes. Requires 1–2 years of medical device regulatory affairs experience, scientific training, Italian and English proficiency, and short quarterly travel to Switzerland.

Supports Regulatory Affairs through technical and regulatory data management, database updates, document workflows, data entry, archiving, and back-office coordination. Uses ERP systems and company applications to maintain accurate, compliant records and improve internal data processes. Requires a technical or scientific bachelor’s degree, intermediate IT skills, strong accuracy, analytical ability, Italian and English proficiency, and willingness to travel to Switzerland for short business trips.

Leads and coordinates cross-functional Market Access projects within the Global RECON Regulatory Affairs Department. Manages timelines, resources, deliverables, risks, and stakeholder communications in a regulated medical device environment. Prepares project reports, implements mitigation strategies, and drives timely execution aligned with company objectives.

Supports regulatory market access for new and modified medical devices across international markets. Prepares submissions, registrations, licenses, and compliance documentation; provides regulatory guidance during product development; manages approvals, re-registrations, and product releases; reviews design and manufacturing changes, labeling, and advertising materials; monitors regulatory requirements; supports audits, training, and cross-functional resolution of regulatory issues.

Supports international regulatory submissions, approvals, renewals, registrations, and ongoing compliance for medical devices. Prepares regulatory documentation, defines approval requirements, reviews product and manufacturing changes, manages regulatory-controlled product releases, and advises cross-functional teams on regulatory issues. Reviews labeling and advertising, monitors changing regulations, maintains audit-ready documentation, provides training, and supports market access planning and product development projects.

Manages a Minnesota sales territory for Enovis Chattanooga and LightForce medical technology products. Develops customer and dealer relationships, achieves revenue targets, identifies and qualifies opportunities, conducts product demonstrations and education, negotiates sales terms, maintains Salesforce records, coordinates technical resources, and supports events and product implementation. The role requires frequent travel to customer accounts, conferences, and trade shows while maintaining compliance with company, healthcare, and industry regulations.

Supervises production cells and assembly employees to meet production plans, quality standards, and timelines. Directs electronic and mechanical assembly operations, interprets diagrams and drawings, performs continuity checks, uses hand and power tools, and conducts quality inspections. Resolves moderately difficult production issues and provides recommendations while guiding employees through repetitive and non-repetitive tasks.

Leads global digital transformation programs across regions, business units, IT teams, and external partners. Responsibilities include managing the corporate website replatforming roadmap, coordinating stakeholders, overseeing timelines, risks, governance, vendors, system integrators, adoption, and executive reporting. The role requires enterprise website replatforming experience, familiarity with CMS and MarTech platforms, and hands-on Optimizely experience. Travel up to 10% is required.

Leads SEO and Generative Engine Optimization governance across Enovis websites and marketplaces. Responsibilities include setting optimization standards, partnering on technical fixes, taxonomy, migrations, content discoverability, reporting, and experimentation. The role translates SEO requirements into technical and content backlogs, monitors rankings and traffic quality, and applies emerging AI search practices across professional and consumer audiences.