Jobs at Enovis

The Demand Planner will enhance forecast accuracy by analyzing data, collaborating with teams, and maintaining data integrity for product planning.

Lead and coach CNC programmers, develop and optimize CNC programs for mills/lathes (including multi-axis and DMG MORI equipment), troubleshoot machining and tooling issues, ensure compliance with cGMP and quality requirements, support production launches and continuous improvement, and collaborate with engineering, quality, and operations to improve throughput and part quality.

The Manager of Process Engineering will lead a team in developing and implementing manufacturing processes for new products while ensuring design transfer to production and improving manufacturing efficiency.

Design, integrate, and optimize system-level architecture for surgical navigation and visualization platforms. Translate clinical requirements into technical specifications, integrate software with cameras and tracking hardware, support real-time AR visualization, ensure system performance and safety, participate in V&V and risk management, troubleshoot integrated hardware/software issues, and document architecture and verification in regulated medical device environments.

Lead cross-functional new product development projects from initiation through commercialization using PMI practices. Build business cases, project plans, budgets, KPIs, and risk mitigation. Coordinate Product Development, Operations, Quality, Marketing, and Commercial teams; run status meetings, dashboards, and leadership updates. Drive accountability, continuous improvement, and change management across matrixed teams to deliver projects on time, within scope, and budget.

Provide technical leadership for quality assurance across new product development and sustaining engineering. Lead design and manufacturing reviews, risk management (DFMEA/PFMEA/ISO 14971), software V&V, audits (FDA, ISO 13485, MDSAP), CAPA investigations, supplier quality, process validation, and continuous improvement while mentoring junior engineers and partnering cross-functionally to ensure regulatory compliance and product quality.

Lead regulatory strategy and submissions for medical devices (hardware and SaMD) across US, EU and Australia. Manage interactions with FDA/Notified Bodies/TGA, support clinical strategy, postmarket surveillance, regulatory assessments, labeling/QMS changes, CAPAs, audits, and cross-functional regulatory support to ensure compliance with relevant standards and regulations.

Design and support system-level architecture for surgical navigation and visualization platforms; translate clinical requirements into technical specifications; integrate software with hardware (cameras, robotics, tracking); develop real-time visualization and AR features; ensure system performance, reliability, safety, and regulatory compliance; participate in V&V, risk management, documentation, and cross-functional design reviews.

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.

Lead technical execution for orthopedic enabling technologies across hardware, software, algorithms, sensors, and visualization from concept to commercialization. Define system architecture, drive computer vision/sensor-fusion/navigation development, ensure regulatory compliance, mitigate technical risks, mentor engineering teams, and support verification, validation, manufacturability, and technology roadmapping.

Lead and manage New Product Development and cross-functional projects from initiation through commercialization. Create and maintain project plans, budgets, timelines, KPIs and risk mitigation. Coordinate Product Development, Operations, Marketing, Quality, and Commercial teams; run status meetings and executive updates; monitor execution, dependencies, and risks; drive accountability and continuous improvement in a matrixed medical device environment.

Lead UX strategy and UI design for a portfolio of MedTech products (SaMD, surgical planning, navigation, AR). Conduct user research, usability testing, workflows, prototypes, and maintain an enterprise design system. Partner with clinical, product, engineering, quality, and regulatory teams to ensure safe, consistent, and efficient clinician-focused experiences.

Lead strategy, roadmap, and commercialization for enabling surgical technologies. Drive cross-functional product development, voice-of-customer activities, market analysis, KOL relationships, and global product launches to improve orthopedic outcomes.

Lead strategy, roadmaps, and commercialization for enabling surgical technologies. Drive product vision, market analysis, KOL engagement, voice-of-customer, cross-functional development, and global launches to improve orthopedic outcomes.

Lead upstream product efforts for the ASTRA enabling technologies platform, translating surgeon and clinical insights into product requirements, driving cross-functional development, maintaining roadmaps, supporting launches, training and sales enablement, and collaborating on forecasting and production planning to deliver cloud-enabled surgical solutions.

Lead global product strategy and lifecycle for upper extremity orthopedic implants. Drive product development and launches, market research, KOL engagement, sales training, cross-functional collaboration (engineering, regulatory, quality, manufacturing, marketing), and business planning. Support surgeon education, create launch materials, analyze market data, and manage product portfolios and strategic roadmaps. Travel domestically and internationally to support launches and clinical engagement.

The role involves participating in all stages of design and development for medical devices used in Total Shoulder Arthroplasty, collaborating with cross-functional teams, creating product designs, ensuring compliance, and managing project schedules.

Responsible for ensuring compliance with quality assurance procedures, conducting audits, supporting product development, and authoring documentation, among other duties.

The Senior Regulatory Affairs Specialist will develop regulatory strategies and manage submissions for medical devices focused on orthopedic technology, ensuring compliance with relevant regulations and standards.

Manage product costing, manufacturing cost analysis, inventory valuation, and ERP cost rolls. Perform month-end cost close, analyze variances, support pricing and profitability, maintain standard costs, improve controls, and partner with operations to optimize manufacturing cost processes.