Jobs at ATEC Spine

Support inventory and cost accounting by preparing journal entries, reconciliations, inventory analyses, and month-end close. Partner with Operations, Supply Chain, and Finance to ensure accurate valuation, costing, and COGS reporting. Support SOX compliance, internal controls, inventory audits, and process improvement in a medical device manufacturing environment.

Design, implement, test, document, and validate C++ software for a surgical navigation and robotics platform on Unix/Linux. Perform integration/system testing, support clinical prototyping and field troubleshooting, maintain version control and unit tests, and collaborate with cross-functional teams to meet FDA quality and reliability standards.

Design, implement, test, and document C++/Linux applications for a surgical navigation and robotics platform. Participate across product development (requirements, design, risk assessment, validation), integrate software/hardware, support clinical prototyping and field-deployed systems, attend surgical cases, and collaborate with cross-functional teams to drive product improvements and regulatory compliance.

Lead design, development, testing, validation, and documentation of C++/Linux surgical navigation applications. Provide technical leadership and mentorship, collaborate cross-functionally for regulatory (510k) approval, support clinical prototyping and surgical evaluations, and manage project planning and feature prioritization. Attend surgeries and travel occasionally.

Coordinate surgical assets and inventory for surgical requirements. Work with the sales team and hospital personnel to track and transport assets.

The SAP SD Analyst supports and optimizes Sales and Distribution processes in SAP S/4HANA, focusing on Order-to-Cash processes, integration, and troubleshooting.

Responsible for SAP FICO configuration, troubleshooting, and integration support across financial modules while collaborating with various stakeholders to ensure system efficiency and compliance.

Primary administrator for HRIS responsible for system configuration, data integrity, integrations, reporting, compliance, and user support. Partners with HR functions and vendors to optimize workflows, deliver reports and analytics, support implementations and audits, and provide training to improve employee experience.

Manage a portion of the neuromonitoring product portfolio from inception to obsolescence. Define requirements, gather surgeon feedback, drive marketing strategy and launches, coordinate cross-functional teams, develop sales collateral and forecasts, maintain customer relationships, support training and events, manage budget, and travel 15–40% to support sales and surgeon engagement.

Responsible for enhancing existing products, creating designs using 3D CAD software, generating design documentation, and assisting in product development and testing processes.

The Sales Representative develops and implements strategies to achieve sales goals and enhance market share, focusing on orthopedic medical devices.

Develop and implement sales strategies, grow business, maintain customer relationships, and achieve sales goals within targeted areas and hospitals.

The Product Manager develops marketing strategies, oversees product management, conducts market research, collaborates with teams, and manages product launch and surveillance to maximize product line value.

The PLM Analyst supports Oracle Fusion Cloud PLM, ensuring compliance and seamless integration with systems like SAP S/4HANA while managing product data and documentation in a regulated medical device environment.

Manage execution of cross-functional Informatics R&D programs for software-intensive medical products (SaMD/SiMD). Maintain plans, schedules, risks, decisions, and action items; coordinate engineering, regulatory, quality, clinical, and product teams; drive status reporting, issue escalation, and controlled documentation to ensure on-time, compliant delivery.

Perform 3D spinal reconstructions and full-body alignment measurements from bi-planar EOS radiographs, conduct quality control and verifications, support research database creation, meet production volumes, and document process feedback for continuous improvement.

Support clinical evidence initiatives by designing CRFs and data management plans, building/curating study databases, cleaning and preparing datasets for analysis, running statistical tests, creating visualizations and reports, managing data queries, and collaborating on study documentation, publications, and SOPs to ensure data accuracy and regulatory compliance.

Lead design and development of implants and instruments using SolidWorks 3D CAD. Drive prototyping, testing protocols, DHF and ECO documentation, and inspection methods. Collaborate with manufacturing, quality, regulatory, marketing, and sales to bring products from concept to launch and support FDA 510(k) submissions.

Design, implement, and maintain Windows-based C#/.NET applications, distributed services, and embedded integrations. Build inter-service communication (e.g., RabbitMQ), perform integration and system testing, maintain CI/CD and documentation, estimate and execute project tasks, and collaborate with global Agile teams in regulated medical-device development environments.

Lead and deliver complex cross-functional Informatics R&D programs for software-intensive medical products (SaMD/SiMD). Own integrated program plans, manage dependencies, risks, and decisions, drive execution cadence, align stakeholders, ensure regulatory and quality controls, and mature program management practices across product lines and platforms.