Jobs at ATEC Spine

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.

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

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

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.

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.

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.

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.

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.

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.

Provide clinical and technical support, training, demonstrations, installations, and troubleshooting for the Valence Robotic Navigation System and related intraoperative technologies. Support surgeons and hospital teams, train local support and sales agents, assist during procedures, collect market data and feedback, and collaborate with sales and marketing to drive regional adoption. High-travel, field-based role requiring credentialing and recordkeeping.

Administer and optimize the company travel & expense platform (Concur/SAP/Workday), manage corporate card reconciliation, prepare T&E reports and dashboards, support month-end accruals, audits, policy updates, train employees, and lead system automation and process-improvement projects.

Lead supplier quality activities for spinal orthopedic implants and related products. Perform supplier audits, drive corrective actions (SCARs/NCRs), manage supplier risk and change, support supplier qualification/validation, statistical process control, and cross-functional supplier development to ensure regulatory compliance and product quality.

The role involves conducting biomechanical evaluations of spinal implants, leading cadaveric studies, collaborating with teams on research studies, and analyzing complex data for scientific dissemination.

The Clinical Scientist II role involves leading clinical research initiatives, managing data analysis, collaborating cross-functionally, and developing technical documentation and scientific communications in spine surgery technologies.

Support Capital Sales from customer engagement through order fulfillment and post-sale support. Prepare quotations, process orders in ERP, maintain Salesforce/CRM data, coordinate onboarding, contracts, renewals, and cross-functional handoffs with Sales, Finance, Legal, Operations, and Service. Track deliveries, produce sales reports, ensure data integrity, and identify process improvements to increase operational efficiency and customer satisfaction.

Support New Product Introduction for spinal surgery devices by managing design controls, supplier qualification, inspections, validations (IQ/OQ/PQ), risk management (FMEA, ISO 14971), MRB/MRB/Supplier/CAPA activities, and regulatory audit support to ensure compliant, safe product launches.