ProMade New Product Development Technician

DJO Tunisie; Austin (TX); On-site; USD 60,000 - 90,000; Full time

Job summary

Enovis is seeking a ProMade Engineering Technician in Austin, Texas, to support product data management and documentation across the orthopedic development lifecycle.

You will perform CT segmentation refinement, manage design history files, and coordinate with engineering, manufacturing, quality, regulatory, and supply chain teams within Agile PLM/PDM to ensure timely product releases and compliance.

Qualifications

• Experience with CT segmentation data handling and product data management.
• Experience with Agile PLM/PDM and end-to-end product lifecycle management.
• Ability to maintain Design History Files and device master records within regulated environments.

Responsibilities

• Support CT segmentation, part number creation, labeling, and product records in Agile PLM/PDM.
• Create and maintain bills of materials and configuration data across the product lifecycle.
• Prepare engineering change and release documentation while ensuring data accuracy.
• Coordinate cross-functional reviews with Engineering, Quality, Regulatory, and Supply Chain.
• Maintain document control and ensure audit readiness for design history files.

Skills

Product data management

Documentation management

CT segmentation refinement

Agile PLM/PDM

Cross-functional teamwork

Tools

Agile PLM/PDM

Design History Files

Job description

Who We Are

ABOUT ENOVIS™ Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company's extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit www.enovis.com .

What You'll Do

At Enovis™ we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence - with the goal of transforming medical technology as we know it. Because that's how we change the lives of patients for the better. And that's how we create better together. Why work at Enovis? See for yourself . As a key member of the Research and Development Team you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Job Title:

ProMade Engineering Technician

Reports To:

Promade Product Development Manager

Location:

Austin Texas

Business Unit Description:

Driven by Enovis' desire to create innovative products that help improve quality of life and restore movement to those suffering from degenerative arthritis, Enovis Surgical provides orthopedic surgeons with modern, patient-focused solutions for total joint arthroplasty. Enovis Surgical offers surgeons and their patients a full range of primary and revision implants for hip, knee, shoulder, and elbow reconstructive joint surgeries, in addition to the tools and digital health technology needed in today's changing healthcare environment.

Job Title/High-Level Position Summary:

The ProMade Engineering Technician provides technical, documentation, imaging-data, and product data management support for the development and lifecycle management of patient-specific orthopedic products. This position supports Product Development Engineers by performing CT segmentation refinement, managing product records, design development documentation, labeling activities, electronic design development files, and workflow execution within Agile PLM/PDM.

Key Responsibilities:

Product Data & Configuration Management Support the part number identification process by coordinating with Product Development, Manufacturing Engineering, Packaging Engineering, Quality, Regulatory Affairs, Supply Chain, and Operations. Create and maintain approved part numbers for patient-specific implants, instruments, packaging components, and associated product records in Agile PLM/PDM. Create and maintain bills of materials, product structures, master data, and configuration records throughout the product lifecycle. Prepare and process engineering change and release documentation while maintaining configuration control and data integrity.

Labeling & Product Identification Support the label creation process for patient-specific products, packaging, and associated identification records. Create and maintain product label requests using released request forms and adjust as necessary through collaboration with the labeling engineer.

Documentation & Electronic Design File Management Create, organize, and maintain electronic Design History Files, Design Development Files, Device Master Record documentation, and other required development records. Collect, organize, and verify completion of required design control deliverables. Maintain documentation in accordance with document control, retention, and audit-readiness requirements.

Agile Workflow Administration Manage document routing, reviewer assignments, and approval workflows within Agile PLM/PDM. Coordinate cross-functional reviews involving Product Development, Manufacturing Engineering, Packaging Engineering, Quality, Regulatory Affairs, Supply Chain, Operations, and other required stakeholders. Monitor workflow status, communicate pending actions, elevate bottlenecks, and support timely closure of approvals.

Cross-Functional Project Support Participate in project meetings and provide updates on CT segmentation, part number, label, documentation, and workflow status. Support project schedules by maintaining readiness of segmentation outputs, product records, labels, design documentation, and release packages. Generate reports and metrics related to documentation status, part number creation, labeling activities, and workflow performance. Facilitate communication across functions to support timely product release activities.

Quality & Compliance Follow applicable quality system procedures, work instructions, data-handling requirements, and regulatory requirements. Support internal and external audits and maintain training and qualifications required for the role. Demonstrate accuracy, thoroughness, and continuous improvement in segmentation, documentation