Project Engineer

Enovis•Dallas, TX

23h•Onsite

About The Position

As a key member of the Recovery Sciences business unit, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes. Enovis Recovery Sciences is the leading global provider of high-quality clinical equipment for rehabilitation and pain management used by physical therapists, occupational therapists, athletic trainers, and chiropractors. Recovery Sciences R&D supports several brands including: Chattanooga, LightForce, Companion, and Compex. The Project Engineer role is dynamic, requiring navigation of all aspects of the value stream and a strategic approach to prioritizing activities. You will lead cross-functional teams to launch new products and maintain globally shipping products, ensuring quality, compliance, and innovation. This role also contributes to strategic initiatives such as acquisition integration, manufacturing transfers, and continuous improvement.

Requirements

Bachelor’s degree in Engineering (or equivalent).
2 - 7 years work experience in Electrical, Mechanical, and/or Systems engineering.
Full-time work authorization in the United States without sponsorship.
Applicants must already have full-time work authorization in the United States, both now and in the future, without requiring sponsorship.

Nice To Haves

Experience with medical device product development is a plus.
Motivation and interest to work in the highly regulated medical devices world.
Ability to influence individuals and groups to resolve conflicts and achieve objectives.
Design controls and/or Quality Systems training.

Responsibilities

Responsible for designing, planning, directing, and coordinating products and processes for Enovis Recovery Sciences brands.
Work may involve studying/modifying schematics, circuit board layouts and component selection of electronic printed circuit board assemblies.
Work may involve studying/modifying solid models, drawings, tooling, mechanism design, chassis design, system integration, material selection and production methods.
Work may involve studying/modifying source code, module design, user interface design, automated test design, and development tool setup/design.
Provides complex technical and engineering support related to key product offerings for the Recovery Sciences portfolio currently in the market in the U.S. as well as globally.
Support includes answering questions from customers and training production associates on product functionality.
Provides technical support and guidance to various groups, such as manufacturing, quality, regulatory and supply chain departments, requiring engineering expertise to investigate and resolve complex problems.
Actively drives root cause problem solving and implementation of appropriate countermeasures.
Provides technical evaluation and analysis for potential adaptation of new techniques and procedures to resolve problems.
Conducts mechanical and electrical design analysis, hands-on troubleshooting in the lab as well as in the production environment, testing, and document review.
Uses sophisticated measurement equipment and engineering tools such as Altium, Solidworks and Jira.
Conducts planning and performs research and development activities related to new product development projects of major magnitude and scope.
Provides design input to new product development based on knowledge gained on existing product manufacturing.
Charged with the design/development of engineering assignments focused on electrical and electromechanical systems.
Duties include performing reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes.
Estimates human resource needs, costs and schedules, and coordinates with engineers, designers and technicians assigned to the projects to develop technical specifications on time.
Evaluates progress and results; recommends major changes in procedures or objectives.
Ensures business operations are in compliance with all Federal, State and local Health, Safety and Environmental regulations.
Understands medical device requirements and the needs of regulatory bodies such as FDA.
Lead cross-functional project teams, including internal and external stakeholders (Marketing, Regulatory, Quality, Supply Chain, Manufacturing, Engineering).
Develop and maintain a plan to achieve the target condition; identify variations to plan and execute corrections as needed.
Manage meetings in support of engineering change orders and all operational activities needed by the change; establish and execute a communication plan to keep all levels of the organization informed as necessary.
Documents all changes appropriately in the Product Lifecycle Management (PLM) system.
Resolve conflicts as they occur; escalate to management situations that could change the plan of record.
Ensure that the sustaining engineering activities achieve the specification, timeline, and cost targets.
Manage project risks and resolve issues.
Develop in collaboration with other departments the necessary changes to product documentation (DHF/DMR), following Enovis procedures.
Work with the cross functional team to improve the product development and sustaining engineering processes.
Develop competency in the most relevant CBS tools, including Accelerated Product Development, Root Cause Countermeasure, and Transactional Process Improvement.