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Software Engineer | Medical Device

Enovis
Dallas, TX, United States
Full-time

Job Description :

At Enovis we sweat the little things. We embrace collaboration with our partners and patients, and we glory in the grind 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.

As a key member of the Recovery Science 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.

Job Title : Software Engineer

Software Engineer

Reports To :

Director, Sustaining Engineering

Location :

Lewisville, Texas (Hybrid)

Business Unit Description :

Enovis Recovery Sciences business 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.

To improve our position even further, Recovery Sciences is focused on accelerating the pace of new product development and better integrating our global product offering to meet the changing needs of clinicians.

Recovery Sciences R&D supports both the Chattanooga, Compex , LightForce and Companion brands.

Job Title / High Level Position Summary :

The Software Engineer will work with a high performing product development team to extend our current product offering with innovative software solutions.

This role will be specifically focused on maintaining software that controls neuromuscular electrical stimulation, ultrasound, laser and mechanical traction devices.

Additionally, this role will contribute to the evolution of connecting devices via network technologies to improve the workflow in clinical settings.

Key Responsibilities :

  • Improve and maintain existing embedded software for electro-therapy products and related documentation (DHF)
  • Investigate software-related issues, perform and document root-cause analysis
  • Coordinate software change activities in collaboration with Project Management, QA, RA, Clinical dept., and product management representatives
  • Setup or extend test infrastructure and software tools
  • Implementation of software change, release, and documentation
  • Organize, document, and participate in software design and code reviews and provides support to manufacturing, servicing and product management department
  • Contribute to new product development project success in a multidisciplinary, international team

Minimum Basic Qualifications :

  • Bachelor's degree in computer science, computer / electrical engineering, information technology or a similar field
  • 5 years experience in software / embedded software development with skills in C#, Javascript, Linux, DevOps, git
  • Medical Device Industry highly desirable with FDA, MDR, 62304, documentation, release process, CAPA, QA, RA
  • Proficient in C, good knowledge of other programming languages including C#, C++, Python, Bash
  • Strong experience in low-level MCU programming like STM32, involving peripherals such as ADC, DAC, UART, SPI, I2C, DMA, USB, Timers
  • Fundamental understanding of electronics, capable of reading and understanding schematic around the MCU
  • Experience with development tools such as debuggers (JTAG), oscilloscopes, logic analyzers, simulators
  • Firmware development expertise is highly desirable

Travel Requirements :

Minima l

Desired Characteristics :

  • Proven track record with low-level software in a MS Windows based environment development
  • Motivation and interest to work in the highly regulated medical devices world
  • Experience with IEC 62304 : 2015 - Medical device software including architecture / documentation / testing of moderate and high level of concern classified products
  • Experience working on Class II Medical Devices and appropriate use of Risk Management standard ISO 14971
  • Experience with FDA guidance documents related to medical device software. Demonstrate an understanding of design control requirements for medical devices and successfully navigate the product development process to release successful products to the market
  • Solid understanding and appreciation of SDLC process and tools (GIT, JIRA, ALM, etc...)
  • Ability to work independently with minimal oversight
  • Ability to work under strong timing and performance pressure
  • Ability to explain complex technical issues and justify solutions with data
  • Capable of transforming business requirements into technical design
  • Strong team spirit and ability to evolve in an international and multi-cultural environment
  • Additional beneficial skills :
  • Experience / knowledge of cybersecurity standards applicable to medical device products
  • Demonstrated understanding of user experience, user centered design and responsive web design
  • Design Controls and / or Quality Management Systems training
  • Experience in battery powered designs with limited resources (battery, processor power, space and costs)
  • Programming experience on mobile platforms (Android and / or iOS) or web frontend and backend

Creating better together". It's the Enovis purpose, and it's what drives us and empowers us every day on a global scale.

We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.

Watch this short video and discover what creating better together means to us at Enovis :

Our Enovis Purpose, Values and Behaviors on Vimeo

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.

Visit www.enovis.com to learn more.

EQUAL EMPLOYMENT OPPORTUNITY :

Enovis provides equal employment opportunities based on merit, experience, and other work-related criteria and without regard to race, color, ethnicity, religion, national origin, sex, age, pregnancy, disability, veteran status, or any other status protected by applicable law.

We also strive to provide reasonable accommodation to employees' beliefs and practices that do not conflict with Enovis policies and applicable law.

We value the unique contributions that every employee brings to their role with Enovis.

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 .

EOE AA M / F / VET / Disability Statement

All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, religion, color, national origin, sex, protected veteran status, disability, or any other basis protected by federal, state or local laws.

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