Software Engineer I

LivaNova•Houston, TX

1d•$75,000 - $85,000•Hybrid

About The Position

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives. The Software Engineer I is responsible for software development and the maintenance of software applications associated with LivaNova’s medical product systems.

Requirements

BS in Computer Science, Electrical Engineering or related field, or relevant experience
Proficient in C#/.NET/Xamarin, C++, Windows and Mobile Application Development

Responsibilities

Lead and coordinate multi-departmental software development projects in accordance with the Product Development Procedure, Quality Policy, and Software Development Procedure.
Apply software engineering knowledge to the design and development of new products as well as product changes and enhancements.
Solve software engineering problems at the subsystem through system level.
Conduct testing utilizing existing test protocols or develop new ones as needed.
Generate written protocols and reports.
Assign work to technicians, temporary workers and others on the project team.
Complete projects (including product enhancements) in a manner consistent with corporate objectives.
Maintain accurate documentation of concepts, designs, architecture, detailed designs, interface specifications, code, code reviews, and testing.
Conduct, lead, and participate in code and design reviews.
Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to company products.
Provide software engineering and technical support of products introduced into both the domestic and international markets as well as physician in service programs.
Oversee outside vendors and consultants as required.
Maintain Quality System compliance in coordination with the Document Control, Clinical, and Quality Assurance functions.
Provide software engineering support in the resolution of product complaints and/or safety issues.
Work with other engineering, manufacturing, clinical affairs, sales and marketing, and quality assurance staff to coordinate pilot production of new products.
Support company goals and objectives, policies and procedures, Quality System Regulations, and FDA regulations.
Chair project meeting and design review.
Perform documentation of software development as required by the product development and quality procedures.
Perform other duties as may be required by management.