Software Engineer

GForce Life Sciences; Florida; Hybrid; USD 100,000 - 140,000; Full time

Job summary

GForce Life Sciences seeks a Consultant, Software Engineer for a 12-month contract in Weston, FL. The role centers on understanding current architecture, designing and developing application software components, and collaborating with the PM and engineers to drive project success.

The candidate will follow SDLC procedures, perform unit and component tests, code reviews, and document activities in the Quality Management System. Strong C++ OO skills in production are required.

Qualifications

• Bachelor's Degree in Software Engineering or Computer Science with 5+ years of experience.
• Demonstrated proficiency in C++ and Object-Oriented programming in a production environment.

Responsibilities

• Understand existing architecture, codebase, and development workflows.
• Independently design and develop application software components per requirements and architecture.
• Collaborate with Project Management and engineers to ensure project success.
• Follow SDLC procedures to ensure software quality through reviews, tests, and defect management.
• Document software engineering activities following R&D procedures in the Quality Management System.
• Communicate progress, risks, and technical decisions.

Skills

C++

Object-Oriented

Education

Bachelor's degree in Software Engineering / Computer Science

Tools

Qt/QML

Linux

Docker

Job description

Consultant, Software Engineer, Medical Device

12-month Contract with potential to extend

Hybrid- Weston, FL

Must be able to work on a W2

Job Duties

• Quickly understand existing architecture, codebase, and development workflows.
• Independently design and develop Application software components per defined requirements and architecture, following design principles and coding standards.
• Collaborate closely with the Project Management team and other engineers to ensure project success as a technical member of the team.
• Follow defined SDLC procedures to ensure software quality through code review, unit and component tests, code analysis, and defect management.
• Author software engineering documentation following R&D procedure per the Quality Management System.
• Clearly communicate progress, risks, and technical decisions.

Requirements

• Bachelor's Degree in Software Engineering / Computer Science or related discipline & 5+ years of work experience.
• Demonstrated proficiency in C++ and Object-Oriented programming in a production environment.

Preferred Qualifications

• Prior contractor or consulting experience with a record of success joining teams mid‑stream and ramping up quickly.
• Experience in Qt/QML framework, Linux, and/or Docker.
• Demonstrated knowledge of full SDLC and Agile software development with tools for static/dynamic analysis, memory management, unit testing, code coverage, CI/CD, security, and task/defect/requirement management.
• Demonstrated knowledge of linear algebra, computational geometry, computer graphics, and software architecture design (e.g., design patterns and software modeling).
• Experience in medical imaging, image processing, computer vision, algorithm development, computer-assisted surgery, or robotics.
• Experience with biomedical software development or software development in a regulated environment.