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Genzeon

Genzeon

via Dice

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Graphics Software Engineer

Anywhere
Contract
Posted 12/22/2025
Verified Source
Key Skills:
3D rendering
OpenGL
Vulkan
C++ (modern)
CUDA
Linux development environment

Compensation

Salary Range

$0K - 0K a year

Responsibilities

Design and optimize 3D rendering pipelines and visualization solutions in a regulated environment.

Requirements

Requires 10+ years of software development, expertise in 3D graphics APIs, and experience with Linux and possibly medical device standards.

Full Description

Genzeon, an AI and automation company with deep engineering and data expertise, dedicated to serving the healthcare and retail industries. Our platform solutions – including HIP One, CompliancePro Solutions, and Patient Engagement Solutions – empower organizations to scale innovation and transform outcomes. Genzeon is a global community of innovators and problem-solvers, with a culture built on inclusion, flexibility, and purpose-driven work. With four global delivery centers, we support providers, payers, Healthtech, and retail organizations worldwide. Genzeon has an exciting opening for Senior Graphics Software Engineer to join our dynamic team. Role: Senior Graphics Software Engineer Location: Langhorne, PA (Locals candidate will be first preference) Duration: 6 Months Required Education and Experience • BSEE/BSCS or science degree – Master’s degree a plus • 10+ years of professional software development experience • 5+ years of recent, hands-on experience in 3D rendering design and implementation • Expertise with OpenGL; Vulkan experience highly desired • Proven experience optimizing existing 3D rendering pipelines, improving performance, and solving complex visualization problems • Strong proficiency in modern C++ (C++14/17/20); CUDA experience is a plus • Experience developing software with a Linux host development environment • Demonstrated ability to work independently as well as collaboratively on a multidisciplinary team. Preferred Qualifications • Experience with requirements analysis, software architecture, and design documentation • Familiarity with FDA 510(k) submissions, medical device development standards, and quality system requirements • Experience working in regulated environments (e.g., ISO 13485, IEC 62304)

This job posting was last updated on 12/29/2025

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