Engineer III

Job Title : Software Engineer

Location : Pleasanton, CA - Hybrid

Duration : 12 months. Will more than likely renew.

Work Schedule - M-F Normal Business Hours

What are the top 3-5 skills, experience or education required for this position :

1. Software in a medical device

2. C# experience on Windows

3. Algorithm development

Job Description :

The software engineer III will work collaboratively with a team to support medical device products from the transfer to production through product end of life. The engineer will have a technical leadership role for supporting components and subassemblies of the body contouring products and will closely interact with a multi-disciplined Engineering team consisting of advanced research, electrical, software and mechanical groups.

The individual works within cross-functional teams and provides software requirements, design and implementation for current generation software and systems projects. He or she develops a thorough understanding of design requirements to ensure that the system's objectives are properly defined and ultimately achieved.

This role is focused on continuous improvement of existing products and in particular algorithm improvements. This individual must have strong technical and data analysis skills complemented by great communications and teamwork qualities. Experience in a software development background in a structured / regulated environment such as medical device development is required.

Major Responsibilities :

• Lead and manage small scale projects for on time deliverable.
• Contribute to requirements definition at the functional level.
• Perform in-depth data analysis and drive improvements to software, algorithms, or product quality.
• Work with cross functional groups.
• Design, develop, and support embedded, Windows embedded and desktop applications.
• Participate in software work product reviews / inspections.
• Interface, integrate, troubleshoot and debug software and hardware components.
• Generate required product development documentation including functional specifications and design documents.
• Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical

Device Regulations, and all other international regulatory requirements with which complies.

Qualifications :

Interviews : Onsite