Associate Systems Engineer - Onsite (Acton, MA)

Insulet Corporation•Acton, MA

1d•$67,100 - $100,625•Onsite

About The Position

The Associate Systems Engineer is an integral member of Insulet’s R&D team, supporting product development for wearable pump technology. The position provides broad exposure to the design and development of wearable medical devices and to Insulet’s design control processes, including product requirements, device integration, verification test methods, troubleshooting and design analysis, and design documentation. The role supports the medical-device design and development lifecycle, including feasibility work, design improvements, regulatory clearances, and commercial release.

Requirements

Bachelor of Science degree in an engineering discipline such as biomedical engineering, electrical engineering, or computer science.
Ability to work in a fast-paced, dynamic environment and a passion for continuous learning.
Passion for improving the lives of others.
Technical writing ability.
Experience with laboratory testing equipment.
Proficiency with Microsoft Office, including Word, Excel, and PowerPoint.
Effective communication skills.

Nice To Haves

One to two years of experience as a Systems Engineer or Project Engineer in the medical-device or another regulated industry, or equivalent.
Working knowledge of engineering principles and scientific methods.
General understanding of communications, mobile technology, or the Internet of Things (IoT).
Experience with software or product lifecycle tools such as Jira, Helix, Bamboo, or Bitbucket.
Hands-on, inquisitive approach and willingness to challenge a design.
General understanding of medical devices and regulations.
Experience with data analysis using MATLAB.
Planning and organization skills.
Experience with SolidWorks or Pro-Engineer.
Ability to organize and prioritize work in a dynamic environment.

Responsibilities

Collaborate with experienced Systems Engineers to troubleshoot design issues and identify improvement methods.
Support all phases of the medical-device design and development lifecycle.
Participate in product design and technical reviews, as well as triage and brainstorming sessions.
Author and review Engineering Change Orders.
Author engineering build requests and manage engineering materials.
Design and set up feasibility tests in a laboratory environment.
Author design feasibility protocols and reports.
Execute design verification testing to support design improvements, FDA and international clearance, or commercial release.
Contribute to team goals by completing related tasks as required.