Associate Systems Engineer - Onsite (Acton, MA)

Insulet Corporation•Acton, MA
•Onsite

About The Position

The Associate Systems Engineer supports the research and development team in the design and development of wearable medical devices, including wearable pump technology. The role provides broad exposure to medical-device development and Insulet’s design control processes, including product requirements, device integration, verification testing, troubleshooting and design analysis, and design documentation. The engineer works with experienced Systems Engineers and contributes throughout the product design and development lifecycle.

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.
  • Experience 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.
  • Demonstrated working knowledge of engineering principles and scientific methods.
  • General understanding of communication, mobile technology, and the Internet of Things.
  • 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, regulatory clearance, and commercial release.
  • Contribute to team goals by completing related tasks as required.

Benefits

  • Medical insurance
  • Dental insurance
  • Vision insurance
  • 401(k) with company match
  • Paid time off (PTO)
  • Employee wellness programs
  • May be eligible for incentive compensation
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