Systems Engineer

Insulet Corporation

. Collaborate with seasoned Systems Engineers on troubleshooting design issues and methods of improvement .

Posted 10/23/2026full-timeActon • Massachusetts • United StatesJuniorMid-Level💰 $81,700 - $122,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in systems engineering within the medical device industry, focusing on design verification, troubleshooting, and risk management. Proficient in technical writing and data analysis, with a strong understanding of regulatory requirements and product lifecycle processes.

Highest-signal resume keywords

Systems EngineeringDesign Verification TestingTechnical WritingData AnalysisMedical Device Regulations

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Systems EngineeringDesign Verification TestingTechnical WritingData AnalysisTroubleshootingRisk ManagementEngineering PrinciplesScientific MethodsSoftware as a Medical Device (SaMD)Feasibility Testing

Soft Skills

Effective CommunicationPlanning and OrganizationStructured Problem-SolvingContinuous LearningPrioritization

Tools & Technologies

Microsoft Office SuiteAmazon Web Services (AWS)Microsoft AzureJiraHelixBambooBitbucketPolarionMATLABPower BI

Industry Keywords

Medical DeviceRegulated IndustryRisk ManagementProduct LifecycleConnected/IoT Systems

Tech Stack

Tools & technologies

AWSAzureCloudIoT

About the role

Key responsibilities & impact

Collaborate with seasoned Systems Engineers on troubleshooting design issues and methods of improvement
Collaborate cross-functionally with Customer Support, Product Support, Software Development, Product Management, and Quality organizations
Lead root cause investigations, risk evaluations, and design change assessments related to on-market product issues
Support seamless transition of information from the field to development and vice versa
Own delivery of post-market initiatives, including field investigations and quality management processes
Manage escalations and inquiries from field-facing partners related to on-market products
Report findings to internal issue management teams when applicable
Support all phases of the design and development lifecycle of a medical device
Author engineering build requests and manage engineering materials
Design and set up feasibility tests in a lab environment
Author design feasibility protocols and reports
Participate in product design, technical reviews, and triage brainstorming sessions
Execute design verification testing supporting design improvements, FDA and international clearance, or commercial release
Contribute to team goals by accomplishing related tasks as required

Requirements

What you’ll need

BS in an Engineering (Biomedical, Computer Science) discipline
At least 2 years' experience as a Systems/Project Engineer in the Medical Device or other regulated industry and/or equivalent
Ability to work in a fast paced, dynamic environment with a passion for continuous learning
Passion for improving the lives of others
Technical writing ability
Experience with lab equipment (testing)
Microsoft Office suite (Word, Excel, PowerPoint)
Effective communication skills
Experience with Software as a Medical Device (SaMD) preferred
Demonstrated working knowledge of engineering principles and scientific methods
Strong systems-thinking and structured problem-solving skills
Experience troubleshooting complex systems consisting of interacting hardware, software, mobile, cloud, connectivity, and/or third-party components
Experience analyzing diagnostic logs, telemetry, system events, or large technical datasets
Working knowledge of cloud systems, mobile technologies, APIs, wireless communications, and connected/IoT (Internet of Things) systems
Experience with Amazon Web Services (AWS) and Microsoft Azure
General understanding of medical device risk and issue management
Experience with software/product lifecycle tools including Jira, Helix, Bamboo, Bitbucket, and Polarion
General understanding of medical devices and regulations
Experience with data analysis tools such as MATLAB, Minitab, or Power BI
Planning and organization skills
Ability to organize and judge priorities in a dynamic environment
Must be able to sit or stand for 8 hours a day

Benefits

Comp & perks

Incentive compensation eligibility
Medical, dental, and vision insurance
401(k) with company match
Paid time off (PTO)
Additional employee wellness programs