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Insulet Corporation

Associate Systems Engineer, V&V

Insulet Corporation

. Support the development of Insulet's wearable medical devices by collaborating with cross-functional R&D teams throughout the product development lifecycle .

Posted 11/10/2026full-timeTijuana • MexicoJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in the design and development lifecycle of medical devices, with strong capabilities in technical writing, data analysis, and the use of engineering software tools. Proven ability to collaborate effectively within cross-functional teams and manage engineering materials in a regulated environment.

Highest-signal resume keywords
BS In EngineeringSystems Engineering ExperienceTechnical Writing AbilityExperience With Lab EquipmentData Analysis With MATLAB

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills
Design Verification TestingEngineering PrinciplesScientific MethodsSolidWorksPro-Engineer
Soft Skills
Effective Communication SkillsPlanning And Organization SkillsAbility To Work In A Fast Paced Environment
Tools & Technologies
Microsoft Office SuiteJiraHelixBambooBitbucket
Industry Keywords
Medical DevicesRegulated IndustryFDA RegulationsIoTProduct Lifecycle

Tech Stack

Tools & technologies
IoT

About the role

Key responsibilities & impact
  • Support the development of Insulet's wearable medical devices by collaborating with cross-functional R&D teams throughout the product development lifecycle
  • Collaborate with seasoned Systems Engineers on troubleshooting design issues and methods of improvement
  • Support all phases of the design and development lifecycle of a medical device
  • Participate in product design or technical reviews
  • Author and review Engineering Change Orders
  • Author engineering build requests with direct responsibility for managing 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 in support of 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, Electrical, Computer Science, etc ) discipline
  • Ability to work in a fast paced, dynamic environment with a passion for continuous learning
  • Passionate about improving the lives of others
  • Technical writing ability
  • Experience with lab equipment (testing)
  • Microsoft office suite (Word, Excel, PowerPoint)
  • Effective communication skills
  • 1-2 yrs experience as a Systems/Project Engineer in the Medical Device or other regulated industry and/or equivalent
  • Demonstrated working knowledge of engineering principles and scientific methods
  • General understanding of communication, mobile technology, IoT (Internet of Things); a strong plus
  • Experience with software / product lifecycle tools – Jira, Helix, Bamboo, Bitbucket; a strong plus
  • Hands-on and inquisitive, not being afraid to challenge a design
  • General understanding of medical devices & regulations
  • Experience with data analysis (MatLAB)
  • Planning and organization skills
  • Experience with SolidWorks or Pro-Engineer
  • Ability to organize and judge priorities in a dynamic environment
  • Must be able to sit or stand for 8 hours a day