Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have improved the lives of hundreds of thousands of patients by using innovative technology that is wearable, waterproof, and lifestyle accommodating.

Position Dates: January 6, 2025- June 27, 2025

Job Title: Co-op: System Engineering, Design Verification (Onsite)

Department: Systems Engineering COE

FLSA Status: Non-Exempt

Position Overview:

Insulet is looking for enthusiastic, team-focused individuals that want to help test great products for the diabetes-care industry and obtain experience in one of the fastest growing and most exciting medical device companies in the greater Boston area! The Systems Engineering Co-op, Systems Design Verification, will be integral in the technical design and development of Insulet’s products by supporting all phases of the Design Verification Process.  The person in this position will be required to assist in the design, execution and reporting on engineering tests, for characterization and Design Verification, as well as participate in the documentation and resolution of product development issues. The Position will be reporting to the Systems Design Verification Leader, within the Systems Engineering COE at Insulet’s Headquarters in Acton, MA.

Responsibilities:

· Design, set up and run feasibility tests in an engineering laboratory environment.

· Strong focus on simulated use testing that simulates typical and non-typical use of the products by end users.

· Assist in / author product characterization and verification tests and report results.

· Perform Verification Testing on various products under development.

· Author product issue records and process these to closure.

· Participate in Technical Reviews and Design Reviews.

· Contribute to Systems team efforts by performing other duties as required.

Education and Experience:

Minimum Requirements:

· Currently enrolled in a Bachelor’s degree program in Biomedical Engineering or a related field from an accredited university.

· Technical writing ability.

· Effective verbal and written communication skills.

· Personal computer skills, word processing, spreadsheet, database.

· Ability to follow written and verbal directions and procedures.

· Ability to generate and maintain accurate records.

Preferred Skills and Competencies:

· Demonstrated working knowledge of engineering principles and scientific methods.

· General understanding of medical devices or other safety-critical technologies; a strong plus

Physical Requirements:

· None

Other Requirements:       

· Transportation to and from the Acton or Billerica locations, as determined by project responsibilities.

· The focus work periods include weekdays as available and if necessary on weekends.

NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite 

Additional Information: