Associate Systems Verification Engineer (Hybrid - Acton, MA)

Job Summary

Be part of a fast-growing, innovative company pioneering “Liveable Technology” to transform diabetes care. We’re hiring an Associate Systems Verification Engineer to help accelerate key initiatives and deliver breakthrough, user-centric solutions in a dynamic, fast-paced environment.



The Associate Systems Verification &Validation Engineer 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 support the development, execution and approvals of system level design verification of products prior to commercial release and for most tasks associated with Design Verification and Validation as part of this COE’s product development efforts. The ideal candidate is someone who thrives in highly collaborative environments, has a high level of curiosity when solving problems and wants to make a direct impact to patient lives by ensuring the products they use achieve world-class safety and usability.  

The position will report to the Manager Systems Design Verification, Advanced Technology & Engineering located at Insulet’s Headquarters in Acton, MA. 

Responsibilities:  

• Work with Systems Engineering and other cross-disciplinary engineering functions to develop Test Cases and Protocols for design verification this Includes obtaining approval from all key stakeholders.  

• Test Cases should properly demonstrate the system performance including “happy path”, as well as properly defined extreme cases.  

• Execute verification and validation tasks according to established timelines.  

• Develop verification and validation of test tools where required. 

• Write reports and log issues for executed verification tests 

• 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: 

• Bachelors’ Degree required (preferred field of study in: Biomedical Engineering, Software Engineering, Computer Science, Mechanical, or Electrical Engineering)

• 0-2 years of relevant industry experience  

Preferred Skills and Competencies:  

• Demonstrated working knowledge of engineering principles and scientific methods. 

• Effective verbal and written communication skills. 

• Ability to follow written and verbal directions and procedures. 

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

• Experience in using any/all of the following software packages: Jira, Helix, Confluence, Arena PLM 

• Ability to generate and maintain accurate records. 

• Previous experience working in medical device or similar regulated environments  

Physical Requirements (if applicable):  

• Not Applicable 

NOTE: This position is eligible for hybrid working arrangements (requires on-site work from an Insulet office). #LI-Hybrid

Additional Information:



Compensation & Benefits:

For U.S.-based positions only, the annual base salary range for this role is $66,500.00 - $99,800.00

This position may also be eligible for incentive compensation.

We offer a comprehensive benefits package, including:
• Medical, dental, and vision insurance
• 401(k) with company match
• Paid time off (PTO)
• And additional employee wellness programs

Application Details:
This job posting will remain open until the position is filled.
To apply, please visit the Insulet Careers site and submit your application online.

Actual pay depends on skills, experience, and education.