Systems Engineer, V&v (hybrid- Acton, Ma)

Insulet

Acton, MA, US
Base: $77,300.00 - $116,000.00; bonus/equity: may ...
Hybrid
Verification and validation management
Medical device testing experience
Systems engineering collaboration
The Systems Engineer V&V is responsible for managing all verification and validation activities and deliverables for new product development and sustaining products at Insulet’s headquarters in Acton, MA

Job Summary

  • The Systems Engineer V&V is responsible for managing all verification and validation activities and deliverables for new product development and sustaining products at Insulet’s headquarters in Acton, MA.
  • This position offers a comprehensive benefits package including medical, dental, vision insurance, 401(k) with company match, paid time off, and employee wellness programs.
  • Insulet is an innovative medical device company dedicated to simplifying life for people with diabetes through its Omnipod product platform and values hiring highly motivated, performance-driven individuals.

Matching Summary

The Systems Engineer V&V is responsible for managing all verification and validation activities and deliverables for new product development and sustaining products at Insulet’s headquarters in Acton, MA.

Salary

Base: $77,300.00 - $116,000.00; Bonus/Equity: May be eligible for incentive compensation; Benefits: Medical, dental, vision insurance, 401(k) match, PTO, wellness programs

Skills & Requirements

Must-have

  • Verification and Validation management
  • Medical device testing experience
  • Systems Engineering collaboration
  • Test case and test run management
  • Compliance with quality policies
  • Hybrid work arrangement

Nice-to-have

  • Automation testing experience
  • Atlassian tools familiarity
  • Technical leadership skills
  • Project team collaboration
  • FDA-regulated device development
  • Problem-solving and communication

Key Requirements

  • Bachelor’s degree in engineering or related field
  • Minimum 3 years medical device testing experience
  • Experience in FDA-regulated device development
  • Knowledge of ISO 13485 and IEC standards
  • Experience leading V&V test programs

Work Rights

Not specified

Tailored Resume

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