Engineer Ii

Merit Medical Systems

United States
Onsite
Bachelor's degree in electrical engineering
2-5 years engineering experience
Experience with electronics and electro-mechanical assemblies
Merit Medical Systems is seeking an Engineer II to support the manufacture and validation of medical devices with electronic and electro-mechanical components. The ideal candidate will have a background in engineering, preferably within the medical device industry, and will be involved in various engineering activities including troubleshooting, compliance, and collaboration with contract manufacturers

Job Summary

  • The role supports the manufacture, validation, and sustainment of medical devices with electronic and electro-mechanical content.
  • Employees will collaborate with third-party contract manufacturers to ensure products are built according to specifications and quality requirements.
  • Merit Medical offers benefits including multiple shift options, onsite medical clinic, cafeteria access, and a 401K plan.

Matching Summary

Match Score: 85

Merit Medical Systems is seeking an Engineer II to support the manufacture and validation of medical devices with electronic and electro-mechanical components. The ideal candidate will have a background in engineering, preferably within the medical device industry, and will be involved in various engineering activities including troubleshooting, compliance, and collaboration with contract manufacturers.

Skills & Requirements

Must-have

  • Bachelor's degree in Electrical Engineering
  • 2-5 years engineering experience
  • Experience with electronics and electro-mechanical assemblies
  • Knowledge of FDA QSR and ISO 13485 standards
  • Troubleshooting manufacturing and test issues

Nice-to-have

  • Medical device industry experience preferred
  • Familiarity with IEC 62304 software lifecycle
  • Experience working with contract manufacturers
  • Strong cross-functional collaboration skills

Key Requirements

  • Bachelor's degree in Electrical Engineering or related field
  • 2-5 years of engineering experience in regulated industry
  • Working knowledge of FDA QSR and ISO 13485

Work Rights

Not specified

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