Design Quality Engineer II

Burlington Permanent USD95,000 - USD115,000 per year
  • Dynamic role in fast growing Medical Device Start-up
  • Work on new products in the bio-materials space

About Our Client

Our client is an oral health care company that delivers advanced, easy-to-use implants, biomaterials and planning software for dental professionals focused on providing the most functional and most aesthetically pleasing outcomes possible.

Job Description

The key responsibilities of The Design Quality Engineer are:

  • Basic tasks associated with this position are as follows:
    • Review and maintain Design History Files for new products and product improvements
    • Revise SOPs and align with regulatory requirements
    • Document critical engineering analyses and studies
    • Develop specifications, test methods/equipment, author verification and validation protocols/reports
    • Maintain risk management files, perform risk assessments/FMEA
    • Interface with critical suppliers during design transfer and resolve technical issues
    • Author and review document change orders

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

The successful Design Quality Engineer are:

  • BS in Biomedical/Mechanical Engineering
  • 1-5 years of medical device experience
  • Important Skills: PFMEA, Verification & Validation(V&V), SOP

What's on Offer

Our client offers a base salary with strong benefits and the flexibility to work from home.

Daniel Hall
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Job summary

Engineering & Manufacturing
Sub Sector
Quality, Technical
Industrial / Manufacturing
Contract Type
Consultant name
Daniel Hall
Job Reference