Medical Device Quality Engineer (Sustaining Engineering)

Regeneron PharmaceuticalsValley, AL
71d$65,200 - $121,400

About The Position

We are currently looking to fill a Quality Engineer position on the Medical Device Sustaining Engineering QA team. This position will provide Quality Assurance oversight and ensure compliance in the support of combination device development life cycles. In this role, a typical day might include the following: Reviewing design and development paperwork and records for compliance to internal procedures and regulations Ensuring accurate justification of statistical analysis and hypothesis testing Reviewing technical reports as well as documents for Design History Files Participating in device risk management activities including UFMEA, DFMEA, PFMEA Aiding in establishing statistical controls in development and transfer to manufacturing processes Reviewing and coordinating with QA Validation for all test method and design validations Reviewing activities related to Design Verification and Design Transfer of Medical Devices Ensuring work product meets regulations Supporting scientific, complaint, and test failure investigations Performing data trend analysis, participating in Phase Reviews, writing Quality Procedures, performing data/statistical analysis.

Requirements

  • Bachelor’s degree in an Engineering subject area
  • 0-2 years of experience for Associate Quality Engineer (related internship preferred)
  • 2+ years of experience for Quality Engineer in combination device or medical device industry

Nice To Haves

  • Knowledge of the combination device development process
  • Experience with device risk management activities
  • Quality mind-set

Responsibilities

  • Reviewing design and development paperwork and records for compliance to internal procedures and regulations
  • Ensuring accurate justification of statistical analysis and hypothesis testing
  • Reviewing technical reports and documents for Design History Files
  • Participating in device risk management activities including UFMEA, DFMEA, PFMEA
  • Aiding in establishing statistical controls in development and transfer to manufacturing processes
  • Reviewing and coordinating with QA Validation for all test method and design validations
  • Reviewing activities related to Design Verification and Design Transfer of Medical Devices
  • Ensuring work product meets regulations
  • Supporting scientific, complaint, and test failure investigations
  • Performing data trend analysis, participating in Phase Reviews, writing Quality Procedures, performing data/statistical analysis

Benefits

  • Health and wellness programs
  • Fitness centers
  • Equity awards
  • Annual bonuses
  • Paid time off for eligible employees
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