Position Overview

Supports the development and manufacture of medical devices. Will work with Manufacturing and R&D to resolve product quality issues. Supports manufacturing process changes, product design improvements, and the implementation of new products. Typical duties include:
  • Works with Manufacturing Engineers to review process changes and resolve product quality issues.
  • Works with suppliers to maintain high quality levels of incoming production materials.
  • Conducts quality audits of suppliers.
  • Work with R&D engineers to support implementation of new products by reviewing quality and testing plans.
  • Works with R&D and manufacturing engineers to develop the DFMEA and PFMEA.
  • Works with R&D and manufacturing engineers to develop test protocols and reports (design verification, design validation, process qualification and process validation)
  • As assigned, maintains various Quality Systems such as CAPA, Non-Conformance (NCR), supplier quality, equipment calibration, internal auditing and quality metrics data analysis.
    • Bachelor’s degree in Engineering or related field
    • Minimum of two (2) years of related experience
    • Strong written and verbal communication skills
    • Proficient computer skills including MS Word, Excel, and statistical software (e.g., MiniTab, Statgraphics, Design of Experiment DOE, etc.)
    Desired qualifications:
    • Knowledge of medical product manufacturing
    • Strong mathematics skills
    • Ability to understand the technology related to MicroVention’s products
    • Knowledge of medical product quality assurance (including the requirements for test protocols and statistical techniques)