Quality Engineer III - Medical Device - (Hillsboro, OR)

A Quality Engineer III is responsible for quality planning and the overall quality of new products being released to the market. This role actively participates in product development activities, ensuring product and process conformance to global standards (including FDA and ISO 13485). The purpose of this position is to serve as a resource to product development and manufacturing to improve product quality, reliability, and process capability and facilitate teams in identifying, documenting, assessing, correcting and presenting quality issues using risk analysis and root cause analysis tools. Duties/Responsibilities • Provide quality leadership to new product development teams in the areas of design control, design verification and validation, design transfer, process validation, risk management, and specification development