Design Quality Engineer 1

Overview

As a Design Quality Engineer 1, you support senior Quality Engineering staff on New Product Development activities for hardware and software products, working under direct supervision.

What you'll do

• Support design control and risk management activities for assigned projects.
• Assist with risk management planning and development of the overall risk management file.
• Participate in core cross-functional teams and provide quality inputs to design and requirements documentation.
• Support design verification, design validation, and usability testing, including protocol/use case development and report writing.
• Develop and release engineering design documentation and support design reviews and design history file compilation/audit activities.
• Support manufacturing quality activities such as measurement systems analysis, incoming inspection, control plans, process summaries, and process FMEA.

What you'll need

• 0–3 years of quality engineering experience in the medical device industry.
• B.S. in engineering or a technically related field.
• Time management and ability to plan and schedule multiple projects and tasks.
• Effective collaboration with cross-functional teams.
• Effective written and oral communication skills.
• Accountability.
• Knowledge of design controls, risk management, testing, statistics, and measurement systems.

Details

• Hybrid work model (for most professional roles).