Work Flexibility: Hybrid or Onsite
This is a permanent hybrid role with full Stryker benefits.
As a Senior(Advanced) Quality Engineer,you will influence Engineering and Advanced Operations to define design requirements and develop manufacturing processes to support new product development projects. You will have the responsibility to drive reliability engineering, human factors engineering, risk management, and design validation, while ensuring compliance to Stryker quality system, FDA Quality System Regulations, ISO 13485 and other medical device regulations.
Engage in design reviews by identifying risks associated with the product used and tracking how the design, documentation, and manufacturing process mitigate those issues throughout the development process.
You will use quality engineering tools, statistical methods, design development methods, process development and control methods, and design verification and validation planning to build quality into new products during development.
Develop, review, and approve inspection plans, routers, and product drawings for new products.
Travel Percentage: 10%