Senior Design Quality Engineer (Hybrid)

at  Stryker Corporation

WHY ENGINEERING AT STRYKER?

At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.
Need another reason to apply? Check out these 8 reasons to join Stryker’s engineering team: https://www.strykercareersblog.com/post/8-reasons-to-join-strykers-engineering-team
We are proud to be named one of the World’s Best Workplaces and a Best Workplace for Diversity by Fortune Magazine! Learn more about our award-winning organization by visiting stryker.com
Stryker is hiring a SENIOR DESIGN QUALITY ENGINEER in Salt Lake City, UT for our Neurovascular division, pushing the boundaries of technology to meet ever increasing product performance requirements, making the goal of assessing and demonstrating safety, performance and compliance an exciting challenge.
Workplace Flexibility: Candidate must reside within a commutable distance to Salt Lake City, UT but is expected to be onsite at the facility at least 3 times/week.

KNOW SOMEONE AT STRYKER?

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Stryker is driven to work together with our customers to make healthcare better. Employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required, depending on customer requirements, to obtain various vaccinations as an essential function of their role

• In this Senior Design Quality Engineer position, you will be involved in supporting fast paced product design change efforts.
• You will be responsible for developing qualification plans, protocols, perform product testing and failure analysis, writing reports.
• You will make regular use of problem solving tools and statistical analysis to perform test method development and validation, design verification, risk assessment and design reviews.
• As a DQE, you will be responsible for product risk management and adherence to design control requirements throughout the product lifecycle.
• You will create and maintain risk files and assess the impact of necessary changes to our products. Remediation of existing risk files will require discussions with Medical Safety, R&D, Marketing, and Regulatory Affairs to bring the files into compliance with current best practices.