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

• As a (Senior) Quality Engineer (m/f/d) you will improve product quality, reliability and customer satisfaction by investigating product field failures and conducting trend analysis.
• You will ensure timely, accurate, and complete failure investigations and root cause analyses through the use of QA tools (Root cause analyses, 4-D, 5 Whys, etc.) and document findings in TrackWise.
• You will organize/lead cross-functional teams to help identify problem issue and drive product improvement.
• You will deploy good design and manufacturing practices/knowledge to make recommendations to prevent future failures.
• You will support the resolution of field issues and work with Research & Development, Advanced Quality Engineering, and Operations in Quality, Product Development and Manufacturing to resolve issues.
• You will lead the development of new and improved quality processes; streamline existing processes.

• You have completed BS in Engineering, Science, or related degree.
• You have gained a minimum of 1 years' experience in medical technology or another regulated sector in the area of quality or R&D. Ideally you have minimum 1 years' experience as a Quality Engineer, or relevant role conducting failure investigations and/or performing failure analysis.
• Ideally you are well-versed in software applications with a solid foundation in computer science/engineering.
• Ideally you have experience working with advanced reliability tools such as Failure Modes Effect Analysis (FMEA), reliability testing, statistical techniques.
• Ideally you have knowledge of FDA and international medical device regulations/standards/directives (ISO 13485, ISO 14971, 21CFR820, 93/42/CE, cGMPs).
• Your English and German language skills enable you to collaborate with colleagues and stakeholders on a global basis as well in the local office.