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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 (https://www.strykercareersblog.com/post/8-reasons-to-join-strykers-engineering-team )

Being a part of this team means that you are working cross functionally to drive our company's mission and strengthen the Stryker brand. You should love solving novel problems in fast paced and stimulating environment.

• Working effectively with respective cross functional stakeholders in product sustenance and assessing health risk

• Own Risk assessment deliverables and review associated design controls

• Strong hold in verification and validation activities with a rigor to drive design philosophy

• Data analysis and use statistical analysis to drive and make inform decisions.

• Minimum of 5+ years' experience in risk management, testing and analysis ideally in a strongly regulated environment such as medical device, military or aerospace industry

• Preferably Bachelor's Degree in Mechanical or Biomedical Engineering or equivalent

• Experience in risk management activities in product sustenance teams by developing risk management plans and reports, conducting risk reviews, verifying implementation and effectiveness of risk controls.

• Experience in the definition of design verification and validation test requirements that ensure appropriate objective evidence is available to support acceptance criteria.

• Participation in design reviews by identifying risks associated with the product use and tracking how the design, documentation, and manufacturing process mitigate those issues throughout the development process.

• Influential partnership with R&D to drive safety and performance during change

• Previous experience in data analysis and statistical techniques to drive appropriate risk management activities and prioritization of issues.

• Effective communication and previous experience in implementing compliance regulations and standards, including 21CFR820, ISO 13485, ISO 14971 throughout the design and development process.

• Working experience in medical device industry is preferred.

• Good knowledge with ISO 13485, ISO 14971, 21 CFR Part 820 standards

• Experience in working in highly engaged teams

About Stryker

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 130 million patients annually. More information is available at stryker.com. (http:)

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.