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

Our benefits include bonuses; commissions; healthcare; insurance benefits; retirement programs; stock based plans; paid time off plans; family and parenting leaves; tuition reimbursement; wellness programs; onsite fitness centers and cafeterias; discount purchase programs; and service and performance awards – not to mention various social and recreational activities.

This position conducts engineering activities and tasks in support of manufacturing requirements.  Activities and tasks are conducted on materials, products, processes, and equipment.

• Ability to work well with others in a team setting.

• Ability to conduct complex statistical, geometric, and mathematical calculations.

• Ability to conduct responsibilities substantially free from routine supervision. 

• Ability to read, understand, create engineering drawings on common engineering software.

• Ability to work efficiently on common personal computer hardware and software.   

• Proficient in Microsoft Office applications

• Demonstrate a primary commitment to patient safety, product quality and compliance with the Stryker, Quality Manual and its governing regulations.

• Document and improve manufacturing processes and operations that control the safety and efficacy of finished devices.

• Conduct qualification, verification, and validation activities for the production of medical devices.

• Analyze, troubleshoot and resolve issues relating to the safety, efficacy, quality, cost, or delivery of components and finished devices.           

• Complete engineering work and contribute to new product development teams and product support, typically including the following activities: technology development, test of materials or products, preparation of specifications, Six Sigma, process study, process improvements, and report preparation.

• Develop manufacturing equipment in compliance with manufacturing safety (e.g., OSHA & EPA) principles.

• Design, procure, and fabricate tooling and fixtures.

• Participate in design control efforts related to risk analysis (FMEA) & design reviews.

• Preferred:  Source component and service suppliers; assess supplier capability and effectiveness.

• Train, develop, and/or provide work direction to operators and technicians.

• Participate in the identification, implementation, and management of production goals.

• Participate on cross-functional project teams. Coordinate, manage, and document project work and progress, and recommend appropriate revisions.

• Design and coordinate engineering tests and experiments. Analyze data, draw conclusions, and summarize test results. Communicate results to manager.

• Interfaces with product builders or extrusion technicians, production supervisors, and engineers in troubleshooting problems on the production floor.

• Participates in project teams typically including one of the following:

• Identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance.

• Designing, performing, and documenting engineering test experiments to evaluate product/process performance.

• Designing, developing, testing, and validating equipment and processes; analyzing and interpreting process models and recommending process improvements.

• Evaluating external process technologies.

• Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.

• Participates in project planning and scheduling.

• Attends and contributes to production core team meetings.

Know someone at Stryker?

Be sure to have them submit you as a referral prior to applying for this position. Learn more about our employee referral program at https://careers.stryker.com/referrals/

About Stryker

Stryker is one of the world’s leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.

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

The future of healthcare starts with you. Customers, patients and employees are at the heart of everything we do at Stryker. As a world-leading medical technology company, we are focused on innovative healthcare solutions not just for today but for tomorrow. The future of healthcare starts with hiring the best talent and providing our employees with flexibility and opportunity to grow their careers in whatever direction their passions take them.