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
Who we want
Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
Curious learners. Engineers who seek out cutting-edge research and information to expand and enhance their ability to design medical devices.
Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.
What you will do
As a Quality Engineer you will provide quality engineering support in quality assurance, control, and preventative activities with a focus on continuous improvement of internal products and processes.
You will support supplier quality issues impacting daily operations.
You will advocate and lead the execution of initiatives and projects to enhance quality performance within the business and for our customers.
You will work closely with operations and the business functions to ensure quality performance of product and processes.
You will collaborates with Divisional QA, cross-functional and suppliers teams to address top quality issues.
You will own identified internal and supplier driven non-conformances and manage the timely closure of NC's within.
You will own or support identified internal CAPAs and manage to timely root cause investigation, implementation and closure.
You will disposition non-conforming product within MRB, issuing NC's as appropriate.
You will communicate with suppliers regarding non-conformances, escalating supplier corrective action requests as required.
You will engage in the development and improvement of the internal manufacturing processes for existing products.
You will performs critical assessment of internal and supplier proposed change management activities.
You will maintain KPIs for monitoring of process and/or product quality, perform analysis, and interpret trends, identifying and activating on appropriate actions as necessary.
You will support execution and analysis of manufacturing related complaints and product field actions and develop understanding of risk management practices and concepts to manufacturing operations.
You advocate of Human Factor practices, familiarity in the science of Human Factor identification, reduction, and mitigation.
You will engage and interface in internal and external audits providing subject matter expertise.
You will support the development and review of process and equipment validation/qualification and MSA of internal processes.
You will support manufacturing transfers to/from other plants/facilities, executing appropriate quality activities.
You will be responsible for initiation, internal containment, communication and support of Commercial Holds for potential product escapes.
What you need
Bachelor's in science and or engineering or related discipline required
0+ years' experience in regulated manufacturing environment.
Knowledge of Quality Concepts (e.g. Risk Management, CAPA, Audits, Statistics) highly preferred
Some travel may be required.
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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. (https://careers.stryker.com/referrals/)