Senior Engineer Quality Assurance

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

• Work closely with operations and the business functions to ensure quality performance of product and processes.
• Collaborates with Divisional QA, cross-functional and suppliers' teams to address top quality issues.
• Own identified internal and supplier driven non-conformances and manage the timely closure of NC's within Trackwise. Own or support identified internal CAPAs and manage to timely root cause investigation, implementation and closure.
• Communicate & collaborate with suppliers regarding non-conformances, escalating supplier corrective action requests as required.
• Engage in the development and improvement of the internal manufacturing processes for existing products.
• Performs critical assessment of internal and supplier proposed change management activities.
• Performs PPAP activities for supplier changes
• Participates and may lead in the creation and/or review of new or modified procedures.
• Maintain KPIs for monitoring of process and/or product quality, perform analysis, and interpret trends, identifying and activating on appropriate actions as necessary.
• Support and Drive Human Factor practices, familiarity in the science of Human Factor identification, reduction, and mitigation.
• Develop understanding of risk management practices and concepts and applies knowledge to manufacturing operations.
• Applies statistical methods of analysis and process control to current operations.
• Engage and interface in internal and external audits providing subject matter expertise
• Support the development and review of process and equipment validation/qualification and MSA of internal processes.
• Execute internal quality deliverables associated with engineering changes, manufacturing transfers and supplier-initiated changes.
• Responsible for initiation, internal containment, communication and support of Commercial Holds for potential product escapes.