Product acceptance engineer
2 weeks ago
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:
Complete Lot Review and Release for The Finished Goods Operations. Complete Sterile load reviews Continuous improvement and development of acceptance and inspection activities in The Finished Goods Operations. Introduction of best practices in acceptance and inspection activities. Co-ordinate with business units to ensure that acceptance and inspection activities are appropriately carried out. Ensure that a consistent approach to acceptance and inspection activities is developed and maintained. Co-ordinate with the business units in relation to non-conformance activities and root cause analysis associated with acceptance and inspection activities, to ensure a consistent approach. Provide effective and responsive QA support to Operations to resolve in-house, customer and supplier issues. Ensure regulatory compliance in area of responsibility to GMP of all medical device's regulatory agencies (, IMB and BSI). Provide functional expertise to other support function on quality related issues. Own and drive NC/CAPA's related to process. Interface with Suppliers for quality Issues. Work cross functionally with such groups as Regulatory, Design Division and Operations to ensure all issues are successfully resolved. Support The Finished Goods Operations in addressing quality metrics, , CAPA, , , Process Changes, , Quality Alert, Product Holds and Recalls. Support site during External Audits. (, IMB and BSI). Support / act as local subject expert for review, creation and training of divisional/corporate procedures. Responsible for input to Quality Metrics. Ensure system transactions Degree in Science or equivalent is required. Minimum of 2 years' experience in a QA role. Good level of technical and analytical skills. Problem Solving Skills and ability to handle multiple tasks in a fast-paced environment. Capable of working as part of a multi-discipline team across multiple continents and time zones. Previous experience in Lot Review and Release would be an advantage The individual should enjoy working in a fast paced, dynamic and results motivated team environment. The individual should be able to work independently to achieve desired goals and results. Competent in working with all Microsoft Office programs (Excel, PowerPoint & Visio etc). Previous experience with ERP systems (SAP, Oracle etc,) would be an advantage. Excellent Communicator.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
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