JOB DESCRIPTION Job TitleSupplier Quality Engineering InternJob DescriptionAre you interested in an Intern opportunity with Philips?
We welcome individuals who are currently pursuing an undergraduate (BS) and/or graduate (MS) degree to participate in 6 month paid internship (prorogation possible) at our site in Alajuela, Costa Rica.
Through this role you will gain meaningful, hands-on experience in engineering for a HealthTech company.In this role, you have the opportunity to make life better Work with all key suppliers of Image Guided Therapy and Cross Functional teams (R&D and Quality) to enhance Supplier maturity through Design Quality and Product Quality.You are responsible forAnalysis of defects for determining if supplier causedSupport Supplier Corrective Action RequestsSupport APQP deliverables as parts of Sustaining ChangesContribute to Supplier performance monitoring, reporting, improvement and developmentSupports with Additions/Changes/Deletion to Approved Supplier ListSupport Supplier audit schedule development and maintenance.Assess and coordinate Supplier Change Requests.You are a part ofAs part of Philips' Image Guided Therapy (IGT) team, this role will support the high-growth Image Guided Therapy Devices business.
With our image-guided therapy solutions we are touching the lives of patients all over the world.
It is our aim to treat patients better by innovating the procedure, which is right at the heart of the Philips purpose of improving peoples lives.
We are doing this by bringing together the most sophisticated imaging systems, smart therapeutic and diagnostic devices, disease-specific software, and services in integrated solutions.
Our solutions help caregivers decide, guide, treat and confirm the right therapy for each patient.To succeed in this role, you should have the following skills and experienceTechnical engineering background to drive root cause analysis to perform problem solving - you should be an active student of Bachelor or Master Degree of Industrial Engineering/ Chemical Engineering/ Electromechanics or similar.Work closely with cross functional team and SQEs across all sites of IGTD to address none-conformances.Visit Suppliers as needed to review corrective actions.Review Design of parts to understand impact to patient safety.
