QLTY & RELIABILITY TECHNICIAN III NIGHT SHIFTAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Job OverviewTE Connectivity's Quality and Reliability Engineering Teams analyze the ability of product and production systems to comply with customer and contractual requirements through established reliability factors. They design, recommend revisions and install quality control systems, develop and document analytical methods for establishing reliability of products and their components and conduct analysis on relative reliability with regards to cost, structure, weight, maintainability, facility of production, and availability of materials and equipment. Our teams develop, implement and monitor company environmental safety programs and policies to ensure compliance with federal, state, and local environmental, health and safety regulations and recommend corrective actions if necessary.
Job DescriptionThe Quality & Reliability Technician is a member of the Quality group. They will work as part of a team to maintain high quality/performance standards on all TE Connectivity products. Reporting to the Area Operations Senior Quality Engineer, the position will be challenging and will require an ability to participate in a cross-functional team and work on own initiative and with minimum supervision. Job ResponsibilitiesWorking with the Manufacturing teams promote the achievement of the health and safety goals.Deliver on all KPIs that help the business achieve its goal.Implement corrective action on issues as they arise.Disposition non-conformances, conduct & determine root cause analysis including corrective actions.Conduct area practice vs procedure/Good Documentation Practice audits and follow up on findings to ensure satisfactory closure.Follow up on Corrective Actions for in-process and customer complaint issues.In-process sampling and testing and subsequent report writing.Conduct First Article Inspections on product as required.Additional ResponsibilitiesProcessing procedure changes.Support all QA related documentation activities (i.e. Raise Change plans, write procedures etc).Review of sterilisation documentation and the release of sterilised product for shipping.Support functional area validation activities.Support Fault Analysis and Scrap Reduction activities.Participate/drive quality improvement projects/activities.Participate in preparing & ongoing maintenance of FMEAs and Control Plans. Reporting function Quality metrics.Support NPI/manufacturing Operations area projects and initiatives e.g. Kaizen, yield improvement, cost reduction etc.Other tasks as directed by the functional area Quality Engineer in line with company goals and objectives.Provide support for internal, customer and external audits to ISO and FDA requirements.Key RequirementsA problem-solving qualification (either green or yellow belt) preferred.Clear understanding of medical device quality systems and requirements.Experience in product inspection techniques.Knowledge of root cause analytical and problem-solving skills.Knowledge of FDA and ISO Quality systems for Medical Device companies desirable.Demonstrated excellent organizational skills and ability to work on own initiative essential.Excellent written and verbal communication skills essential.Computer literate, MS Word, Excel, PowerPoint.What your background should look like:Level 6 degree in Science / Engineering / Quality Management or related fields essential is a minimum requirement. A level 8 degree in one of these areas would be a distinct advantage.Minimum of 1 years' industry experience in a manufacturing environment.CompetenciesValues: Integrity, Accountability, Inclusion, Innovation, Teamwork
Location: GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: None
Requisition ID: 124741
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