Quality Engineer 2, Product Analysis Lab Job
Intermediate level job Irvine (Orange County) Design / Civil engineering / Industrial engineering
Job description
Quality Engineer 2, Product Analysis Lab-5170150422DescriptionAdvanced Sterilization Products Division of Ethicon, Inc., a member of Johnson & Johnson's Family of Companies, is currently recruiting for Quality Engineer II, Product Analysis Lab, located in Irvine, CA.ASP (Advanced Sterilization Products), a member of the Johnson & Johnson Family of Companies, is a leading designer and developer of innovative instrument sterilization, high-level disinfection and cleaning technologies. The company is dedicated to providing infection prevention solutions that create the safest possible environments for patients, healthcare providers, and communities. ASP is based in Irvine, California with offices around the world. For more information, please visit www.aspjj.com or follow us at www.
Twitter.com/aspjj.
The Quality Engineer II, Product Analysis Lab is responsible for providing engineering support to the complaint investigation process at ASP. This person maintains failure analysis test methods, tools, and capabilities. Completes investigations to determine root cause of product issues, presents results, and proposes corrective and preventative actions as required. S/he uses knowledge to improve company knowledge, products and processes. S/he collaborates and interacts with other company engineering teams, including teams representing Manufacturing, R&D, Product Quality, and Supplier Quality.
Under general supervision this person proposes improvements to methods for inspecting, testing and evaluating complaint-related product; maintains failure analysis test tools, fixtures, and equipment; proposes improvements to tests and methods to locate, reproduce, identify, and analyze complexpart failures; and analyzes design, reliability, or yield issues to determine the root cause of their failure.
S/he characterizes problems related to the company technologies. Reviews historical production dataand other quality data as part of the investigation and collaborates with other laboratory team members and engineers in diagnosis of technically challenging problems. This individual authors technical reports of findings, including probable cause of failures, and provide recommendations to prevent failure recurrence. S/he participates in proposal, presentation and implementation of corrective and preventative actions as required. S/he presents results of analysis to all levels of organization; generates monthly status reports on individual and team activity; and maintains Product Analysis Laboratory.
J2W:LI NAQualificationsA combination of one of the following is required: BS degree in a technical field (for example, Electrical Engineer, Mechanical Engineering, Industrial Engineering, Chemical Engineering, etc.) and 2-4 years of experience in engineering design or root cause analysis, or MS in a relevant discipline and 1-2 years of experience in engineering design or root cause analysis. Proficiency with common office computer software programs such as MS-Word, Excel, PowerPoint and basic UNIX system operation is required. Ability to read and understand electrical and mechanical schematics is required. Solid theoretical knowledge of analog, digital, and RF electronics is preferred. Understanding and experience in failure analysis and test of systems, parts and/or materials is required. Demonstrated experience using common failure analysis tools including visual inspection, electronic test equipment, mechanical/test equipment, chemical analysis, and dimensional measurement is required. Experience in trouble shooting, failure analysis, fish bone diagrams, decision trees, FMEA’s and other quality tools is required. Ability to design and implement test apparatus, sample preparation, and other methodologies to facilitate root cause identification and product reliability is required. Understanding of Failure Modes and Effects Analysis and Fault Tree Analysis is required. Understanding of test method and equipment validation is required. Ability to write and communicate clearly, including generating and presenting well-written reports is required. Demonstrated ability to work effectively with cross-functional teams for complaint investigation and root cause analysis is required. Able to multi-task with an established track record of meeting milestone schedules. Demonstrated leadership skills and ability to work in environments with fluctuating and competing environments.
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Primary Location:North America-United States-California-IrvineOrganization: Advanced Sterilization Products (ASP)Job Function: Quality AssuranceCertain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law. EEO is the Law EEO is the Law GINA Supplement