SR. SOFTWARE VALIDATION ENGINEER-00000QU3
Description
Advanced Sterilization Products Division of Ethicon, Inc., a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Senior Software Validation Engineer, 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.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The Senior Software Validation Engineer will be responsible for supporting the goals and objectives of ASP by developing and reviewing software validation plans, test protocols, test data and test reports for embedded medical device. This individual will execute test cases per protocol and document the results. This individual will participate in the development and review of software requirements. S/he will contribute to the design and implementation of Software Validation processes on projects. S/he will work closely with Software Engineering team to ensure implementation and application of Software Validation principles throughout the development process. S/he will provide technical direction and hands-on assistance for testing projects. This individual may represent Software Engineering on teams for projects involving software.
Qualifications
A minimum of a Bachelor’s of Science in Computer Science, Electrical Engineering, Bioengineering, System Engineering, or Quality Engineering is required. An advanced Degree of in Computer Science, Electrical Engineering, Bioengineering, System Engineering, or Quality Engineering is preferred. A minimum of 5 years of industry experience in software engineering is required. Software engineering experience in a regulated industry: FDA 21 CFR 820, the Quality System Regulation, ISO 13485, and IEC 62304 are required. Experience in software testing, verification, and validation, including an understanding of "white box" and "black box" testing, test design, test tools and methods, test documentation, test management, test traceability, defect management and tracking is required. The successful candidate will have experience in defining test strategy, designing and developing test cases from software requirements, architecture designs, and code of complex embedded real-time systems. Technical ability to understand the mechanical, electrical and software of the system is required. The successful candidate will have knowledge in C/C++/Java programming languages. Knowledge of real-time operating systems such as QNX and Linux is required.
The successful candidate should have effective written and oral communication. Excellent problem-solving and trouble-shooting skills, and ability to work independently are required. Excellent organizational skills and attention to details are required. Good interpersonal skills are required. Experience in embedded software development and testing is preferred. Experience in requirements specification is highly preferred, but not required. Experience in using Static Code Analysis tools is preferred. Experience in leading other verification and validation engineers or contractors is preferred, but not required. Experience in defining and collecting software quality metrics is preferred. The position will require up to 20% travel (Domestic/international).
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J2W:LI NA
Primary Location:North America-United States-California-Irvine
Organization: Ethicon Inc. (6045)
Job Function: R&D Engineering (R&D)
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