Medical Device System Test Engineer Position Available In Wake, North Carolina
Tallo's Job Summary: The Medical Device System Test Engineer is responsible for developing design specifications, configurations, and test methods for medical devices. They serve as technical support for key products, prototype and test circuit boards, and ensure compliance with design control methodology. Requirements include experience with standards compliance, technical writing, and a Bachelor's degree. Employers are looking for individuals with exceptional organizational and communication skills.
Job Description
Medical Device System Test Engineer
Responsibilities:
Develop system and subsystem-level design specifications based on requirements. Develop system and subsystem-level configurations. Develop system and subsystem-level test methods and protocols. Serve as design transfer liaison to Manufacturing, Service, Support, and Training. Serve as technical support for key products to our customers, dealers and field engineers. Prototype and test new circuit boards and improved revisions of existing circuit boards following medical devices design control methodology. Complete and submit all required design control documentation on time and accurately. Completes assigned training and development courses assigned by management team. Provide emergency on-call services as needed in partnership with Service and Support. Serves as a Representative for conventions and shows. Understands and Complies with all FSE Guidelines as applicable to the role. Must comply with Radiation Safety Policy including the timely replacement of used badges Completes the Corrective Actions Policy as prescribed Displays highly developed organizational skills. Ability to prioritize, plan, and execute are key success factors in this position. Utilize exceptional interpersonal and communication skills for problem situations with customers and/or staff. Completion of additional projects and assignments as given by management.
Requirements:
Medical Device Test. User Requirements Defining and Managing. Verification and Validation and Testing. Documentation Technical Writing. Experience with standards compliance such as
IEC 60601, ISO
13485, and/or
ISO 14971. FDA
regulated industry or willing to learn. Bachelor’s degree. Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
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Dice Id:
91116760
Position Id:
fa7ad0dc5501ac2f4182ad9de9ca5029
