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regulations and standards. Medical Device product development experience a strong plus. Experience working in a regulated environment. Prior experience leading HF input for product submissions and interfacing
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in a regulated environment. Prior experience leading HF input for product submissions and interfacing with regulatory agencies. Other: This position is based in Santa Clara, CA and requires up to 10
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product development cycle. Support usability and validation-related activities such as large Human Factors studies assessing critical workflows end-to-end in simulated environments. Support generation
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process. Conduct usability and validation-related activities such as large human factors studies assessing critical workflows end-to-end in simulated environments. Generate deliverables such as Usability