Roles and ResponsibilitiesWork with the Chief Technology officer to perform R&D and prototype new data capabilities that make existing features more intelligent or enable new classes of intelligent product featuresParticipate in demand analysis, product planning, prototype design, process system document and technical regulation document writing for B-oriented artificial intelligence medical device softwareBe responsible for project execution and effect evaluationBe responsible for demand feedback collection, product customization and subsequent development during deploymentAssist the regulatory team to customize the clinical functions of the software, test, and provide quality control of the delivered products, assisting the regulatory team in writing relevant documents, and cooperating with the registration tasks throughout the cycleLead a team of engineers to maintain, deploy and support the product based on existing set protocols and standard operating procedures in alignment with ISO13485 standardsRequirementsBachelor degree and above, with at least 2 years of software product development experienceIn-depth understanding of software product development process, familiar with software testing and quality control methods, strong logic and expression skills, and good communication skillsGood English document writing skills, and able to communicate fluently in EnglishNice to haveMedical software product or AI product developer/manager work experienceRelevant experience in medical device software regulatory processA good attitude to learn and be willing to work with different age groups in a startup and research environmentJob Type: Full-timeSalary: $7,500.00 - $9,000.00 per monthBenefits:
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