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醫藥法規專員（RA）將負責管理和執行公司醫療器材相關的法規事務，確保公司的產品在全球範圍內合法上市。主要職責包括但不限於： 建立和維護TFDA、FDA、CE等相關醫療器材產品許可證的文書作業

【HTC】 Job Responsibilities • Analyze, propose, and validate solutions to vaguely defined technical problems • Create and manage the structure of software projects, defining components, and interfaces that is flexible for collaboration and feature expansion • Work closely with key stakeholders in design, user research and program management to define new kinds of XR experiences and find creative ways to prototype the future with today’s technology • Play a key role in building and iterating on in