智合精準醫學科技股份有限公司

1. 例行會計帳務處理、每月財務報表及科目餘額表編製、配合會計師查帳作業 2. 申報營業稅、營所稅、各類所得扣繳申報等各項稅務作業 3. IPO事項協助 4. 其他主管交辦事務

As a patent engineer at Biogate, you will play a pivotal role in advancing Biogate's innovation to gain a competitive edge. You will collaborate with our different teams to fortify our intangible assets and ensure they align with strategic goals. Responsibilities: 1. Collaborate with our research and product development teams for patent mining and portfolio diversification. 2. Draft patent applications and work closely with the in-house legal team and outside counsel for patent prosecution, license, invalidation, and litigation matters. 3. Conduct patent searches and analyses to identify gaps in the competitive landscape and opportunities for patenting inventions. 4. Provide patent analysis and advisement in non-infringement, invalidity, FTO, etc. 5. Continuously evaluate the patent portfolio to assess its relevance and validity and to ensure alignment with business goals. 6. Provide support in internal and cross-department projects. 7. Provide intellectual property training to Engineering personnel. Requirements: 1. Good English communication ability with a TOEIC score of 800 or above is required. 2. Familiar with patent laws and practices in various jurisdictions is a plus; familiar with patent prosecution and , including the U.S. and Taiwan, is a must. 3. At least 5-y related experience in patent application and management is preferred.

本公司正積極布局次世代抗體藥物的開發，包含雙特異性抗體（bispecific antibody）、三特異性抗體（trispecific antibody）以及免疫細胞激素融合蛋白（immunocytokine）等新型療法。為推動相關研發，我們誠摯邀請具備以下背景的人才加入： 1. 具抗體工程經驗，熟悉分子設計、抗體格式（IgG-like、scFv、Fab、nanobody 等）以及 蛋白質結構優化。 2. 熟悉免疫學與腫瘤免疫學，能針對免疫檢查點、細胞因子或腫瘤相關抗原設計多特異性分子。 3. 具備細胞功能驗證與作用機制研究能力（例如 T cell engager、NK cell engager、cytokine signaling assay）。

工作經驗專長說明: 1. 臨床試驗專案的執行，包括試驗之啟動準備工作，聯繫庶務行政工作等。 2. 與醫院試驗CRO團隊等溝通操作事宜。確保專案符合GCP 規範與順利推進。定期瞭解試驗進度並書面報告高層。 3. 協助定期維護試驗相關作業，例IRB報告的drafting, review與遞交，個案報告書即時通報台灣FDA與審查/法規單位。 4. 處理專案的vendors管理與外包實驗室協調，如all parties保密協定處理，budget negotiation，控管專案預算與費用報銷等。 5. 臨床試驗文件歸檔與系統管理，會議協調安排。確保文件品質符合規範。試驗資料轉換整合處理。 6. 執行主管交辦其他任務。