「資深研究員 (肝臟疾病研發處)」的相似工作

1. 獨立完成大小鼠動物實驗，需熟悉動物保定、注射、給藥、採血、犧牲、組織處理等技術。 2. 負責相關實驗操作與資料的紀錄，可獨立收集和數據分析，彙整結果撰寫實驗記錄與口頭報告，並能加以解讀實驗結果並解決問題。 3. 參與專案管理，跨部門團隊合作，確保專案從早期研究順利推進至臨床階段。 4. 協助執行臨床試驗計畫。 5. 新藥市場相關研究文獻收集與更新整理。 6. 協助主管完成各項交辦工作和任務。

1. 負責臨床試驗專案的推動、管理、醫學評估，包括IND申請文件準備、試驗執行與GCP查核。 2. 協調內部與委外之工作，維持臨床專案品質並有效掌握專案時程。 3. CRO服務的評估、監督、審核及管理，確保其服務品質與合規性。 4. 藥物臨床試驗之法規遵循。 5. 跨部門相關事務之協助及臨時交辦事項。

1. 獨立完成大小鼠動物實驗，需熟悉動物保定、注射、給藥、採血、犧牲、組織處理等技術。 2. 負責相關實驗操作與資料的紀錄，可獨立收集和數據分析，彙整結果撰寫實驗記錄與口頭報告，並能加以解讀實驗結果並解決問題。 3. 參與專案管理，跨部門團隊合作，確保專案從早期研究順利推進至臨床階段。 4. 協助執行臨床試驗計畫。 5. 新藥市場相關研究文獻收集與更新整理。 6. 協助主管完成各項交辦工作和任務。

協助醫學專業人士或藥廠優化研究設計，並以英文撰寫與修改學術文件及研究計畫，確保內容的專業性與準確性。 與醫療機構及研究單位建立長期穩健的合作關係，依照客戶情況提供專業建議，解讀臨床數據，搜尋學術文獻找出臨床研究的價值，協助解決研究過程中的挑戰，以提升研究品質與學術產出價值。

Please do submit English resume via our company website. https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2284?utm_medium=jobboard Reporting to: Lab Director, or Lab Manager Position Description: The Researcher is responsible for the conduct of analysis related works according to GCP, GLP, CAP, Standard Operating Procedures (SOP), applicable Study Specific Procedures (SSP), and local regulatory requirements. The report writer/QC is responsible for writing correspond study report/method according to study plan and Standard Operating Procedures (SOP). And to perform the quality control works. Responsibilities: General Responsibilities • Conduct analysis work following related SOPs and guidance. • Draft/check/review/approve documents, such as SOP, protocol, analytical result, report and method. • Involve in lab logistics (general affair) management, such as purchasing, inventory controlling, payment applying. • Responsible for instrument maintenances, workspace cleaning/maintenance. • Delegated /assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc. • Participate in CAP/GCP/GLP/ regulatory related training courses. • Provide temporary supporting assigned by line manager. • Refer to additional Study Based Responsibilities while being assigned in analytical project. • Involve in sample collection kit/label preparation. • Involve in analytical study project management. • Other tasks assigned by line manager. Study Based Responsibility (if needed) Study Personnel in Study • All personnel involved in the conduct of the study must be knowledgeable in those parts of the Principles of Good Laboratory Practice which are applicable to their involvement in the study. • Study personnel will have access to the study plan and appropriate Standard Operating Procedures applicable to their involvement in the study. It is their responsibility to comply with the instructions given in these documents. Any deviation from these instructions should be documented and communicated directly to the Study Director, and/or if appropriate, the Principal Investigator(s). • All study personnel are responsible for recording raw data promptly and accurately and in compliance with these Principles of Good Laboratory Practice, and are responsible for the quality of their data. • Study personnel should exercise health precautions to minimize risk to themselves and to ensure the integrity of the study. They should communicate to the appropriate person any relevant known health or medical condition in order that they can be excluded from operations that may affect the study. Report Writer/Quality Control • As QC person, check and review the study data, document, report. • Involve in reference compound management, such as planning, shipping, receiving, using, storing, and disposing. And as the backup of sample manager. Qualifications: Education and Experience: • Secondary Technical school, Junior colleague, BS (Bachelor of Science) degree in Biochemistry, Biotechnology and Laboratory Science, Chemistry, or a related field. Advanced degree is a plus for Associate Researcher/ Senior Researcher. • License of Medical Technician is required for Associate Researcher/ Senior Researcher in Central Lab. Skills and Competencies: • Familiar with all lab operation activities. • Good working knowledge of CAP/GCP/GLP, applicable law (local and country) and regulatory requirements. • Good communication skills. • Good verbal and written English or other second language skills. • Good problem-solving skills. • Effective time management and prioritization skills.

• 參與ADC(Antibody Drug Conjugate)藥物研發，開發並優化偶聯技術(Conjugation Technology)。 • 建立多元化的偶聯平台。 • 負責早期抗體偶聯藥物的偶聯與純化方案規劃與執行。 • 負責抗體偶聯藥物的相關製程開發，進行跨部門合作。 • 負責偶聯樣品純化與質量分析（UV, HPLC, LC-MS）等工作。 • 配合專案執行, 確保偶聯實驗銜接上下游物流，及實驗室管理和儀器設備維護保養，管控物料庫存量等，不拖延專案時程，按時交付偶聯產品。 • 專利文獻技術分析、持續掌握偶聯技術和ADC開發的最新趨勢，定期分享該領域相關期刊。

＊⽣物醫學研發資料搜尋、藥物臨床試驗法規評估 ＊新藥開發臨床試驗管理、醫學評估 ＊國內、外新藥臨床試驗申請文件撰寫 ＊其他主管交辦事項

1.產業導向的嗅覺科學(Olfactory Science) 相關產品研發及企劃工作。 2.嗅覺科學(Olfactory Science)與 Endocrine System, Immune System及Central Nervous System 等相關研究。 。 3. 產品相關資訊調查及收集。 4. 期刊論文撰寫。

1. 微針處方設計與開發 2. 微針處方與成品之物化性檢測及規格確立 3. 開發微針成品所需之檢測分析方法 5. 研發技術文件撰寫 6. 實驗數據整理及報告撰寫 7. 安定性試驗執行 8. 其他主管交辦事項 工作地點：台北生技園區（捷運南港站2號出口）

協助醫學專業人士或藥廠優化研究設計，並以英文撰寫與修改學術文件及研究計畫，確保內容的專業性與準確性。 與醫療機構及研究單位建立長期穩健的合作關係，依照客戶情況提供專業建議，解讀臨床數據，搜尋學術文獻找出臨床研究的價值，協助解決研究過程中的挑戰，以提升研究品質與學術產出價值。

1. Oversee and manage non-clinical studies with Contract Research Organizations to support the research and clinical product development. 2. Design and conduct laboratory experiments related to the company's discovery and pre-clinical pharmacology activities. 3. Draft preclinical-related documents to support clinical trial submissions according to project timelines. 4. Collect and present research findings to the project teams. 5. Perform any other job-related duties as assigned.

1.負責外泌體相關產品或技術平台的研究與開發（應用領域包含：癌症早篩、神經退化疾病、液體活檢、再生醫學等）。 2.建立與優化外泌體的分離純化方法（超高速離心、Size exclusion、商用kit、微流體技術等）。 3.開發與執行外泌體的定性與定量分析技術（如：NTA、Western blot、ELISA、qPCR、TEM、flow cytometry等）。 4.協助開發外泌體為基礎之診斷試劑、標記技術或生物載體（drug delivery）。 5.撰寫研發報告、實驗紀錄、技術規格文件與專案簡報。

Pythia Biotech is a Taiwan-based startup dedicated to accelerating cancer drug development, immunotherapy, and precision medicine through Organ-on-a-Chip (OoC) technologies. We are expanding our team and seeking a Head of R&D to lead research, drive innovation, and advance translational applications. This is a rare opportunity to join a fast-growing startup, work alongside a world-class advisory team, and take on a pivotal leadership role as the company scales. Job Responsibilities •Develop and execute R&D strategies to support oncology and immunotherapy research. •Lead the development and validation of the TME-Chip platform. •Manage project timelines and resources to ensure successful delivery. •Support and communicate with partners to integrate resources and promote R&D progress. •Ensure that R&D complies with relevant laws, regulations and standards. •Prepare investment presentations, represent the company at academic and industry conferences to raise visibility. Qualifications •Ph.D. in Oncology, Immunology, Biomedical Engineering, Pharmacology, or a related field. •Minimum 2 years of experience in biotech or pharmaceutical R&D; prior leadership experience is a plus. •Familiarity with tumor biology, immuno-oncology, organoids, or Organ-on-a-Chip-related technologies. •Experience in cross-functional collaboration and project delivery in dynamic or startup environments. • Strong communication skills in both Mandarin and English; able to represent the company externally.

The Researcher is responsible for the conduct of analysis related works according to GCP, GLP, CAP, Standard Operating Procedures (SOP), applicable Study Specific Procedures (SSP), and local regulatory requirements. Manage the operation of MT and aid physicians in the diagnosis, treatment, and prevention of diseases by testing patient specimens, correlating data, and reporting results in a timely manner to effect quality patient care. Responsibilities: Perform analysis work according to SOPs and guidance. Prepare, review, and approve various documents, including SOPs, protocols, reports, and analytical methods. Manage lab logistics, including purchasing, inventory control, and payment processing. Maintain instruments and ensure cleanliness and maintenance of the workspace. Take on the role of system owner for computerized systems, performing tasks such as validation tests, periodic reviews, and reporting. Attend training courses related to CAP/GCP/GLP/regulatory requirements. Study Based Responsibility (if needed) Analytical Study Director in Study Work as the Study Director, responsible for the overall conduct and final report of the study. Approve the study plan and any amendments by signature, and ensure Quality Assurance personnel receive timely copies. Make study plans, amendments, and SOPs available to study personnel. Ensure procedures in the study plan are followed and document deviations and take corrective action if necessary. Document and record all generated raw data. Validate computerized systems used in the study, sign and date the final report to indicate acceptance of responsibility for data validity, and ensure study materials are archived after completion. Study Personnel in Study Ensure personnel are knowledgeable in relevant Principles of Good Laboratory Practice. Provide study personnel with access to study plans and SOPs applicable to their involvement, with a responsibility to follow instructions and document any deviations. Emphasize the responsibility of all study personnel to promptly and accurately record raw data, comply with Good Laboratory Practice principles, and exercise health precautions to safeguard the integrity of the study.

Dazzeon develops the world’s highest-purity acemannan (MannanPRO®, ≥90%) from Aloe vera for applications spanning immunity, mucosal/wound repair, oncology adjuvancy, and drug delivery. We operate ISO-22000/HACCP facilities and are building toward ISO-13485/GMP for devices and botanical drug pathways. The Opportunity We have a rich dataset (cell assays, organoids, RNA-seq, ROS/ferroptosis, wound healing, antiviral ALI models, nanogels, SHIME gut model data, etc.) and several commercialization tracks (B2B ingredient, medical device, oncology adjuvant). We need a creative, independent, and critical thinker who can connect the dots, propose smart next steps, and execute. What You’ll Do • Synthesize evidence: Audit and integrate internal datasets (HCT116 anti-tumor/ROS, ferroptosis signals, 5-FU co-treatment wound-healing rescue, NHBE ALI antiviral/TEER, RNA-seq DEGs, nanogel DLS/loading) into clear narratives and decision docs. • Design & run experiments: Plan and coordinate in-vitro (cell culture, wound healing, viability, flow cytometry, RT-qPCR, western blot, etc), organoid studies, and small animal pilots via CROs/academia or internally as needed. • Translate science to product: Convert findings into specifications for (a) oral MannanPRO® supportive-care use (e.g., 10 mg/10 mL/day), (b) mucosal medical device claims (ISO-10993 strategy), and (c) oncology adjuvant positioning. • Regulatory & documentation: Draft protocols, statistical plans, reports, white papers, and submission-ready materials (e.g., device technical files, literature reviews, risk/benefit rationales). • IP & publications: Scout prior art, support patent claims, and prepare manuscripts/abstracts with clean figures and reproducible methods. • External partnerships: Source, brief, and manage CROs/academic labs; negotiate timelines, QC data, and budget. • Data hygiene: Stand up an electronic lab notebook (ELN) and a lightweight data room (protocols, raw data, scripts, COAs). What You’ll Bring • MS/PhD (or equivalent experience) in Biomedical Science, Pharmacology, Biotech, or related. • Proven independence in experimental design, critical analysis, and hypothesis generation. • Experience interfacing with CROs/academia; comfortable writing SOPs, protocols, and reports. • Excellent scientific writing (English a must; Mandarin a plus). Clear slides and figures. • Bias for action, ownership, and pragmatic problem-solving in fast, changing contexts. Nice to Have • Oncology or mucosal biology background; familiarity with 5-FU models and adjunctive care. • Organoid systems, RNA-seq analysis, DLS/zeta for nanomaterials, or device biocompatibility (ISO-10993). • Regulatory familiarity (ISO-13485/QMS, TFDA/FDA device files, botanical drug pathways). Success in Your First 90 Days • Deliver a gap analysis that maps current evidence → near-term claims for (1) oncology supportive care and (2) medical device. • Run/coordinate one confirmatory experiment (e.g., 5-FU + MannanPRO® wound-healing rescue with stats and visuals) and one translational pilot (e.g., palatability/PK-adjacent marker readouts for 10 mg/day oral use). • Produce a publishable white paper (sales-ready) and a CRO workplan with timelines, budgets, and success criteria. Contract & Compensation • Project-based retainer or milestone structure; competitive and negotiable. • Option to convert to full-time with equity participation. • IP/confidentiality assignment required; occasional travel to partner labs.

哥吉生技以醣生物學為核心，開發學研與臨床診斷試劑。公司正在尋找具蛋白質生物工程背景之博士級研究員，開發初期製程與產品應用。工作項目包含： 1. 篩選及優化特定功能之蛋白質與酵素。 2. 建立目標蛋白質小量製程 3. 建立品質測定法。 4. 表現用之菌種、細胞株篩選與優化。 5. 功能性驗證方法開發。 6. 蛋白質製劑配方開發。 7. 跨部門協調團隊溝通。 8. 其他主管交辦事項。 Glycogenetics is a research-centric biotechnology company with a keen focus on solving technological challenges in glycobiology. We are looking for a protein scientist to join our R&D team to be responsible for the following tasks: 1. Functional candidate screening for protein production pipeline; 2. Establishing small scale production processes for proteins; 3. Quality control assay development; 4. Production strains host optimization; 5. Protein functional assay development; 6. Protein formulation development; 7. Coordinate cross-team communication; 8. Routine R&D labwork. A qualified candidate should demonstrate a strong research experience in protein biochemistry or related fields. The candidate should also demonstrate the ability to communicate with colleagues of different research disciplines.

◖為什麼你該加入台美檢驗Superlab◗ 我們是全國唯一橫跨醫學、化學及生物相關領域的檢驗科技公司。 擁有最齊全的設備、最先進儀器、最頂尖創新檢驗技術的全方位實驗室，服務項目包含一般食品、藥品、中藥、健康食品、化妝品、環境水質、化學品、紡織品、奈米產品、飲用水、醫療器材、生醫材料等。 邀請你和我們一起為消費大眾的衛生安全把關，並確保每一階段都能達到法律規範和個人期望的高標準。 ◖你將在團隊參與◗ 1. 健康食品/醫療器材/藥品臨床前試驗研究主持人 2. 臨床前試驗規劃開發、試驗流程優化、數據合理性分析 3. 實驗室GLP品質系統維運與優化 ◖我們期待優秀的☞研究主持人☜具備這樣的能力◗ 1. 具三年以上以上細胞或病毒實驗經驗 2. 具執行多年期計畫或專案經驗 ◖如果你有這樣的條件，那就太好了◗ 1. 有ISO/IEC 17025 測試實驗室管理經驗尤佳 2. 有細胞治療或再生醫療相關產業經驗尤佳

1.細胞培養以及生物醫學研究 2.細胞製程開發相關研發 3.從事新穎細胞培養媒介物及相關產品的研究、開發與改良 4.專案管理 5.其他主管交辦事項 其他說明 由公司補助交通費用(含機票)、海外住宿 ★★★須具備細胞培養經驗1年以上。★★★ 很抱歉，若無實務經驗者請勿投遞履歷

我們是智新生技，專注於新藥開發與 GMP 製造，現正尋找對「微生物分析與環境監控」有熱情的你，一起打造高標準、符合法規的製藥品質實驗室！ ｜職務說明｜ · 執行微生物分析方法之開發與確認作業 · 建立與維護 GMP 微生物實驗室相關標準作業程序（SOP） · 進行潔淨室環境監控 · 執行一般日常檢驗作業 · 管理與維護微生物實驗室使用之相關設備 · 辦理藥品微生物檢驗及試劑管理作業 · 執行微生物實驗室檢驗設備之維護、校正與操作 · 配合完成其他主管交辦事項 ｜Job Description｜ · Development and validation of microbiological analysis methods · Eestablishments and maintenance of SOPs related to GMP microbiological laboratories · Clean room environment monitoring · General daily experiment · Management and maintenance of equipment used in microbiology laboratories · Pharmaceutical microbiological testing and reagent management · Maintenance, calibration and operation of microbiological laboratory testing equipment · Other matters assigned by the supervisor

1. 開發醫藥委託開發暨製造服務(CDMO)的潛在商機(以日本、美歐、台灣市場為主)。 2. 開拓新客戶，並促進現有客戶的業務增長。 3. 客戶進行討論委託內容，達到簽署合約的目標 。 4. CDMO 提案準備/COG 分析/基本市場分析和競爭分析。 5. 協助規劃及參與 CDMO 之行銷活動與推廣(研討會/展會為主) 。 6. 跨部門團隊協作，確保專案提案及執行順利進行。