「微流體工程助理」的相似工作

1. 有免疫或細胞、CTC（循環腫瘤細胞）培養經驗背景可與主管討論研發事宜 2. 負責準備、監控、實施專案並須符合公司標準作業流程 3. 產品研發、 臨床測試和製程規劃改善及追蹤 4. 產品測試確保品質、打樣生產 5.紀錄所有實驗過程，撰寫研發紀錄簿，產品品質改良，做日後公司資產並避免日後智產權糾紛 6.其他主管交辦事項

1. 中西藥交互作用研究 (包括：重組蛋白、細胞、動物實驗)。 2. 處理文書業務及其他交辦之行政與研究相關事項。 雇用期限：114年10月1日至115年12月31日止

生醫材料、原料之產品開發與推廣。

1. 進行細胞培養、建立相關技術、細胞製程優化(有相關經驗者佳)。 2. 協助對岸實驗室運作。 3. 資料搜索、整理，文獻探討。 4. 協助建立、管理、遵從品質四階文件。 5. 其他主管交辦事項

須熟悉下列實驗操作 1.分生實驗(DNA extraction, PCR等) 2.ELISA實驗 3.Western Blotting相關實驗 4.完成主管交辦工作事務

Job Summary As a member of the Central Lab team, you will be primarily responsible for the development, optimization, validation, and testing of Potency Assays based on cellular and immunological principles, as well as ELISA, cell culture, and functional assays. You will help define validation requirements and establish compliant processes under the supervision of the line manager, enabling the Central Lab to successfully develop, validate, and deliver high-quality assays to support clinical trials and regulatory submissions. This role also offers the opportunity to closely collaborate with clinical trial teams as you define and execute the start-up activities required to establish these assay capabilities and technical expertise within the Central Lab. You will lead or contribute to method development, optimization, validation, and transfer of assays, including cell-based functional assays, ELISA, and other immunoassays, while ensuring full GLP compliance. The role involves performing mammalian cell culture, advanced analytical techniques (e.g., Flow Cytometry, qPCR/dPCR), and driving method transfer and validation from external partners. Additionally, you will be responsible for supporting computer system validation, ensuring data integrity, audit readiness, and regulatory compliance across lab operations. General Responsibilities: 1. Collaborate with external groups to identify technology, method evaluation and business processes that will establish potency assay expertise at Central lab. 2. Conduct analytical testing in compliance with established SOPs and relevant guidance. 3. Review data and evaluate against established acceptance criteria. 4. Define requirements for laboratory equipment and support purchasing. 5. Evaluate data to identify trends and/or establish limits. 6. Participant in discrepancy investigations and corrective actions. 7. Provide training to department team member, especially in potency assay techniques. 8. Lead assay development, optimization, transfer and validation activities. 9. Write, review or approve equipment qualification/maintenance life cycle documents. 10.Draft, check, review documents, such as SOP, protocol, analytical result, report and method under limited supervision. 11.Support internal, external, and regulatory inspections. 12.Other tasks assigned by line manager. Qualifications: Education and Experience: 1. Master’s degree in Biotechnology, Biochemistry, Pharmaceutical Sciences, Laboratory Science, or related field. 2. 3+ years of experience in potency assay, ELISA, and/or cell-based assay development, preferably from CDMO, CMO, CRO, or GMP-regulated laboratories. 3. Familiarity with assay development for vaccines, biologics, ADC, or cell therapies is a plus. 4. With direct experience in flow cytometry method development is preferred. 5. Demonstrated ability to apply knowledge of potency assay theories, principles, and techniques. 6. Medical technologist license is a plus, but not required. Skills and Competencies:  Strong expertise in assay validation, method lifecycle management, and data analysis.  Familiarity with clinical trial lab operations and regulatory compliance.  Excellent documentation skills for regulated environments.  Effective communication and collaboration with cross-functional teams and clients.  Strong troubleshooting and problem-solving abilities.  Good verbal and written communication in English.  Ability to manage multiple priorities and meet deadlines in a dynamic CRO setting.

1. 執行動物實驗、細胞試驗與分生試驗 2. 執行藥物篩選與臨床前試驗(藥理、毒理) 3. 試驗方法整理與數據分析整理 4. 藥物開發相關參考文獻搜尋與整理

1. 金屬複合材料開發協助 2. 材料物化性分析 3. 材料測試 4. 表面處理打樣測試

1. ESD /FET新產品驗證/測試 2. 負責測試文件之建檔與管理。 3. 共同研討元件設計及封裝結構 4. 評估數據及書寫報告，以確認或顯示與現有標準之間的差異。 5. 會同參與專案工作 6. 參與設計產品應用電路討路

1. 依品質系統與標準作業流程執行臨床檢體檢測，並確實記錄檢測流程參數及數據 2. 按時程完成數據分析和出具檢測報告 3. 依需求建立新的檢測程序與檢測方法確效或優化現有的檢測方法 4. 需撰寫技術類程序書與標準書，並定期審視現有版本及優化改版 5. 其他主管交辦事項。

About Us We're a biotech startup on a mission to make microfluidic chips accessible for research and product development through our proprietary technology. Our team brings together a serial entrepreneur, a PhD in microfluidics, and an ex-MBB consultant. What You Will Do • Outbound Lead Generation: Research and reach out to prospective clients via LinkedIn and other channels • Inbound Lead Generation: Set up and manage our professional website and LinkedIn presence • Sales Support: Assist in preparing proposals, presentations, and marketing content What We're Looking For • Currently pursuing or holding a degree in Business, Marketing, Economics, or related field • Experience in B2B international business development is a plus • Self-motivated, adaptable, and eager to learn • Able to commit at least 16 hours/week for a minimum of 3 months • Location: flexible What You'll Gain • Hands-on experience in business development and startup growth • Working closely with the Ex-MBB consultant who loves to mentor and coach • Attractive result-based incentives and sales commission

1. 執行 CAR-T 及其他細胞治療產品之製程品質檢測，確保產品品質與臨床使用安全性。 2. 負責臨床檢體之檢測、數據分析與結果解讀，支持臨床試驗與研發計畫。 3. 建立並優化符合 GxP 規範之分析方法，並執行方法確效與驗證。 4. 撰寫並維護相關分析方法、確效與驗證之技術文件及報告。 5. 進行實驗儀器日常維護、校正與紀錄，確保檢測準確性與實驗室合規。 6. 協助品質體系之持續改進與合規運作。 7. 完成主管交辦之其他專案與任務。

我們正在尋找一位專業且富有熱忱的科學家，負責抗體藥物的臨床前開發，並參與專利撰寫、學術發表及國內外研討會報告。理想的候選人需具備良好的抗體藥物開發與分析能力，能夠整理研發結果，並與跨部門團隊合作推動抗體藥物從研究階段向臨床開發邁進。 如果您對抗體藥物的創新開發充滿熱情，並希望參與推動突破性的生物製藥研究，歡迎加入我們的團隊！ 主要工作內容： ‧領導並分析抗體藥物的臨床前開發策略，推動專案進展。 ‧整理與解析研發數據，為藥物開發提供決策依據。 ‧撰寫專利申請，保護技術創新。 ‧發表研究成果，撰寫學術論文，並於國內外研討會進行報告。 ‧與跨部門團隊合作，確保專案從早期研究順利推進至臨床階段。

Job Summary： As a member of Central lab team, you will be supporting the start-up of a cell-based assay and flow cytometry analysis. You will help define the requirements for validation and will establish processes under line manager's supervision that will enable the Central lab to operate successfully with regard to the analysis and characterization of cell-based therapies or vaccines; specifically as a flow cytometry scientist. This role provides the opportunity to closely partner with the vaccine development and clinical trials as you define and execute the start-up activities associated with establishing flow cytometry / cell-based assay capabilities and expertise at Central lab. Responsibilities include flow cytometry / cell-based assay method development, validation, qualification, transfer and troubleshooting. In addition, the candidate will be expected to write the validation / analytical protocol and report. Additional responsibilities include validation of computer systems, and management/administration of equipment (e.g. instrument, etc.). General Responsibilities: 1.Collaborate with external groups to identify technology and business processes that will establish flow cytometry / cell-based assay expertise at Central lab. 2.Conduct analysis work following related SOPs and guidance. 3.Review data and evaluate against established acceptance criteria 4.Define requirements for laboratory equipment and support purchasing. 5.Evaluate data to identify trends and/or establish limits 6.Participant in discrepancy investigations and corrective actions 7.Receive and provide training 8.Lead assay development, transfer and validation activities 9.Write, review or approve equipment qualification/maintenance life cycle documents 10.Draft, check, review or approve documents, such as SOP, protocol, analytical result, report and method. 11.Write protocols and reports under limited supervision 12.Assure and apply GCP/CAP throughout operations 13.Participate in CAP/GCP/GLP/ regulatory related training courses. 14.Support internal, external, and regulatory inspections 15.Work to meet schedules, timelines, deadlines 16.Participate in and/or lead projects and process improvements 17.Delegated /assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc. 18.Provide input or set personal performance goals and departmental objectives Establish work priorities to meet targets and timelines; manage competing priorities Other tasks assigned by line manager. Clinical Lab Service Scientist 1.Participate in and/or lead projects and process improvements Delegated /assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc. 2.Provide input or set personal performance goals and departmental objectives Establish work priorities to meet targets and timelines; 3.Manage competing priorities Other tasks assigned by line manager.

1. 市場資訊收集及分析，包含文獻、專利檢索，以支援研發決策。 2. 負責產品測試、品質檢驗、及標準品維護。 3. 制定、更新並執行 QC 標準作業流程（SOP），協助優化品質管理。 4. 配合主管交辦事項，並跨部門協調以確保專案順利推進。 5. 需具備細心、主動回報進度，並展現良好的溝通、協調、解決問題能力。

Please do submit English resume to our company website. https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com:443/hcmUI/CandidateExperience/en/job/1488?utm_medium=jobboard General Responsibilities: Manage staff in accordance with organization's policies and applicable regulations, including without limitation: planning, assigning, and directing work; managing performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems; acting as a coach and mentor for subordinates as they develop in their role. Participate in the selection and onboarding process for new staff by conducting candidate review and participating in the interviewing process. Conduct onboarding training for new staff in conjunction with Human Resources and Learning and Development training programs. Ensure that staff have the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and mentored training experiences, as applicable. Maintain lab daily operation. Ensure the quality and timely of lab deliverable. Perform the tasks assigned by line manager. Refer to additional GLP/GCP Regulation Required Responsibilities while involved in GLP organization. As the member of test facility/site management. Delegated /assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc. GLP/GCP Regulations Required Responsibilities (if needed): Lab Manager Maintain an internal responsibility chart which identifies the individual(s) within a test facility who fulfil the responsibilities of management as defined by the Principles of Good Laboratory Practice. Ensure that a sufficient number of qualified personnel, appropriate facilities, equipment, and materials are available for the timely and proper conduct of the study. Ensure the maintenance of a record of the qualifications, training, experience and job description for each professional and technical individual. Ensure that personnel clearly understand the functions they are to perform and, where necessary, provide training for these functions. Ensure that for each study an individual with the appropriate qualifications, training, and experience is designated by the management as the Study Director before the study is initiated. Replacement of a Study Director should be done according to established procedures, and should be documented. Ensure, in the event of a multi-site study, that, if needed, a Principal Investigator is designated, who is appropriately trained, qualified and experienced to supervise the delegated phase(s) of the study. Replacement of a Principal Investigator should be done according to established procedures, and should be documented. Ensure documented approval of the study plan by the Study Director. Ensure that the Study Director has made the approved study plan available to the Quality Assurance personnel. Ensure the maintenance of a master schedule. Ensure that test facility supplies meet requirements appropriate to their use in a study. Ensure for a multi-site study that clear lines of communication exist between the Study Director, Principal Investigator(s), the Quality Assurance Programme(s) and study personnel. Ensure that test and reference items are appropriately characterized. Ensure that appropriate and technically valid Standard Operating Procedures are established and followed, and approve all original and revised Standard Operating Procedures. If necessary, function as Study Director for specific study, in this case, he/she must not have the responsibility of test facility/site management role in the study.

1. 產品配方開發與打樣 2. 實驗室原料建檔及配方建立 3. 量產配方的製程及異常分析處理 4. 化妝品、保養品有效性/安全性/穩定性評估測試 5. 客戶文件需求 6. 其他主管交辦事項

1.抗老相關實驗 2.基因,病毒研究及分析 3.貼複型,免疫,懸浮細胞培養 4.培育NK,MSC,EPC 經驗 5.發表論文經驗 生物科技是當今最具發展前景的行業之一，擁有技術專業的生物科技研發人員在產品開發和研究領域上扮演著關鍵角色。此職位是一個從事生物科技研發的機會，擁有豐富的成長空間和良好的薪酬福利。 我們期待有才華和熱情的人加入我們的團隊，如果你符合以上要求，歡迎提交你的申請。

1. 協助工程師IC電氣特性及功能驗證測試. 2. 協助工程師IC可靠度驗證測試 3. 協助工程師測試數據的整理及分析 4. Proficient with electronic welding skills. Skill any of the following is a plus: Any college students in electrical engineer related field. Patience and attentive are preferred. Basic Excel skills are required Have flexible schedule. Self-motivated and aggressive to learn. Please bring relevant transcript to the interview. KaiKuTek is the world's leading provider for 3D gesture sensor using mmWave Radar with embedded AI accelerator. We possess key technologies in areas such as Antenna-in-Package (AiP), ML algorithm, AI accelerator, as well as 60 GHz radar transceiver design. With recent merger by JMicron, founded in 2001 and located in Hsinchu Science Park, our product portfolio expands to high speed SerDes bridge controller SOC's mainly in storage application utilizing USB, PCIe, and SATA. This new sensing technology will change and redefine human-machine interface as we know today, and mmWave technology combined with high speed SerDes will open door to many new possibilities and application frontiers. KaiKuTek is looking for enthusiastic test Intern engineers willing to take upon new challenges of working closely with cross functional teams, including digital IC designers, analog/RFIC designers, firmware engineers, packaging engineers, production and testing as well as marketing and FAE, to optimize the overall SoC performance in terms of power, area, functionality, testability as well as to create proof-of-concept for new customer engagement.

負責IronCAD，ENCY CAM軟體售前DEMO、客戶教育訓練、售後技術服務、教材製作....等工作