工作職責 / Responsibilities:
1.醫用高分子原料開發(高分子合成改質)
1.Development of medical-grade polymer materials (polymer synthesis and modification).
2.執行相關研發計畫
2.Execution of related research and development projects.
3.主管交辦事項
3.Other tasks assigned by supervisors.
1.滿足日常藥物研發需求-取得和提取動物組織,使用放射性標記配體執行受體結合實驗*
(*我們實驗室採用高於法規規定的防護策略和徹底的輻射防護訓練)
2.科學創新和重塑** - 根據觀察和研究證據分析和完善工作流程
3.發現新的可能性** - 設計、測試和驗證新的檢測方法和平台
4.建立關係和溝通網絡 - 建立良好的人際溝通能力並與團隊成員合作
5.其他分配的任務 - 設備和實驗室環境的日常維護
** 碩士學位候選人必須具備
1. Fulfil daily drug discovery demand - acquire and extract animal tissue, execute receptor binding assays with radio-labeled ligands*
(*A higher-than-regulation protecting strategy and a thorough radiation protection training are applied in our laboratory)
2. Scientific innovation and reinvention** - analyze and refine the workflow based on observations and research evidences
3. Discover new possibilities** – design, test, and validate new assays and platforms
4. Building relationships and communication network- establish good interpersonal skills and collaborate with team members
5. Other assigned tasks – routine maintenance of equipment and laboratory environment
** Obligatory for Master’s degree candidates
Key responsibilities include the following, but are not limited to:
1. Generate Quotations:
- Coordinate CDA/agreements execution
- Coordinate internally to gather information required for quotation
- Provide quotations/project proposal to Client and follow-ups
2. Client Communication Management
- Serves as a central hub of internal/external communications with existing clients/third parties for project and product changes
- Serves as a central hub of internal/external communications with potential new clients /third parties to provide proposal to meet their needs and to enhance company business opportunities
- Schedule and arrange project meetings and task assignments, communicate expectations and record meeting minutes
3. Project Planning:
- Establishes project charter and plan to define project scope and timeline
- Assign tasks and perform follow-ups to ensure timely deliverables
- Identify potential issues and risks, and solutions.
4. Project Execution and Delivery:
- Drive project activity execution to meet goals/objectives and the agreed plan without compromising project deliverables or relationships
- Work with Subject matter experts to propose solutions on a variety of issues with low to moderate complexity and changes
- Coordinate Client Budget management including invoice management to client.
- Leverage robust project management skills and co-work with project managers to drive key decisions and milestones according to the endorsed plans, timelines, costs, and quality parameters
5. Perform other PMO-related duties/tasks as assigned by Management
工作內容
1. 開發委託開發/代工(CDMO)業務、準備委託案報價單及合約簽訂 2. 負責委託開發/代工(CDMO)專案進度追蹤(業務端)與文件管理、客戶端聯繫窗口 3. 協調廠內PM與客戶溝通事宜 4. 委託開發/代工(CDMO)業務監督與管理:各專案進度掌握與彙整、收款進度管理、BD 專案人員管理
奈米化藥物劑型研發,藥物奈米化技術平台開發,及其它交辦的各項工作。
【Description】
Formosa Pharmaceuticals seeks an independent, motivated, and team-oriented researcher to learn and implement our proprietary APNT® formulation technology and join the team in Taoyuan. The successful candidate will be passionate about contributing to our ongoing growth and success.
【Responsibilities】
1. Develop and optimize APNT@ and pharmaceutical nanoformulations.
2. Practical implementation of drug delivery and formulation techniques for the purpose of generating novel and/or enhanced drug candidates.
3. Understand project strategy and work toward achieving company goals
4. Regular submission of progress reports and summaries
5. Prepare technical documentation for communication, including transfer and validation of pharmaceutical manufacturing processes.
6. Maintenance of a detailed lab notebook and clean lab bench/hood area
7. Foster teamwork, contributing to a positive and collaborative environment with employees both within and outside the group
8. Involvement in cross-functional aspects of projects and assist in the completion of any required tasks.
9. Report to Staff Scientist or Director of Nanotechnology
【Technical requirements】
1. Understanding of GMP regulations and extensive experience in pharmaceutical analysis techniques.
2. Experience in the usage of drug delivery and formulation techniques and instrumentation
3. Knowledge of biological consequences related to formulation is a plus.