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.
As QC Biochemical Scientist be major responsible as below:
1. 負責生物化學成品實驗室的測試並確保測試行為並符合PICS/GMP和中裕新藥PMS的要求。 Be responsible for biochemical-drug product tests and make sure the test practice is complied with both PICS/GMP and Taimedbio PMS requirements.
2. 按時完成中控樣品測試,成品測試及穩定性樣品測試。Complete the test for in-process control samples, release product and stability test on time.
3.負責起草/修訂生物化學測試相關的SOP。Be responsible for the SOP draft/revision in QC biochemistry lab.
4. 根據GMP and GLP要求有序,有組織地書寫分析報告。To prepare the analytical reports in order and organized format.
5. 負責化學實驗室的5S管理與儀器校正及維護。perform 5S management and instrument calibration and maintenance for biochemical lab.
6. 持續優化測試效率、專業知識和設備操作/維修技能Continuous improvement on testing efficiency, analytical knowledge and equipment operation / maintenance skills
7. 準備/制定實驗室標準操作程序、在職訓練和確校計畫書與報告書 Prepare / drift lab SOPs, OJT and validation protocols/reports.
8. 直屬主管交辦的其他任務Other tasks assigned by line manager.
1. Formulation design of oral, parenteral and topical product.
2. New drug delivery platform development for 505(b)2 candidate.
3. CMC preparation global submission.
4. Patent survey for new candidate and by-pass formulation design.
5. Trouble-shooting of existing commercial products.