Job Responsibilities/崗位職責:
1.Responsible for process characterization, process validation, and risk assessment of related projects to ensure the robustness and reliability of conjugation processes.
負責相關(guān)項目的工藝表征、工藝驗證和風(fēng)險評估,確保偶聯(lián)工藝的穩(wěn)健性和可靠性;
2.Responsible for the preparation of ADC samples (from milligram to gram scale) and development of conjugation process for preclinical-stage projects, including both site-specific and non-site-specific conjugation strategies, as well as the development, optimization, and purification process development, and draft conjugation process development research protocols, study reports and related regulatory submission documents.
負責臨床前階段項目的ADC樣品的制備(毫克到克級別)和偶聯(lián)工藝開發(fā)工作,包括定點偶聯(lián)和非定點偶聯(lián)工藝的開發(fā)、優(yōu)化及純化工藝的開發(fā),并撰寫偶聯(lián)工藝開發(fā)研究方案、研究報告及相關(guān)申報資料;
3.Execute technical transfer and process scale-up activities as required, and support pilot-scale production for toxicology batches.
按要求完成技術(shù)轉(zhuǎn)移與工藝放大的工作,輔助毒理批中試生產(chǎn);
4.Participate in laboratory document management, training, self-inspection, and rectification, and cooperate with QA inspections to ensure compliance with quality management requirements.
參與實驗室文件管理、培訓(xùn)及自查整改工作,配合研發(fā)QA的監(jiān)督檢查,確保實驗室符合質(zhì)量管理要求;
5.Manage laboratory equipment and instruments, including acceptance, validation, maintenance, and calibration, to ensure smooth laboratory operations.
負責實驗室工藝開發(fā)相關(guān)設(shè)備儀器的驗收、驗證、維護及管理,參與實驗室儀器操作SOP的起草、培訓(xùn)及修訂工作;
6.Implement EHS (Environment, Health, and Safety) requirements, handle hazardous waste and liquid disposal, and maintain laboratory hygiene standards.
執(zhí)行EHS(環(huán)境、健康與安全)要求,處理實驗室危險廢棄物及廢液,確保實驗室環(huán)境衛(wèi)生符合標準。
Job Requirements/崗位要求:
1.Master’s degree or higher in pharmacy, chemistry, bioengineering, biopharmaceutics, or related fields.
碩士及以上學(xué)歷,藥學(xué)、化學(xué)、生物工程、生物制藥等相關(guān)專業(yè);
2.3+ years of experience in ADC conjugation R&D, process development, or technology transfer, or experience in downstream biopharmaceutical process development.
3年以上ADC偶聯(lián)研發(fā)、工藝開發(fā)或技術(shù)轉(zhuǎn)移經(jīng)驗,或生物制藥下游工藝開發(fā)經(jīng)驗;
3.Familiar with biopharmaceutical CMC processes, conjugation chemistry, and process development; proficiency in protein purification and chromatography system operation.
熟悉生物藥CMC流程,掌握偶聯(lián)化學(xué)及工藝開發(fā)知識,具備蛋白純化和層析系統(tǒng)操作等技能;
4.Skilled in the operation of advanced bioprocessing equipment, including ultrafiltration/diafiltration (UF/DF), tangential floe filtration (TFF), and fast protein liquid chromatography system such as AKTA. Familiar with the analytical methods for assessing critical quality attributes (CQA) of ADC.
熟練使用超濾/滲濾系統(tǒng)(UF/DF)、切向流過濾(TFF)、快速蛋白純化儀(FPLC,AKTA)等設(shè)備,了解ADC關(guān)鍵質(zhì)量屬性(CQA)的檢測方法;
5.Strong English reading and writing skills for report preparation and literature review; excellent communication, teamwork, and problem-solving ability.
具備良好的英語讀寫能力,能夠撰寫英文報告及文獻檢索;具備較強的溝通能力、團隊協(xié)作精神及解決問題的能力。