Job responsibility 工作职责
Process Development工艺开发
61 Research the formulation of protein, process development and optimization.
研究蛋白质的处方、完成工艺开发和优化。
61 Develop process plan, provide clear prescription process, and guide the workshop to complete manufacture.
制定工艺计划,提供明确的工艺流程,指导车间完成生产。
61 Prepare qualified samples to ensure the smooth operation of pre-clinical.
准备合格的样品,确保临床前的顺利进行。
61 Draft the original experiment record and filing documents for IND.
为IND起草原始实验记录和归档文件。
61 Collecting the supporting documents of excipient and package materials.
收集辅料和包装材料的证明文件。
Site Safety and Environmental compliance现场安全和环境合规
61 Take part in the site safety;
参与到工作现场的安全中。
61 Adhere to the Company’s safety and environmental protection procedures.
61 遵守公司的安全环保程序。
Quality Assurance 质量要求
61 Comply with the Company Quality Management System for development activities.
遵守公司制定的研发质量管理体系。
General常规要求
61 Take responsibility of the general operation of the protein formulation laboratory facilities;
负责蛋白质处方实验室设施的一般操作;
61 Maintain effective, collaborative, and frequent interactions with other department to ensure harmonization in scientific and technical approaches;
与其他部门保持有效、协作和频繁的沟通,以确保科学和技术方法的协调。
61 Comply with Company Policies and Procedures and contribute positively to Company Morale;
遵守公司政策和程序,积极提升公司士气;
61 Plans, executes and manages both routine and non-routine projects simultaneously with general criteria for results
根据一般标准的结果,同时计划、执行和管理常规项目和非常规项目
61 Other reasonably duties as requested by Company Senior Management from time to time.
完成领导提出的其他任务。
Qualifications 任职资格
61 Major in Pharmaceutics, Pharmaceutical Science or related field;
药剂学、药学或者其他相关专业。
61 Advanced post-graduate qualification (BS or MS) related to bioprocessing or biopharmaceutical production.
相关专业的本科或硕士学历。
Essential Experience必要经验
61 BS degree with a minimum of 0~3 years and MS degree with a minimum of 0~2 years of large Biomolecule formulation experience;
本科0~3年,硕士0~2年相关生物大分子制剂经验
61 Mastered the theoretical knowledge of pharmaceutical;
掌握药学的理论知识
61 Familiar with the literature retrieval and relevant information inspection, and familiar with the IND filing;
熟悉文献检索及相关信息检查,熟悉IND备案。
61 Strong communication and execution ability;
较强的沟通和执行能力。
61 Ability to bear certain stresses. Advanced computer system skills for Microsoft Office suite (Word, Excel, Powerpoint, Project, Outlook);
熟练使用Microsoft Office办公软件(Word、Excel、Powerpoint、Project、Outlook)
Preferred Experience优先考虑
61 Project management of CMC filing for US, EU, and China IND/CTA;
具有美国、欧盟和中国项目申报方面的管理经验。
61 Familiar with office software and proficient in reading professional English;
熟悉办公软件,熟练阅读专业英语;
61 Sound knowledge of Good Manufacturing Practices including NMPA, PIC/S, and US-FDA guidelines with focus on biologic API production for clinical trials;
具备良好的生产实践知识,并注重关于API产品的临床试验的NMPA、PIC/S和US-FDA法规指南,
61 Project management training;
具有项目管理能力
61 Formal root-cause analysis training;
严谨的问题分析能力
61 Formal root-cause analysis training;
严谨的问题分析能力;