岗位职责:
1. 负责跟进、落实制剂研发实验室的规划、设备物料及耗材的采购；规章制度、良好操作规范和5S的建设及监督执行。
Responsible to follow up and implement the planning of DP R&D lab, procurement of equipment materials and consumables; develop and supervise rules and regulations, good practices and 5S implementation.
2. 负责制剂处方的开发计划/方案及其他相关研究报告的起草/审核。
Responsible for the drafting/review of formulation development plans/schemes and other related research reports.
3. 负责推进制剂处方工艺开发工作，包括早期成药性研究、临床制剂处方筛选、工艺优化、运输条件、稳定性考察等相关研究方案的制定、实施、评价、审核等工作。
Responsible for promoting the development of formulation prescription process, including the development, implementation, evaluation and review of early drug-forming studies, clinical formulation prescription screening, process optimization, transportation conditions, stability investigation and other related research programs.
4. 确保各项实验按照拟定的计划、方案执行；控制实验成本、进度和质量；审核实验记录。
Ensure that all experiments are executed according to the proposed plans and protocols; control the cost, progress and quality of experiments; review experimental records.
5.负责制剂项目管理、不断完善制剂研发平台。
Responsible for formulation project management and continuous improvement of formulation R&D platform.
6.负责落实与制剂相关的IND申报资料和原始记录的整理、汇总和审核；配合药品注册现场检查。
Responsible for organizing, summarizing and reviewing information and original records related with DP for the IND filing; cooperate with on-site inspection for drug registration.
任职要求:
1.本科或以上学历，生产经验丰富者可放宽要求
High school, college or above; the requirement can be relaxed for candidate with rich manufacture experience
2.两年制剂相关的工作经验；优先考虑有制剂研发工作经验。
Two years working experience related to DP; priority will be given to those who have pharmaceutical work experience and are familiar with the work flow and equipment operation in the production plant.
3.良好的学习能力和表达能力
Good learning ability and expression ability.
4.熟练使用各种办公软件
Proficiency in using various office software.
5.具有良好的语言表达能力和书面写作能力
Good language skills and written skills.
6.具有良好的职业操守，有责任心及团队合作精神
Good professional conduct with responsibility and teamwork spirit.