研发制剂主管
昆山龙灯瑞迪制药有限公司
- 公司规模:150-500人
- 公司性质:外资(非欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2017-06-02
- 工作地点:昆山
- 招聘人数:1人
- 工作经验:5-7年经验
- 学历要求:本科
- 语言要求:英语 良好
- 职位月薪:0.8-1万/月
- 职位类别:医药技术研发管理人员
职位描述
职位描述:
1负责各个项目的技术转移及新项目的处方工艺筛选、优化、放大及工艺验证,负责解决项目工艺放大中遇到的的技术问题;
Responsible for the technology transfer process of the projects ,
Responsible for formulation and process development, opitimizaion , scale up & process validation ,
Responsible for solving technical problems encountered in process scale up;
2、负责制剂研发产品研究方案、研究计划、实验记录、研究报告、注册资料的指导,及时整理和归档产品开发技术资料和报告
Responsible for guidance of the project research proposal,
research plan, experimental records and report, registration document,
Sorting and filing product development technical data and report in time.
3负责公司内部相关部门的沟通协调工作,以保证研发项目的顺利开展;
Responsible for the company's internal communication and coordination with other related department, Ensure the R&D project process smoothly;
4指导制剂研究员按照研究方案开展工作,确保试验数据的准确性,可靠性,加快推进实验项目进展,在保证质量的前提下,确保注册部门申报工作按时完成。
Guide researcher to work according to the research protocol, ensure the accuracy of and reliability of the experiment results,
cooperate with new product registration filing work to ensure declaration quality and schedule
6、参与制定研发人员成长规划和和年度培训计划;
Participate in research and development personnel growth plan and annual training plan;
7完成部门领导安排的其他临时性工作任务。
Complete other temporary tasks arranged by department leader.
职位要求:
1、2年以上的团队管理经验;
more than two years experience in team management;
2、具备口服固体制剂新技术、新剂型产品开发能力和经验的更佳。
It is better that if someone have the ability of developing new technology or new dosage form or relative experience
3、精通口服固体制剂开发小试、中试、大生产的各个环节;
Be proficient in every part of small scale 、pilot scale、scale up of solid oral dosage form preparation。
4、 具有扎实的药剂学理论基础和丰富的项目经验;
Have a solid theoretical pharmacy foundation and rich experience
in pharmacy project development;
5、熟悉CFDA药品法律法规及要求;
Familiar with the CFDA drug laws and regulations and requirements;
6、 具有组织协调、人际沟通能力,有良好的管理经验。
Has the ability of the organization and coordination、interpersonal communication, good management experience.
7、具有很强的科研计划和执行能力,出色的解决问题的能力,能够承受一定压力。
Has a strong ability of scientific research plan and execution ability, good problem solving skills, be able to withstand a certain pressure.
8 、 有缓控释微丸等缓释制剂开发经验者优先;
It is prefered that if someone have controlled-release pellets preparation development experience
举报
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1负责各个项目的技术转移及新项目的处方工艺筛选、优化、放大及工艺验证,负责解决项目工艺放大中遇到的的技术问题;
Responsible for the technology transfer process of the projects ,
Responsible for formulation and process development, opitimizaion , scale up & process validation ,
Responsible for solving technical problems encountered in process scale up;
2、负责制剂研发产品研究方案、研究计划、实验记录、研究报告、注册资料的指导,及时整理和归档产品开发技术资料和报告
Responsible for guidance of the project research proposal,
research plan, experimental records and report, registration document,
Sorting and filing product development technical data and report in time.
3负责公司内部相关部门的沟通协调工作,以保证研发项目的顺利开展;
Responsible for the company's internal communication and coordination with other related department, Ensure the R&D project process smoothly;
4指导制剂研究员按照研究方案开展工作,确保试验数据的准确性,可靠性,加快推进实验项目进展,在保证质量的前提下,确保注册部门申报工作按时完成。
Guide researcher to work according to the research protocol, ensure the accuracy of and reliability of the experiment results,
cooperate with new product registration filing work to ensure declaration quality and schedule
6、参与制定研发人员成长规划和和年度培训计划;
Participate in research and development personnel growth plan and annual training plan;
7完成部门领导安排的其他临时性工作任务。
Complete other temporary tasks arranged by department leader.
职位要求:
1、2年以上的团队管理经验;
more than two years experience in team management;
2、具备口服固体制剂新技术、新剂型产品开发能力和经验的更佳。
It is better that if someone have the ability of developing new technology or new dosage form or relative experience
3、精通口服固体制剂开发小试、中试、大生产的各个环节;
Be proficient in every part of small scale 、pilot scale、scale up of solid oral dosage form preparation。
4、 具有扎实的药剂学理论基础和丰富的项目经验;
Have a solid theoretical pharmacy foundation and rich experience
in pharmacy project development;
5、熟悉CFDA药品法律法规及要求;
Familiar with the CFDA drug laws and regulations and requirements;
6、 具有组织协调、人际沟通能力,有良好的管理经验。
Has the ability of the organization and coordination、interpersonal communication, good management experience.
7、具有很强的科研计划和执行能力,出色的解决问题的能力,能够承受一定压力。
Has a strong ability of scientific research plan and execution ability, good problem solving skills, be able to withstand a certain pressure.
8 、 有缓控释微丸等缓释制剂开发经验者优先;
It is prefered that if someone have controlled-release pellets preparation development experience
职能类别: 医药技术研发管理人员
关键字: 制剂 制剂主管 主管 工程师
公司介绍
昆山龙灯瑞迪制药有限公司是由加拿大龙灯集团与印度瑞迪博士制药有限公司及昆山双鹤制药有限公司三方合资的一高新技术制药企业,公司主要生产经营医药原料及制剂产品。“引导健康新生活”是公司的核心目标,我们立志为人类健康事业做出应有的贡献。公司诚邀各界有识之士加盟“龙灯瑞迪”,共同创造美好未来。
联系方式
- 公司地址:广州增城