R&D supervisor 研发主管
迪氏曼医药化学（上海）有限公司
- 公司规模：50-150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：2015-05-18
- 工作地点：上海-奉贤区
- 招聘人数：1
- 工作经验：5-7年
- 学历要求：本科
- 语言要求：英语熟练
- 职位月薪：面议
- 职位类别：生物工程/生物制药 医药技术研发人员
职位描述
R&D supervisor
Job description:
1, Factory research and development, management, maintenance, Shanghai analysis laboratory apparatus and make its continued in efficient, clean and safe condition;
2, Management, training and motivating team members to make team members to make the team to maintain good working condition and high business level to ensure the efficient of the research and development tasks to complete;
3, Organize, and participate in the development of pharmaceutical analysis method, the transfer and validation; In all kinds of experimental drugs;
4, To process the team to provide daily analysis services;
5, In the production phase analysis method for from the transfer of technology research and development department to the quality control department;
6, Research and development, report writing and drug registration documents.
7, Assist R&D director to finish other tasks.
8, The successful candidate will be expected to gradually assume all responsibilities for research and development (become the head of department), as well as plant support and deviation investigation. Training will be provided for this demanding role.
Requirements:
1, Bachelor 's degree or above, chemical or pharmaceutical chemistry;
2, 5 years or above in pharmaceutical enterprise (or scientific research units) research and development department (R&D) work experience;
3, Have a certain organization management ability, it is better to have experience with team;
4, Good inter-departmental communication ability;
5, Good listening, speaking, reading and writing in both Chinese and English, skilled use of English in the project implementation;
6, Laboratory management and equipment maintenance experience;
7, Familiar with the development of pharmaceutical analysis method;
8, Familiar with the analytical method validation, methodology research;
9, Familiar with drug raw materials, intermediates of the establishment of quality standard;
10, Be familiar with GMP guidelines and national pharmacopoeia;
11, Have certain writing experience better drug registration file.
Job description:
1, Factory research and development, management, maintenance, Shanghai analysis laboratory apparatus and make its continued in efficient, clean and safe condition;
2, Management, training and motivating team members to make team members to make the team to maintain good working condition and high business level to ensure the efficient of the research and development tasks to complete;
3, Organize, and participate in the development of pharmaceutical analysis method, the transfer and validation; In all kinds of experimental drugs;
4, To process the team to provide daily analysis services;
5, In the production phase analysis method for from the transfer of technology research and development department to the quality control department;
6, Research and development, report writing and drug registration documents.
7, Assist R&D director to finish other tasks.
8, The successful candidate will be expected to gradually assume all responsibilities for research and development (become the head of department), as well as plant support and deviation investigation. Training will be provided for this demanding role.
Requirements:
1, Bachelor 's degree or above, chemical or pharmaceutical chemistry;
2, 5 years or above in pharmaceutical enterprise (or scientific research units) research and development department (R&D) work experience;
3, Have a certain organization management ability, it is better to have experience with team;
4, Good inter-departmental communication ability;
5, Good listening, speaking, reading and writing in both Chinese and English, skilled use of English in the project implementation;
6, Laboratory management and equipment maintenance experience;
7, Familiar with the development of pharmaceutical analysis method;
8, Familiar with the analytical method validation, methodology research;
9, Familiar with drug raw materials, intermediates of the establishment of quality standard;
10, Be familiar with GMP guidelines and national pharmacopoeia;
11, Have certain writing experience better drug registration file.
公司介绍
迪氏曼医药化学（上海）有限公司于2006年在上海金山化学工业园区成立，投资总额为1250万美元，公司总部位于印度，在全球拥有数十家子公司，是一个提供无限创意及全球化策略的公司，迪氏曼医药化学（上海）有限公司向您提供良好的职业发展机会，独特的企业文化让我们重视创意、鼓励创新，并且非常注重个人领导能力。所有的这些共同造就了我们“高品质的化学品”。如今，我们在寻求致力于在化学领域开创领导事业的各类英才。我们向员工提供的不仅仅是优厚的薪资和福利待遇，还有非常广阔的个人发展空间。
公司在莘庄地铁站设有班车，便于公司员工上下班。
公司在莘庄地铁站设有班车，便于公司员工上下班。