m****s 发帖数: 18160 | 1 【 以下文字转载自 Postdoc 讨论区 】
发信人: Chum23 (喜欢春天的人), 信区: Postdoc
标 题: 国内上市企业高薪职位
发信站: BBS 未名空间站 (Tue Mar 4 23:28:49 2014, 美东)
代友转发:诚聘固体制剂研发总监 (职位描述如下)和药物注册专家,有意者请投简
历至Jim Li
-----------------------------------
Process R&D Director of Solid Oral Formulation
Hainan Shuangcheng Pharmaceuticals Co., Ltd. (海南双成药业有限公司)
Location:
China
Contact:
Jim Li
Salary:
80,000.00 - 120,000.00 USD
Type:
Full Time - Experienced
Sector:
Private Industry
Discipline:
Academic / Research
Preferred Education:
Masters
Hainan Shuangcheng Pharmaceuticals Co., Ltd.
Hainan Shuangcheng Pharmaceuticals Co., Ltd. (HNSP) was found in 2000. It is
a high-tech company which is characterized by its chemical synthesis
peptide drugs. The company is focusing on drug’s research and development,
application and registration, manufacturing and marketing. HNSP successfully
developed Jitai® (Thymalfasin for Injection), Somatostatin for
injection, and Thymopentin for Injectio ...n in domestic market, meanwhile
we have several chemical synthesis peptide drugs under application. The
Peptide API Workshop has a production capacity of 10kg/year, and the two
Lyophilized Formulation Workshops are complied with Chinese GMP and managed
by experienced personnel, the Lyophilized Formulation Workshops has the
capacity of approximate 30 million vials per year. Besides these, we also
have a Chinese GMP-conformed Solid Formulation Workshop. Since the company
set up, it keeps rapid growth. The sales network covers 28 administrative
regions in the mainland. The terminal sales for the peptide drugs are 352
million. The company adheres to philosophy of “To Fulfill Your Wishes, and
To Fulfill Ours” which is embodied in delivering health with our good faith
and creating a bright future by hardworking. Besides focus on company
development, we also actively perform our social responsibilities in return.
In the future, HNSP’s development strategy is to become a leading global
peptide API supplier and generic peptide drugs and drug products
manufacturer.
Guide and manage the R&D, improvement, technology transfer and validation of
process of solid oral formulations.
1. Bachelor or master degree in pharmacy, organic chemistry or
pharmaceutical chemistry and relevant major, with more than 6 years
experience in process R&D, or; PhD degree with more than 4 years experience
in process R&D. 2. Extensive knowledge and experience of solid oral
formulations (tablet, capsule, particulate and sustained release formulation
), familiar with the characteristic of different kinds of solid oral
formulations and have success experience in developing different formulas of
solid oral formulation. Be Capable of designing new formula, reverse
engineering and solving the technical problems during R&D procedure. 3.
Proficient in understanding characteristic and function of different
excipient, choose the proper and effective percipients to ensure the success
of the formula and process. 4. Familiar with sustained release and control
release solid oral formulations and process development, can choose the
reasonable excipients, formula and process base on the physical and chemical
characteristics of drug substances. 5. Have strong understanding of the
characteristic of packing materials, can choose the reasonable packing
materials base on the characteristic and requirements of solid formulation,
can do the packing materials verification. 6. Familiar with the advanced
solid oral formulation research and development process and means, such as
DOE, QbD, risk analysis and risk control, process scale-up, change control,
technical transfer, validation etc. 7. Familiar with international guidance
(including ICH, FDA and EMA) of medicine research, and cGMP regulatory
requirements. 8. Familiar with the principle, performance and quality of
solid oral formulations R&D and manufacturing equipments. 9. Abundant
experience in management and leadership, and good ability of communication
and negotiation, strong sense of responsibility, provide the R&D personnel
with guidance and training. 10. Lead the R&D project team to fulfill the
process research and development tasks. 11. Strong document writing skills
and good at using MS software. 12. Good command of chemical and
pharmaceutical English, capable of communicating with foreign customers
through listening, speaking, reading and writing. 13. Oversea studies and
working experiences of related industry in foreign countries will be
preferred.
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