Pharmaceutical R&D Director
Hinye Pharmaceutical Co., Ltd. was founded in August 2006 under the modern enterprise system, which has been a comprehensive modern pharmaceutical enterprise that is market-oriented, R&D-driven and science, industry and trade-integrated. Hinye lies in Liuyang Bio & Information Industry Park. It covers an area of 40,000 square meters and 20,000 square meters building area included now. A manufacturer building over 15,000 square meters is being built. And another 267, 000 square meters of land has been bought to built a production workshop under the criteria of USA FDA and Europe FDA. The strategic objectives of Hinye is creating a company that is meaningful and valuable to society. Its Business Philosophy is Patient-centered cooperation and win-win relationship. Therefore, a large number of young people who have entrepreneurship and dreams are gathering here.More than 60 researchers are working in Hinye R&D center (The key member were Master Degree or Ph.D.). Hinye has established 3 R&D systems that include synthesis laboratory, formulation laboratory and analysis laboratory. It has owned pilot scale synthesis platform, pilot scale formulation production platform and analysis platform. By the end of 2017, our company had undertaken 2 national science and technology projects, 6 provincial scientific research projects, 9 invention patent certificates and 8 design patents. More than 90 trademarks were filed with the State Trademark Office, and nearly 80 trademarks were obtained. Hinye is a famous trademark of Hunan Province now. Our company is a national high-tech enterprise. Hunan Province certified enterprise technology center, Hunan Province bone and joint disease drug engineering technology research center, Hunan Province drug quality evaluation engineering technology research center, 2016 Hunan province contract-honoring and credit enterprise, 2017 industrial brand cultivation Pilot companies.
Requirements and Key Responsibilities (include but not limited to)
1. A PhD required in pharmacy or related subjects.
2. Extensive experience in pharmaceutical research and project management; familiarity with the overall management of pharmaceutical projects; experience in taking charge of original drug information retrieval, prescription screening, process verification, small testing, pilot production, writing of relevant documents, and technical handover of the workshop.
3. Familiarity with the process of prescription and technology research of solid oral medicines, Western conventional preparations, Western sustained-release tablets, etc.
4. Proficiency in various experimental design methods and ability to apply them in the research process to ensure overall project management and improve the overall research efficiency.
Base on Changsha, Hunan Province.
API, Drug Substance, drug product technology transfer, Drug Corporation