Director, Microbial Fermentation

KLUS PHARMA INC Cranbury, NJ
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科伦è¯ä¸š Kelun Pharmaceutical CO, LTD

  • 拥有海内外90余家下属ä¼ä¸šçš„现代化è¯ä¸šé›†å›¢ï¼Œæ˜¯ä¸­å›½åŒ»è¯è¡Œä¸šçš„领军ä¼ä¸š
  • å…¨çƒè§„模最大的输液专业制造商和全çƒè§„模最大抗生素中间体制造商 A股上市公帠(股票代ç ï¼š 002422)
  • 全国医è¯åˆ¶é€ ä¸šå‰10强
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  • A leading Pharmaceutical Company in China with over 90 subsidiaries globally;
  • The biggest producer of injectable and infusion products in the world;
  • The biggest in antibiotic intermediate production in the world;
  • Public-Traded company in China (Stock Code; 002422);
  • A Top 10 Chinese Pharmaceutical Company;
  • 2016 sales revenue of RMB 40 billion with profit RMB 2 billion

科伦è¯ç‰©ç ”究院Kelun Pharmaceutical Research Institute

  • 现拥有è¯ç‰©ç ”å‘人员1000余人;
  • 构建了以中央研究院(æˆéƒ½ï¼‰ä¸ºæ ¸å¿ƒï¼Œä»¥å—方(è‹å·žï¼‰ã€åŒ—æ–¹ï¼ˆå¤©æ´¥ï¼‰ç ”ç©¶åˆ†é™¢ã€æµ·å¤–(美国新泽西,圣地亚哥)研究分院为分支的集约化研究体系,
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  • Over 1000 R&D staff;
  • HQ in Chengdu with satellite research centers in Tianjin, Suzhou, New Jersey and San Diego, CA
  • A highly-integrated research platform on generic, NDDS, small molecules and biologics discoveries;
  • Focusing on highly unmet medical needs on oncology, diabetes, liver, cardiovascular and other diseases;

 

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Job Title: Director, microbial fermentation

Job Location: Chengdu, China

Job Type:  Full-time

Job Description:

1. Responsible for the development, scale-up and production of antibiotics, peptides and protein products, to solve key technical problems;

2. Responsible for project management and IND application, to ensure compliance with regulatory requirements and future trends;

3. Responsible for the establishment of production documents in accordance with the requirements of cGMP system, responsible for the production process control and improvement in production to ensure the smooth operation of the production line.

 

Job Requirements:

1. Education: Bachelor degree or above in Fermentation Engineering, bio-engineering, cell biology, bio-pharmaceutical and other related fields;

2. Language: capable to communicate in Chinese (Mandarin);

3. Working Experience:

(1) At least 5 years’ experience in Prokaryotic or yeast microbial screening, optimization and fermentation process development;

(2) Responsible for pilot or production-scale fermentation process research in pilot or production-scale, completing IND filing or production applications;

(3) Oversea industry experience preferred;

4. Qualifications:

(1) Familiar with the global biologics R & D, EMA/FDA/CFDA regulations, and relevant clinical submission requirements;

(2) Proficient in prokaryotic or yeast fermentation process research and industrial production processes and technologies;

(3) Familiar with antibiotics, peptides, protein drugs GMP workshop design, management and operation;

(4) Managerial and leadership experience in building and developing R & D team;

(5) Capable to provide coaching and mentorship;

5. High degree of loyalty, responsibility and professionalism.

 

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