Director of Biotechnology (Purification Process Development and Scale-up)

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;
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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;

èŒä½å称:生物工艺总监(纯化工艺开å‘与放大)

工作地点:中国.æˆéƒ½

工作类型:全èŒ

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Job Title: Director of Biotechnology (Purification Process Development and Scale-up)

Job Location: Chengdu, China

Job Type: Full-time

Job Description:

1. Process development and scale-up of recombinant protein/antibody purification;

2. Build-up and continuous optimization of recombinant protein, /antibody purification platform, management of pilot lab active participation in design and construction of manufacturing facility;

3. Being responsible for managing relevant projects and documents on product purification in compliance with CFDA/FDA/EMA regulations.

Job Requirements:

1. Education: MasterDegree or above;

2. Major: Biochemistry, Chemical Engineering, Biophysical Chemistry or related fields;

3. Experience:

(1) 5+ years management experience in bio-pharmaceutical companies, skilled in process development and scale-up of protein purification;

(2) Hands-on relevant experience in overseas pharmaceutical company preferred;

4. Qualifications:

(1) Familiar with FDA/CFDA regulations onbiologics products at different stages;

(2) Strong capabilities in experiment design, project management and trouble-shooting with proven track records;

(3) Sophisticated skills on team management able to provide guidance and training for professional personnel with different functions and levels;

(4) Requirement for leadership and willing to take more responsibilities. 

5. Language: Good communication skills, both oral and writing, in English and Chinese.

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