北京民海生物科技有限公司
北京民海生物科技有限公司是深圳康泰生物制品股份有限公司（股票代码300601）旗下的全资子公司之一，是一家以人用疫苗产品研发、生产和销售为主营业务的国家新技术企业。公司创立于2004年，坐落在中关村科技园区北京大兴生物工程与医药产业基地思邈路35号，拥有国内领先的新型疫苗研发中心，以及由十几个GMP生产车间组成的现代化人用疫苗生产基地。目前公司注册资本人民币7.7亿元，公司现有员工近千人；投资规模近人民币20亿元，总占地面积235亩。公司自主承担和参与多个“863”国家重点攻关项目和科技部重大专项，以及40多个国家和省市级科技项目，获得国家发明专利证书20余项。公司2009年被认定为“高新技术企业”并分别于2012年、2015年、2018年通过再认定。2010年入选北京市首批“G20企业”，2011年被北京市科委授予为“结合疫苗新技术研究北京市重点实验室”；2012年被北京市发改委授予为“新型疫苗北京市工程实验室”，获科技部首届中国创新创业大赛“优秀企业”称号；2013年经国家人保部批准设立“博士后科研工作站”；2014年经北京市科协批准设立“院士专家工作站”、被北京市科委认定为“新型联合疫苗北京市工程技术研究中心”及“新型疫苗北京市国际科技合作基地”、被北京市知识产权局认定为“北京市专利示范单位”；2015年被国家发改委认定为“新型疫苗技术研制国家地方联合工程实验室”；2017年通过第20批北京市企业技术中心认定；2018年新型疫苗研究与开发“刘建凯创新工作室”获得了“全国工人先锋号”的荣誉称号等等。公司与世界卫生组织（WHO）等国外许多机构建立了良好的技术合作关系。公司的质量体系借鉴了美国FDA、欧盟的质量管理体系模式优点，严格执行国家2010版GMP标准，全面消化和吸收美国默克集团、法国巴斯德生物制药有限公司相关产品的综合研发和产业化管理经验，探索出了一条具有国际化视野，符合中国国情，以研发为先导，高效产业化的疫苗发展道路。公司在研产品25个，截止目前有4个疫苗产品获批上市销售并覆盖全国，部分产品已经进入国际市场。其中自主研发的产品“无细胞百白破b型流感嗜血杆菌联合疫苗”为国内首创四联疫苗。公司近三年销售收入逐年增长50%以上，2018年销售收入达14.97亿元。
公司秉承“诚信、高效、创新、凝聚、卓越”的管理理念，建立了一套科学的激励机制，为优秀人才提供发挥才能、成就事业的舞台。在为员工提供有竞争力的薪酬、技术及管理双通道发展规划外，还提供高于同行业的良好福利，帮助新人制定职业发展规划，使每一位民海的员工都可以在公司提供的平台上成就一番事业。
欢迎致力于生物疫苗及人类健康守护事业的有识之士加入。
Recruitment Profile
Beijing Minhai Biotechnology Co., Ltd. is one of the wholly-owned subsidiaries of Shenzhen Kangtai Biological Products Co., Ltd. (Stock Code 300601).It is a National high and new technology enterprise which is engaged in human vaccine R&D, production and distribution in the biomedical industry. Minhai established in 2004 with a registered capital of 770 million RMB and a total investment of 2 billion RMB, which has nearly 1,000 employees and has 235 mu of total area, located at No.35 Simiao Road, DaXing Biomedical Base of Zhongguancun Science and Technology Park, Beijing, which has a leading new type of vaccine R&D center in China, and a dozen GMP standard (2010 version GMP) modern vaccine manufacturing site for human vaccines.
Many core technical personnel are independently responsible for or participate in a number of “863” national key research projects and major special projects of the Ministry of Science and Technology, as well as more than 40 national and provincial and municipal science and technology projects, and has obtained more than 20 national invention patent certificates. The company Obtained “National High-tech enterprise certificate” in 2009 and re-recognized in 2012, 2015 and 2018 respectively; listed in “G20 project” (The Great-leap-forward Development Project for Beijing Biomedical Industry)in 2010, and awarded as “Key laboratory of Novel technology of conjugate vaccines” by Beijing Municipal Science and Technology Commission in 2011;awarded as "Beijing Engineering Laboratory of Novel Vaccine" by Beijing Development and Reform Commission, and awarded as the title of "Excellent Enterprise" in the First China Innovation and Entrepreneurship Competition of the Ministry of Science and Technology in 2012;awarded as “Postdoctoral R&D station” approved by the Ministry of Human Resource and Social Security of PRC in 2013;obtained"academician expert workstation" approved by the Beijing Association of Science and Technology, recognized as "Beijing Engineering Technology Research Center for Novel Conjugate Vaccines" and “International collaboration base of novel vaccines” by the Beijing Municipal Science and Technology Commission, and recognized as "Beijing Patent Demonstration Unit" by the Beijing Intellectual Property Bureau in 2014;recognized as "National and Local Joint Engineering Laboratory for Novel Vaccine Technology Development" by the National Development and Reform Commission in 2015;recognized through the 20th.batch of Technical Certification by the Beijing Enterprise Technology Center in 2017;Liu Jiankai Innovation Studio for Novel Vaccine R&D was awarded as "National Worker Pioneer" in 2018, and so on.
The company has established good technical cooperation relations with many international organizations such as the World Health Organization (WHO). The company's quality system draws lessons from the advantages of FDA of US and quality management system of EU, strictly implements the national GMP standard published in 2010, comprehensively digests and absorbs the comprehensive R&D and experience of industrialization related products of Merck Group from US and Pasteur Biopharmaceutical Co., Ltd. from France, and explores an international perspective vaccine development path with R&D as the guide and high efficient industrialization in line with China's conditions. The total research products amount for 25,and there are four commercialized vaccine products have been approved for sale and covering the whole nation till now, and some of them have entered the international market.Among them, the self-developed product "DTaP-Hib conjugate vaccine" is the initiative in China. The company's sales revenue has increased by more than 50% year by year in recent three years, reached 1.497 billion yuan in 2018.
Adhering to the management concept of "Faith, Efficiency, Innovation, Cohesion and Excellence", the company has established a set of scientific incentive mechanism to provide a stage for talents to bring their talents into full play and build their careers. In addition to providing a competitive salary, technology and management dual-channel development plan for employees, it also provides better material benefits than the same industry, and helps new employees to make career development plans so that every employee in Minhai can achieve a career on the platform provided by the company.
Welcome the man of insight who devote themselves to the cause of biological vaccine and human health protection to join us.
Vaccine researcher(Cell and virus culture)
Essential Duties and Responsibilities include, but are not limited to, the following:
Be responsible for the operation and control of large-scale cell platform for culture technology;
Be responsible for the operation and control of large-scale virus on culture technology;
Be responsible for the design and implementation of optimization test program of cell and virus on culture technology;
Be responsible for the validation of cell and virus on culture technology and related equipment;
Be responsible for equipment use and daily maintenance during cell and virus culture;
Required Skills and Experience:
Master degree or above, majored in biology or relevant profession;
Preferred in cell and tissue culture skills;
Be practical and serious, strong sense of responsibility, initiative, good at communication, have team work spirit;
Good command of both spoken and written English, CET-6 or above
R & D Verification Engineer
Essential Duties and Responsibilities include, but are not limited to, the following:
Responsible for the detection of vaccine samples and can skillfully use analytical instruments to detect vaccine samples;
Analyze the test results and provide data support for relevant conclusions;
Responsible for completing the optimization, development, verification and validation of relevant detection methods;
Responsible for the research and establish new detection methods, and complete the verification of methodology;
assist in drug (vaccine) stability research;
Responsible for daily management, maintenance and verification of analytical instruments;
Be responsible for the query and translation of documents related to analytical instruments and sterility test.
Required Skills and Experience:
Master or equivalent in Biotechnology or related field;
Preferred experience in mass spectroscopy, ion chromatography, NMR related instruments ;
Preferred experience in high performance liquid chromatography and proteomics;
Devoted in technical work, have strong scientific research ability, can work stably for a long time.
R&D post which get a Beijing residence permit
Required Skills and Experience:
Master or equivalent in Biotechnology,immunology,,fermentation engineering,preventive medicine or related field;
Willing to work in vaccine R&D, production technology post and other related technical posts for a long time;
Preferred in vaccine development or testing;
Excellent academic performance.
International cooperation specialist
Essential Duties and Responsibilities include, but are not limited to, the following:
Collect, translate and supplement registration documents;
Go through customs inspection procedures;
Receive international conferences;
Accomplish the other work assigned by the company leader;
Required Skills and Experience:
Bachelor or equivalent in Biotechnology or international trade related field;
Fluent oral and written English skills;
Have related import and export trade, familiar with import and export process, freight and inspection system;
Have strong communication skills.
Quality Compliance Officer
Essential Duties and Responsibilities include, but are not limited to, the following:
Ensuring compliance with all aspects of the QMS program;
Provide advice on all QMS matters within the organization;
Administration and oversight activities for the site quality system;
Participates in WHO prequalification project, and review procedures, policies and other instructional documents relating to QMS to ensure compliance with WHO PQ requirements;
Follow up on the WHO Prequalification schedule to make sure the project moving forward as planed;
Ensure company's QMS compliance in accordance with company policy, as well as applicable worldwide regulations and standards (WHO, EU, FDA and others), identify and implement improvement opportunities within the organization;
Participates in regulatory and customer audits especially the regulatory audits from oversea NRAs (including WHO);
Collaborates with functional departments to resolve issues and maintain compliance;
Required Skills and Experience:
Bachelor or equivalent in Biotechnology or related field;
Minimum 3+ years of relevant work experience within the pharmaceutical or biopharmaceutical or related industry with at least 1+ year experience in quality management;
Familiar with drug/vaccine regulations and standards, especially WHO
Direct working experience in WHO PQ preferred;
Proficient at report generation using Excel and other MS Office applications;
Fluent oral and written English skills.
Senior Quality Compliance Officer
Essential Duties and Responsibilities include, but are not limited to, the following:
Ensuring compliance with all aspects of the QMS program;
Provide advice on all QMS matters within the organization;
Administration and oversight activities for the site quality system;
Participates in WHO prequalification project, and review procedures, policies and other instructional documents relating to QMS to ensure compliance with WHO PQ requirements;
Follow up on the WHO Prequalification schedule to make sure the project moving forward as planed;
Ensure company's QMS compliance in accordance with company policy, as well as applicable worldwide regulations and standards (WHO, EU, FDA and others), identify and implement improvement opportunities within the organization;
Participates in regulatory and customer audits especially the regulatory audits from oversea NRAs (including WHO);
Collaborates with functional departments to resolve issues and maintain compliance;
Provision of monitoring and trending metrics associated with QMS;
Develop methodology for company Quality Audit programme, and establish the indicators used to evaluate the performance of company’s QMS;
Identify gaps in systems and works with management to develop feasible plans for correction;
Participates in company’s overall Quality Strategy making, and provides insight and advice to the senior management team.
Required Skills and Experience:
Bachelor or equivalent in Biotechnology or related field;
5+ years of relevant work experience within the pharmaceutical or biopharmaceutical or related industry with at least 3+ year experience in quality management;
Experience in quality auditing;
Familiar with drug/vaccine regulations and standards, especially WHO
Direct working experience in WHO PQ preferred;
Experience in the pharmaceutical industry with proven experience in leading cross functional teams preferred.
Fluent oral and written English skills.
