中山康源基因技术科技有限公司

——国内首家原创基因芯片研发应用高新企业

  中山康源基因技术科技有限公司（以下简称“康源基因”），设立于中山市火炬开发区国家健康产业基地，是2014年“中山市3.28招商引资”项目，并于2014年12月30日完成工商注册，注册资本为3409万元，是由美籍华人科学家蔡伟文博士为带头人的海归创业团队创办的企业。公司主要业务为研发和生产基因芯片及其他生物试剂和仪器，并从事自产产品同类商品的检测服务。公司拥有8项发明专利、2项实用新型专利、500平方米符合GMP要求的10万级洁净生产车间。                        

  康源基因是一家以自主知识产权的高特异性高灵敏度基因芯片制造技术为核心，以基因芯片以及定量微生物芯片，基因组大数据分析解决方案提供商为主导，以发展为分子检测产业上游供应商为目标，集研发、生产、销售和科研服务于一体的高新技术企业。目前公司已建成具有国际水平的生物芯片研发，生产和检测平台；建立了针对微生物定量分析，呼吸道感染检测，抗生素耐药性检测等产品系列。业务双轨制推进，建立了基因检测和定制两大体系，应用于IVD体外检测及公共安全、环境生态等行业。

  目前，国内分子产业尚未有一家企业完全拥有自主知识产权基因芯片制备技术；基因测序原材料（试剂与耗材）设备仪器等依赖进口；aCGH芯片生产所需原材料（试剂与耗材）设备仪器等均高度依赖进口。以上导致市场上主流的分子检测手段使用门槛较高，市场上缺乏一种能够定量、快速、操作简便的分子检测手段，这是国内在分子检测这一领域的潜在经济效益。

  康源基因拥有完整先进的研发平台，可快速且低成本研发各种定制产品。通过康源基因拥有自主化基因芯片制造工艺和检测技术，其芯片检测方法具有操作简便，检测结果精确，成本低，可大规模推广使用等特点，再加上国家政策号召促进全民大健康的背景下，利用此技术开发的芯片检测产品在科研与临床应用方面具有广阔的发展潜力。康源基因的发展宗旨成为中国市场上应用级基因芯片的主导者，让分子检测手段平民化。

康源使命，专芯惠民——做老百姓用得起的原创基因芯片！   

                                  招聘岗位 

一、研发工程师

工作内容：

1.协助公司研发项目设计、实施及优化工作；
2.负责组织和协调相关部门进行公司产品小试、中试，新产品的测试；
3.完成上级安排的实验任务，做好相关实验记录；

4.协助新产品、新技术等知识产权申报工作，保护公司及相关人员的研发成果。

任职条件：

1. 本科以上学历，生物化学、分子生物学、遗传学等相关专业；
2.了解PCR、基因芯片等分子诊断技术，熟练的分子生物学相关实验技能；
3.有长期稳定发展意愿。

二、市场专员

工作内容：

1.负责基因芯片及试剂耗材市场的开发与维护;

2.解决客户的技术要求及疑问；

3.负责合同、质量保证协议的签订；

4.负责产品售后服务工作。

5.维护客户关系，定时拜访客户；

6.本岗位非医药代表。

任职条件：

1. 生物技术类、分子生物学、遗传学等相关专业优先;
2.有相关工作经验优先，可接受应届毕业生;
3.能够承受较强的工作压力,能适应出差。

三、检测主管

工作内容：

1.根据样品量合理安排检测工作，保证检测任务按时按量完成；

2.负责样本接收、登记、保存制度的制定与监督实施，确认检测数据及报告； 

3.负责检测设备日常管理及维护，并与其他相关部门协调设备的维修、使用； 

4.指导并解决检测过程出现的问题，优化检测流程，并定期向上级汇报部门情况；

任职条件：

1.硕士以上学历，医学检验专业、生物制药、分子生物学、微生物研发、细胞生物学、生物工程等相关专业毕业，2年以上工作经验。

2.有医院实习经验、分离纯化、PCR、GMP等相关工作经验者优先考虑。

3.做事认真、细心，负责。

四、检测员

工作内容：

1.负责样本采集及各项检验检测工作；

2.按照有关的检验操作规程及时准确地完成检验任务；

3.负责认真填写检验原始记录和辅助记录；

4.负责仪器的日常维护和管理。

任职条件：

1.大专学历，医学检验专业、生物制药、分子生物学、微生物研发、细胞生物学、生物工程等相关专业毕业（接受应届毕业生）。 

2.有医院实习经验、分离纯化、PCR、GMP等相关工作经验者优先考虑。

3.做事认真、细心，负责。

Halgen Limited

--- The First High-tech Enterprise of Original Gene Chip R&D and Application in China

Halgen Limited (hereinafter referred to as “Halgen”), established in the National Health Technology Park of Huoju Development Zone, Zhongshan City, is a project of “3.28 Inviting Outside Investment in Zhongshan City” in 2014, and completed its industrial and commercial registration on December 30, 2014, with a registered capital of RMB 30million. Founded by a returnee entrepreneurial team led by Chinese-American scientist Dr. Cai Weiwen, it is engaged in the R&D and production of gene chip and other biological reagents and instruments, along with the testing service for self-produced products and similar products. The Company enjoys 8 invention patents, 2 utility model patents, and 500 square meters of 100,000-class clean production workshop up to GMP.

As a high-tech enterprise, Halgen takes independent intellectual property rights of high specificity and high sensitivity gene chip manufacturing technology as its core, gene chip and quantitative microbial chip, genomic big data analysis solution providers as its leading factor, developing into the upstream supplier of molecular detection industry as its goal, and integrates R&D, production, sales and scientific research services. Now, the Company has built an international level biochip R&D, production and testing platform, and established a series of products for microbial quantitative analysis, respiratory infection detection, antibiotic resistance detection, etc. The Company has promoted the double-track business system, and established two major systems of genetic testing and customization, which are applied to IVD in vitro testing, public safety, environmental ecology as well as other industries.

At present, there have not been any enterprises in the domestic molecular industry that own the technology of gene chip preparation with independent intellectual property rights; gene sequencing raw materials (reagents and consumables), equipment and instruments rely on imports; the raw materials (reagents and consumables), equipment and instruments required for the production of aCGH chips are highly dependent on imports. The aforesaid reasons impose the high threshold of the mainstream molecular detection in the market, and there is a lack of molecular detection method in the market that is featured with quantity, rapidness and handy operation, enabling the potential economic benefit in the field of molecular detection in China.

Halgen has a complete and advanced R&D platform, which can develop various customized products at a quicker pace and a lower cost. As Halgen has been equipped with independent gene chip manufacturing process and testing technology, the chip detection method is featured with simple operation, accurate detection results, lower cost and great potentials of application. Besides, under the background of national policy calling for the promotion of national health, the chip detection products developed by this technology enjoy broad development potential in scientific research and clinical application. The development purpose of Halgen is to become the leader of application level gene chip in the Chinese market so that it may make molecular detection methods popular.

Halen’s is committed to specializing in chip and benefiting the people---- Manufacturing original gene chips that ordinary people can afford!

                                                                                                      Job Vacant

R&D Engineer

Job Description：

1. Assist the company in R&D project design, implementation and optimization;

2. Responsible for organizing and coordinating the relevant departments to carry out the company’s product casual tests, pilot tests and new product tests;

3. Complete the experimental tasks assigned by the superior, and make relevant experimental records;

4. Assist in the declaration of new products, new technologies and other intellectual property rights, and protect the R&D achievements of the company and relevant personnel.

Job Qualifications：

1. Bachelor degree or above, major in biochemistry, molecular biology, genetics, etc.;

2. Expertise with PCR, gene chips and other molecular diagnostic techniques, proficient in molecular biology-related experimental skills;

3. Willing to have a long-term stable development in our company.

Marketing Officer

Job Description：

1. Responsible for the development and maintenance of gene chips and reagent consumables market;

2. Solve customer’s technical requirements and questions;

3. Responsible for signing contract and quality assurance agreement;

4. Responsible for after-sales service;

5. Maintain customer relationship and visit customers regularly;

6. You are not working as a medical representative at this post.

Job Qualifications：

1. Biotechnology, molecular biology, genetics and other related majors are preferred;

2. Relevant working experience is preferred, and fresh graduates will be acceptable;

3. Able to take high pressure, and adaptable to business trips.

Test Supervisor

Job Description:

1. Arrange the testing work according to the sample quantity to ensure that the testing task is completed on time;

2. Responsible for the formulation and implementation of sample receiving, registration and preservation system, and confirm the test data and reports;

3. Responsible for the daily management and maintenance of testing equipment, and coordinate with other relevant departments for the repair and use of equipment;

4. Guide and solve the problems in the testing process, optimize the testing process, and report to the superior regularly;

Job Qualifications:

1. Master degree or above in medical laboratory, biopharmaceutical, molecular biology, microbial research and development, cell biology, bioengineering and other related majors, with more than 2 years of working experience;

2. Experience in hospital practice, separation and purification, PCR, GMP and other related work experience is preferred;

3. Equip with conscientiousness, carefulness and a sense of responsibly.

Inspector

Job Description:

1. Responsible for sample collection and inspection;

2. Complete the inspection task timely and accurately according to the relevant inspection procedures;

3. Responsible for filling in the original inspection records and auxiliary records;

4. Responsible for instrument daily maintenance and management.

Job Qualifications:

1. College degree in medical laboratory, biopharmaceutical, molecular biology, microbial research and development, cell biology, bioengineering and other related majors (fresh graduates will be acceptable);

2. Experience in hospital internship, separation and purification, PCR, GMP and other related work experience;

3. Equip with conscientiousness, carefulness and a sense of responsibly.