Job Description：
1、Design and conduct gene editing experiments and subsequent identification at the cell level；

2、Design and conduct molecular biology experiments related to gene editing；

3、Developing new gene-editing technologies.

Core qualifications：

1、Master degree or above;

2、Experience in stem cell culture, stem cell gene editing and functional genome screening is preferred;

3、At least 6 years (director scientist) /3 years (senior scientist) /1 year (scientist) working experience;

4、Proficient in gene editing operations represented by CRISPR-Cas9;

5、Proficient in experimetal skills of cell and molecular biology.

Resume Delivery E-mail：hr@xellsmart.com

Job Description：

1、Responsible for the quality tests of the intermediate and final products of stem cells, and fill in the test records, instrument and equipment usage records, test reports, etc；

2、Participate in the quality testing of stem cell products in the process of quality research, methodology development, validation and transfer, process optimization, stability research, etc;

3、Participate in QC laboratory, equipment daily cleaning and maintenance;

4、Complete other work assigned by superior.

Core qualifications：

1、Bachelor degree or above, major in microbiology, molecular biology, cell biology or pharmacy, with at least 1 year working experience;

2、Experience in microbiological testing (asepsis, mycoplasma, virus, endotoxin, etc.), or familiar with flow cytometry, ELISA, qPCR is preferred

3、Have working experience in cell therapy industry, master cell culture routine technology, have certain aseptic operation consciousness is preferred;

4、Strong sense of responsibility, good at communication and coordination, team spirit, can bear hardships and stand hard work, have a strong sense of confidentiality;

5、Have the willingness and motivation to study independently (literature, laws and regulations, experimental techniques, training, etc.), try new challenges, and strive to improve yourself.

Resume Delivery E-mail：hr@xellsmart.com

Job Description：

1、Plan and maintain the quality system and document control system to ensure the stability and compliance of the quality system and procedures
2、Implement strict internal control and internal audit according to quality internal audit plan, support external audit;

Core qualifications：

1、Master degree or above;

2、Experience in leading or participating in the whole process of cell drug QA is preferred (including stem cell investigator-initiated clinical trial project);

3、Familiar with GMP quality control is preferred; Familiar with clinical-grade cell bank establishment, quality control system and quality methodology verification is preferred;

4、At least 2 years experience in QA system construction and implementation;

Resume Delivery E-mail：hr@xellsmart.com

Job Description：

1、Plan the application and registration of the company's products and pipelines, and promote the preparation of application materials and other registration according to the requirements of drug regulations；
2、Organize timely communication with regulatory authorities and coordinate with other departments to complete the rectification；
3、Organize, coordinate and supervise the preclinical CRO trials of the company's products and the third party application according to the requirements of the registration program

Core qualifications：

1、Master degree or above;

2、Successful experience in leading or participating in the application of IND for cell drugs is preferred (including stem cell investigator-initiated clinical trial project)；

3、At least 2 years of drug registration experience.

Resume Delivery E-mail：hr@xellsmart.com