Job Description

(1) Mainly responsible for assisting recruitment, including but not limited to: recruitment channel maintenance, resume screening, personnel invitation, interview arrangement, interview data statistics and other work.

(2) Assisting other human resources work according to the needs of department work.

Job Requirements

(1) Bachelor degree, human resources management, industrial and commercial management, administrative management and other management major;

(2) 2023 graduates, with an internship cycle of at least half a year; they are interested in engaging in recruitment;

(3) mastering the commonly used office software operation and having certain written organization and coordination ability;

4. High sense of responsibility, good professional ethics, certain stress resistance, result-oriented, active learning and strong execution.

Job Description

(1) Analyzing the demand and supply of organizations, formulating recruitment plans, and providing high-quality talent supply for business development;

(2) Establishing internal and external recruitment channels, making overall use of internal and external human resources of the organization, and realizing the efficient allocation of organization personnel;

(3) Implementing recruitment, reserve talents inside and outside the organization, establishing a talent reserve mechanism, and providing efficient staffing for the business development of all business departments;

(4) Sorting out and optimizing the recruitment system and process;

(5) other tasks arranged

Job Requirements

(1) Having a college degree or above, and majoring in human resources, industrial and commercial management, psychology, biotechnology or bioengineering;

(2) Having more than 2 years of recruitment experience and practicing experience in the biomedical industry;

(3) Understanding the business process and norms of human resources, having certain professional skills and practical experience in recruitment, and having biomedical headhunters' work experience first;

(4) Be skilled in operating OFFICE software;

(5) High sense of responsibility, initiative and execution; self-driven working mode, strong willingness and ability to learn, and good communication and expression ability and teamwork spirit.

Job Description

1. be responsible for in vitro and in vivo efficacy, pharmacokinetics and toxicological tests of new anti-tumor drug application projects, including literature research, design and implementation of trial protocols, and analysis and evaluation of trial results;

2. Be responsible for connecting with the CRO institution carrying out the trial, timely and effectively communicating and solving the problems encountered in the trial design and trial, and ensuring the quality and progress of the trial;

3. Be responsible for writing preclinical pharmacological and toxicological application dossiers and cooperate in completing IND application.

Job Requirements

1. Master degree or above, pharmacology, toxicology, immunology, oncology and other related major; published articles with SCI of 6 points or more;

2. Be familiar with pharmacological and toxicological related experimental methods, and have experience in the construction and evaluation of in vitro and in vivo pharmacodynamic models of new drugs or the analysis of in vivo pharmacokinetic studies in animals;

3. Be familiar with common molecular biology experimental methods and principles, and be able to independently complete the experimental design and data analysis;

4. Be familiar with domestic and foreign regulations and guidelines related to preclinical pharmacological and toxicological studies and review and approval;

5. Have excellent English reading and writing ability and be skilled in searching and inquiring literatures;

6. Adapt to long business trips.

Job Description

1 Be responsible for training management, equipment management, validation and follow-up of plasmid workshop, virus workshop and cell workshop;

2 Issue production plan and inspection plan;

3 Be responsible for the inventory control of key materials, purchase statistics and purchase application of materials and materials within the department;

4 Be responsible for document management of three workshops, regularly filing relevant documents and records, and connecting with QA;

5 Follow up the sanitary cleaning and disinfection work of three workshops;

6 Follow up the progress of internal deviations and CAPA handling;

7. Be responsible for relevant internal notification and external coordination of the department;

8. other tasks arranged

Job Requirements

(1) Biotechnology, bioscience, bioengineering, pharmaceuticals and other related major, college degree or above; more than 1 year of relevant work experience;

(2) Being diligent and dedicated, having a strong sense of service and responsibility, having good communication ability and execution ability, and having a high sense of responsibility and teamwork spirit;

(3) Have certain GMP drug company related experience is preferred.

Job Description

1) Completes the analytical method development, optimization, training and transfer tasks of the project under the allocation of the analytical method development supervisor;

2) Supporting the corresponding process development project team and providing testing and analysis services;

3) According to the project requirements, summarize the analytical method development data and other data on a regular basis;

4) Carry out close technical exchange and cooperation with process developers or other technicians;

5) Completing the in-process control sample detection of the responsible project;

6) Carry out analytical method development according to ICH and pharmacopoeia requirements, and provide compliant and effective analytical data for IND/BLA-related applications;

7) Assisting in establishing and improving product quality

8) other tasks arranged 

Job Requirements

1) Bachelor degree or above, cell biology, immunology, molecular biology live drug analysis, biochemistry or biotechnology related major; related major graduate master 's degree is also acceptable;

2) More than 2 years of experience in the development of biopharmaceutical analytical methods, more than 1 year of experience in the development of cell and gene drug analytical methods or recent graduates of master 's degree in related major;

3) Having experience in developing a variety of analytical methods, and at least being very familiar with more than two professional directions such as physicochemical, molecular, and biochemical directions;

4) Having IND application experience for pharmaceutical products;

5) Understand ICH Q14 analytical method development and ICH Q2 analytical method validation;

6) Be skilled in using English for listening, speaking, reading and writing, and be familiar with literature consultation;

7) Confident optimism and eager to learn, love to study, have independent thinking ability, and have a high sense of responsibility.

Job Description

1. carry out material, on-site cleaning, instrument and equipment cleaning, buffer preparation, column loading of chromatographic column, balance and other production preparations according to the production plan and production instructions;

2. prefiltration, ultrafiltration concentration, chromatographic filtration of plasmids and viruses, cleaning of chromatographic columns, and dispensing of preparations according to process procedures, operating procedures, and batch records;

3. Strictly control various process parameters according to the production process, complete the production task with quality and quantity guarantee, timely feed back to the superior in case of deviation, and participate in the investigation and handling of deviation;

4. carry out cleaning and disinfection of clean workshops as required;

5. Timely fill in batch production records, equipment use records and cleaning and disinfection records;

6. participate in the drafting, preparation, revision and training of SMP and SOP;

7. Be responsible for the maintenance and repair of relevant equipment in the purification process;

8. Writing regular work summaries and reports.

Job Requirements

1. biotechnology, bioscience, bioengineering, pharmaceutical related major, college degree or above;

2. Have solid professional theoretical knowledge and be familiar with molecular sieve chromatography, ion chromatography, affinity chromatography and other process theoretical knowledge;

3. Be diligent and dedicated, have a strong sense of service and responsibility, have good communication ability and execution ability, and have a high sense of responsibility and teamwork spirit.

Job Description

1. According to the inventory, be responsible for the establishment of seed banks at three levels: seed bank, main bank and working bank;

2. carry out material, on-site cleaning, instrument and equipment cleaning, medium preparation, sterilization and other production preparations according to the production plan and production instructions;

3. Resuscitation, expansion culture, reactor fermentation culture, collection of viable bacteria and plasmid lysis of strains shall be carried out according to technological procedures, operating procedures and batch records;

4. Strictly control various process parameters according to the production process, complete the production task with quality and quantity guarantee, timely feed back to the superior in case of deviation, and participate in the investigation and handling of deviation;

5. Carry out cleaning and disinfection of clean workshops as required;

6. Timely fill in batch production records, equipment use records and cleaning and disinfection records;

7. Participating in the drafting, preparation, revision and training of SMP and SOP;

8. Being responsible for the maintenance and repair of relevant equipment in the fermentation process;

9. Writing regular work summaries and reports.

(5) Carrying out the cleaning and disinfection of clean workshops as required;

(6) Filling in batch production records, equipment use records and cleaning and disinfection records in a timely manner;

(7) Participating in the drafting, preparation, revision and training of SMPs and SOPs;

(8) Being responsible for the maintenance and repair of relevant equipment in the fermentation process;

9. Writing work summaries and reports on a regular basis.

Job Requirements

1. biotechnology, bioscience, bioengineering, fermentation engineering related major, college degree or above;

2. have solid professional theoretical knowledge and theoretical knowledge related to fermentation processes;

3. Be diligent and dedicated, have a strong sense of service and responsibility, have good communication ability and execution ability, and have a high sense of responsibility and teamwork spirit.

Job Description

1. Responsible for cell recovery, passage and banking experiments;

2. responsible for cell monoclonal construction experiments;

3. responsible for cell biological activity testing;

4. be responsible for the drafting and collation of data and reports;

Job Requirements

1. Bachelor degree or above, cell biology, medical immunology and other related major;

2. have more than 1 year of experience in cell culture laboratories;

3. Good communication ability, learning ability and certain literature retrieval ability are preferred.

4. Careful and practical, having rich sense of responsibility, and full enthusiasm for the work; good teamwork spirit, strong execution, and willingness to grow with the company.

Job Description

(1) Strictly implementing the regulatory requirements, be responsible for the sterility and endotoxin inspection of products in all items of the company;

(2) Being responsible for the sterility, endotoxin and relevant inspection of all materials of the company;

(3) Being responsible for the validation of sterility and endotoxin of all product projects (plasmids, lentiviruses & cell preparations) of the company and meeting the requirements for IND application;

(4) Establishing and optimizing the inspection methods for this post in accordance with the design scheme of the upper leaders.

(5)Writing work summaries and reports on a regular basis.

Job Requirements

1. Bachelor degree or above, microbiology related major;

2. Be familiar with GMP regulations, Chinese Pharmacopoeia, and have microbiome-related experience

3. Understand the correlation between microbial culture and Gram staining;

4. Be familiar with the sterility and microbiological examination in the Chinese Pharmacopoeia and aseptic operation.

5. Proficient in the use of relevant inspection instruments in molecular laboratories (such as bacteria collection instruments, rapid microbial detection systems, microbial identification systems, etc.)