Job Requirements 

1. Master degree or above; 

2. more than 3 years of experience in research reagents, sales or marketing management;

3. good organisation, planning, control and coordination skills, good interpersonal skills, strong communication and management skills;

4. Familiar with the current situation of life science products at home and abroad, understand the main customers and distributors demand information; 

5. strong sense of responsibility, able to withstand intense work pressure and travelling, with teamwork spirit; 


Job responsibilities 

1. be responsible for the market development and promotion of the company's reagents and other products in the field of life sciences; 

2. Responsible for the management of the national agents of the relevant products, market channel development, etc.; 

3. specialising in brand households and agents, dealers customer development and promotion; 

4. to develop and improve the company's overall product marketing strategy, implementation of the programme, to assist in completing the product marketing planning in the development of relevant organizations and institutions, liaison, coordination, etc.; 

5. assist in market research, coordination of the company's new product development and the original product improvement; 

6. other work assigned by the superior;

Work location: Shanghai
Please submit your CV to: wangxx@hillgene.com

Job Responsibilities

1. be responsible for the management of clinical trial projects, carry out comprehensive quality control and progress management, and ensure that the clinical trial projects are carried out in strict accordance with GCP, SOP, trial protocols and relevant laws and regulations;

2. formulate management plans in line with project requirements, assist in the completion of the progress plan of each centre, and promote the comprehensive initiation, execution and completion of clinical research projects in accordance with the plan; and 

3. be responsible for the daily management of the clinical research project, and hold regular project progress and communication meetings.

4. Maintain timely and effective communication with PIs to ensure accurate and complete delivery of project-related information, and cultivate and maintain a good working relationship with investigators (research centres).

5. Responsible for organisational development, formulation of project management rules and SOPs, and regular training for project team CRAs and related personnel.

6. Responsible for other tasks assigned by supervisor;


Qualifications

1. Bachelor degree or above in clinical, pharmacy, biology or other related majors, with English as working language;

2. more than 5 years of drug clinical research work experience (with CRC, CRA work experience), more than 3 years of clinical project management experience.

3. working experience in large-scale well-known CRO companies is preferred, and independent working experience in clinical phase I, II, III projects and experience in cooperating with on-site verification is preferred.

4. Familiar with clinical research in the field of oncology and autoimmune diseases is preferred.

5. Comprehensive knowledge of ICH, GCP, technical guidelines for clinical research and relevant laws and regulations on drug management.

6. Project Management Professional certification (PMP certificate) or training experience is preferred.

7. Strong sense of responsibility, good teamwork, good communication and coordination skills.

Work location: Suzhou
Please submit your CV to: wangxx@hillgene.com

Job responsibilities 

1. be responsible for drafting and revising the relevant test protocols, test records, equipment operation procedures and other documents of the immunoassay group, to ensure that the testing activities of the biochemical group are within the control range; 

2. responsible for the development, optimisation and confirmation of immunoassay methods; 

3. be responsible for drafting the confirmation and validation plan for immunoassay methods involved in the process of technology transfer within the company, and execute the confirmation/validation of analytical methods in accordance with the approved confirmation/validation plan for analytical methods, and write the confirmation/validation report to regulate the testing operation of technology transfer; 

4. Test, record and collate raw data of R&D samples, stock solutions, intermediate products, finished products, stability study samples, cell bank samples, materials, etc. in accordance with relevant protocols to ensure data integrity and traceability; 

5. Responsible for the installation and commissioning confirmation of immunoassay related instruments and equipment; 

6. be responsible for the routine maintenance of immunoassay-related instruments and the implementation of validation plans; 

7. be responsible for the inventory management of immunoassay group materials to ensure the continuous operation of the group. 


Qualifications 

1. Full-time undergraduate degree, postgraduate degree is preferred. 2. at least 5 years of experience in biotechnology in a pharmaceutical company; 

2. at least 5 years of experience in biopharmaceutical analysis in a pharmaceutical company; 

3. good language skills, teamwork ability; 

4. experience in the development and validation of immuno-related analytical methods; 

5. positive and enthusiastic about work; 

6. have the ability to resist pressure; 

7. good GMP awareness, experience in new drug submission and official site audits is a plus.


Work location: Suzhou
Please submit your CV to: wangxx@hillgene.com

Job responsibilities 

1. be responsible for drafting and revising the relevant test protocols, test records, equipment operation procedures and other documents of the cell group, to ensure that the testing activities of the biochemical group are within the controlled scope; 

2. be responsible for the development, optimisation and validation of cell-based assays; 

3. be responsible for the drafting of analytical method validation and verification plan for the internal technology transfer process, and execute analytical method validation/verification according to the approved analytical method validation/verification plan, and write validation/verification report to standardise the testing operation of technology transfer; 

4. Test, record and organise raw data of R&D samples, stock solutions, intermediate products, finished products, stability samples, cell bank samples, materials, etc. in accordance with relevant protocols, to ensure the integrity and traceability of the data; 

5. Responsible for the installation and debugging confirmation of cell testing related instruments and equipment; 

6. be responsible for the daily maintenance and repair of cellular testing instruments and the implementation of the validation plan; 

7. be responsible for the inventory management of materials in the cellular testing group to ensure the continuous operation of the group; 

8. be responsible for the management of cell bank for testing, cell resuscitation, passaging and freezing; 

9. Other duties as assigned by the supervisor. 


Job Requirements 

1. Full-time undergraduate degree, postgraduate degree is preferred; 

2. at least 5 years of experience in biopharmaceutical analysis in a pharmaceutical company; 

3. good language skills, teamwork ability; 

4. Positive and enthusiastic about work; 5. Ability to resist pressure; 

6. good GMP awareness, experience in new drug reporting and official site audits is a plus.


Work location: Suzhou
Please submit your CV to: wangxx@hillgene.com

Job responsibilities 

1. be responsible for drafting and revising relevant test protocols, test records, equipment operation procedures and other documents of the molecular group to ensure that the testing activities of the biochemical group are under control; 

2. be responsible for the development, optimisation and validation of molecular testing methods; 

3. be responsible for the drafting of analytical method confirmation and validation plan for internal technology transfer, and execute the confirmation/validation of analytical methods according to the approved analytical method confirmation/validation plan, and write confirmation/validation reports to standardise the testing operation of technology transfer; 

4. Test, record and organise raw data of R&D samples, stock solutions, intermediate products, finished products, stability samples, cell bank samples, materials, etc. in accordance with relevant protocols, to ensure the integrity and traceability of the data; 

5. Responsible for the installation and debugging confirmation of molecular testing related instruments and equipments; 

6. responsible for the routine maintenance of molecular testing instruments and the implementation of validation plans; 

7. Responsible for the inventory management of molecular testing materials to ensure the continuous operation of the group; 

8. Other duties as assigned by the supervisor.


Job Requirements 

1. Full-time undergraduate degree, graduate degree is preferred; 

2. at least 5 years of experience in biopharmaceutical analysis in a pharmaceutical company; 

3. good language skills, teamwork ability; 

4. Positive and enthusiastic about work; 

5. able to withstand a certain degree of pressure, good resistance to pressure; 

6. good GMP awareness, experience in new drug submission and official site audit is an advantage.


Work location: Suzhou
Please submit your CV to: wangxx@hillgene.com