Job Responsibilities:

1、 Conducted feasibility analysis and advanced analysis of preparation technology for the proposed project, and put forward proposals and opinions for the project.

2、Guided and supervised the formulation and implementation of project preparation research and development plan; Regularly check the authenticity, integrity and compliance of the research work, and carry out acceptance inspection on key R&D nodes; Responsible for preparation process development and production amplification; Responsible for the examination of registration and application materials; Be responsible for the inspection of development site and production site.

3、Periodically conduct risk assessment of the project according to the latest drug development laws and regulations of FDA, ICH and CFDA.

4、Formulated and improved relevant systems such as team management and product development life cycle management, and supervised their implementation.

5、Conducted training for employees on technology, regulations, document writing and other related contents, and formulated annual training plan and incentive plan for employees.

6、Analysis of domestic and foreign drug research and development trend; Collect pharmaceutical industry information, market information, research and development institutions information, and continue to follow up;

7、Completed other tasks assigned by leaders.

Ability Requirements:

1、Master degree or above in pharmaceutical preparation, pharmaceutical engineering or related major;

2、Have strong experience in preparation process development, production amplification, registration and declaration.

3、Doctor 1 year, Master 4 or above working experience in related functional or professional field.

Qualifications:

Salary: negotiable, excellent candidates can be negotiable.

Job Responsibilities:

1、Sorted out pharmaceutical materials and wrote clinical review materials.

2、Organized and supervised the group's self-examination before the current examination; Responsible for the comprehensive filing and submission of declaration materials.

3、Supervise cooperative R&D enterprises and group production enterprises to complete research and development and on-site production assessment.

4、Follow up the drug test report of the drug control bureau.

5、Check the completed work content with the Commissioned Party monthly according to the plan, and check the integrity and accuracy of the original records and data.

6、Periodically review and summarize newly approved listed drugs in China, Europe, Japan and the United States;

7、Wrote pharmacology and toxicology, clinical review materials, and reviewed the application materials;

Ability Requirements:

1.Bachelor degree or above, majored in Chemistry, Pharmacy, Biology, etc., with more than 5 years of working experience.

2.Familiar with the registration regulations of chemical drugs or biological products. Participated in the application of generic drugs or successful application of chemical drugs 3 categories, 4 categories of product registration experience. Experience in pharmaceutical or biological product development or quality research is preferred.

3.Skilled use of common office software, good literature retrieval ability.

4.Good communication skills, organization and coordination ability, and self-learning ability.

5.Fluent in English, reading and writing.

Qualifications:

Salary: negotiable, excellent candidates can be negotiable.

Job Responsibilities:

1、Manage the progress and quality of clinical projects, connect and coordinate with CRO clinical operation department;

2、Make specific plans for personnel, progress, funds, quality, data and other aspects of the project implementation;

3、Responsible for communicating with project implementation personnel (CRA, CRC, researchers, etc.) before and during the implementation;

4、Follow up and monitor the work progress and quality of related CRA or CRC;

5、Familiar with the storage, transportation and registration of experimental drugs;

6、Participate in the progress and communication of ethics submission, first research meeting, launch meeting, etc.;

7、Responsible for the organization and implementation of the late project and various works delivered by the bidder;

8、Made training courseware and provided necessary training to new employees.

Ability Requirements:

1、Bachelor degree or above in medicine, pharmacy or clinical related major;

2、More than 2 years of clinical research and medical support experience in multiple projects;

3、Familiar with drug registration management, GCP regulations and related regulations of clinical research;的相关法规;

4、Calm personality, careful, independent, team spirit, strong sense of responsibility, strong ability to work under pressure, can adapt to business trip.

Qualifications:

Salary: negotiable, excellent candidates can be negotiable.

Job Responsibilities:

1、Communicated with CRO company and communicated with the medical department of CRO company;

2、Responsible for archiving, proofreading and checking the company's technical documents;

3、Assist in clinical research program and manage experts;

4、Manage and improve the data and reports of clinical research projects in my charge.

5、Provide medical and pharmaceutical background knowledge of related products;

6、Responsible for related medical support, including PPT making of relevant medical knowledge;

7、Dealing with medical problems encountered in clinical research and timely reporting to leaders;

8、Trained the basic medical knowledge of the sales team and answered medical questions;

Ability Requirements:

1、Master degree or above in Medicine, Pharmacy or Biology;

2、Familiar with drug registration management, GCP regulations and related regulations of clinical research;

3、More than 1 year working experience in clinical CRO company is preferred;

4、Have experience in writing clinical trial program and BE program, and have strong ability in English literature review and reading;

5、Strong communication skills and ability to work under pressure.

Qualifications:

Salary: negotiable, excellent candidates can be negotiable.

Job Responsibilities:

Ability Requirements:

1、Master degree or above, major in pharmaceutical analysis, analytical chemistry or related;

2、Experience in analytical method development, pharmaceutical quality research, registration and application;

3、Ability of project management;

4、Skilled in written English translation and oral expression;

5、Active learning ability;

6、Good ability to work under pressure, travel on business from time to time and work overtime to a certain extent. Qualifications:

Qualifications:

Salary: 18,000-30,000 RMB/month, excellent candidates can be negotiated.

Job Responsibilities:

1.Improve the group's daily tax management workflow;

2.Responsible for the filing management of the group's tax work, assisting in the annual audit and the final settlement of annual income tax;

3.Regularly collect and sort out relevant fiscal and tax policies, analyze their impact on business and use them for business guidance;

4. Intra-group tax-related consultation and organizing related tax training;

5.Tracked and analyzed the completion of tax-related matters of companies in various sectors of the Group;

6.Due diligence tax adjustment for investment

7.Assisted in formulating and improving the tax management regulations of the Group, assisted in completing tax planning, coordinated the relationship between tax enterprises,

8.Complete other work of tax department.

Ability Requirements:

1. Bachelor degree or above, majored in finance or economics. Certificate of CPA or CPA is preferred;

2. At least 3 years working experience in taxation, familiar with relevant laws and regulations of finance and taxation, tax office experience is preferred;

3. Have strong communication and coordination ability, learning ability, good team work ability, can work under great pressure.

4. Proficient in financial software and office software;

Qualifications:

Salary: negotiable, excellent candidates can be negotiable.

Job Responsibilities:

1.Responsible for data collection, collation and analysis of the industry background, competitive environment, laws and regulations of the pharmaceutical and big health industries, digging deep into information, and observing the changes of the external environment;

2.Assisted in studying the development strategy and management mode of benchmarking enterprises, and summarized the experience with reference significance;

3.Conducted research and evaluation on the core competence and internal resource capability of each enterprise of the Group;

4.Implement project management, formulate project plans, organize and coordinate related resources, mobilize and lead team members, promote the implementation of project plans, and ensure and control the project outputs;

5.On the basis of the above work, assist in formulating the strategic development direction and business development model of the Group, and innovate and design the business model of emerging businesses;

6.Participate in the strategic management of the company, assist other functional departments to complete the organizational structure design, business process sorting, human resources system construction, etc., participate in the construction of management system suitable for the company and assist in the establishment of relevant systems and processes;

7.Conducted targeted research on relevant research topics and formed research reports to provide support for management decision-making.

Ability Requirements:

1.Excellent data analysis skills, text synthesis and expression skills, and report writing skills;

2.Extremely strong drive, active in trying, bold innovation, willing to contribute to the organization to open up a new situation, take responsibility;

3.Prospective thinking, keen perception and insight, excellent logical thinking ability, analytical and judgment ability, research ability and continuous learning ability;

4.Good communication and coordination skills, high interpersonal acuity.

Qualifications:

1、Have one of the following relevant work experience:

- Consulting experience in well-known management consulting companies;

- Senior management experience in pharmaceutical or consumer products industry;

- Experience in consulting companies or large enterprises, financial institutions related industry research;

- Experience in strategic planning and management consulting

2、Others：

- Education requirement: Bachelor's degree or above in medicine or management, master's degree preferred;

- Language requirement: English proficiency;

- Age requirement: 28-45;

- Years of working: More than 5 years

Salary: 20-25K, excellent candidates can be negotiated.

Job Responsibilities:

1、Implement national labor and personnel policies and regulations, be familiar with the six personnel modules, and be responsible for the management of the company's personnel system based on the company's production and operation scale and development needs;

2、Responsible for handling the social security of the company's employees, increasing or decreasing the number of employees, and consulting and answering the social security of the employees;

3、Responsible for employee salary accounting, payroll preparation and reporting;

Ability Requirements:

1、Education: Bachelor degree or above;

2、Major: Human Resource Management, Management and other related majors;

3、Qualifications and experience: related personnel work experience, with the drug company human resources work experience is preferred;

4、Essential professional skills: familiar with policies and procedures related to Harbin social security work, proficient in using office software, Excel spreadsheet making, good language expression ability, strong executive power;

5、Professional ethics: responsible, adhere to the principle, to the interests of the company.

6、Living in Harbin bungalow area is preferred

Qualifications:

Salary: 4.5-6 thousand/month, excellent candidates can be negotiated.

岗位职责：

Ability Requirements:

Qualifications:

Salary: negotiable, excellent candidates can be negotiable