太阳集团见好就收9728(中国)有限公司

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    Respect Talents

    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

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    About Us

    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

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    Registration Declaration

    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

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    2. Psychotropic Drugs
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    R & D field

    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

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    R&D Equipment

    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

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    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

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    External Information

    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

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    Contact Us

    VAYUAN focuses on drug synthesis, formulations, quality analysis, drug packaging compatibility research, microbiology, standard physical and chemical testing, drug registration and application, and other comprehensive drug development and drug clinical trial research.

MORE +Drug Analysis Researcher

    岗位职责

    In accordance with the requirements of IND and ANDA declarations, conduct analytical method development and verification, release and stability studies of standardized samples of reference substances;

    In accordance with the requirements of SOP and relevant regulations, carry out laboratory analysis work, participate in the maintenance of laboratory HPLC, GC and other analytical instruments and routine instrument troubleshooting, and propose corresponding solutions;

    Drafting and reviewing analytical method development reports, method verification plans and reports, stability plans and reports, and various test documents;

    Record, sort out and review the original data of the test to ensure the authenticity, reliability and completeness of the test results;

    According to the requirements of the project schedule, complete the work objectives regularly, and give feedback on the progress of the experiment in time;

    Obey the arrangement and complete the work designated by the person in charge of project analysis and the supervisor;

    Cooperate with the application team to complete the sorting and confirmation of drug R&D application materials and on-site verification of the application project;


    岗位要求

    Master degree or above, major in analytical chemistry, pharmacy and related fields;

    More than three years of experience in drug analysis and analytical method development and verification;

    Familiar with the basic principles of HPLC, GC and common physical and chemical detection methods and the routine operation and maintenance of the instrument;

    Familiar with the pharmacopoeia and ICH related guidelines, familiar with the analysis method development process and requirements of raw materials, intermediates, APIs and preparations;

    English level 4 or above, with the ability to search and read related English documents, and be able to write English experiment records and reports;

    Good health, honesty and dedication, and team spirit;

    Have IND or ANDA declaration, GLP/GMP laboratory related work experience is preferred.

    hr@vayuan.com 申请职位

MORE +QC Specialist

    岗位职责

    Responsible for chemical, physical and biological test analysis and review of raw materials, packaging materials, intermediates and finished products in accordance with standard operating procedures, and issue inspection reports;

    Responsible for the normal operation and use of test instruments and equipment, daily maintenance and simple repairs;

    Responsible for the preparation, storage and use of standards, standard solutions, control solutions, daily reagents, and indicators;

    Provide test data for product process verification and verification, equipment verification, and cleaning verification;

    Responsible for testing and analyzing the stability inspection samples;

    Verify and confirm inspection methods and inspection equipment.


    岗位要求

    Bachelor degree or above, graduated in chemical analysis, pharmaceutical analysis, organic chemistry or related majors, 2 to 3 years working experience in analytical work;

    GMP experience in QC laboratory is preferred;

    Proficiency in the use of HPLC, GC and other conventional chromatographic or physical and chemical analysis instruments, and simple maintenance;

    Good communication skills;

    Good teamwork ability.

    hr@vayuan.com 申请职位

MORE +Director of Pharmaceutical Preparations

    岗位职责

    Responsible for the daily management of the department and establish an efficient team;

    Undertake and support the management of the company's preparation project;

    Responsible for the literature research of the preparation project, the formulation, implementation, and evaluation of the process research plan;

    Cooperate with the application team to complete the registration of drug R&D application materials;


    岗位要求

    Master's degree or above, pharmacy, pharmaceutical preparations and related majors, more than five years of R&D and management experience in related professional fields in pharmaceutical companies or global R&D companies;

    Familiar with the relevant requirements of FDA/CFDA, understand EMEA and CFDA regulations, guidelines, GMP and drug product development process;

    Have the ability to analyze and solve problems, and have strong leadership and management skills;

    Have a high sense of responsibility for work, be able to withstand greater work pressure, have good communication, coordination and team management skills;

    hr@vayuan.com 申请职位

MORE +Formulation Researcher

    岗位职责

    Responsible for literature research, prescription screening, process optimization and amplification of preparation projects;

    Responsible for the formulation, implementation, and evaluation of preparation process research plans (prescription formulation screening, preparation process optimization, packaging design, transportation conditions, preparation stability investigation and other new drug preparation related research);

    Conduct formulation research and development in accordance with domestic and international quality requirements and GMP requirements;

    Standardize research in accordance with the requirements, prepare relevant original records, organize, compile and file data, and write research reports and review application materials related to preparation process research;

    Responsible for the use and maintenance of related test equipment.


    岗位要求

    Master's degree or above, major in pharmacy, pharmacy, pharmaceutical engineering, chemistry, drug analysis, etc.;

    More than 3 years of pharmaceutical R&D work experience, proficient in the research technology and skills of a variety of dosage forms, with pharmaceutical company engaged in related R&D work experience is preferred;

    Be proficient in operating and maintaining preparation equipment;

    Understand GMP and drug production registration related regulations; experience in new drug application and development and familiar with ICH regulations is preferred;

    Have a high sense of responsibility and teamwork, good communication skills and work execution.

    hr@vayuan.com 申请职位

MORE +Head of Pharmaceutical Chemistry R&D

    岗位职责

    Responsible for project operation and team management, including supervising the progress of each project and solving technical difficulties;

    Coordination of resources and feasibility assessment of project requirements put forward by customers;

    Solve various problems encountered during project implementation;

    Independently complete literature review and map analysis, and complete compound synthesis route design based on literature;

    Cooperate with the application team to complete the registration of drug R&D application materials;



    岗位要求

    Master's degree or above, organic chemistry, medicinal chemistry and other related majors, at least five years of work experience in the pharmaceutical industry, three years of management work experience in the pharmaceutical industry, overseas study experience in Europe or the United States or management experience in multinational biopharmaceutical or large CRO industry is preferred;

    Have excellent R&D and project management capabilities, able to solve problems encountered in the process of project management and R&D;

    Have the ability to analyze and solve problems, and have strong communication, leadership and management skills, and excellent professionalism and teamwork spirit;

    Experience in Chinese medicine research and development is preferred;

    Fluent in listening, speaking, reading and writing in Chinese and English;

    hr@vayuan.com 申请职位

MORE +Organic Synthesis Researcher

    岗位职责

    Independently complete the literature review and map analysis, and complete the preliminary design of the compound synthesis route based on the literature;

    Complete chemical reactions proficiently, make a more comprehensive analysis of the results, and complete research projects independently;

    Compile and organize experiment records, and complete experiment reports;

    Complete the writing of relevant materials for drug application materials;

    Solve the problems in the experiment, sort out and summarize the project in time;

    Complete experimental data and experimental report clearly and completely;


    岗位要求

    Master's degree or above, organic chemistry or medicinal chemistry and related majors, more than two years of work experience in chemical synthesis, familiar with organic synthesis unit operations, and have strong analytical and problem-solving capabilities;

    Experience in Chinese medicine research and development is preferred;

    Good Chinese and English listening, speaking, reading and writing skills;

    Have a high sense of responsibility and good communication skills, strong learning ability, rigorous and serious working attitude and good teamwork spirit;

    hr@vayuan.com 申请职位

MORE +Process Researcher

    岗位职责

    Independently complete literature review and map analysis, and complete the preliminary design of the compound and API synthesis route;

    According to different project requirements, optimize the synthesis process parameters, and make a more comprehensive analysis of the results, and work with the department head to complete the drug quality research work, including impurity synthesis, separation and identification;

    Solve the problems in the experiment, be able to foresee the problems that may occur in the production scale-up process, and propose corresponding solutions;

    Refer to the corresponding laws and regulations and guidance documents, complete the experiment, data, and materials, and carry out the process transfer;

    Complete experimental records clearly and completely, and initially compile project progress reports, project summary reports and API declaration related materials;

    Work closely with production personnel, quality assurance department, and quality control department to complete the process optimization and transfer of the project;

    Responsible for the daily maintenance of laboratory equipment and facilities.


    岗位要求

    Master's degree or above, major in organic chemistry, medicinal chemistry, pharmaceutical engineering, applied chemistry, chemical engineering, fine chemical engineering and related majors; more than two years of process research and development experience;

    Ability and enthusiasm to learn new chemistry, and the ability to independently operate experimental equipment;

    Experience in Chinese medicine research and development is preferred;

    Possess certain scientific research capabilities;

    Have the ability to find corresponding scientific literature;

    Experience in GMP is preferred;

    hr@vayuan.com 申请职位

MORE +Head of Drug Analysis

    岗位职责

    Lead and manage the analysis team, guide the completion of product research and development project analysis, the formulation of project plans, and personnel arrangements;

    Supervise the execution of the plan of the analysis team, and solve the difficulties and various problems encountered by the analysis team in the drug analysis work;

    Write SOP and lead the team to strictly follow SOP implementation;

    Review the analysis method development report, method verification plan and report, stability plan and report;

    Cooperate with the application team to complete the registration of drug application materials;


    岗位要求

    Master's degree or above, major in chemistry, applied chemistry, pharmaceutical analysis and related fields, more than five years of work experience in chemical drug quality research and application, and rich experience in analytical method development;

    Be able to independently formulate experimental plans for quality research and stability research, carry out quality research and stability research on new drugs and generic drugs, and be competent in writing and modifying CTD documents for new drug applications;

    Have a high sense of responsibility for work, be able to withstand greater work pressure, have good communication, coordination and team management skills;


    hr@vayuan.com 申请职位

Qingdao Vayuan Pharmaceutical Technology Ltd.

电话:0532-55678600

邮箱:ad@vayuan.com

传真:0532-55678586

地址:11th Floor, No.377 Nanjing Rd. Qingdao City, Shandong Province, China

时间:周一至周五 8:30~12:00;13:00~17:30

公司电话

+86-0532-55678600

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