Job Responsibilities
1. Design toxicological tests, write test protocols and test reports, analyze and interpret test results, etc., take overall responsibility for the operation and management of toxicological tests and the content of the summary report;

2. Supervise the test process, including in life, biological analysis, clinical pathology and pathology and other test processes;

3. Familiar with NMPA, ICH, OECD guidelines, familiar with NMPA, US FDA, OECD GLP regulations, to ensure that the toxicology research undertaken is designed and implemented in accordance with sound scientific, ethical and appropriate GLP standards;

4. Communicate with customers in a timely manner, including experimental program design, reporting experimental progress, etc.;

5. Solve the problems encountered during the experiment and ensure that customers and leaders have a comprehensive understanding of the progress of the experiment.

Job Responsibilities

1. Assist the subject leader (SD) to participate in the management and coordination of the project, including preparing the experimental plan and the draft of the experimental report, tracking the progress of the trial and reporting to the subject supervisor in a timely manner, etc.

2. Familiar with NMPA, ICH, OECD guidelines, familiar with NMPA, US FDA, OECD GLP regulations, to ensure that the toxicology research undertaken is designed and implemented in accordance with sound scientific, ethical and appropriate GLP standards.

3. Communicate with customers in a timely manner, including experimental program design, reporting experimental progress, etc.;

4. Implement competent experimental technical operations after assessment, and participate in technical operations such as drug administration and dissection if necessary.

Those with good performance can apply for the post of thematic leader.

 

Job Requirements

1. Bachelor degree or above in pharmacy, pharmacology, toxicology, clinical medicine and other related majors;

2. Passed CET 4;

3. Ability to withstand pressure;

4. Have a strong team spirit and a strong sense of responsibility; have strong learning and problem-solving skills;

5. Those with GLP work experience are preferred;

For fresh graduates or those with no relevant experience, professional training will be conducted after entering the company.

Job Responsibilities

1. Master (or be able to master through training) the operation of various experimental animals such as rats, rabbits, beagle dogs and monkeys (such as drug administration, observation, weighing, blood collection, etc.);

Make experimental records in accordance with GLP specifications and relevant SOP requirements;

2. Do a good job in the sorting and temporary storage of experimental data.

 

Job Requirements

1. Have a professional background in animal medicine, veterinary medicine, laboratory zoology, animal science, etc.;

2. Those with more than 1 year working experience in laboratory animal center;

3. Familiar with the basic operation of large and mouse experimental animals;

4. Possess certain English ability, can read relevant literature independently, and collect and organize relevant information;

Has a strong sense of responsibility, is serious and responsible for work, and can bear hardships and stand hard work.

Job Responsibilities

1. Responsible for the implementation of DMPK-related biological analysis projects, skilled use of LC-MS/MS instruments, including biological samples under various biological matrices (plasma, urine, feces, heart, liver, kidney, lung, intestine, etc.) Quantitative method development, establishment, validation and sample testing; 

2. Ability to use high-resolution mass spectrometry (LC-TOF MS) bioanalytical technology for structural identification of metabolites of specific compounds;

3. Ability to identify drug metabolites from liver microsomes, hepatocytes, plasma, urine, bile and tissue; 

4. Have a deeper understanding of DMPK and solid practical experience, can solve the problems encountered to a certain extent and ensure the smooth progress of the project; 

5. Review data quality to ensure reliable data quality and compliance with relevant systems for bioanalysis compliance; write experimental reports and explain research results; 

6. Write, maintain and upgrade SOPs, and carry out bioanalytical testing in strict accordance with SOPs;

Responsible for instrument maintenance, especially routine maintenance and troubleshooting of LC/MS/MS and LC-TOF MS;

 

Job Requirements

1. Major in biology, pharmacokinetics or drug analysis;

2. Serious and responsible work, positive attitude, good at communication, good teamwork spirit; strong learning and problem-solving ability;

Good literature retrieval skills, English reading and writing skills, oral and written expression skills.

Job Responsibilities

1. In vitro ADME assays (such as liver microsomal metabolic stability, CYP enzymatic inhibition and induction, CYP phenotype confirmation, plasma protein binding    permeability, etc.), generating samples, processing data, writing reports, filing materials, etc.;

2. Review the data quality, in line with the company's relevant systems; write experimental reports in a timely, true and accurate manner, and explain the research results;

3. It is necessary to communicate with test analysts and laboratory support personnel in a timely manner to efficiently complete the project to ensure the quantity, quality and delivery time of the work. and comply with relevant regulations and requirements;

4. Write, maintain and upgrade SOPs, and carry out in vitro ADME experiments in strict accordance with SOPs;
5. Comply with the company's rules and regulations, and obey other work arranged by the superior.

 

Job Requirements

1. Major in pharmacy, bachelor degree or above; relevant work experience is preferred;

2. Familiar with the preclinical research and development process of drugs; directly engaged in relevant work experience in ADME; working experience in pharmaceutical companies is preferred;

3. Able to independently design, complete and analyze ADME experiments; be able to write relevant professional reports, with good English;

Team spirit, serious and responsible work, positive attitude, good at communication, strong learning and problem-solving ability.

Job Responsibilities

1. According to the relevant guiding principles and scientificity, conduct experimental program writing, experimental schedule arrangement, resource allocation, data and experimental report approval;

2. Take overall responsibility for the scientific, technical and regulatory compliance of the project in charge, directly communicate with the contact person of the entrusting party, report the progress of the experiment to the entrusting party on a regular basis, and ensure that the customer is aware of the progress of the project and the problems that arise;

3. Ensure that the project is completed on time and in compliance with applicable regulations;

4. Provide countermeasures to solve the technical and regulatory compliance problems encountered during the experiment, and record the problems and solutions in detail and the impact on the experiment;

5. Supervise and track the progress of the entire experiment, and provide solutions to problems. Examine various laboratory records to ensure they are timely, direct, clear and accurate;

6. Ensure that the staff involved in the research are clear about the work they undertake and are familiar with the corresponding standard operating procedures;

7. Review and approve the analytical data according to the experimental protocol and SOP, and accept the standard curve, quality control, test samples and chromatograms;

8. Respond to the problems in the QC inspection in time, and take relevant measures to deal with common problems;

9. At the end of the experiment, archive the experimental plan, original data, specimens to be preserved, various related record documents and summary reports;

Cooperate with the commissioning party and the regulatory agency to verify the experiment.

 

Job Requirements

1. Pharmaceutical analysis/pharmacy/pharmacokinetics and other related majors, master's degree or above, two years of work experience;

2. The DMPK knowledge structure is complete and can continuously update the knowledge structure to adapt to the development of the industry;

3. Understand various guiding principles related to the DMPK industry;

4. College English CET 6 and above or equivalent, able to read foreign literature proficiently;

5. Good interpersonal communication skills, strong execution;

6. Good pressure bearing capacity.

Job Responsibilities

1. Independently carry out DMPK research, responsible for DMPK trial design, trial development, data interpretation, report writing, etc.;

2. Guarantee the quality of the DMPK project and ensure the authenticity and scientificity of the test results;

3. Assist the DMPK supervisor in the overall management of DMPK projects, including IND application projects and early screening projects;

4. Assist DMPK in charge of building and maintaining the quality system and project operation process within the department;

5. Assist the DMPK supervisor to build and maintain the relevant test platforms in and out of the department;

6. Assist DMPK supervisor in personnel recruitment and personnel training;

7. Responsible for communication with other department heads or related personnel to promote the smooth progress of the project;

8. Responsible for regularly reporting project progress to the entrusting party, and communicating with the entrusting party in a timely manner when encountering project problems.

 

Job Requirements

1. Doctorate degree; or master degree, more than 2 years of work experience; or bachelor degree, more than 5 years of work experience;

2. Majors in pharmacokinetics, pharmacology, drug analysis, analysis, etc.;

3. Have in-depth understanding and solid practical experience of DMPK;

4. Able to use and maintain LC-MS/MS systems, including method development and instrument troubleshooting;

5. Proficiency in the use of pharmacokinetic calculation software, such as Winnonlin, etc.;

6. Strong communication skills, calm, patient in work, and team management experience;

7. Have good English reading and writing skills.

Job Responsibilities

1. Participate in the gross autopsy of routine experimental animals for the evaluation of various preclinical new drugs. The specific operations include in vivo multi-system tissue/organ extraction, weighing, fixation, and macroscopic morphological observation and evaluation. The species of experimental animals mainly include non-human primates, dogs, rats, mice, rabbits, etc.;

2. Preparation of various fixatives involved in dissection and related operations and replacement of reagents after the test. Trimming and collecting various animal tissues/organs according to experimental requirements or regulations;

3. With the help of instruments and a variety of equipment to complete the routine production of animal tissues/organs, such as dehydration, wax dipping, embedding, tissue thin sectioning, HE staining and resin sealing;

4. Familiar with the use and simple maintenance of multiple instruments in the production process, including dehydrators, dyeing machines, etc., and be proficient in conventional experimental instruments such as electronic scales, electronic balances, mixers, etc.;

Collect fresh tissue for rapid freezing and make thin sections of frozen tissue, and participate in various immunohistochemical experiments and cross-reaction of various genera in the later stage.

 

Job Requirements

1. College degree or above in biology, veterinary medicine, medicine, pharmacy, etc.;

2. Understand the anatomical structure and physiological functions of different animals;

3. Have strong experimental and practical ability.

Job Responsibilities

1. Familiar with and follow GLP principles;

2. Receive and analyze biological samples in accordance with thematic protocols and method documents;

3. Proficient in operating analytical instruments, and timely and faithfully recording the records required for the analytical process;

4. Able to independently complete daily sample analysis work and manage the reagents required for related analysis work;

Participate in the work of developing and validating new detection methods, and the work is serious, responsible and meticulous.

 

Job Requirements

1. College degree or above, major in medical laboratory;

2. Be able to use automatic biochemical analyzers, blood cell analyzers, blood coagulation analyzers and other analytical instruments;

3. Be able to use Word, Excel, Powerpoint and other computer software;

4. Have good communication skills;

5. Have good professionalism and teamwork spirit.

Job Responsibilities

1. Review of the experimental protocol: Participate in the formulation and review of pathology in the preclinical toxicology experimental protocol of new drugs, provide opinions and suggestions from a professional perspective, and ensure that the methods used in the pathological part of the experimental protocol are scientific and correct. Provide professional advice as much as possible in other areas of the experimental protocol;

2. Anatomy supervision: Responsible for the quality of the anatomy, ensure that the anatomy process meets the requirements of the experimental program and follow the relevant experimental operating procedures, and report any special emergencies in the anatomy process to the person in charge of the experimental subject and make corresponding processing and records;

3. Histological diagnosis: record and interpret the pathological changes in the readings. At the same time, it is necessary to ensure that the organs required by the test plan have been prepared and the consistency of the sampling site and the consistency of staining; the standard of diagnostic terms used is unified, and the degree of diagnostic grading is consistent;

4. Pathology report writing: After the reading, the pathology subject leader is responsible for writing the pathology report according to the corresponding SOPs or completing the pathology part of the general report, and describing the changes related to drug treatment and other important findings in the report, and giving corresponding Possible explanations and connections to other data, such as clinical data, are stated in the discussion. Also ensure that the report is accurate and fully reflects the original results;

5. Quality control: No matter what method is used for recording, such as electronic data acquisition system, paper documents, etc., it is necessary to ensure the integrity and accuracy of experimental data and that the experimental protocol and corresponding SOPs in the experimental process are followed. Perform quality checks after forms and reports are generated and before filing and QA review;

During the whole experiment, maintain good communication with the person in charge of the experiment, and report any situation in the experiment to him in time. Any comments and questions from the test quality assurance department will be answered and resolved as soon as possible.

 

Job Requirements

1. Master's degree or above in pathology, comparative tissue and anatomy of experimental animals, hematology, physiology and medicine, biology, veterinary medicine, experimental design, statistical analysis, etc.;

2. Deeply understand the principles and requirements of GLP in toxic pathology, and possess the core skills and knowledge required for the position;

3. Familiar with pathological auxiliary diagnosis techniques and methods, such as light microscopy, electron microscopy, special staining and immunohistochemistry;

4. Familiar with clinical detection indicators and the biological significance of each indicator, cytology, hematology and their possible connections with some pathological phenomena;

5. Basic familiarity with laser confocal, fluorescence microscopy, morphometric techniques and some modern molecular biology techniques, such as in situ hybridization, laser capture microdissection;

6. Understand the basic knowledge of pharmacokinetics, toxicokinetics and genomics, proteomics, metabolomics, etc.

Familiar with the basic principles and requirements of animal welfare.

Job Responsibilities

1. Responsible for the prevention, identification, diagnosis, treatment and treatment of diseases in laboratory animals;

2. Responsible for the reception and quarantine of experimental animals;

3. Responsible for laboratory animal surgery and postoperative care;

4. Participate in the management of the operation of experimental animal facilities;

5. Responsible for the welfare management of experimental animals.

 

Job Requirements

1. Bachelor or master degree in animal medicine, animal husbandry and veterinary related majors;

2. Those with a practicing veterinary qualification are preferred;

3. Able to read English literature fluently;

4. Be sincere, positive, good at communication, have a good sense of teamwork; work rigorously, seriously, with a strong sense of responsibility and professionalism.

Job Responsibilities

1. The methods of grasping and administration of various animals, such as gavage, blood collection, tail vein injection, etc., biological sample collection, dissection, etc.;

2. Experience in the culture of primary cells and tumor cells, including cell recovery, culture, cryopreservation, primary isolation and culture, drug efficacy evaluation, etc.;

3. Timely, accurate and clear experimental observation records; have the ability to collect and analyze experimental data, understand the principles of statistical analysis and related software applications.

 

Job Requirements

1. Biomedical related majors such as veterinary medicine, biology, pharmacy or nursing (undergraduate degree or above);

2. Willing to engage in animal experiments, responsible and team spirit;

3. Diligent and studious, willing to accept challenges, practical work, and able to strictly abide by the standard operating specifications.

Job Responsibilities

1. Carry out the experimental plan and arrangement of animal (small animal) pharmacology and pharmacodynamics according to the requirements of the experiment;

2. Have relevant research experience in animal disease models or tumor models, and be proficient in culturing primary cells and tumor cells;

3. Relevant immunology and cell activity evaluation, including ELISA, WB, flow cytometry and other tests;

4. Complete technical research and development tasks independently, demonstrate data, express opinions, etc.;

5. Proficiency in literature retrieval and establishment of new methods; data analysis, experimental report writing;

  Participate in experiments, collect data, analyze, track the progress of experiments, control the quality of experiments, discover problems in experiments in time and propose solutions;

 

Job Requirements

1. Major in pharmacy, medicine, biology or other related biomedicine, with experience in pharmacology or pharmacodynamics research, bachelor degree or above;

2. Quick thinking, calm in case of trouble, positive work attitude, teamwork and professionalism.

Job Responsibilities

1. According to the requirements of the GLP specification and experimental plan, be responsible for the preparation of the test product and the control, including arranging the preparation, solvent preparation, solution and suspension preparation and recording, sampling, cleaning, waste disposal, etc. according to the research plan ;

2. Ensure that all data are properly recorded and SOP deviations are recorded in a timely manner and reported to SD;

3. Manage and maintain preparation-related equipment;

4. Coordinate and maintain daily experimental consumables and preparation accessories;

5. Deal with the problems found by the QA department, take practical and effective measures and correct them in time;

6. Experimental process confirmation and QC.

 

Job Requirements

1. Major in pharmacy, pharmaceutical preparations, college degree or above;

2. Have good written and oral communication skills and teamwork spirit;

3. Strong sense of responsibility, patient and meticulous in work, good ability to summarize and organize, and strong in organization;

4. Possess a certain level of English and basic computer skills.

Job Responsibilities

1. Responsible for preparation analysis according to GLP guidelines and protocols. Including arranging the analysis time point according to the experimental plan, ensuring that all data are properly recorded, and recording the deviation in time, and reporting it to SD; replying to the problems found by the QA department, taking effective measures and correcting them in time, confirming the experimental process and QC;< /div>

Job Responsibilities

1. According to GLP requirements, complete the development and validation of LC-MS/MS bioanalytical methods;

2. Complete PK/TK biological sample analysis according to GLP requirements;

3. Use WinNonlin to calculate PK/TK parameters and assist in writing PK/TK reports;

   Review of data and reports in accordance with GLP requirements.

 

Job Requirements

1. Majors in pharmacy, medical testing, analytical chemistry, pharmaceutical preparation analysis, biology, etc.

Job Responsibilities

1. Manage the biological analysis team, reasonably arrange the resources, personnel and experimental progress in the team, and ensure that the team work conforms to the relevant standard operating procedures. Ensure that the quality of experimental data meets GLP requirements;

2. Assist in optimizing departmental processes, solve problems in departmental operations, and provide relevant training to departmental staff;

3. Participate in the experimental work of the department, as the subject leader of the bioanalytical verification project or the leader of the analysis project, responsible for controlling the quality and progress of the project, which is the key control node of the project. Solve technical problems in the project and reply to the finding of QA in the project;

4. Write and update department-related SOPs;

5. Participate in customer visits and reviews, and communicate with customers;

6. Make and update relevant analysis documents and related tables of the department;

7. Write and review the department's experimental plan and report; review the experimental data and related documents;

8. Carry out biological analysis calculations, use WinNonlin and other software to calculate relevant parameters, and evaluate the analysis results;

9. Carry out routine maintenance and calibration of the instrument according to the corresponding SOP. Participate in equipment management. As departmental LC/MS system owner, manage computerized systems;

10. As a translator of documents and reports, translate relevant source records and related documents, as well as schemes, methods and reports, etc. As a translation reviewer, review the translated material to confirm that the translation is consistent with the original;

Other department-related matters, such as ordering and management of reagent consumables, etc.

 

Job Requirements

1. Bachelor degree or above in pharmacy or related majors;

2. More than 2 years experience in bioanalytical laboratory management 

3. Received training on relevant GLP regulations and norms of FDA, OECD and CFDA, familiar with GLP regulations and have corresponding work experience and technical requirements;

4. Possess a highly conscientious and responsible working attitude, good communication and coordination skills, and is fluent in English speaking and writing.

Job Responsibilities

1. Arrange the audit work of the QA department and train the junior auditors;

2. Audit the trial project, including reviewing the trial protocol and related amendments, key stages, original data and trial final reports, writing and signing QA reports, and issuing quality assurance statements;

3. Conduct audits of facilities and computerized systems and assess their compliance with the GLP;

4. Conduct external audits to assess their organization's compliance with GLP or other quality standards;

5. Drafting, reviewing and training QA SOPs, and reviewing the SOPs of various functional departments of Anling;

6. Proactively provide professional advice on GLP implementation quality improvement;

7. Provide training on GLP regulations and GLP compliance for laboratory staff, subject leaders and management;

8. Always pay attention to and identify the development of GLP, GCP, GMP regulations and related GLP, GCP, GMP regulations, and give explanations and provide reasonable and constructive suggestions for the development of the organization in accordance with the development of regulations;

9. Receive and support NMPA, OECD, FDA and other official audit work, and answer official inspection questions;

10. Maintain documentation of the quality assurance department;

11. Support the audit of the regulatory department and customer of the corresponding country or institution;

12. Obey the external training arranged by the company, as well as the GLP, GCP, GMP regulations training for the employees of the group company (Shanghai, Hong Kong, Zhongke);

    Complete other tasks assigned by the department head.

 

Job Requirements

1. Bachelor degree or above;

2. Chemistry, pharmacy, pharmacy related majors;

3. CET-4, fluent in listening, speaking and writing;

4. Familiar with GLP, GCP, GMP regulations and related knowledge of quality assurance;

5. Have good teamwork, communication and interpersonal skills;

6. Those with more than 3 years of relevant work experience are preferred.

Job Responsibilities

1. Audit the trial project, including reviewing the trial protocol and related amendments, key stages, original data and trial final reports, writing and signing QA reports, and issuing quality assurance statements;

2. Conduct audits of facilities and computerized systems and assess their compliance with the GLP;

3. Always pay attention to and identify the development of GLP, GCP, GMP regulations and related GLP, GCP, GMP regulations, and give explanations and provide reasonable and constructive suggestions for the development of the organization in accordance with the development of regulations;

4. Receive and support NMPA, OECD, FDA and other official audit work, and answer official inspection questions;

5. Maintain documentation of the quality assurance department;

6. Support the audit of the regulatory departments and customers of the corresponding countries or institutions;

7. Obey the external training arranged by the company, as well as the GLP regulations training for the employees of the group company (Shanghai, Hong Kong and Zhongke);

8. Complete other tasks assigned by the department head.

 

Job Requirements

1. Bachelor degree or above;

2. Chemistry, pharmacy, pharmacy related majors;

3. CET-4, fluent in listening, speaking and writing;

4. Have good communication skills, strong learning ability and positive attitude.

Job Responsibilities

1. According to the company's overall strategic development needs, be responsible for finding cooperation opportunities for domestic and foreign biopharmaceutical companies and research institutions;

2. Propose and implement business development strategies according to market characteristics and trends, and promote the company's external service business; 

3. Responsible for the preparation and implementation of business development plans and related project foreign cooperation negotiations, and responsible for the progress follow-up and management of cooperative projects; responsible for project plan review, contract review, and on behalf of the company and customers to discuss contract terms

4. Achieve annual business goals and customer growth rates;

5. Collect information on major competitors, customers, and markets, and write analysis reports based on the information;

6. Plan, organize and supervise the marketing activities of the project in charge of the project, etc.

Establish and maintain a normal and stable relationship with partners to ensure good business development.

 

Job Requirements

1. Major in medicine, pharmacy or biology, bachelor degree or above; 

2. Understand and be familiar with the domestic and foreign pharmaceutical market and commercial marketing business operation process, with relevant work experience in the CRO industry is preferred, with a customer relationship network, and more than three years of work experience in the same position;

3. Entrepreneurial enthusiasm and persistence, keen business insight and analytical skills;

4. Good teamwork skills, interpersonal communication skills, planning and execution skills;

5. Active creative thinking, highly sensitive to new things, strong written and oral expression skills;

   Able to work under great pressure, have the courage to accept challenging work, and have a strong self-driving force.