Recruitment

We Are Hiring!
We offer competitive salaries and benefits and are welcome to join our team.
Contact: Email: info@sungening.com (Please specify the position you are applying for)

Recruitment

  • Job Description:

    1. Manager and coordiante the New drugs R&D Project.
    2. Ability to complete the background research, data collection of New drug projects, and creat feasibility report
    3. Related drug information research, literature patent tracking
    4. Ability to draft and adjust the experimental protocal to promote project progress
    5. Responsible for project management, arrange the tasks of team members, coordinate the relationship between team members, and ensure the completion of the project
    6. Participate in external project cooperation and technical exchanges
    7. Summarize the work in time and complete project progress report
    8. Other work assigned by leader.

    Position Requirement:

    1. Major: Organic chemistry, pharmaceutical chemistry or related major. Bachelor/ master’s degree or above, more than 2 years of experience in small molecular innovation drug research and development experience
    2. Have a certain research and development team management experience. Prefer candidate who participate in the application of type 1 small molecule new drugs application
    3. Good team consciousness and collaboration spirit, good at communication, strong sense of responsibility, hard work, strong execution
  • Job Description:

    1. Undertaking the overall research of vivo and vitro DMPK projects: including experimental design, implementation, data generation, processing analysis, interpretation, reporting, etc., and providing DMPK -related scientific support for the project team
    2. Responsible for writing, reviewing and modifying the DMPK part of the relevant projects in the IND application.
    3. Establish a research method for vivo and vitro DMPK to enrich platform research strength
    4. Contact with CRO to ensure the smooth implementation of the outsourced DMPK experiment project
    5. Responsible for the drafting department SOP and organization related training
    6. Other work assigned by leader.

    Position Requirement:

    1. Major: Pharmacology, pharmacokinetics, pharmaceutical analysis or related major. master’s /Doctor’s degree or above, more than 2 years of biological analysis and DMPK working experience
    2. Master the conduct of pharmacokinetic samples, compound pharmaceutical analysis methods, and instruments such as LC/MS and other
    3. Familiar with CFDA, FDA and OECD GLP regulations and related guidelines
    4. Understand the pharmaceutical research and development process and have other aspects of acknowledge of pharmacology, pharmacokinetics, and toxicology
    5. With project management or team management capabilities
    6. Fluent Listening, speaking, reading and writing. Strong learning ability and willingness.
  • Job Description:

    1. Responsible for guiding the quality research of new drugs including the method development, verification, release and stability research, and finally establish drugs specification.
    2. Responsible for the drafting or review of various documents in the project, and to deal with the deviation in the process of quality research in time
    3. Responsible for writing or reviewing the application documents and original records of drug analysis, which can accurately and clarify the content of quality research to meets the application requirements of the drug regulatory bureau then complete the drug listing.
    4. Responsible for retrieval Chinese and English literature, follow the latest domestic and foreign updation of research progress and regulations of each Agency.
    5. Arrange the assignment of each project reasonably, and facing the problems of analysis, solutions can be proposed in a timely manner to ensure the smooth progress of the project
    6. Responsible for daily management of the laboratory, and training of analysts, etc.
    7. Other work assigned by leader.

    Position Requirement:

      1. Major: Pharmaceutical preparation, parmacy or related major. master’s /Doctor’s degree or above, more than 2 years of New drugs R&D working experience
      2. Familiar with cGMP、ICH、FDA related research guidelines, Familiar with domestic and foreign registration declaration and review requirements

       

      1. Proficiency in analytical instruments such as the moisture meter, dissolution tester, HPLC, LC-MS, etc., Ability to develop and verify methods independently.
      2. Proficiency in the technologies of various administration and dosage form of finished drugs. Experience and ability for pre -research of biopharmaceuticals, chemical preparation prescriptions, preclinical testing agent development, preparation process research, and process amplificatio.
      3. Ability to retrieve and review professional foreign language literature, have a certain level of English writing, can draft English listing documents.
      4. With strong time management and execution capabilities, the progress of multiple projects can be planned at the same time
  • Job Description:

    1. Responsible from the choice of candidate compounds to the biology research in the early clinical stages, including deeply understanding of signal conduction pathways and in vitro and in vivo pharmacology
    2. Leading project team design and pharmacological research to support biomarker strategies and clinical trial design. Analyze the data/results and convey it to the project team and leader.
    3. Cooperate with team members, determine and evaluate CROs company, provide scientific and reasonable support for the company’s research, and be responsible for outsourced research solutioner to accelerate the completion of the project’s milestone.

    Position Requirement:

    1. Major: Pharmacology, biology, animal medicine or related major. master’s /Doctor’s degree or above, more than 2 years of New drugs Pharmacology and toxicology working experience
    2. Familiar with the evaluation method of the vivo and vitro, Have 1-3 years experience in the establishment of the vivo and vitro efficacy screening platform.
    3. Experience of non -clinical application of new drug projects, very familiar with the guidance principles and knowledge of DMPK, non -clinical toxicology research
    4. Ability to review Chinese and English literature and translate foreign literature independently
    5. Clear ideas, strong logical thinking ability, communication ability, can evaluate and adjust the experimental scheme, and have strong analysis and summary ability of the experimental results.