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A pharmaceutical company  

A company willing to dream with you

A Wonderful Land worthy of your lifetime career

phone:0512-6296-5186

email:guoruiying@totbiopharm.com
fandandan@totbiopharm.com

  • Engineer of liquid chromatography and mass spectrometry

    The function

    1、The characterization of biological drugs, including antibody drugs, ADC drugs and fusion proteins, was analyzed by lc-ms;

    2、The metabolites of cell culture were qualitatively and quantitatively analyzed by lc-ms.

     

    Post requirements

    1、Master degree or PhD in biological analysis or chemical analysis, bachelor degree or above 3 years analytical experience;

    2、Experience in using liquid chromatography or mass spectrometry, including q-tof biological macromolecule characterization or QQQ small molecule quantitative analysis;

    3、Experience in the analysis of biological macromolecules (recombinant proteins and antibodies) is preferred.

    4、Team spirit, serious and responsible in work.

    Apply for the position

  • Engineer of biological medicine physics and chemistry research and development analysis

    The function

    1、Responsible for physical and chemical detection of small test and medium test protein samples, such as molecular exclusion chromatography, ion exchange chromatography, hydrophobic chromatography, reverse phase chromatography, protein content determination, CE analysis, etc. Report the results in time, and follow up the problems occurred in the inspection.

    2、Participated in the development of physical and chemical analysis methods of biological drugs and validation of methodology;

    3、Assisted superior supervisor in data summary, preparation of new drug declaration materials and laboratory management.

     

    Post requirements

    1、Master degree of at least 1 year or bachelor degree of at least 4 years relevant working experience, excellent master of biopharmaceutical or pharmaceutical analysis is acceptable;

    2、Familiar with the operation and data analysis of UPLC, HPLC, GC, capillary electrophoresis, ultraviolet spectrophotometer and other instruments;

    3、Capable of literature review and learning;

    4、Strong sense of responsibility, good team cooperation ability and analytical and solving ability.

    Apply for the position

  • Structural verification engineer

    The function

    1、Responsible for physical and chemical special test of biological drug products, such as molecular exclusion chromatography, ion exchange chromatography, peptide diagram, capillary electrophoresis analysis, etc., timely report the results, timely report problems occurred in the test, and responsible for treatment and tracking;

    2、Participated in the development of physical and chemical analysis methods of biological drugs and validation of methodology;

    3、Assisted superior supervisor in data summary, preparation of new drug declaration materials and laboratory management.

     

    Post requirements

    1、Master degree of at least 1 year or bachelor degree of at least 4 years relevant working experience, excellent master of biopharmaceutical or pharmaceutical analysis is acceptable;

    2、Familiar with the operation and data analysis of UPLC, HPLC, GC, capillary electrophoresis, ultraviolet spectrophotometer and other instruments;

    3、Capable of literature review and learning;

    4、Strong sense of responsibility, good team cooperation ability and analytical and solving ability.

    Apply for the position

  • Microbiology analyst

    The function

    1、Complete the microbiological examination of raw materials, auxiliary materials, finished products and stable products, including limit test, sterility test, bacterial endotoxin test, etc.;

    2、Methods for microbial limit, asepsis and endotoxin analysis were established.

    3、Sampling of raw and auxiliary packaging materials;

    4、Diversity management;

    5、Responsible for the management of cleaning and disinfection of microbial clean area and sampling room;

    6、Responsible for the sanitation, instrument maintenance and instrument calibration of the whole area under my jurisdiction;

    7、Responsible for document preparation within the scope of responsibility, and cooperate with OOS and deviation investigation;

    8、Participate in the verification work of the verification department.

     

    Post requirements

    1、Pharmacy related major, familiar with Chinese pharmacopoeia, American pharmacopoeia, ICH, GMP and other regulations is preferred;

    2、Honest and trustworthy, responsible and positive.

    Apply for the position

  • Biometric engineer

    The function

    1、Responsible for in vitro binding detection of antibody drugs, including antigen and antibody binding activity detection;

    2、Responsible for quality control and detection of exogenous substance residues of biological drug stock solution and finished products, including DNA residue, protein A residue, host protein residue, etc.

    3、Responsible for the detection of cell activity of biological drugs;

    4、Responsible for the testing of intermediates, raw liquid and finished product release, stability sample, etc.

     

    Post requirements

    1、Bachelor degree or above, major in biochemistry, molecular biology, cell biology, etc.

    2、Theoretical knowledge background or work experience related to ELISA detection is required; ;

    3、Experience in cell culture.

    Apply for the position

  • Physical and chemical analyst

    The function

    1、Formulated quality standards and inspection operation procedures for raw and auxiliary materials, packaging materials, etc.;

    2、Responsible for sampling and testing of daily raw and auxiliary materials and process water;;

    3、Daily management of reagent, test solution and reference substance;

    4、Maintenance and daily calibration of inspection instruments;

    5、Receiving and distributing samples, applying for and distributing inspection records;

    6、Daily management of sample retention and stability.

     

    Post requirements

    1、Pharmacy and related major, GMP background is preferred;

    2、Good communication and learning skills, initiative and teamwork spirit.

    Apply for the position

  • QA engineer

    The function

    1、Assisted in the writing, modification, training and execution of quality system documents;

    2、Responsible for the review, processing and follow-up of deviations and changes;

    3、Responsible for the review and follow-up of CAPA;

    4、Organize departments to recommend themselves regularly and review annual production/quality, and complete corresponding reports;

    5、Responsible for maintenance of supplier management procedures to ensure that supplier management meets GMP requirements;

    6、Responsible for drafting annual audit plans and on-site audit plans of suppliers, participating in on-site audit and completing reports;

    7、Organized supplier evaluation and audit, including supplier questionnaire, on-site audit, quality agreement signing, etc.;

    8、Responsible for supplier qualification review and file arrangement, and regularly update the list of qualified suppliers and related materials;

    9、Participate in material related deviation, change processing and supplier risk management;

    10、Responsible for maintenance of training management procedures to ensure that training activities meet GMP requirements;

    11、Organized the drafting of annual training plan and organized and coordinated all departments to complete the training;

    12、Responsible for the implementation and follow-up of GMP training for new employees;

    13、Organize all employees of biological medicine to participate in external training and carry out retraining within the department.

     

    Post requirements

    1、Bachelor degree or above, major in pharmacy or biology, familiar with production process of biological medicine is preferred;

    2、Familiar with GMP /GLP requirements, GMP certification experience is preferred;

    3、Good command of English, proficiency is preferred;

    4、Good communication skills, adaptability, attention to details and strong execution ability.

     

    Apply for the position

  • Verification engineer

    The function

    1、Responsible for validation of sterilizing equipment and incubator;

    2、Periodic re-evaluation and re-verification of other process equipment;

    3、Organize and coordinate the periodic re-evaluation and re-verification of air conditioning system, water system and other public engineering systems;

    4、Followed up and coordinated the work of the verification service company, and sorted out and reviewed the reports of the verification service company;

    5、Draft verification plan and verification report for the verification work;

    6、Responsible for the quality risk assessment related to the validation in charge and the development and follow-up of the validation related to deviations and changes;

    7、Responsible for the management of on-site validation status related to the validation project carried out.

     

    Post requirements

    1、Bachelor degree or above, major in pharmacy;

    2、Experience in GMP certification is preferred;

    3、Honest and practical, with strong systematic thinking ability.

     

    Apply for the position

  • CRA

    The function

    1、Relevant investigation business before the start of clinical trial;

    2、Screened main researchers and participating research institutions, drafted data confidentiality agreement and clinical trial agreement, and assisted CRO to complete agreement signing and payment verification;

    3、Participate in organizing various researcher meetings (program seminar/pilot start meeting/mid-term meeting/conclusion meeting, etc.);

    4、Prepare and/or review test inspection plan, prepare collaborative inspection plan and implement it with PM;

    5、Complete the closing of each participating research center;

    6、Assisted in writing and revising clinical trial data;

    7、Prepare the filing materials to the ethics committee (IRB);

    8、Cooperate with inspection of drug regulatory department and internal and external inspection of the company.

     

    Post requirements

    1、Experience in tumor clinical research is preferred;

    2、Work with a strong sense of responsibility and autonomy, strong ability to work under pressure. ;

    Location: Suzhou, Beijing, Shanghai.

     

    Apply for this position

  • Academic promotion staff

    The function

    1、Achieved sales target through professional and academic promotion
      (1)achieve the sales target and control the cost within the budget;
      (2)carry out various promotional activities of the hospitals under the jurisdiction;
      (3)frequent and effective visits;
      (4)organize and take charge of small academic activities;
      (5)communicate with doctors about case collection and other research activities;
      (6)responsible for product development and admission to the assigned hospital.

    2、Establish good relationship with key customers
      (1)understand and tap potential customer needs, and provide professional services;
      (2)establish good relationship with relevant customers.

    3、Carry out self-management according to the requirements of the enterprise
      (1)timely feedback on competitive product strategies and various activities;
      (2)discuss product materials and actively participate in product training;
      (3)complete all required reports and statements;
      (4)attend regular and irregular sales meetings;
      (5)timely report adverse drug reactions and adverse drug events.

     

    Post requirements

    1、Bachelor degree or above, major in medicine or related.

    Location: all over the country

     

    Apply for the position