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Talent Recruitment

The international environment within Canton Biologics has attracted global talents from 7 different countries (including theUnited States, Germany, South Korea, Switzerland and others) to join.  Proudly, Canton Biologics has also been grantedthe fame of National high-tech Enterprise and > 50% employees hold MS andPh.D. degrees. Graduates from Oxford University, ETH, California Institute ofTechnology, Sun Yat-sen University, University of Science and Technology ofChina,  Hong Kong University of Scienceand Technology and other top universities already joined Canton Biologics and arecreating value for the society.

Your Gains:
1、Corporate culture and compliance training
2、Comprehensive experimental skills training: covering a variety of biological in vitro/in vivo experimental skills in biotechnology
3、Training for automated instrument operation
4、Trainings for drug development process
5、Communication and management skills trainings
6、Cross-functional training and rotation
Career Development:
1、We help you quickly grow into a biological andtechnical expert and familiarize yourself with the key aspects of drugdevelopment through systemic trainings
2、Through courses and training in the job, youwill gain a deeper understanding of all compliance issues related to CDMO and drugdevelopment as a whole
3、Regardless of your past academic records, a performance-basedrewarding and incentive plan will accelerate your career development
4、Discover your management potential and leverageyour professionalism, dual development tracks (management and technical) will lightyou up during your career development

* All qualified candidates can apply, regardless of race, color, religion, nationality, etc.

Social Recruitment

Position Classification
Director Manager Researcher
City
Guangzhou

Associate Scientist/Scientist Biomolecule Characterization and Analytical Development

Responsibility:
1. Glycoprotein analysis: Perform mass spectrometry based characterization of biotherapeutics (mAb, bsAb, Fc-fusion proteins, ADCs etc.). Complete and deliver analysis results accurately and in time. Collaborate with other departments, such as upstream and downstream processing.
2. Glycan composition analysis: Deliver high-quality characterization results in in time.
3. Peptide mapping: Complete the peptide profile analysis of samples, including post-translational modification, sequence identification, peptide assignment and other tests.
4. Free Disulfide bond characterization: Identify and confirm disulfide bonds and disulfide bond mismatches for simple and complex proteins.
5. Innovation: Drive innovation by closely following：advances/developments/international literature and contribute this know-how to method development.
Qualifications：
1. Master Degree in Analytical Chemistry with focus on mass spectrometry on macromolecules. Fast and motivated learners with background in biotherapeutics characterization and other related majors (e.g. pharmaceutical sciences, biology) are also welcome to apply.
2. At least half-a-year of relevant work experience with macromolecules.
3. Ideal candidates have a proven track record in the structural characterization of antibody drugs, peptide drugs and fusion protein drugs for more than one year. This includes ability to apply mass spectrometry, high performance liquid chromatography and performing related maintenance for LC-MS, Native MS, Proteomics etc.. The candidate should be familiar with glycoprotein characterization, glycan profiling, glycopeptide analysis, impurity analysis, protein molecular weight, peptide mapping, disulfide bond, post-translational modification and other structural characterization.
4. The ability to learn fast and having a responsible and quality-driven attitude are essential attributes.

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020-31800171-803

Job@cantonbio.com

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Senior Director Biomolecule Analysis Development Department

Responsibility:
1. Lead a high-performing biotherapeutics analytical department for our R & D projects. This includes leading the overall strategy, drive innovation (assay development, qualification, validation), guide teams of motivated PhD and MSc scientists, and covering all relevant activities of the AD department for our pre-clinical and clinical development.
2. Allocate and utilize the resources and personnel according to the needs of the project. This will include creating work plans, giving guidance to the technical problems in the R & D process and ensuring efficient and qualitatively excellent completion of tasks.
3. Establish new technology platforms by identifying and leveraging cutting-edge technologies and creating an environment which supports and encourages innovation.
4. Guide and audit all laboratory standard operating procedures and be responsible for the improvement of laboratory quality control system.
5. According to the requirements of drug registration and approval, organize the audit of relevant application materials and original records, and cooperate with the completion of application and on-site verification.
6. Guide the analysis team, conduct training. Set up the Department personnel training and career development plan.
Qualifications：
1. Doctor's degree and more than 10 years working experience in related industry, with working experience in API or analytical method development / method validation / method transfer, and more than 8 years team management experience. Significant experience in drug registration process.
2. Proficiency in one or more areas of macromolecular protein analysis related research, such as physical and chemical characterization, structural characterization or bioassays.

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020-31800171-803

Job@cantonbio.com

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Scientist Physical and Chemical Characterization of Biopharmaceuticals

Responsibility:
1. Leading the development, optimization and technology transfer for phys.-chem. characterization of biopharmaceuticals (mAbs, bsAbs, ADCs, Fc-fusion, etc.). , including but not limited to SEC-HPLC, IEX-HPLC, RP-HPLC, HIC-HPCL and other liquid chromatography methods (e.g. peptide map, glycan profiling type, etc.).
2. Complete the audit of internal projects and process analytical data of physical and chemical platform; Review the relevant work plans, reports and experimental plans for method development and audit our platform SOPs.
3. Responsible for delivering customer commissioned analytical method development and reliable method development data.
4. Drive innovation by closely following international literature/recent developments, designing and developing new methods, and optimizing the methods of the physical and chemical analysis platform.
Qualifications:
1. Master degree or above in analytical chemistry, pharmaceutical sciences, biology or related majors.
2. At least 5 years working experience in macromolecular biotherapeutics analysis, 3 years working experience as supervisor or senior supervisor.
3. Strong English communication skills are a must to ensure barrier free communication and smooth project progress.

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020-31800171-803

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Biochemical Analysis Senior Manager

Responsibility:
1. Manage and arrange the work of the people in the team, coordinate the resources inside and outside the team to complete the project according to the project timeline.
2. Complete biochemical analysis development experiments and make relevant records, complete the relevant inspection records of the assigned instruments.
3. Complete the assigned development plan, development report, and test plan on time, complete the summary analysis and submission of the third-party test result report on time, and complete the assigned SOP, SMP and various related records on time.
4. Timely solve or feedback the problems encountered during the method development within the team; Assist supervisors in team management and laboratory management.
Qualifications：
1. More than 5 years of analysis experience of macromolecular protein drugs.
2. Required experimental skills: good primary cell and subculture cell culture experience, certain experience in macromolecular interaction research (Octet or Biacore), familiar with flow cytometry analysis, familiar with Elisa related operations Have certain knowledge or experience of ADCC, ADCP, CDC and in vitro cell killing activity.
3. Equipment operation ability: familiar with the use and maintenance of flow cytometry, Octet molecular interaction instrument, Biacore biological macromolecule interaction instrument, automatic cell counter, CO2 incubator, microplate reader.
4. Able to develop methods in accordance with the relevant legal requirements of Pharmacopoeia, ICH, etc. Can solve problems in a reasonable and compliant manner according to relevant requirements.

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020-31800171-803

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Formulation Scientist/Senior Scientist

Responsibility:
1. Perform feasibility studies for new projects, including: drug delivery system research report and overall project feasibility analysis.
2. Propose experimental protocols, perform implementation and provide supporting experimental data.
3. Create technical and process development reports.
4. Communicate with team leader to develop project plans and deliver results on time and with high quality standards.
5. Regularly report the experimental results and project progress supervisor.
Qualifications：
1. Master or above in pharmaceutical sciences, biology, etc., with overseas background preferred. (2021 graduate student also welcome)
2. Having relevant work experience in drug delivery system (nanoparticles, liposomes, microspheres, etc.) is required. Proven track record in the ability to independently work on projects. Basic knowledge of biological drugs, as well as the entire preparation and development process is preferred.
3. Excellent communication skills in English (listening, speaking, reading and writing), and ability to independently complete the English literature research and report writing required in the daily work.
4. Highly organized person with responsible attitude and the ambition to actively asking for help and learning fast.

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020-31800171-803

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Upstream Process Development Director

Responsibility:
1. Develops cell culture processes using ambr15, ambr250, 2L/5L bench-scale, and up to 200L disposable bioreactor systems for the production of antibody and recombinant protein.
2. Performs hands-on experiments to develop/improve bioreactor processes using chemically defined media and feeds.
3. Interprets results to make process improvements and further design next studies.
4. Executes process monitoring and control strategies for robust process design.
5. Collaborates with downstream and analysis development teams to coordinate material needs.
6. Authors Standard Operating Procedures, technical reports, and process descriptions including data interpretation and procedures.
Qualifications：
1. More than 6 years working experience in cell culture process development.
2. Experience with mammalian cell culture aseptic techniques.
3. Experience with suspension cell lines used in protein production.
4. Experience with high-throughput (e.g. ambr) and benchtop stirred tank bioreactor.
5. Experience with bioreactor scale-up is preferred.
6. Knowledge of Design of Experiments and statistical data analysis.
7. Technical proficiency and knowledge of scientific concepts.
8. Strong verbal and written communication skills and ability to communicate within the organization as well as externally.
9. Detail-oriented and able to prioritize assignments with excellent team work and communi-cation skills.

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020-31800171-803

Job@cantonbio.com

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