Active Analysis Direction

Job Responsibilities

1. Responsible for the development, optimization, validation, and transfer of bioactivity methods (including ELISA, cell-based assays, etc.), biological residue and safety analysis methods (including residual HCP, residual DNA, residual Protein A), writing and revising relevant documents to support project progress;
2. Responsible for the evaluation and application of new technologies/instruments;
3. Formulate and execute monoclonal antibody characterization plans for IND and BLA submissions, mainly providing support for formulation development through structural and degradation pathway characteristics and stability-related studies;
4. Possess cross-departmental communication skills, effectively follow up and communicate project progress;
5. Analyze and solve abnormal problems encountered in experiments, promptly organize and analyze data to support project progress;
6. Able to proactively undertake various responsibilities and possess good decision-making abilities.

Job Requirements

1. Bachelor’s degree or above in cell biology, molecular biology, biochemistry, pharmacy, immunology, biotechnology, basic medicine, or related fields;
2. Experience in optimizing and constructing expression vectors, transfection, Western, ELISA, cell-based assays, cell proliferation inhibition, apoptosis, phagocytosis, ADCC, CDC, enzyme activity, flow cytometry, etc. is preferred. Candidates with statistics knowledge/mathematical background are preferred;
3. Familiarity with cGMP, pharmacopoeial testing, and biological drug application and registration regulations is preferred;
4. Ability to conduct literature searches, excellent English skills, able to read and translate English literature fluently;
5. Strong curiosity for learning new things;
6. Possess good professionalism, team spirit, and communication and coordination abilities.

HR Email: hr@biotech-pack.com (If interested, please contact us through this email or directly submit your resume)