Custom Protein Generation

Drug Substance Manufacturing

Drug Product Fill & Finish




Antibody Drug Conjugates

Technologies & Platforms

• Generate and review technical documents such as methods protocol, method transfer/qualification/ validation protocols and reports.
• Perform analytical method optimization, transfer /qualification/ validation and sample testing under cGMP.
• Perform QC in-process/release/stability testing.
• Serve as technical lead to solve technical challenges and support laboratory investigations of OOS/OOT or deviation.
Basic Qualifications:
• Graduate degree in biochemistry, molecular/cell biology, immunology or related fields.
• Relevant industrial working experience, BS or MS degree with 2+ year GMP experience.
• Extensive knowledge and hands-on experience in the following fields.
• Biochemical assays such as UV, SDS-PAGE, WB, ELISA and qPCR.
• Experience on developing and characterizing biochemical analytical methods.
• Strong communication skills in English and Chinese, fluent in speaking, writing and reading.
• Critical thinking, scientific reasoning and problem solving skills.

1.Sending email to with subject”Apply for+Position+Location”