Genovior Biotech Corporation jobs and careers

About Genovior Biotech Corporation

Genovior Biotech Corporation operates several aseptic GMP production facilities capable of producing clinical or commercial materials based on CDMO. We have a robust quality assurance procedure and are currently carrying out several CDMO projects about API and injection, which are scheduled to be released in 2022/23. Please contact us to discuss your project requirements. 1. GMP certificate: PIC/S cGMP certificated by Taiwan's FDA 2. One-stop service from Drug Substance (DS/API) to finished product (DP/FDF) 3. CDMO/CMO: Drug Substance/API: HPAPI, Peptide, Protein (E. Coli. & CHO) Drug Product/FDF: Lyo-vial, Liquid-vial, Pre-Filled Syringe (PFS), Cartridge, Pen 4. Field of Manufacture: Oncology/Peptides/Biosimilar/mAb 5. Core technology: Lyophilization/up-&downstream (Fermentation&Purification) 6. Batch size: from pre-clinical trials, clinical trials, commercial trials