CAR-T（Chimeric Antigen Receptor T-Cell）
- A minimum of a Master degree in Engineering, Science, Chemical, Pharmaceutical or related field or equivalent experience required.
- Minimum 8 years of experience within a cGMP driven environment in the biotech / biopharma industry. Cell and Gene Therapy Experience is a must.
- Experience in the execution (design, build, start-up) of capex projects for drug substance and drug product manufacturing.
- Ability to work cross-functionally and successfully.
- High organizational skills: prioritize and manage multiple tasks simultaneously. Must be able to manage shifting priorities to meet multiple clients in a multiple country location environment.
- Good communication skills in English and Chinese (both written and oral).
- An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment among clients and suppliers.
- Strong analytical, problem solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability.
- Working location based in Shanghai and can accept travels to the project site
- Contract Type: Fixed Term Contract (UNfixed Wkg Hrs for management, which is No overtime payment)
