Responsibilities

 Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes.

 Manage project workflow to ensure on time delivery: from initial planning, experiment execution, to data evaluation.

 Design and execute lab-scale experiment in supporting downstream process development, verification, characterization, and tech transfer. Perform independent data analysis and interpretation and develop strategies for optimization and troubleshooting.

 Represent Vaccine Downstream Process Development Group in internal cross-functional teams and external communication with client.

 Manage technical transfer of processes into the non-GMP pilot plant or GMP production facility.

 Document development work in concise reports and provide project updates in written and oral presentations.

 Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers

Qualifications

 The candidate should have background in one of the following fields: chemical engineering, biochemical or biological engineering, cell/molecular biology, biochemistry, or microbiology.

 Hands-on experience in downstream process unit operations and lab scale experimental execution.

 PhD degree and 0-2 years industry experience, or with MS degree and at least 3 years industry experience.

 Strong written and verbal communication skills are required, as well as ability to take on multiple tasks simultaneously.

 Excellent communication and good interpersonal skills, work well with diverse team members