$80K - $100K*
Design, execution, and data interpretation of Chromatography and Filtration experiments.
Support process scale-up activities in the pilot plant and clinical and commercial manufacturing sites. Prepare/review technical documents including process development reports, tech transfer documents, process characterization reports, and in-process control strategy documents, as well as CMC regulatory submissions.
Participate on cross-functional teams to progress both early and late stage drug candidates. Conceptualize and implement upcoming technologies for biologics manufacturing.
Ph.D. in Chemical/Biochemical Engineering, Biochemistry or equivalent with 0-3 years of industry experience.
Prior experience in downstream process development. Demonstrated ability to work in matrix teams.
Knowledge of analytical techniques.
Knowledge of statistical experimental design and data analysis. Excellent ora
Valid through: 2020-5-20