$100K - $150K
Designs and develop preformulation, and conduct formulation screening and optimization studies for parenteral liquid and lyophilized biologic drug products to ensure stability and manufacturing feasibility for pre-clinical and clinical trials. This position contributes to and supports the company's research and product development efforts to create high value therapeutics to address unmet medical needs.
Responsible for design and development of new biologics drug formulations. Also responsible for formulation optimization with a view to establish the quality and stability of drug products. Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining optimal results. Designs, executes, and interprets formulation studies based on defined deliverables, planning activities to meet project t
Valid through: 2020-1-20