Currently I have an opening for an Associate Scientist located in Kansas City, MO. Details for the position are as follows:

Job Description:

• Primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.


• Reads and follows Standard Operating procedures with attention to details


• Successfully trains on 1-2 methods and/or techniques mentioned above and performs ad hoc sample testing activities under cGMP as required


• Applies basic scientific and laboratory concepts and theories related to specific testing in the group


• Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports.


• Adheres to policies, processes, and procedures for ...