Senior chemist - (Windsor, CT)

Summary: Under the direction of a Chemistry Manager, the Senior Chemist performs method development of UPLC potency assays for injectable drug products. The methods will be developed as stability-indicating, and, following validation, will be utilized for stability and QC testing. The analyst must be familiar with the workings of a GMP chemistry lab, equipment and documentation requirements, including following standard operating procedures, using proper documentation, performing forced degradation, method validation, preparing samples and analyzing results. Key functions: Develop stability-indicating UPLC potency assays for small-molecule injectable drug products. Execute forced-degradation experiments in support of the method development. Become familiar with, and adhere to, requirements as documented in SOPs for Good Manufacturing Practices. Clearly document all laboratory activities using proper documentation. Perform thorough peer reviews to ensure accuracy of raw data and calculations.