Description
The Associate Scientist, QC will support quality control and stability testing in a cGMP-regulated pharmaceutical laboratory. Responsibilities include analytical testing of raw materials, in-process samples, finished products, and stability samples; data review and reporting; laboratory investigations; protocol and specification authoring; sampling; inventory management; and collaboration with Quality Assurance, Manufacturing, and clients. The role requires a bachelor's degree in Chemistry or a related scientific discipline, at least three years of pharmaceutical analytical laboratory experience with a B.S. degree or an equivalent education and experience combination, and experience in a cGMP and/or GLP environment.
