Please note this is a 3 month contract position. Requires minimal supervision, reporting to the Engineering Laboratory manager. Chemist activities include routine analytical testing to support research and development, product release, QC investigations, customer complaints, and other. He/She supports the ongoing development, manufacture, and distribution of medical devices in compliance with local procedures, corporate policies, and the regulatory requirements of the U.S. Food and Drug Administration. Key responsibilities include but are not limited to: Routine analytical testing of samples supporting incoming raw materials, in-process production, finished product, and validation. Use analytical instrumentation such as FTIR, HPLC, GC, UV/VIS, and refractometer. Perform instrument calibration and preventive maintenance Documents/reviews laboratory work using laboratory notebooks/worksheets that is detailed, timely and in compliance with GLP/cGMP requirements. Order chemicals and laboratory supplies as needed Maintains strictest standards of hygiene in laboratory area Assumes other duties as assigned by area management For consideration please include Dice # 1621.