Quality Control Analyst III

Pay Rate Low: 30.63 | Pay Rate High: 45.95 Astrix is proud to partner with our client- a leading force in contract research, development, and manufacturing within the pharmaceutical and biotech space- to find top-tier talent. We are currently seeking a Quality Control Analyst II to join a growing QC team in Rensselaer, NY for a 6 month contract agreement with the possibility of extension. This role is ideal for an analytical scientist with pharmaceutical laboratory experience who enjoys hands‑on testing, problem solving, and working in a regulated environment supporting drug product quality. If you are passionate about science and want to contribute to the development and manufacturing of life‑saving therapies, this is an exciting opportunity to make a meaningful impact. Schedule: 6:00 PM – 6:00 AM Responsibilities Perform analytical testing of incoming raw materials, in‑process samples, finished products, and stability samples using laboratory equipment such as balances, pipettes, pH meters, UV/Visible spectrophotometers, and Total Organic Carbon analyzers. Conduct chromatographic analysis including HPLC, GC, and UPLC with minimal supervision following established methods and procedures. Perform wet chemistry and analytical assays, including testing by HPLC, GC, IR, UV, and other analytical techniques. Support raw material testing and sampling in accordance with established quality procedures. Provide backup support for QC analytical instrument maintenance and calibration. Maintain general laboratory equipment, ensure proper laboratory housekeeping, and support preparation activities for internal and external audits. Perform or assist with method qualifications, method transfers, and validation activities within the QC laboratory. Assist with analytical method development initiatives. Support cleaning validation studies and related testing activities. Assist in the evaluation and implementation of new laboratory equipment and processes. Review QC data and provide summaries and reports to management as needed. Assist QC management with investigations related to OOS results, deviations, and CAPAs. Provide backup support for analytical sample receipt and logistics, including sample login, shipment to external labs, tracking, distribution of test results, and documentation closure. Qualifications Bachelor’s degree in Chemistry or a related scientific discipline 3–5 years of experience in a pharmaceutical or regulated laboratory environment, or an equivalent combination of education and experience Preferred Qualifications Experience working in a cGMP or GLP pharmaceutical environment Hands‑on experience with chromatographic techniques (HPLC, GC, UPLC) and analytical instrumentation Experience supporting method validation, method transfer, or quality investigations This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you. #J-18808-Ljbffr