Description
The Pharmaceutical Quality Control Laboratory Analyst performs routine analytical testing of raw materials, in-process materials, commercial products, and clinical supplies under GMP. The role includes independent assay execution, data documentation, laboratory investigations, instrumentation operation and troubleshooting, and analysis of manufacturing and stability data. Candidates need a bachelor’s degree in science or a related field, 2–5 years of relevant cGMP pharmaceutical QC experience, or at least one year with a master’s degree, along with HPLC, GC, FTIR, data analysis, and regulatory knowledge. The position offers a base salary starting at $41 per hour and includes health and other benefits plus an annual target bonus for full-time positions.
