Associate Scientist II, Quality Control

Role: Associate Scientist II, Quality Control, supporting analytical testing of pharmaceutical raw materials, in-process samples, finished drug substances, drug products, and stability samples within a cGMP environment. Responsibilities: perform routine analytical assays (e.g., HPLC, GC, FT-IR), conduct environmental monitoring, support testing for GLP toxicology and clinical trial materials, ensure compliance with SOPs and cGMP standards, and assist in troubleshooting instrumentation and analytical issues. Requirements: B.S. in Microbiology, Chemistry, or related field; 1-3 years' relevant lab experience with familiarity in cGMP operations and analytical instrumentation. Preferred: experience in environmental monitoring, microbiology, and cleanroom procedures; strong technical writing and data analysis skills; proficiency with chromatography and laboratory software. HighValue: biopharma (pharmaceutical manufacturing), cGMP compliance, analytical testing, environmental monitoring, GLP, clinical trial support, biotech manufacturing environment; role reports to QC-EM Scientist. WorkSetup: on-site in Wisconsin, with salary range $70K-$85K.