Bachelor's degree in Chemistry, Pharmaceutical Sciences, Microbiology, or a related scientific field.
5+ years of Quality Control experience in the pharmaceutical industry.
Hands-on experience with GC, FTIR, TOC, UV-Vis, and other analytical instrumentation.
Experience supporting sterile injectable manufacturing environments.
Strong knowledge of cGMP, GLP, FDA regulations, USP, ICH guidelines, and data integrity requirements.
Experience with method validation, equipment qualification (IQ/OQ/PQ), and laboratory investigations.
Familiarity with LIMS and electronic laboratory systems.