Associate degree in Microbiology, Biology, Biotechnology, or a related scientific discipline preferred.
Experience working in a cGMP-regulated pharmaceutical, medical device, or biotechnology environment.
Hands-on experience with environmental monitoring, bioburden testing, microbial identification, or sterility testing.
Familiarity with laboratory systems, data management software, and electronic documentation practices.
Knowledge of USP microbiological testing requirements and contamination control principles.