Job Description

Preferred candidates will have Validation Experience in Parenteral Manufacturing. Specifically, experience focused in Aseptic Process Validation, Aseptic Techniques, Environmental Monitoring Performance Qualifications, Environmental Characterizations, Airflow Visualization (Smoke Tests). Experience writing protocols and reports and executing inside clean rooms. Requirements Doctorate OR Masters + 2 years of directly related experience OR Bachelors + 4 years of directly related experience OR Associates + 8 years of directly related experience OR High school/GED + 10 years of directly related experience. Microbiology/Life Sciences/Engineering

5+ years

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