About the Role
Sr Validation Scientist with experience in Parenteral Manufacturing. Specifically, experience focused on 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 Bilingual (Spanish/English)(Write/Speak) Computer Literacy
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