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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