Found 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.
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