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.

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