Ryan Rice

Senior Manufacturing Engineer @Wesley Pharmaceuticals

Orlando, FL, US

Ensure compliance with FDA regulations, cGMP standards, and internal SOPs in a sterile, aseptic pharmaceutical manufacturing environment.Monitor and support aseptic processes including cleanroom operations, environmental monitoring, and sterile filling activities.Conduct investigations, root cause analyses, and implement CAPAs for deviations and nonconformances related to sterile operations.Participate in media fill validation, aseptic gowning qualification, and cleanroom behavior monitoring to uphold sterility assurance.Collaborate with cross-functional teams to drive continuous improvement in aseptic technique, contamination control, and batch record accuracy.Review and approve quality documentation including batch records, SOPs, and validation protocols related to aseptic production.Support internal and regulatory audits; provide documentation and responses related to sterile manufacturing operations.Maintain and report quality metrics focused on environmental control, batch sterility, and deviation trends.

Utah Valley University

Associates, University Studies

University of Utah

Master's Degree, Petroleum Engineering

University of Utah

Bachelors, Chemical Engineering