She has broad engineering background and extensive experience in pharmaceutical manufacturing operations, technology transfer and validation of pharmaceutical processes and facilities for tablets, capsules, powders, and aerosols, full understanding of validation principles, Good Manufacturing Practices, FDA regulations and guidelines, and compliance concepts. Her full-time job is a Technical Manager – Validation and Process Management in the Global Technical Services group at Schering-Plough, where she provides technical expertise and detailed project support to manufacturing sites and global corporate teams for technology transfer and process validation of new and existing solid oral dosage forms. Such support ranges from consultation services, problem solving and troubleshooting, to preparation, development, execution, and documenting validation studies. |
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