Vanessa Chamoun

Creation of a database to optimize QC test tracking and inventory management for all materials stored at CordenPharma.

• Development of an Excel database designed to enhance the monitoring of QC laboratory tests and analytical equipment performance (KF, HPLC).
• Implementation of a centralized database consolidating specifications, characteristics, and detailed information related to each raw, intermediate, and finished material (active or inactive) stored or utilized at CordenPharma.

Optimization of the synthesis of a lipid adjuvant for the shingles vaccine.

• Improvement of synthesis steps to enhance industrial feasibility.
• Increase in yields and purity of the final product through precise adjustments of reaction and purification conditions.
• Resolution of technical challenges related to filtration, by-products, and reproducibility.
• Adaptation of the process for large-scale production, ensuring industrial viability.

Managed a reference standard characterization project for an API and internalized a lyophilization process within GMP conditions, completed in 4 months instead of the planned 6.

• Successfully coordinated cross-functional teams to deliver 2 × 500 vials of impurity reference standards to the client within tight deadlines.
• Developed and validated a lyophilization process including feasibility tests (KF analysis, characterization).
• Managed GMP documentation with a thorough understanding of pharmaceutical regulatory requirements.
• Interacted with external laboratories.
• Created a database for managing the inventory of reference standards (PM/QC collaboration).