A. Tataji

• Conducted method development activities across multiple products.
• Performed forced degradation studies to evaluate product stability.
• Managed analytical method transfers to ensure effective implementation.
• Addressed analytical-related regulatory queries
• Prepared and reviewed analytical methods, validation protocols, reports, and method development documents.
• Planned HPLC and GC analyses for various projects.
• Executed method validations and verifications for CMO and CRO projects.

Executed method development activities for multifil products, enhancing analytical capabilities.

• Conducted formulation compatibility and stability studies to ensure product integrity.
• Led forced degradation studies to assess stability under stress conditions for various products.
• Facilitated analytical method transfers, ensuring consistency across multiple sites.
• Addressed regulatory queries related to analytics while maintaining compliance with GLP standards.
• Prepared and reviewed analytical methods and validation protocols to support product integrity.
• Conducted verifications and validations of analytical methods for active pharmaceutical ingredients and finished products.