Matias Anton

• Managed team of 5 employees. • Managed and oversaw the daily activities of all team members • Wrote, approved and implemented end product and raw material specifications and methods of analysis. Reviewed laboratory standard operative procedures. • Reviewed and approved laboratory records. • Managed OOS and OOT investigations.

•Performed quantitative and qualitative analysis on raw materials, intermediate products and end products using HPLC, UV-Vis Spectroscopy, Particle size distribution, IR Spectroscopy and wet methodologies. • Wrote method validation protocols and method validation reports. • Executed method validation protocols according to ICH guidelines and reported results for further registration of new products in the local sanitary authority. • Developed new HPLC analytical methods .

Wrote method validation protocols as well as method validation reports. Executed method validation protocols according to ICH guidelines and reported results for further registration of new products in the local sanitary authority. Developed new HPLC analytical methods of analysis. Wrote analytical methods of analysis (English, Spanish). Performed dissolution profiles to evaluate in-vitro bioequivalence of products using different dissolution media (including biorelevant media).

Conducted quality control tests on raw materials (API’s and excipients), intermediate products and end products using HPLC, UV-Vis spectroscopy and wet methodologies. Performed on going stability studies of end products in varied dosage forms: tablets, topical creams and ointments, metered dosed inhalators among others. Performed daily checks on analytical balances and pH-meters as well as basic maintenace of said equipment.

•Performed analysis on raw materials and end product using GC and diverse wet methods. • Kept laboratory material inventory. • Sampled raw materials.