• Responsible for Product Quality related activities for Sanofi Canada’s importation and distribution serving as backup capacity to Product Quality Lead and other QA Specialists for their respective responsibilities. • Provide QA expertise to internal and external partners to establishing and maintaining high quality and compliance status of all products handled by Sanofi Canada to meet all Canadian cGMP regulations as well as Corporate requirements.• Responsible for Stability Program Review to ensure Canadian regulatory requirements are consistently met in a streamlined fashion, actively working with external manufacturing sites, collecting and analyzing PQRs, stability reports, and associated deviations and change controls.• Plan and coordinate daily, weekly, and monthly release activities. Review documentation and release Clinical Supply Materials, products under the programs Special Access to Drugs and Health Products and Access to Drugs in Exceptional Circumstances.• Issue and execute Change Requests, Deviations, Investigations and CAPAs.• Utilized spreadsheets and MS Office, SharePoint, Adobe, SAP, Phenix and Veeva systems daily to complete tasks.

• Engaged in research projects in the field of Artificial intelligence and bioremediation applied to Agriculture. • Performed media and solutions preparation to be used for students and faculty members in their courses and projects, respectively.• Assisted to volunteer research students to perform their techniques.

● Provided QA technical support to manufacturing, maintenance, and quality control departments.● Ensured GMP activities, company ́s global quality requirements and HSE directives.● Promoted continuous improvement of compliance with standards.● Reviewed and approved of Standard Operating Procedures (SOPs), specifications, change controls, and deviation reports ensuring a proper root cause analysis and robust CAPAs.● Trained and coached permanent and new employees.● Performed Quality Audits to suppliers and internal departments. ● Supported company with a focus on quality, communication, collaboration, integration, and teamwork.● Utilized spreadsheets and Microsoft Office daily to complete tasks.

● Reviewed batch records and released finished product.● Reviewed and approved SOPs.● Participated in internal audits.● Handled CAPAs, change controls, deviations and customer complaints.

● Conducted tests to determine quality and stability of pharmaceutical finished products using HPLC, GC, UV-V Spectroscopy, KF, IR.● Executed validations or transfers of analytical methods in accordance with applicable policies and guidelines.● Completed tasks in compliance with cGMP, cGLP, cGDP, pertinent legislation and regulations, as well as pharmaceutical standards and guidelines.● Performed OOS/OOT Investigations and proper reporting procedures.● Wrote technical reports, lab procedures and deviation reports.● Collaborated with Quality Control Supervisor to coordinate activities of analysts.

● Tested final products. ● Audited suppliers.● Handled gas chromatography.● Coordinated the non-conforming product circuit.

● Conducted raw materials, semi-finished and finished product tests by HPLC. ● Analysed and reported results.● Investigated non-conformities.● Participated in audits.● Provided technical support to Manufacturing and Sales departments.

● Supported development team to define and implement customer change requests to enhance product functionality.● Developed experimental formulae of label adhesives to support Marketing operations.● Created spreadsheets using Microsoft Excel for daily, weekly, and monthly reporting.● Analyzed polymer and resin materials to evaluate nature, reactivity and other factors affecting use in adhesive applications.

● Chemistry and Physics Secondary Professor at Integral Institute of Education(Buenos Aires, Argentina). July 2010 – October 2010● Chemistry Professor at School of Secondary Education nº1 D.E 3 (BuenosAires, Argentina). June 2010 – October 2010

Introduction to research for advanced students (Resolution: CSU-064 /07). Topic: Quality control in regional honeys. Antibiotic ́s determination.

Teaching assistant in analytical chemistry at National University Of The South(Resolution CD-189).