Experience

HealthPoint Pharmacy

• Retail
• 1 - 100 Employee

• Pharmacy Technician

  • Nov 2022 - Present

  • Front of shop: Tills (include cashing up & lodgment), Customer Queries (incl. phone), Stock (incl. order), Accounts (incl. resolve issues with suppliers). • Dispense (incl.blister packs). • Pharmaceutical Care (inc. health check of arterial pressure, flow rate, blood glucose, BMI) • Front of shop: Tills (include cashing up & lodgment), Customer Queries (incl. phone), Stock (incl. order), Accounts (incl. resolve issues with suppliers). • Dispense (incl.blister packs). • Pharmaceutical Care (inc. health check of arterial pressure, flow rate, blood glucose, BMI)



FARMACIAS ABC

• Argentina

• Second Pharmacyst

  • Oct 2020 - Oct 2022

  --Argentine pharmacy chain with more than 18 pharmacies and one wholesale. -- Management position of the late shift, severally liable with any medical issue in a store that include non license & high tech products. Pharmaceutical Care that includes application of vaccines. --Argentine pharmacy chain with more than 18 pharmacies and one wholesale. -- Management position of the late shift, severally liable with any medical issue in a store that include non license & high tech products. Pharmaceutical Care that includes application of vaccines.



GEMA Biotech

• Argentina
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• International Regulatory Affairs Analyst

  • Feb 2019 - Nov 2020

  -- Biopharmaceutical platform that integrates development and production operations, designing all processes, from the selection of clones to the production of purified protein and the formulation of the finished product with the MR Pharma collaboration. Part of the group MEGALABS, consisting of several LATAM laboratories with customers in all LATAM (incl. Mexico, Paraguay, Uruguay, Chile, Bolivia & Brasil), Africa (incl Marrocco & Libya) & Asia (incl. Sri Lanka, Myanmar, Oman & Philippines). -- My tasks were (with interaction with R&D, QC & Medical department) to prepare the Common Technical Document (from the Argentinian version that was not following the CTD structure) or update it on-demand of the health Authorities of the African & Asian customers. Show less



GSK

• United Kingdom
• Pharmaceutical Manufacturing
• 700 & Above Employee

• R&D Analyst (covering a maternity leave)

  • Jul 2018 - Feb 2019

  Stability tests, new methods of analysis & analytical transfers testing, trials process change support and support tests for the QC department (incl. a lot of UV & High Performance Liquid Chromatography) Stability tests, new methods of analysis & analytical transfers testing, trials process change support and support tests for the QC department (incl. a lot of UV & High Performance Liquid Chromatography)



Gador

• Argentina
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Validation and Stability Analyst

  • Nov 2017 - Jun 2018

  -- One of the top 5 local pharmaceutical companies, where I covered a license with a temporary contract that was not renewed due to the economic impact of a big political change: the government demanded to halve the prices of the pension scheme. -- •Stability On Going: Quality Control Tests for Stability study. •Process Validation: Taking of Drugs-Technical data (hardness, weight, thickness, diameter / length, reliability and disintegration) and its subsequent statistical analysis with Minitab for DQ and PQ. •Cleaning Validation: Microbiological swab and swab for FOAM detergent residue detection. Show less



Novartis

• Switzerland
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Regulatory Affairs Analyst (in a temporal project)

  • Oct 2016 - May 2017

  --Inside Novartis offices & under their Tenical Director/RA manager untill Seqirus was born officialy. Seqirus: One of the world’s largest influenza vaccine companies. Created when CSL Limited, acquired the Novartis influenza vaccine business and combined it with vaccine subsidiary, bioCSL. During that “brith” I was half of the LATAM RA team. -- Argentina/Local work: Made all the usual changes of the Products Registers: requests the change of strains and the authorization of new labels and prospectus, change of businesses names, their attestations, etc. The reinscription request of a Register. Made the Inscription dossier of a full register. Southern Cone: With the manager, be the nexium of the countries with the heads offices of Novartis and Seqirus (Australia). Show less



Boehringer Ingelheim

• Germany
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Validation Analyst (A temporal International Proyect)

  • Nov 2015 - Oct 2016

  -- Huge German Pharmaceutical Company. I really enjoy being part of the International GBP (Global Business Services) Project at the Boehringer Ingelheim Laboratory, with its very cozy work environment. Unfortunately, the first possibility of renewal (an internship) was not allowed by the collage (since they considered it a precarious job) and for the 3rd job offer I made the mistake of rejecting it because I had started in Novartis. -- My main tasks were based on SOP (Standard Operating Procedures): in their own elaboration, support, monitoring and correction of their preparation or updating by more than 42 colleagues from different areas (SCM, OPS, A2R, O2C, MDM, P2P ) and different countries (Argentina, Uruguay, Chile, Bolivia, Peru, Ecuador, Venezuela, Colombia and Regional itself) and granting its weekly report of the advances and inconveniences. Also carry out the support and monitoring of the Risk Mitigation tables among other tasks of the Validation Area Show less



Boston Scientific

• United States
• Medical Equipment Manufacturing
• 700 & Above Employee

• Local Quality Assurance Analyst

  • May 2014 - Oct 2015

  --Commercial representation in Southern Cone (incl. Argentina, Chile, Uruguay, Paraguay, Bolivia) of the EEUU medical devices company. -- • Implementation of GMP and GDP standards. • Drafting and Updating of SOPs (SOP) in order to guarantee GMP, compliance with Local Legislation and Alignment with regional, international and Global SOPs of the Corporation. • Reclaims Report (in the Global Corporate System) • Translation and presentation of the adverse event report to the Ministry of Public Health of Uruguay ("Medical-Device-vigilance Product"). • Advice, incorporation and audits of suppliers that affect product quality. • The "CAPA" Tasks: Registration, Immediate Containment Actions, Risk Assessment, Long-term Containment Action and Investigation of Non-Conformities (all written in English, intervening with the other areas and meeting strict deadlines) • Implementation of methodologies for sampling materials used in the production of medical products (packaging). • Products release and label inspection according to local regulations. • Monitoring and documentary support (and proactive) in compliance with pest maintenance control; environmental storage conditions (thermostat calibration); destruction of hazardous waste (quarantined products). • Internal Auditors to the Deposit and Logistics Area. Show less