Experience

• 

  Isel - instituto superior de engenharia de lisboa

  Apr 2015 - Jul 2015

  Estagiário em investigação no ceeq - centro de estudos de engenharia química

  Development of laboratory analysis techniques (spectrophotometric techniques in UV-VIS in food analysis)Coordination of stages of the Ciência Viva programmesDissemination of secondary school experiences to motivate young people in the area of ​​science

• 

  Hikma pharmaceuticals

  Aug 2015 - May 2016

  Trainee, hikma 2 quality unit - wetchemistry

  Reception of raw materials and analysis of final product.Chemical analysis of waterSampling and analysis of packaging components: package inserts, cartons, jars, stoppers.Analysis of raw materials and final product through FT-IR, UV, optical rotation, determination of water content by Karl-Fisher.Calibration of equipment.

• 

  Recipharm

  Jun 2016 - Sept 2016

  Quality control analyst
• 

  Azbil telstar

  Apr 2017 - Jul 2021

  Process validation, equipment and csv consultant -pharma division

  Quality Assurance- Issuance of Product Quality Review- Issuance and review of GMP procedures Process Validation:- Issuance of PVP and PVR- Issuance and revision of Criticality Analysis- Issuance and revision of Continued Process Verification Protocols and Continued Process Verifcation Reports Equipment Qualification:- Issuance of Impact Assessment, IQ, OQ and PQ Protocols- Execution of IQ, OQ and PQ protocols- Issuance of Qualification Reports- Revision of executed IQ, OQ and PQ Protocols- Issuance and Revision of Qualification Reports.Computerized System Validation- Issuance of VP, URS, Risk Analysis, DQ, IQ, OQ and PQ.- Issuance and revision of Validation ReportsData IntegrityExcel spreadsheets validation Show less

• 

  Hovione

  Jul 2021 - now

  Engineer | compliance

  Equipment Qualification:- Issuance of Impact Assessment, IQ, OQ and PQ Protocols- Execution of IQ, OQ and PQ protocols- Issuance of Qualification Reports- Revision of executed IQ, OQ and PQ Protocols- Issuance and Revision of Qualification Reports.Quality Assurance-Review and Implementation of SOP, IOP-Supplier Qualification-Internal Audit participation- Inspection from Health Authorities - Deviations Management