Miguel Ângelo Pereira Silva Mateus

Experience

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  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

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  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.

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  Recipharm

  Jun 2016 - Sept 2016

  Quality Control Analyst
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  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

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  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