Experience

Intertek Melbourn

• United Kingdom
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Senior Scientist

  • Mar 2023 - Present



Herbarium Laboratório Botânico

• Pharmaceutical Manufacturing
• 400 - 500 Employee

• R&D ANALYST – STABILITY

  • Aug 2020 - Nov 2020

  - Work in the Quality Control department (Research and Development) being responsible for managing the stability activities, statistics data analysis and generation of stability reports. - Analyse phytomedicines using various methods (including HPLC, GC and UV). - Work in the Quality Control department (Research and Development) being responsible for managing the stability activities, statistics data analysis and generation of stability reports. - Analyse phytomedicines using various methods (including HPLC, GC and UV).



Sanofi

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Control Analyst

  • May 2018 - Dec 2019

  - Work in the Quality Control department (Chemistry & Biochemistry) carrying out the transfer/validation of analytical methods. - Analyse drug products and drug substances using various chemistry/biochemistry techniques as per GMP requirements (HPLC, LC-MS, GC, SPR-Biacore, SDS-PAGE) - Stability Coordinator: responsible for management of stability activities, statistics data analysis and generation of stability reports. Liaising with Quality Assurance, Regulatory Affairs and Quality Management to keep track of stability studies and expected shelf-life determination. - Supporting Laboratory Investigations (OOS, OOT and atypical results. Show less



Intertek Melbourn

• United Kingdom
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Scientist

  • Jun 2017 - May 2018

  - Work in the Formulation department for Research and Development of Investigational Medicinal Products (IMP). - Manufacture of IMPs in a clean room environment including suspensions, solutions, DPI, pMDI, gels and others. - Work in the Formulation department for Research and Development of Investigational Medicinal Products (IMP). - Manufacture of IMPs in a clean room environment including suspensions, solutions, DPI, pMDI, gels and others.



Sanofi

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Control Analyst

  • Apr 2016 - May 2017

  - Work in the Quality Control department (Chemistry & Biochemistry) in the Analytical Technical Transfer team responsible for transfer of analytical methods. - Support primary manufacturing quality control testing and secondary operations. - Working with the Quality Management System (CAPA, event, change control, effectiveness review, etc.) - Work in the Quality Control department (Chemistry & Biochemistry) in the Analytical Technical Transfer team responsible for transfer of analytical methods. - Support primary manufacturing quality control testing and secondary operations. - Working with the Quality Management System (CAPA, event, change control, effectiveness review, etc.)



ALS

• Australia
• International Trade and Development
• 700 & Above Employee

• Laboratory Analyst

  • Apr 2014 - Apr 2016

  - Worked in the Vitamins and Additives department, carrying out the maintenance of instrumentation, performing equipment checks and calibrations. - Supported the Nutritional Chemistry Department analysing food, supplements and pharmaceuticals with a large range of techniques that included HPLC, polarimetry, spectroscopy, centrifugation, distillation and titrations. - Worked in the Vitamins and Additives department, carrying out the maintenance of instrumentation, performing equipment checks and calibrations. - Supported the Nutritional Chemistry Department analysing food, supplements and pharmaceuticals with a large range of techniques that included HPLC, polarimetry, spectroscopy, centrifugation, distillation and titrations.



IGUAÇU Embalagens Industriais Ltda.

• Brazil
• Paper and Forest Product Manufacturing
• 200 - 300 Employee

• Chemical Technician

  • Apr 2008 - Dec 2008

  - Work in a Paper Manufacturer performing the analysis of paper in the quality control department. Test raw materials and chemicals when arrived at factory facilities prior to be included in the process flow. - Analyse water and waste effluents from plants and production process. Analysis include: BOD/COD; turbidity; Jar test; Imhoff cone TSS; alkalinity; water hardness; chloride; sulfite; conductivity and pH. - Work in a Paper Manufacturer performing the analysis of paper in the quality control department. Test raw materials and chemicals when arrived at factory facilities prior to be included in the process flow. - Analyse water and waste effluents from plants and production process. Analysis include: BOD/COD; turbidity; Jar test; Imhoff cone TSS; alkalinity; water hardness; chloride; sulfite; conductivity and pH.