Experience

QUINTA-ANALYTICA

• Czechia
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Analyst at Biopharmaceutical Analysis Department

  • Aug 2018 - Present

  Method validation and routine testing of pharm products using LC, LC-MS/MS, LC-HRMS (QExactive) in accordance with GMP rules. Method development, validation and routine testing using capillary electrophoresis (CE-UV) in accordance with GMP rules. Basic experience with method development and validation of immuno method to determine anti-drug antibodies (ADA) in plasma using electrochemiluminiscence detection. Preparation of validation documents (protocol, report), data review (GMP). SW experience with LIMS, Empower, Chromeleon, Karat32, MethodicalMind,Gen5. Show less



Zentiva

• Czechia
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Junior Analyst

  • Aug 2017 - Jul 2018

  API-Separation methods (HPLC) - method development, validation and routine testing of API using LC-UV/PDA. Validation documents preparation. API-Separation methods (HPLC) - method development, validation and routine testing of API using LC-UV/PDA. Validation documents preparation.



ALS Czech Republic

• Czechia
• Environmental Services
• 100 - 200 Employee

• Trainee programme

  • Aug 2015 - Jul 2017

  HPLC section: Sample preparation, HPLC maintance, data interpretation, administration HPLC section: Sample preparation, HPLC maintance, data interpretation, administration



Zentiva

• Czechia
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Laboratory Assistant

  • Jul 2016 - Jul 2016

  Department of Solid State Development: Sample preparation and measurement using methods of Infrared spectroscopy, Raman spectroscopy and Scanning electron microscopy Department of Solid State Development: Sample preparation and measurement using methods of Infrared spectroscopy, Raman spectroscopy and Scanning electron microscopy