Experience

LAVET Pharmaceuticals Ltd.

• Hungary
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• • Mar 2022 - Present

  QA Engineer at Release Team:QA review of Batch Records for the QPReview of Batch Release related quality events (i.e. deviations, OOS, Change Controls)Product Quality Review (PQR) preparation

• • Nov 2018 - Feb 2022

  QA Engineer at Compliance Team:Complaint management;Deviation management: knowledge of investigation technics, root cause analysis, FMEA;SOP revision



Mylan

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• QA Specialist

  • Nov 2015 - Nov 2018

  Supplier Complaint Coordinator at Quality Compliance Team - Supplier complaint management - Analyzes data and prepares periodic reports relating to complaints, product problems, etc. Quality Assurance Specialist at QA Packaging Team - QA support in the planning of manufacturing - Supervision of supplier documentation - Preparing Batch Packaging Records - Occasional QA review support at Quality Control department Supplier Complaint Coordinator at Quality Compliance Team - Supplier complaint management - Analyzes data and prepares periodic reports relating to complaints, product problems, etc. Quality Assurance Specialist at QA Packaging Team - QA support in the planning of manufacturing - Supervision of supplier documentation - Preparing Batch Packaging Records - Occasional QA review support at Quality Control department



Egis Pharmaceuticals PLC

• Hungary
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Analytical Chemist

  • Apr 2012 - Jul 2015

  Working in the Laboratory of Polymorphism Duties: - measuring generic and original API’s and finished products by solid state analytical methods according to GMP (XRPD, TGA, DSC, DVS, PSD, PLM) - investigating OQ and PQ tests of laboratory instruments - giving advice in the field of polymorphism to the running R&D projects - writing polymorphism chapter of DMF’s to the Regulatory Affairs Working in the Laboratory of Polymorphism Duties: - measuring generic and original API’s and finished products by solid state analytical methods according to GMP (XRPD, TGA, DSC, DVS, PSD, PLM) - investigating OQ and PQ tests of laboratory instruments - giving advice in the field of polymorphism to the running R&D projects - writing polymorphism chapter of DMF’s to the Regulatory Affairs



Richter Gedeon Nyrt. / Magyarország

• Hungary
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Pharmaceutical researcher

  • Jun 2010 - Apr 2012

  Working at the Scale-up laboratory Duties: - planning and executing novel synthetic routes of API’s - issuing tasks to the laboratory assistant - co-working with the pilot plant in various projects - take part in the patent writing Working at the Scale-up laboratory Duties: - planning and executing novel synthetic routes of API’s - issuing tasks to the laboratory assistant - co-working with the pilot plant in various projects - take part in the patent writing



CF Pharma

• Hungary

• Researcher

  • Mar 2007 - May 2010

  Working at R&D laboratory Duties: - planning and executing novel synthetic routes of API’s - structure determination by IR and NMR methods - issuing tasks to the laboratory assistant Working at R&D laboratory Duties: - planning and executing novel synthetic routes of API’s - structure determination by IR and NMR methods - issuing tasks to the laboratory assistant