May 2017 - present- Joined LabtimMar. 2014 - May 2017- Joined Instrumentalia Adria as Application specialistMar. 2009 - Mar 2014- Joined PLIVA Hrvatska d.o.o.-TAPI R&D as Analytical development coordinator.Nov. 2007 – Mar. 2009- Joined PLIVA d.d. Human resources – PLIVA LEARNING DEPARTMENT as Laboratory Trainer, with responsibility for development of learning modules and coordination of laboratory personnel skill improvement. Department introduced computerization of training and training records management for which I have created several web applications. Involved in implementation of several new documentation management software (GMP docs). 2005 – Nov. 2007- developed over 30 instrumental analytical methods, and validated over 20 instrumental (HPLC/GC) analytical methodsNov. 11st. 2005- Joined Pharma Chemicals - Process Development as Coordinator of Analytical Development; with responsibility for development and validation of analytical methods for HPLC, GC and other instrumental techniques2003 - 2005- Performed several internal and external audits according to cGMP, US CFR regulationsNov. 1st. 2003- Promoted to position of Manager of HPLC laboratories in Quality Control, PLIVA Hrvatska d.o.o.; with full responsibility for all operations and financial activities for over 30 persons and 32 HPLC instruments valued over 16 millions kuna- Was inspected by US FDA in 2002 within audit of PLIVA Hrvatska d.o.o.Since 2002- After year and half of experience in analytical method development and validation, and after several successfully passed external audits (Novartis, GSK, Pfeizer, MCA,FDA) promoted to position Analyst IIISep. 3rd 2001- Working as Physical-chemical Analyst I in HPLC laboratories, Quality Control, Pliva Hrvatska d.o.o.; working in ”Laboratory for improvement of analytical measurements” as analyst operating HPLC instruments