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no compromise in quality! it focuses on continuous work on personal Training and development; reduce uncertainty, inefficiencies and high costs of production, Quality Control, Quality Assurance, the search for better solutions and achieve better quality and efficiency. work on personal Communication Skills and understanding the needs of other people. professional experience of over 24 years of working experience includes: - responsibility for physico-chemical and microbiological Testing of raw materials, semi-finished products and control conditions and environmental protection in production - stability studies / write science)" >Protocol and stability evaluation results in accordance with the directives of ich - preparation of ctd module / registration dossier for the drug (module 3 quality) - experience with local GMP inspections - responsible for the implementation of Quality Systems Laboratory (qualifications, Training, Validation) - responsible for the purchase of analytical equipment according to customer requirements (urs) - audit manufacturers under contract and qualifying suppliers - responsible for the development and establishment of Quality Control laboratories in the new factory - the Leader or Member of several projects: the implementation of GMP directives in production and Quality Control of medicines, ISO 17025, iso 14000, HACCP - Member of the team for the implementation of microsoft dynamics ax


Current Experience

  • Senior Consultant

    Since May 2015

Past Experience

  • Person responsible for quality control medical device

    July 2014 --- March 2015

  • Head of Quality Control

    September 2010 --- July 2014

  • Quality Director

    January 2009 --- August 2010
    responsible for the quality sector, which includes Quality Control, development and Validation and Quality Assurance. responsible for the overall business is conducted in accordance with applicable legislation, GMP and ISO 9001: 2008.


LinkedIn Assessment :
Cleaning ValidationGMPPharmaceutical IndustryValidationSOPRegulatory RequirementsQuality SystemRegulatory affairsCAPAQuality AssuranceChange ControlPharmaceuticsStability TestingMethod TransferDissolutionDissolution TestingAnalytical R&DAnalytical Method ValidationQuality by DesignQuality AuditingV&VRegulatory submissionsQuality ControlGLPFDALaboratory


  • Bachelor's Degree in Biochemistry from University of Belgrade in 1986
  • Master of Science (M.Sc.) in Organic Chemistry from University of Belgrade in 0000

Training and Certification

  • Duolingo German Fluency: Elementary in 2015 Certification

Area / Region



Driving License
  • Yes

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