Vesna Logomerac
About Vesna Logomerac
Vesna Logomerac is a Senior Manager of Regulatory Affairs at Dechra Pharmaceuticals PLC, where she has worked since 2020. She has extensive experience in quality control and regulatory affairs, with a background in various pharmaceutical companies and a strong academic foundation in science.
Work at Dechra Pharmaceuticals
Vesna Logomerac has been serving as the Senior Manager of Regulatory Affairs at Dechra Pharmaceuticals plc since 2020. In this role, she is responsible for overseeing regulatory compliance and ensuring that the company's products meet the necessary legal and safety standards. Her experience in regulatory affairs is critical to the company's operations in the pharmaceutical industry.
Education and Expertise
Vesna Logomerac completed her Bachelor of Science degree at the University of Zagreb from 1993 to 1999. She furthered her education by obtaining a Master of Science degree from the same institution between 2002 and 2006. Her academic background provides her with a solid foundation in the scientific principles relevant to her work in regulatory affairs and quality control.
Background in Quality Control and Assurance
Vesna Logomerac has extensive experience in quality control and assurance. She worked as the Head of Quality Control at Pharmas d.o.o. from 2012 to 2015. Additionally, she served as the Head of Quality Assurance and Environment at Piramida d.o.o. for a brief period in 2017. Her roles have involved managing quality systems and ensuring compliance with industry standards.
Previous Roles in the Pharmaceutical Industry
Throughout her career, Vesna Logomerac has held various positions in the pharmaceutical sector. She worked as an Analyst Specialist at Pliva from 2008 to 2011, focusing on the development and introduction of new methods. She also served as a Quality Control Analyst at Pharmas d.o.o. for nine months in 2011 and as an external associate at Supera Kvaliteta d.o.o. from 2013 to 2015.
Experience in Veterinary Medicinal Products
Vesna Logomerac has experience in the analysis of veterinary medicinal products, having worked as an Assistant in the Laboratory for Veterinary Medicinal Products Analysis at the Croatian Veterinary Institute from 2002 to 2007. This role contributed to her understanding of regulatory requirements specific to veterinary pharmaceuticals.