Regulatory Affairs Associate
Samra Hodžić joined the Qserve Group early 2022 to join our team of global registrations as a Regulatory Affairs Associate and is based in the Netherlands. She’s involved in the review of documentation for the registration of medical devices and IVD manufacturers and their products in various countries outside the EU, with focus on the UK.
Samra about working at Qserve
When I started at Qserve I had a really warm welcome and I felt a really calming ambiance in the company. Working in a very multicultural environment makes people feel accepted and respected and it is always interesting to learn more about different types of habits and traditions. Everyone is open and ready to help if they can.
Samra has a bachelor’s degree in Food Technology and a master’s degree in Quality Control of Food and Beverages from University of Sarajevo in Bosnia and Herzegovina. She now has been living in The Netherlands for 6 years.
Earlier she worked as a quality officer at a food company for retailers. She was responsible for the quality control in production and supported the maintenance of the quality management system. There she learned a lot about quality systems in food and in food production.
In 2018, she switched jobs to the role of Regulatory Affairs Consultant for Food Labeling. There she was responsible for the legal control and monitoring of labelling according to the Dutch and European Regulations.
The medical device industry has always been an interest for her and in 2022 it was the right time to take on an opportunity within this field at Qserve. In her current role, she maintains contact with the clients, communicates about registration requirements for market access, with a focus on the UK, and collects the relevant documentation to build registration files for clients. She also supports the global registration team in various countries.
The key expertise areas of Samra:
Legislation and database registration, with a focus on the UK
Support in Global registrations in various countries
Review and submit documentation for the registration of medical device and IVD manufacturers also outside the EU
Fulfill the registration process for customers by communicating with local competent authorities