Kacper Budek

I'm Quality Director of ICM Farmak, which is a Spanish company recently certified on EU-GMP regulations, acting mainly as a CDMO, for development, importing, manufacturing, batch control and batch release of sterile injectables Final Dosage Forms. I have a Pharmaceutical Degree and from the very beginning, my career was focused on pharmaceutical industry and public health environment, having the opportunity to represent as delegate for some health stakeholders on 68th World Health Assembly by WHO, as well other working groups focused on defense of bioethics and nonprofit cooperation. In terms of experience inside Pharmaceutical Industry, I'm working over ten years, taking mostly experience as Regulatory Affairs Specialist and Quality Assurance Manager inside different pharmaceutical markets and sectors. The ICM Farmak project, bring to me the opportunity to open a new facility managing the creation of QMS foundations and its implementation, by main support of the Quality Department Team.