I am trained as a pharmacist and since 2000 I gained working experience in Regulatory Affairs, first at the national competent authority as a pharmaceutical assessor and later as a RA project manager at a generic development company, responsible for the life cycle management of many products. I later made a move to a contract manufacturer (food/pharma) and worked as RA manager and project manager for among others new product developments and technology transfers. I also worked for more than two years as a QA Specialist and QP for a large biotechnology company where I gained experience in e.g. GMP, product disposition, change controls and deviations. In all these positions, I learned to maintain high standards and to work at high speed without neglecting accuracy. At Starodub I’m looking forward to work with our clients on a broad variety of projects and find the most efficient way to achieve the agreed goals in a timely manner.