I am an expert in protein purification and biological drug development with over 7 years of experience in the biotechnology and pharmaceutical industry. Throughout this journey, I have developed deep knowledge of biomolecule purification (peptides and proteins) by liquid chromatography (downstream) and applied high performance processing techniques, gaining experience in the use of various equipment and strategies for recovery, concentration, diafiltration (TFF) and process control, ensuring quality results. I have been involved in the development of protocols for characterizing biological activity, standardization and validation of potency and immunogenicity assays, collaborated in the development of a method for determining in vitro potency based on antigen-antibody avidity, in-house production of reference materials and internal quality control.I have experience in technology transfer processes, gap analysis, risk analysis, technical report preparation, knowledge of ICH Guides, preparation of documentation in CTD format, development and registration of new products.Currently, I am a galenic development researcher, responsible for conducting research and development projects of innovative products for the NC Group - EMS.