Graduated in Industrial Pharmacy (2005), postgraduate in Pharmaceutical Chemistry (2012) and Pharmaceutical Auditing (2013). With over 20 years of experience in pharmaceutical industries, both national and multinational, I have built a solid career in the area, working on Analytical Laboratory and Technical Documentation projects.
My work encompasses several areas, such as:
• Development and Validation of Analytical Methodologies
• Quality Control and Stability Studies
• Preparation of Protocols, Reports and Technical Justifications
• Validation of Cleaning Residuals and Gap Analysis
• Review of technical documents
• Support in response to regulatory requirements and specialized training
In the field of technical consultancy, I offer full support in the preparation of:
• Technical justifications for regulatory requirements
• Analytical Validation Protocols and Reports in accordance with RDC 166/2017
• Complete assessment (Gap Analysis) and forced stress studies
• Review of documents related to quality and change control
My passion is to disseminate knowledge and promote the exchange of experiences in the pharmaceutical area. If you wish to explore a specific topic or need technical support, I am available to talk and collaborate.