Jorge Mercado Portilla
About Jorge Mercado Portilla
Jorge Mercado Portilla is a Quality Assurance Quality Control professional at QuVa Pharma, Inc., with expertise in stability analysis of drug products using advanced techniques. He has extensive experience in analytical testing and has been with the company since 2018.
Work at QuVa Pharma
Jorge Mercado Portilla has been employed at QuVa Pharma, Inc. since 2018, where he holds the position of Quality Assurance Quality Control. In this role, he is responsible for ensuring that all quality control testing data complies with Standard Operating Procedures (SOP), current Good Manufacturing Practices (cGMP), and Good Documentation Practices. His work involves collaborating with cross-functional groups to identify root causes of issues and implementing Corrective and Preventive Actions (CAPAs) to enhance product quality.
Education and Expertise
Jorge Mercado Portilla studied at Interamerican University, where he earned a degree in Chemistry, achieving the title of Barchiller in 1989. He possesses expertise in performing stability analysis on drug products using advanced techniques such as High-Performance Liquid Chromatography (HPLC) and Ultra-Performance Liquid Chromatography (UPLC). His educational background and technical skills contribute to his proficiency in analytical testing across various drug forms.
Background
Jorge Mercado Portilla has extensive experience in the pharmaceutical industry, particularly in analytical testing for a diverse range of drug forms, including parenterals, ophthalmic solutions, and creams. His background in chemistry and quality assurance positions him as a knowledgeable professional in the field, capable of addressing complex quality control challenges.
Achievements
Throughout his career, Jorge Mercado Portilla has demonstrated a commitment to quality assurance and control in the pharmaceutical sector. His role at QuVa Pharma involves conducting thorough reviews of quality control testing data, ensuring compliance with industry standards, and actively participating in quality improvement initiatives. His contributions help maintain high standards in drug product stability and safety.