Quality and RA Director
Liliana Joachín-Rodríguez is the Quality and Regulatory Affairs Director at PROBIOMED, a Mexican enterprise oriented to the research, development, production and commercialization of biopharmaceutical products from the gene to the finished medicine – including hormones, cytokines, monoclonal antibodies, fusion proteins and vaccines. Liliana has 22 years of experience in the biotechnology industry and has held various leadership roles managing analytical development, quality control and quality assurance departments at the API manufacturing facility of recombinant proteins and monoclonal antibodies of PROBIOMED. Additionally, she has been responsible for the regulatory life cycle management of biotech and generic products, as well as medical devices of the company, including development of regulatory strategies to achieve new marketing authorizations, registration maintenance and change registration control. Her team also provides guidance about technical information and GMP compliance required to support quality, safety and efficacy of the products for their registration in Mexico and other countries, including LatAm. She holds a bachelor´s degree in Biotechnological Engineering from the National Polytechnic Institute, Mexico and a master´s degree in Biomolecular Sciences (with a Regulatory Sciences profile) from the Utrecht University, The Netherlands.