Alan Serres
About Alan Serres
Alan Serres is a Project Manager for Latin America Regulatory at Bristol Myers Squibb in Argentina, with extensive experience in the pharmaceutical industry and a background in microbiology and biotechnology.
Current Position at Bristol Myers Squibb
Alan Serres is currently employed at Bristol Myers Squibb as a Project Manager, focusing on Latin America Regulatory operations in Argentina. His role involves managing regulatory projects across the Latin American region, ensuring compliance with local and international standards. Alan brings over a decade of experience in the pharmaceutical industry to his current position, leveraging his background in microbiology and quality assurance to enhance the company's regulatory processes.
Professional Experience at Fortbenton Co. Laboratories
Before his current role, Alan Serres worked at Fortbenton Co. Laboratories as a Senior Analyst in Microbiology Quality Assurance for ten years, from 2011 to 2021, in Argentina. During his tenure, he gained extensive experience working under GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice) standards. His responsibilities included ensuring the quality and safety of pharmaceutical products through rigorous microbiological testing and validation processes.
Past Role at Blipack Pharma SA
Prior to his position at Fortbenton Co. Laboratories, Alan Serres worked at Blipack Pharma SA as a Microbiology Analyst from 2009 to 2011 in Provincia de Buenos Aires, Argentina. In this capacity, he performed microbiological analyses to support product development and regulatory compliance, contributing to the overall quality assurance processes within the organization.
Educational Background and Biotechnology Studies
Alan Serres pursued his Higher Education at UADE, where he studied Biotechnology and earned a Bachelor's degree (Licenciatura) in 2022 after two years of study. Additionally, he has a Technical Degree (Tecnicatura Superior) in Chemistry and Biotechnology from ORT Argentina, completed between 2013 and 2016. His academic background has provided a solid foundation in scientific principles, supporting his professional expertise in the pharmaceutical industry.
Experience in GMP/GLP Standards
With over a decade of professional experience in the pharmaceutical industry, Alan Serres has extensive expertise in working under Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards. His deep understanding of these regulatory frameworks has enabled him to effectively manage and ensure the compliance of pharmaceutical processes and products, contributing significantly to his roles in quality assurance and regulatory affairs.