Victor Ramos
About Victor Ramos
Victor Ramos is a Validation Manager at Organogenesis with over 25 years of experience in aseptic GMP environments for pharmaceutical and medical device manufacturing. He has held various managerial roles in the industry and is well-versed in compliance with regulatory standards.
Work at Organogenesis
Victor Ramos has served as the Validation Manager at Organogenesis since 2014. In this role, he is responsible for maintaining the validated state of the facility, utilities, equipment, processes, and computer systems. His responsibilities encompass direct engagement with all aspects of the quality system, including Corrective and Preventive Actions (CAPA), Risk Assessment, Product Development, Technology Transfer, and Change Control. His extensive experience in aseptic GMP environments supports his effectiveness in this position.
Previous Experience in Manufacturing
Before joining Organogenesis, Victor Ramos held significant positions in the manufacturing sector. He worked as a Manufacturing Supervisor at Advanced BioHealing from 2008 to 2011, where he contributed for three years. Prior to that, he was the Production Manager at Artes Medical from 2005 to 2008, also for three years. These roles provided him with a solid foundation in manufacturing processes and compliance within the pharmaceutical and medical device industries.
Education and Expertise
Victor Ramos earned a Bachelor of Science degree in Biochemistry Engineering from Instituto Tecnológico de Tijuana, studying from 1980 to 1985. He furthered his education by obtaining a Professional Certificate in Biotechnology Manufacturing from UC San Diego, completing the program from 2004 to 2005. His educational background, combined with over 25 years of experience in aseptic GMP environments, equips him with a strong understanding of industry standards and practices.
Compliance and Standards Knowledge
Victor Ramos possesses extensive knowledge of regulatory compliance, specifically with CFR Title 21, Parts 11, 210, 211, 800, and 820, as well as ISO 13485 standards. His expertise in these areas is critical for ensuring that manufacturing processes meet the necessary regulatory requirements in the pharmaceutical and medical device sectors. This compliance knowledge is integral to his role at Organogenesis and his previous positions.